TITLE OF THE INVENTION

METALLO-BETA-LACTAMASE INHIBITORS

FIELD OF THE INVENTION

This invention relates to novel metallo-p-lactamase inhibitors and their uses. A preferred use of the metallo-p-lactamase inhibitors is for reducing bacterial beta-lactam antibiotic resistance.

BACKGROUND OF THE INVENTION

Bacterial antibiotic resistance has become one of the most serious threats to modern health care. Infections caused by resistant bacteria frequently result in longer hospital stays, higher mortality and increased cost of treatment. See, e.g., Cohen, Science 1992,

257: 1051-1055. The need for new antibiotics will continue to escalate because bacteria have a remarkable ability to develop resistance to new agents rendering them quickly ineffective. See, e.g., Neu, Science 1992, 257: 1064-1073. The spread of antibiotic resistance has been referred to as a pandemic and that a solution to the growing public health threat will require an

interdisciplinary approach. See, e.g., Anderson, Nature America 1999, 5: 147-149. See also Bush et al, Nature Reviews in Microbiology 2011, 9: 894-896; Levy and Marshall, Nature Medicine 2004, 10: S122-S129; Livermore, Clinical Infectious Diseases 2003 , 36: S11-S23; and Roberts et al. Clinical Infectious Diseases 2009, 49: 1175-1184.

The present crisis has prompted various efforts to elucidate the mechanisms responsible for bacterial resistance. The widespread use of penicillins and cephalosporins has resulted in the emergence of β-lactamases, a family of bacterial enzymes that catalyze the hydrolysis of the β-lactam ring common to numerous presently used antibiotics. See, Coulton et al, Progress in Medicinal Chemistry 1994, 31 : 297-349. This family of bacterial β-lactamases is further divided into four sub-families: A, C, and D which have a serine at the active site that catalyzes the hydrolysis of β-lactam antibiotics and a B family β-lactamases which are zinc metalloenzymes. Resistance mediated by β-lactamases is a critical aspect at the core of the development of bacterial antibiotic resistance. See, Dudley, Pharmacotherapy 1995, 15: 9S-14S. Clavulanic acid, which is a metabolite of Streptomyces clavuligerus, and two semi-synthetic inhibitors, sulbactam and tazobactam, are currently available semi-synthetic or natural product β-lactamase inhibitors. Synthetic β-lactamase inhibitors have also been described. See, U.S. Patent Nos. 5,698,577; 5,510,343; 6,472,406; Hubschwerlen et al, J. Med. Chem. 1998, 41 : 3961 ; and Livermore et al, J. Med. Chem. 1997, 40: 335-343. Poole, Cell. Mol. Life Sci. 2004, 61 : 2200-2223 provides a review of the resistance of bacterial pathogens to β-lactam antibiotics and approaches for overcoming resistance. For a review of inhibitors of metallo β-lactamases, see Fast and Sutton, Biochimica et Biophysica Acta - Proteins and Proteomics 2013, 1834(8): 1648-1659.

U.S. Patent Application Publication No. US 2003/0199541 Al discloses certain azabicyclic compounds including certain 7-oxo-6-diazabicyclic[3.2.1]octane-2-carboxamides and their use as anti-bacterial agents. U.S. Patent Application Publication No. US 2004/0157826 Al discloses heterobicyclic compounds including certain diazepine carboxamide and diazepine carboxylate derivatives and their use as anti-bacterials and β-lactamase inhibitors. International Patent Application Publication No. WO 2008/039420 A2 discloses 7-oxo-2,6- diazabicyclo[3.2.0]heptane-6-sulfooxy-2-carboxamides and their use as β-lactamase inhibitors.

Zheng et al, in PLOS One 2013, 8(5), e62955, discloses substituted 2,5-bis- tetrazolylmethyl-thiophenes and their use as β-lactamse inhibitors. Chinese Patent Application Publication No. CN103130686 A discloses Ν,Ν' -diary 1-ureas and their use as inhibitors of metallo β-lactamases. Chinese Patent Application Publication No. CN103191091 A discloses substituted arylsulfonamides and their use as inhibitors of metallo β-lactamases.

U.S. Patent Nos. 4,786,31 1; 4,746,353; 4,838,925; European Patent Application Publication Nos. EP204513A2, EP244166A2, and Chinese Patent Application Publication No. CN1095549A disclose substituted 2-(lH-tetrazol-5-yl)benzenesulfonamides and their use as herbicides.

SUMMARY OF THE INVENTION

The present invention is directed to certain substituted 1H- and 2H-tetrazol-5-yl sulfonamide compounds which are metallo^-lactamase inhibitors. The compounds, and their pharmaceutically acceptable salts, are useful, for example, in combination with β -lactam antibiotics for the treatment of bacterial infections, particularly antibiotic-resistant bacterial infections. More particularly, the present invention includes compounds of Formula I:

or a pharmaceutically acceptable salt thereof,

wherein:

X ² is N or CR ^B ;

X ³ is N or CR ^C ;

X ⁴ is N or CR ^D ;

wherein no more than 2 of X ² , X ³ , and X ⁴ are N:

Z is tetrazolyl, wherein Z is linked to the six membered ring (containing X ² -X ⁴ ) through a carbon to carbon bond;

R ^A is H, Ci-Ce alkyl, -(CH ₂ )o-3-C ₃ -C8 cycloalkyl, -C ₃ -C ₆ cycloalkenyl, -CF ₃ , Ci-C ₆ alkoxy, -COOR ^a , -CN, -NR ^a R ^b , -(CH ₂ ) ₀ - ₃ HetA, -(CH ₂ ) ₀ - ₃ -AryA, -(CH ₂ ) ₀ -i-O-AryA,

-NR ^a (CH ₂ ) ₀ - ₂ -C ₃ -C ₈ cycloalkyl, -NR ^a (CH ₂ )i_ ₂ -phenyl, -C≡C-pyridinyl, -C≡C-CH ₂ -HetC, or -C≡C-CH ₂ -0-HetC; wherein the R ^A Ci-C ₆ alkyl or any R ^A C ₃ -C ₈ cycloalkyl is optionally substituted with 1, 2, or 3 substituents independently selected from C1-C6 alkoxy,

C ₃ -C ₇ cycloalkyl, -OH, F, -CF ₃ , -CN, -(CH ₂ ) ₀ - ₃ NR ^a R ^b , -C(=NH)NH ₂ ; -CONR ^a R ^b ,

-(CH ₂ )o-iNHC(=NH)NH ₂ ; -NHCONR ^a R ^b , -NHCO-diaminoC ₂ alkyl,

-NH(CH ₂ ) ₀ -i-C ₃ -C ₆ cycloalkyl; -NHS0 ₂ -Ci-C ₆ alkyl, -S0 ₂ -Ci_C ₆ alkyl, -S0 ₂ -C ₃ _C ₆ cycloalkyl, -S0 ₂ NR ^a R ^b , AryB, -NH(CH ₂ ) ₀ -i-AryB, HetB, and -NH(CHR ^a ) ₀ -i-HetB, and wherein any C ₃ - C ₆ cycloalkyl is optionally substituted with -(CH ₂ ) ₀ - ₂ NH ₂ , wherein -C ₃ -C6 cycloalkenyl is optionally substituted with cyano; and the pyridinyl is optionally substituted with 1 or 2 substituents independently selected from -CH ₂ OH and-NH ₂ ;

R ^B is H, Ci-Ce alkyl, -OH, Ci-C ₆ alkoxy, -CN, F, CI, Br, or -NR ^a R ^b , wherein the R ^B Ci-C ₆ alkyl can optionally be substituted with 1, 2 or 3 substituents selected from -OH, -F, -NR ^a R ^b , -CF ₃ , Ci-Ce alkoxy, and -CONR ^a R ^b ;

or R ^A and R ^B together with the atom(s) to which they are attached form a 5-7 membered fused ring containing 0, 1, or 2 heteroatoms independently selected from N, O and S, wherein N is optionally substituted with R ^d ; R is H, Ci-C ₆ alkyl, F, CI, -CF ₃ , -COOCH ₃ , -C(0)NH ₂ , or AryC;

R ^D is H, C1-C6 alkyl, C1-C6 hydroxyalkyl, -(CH ₂ )o-2C3-C6 cycloalkyl, -C ₃ -C6 cycloalkenyl, -(CH ₂ ) ₂ C(0)OH, -CF ₃ , F, CI, Br, -(CH ₂ ) ₀ -iAryA, or -(CH ₂ ) ₀ - ₂ HetA, wherein the R ^D Ci-C ₆ alkyl or R ^D C ₃ -C6 cycloalkyl is optionally substituted with 1, 2, or 3 substituents independently selected from C ₃ -C ₆ cycloalkyl, -OH, F, -CN, -(CH ₂ ) ₀ - ₃ NR ^a R ^b , -CF ₃ , -(CH ₂ ) ₀ - ₂ HetB,

-(CH ₂ )o- ₂ AryB, -(CH ₂ ) ₀ -iNHC(=NH)NH ₂ ; -S0 ₂ -Ci_C ₆ alkyl, -S0 ₂ -C ₃ _C ₆ cycloalkyl, -S0 ₂ NR ^a R ^b , C1-C6 alkoxy, and -(CH ₂ )o-4CONR ^a R ^b , and wherein the -C ₃ -C6 cycloalkenyl is optionally substituted with cyano;

wherein when R ^A , R ^B , R ^c and R ^D are all present, then 1, 2 or 3 of R ^A , R ^B , R ^c and R ^D are H; wherein when 1 or 2 of X ² , X ³ , X ⁴ are N, then at least one of R ^A , R ^B , R ^c , and R ^D , if present, is not H;

AryA is an aromatic ring system selected from:

1) a 5-6 membered monocyclic ring with 0, 1, 2 or 3 heteroatom ring atoms

independently selected from , O and S, optionally substituted with 1, 2 or 3 substituents independently selected from:

a) -Ci-Ce alkyl,

b) -C ₂ -C ₆ diaminoalkyl;

c) -C1-C6 hydroxyalkyl,

d) -C1-C6 dihydroxyalkyl,

e) -C ₃ -C6 cycloalkyl optionally substituted with 1 or 2 substituents selected from -OH and -NR ^a R ^b ,

f) -C ₃ -C6 cycloalkenyl optionally substituted with -CN,

g) (CH ₂ )o- ₆ NR ^a R ^b ,

h) CH(OH)R ^e ,

i) CH ₂ OR ^a ,

j) (CH ₂ )o- ₂ C(0)NR ^a R ^b ,

k) CH ₂ NR ^a -C ₂ -C ₄ alkyl-NR ^a R ^b ,

1) C(=NH)NHR ^b ;

m) CH ₂ NHCH(=NH);

n) CH ₂ NHCH ₂ C(0)NR ^a R ^b ,

0) (CH ₂ )o- ₂ C(0)OR ^a ,

P) CH ₂ NR ^a -Ci-C ₃ alkyl-C(0)OR ^a , q) -CH ₂ NH-CH[C(OH)CH ₃ ][C(0)OR ^a ],

r) -CH ₂ NR ^a -Ci-C ₆ hydroxyalkyl,

s) -(CHz^SOz-d-Ce alkyl,

t) -NR ^a S0 ₂ -C ₃ -C ₆ cycloalkyl,

u) -NR ^a S0 ₂ -Ci-C ₆ alkyl,

v) -NR ^a S0 ₂ -NR ^a R ^b ,

w) -CH ₂ NHC(=NH)NHR ^b ;

x) -NHC(=NH)NH ₂ ;

y) -OR ^a ,

z) -O(CH ₂ ) ₀ - ₆ NR ^a R ^b ;

aa) -O-C 1-C6 hydroxyalkyl,

bb) -(CH ₂ )o. ₁ S0 ₂ (CH ₂ )o. ₂ NR ^a R ^b ,

cc) -S0 ₂ (CH ₂ )o- ₂ OH,

dd) -CN,

ee) halogen,

ff) -CF ₃ ,

gg) -CH ₂ NR ^a (CH ₂ Vi-C ₆ -C ₆ cycloalkyl op

NR ^a R ^b or 2 F,

hh) -(CH ₂ )o-i-AryB,

ϋ) -CH ₂ NR ^a -Ci-C ₃ alkyl-AiyB,

jj) -CH ₂ NR ^a -CH(COOH)CH ₂ -AryB,

kk) -C ₀ -C ₂ alkyl-HetB,

11) -CH(OH)-HetB,

mm) -(CH ₂ )o-iNR ^a (CH ₂ )o- ₂ -HetB,

nn) -C(=NH)NH-HetB;

oo) -O(CH ₂ ) ₀ - ₂ -HetB,

P) -C(0)-HetB, and

qq) -C(O)NR ^a (CH ₂ ) ₀ - ₂ -HetB; or

a 9- or 10-membered bicyclic ring with 1, 2, 3 or 4 heteroatom ring atoms selected from N, O and S, wherein an N atom is optionally in the form of a quaternary amine and wherein the ring is optionally substituted with 1 , 2 or 3 substituents independently selected from Ci_C ₆ alkyl, C ₃ -C ₆ cycloalkyl, Ci_C ₆ alkoxy, d-C ₆ hydroxyalkyl, Ci_C ₆ aminoalkyl, -CF ₃ , -C(=NH)NH ₂ , -COOR ^a , -(CH ₂ ) ₀ -iC(O)NR ^a R ^b , -CN, -(CH ₂ ) ₀ - ₃ NR ^a R ^b , -NHCH ₂ CH ₂ N(CH ₃ ) ₂ , -NH-C ₃ -C ₆ cycloalkyl, -NHC(=NH)NH ₂ , -NH-HetB, -OR ^a , -S0 ₂ -Ci-C ₆ alkyl, -S0 ₂ -phenyl, halogen, and oxo, wherein the C ₃ -C6 cycloalkyl is optionally substituted with -NH ₂ ;

AryB is

1) a 5-6 membered monocyclic aromatic ring with 0, 1, 2, 3, or 4 ring atoms selected from N, O and S, optionally substituted with 1 or 2 substituents selected from Ci_C ₆ alkyl, -CH ₂ NH ₂ , -CONH ₂ , -CH ₂ OH, -NH ₂ , -OH, -CH(OH)R ^e , halogen, -CF _3; and pyrrolidinyl; or

2) a 9- or 10-membered bicyclic ring with 1, 2 or 3 N ring atoms optionally

substituted with 1 or 2 substituents selected from Ci_C6 alkyl, Ci_C6 hydroxyalkyl, Ci_C ₆ aminoalkyl, -CONH ₂ , -NH ₂ , -OH, -CH(OH)R ^e , halogen, -CF _3, piperidinyl, pyrrolidinyl, and oxo;

AryC is

1) phenyl optionally substituted with -CONH ₂ ;

2) a 5-6 membered monocyclic aromatic ring with 1 or 2 N ring atoms, optionally substituted with -CH ₃ or -OH; or

3) a 9-membered bicyclic ring with 1 N ring atom optionally substituted with oxo; AryD is a 5-membered monocyclic aromatic ring with 2 N ring atoms, optionally substituted with -CH ₃ ;

HetA is

1) a 4-6-membered saturated or monounsaturated monocyclic ring with 1 or 2

heteroatom ring atoms independently selected from N, O and S, wherein an N atom is optionally in the form of a quaternary amine and wherein the ring is optionally substituted with 1 or 2 substituents independently selected from a) Ci-C ₆ alkyl,

b) -C1-C6 hydroxyalkyl,

c) C ₃ -C ₆ cycloalkyl optionally substituted with -NH ₂ ,

d) -C(0)-C ₃ -C ₆ cycloalkyl optionally substituted with phenyl, e) -(CH ₂ ) ₀ - ₄ NR ^a R ^b ,

f) -C(=NH)NH ₂ ; g) -(CH ₂ )o_ ₁ C(0)NR ^a R ^b ,

h) -(CH ₂ ) ₀ - ₂ C(O)OR ^a ,

i) -(CH ₂ )a.2S02-Ci-C6 alkyl,

j) -CN,

k) -NHC(=NH)NH ₂ ;

1) -0R ^a ,

m) F,

n) -CF ₃ ,

o) -(CH^o- _! -AryB,

P) -O-AryB,

q) -Co-C ₂ alkyl-HetB, and

r) oxo; or

2) a 6- 11 -membered bicyclic ring with 1 to 3 heteroatom ring atoms selected from N and O, optionally substituted with -CH ₂ OH, -C(=NH)NH ₂ ;

-CH ₂ C3-C ₆ cycloalkyl, -C(=0),-NH ₂ , or oxo, wherein the rings in the bicyclic ring are bridged, fused or spirocyclic, and wherein the C3-C ₆ cycloalkyl is optionally substituted with -NH ₂ ;

HetB is

1) a 4-7 membered saturated or monounsaturated monocyclic ring with 1 or 2 heteroatom ring atoms independently selected from N, O and S, wherein an N atom is optionally in the form of a quaternary amine and wherein the ring is optionally substituted with 1, 2 or 3 substituents independently selected from -CF ₃ , F, C1-C6 alkyl, C1-C6 hydroxyalkyl, C ₂ -C6 aminoalkyl, C1-C6 haloalkyl, -CH ₂ CH ₂ N ⁺ (CH ₃ ) ₃ ; -(CH ₂ )o-iC ₃ -C ₆ cycloalkyl, -OH, Ci-C ₆ alkoxy, -C(0)OR ^a , -C(0)NH ₂ , -CH(=NH), -C(=NH)NH ₂ , -CN, -C(OH)(CH ₃ ) ₂ , -CH(OH)(CH ₃ ), -(CH ₂ ) ₀ - ₂ NR ^a R ^b , -CH ₂ CHR ^f -(CH ₂ )o- ₂ -NHR ^g , -CH ₂ -AryD, -(CH ₂ ) ₀ - ₂ -HetD, oxo, and -S0 ₂ -Ci-C6 alkyl, wherein the cycloalkyl is optionally substituted with -(CH ₂ ) ₀ - ₂ NHR ^a ; or

2) a 7- 11 -membered bicyclic ring with 1 or 2 N ring atoms optionally substituted with methyl, wherein the bicyclic ring is bridged, fused or spirocyclic;

HetC is a 5-6 membered saturated monocyclic ring with 1 or 2 heteroatom ring atoms independently selected from N, O and S, optionally substituted with 1 or 2 oxo substituents; HetD is

1) a 4-6 membered saturated monocyclic ring with 1 or 2 heteroatom ring atoms independently selected from N and O;

2) 7-9 membered bicyclic ring with 1 N heteroatom ring atom, wherein the bicyclic ring is bridged or spirocyclic;

R ^a is H or Ci-C ₆ alkyl;

R ^b is H, -OH, C1-C6 alkyl, C1-C6 alkoxy, C2-C6 hydroxyalkyl, C2-C6 aminoalkyl,

C2-C6 dihydroxyalkyl, C2-C6 diaminoalkyl, dimethylaminoC2-C ₆ alkyl,

C ₂ -C ₆ hydroxyaminoalkyl, -(CH ₂ )o-i-C ₃ -C ₆ cycloalkyl, -C(0)Ci-C ₆ alkyl, or -CH ₂ C(0)NHOH; or

R ^a and Rb together with the atom(s) to which they are attached form a 3-7 membered cycloheteroalkyl ring with 0, 1 or 2 additional heteroatom ring atoms independently selected from N, O and S, wherein N is optionally substituted with R ^d ;

R ^d is H, Ci-C ₆ alkyl, C ₃ -C ₆ cycloalkyl, -C(0)-Ci-C ₆ alkyl, -C(0)-AryC, -S0 ₂ -Ci-C ₆ alkyl, or -S0 ₂ -AryC;

R ^e is Ci-C ₆ alkyl, -CF ₃ or -CHF ₂ ;

R ^f is Ci-C ₆ alkyl, -CH ₂ OH, -(CH ₂ )i- ₄ NH ₂ , -(CH ₂ )i-3CONH2, -CH ₂ -imidazole, or benzyl; and

R ^s is H or Ci-C ₆ alkyl; or

f

R and R ^s together with the atom(s) to which they are attached form a 4-6 membered cycloheteroalkyl ring with 0, 1 or 2 additional heteroatom ring atoms independently selected from N, O and S. In one aspect, a N ring atom on HetB can be substituted with 2 methyl groups to afford a positively charged quaternary amine.

Compounds of Formula I inhibit metallo-p-lactamases and can synergize the antibacterial effects of β-lactam antibiotics (e.g., imipenem, ceftazidime and piperacillin) against microorganisms normally resistant to β-lactam antibiotics as a result of the presence of the metallo-p-lactamases. The compounds of the present invention are effective against metallo- β-lactamases and their combination with a β-lactam antibiotic, such as imipenem, ceftazidine or piperacillin, can provide for effective treatment of bacterial infections caused by metallo- p-lactamase producing microorganisms. Accordingly, in certain embodiments, the present invention includes combinations of a compound of Formula I with a β-lactam antibiotic suitable for use against metallo-p-lactamase producing bacteria such as Pseudomonas spp.and Klebsiella spp. The invention also includes compositions comprising a compound of Formula I or its pharmaceutically acceptable salt, and a pharmaceutically acceptable carrier. The invention further includes methods for treating bacterial infections and inhibiting bacterial growth by use of a compound of Formula I or its salt or a combination or composition containing the compound or its salt.

Embodiments, sub-embodiments, aspects and features of the present invention are either further described in or will be apparent from the ensuing description, examples and appended claims.

DETAILED DESCRIPTION OF THE INVENTION

As noted above, the present invention includes compounds of Formula I, wherein the compounds are metallo-p-lactamase inhibitors suitable for use in combination with β-lactam antibiotics and class A, C, and D β-lactamase inhibitors for the treatment of bacterial infections.

In a first embodiment of the invention, the compound is a compound of formula (I), or a pharmaceutically acceptable salt thereof, wherein:

R ^A is H, Ci-C ₆ alkyl, -(CH ₂ )o-2-C ₃ -C ₈ cycloalkyl, -CF ₃ , Ci-C ₆ alkoxy, -COOR ^a , -CN, -NR ^a R ^b , HetA, -(CH ₂ )o- ₂ -AryA, -(CH ₂ ) ₀ -i-O-AryA, -NR ^a (CH ₂ ) ₁ . ₂ -C ₃ -C ₈ cycloalkyl,

-NR ^a (CH ₂ ) _! _ ₂ -phenyl, -C≡C-pyridinyl, or -C≡C-CH ₂ -HetC; wherein the R ^A d-C ₆ alkyl or any R ^A C ₃ -C ₈ cycloalkyl is optionally substituted with -OH, -(CH ₂ ) ₀ - ₂ NR ^a R ^b , -NHS0 ₂ -Ci-C ₆ alkyl, AryB, or HetB;

R ^B is H, Ci-C ₆ alkyl, -OH, Ci-C ₆ alkoxy, -CN, F, or -NR ^a R ^b ;

or R ^A and R ^B together with the atom(s) to which they are attached form a 5-6 membered fused aromatic ring containing 0, 1, or 2 heteroatoms independently selected from N, O and S, wherein N is optionally substituted with R ^d ;

R ^c is H, Ci-C ₆ alkyl, F, CI, -COOCH ₃ , -C(0)NH ₂ , or AryC;

R ^D is H, Ci-C ₆ alkyl, -(CH ₂ ) ₀ -iC ₃ -C ₆ cycloalkyl, -CH ₂ -phenyl, -CH ₂ -azetidinyl,

-(CH ₂ )i_ ₂ -piperidinyl, or -CH ₂ -pyrrolidinyl, -CF ₃ , -CN, CI, or Br, wherein the cycloalkyl is optionally substituted with -(CH ₂ )o-iNH ₂ and the piperidinyl is optionally substituted with fluoro;

AryA is an aromatic ring system selected from:

1) a 5-6 membered monocyclic ring with 0, 1, 2 or 3 heteroatom ring atoms independently selected from N, O and S, optionally substituted with 1 or 2 substituents independently selected from:

a) -Ci-C ₆ alkyl,

b) -C1-C6 hydroxyalkyl,

c) -C ₃ -C6 cycloalkyl optionally substituted with -OH, d) -C ₃ -C6 cycloalkenyl optionally substituted with -CN, e) -(CH ₂ ) ₀ - ₆ NR ^a R ^b ,

f) -CH ₂ NHCH=NH;

g) -CH(OH)R ^e ,

h) -CH ₂ OR ^a ,

i) -(CH ₂ ) ₀ -iC(O)NR ^a R ^b ,

j) -CH ₂ NR ^a -C ₃ -C ₄ alkyl-NR ^a R ^b ,

k) -CH ₂ NHCH ₂ C(0)NR ^a R ^b ,

1) -(CH ₂ ) ₀ - ₂ C(O)OR ^a ,

m) -CH ₂ NR ^a -Ci-C ₃ alkyl-C(0)OR ^a ,

n) -CH ₂ NH-CH[C(OH)CH ₃ ][C(0)OR ^a ],

0) -CH ₂ NR ^a -Ci-C ₆ hydroxyalkyl,

p) -(CH ₂ )o- ₂ S0 ₂ -Ci-C ₆ alkyl,

q) -NR ^a S0 ₂ -Ci-C ₆ alkyl,

r) -OR ^a ,

s) -O(CH ₂ ) ₀ - ₆ NR ^a R ^b ;

t) -0-Ci-C ₆ hydroxyalkyl,

u) -S0 ₂ NR ^a R ^b ,

v) -CN,

w) halogen,

x) -CH ₂ NR ^a (CH ₂ ) ₀ -i-C ₃ -C ₆ cycloalkyl optionally substituted with -OH,

NR ^a R ^b or 2 F,

y) -(CH ₂ )o- _! -AryB, z) -CH ₂ NR ^a -Ci-C ₃ alkyl-AryB,

aa) -CH ₂ NR ^a -CH(COOH)CH ₂ -AryB,

bb) -C ₀ -C ₂ alkyl-HetB,

cc) -(CH ₂ )o-iNR ^a (CH ₂ )o- ₂ -HetB,

dd) -0(CH ₂ )o- ₂ -HetB,

ee) -C(0)-HetB, and

ff) -C(O)NR ^a (CH ₂ ) ₀ - ₂ -HetB; or

2) a 9- or 10-membered bicyclic ring with 1, 2 or 3 heteroatom ring atoms selected from N, O and S, optionally substituted with 1 or 2 substituents independently selected from Ci_C ₆ alkyl, Ci_C ₆ alkoxy, -NH ₂ , Ci_C ₆ aminoalkyl, -CF ₃ , -COOR ^a , -CONH ₂ , -S0 ₂ -Ci-C ₆ alkyl, -S0 ₂ -phenyl, -CN, CI, and oxo;

AryB is

1) a 5-6 membered monocyclic aromatic ring with 0, 1, 2, 3, or 4 ring atoms selected from N, O and S, optionally substituted with Ci_C ₆ alkyl, -CH ₂ NH ₂ , -NH ₂ , -CH(OH)R ^e , or pyrrolindinyl; or

2) a 9-membered bicyclic ring with 2 or 3 N ring atoms optionally substituted with

-CH ₃ ;

AryC is

1) phenyl optionally substituted with -C(=0)NH ₂ ;

2) a 5-6 membered monocyclic aromatic ring with 1 or 2 N ring atoms, optionally substituted with -CH ₃ or -OH; or

3) a 9-membered bicyclic ring with 1 N ring atom optionally substituted with oxo;

HetA is

1) a 6-membered monounsaturated monocyclic ring with 1 heteroatom ring atoms independently selected from N, O and S, optionally substituted with 1 or 2 substituents independently selected from C1-C6 alkyl, -CN, and oxo;

2) a 6-membered saturated monocyclic ring with 1 N ring atom, optionally

substituted with 1 substituent selected from

a) -C1-C6 hydroxyalkyl,

b) C(0)-C ₃ -C ₆ cycloalkyl,

c) (CH ₂ ) ₁ . ₂ NR ^a R ^b ,

d) (CH ₂ )o- _! C(0)NR ^a R ^b , e) -(CH ₂ ) ₀ _ ₂ C(O)OR ^a ,

f) -(CH ₂ )o- ₂ S0 ₂ -C ₁ -C ₆ alkyl,

g) -OH,

h) -(CH.VrAryB,

i) -O-AryB, and

j) -Co-C ₂ alkyl-HetB; or

3) a 10-11-membered spirocyclic ring with 2 or 3 N ring atoms optionally

substituted with oxo;

HetB is

1) a 4-6 membered saturated or monounsaturated monocyclic ring with 1 or 2

heteroatom ring atoms independently selected from N, O and S, optionally substituted with 1, 2 or 3 substituents independently selected from -CF ₃ , F, C1-C6 alkyl, C1-C6 hydroxyalkyl, C3-C6 cycloalkyl, -OH, C1-C6 alkoxy, -C(0)OR ^a , -C(0)NH ₂ , -C(=NH ₂ )NH ₂ , -CN, -C(OH)(CH ₃ ) ₂ , -CH(OH)(CH ₃ ), -NH ₂ , -N(CH ₃ ) ₂ , and oxo; or

2) 8-methyl-8-azabicyclo[3.2.1]octane with the point of attachment being the 3- position of the bridged bicycle;

HetC is a 5-6 membered saturated monocyclic ring with 1 or 2 heteroatom ring atoms independently selected from , O and S, optionally substituted with 1 or 2 oxo substituents; R ^a is H or Ci-C ₆ alkyl;

R ^b is H, -OH, Ci-C ₆ alkyl, Ci-C ₆ alkoxy, d-C ₆ hydroxyalkyl, Ci-C ₆ dihydroxyalkyl,

C ₃ -C ₆ cycloalkyl, -C(0)Ci-C ₆ alkyl, -CH ₂ C(0)NHOH, or Ci-C ₆ aminoalkyl; or

R ^a and Rb together with the atom(s) to which they are attached form a 3-7 membered cycloheteroalkyl ring with 0, 1 or 2 additional heteroatom ring atoms independently selected from N, O and S, wherein N is optionally substituted with R ^d ;

R ^e is -C1-C6 alkyl, -CF ₃ or -CHF _2; and the other groups are as provided in the general formula I above.

In a second embodiment of the invention, the compound is a compound of formula I, or a pharmaceutically acceptable salt thereof, wherein R ^A is C1-C6 alkyl,

-(CH ₂ )o- ₂ -C ₃ -C ₈ cycloalkyl, -CF ₃ , Ci-C ₆ alkoxy, -COOR ^a , -CN, -NR ^a R ^b , HetA,

-(CH ₂ )o- ₂ -AryA, -CH ₂ -0-AryA, -NR ^a (CH ₂ ) ₁ . ₂ -C ₃ -C ₈ cycloalkyl, -NR ^a (CH ₂ ) ₁ . ₂ -phenyl, -C≡C-pyridinyl, or -C≡C-CH ₂ -HetC; wherein the R ^A cycloalkyl is optionally substituted with -OH, -(CH ₂ ) ₀ _ ₂ NH ₂ , -NHSO2-C1-C6 alkyl or HetB, and the other groups are as provided in the general formula I above, or as in the first embodiment.

In a third embodiment of the invention, the compound is a compound of Formula I, or a pharmaceutically acceptable salt thereof, wherein Formula I is

wherein

R ^A is Ci-C ₆ alkyl, -(CH ₂ )o- ₂ -C ₃ -C ₈ cycloalkyl, -CF ₃ ; Ci-C ₆ alkoxy, -COOR ^a , -CN, -NR ^a R ^b , HetA, -(CH ₂ ) ₀ -2-AryA, -CH ₂ -0-AryA, -NR ^a (CH ₂ ) ₁ _ ₂ -C ₃ -C8 cycloalkyl, -NR ^a (CH ₂ ) _! _ ₂ -phenyl, -C≡C-pyridinyl, or -C≡C-CH ₂ -HetC; wherein the R ^A cycloalkyl is optionally substituted with -(CH ₂ ) ₀ -iNR ^a R ^b , AryB, or -OH;

R ^B is Ci-C ₆ alkyl, -OH, Ci-C ₆ alkoxy, -CN, F, or -NR ^a R ^b ,

R ^c is Ci-C ₆ alkyl, CI, -COOCH ₃ , -C(0)NH ₂ , or AryC; and

R ^D is Ci-C ₆ alkyl, -(CH ₂ )o-iC ₃ -C ₈ cycloalkyl, -CH ₂ -phenyl, -CH ₂ -azetidinyl,

-(CH ₂ )i_ ₂ -piperidinyl, or -CH ₂ -pyrrolidinyl, -CF ₃ , CI, or Br, wherein the cycloalkyl is optionally substituted with -(CH ₂ ) ₀ -iNH ₂ and the piperidinyl is optionally substituted with fluoro; and the other groups are as provided in the general formula I above, or as in the first or second embodiment.

In a fourth embodiment of the invention, the compound is a compound of formula

I, or a pharmaceutically acceptable salt thereof, wherein AryA is phenyl optionally substituted with:

a) -d-C ₆ alkyl,

b) -C1-C2 hydroxyalkyl,

c) -(CH ₂ )i_ ₃ NR ^a R ^b ,

d) -CH ₂ NHCH=NH;

e) -CH ₂ NHC(=NH)NH ₂ ;

f) -CH(OH)R ^e ,

g) -CH ₂ OR ^a ,

h) -CH ₂ NR ^a -Ci-C ₆ hydroxyalkyl,

i) -(CH ₂ ) ₀ -iC(O)NR ^a R ^b ,

j) -C(0)OR ^a ,

k) -NHS0 ₂ -Ci-C ₆ alkyl,

1) -OR ^a ,

m) -OCH(CH ₃ )CH ₂ OH,

n) -S0 ₂ -Ci-C ₆ alkyl,

0) -S0 ₂ NR ^a R ^b ,

p) halogen,

q) -CN,

r) -CH ₂ NR ^a (CH ₂ ) ₀ -i-C ₃ -C ₆ cycloalkyl optionally substituted with -OH, NR ^a R ^b or 2 F,

s) AryB,

t) -CH ₂ NR ^a -C ₃ -C ₄ alkyl-NR ^a R ^b ,

u) -CH ₂ NHCH ₂ C(0)NR ^a R ^b ,

v) -CH ₂ NR ^a -Ci-C ₃ alkyl-C(0)OR ^a ,

w) -CH ₂ NH-CH[C(OH)CH ₃ ][C(0)OR ^a ],

x) -CH ₂ NR ^a -Ci-C ₆ alkyl-AryB,

y) -CH ₂ NR ^a -CH(COOH)CH ₂ -AryB,

z) -Co-C ₂ alkyl-HetB,

aa) -C(0)-HetB,

bb) -(CH ₂ )o-iNR ^a (CH ₂ ) ₀ -2-HetB,

cc) -C(O)NR ^a (CH ₂ ) ₀ -2-HetB, or

dd) -O(CH2) ₀ - ₂ -HetB; or 2) dihydroindenyl substituted with -NH ₂ or -NHC(=NH)NH ₂ ; and the other groups are as provided in the general formula I above, or as in any of the first through third

embodiments.

In a fifth embodiment of the invention, the compound is a compound of formula I, or a pharmaceutically acceptable salt thereof, wherein AryA is an aromatic ring system selected from:

a) a 5-6 membered monocyclic ring with 1 or 2 heteroatom ring atoms

independently selected from N, O and S, optionally substituted with 1 or 2 substituents selected from Ci-Ce alkyl; Ci-Ce hydroxyalkyl; Ci-Ce alkoxy; Ci-C ₆ aminoalkyl; C ₃ -C ₆ hydroxycycloalkyl; -CH ₂ CH ₂ C(0)OCH ₂ CH ₃ ; -CN; -(CH ₂ )o- ₂ S0 ₂ CH ₃ ; -NR ^a R ^b , -N(R ^a )S0 ₂ CH ₃ ; -OH;

-O(CH ₂ ) ₀ - ₆ NR ^a R ^b ; dioxolanyl substituted with -CF ₃ ; halogen;

-(CH ₂ )o-i-AryB; -C ₀ -C ₂ alkyl-HetB; and -(CH ₂ ) ₀ -iNR ^a (CH ₂ ) ₀ - ₂ -HetB; or b) a 9- or 10-membered bicyclic ring with 1 , 2 or 3 heteroatom ring atoms selected from N, S and O, optionally substituted with 1 or 2 substituents independently selected from Ci_C6 alkyl, Ci.Ce alkoxy, -NR ^a R ^b , d-Ce aminoalkyl, -CF ₃ , -C(=NH)NH ₂ , -COOR ^a , -CONH ₂ ,

-S0 ₂ -Ci-C6 alkyl, -S0 ₂ -phenyl, -CN, CI, and oxo; and the other groups are as provided in the general formula I above, or as in any of the first through third embodiments.

In a sixth embodiment of the invention, the compound is a compound of formula I, or a pharmaceutically acceptable salt thereof, wherein AryA is an aromatic ring system selected from:

a) a monocyclic ring selected from furanyl, imidazolyl, morpholinyl, pyrazinyl, pyrazolyl, pyridazinyl, pyridinyl; pyrimidinyl, thiazolyl, and thiophenyl, wherein the monocyclic ring is optionally substituted with 1 or 2 substituents selected from Ci-Ce alkyl; Ci-Ce hydroxyalkyl; Ci-Ce alkoxy; Ci-Ce aminoalkyl;

C ₃ -C ₆ hydroxycycloalkyl; -CH ₂ CH ₂ C(0)OCH ₂ CH ₃ ; -CN; -(CH ₂ ) ₀ - ₂ SO ₂ CH ₃ ; -NR ^a R ^b , -N(R ^a )S0 ₂ CH ₃ ; -OH; -O(CH ₂ ) ₀ - ₆ NR ^a R ^b ; dioxolanyl substituted with -CF ₃ ; halogen; -(CH ₂ ) ₀ -i-AryB; -C ₀ -C ₂ alkyl-HetB; and

-(CH ₂ )o-iNR ^a (CH ₂ )o- ₂ -HetB; or b) a bicyclic ring selected from lH-benzo[d]imidazolyl, benzodiimidazolyl, benzooxadiazolyl, benzo[d]thiazolyl, benzothiophenyl, benzotriazolyl, dihydrobenzimidazol, dihydrobenzodioxinyl, dihydrobenzooxazinyl, dihydrochromenyl, dihydroisoindolyl, dihydroindolyl, dihydroquinazolinyl, furopyridinyl, imidazopyridinyl, indazolyl, indolinyl, indolyl, isoindolinyl, isoquinolinyl, naphthyridinyl, pyrazolopyrazinyl, pyrazolopyridinyl, pyrrolopyrazinyl, pyrroloppyridinyl, quinolinyl, tetrahydroimidazopyridinyl, tetrahydropyrazolopyridinyl, tetrahydroquinolinyl, and triazolopyridinyl; wherein the bicyclic ring is optionally substituted with 1 or 2 substituents independently selected from Ci_C ₆ alkyl, Ci_C ₆ alkoxy, -NR ^a R ^b , d_C ₆ aminoalkyl, -CF ₃ ,

-COOR ^a , -CONH ₂ , -S0 ₂ -Ci-C ₆ alkyl, -S0 ₂ -phenyl, -CN, CI, and oxo; and the other groups are as provided in the general formula I above, or as in any of the first through third embodiments.

In a seventh embodiment of the invention, HetB is azabicyclo[3.2.1]octyl, azetidinyl, 1,1-dimethylazetidin-l-ium, 1, 1-dimethylpiperidin-l-ium, dioxolanyl, morpholinyl, oxoimidazolidinyl, oxazolidinyl, oxopiperazinyl, oxopiperidinyl, oxopyrrolidinyl, oxazolidinyl, piperidinyl, piperazinyl, pyrazolyl, pyrrolidinyl, tetrahydrofuranyl, tetrahydropyranyl, or thiazolidinyl; wherein HetB is optionally substituted with 1, 2 or 3 substituents independently selected from -CF ₃ , F, C1-C6 alkyl, -C1-C6 hydroxyalkyl, C3-C6 cycloalkyl, -OH, C1-C6 alkoxy, -C(0)OR ^a , -C(0)NH ₂ , -CH(=NH), -C(=NH ₂ )NH ₂ , -CN, -C(OH)(CH ₃ ) ₂ , -CH(OH)(CH ₃ ),

-NH ₂ , -N(CH ₃ ) ₂ , -(CH ₂ )-azetidinyl, and oxo; or HetC is dioxidothiomorpholinyl, morpholinyl, piperidinyl, or pyrrolidin-l-yl; and the other groups are as provided in the general formula I above, or as in any of the first through sixth embodiments.

In an eighth embodiment of the invention, the compound is a compound of a formula below, or a pharmaceutically acceptable salt thereof,

wherein

R ^A is 1) -(CH ₂ )o- ₂ AryA optionally substituted with a) -d-C ₆ alkyl,

b) -C1-C2 hydroxyalkyl,

c) -(CH ₂ ) ₀ - ₃ NR ^a R ^b ,

d) -C(=NH)NH ₂

e) -CH ₂ NHCH=NH;

f) -CH ₂ NHC(=NH)NH ₂

g) -(CH ₂ ) ₀ -iC(O)NR ^a R ^b ,

h) -NHC(=NH)NH ₂ ;

i) -NHS0 ₂ -Ci-C ₆ alkyl,

j) -OH,

k) -S0 ₂ NR ^a R ^b , or

1) HetB, or

2) -(CH ₂ )o- ₂ C3-C6-cycloalkyl, wherein the C3-C6 cycloalkyl optionally substituted with -OH or -(CH ₂ ) ₀ - ₂ NR ^a R ^b ;

HetB is

1) a 4-6 membered saturated or monounsaturated monocyclic ring with 1 N ring atom, optionally substituted with 1 or 2 substituents selected from -CH(=NH), -C(=NH)NH ₂ , -NH ₂ , and -OH; or

2) a 4-6 membered saturated monocyclic ring with 1 N ring atom, in the form of a quarternary amine, wherein the N ring atom is substituted with 2 methyl groups;

R ^c is CI;

R ^D is Ci-C ₆ alkyl, C ₃ -C ₆ cycloalkyl, -CF ₃ , CI, Br, -CH ₂ -cyclohexyl-(CH ₂ ) ₀ -iNH ₂ ,

-CH ₂ -azetidinyl, -(CH ₂ )i_ ₂ -piperidinyl, or -CH ₂ -pyrrolidinyl, wherein the piperidinyl is optionally substituted with fluoro;

R ^a is H or CH ₃ ;

R ^b is H or CH ₃ ; and the other groups are as provided in the general formula I above, or as in the first embodiment.

In a ninth embodiment of the invention; the compound is a compound of a formula in the eighth embodiment; or a pharmaceutical salt thereof; wherein AryA is phenyl substituted with 1) -CH ₃ , 2) -CH ₂ CH ₂ CH ₃ , 3) -CH ₂ OH, 4) -CH ₂ NH ₂ , 5) -CH ₂ NHCH=NH, 6) -CH ₂ NHC(=NH)NH ₂ , 7) -CH ₂ CH ₂ NH ₂ , 8) -CH ₂ CH ₂ CH ₂ NH ₂ , 9) -C(0)NH ₂ ,

10) -(CH ₂ )C(0)NH ₂ , 11) -NHS0 ₂ CH ₃ , 12) -S0 ₂ NH ₂ , 13) -S0 ₂ NHCH ₃ , 14) dimethylazetidinium, 15) azetidinyl optionally substituted with -C(=NH)NH ₂ or -OH,

16) piperidinyl optionally substituted with 1 or 2 substituents selected from -NH ₂ ,

17) -C(=NH)NH ₂ , 18) -CH(=NH), 19) -CH-azetidinyl, or 20) pyrrolidinyl optionally substituted with -OH or 2,5-dihydro-lH-pyrrolyl, and the other groups are as provided in the eighth embodiment.

In a tenth embodiment of the invention, the compound is a compound of a formula in the eighth embodiment, or a pharmaceutical salt thereof, wherein AryA is pyridinyl substituted with -NH _; and the other groups are as provided in the eighth embodiment.

In an eleventh embodiment of the invention, the compound is a compound of a formula in the eighth embodiment, or a pharmaceutical salt thereof, wherein AryA is benzodimidazolyl substituted with -NH ₂ ; benzothiophenyl; benzothiazolyl substituted with -NH ₂ or -C(=NH)NH ₂ ; dihydrobenzimidazol; dihydroindenyl substituted with -NH ₂ or -NHC(=NH)NH ₂ ; dihydroisoindolyl substituted with oxo; imidazopyridinyl; indazolyl optionally substituted with -NH ₂ ; isoindolinyl optionally substituted with -CH(=NH)NH ₂ ; pyrazolopyridinyl; pyrrolopyrazinyl; pyrrolopyridinyl; quinolinyl optionally substituted with -CH ₂ NH ₂ ; or tetrahydroimidazopyridinyl; and the other groups are as provided in the eighth embodiment.

In another embodiment of the invention, the compound of the invention is selected from the exemplary species depicted in Examples 1-840 shown below, and

pharmaceutically acceptable salts thereof.

In another embodiment of the invention, the compound of the invention is selected from the exemplary species depicted in Examples 131, 132, 134, 168, 178, 180, 181, 198, 259, 260, 264, 265, 267, 268, 269, 270, 271, 272, 273, 274, 275, 276, 284, 285, 286, 298, 312, 315, 423, 425, 433, 434, 435, 436, 437, 438, 439, 440, 441, 442, 443, 446, 447, 455, 456, 457, 460, 463, 464, 468, 469, 474, 481, 482, 494, 499, 544, 545, 551, 574, 590, 596, 597, 610, 612, 671, 783, and 820 shown below, and pharmaceutically acceptable salts thereof.

Other embodiments of the present invention include the following:

(a) A pharmaceutical composition comprising an effective amount of a compound of Formula I as defined above, or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier.

(b) The pharmaceutical composition of (a), further comprising an effective amount of a β-lactam antibiotic. (c) The pharmaceutical composition of (b), wherein the β-lactam antibiotic is selected from the group consisting of imipenem, ertapenem, meropenem, doripenem, biapenem, panipenem, ticarcillin, ampicillin, amoxicillin, carbenicillin, piperacillin, azlocillin, mezlocillin, ticarcillin, cefoperazone, cefotaxime, ceftriaxone, and ceftazidime.

(d) The pharmaceutical composition of (b), wherein the β-lactam antibiotic is imipenem.

The pharmaceutical composition of (b), wherein the β-lactam antibiotic is ceftazidime.

The pharmaceutical composition of (b), wherein the β-lactam antibiotic is piperacillin.

(g) The pharmaceutical composition of (a), further comprising effective amounts of a β-lactam antibiotic and a renal dehydropeptidase (DHP) inhibitor.

(h) The pharmaceutical composition of (g), wherein the β-lactam antibiotic is imipenem, and the DHP inhibitor is cilastatin or a pharmaceutically acceptable salt thereof.

(i) A combination of effective amounts of a compound of Formula I as defined above, or a pharmaceutically acceptable salt thereof, and a β-lactam antibiotic.

(j) The combination of (i), wherein the β-lactam antibiotic is selected from the group consisting of imipenem, ertapenem, meropenem, doripenem, biapenem, panipenem, ticarcillin, ampicillin, amoxicillin, carbenicillin, piperacillin, azlocillin, mezlocillin, ticarcillin, cefoperazone, cefotaxime, ceftriaxone, and ceftazidime.

(k) The combination of (i), wherein the β-lactam antibiotic is imipenem. (1) The combination of (i), wherein the β-lactam antibiotic is ceftazidime.

(m) The combination of (i), wherein the β-lactam antibiotic is piperacillin.

(n) A combination of effective amounts of a compound of Formula I as defined above, or a pharmaceutically acceptable salt thereof, a β-lactam antibiotic and a DHP inhibitor.

(o) The combination of (n), wherein the β-lactam antibiotic is imipenem, and the DHP inhibitor is cilastatin or a pharmaceutically acceptable salt thereof.

(p) A method for treating a bacterial infection which comprises administering to a subject in need of such treatment a therapeutically effective amount of a compound of Formula I, or a pharmaceutically acceptable salt thereof, optionally in combination with an effective amount of a β-lactam antibiotic. (q) A method for treating a bacterial infection which comprises administering to a subject in need of such treatment a therapeutically effective amount of a compound of Formula I, or a pharmaceutically acceptable salt thereof, in combination with effective amounts of a β-lactam antibiotic and a DHP inhibitor.

(r) A method for treating a bacterial infection which comprises administering to a subject in need of such treatment a therapeutically effective amount of the composition of (a), (b), (c), (d), (e), (f), (g) or (h).

(s) A method for treating a bacterial infection which comprises administering to a subject in need of such treatment a therapeutically effective amount of the combination of (i), (j), (k), (l), (m), (n) or (o).

(t) A method of treating a bacterial infection as set forth in (p), (q), (r), or (s), wherein the bacterial infection is due to Pseudomonas spp., Klebsiella spp., Enterobacter spp., Escherichi spp.a, Morganella spp., Citrobacter spp., Serratia, spp. or Acintetobacter spp.

The present invention also includes a compound of Formula I, or a pharmaceutically acceptable salt thereof, (i) for use in, (ii) for use as a medicament for, or (iii) for use in the preparation (or manufacture) of a medicament for, inhibiting beta-lactamase activity or treating bacterial infection. In these uses, the compounds of the present invention can optionally be employed in combination with one or more β-lactam antibiotics and/or one or more DHP inhibitors.

Additional embodiments of the invention include the pharmaceutical compositions, combinations and methods set forth in (a)-(t) above and the uses set forth in the preceding paragraph, wherein the compound of the present invention employed therein is a compound of one of the embodiments, sub-embodiments, classes or sub-classes described above. The compound may optionally be used in the form of a pharmaceutically acceptable salt in these embodiments.

In the embodiments of the compounds and salts provided above, it is to be understood that each embodiment may be combined with one or more other embodiments, to the extent that such a combination provides a stable compound or salt and is consistent with the description of the embodiments. It is further to be understood that the embodiments of compositions and methods provided as (a) through (t) above are understood to include all embodiments of the compounds and/or salts, including such embodiments as result from combinations of embodiments. Additional embodiments of the present invention include each of the

pharmaceutical compositions, combinations, methods and uses set forth in the preceding paragraphs, wherein the compound of the present invention or its salt employed therein is substantially pure. With respect to a pharmaceutical composition comprising a compound of Formula I or its salt and a pharmaceutically acceptable carrier and optionally one or more excipients, it is understood that the term "substantially pure" is in reference to a compound of Formula I or its salt per se; i.e., the purity of the active ingredient in the composition.

The term "metallo-p-lactamase inhibitor" refers to a compound which is capable of inhibiting metallo-p-lactamase activity. As used herein, inhibiting metallo-p-lactamase activity means inhibiting the activity of a class B metallo-p-lactamase. For antimicrobial applications inhibition at a 50% inhibitory concentration is preferably achieved at or below about 100 micrograms/mL, or at or below about 50 micrograms/mL, or at or below about 25 micrograms/mL. The terms "class A", "class B", "class C", and "class D" β-lactamases are understood by those skilled in the art and are described in S. G. Waley, β-lactamase: mechanisms of action, in The Chemistry of β-Lactams, M. I. Page, Ed.; Chapman and Hall, London, (1992) 198-228.

The term "metallo-p-lactamase" denotes a metalloprotein capable of inactivating a β-lactam antibiotic. The β-lactamase can be an enzyme which catalyzes the hydrolysis of the β-lactam ring of a β-lactam antibiotic. Of particular interest herein are microbial metallo- β-lactamases. The metallo^-lactamase can be, for example, a zinc metallo^-lactamase.

β-Lactamases of interest include those disclosed in, e.g., S. G. Waley, β-lactamase: mechanisms of action, in The Chemistry of β-Lactams, M. I. Page, Ed.; Chapman and Hall, London, (1992) 198-228. β-Lactamases of particular interest herein include a metallo^-lactamases of

Escherichia coli (such as New Delhi Metallo-b-lactamase, NDM), Serratia marcescens(such as IMP), and Klebsiella spp. (such as Verona integron-encoded metallo^-lactamase, VIM)).

Additional metallo^-lactamases of interest herein include SPM-, GIM-, SIM-, KHM-, AIM-, DIM-, SMB-, TMB-, and FIM-type enzymes.

The term "antibiotic" refers to a compound or composition which decreases the viability of a microorganism, or which inhibits the growth or proliferation of a microorganism. The phrase "inhibits the growth or proliferation" means increasing the generation time (i.e., the time required for the bacterial cell to divide or for the population to double) by at least about 2-fold. Preferred antibiotics are those which can increase the generation time by at least about 10-fold or more (e.g., at least about 100-fold or even indefinitely, as in total cell death). As used in this disclosure, an antibiotic is further intended to include an antimicrobial, bacteriostatic, or bactericidal agent. Examples of antibiotics suitable for use with respect to the present invention include penicillins, cephalosporins and carbapenems.

The term "β-lactam antibiotic" refers to a compound with antibiotic properties that contains a β-lactam functionality. Non-limiting examples of β-lactam antibiotics useful with respect to the invention include penicillins, cephalosporins, penems, carbapenems, and monobactams.

The term "about", when modifying the quantity (e.g., kg, L, or equivalents) of a substance or composition, or the value of a physical property, or the value of a parameter characterizing a process step (e.g., the temperature at which a process step is conducted), or the like refers to variation in the numerical quantity that can occur, for example, through typical measuring, handling and sampling procedures involved in the preparation, characterization and/or use of the substance or composition; through inadvertent error in these procedures;

through differences in the manufacture, source, or purity of the ingredients employed to make or use the compositions or carry out the procedures; and the like. In certain embodiments, "about" can mean a variation of ± 0.1, 0.2, 0.3, 0.4, 0.5, 1.0, 2.0, 3.0, 4.0, or 5.0 of the appropriate unit. In certain embodiments, "about" can mean a variation of ± 1%, 2%, 3%, 4%, 5%, 10%, or 20%.

Another embodiment of the present invention is a compound of Formula I, or a pharmaceutically acceptable salt thereof, as originally defined or as defined in any of the foregoing embodiments, sub-embodiments, aspects, classes or sub-classes, wherein the compound or its salt is in a substantially pure form. As used herein "substantially pure" means suitably at least about 60 wt.%, typically at least about 70 wt.%, preferably at least about 80 wt.%, more preferably at least about 90 wt.% (e.g., from about 90 wt.% to about 99 wt.%), even more preferably at least about 95 wt.% (e.g., from about 95 wt.% to about 99 wt.%, or from about 98 wt.% to 100 wt.%), and most preferably at least about 99 wt.% (e.g., 100 wt.%) of a product containing a compound of Formula I or its salt (e.g., the product isolated from a reaction mixture affording the compound or salt) consists of the compound or salt. The level of purity of the compounds and salts can be determined using a standard method of analysis such as thin layer chromatography, gel electrophoresis, high performance liquid chromatography, and/or mass spectrometry. If more than one method of analysis is employed and the methods provide experimentally significant differences in the level of purity determined, then the method providing the highest level of purity governs. A compound or salt of 100% purity is one which is free of detectable impurities as determined by a standard method of analysis.

With respect to a compound of the invention which has one or more asymmetric centers and can occur as mixtures of stereoisomers, a substantially pure compound can be either a substantially pure mixture of the stereoisomers or a substantially pure individual diastereomer or enantiomer.

Definitions:

"Alkyl" means saturated carbon chains which may be linear or branched or combinations thereof, unless the carbon chain is defined otherwise. Other groups having the prefix "alk", such as alkoxy and alkanoyl, also may be linear or branched, or combinations thereof, unless the carbon chain is defined otherwise. Examples of alkyl groups include methyl, ethyl, propyl, isopropyl, butyl, sec- and tert-butyl, pentyl, hexyl, heptyl, octyl, nonyl, and the like.

"Aminoalkyl" means saturated carbon chains which may be linear or branched or combinations thereof which are substituted with one amino group which may be terminal (-NI¾) or internal (-NH-).

"Hydroxyalkyl" means saturated carbon chains which may be linear or branched or combinations thereof which are substituted with one hydroxyl (-OH) group.

"Diaminoalkyl" means saturated carbon chains which may be linear or branched or combinations thereof which are substituted with two amino (-NH ₂ ) groups.

"Dihydroxyalkyl" means saturated carbon chains which may be linear or branched or combinations thereof which are substituted with two hydroxyl (-OH) groups.

"Hydroxyaminoalkyl" means saturated carbon chains which may be linear or branched or combinations thereof which are substituted with one hydroxyl (-OH) group and one amino (-NH ₂ ) group .

"Alkenyl" means carbon chains which contain at least one carbon-carbon double bond, and which may be linear or branched, or combinations thereof, unless otherwise defined. Examples of alkenyl include vinyl, allyl, isopropenyl, pentenyl, hexenyl, heptenyl, 1-propenyl, 2- butenyl, 2-methyl-2-butenyl, and the like.

"Aromatic ring system" means monocyclic, bicyclic or tricyclic aromatic ring or ring system containing 5-14 ring atoms, wherein at least one of the rings is aromatic. The term may be used to describe a carbocyclic ring fused to an aryl group. For example, a 5-7-membered cycloalkyl can be fused through two adjacent ring atoms to a 5-6-membered heteroaryl containing 1, 2, or 3 heteroatom ring atoms selected from N, O, and S. In other example, a heteromonocyclic ring is fused through two ring atoms to a phenyl or 5-6-membered heteroaryl containing 1, 2, or 3 heteroatoms selected from N, O, and S. In the case of a heteromonocyclic ring containing one or more N atoms, the N can be in the form of quarternary amine.

"Aryl" means a monocyclic, bicyclic or tricyclic carbocyclic aromatic ring or ring system containing 5-14 carbon atoms, wherein at least one of the rings is aromatic. Examples of aryl include phenyl and naphthyl. In one embodiment of the present invention, aryl is phenyl.

"Cycloalkyl" means a saturated monocyclic, bicyclic or bridged carbocyclic ring, having a specified number of carbon atoms. Examples of cycloalkyl include cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, indanyl, 1,2,3,4-tetrahydronaphthyl and the like. In one embodiment of the present invention, cycloalkyl is selected from: cyclopropane, cyclobutane, cyclopentane and cyclohexane.

"Cycloalkenyl" means a nonaromatic monocyclic or bicyclic carbocylic ring containing at least one double bond. Examples of cycloalkenyl include cyclopropenyl, cyclobutenyl, cyclopentenyl, cyclohexenyl, cycloheptenyl, cyclooxtenyl and the like.

"Cycloheteroalkyl" or "heterocycloalkyl" means a saturated or partly unsaturated non-aromatic monocyclic, bicyclic or bridged carbocyclic ring or ring system containing at least one ring heteroatom selected from , S (including SO and SO2) and O. The cycloheteroalkyl ring may be substituted on the ring carbons and/or the ring nitrogen(s). Examples of cycloheteroalkyl include tetrahydrofuran, piperazine, piperidine, morpholine, oxetane, tetrahydropyran, indolinyl, isoindolinyl, azabicyclooctane, hexahydrofuro[3,2-b]furan, and 2,3,3a,5,6,6a-hexahydrofuro[3,2-b]furan. Where the ring or ring system contains one or more N atoms, the N can be in the form of quarternary amine.

"Heteroaryl" means monocyclic, bicyclic or tricyclic ring or ring system containing 3-14 carbon atoms and containing at least one ring heteroatom selected from N, S (including SO and SO2) and O, wherein at least one of the heteroatom containing rings is aromatic. In the case of a heteroaryl ring system where one or more of the rings are saturated and contain one or more N atoms, the N can be in the form of quarternary amine. Examples of heteroaryl include pyrrolyl, isoxazolyl, isothiazolyl, pyrazolyl, pyridyl, oxazolyl, oxadiazolyl, thiadiazolyl, thiazolyl, imidazolyl, triazolyl, tetrazolyl, furanyl, triazinyl, thienyl, pyrimidyl, pyridazinyl, pyrazinyl, benzisoxazolyl, benzoxazolyl, benzothiazolyl, benzimidazolyl, benzopyrazolyl, benzofuranyl, benzothiophenyl (including S-oxide and dioxide), benzotriazolyl, furo(2,3-b)pyridyl, quinolyl, indolyl, isoquinolyl, quinazolinyl, dibenzofuranyl, and the like.

"Halogen" includes fluorine, chlorine, bromine and iodine.

Where any amine is present in the compound, the N atom may be optionally in the form of a quaternary amine having an appropriate additional substitution.

When any variable (e.g., Rl, R ^a , etc.) occurs more than one time in any constituent or in formula I, its definition on each occurrence is independent of its definition at every other occurrence. Also, combinations of substituents and/or variables are permissible only if such combinations result in stable compounds. A squiggly line across a bond in a substituent variable represents the point of attachment.

Under standard nomenclature used throughout this disclosure, the terminal portion of the designated side chain is described last, preceded by the adjacent functionality toward the point of attachment.

In choosing compounds of the present invention, one of ordinary skill in the art will recognize that the various substituents, i.e. R1, R^, etc., are to be chosen in conformity with well-known principles of chemical structure connectivity and stability.

The term "substituted" shall be deemed to include multiple degrees of substitution by a named substitutent. Where multiple substituent moieties are disclosed or claimed, the substituted compound can be independently substituted by one or more of the disclosed or claimed substituent moieties, singly or plurally. By independently substituted, it is meant that the (two or more) substituents can be the same or different.

In the compounds of formula I, the atoms may exhibit their natural isotopic abundances, or one or more of the atoms may be artificially enriched in a particular isotope having the same atomic number, but an atomic mass or mass number different from the atomic mass or mass number predominantly found in nature. The present invention is meant to include all suitable isotopic variations of the compounds of formula I. For example, different isotopic forms of hydrogen (H) include protium (¾) and deuterium ( ² H or D). Protium is the predominant hydrogen isotope found in nature. Enriching for deuterium may afford certain therapeutic advantages, such as increasing in vivo half-life or reducing dosage requirements, or may provide a compound useful as a standard for characterization of biological samples.

Isotopically-enriched compounds within formula I can be prepared without undue

experimentation by conventional techniques well known to those skilled in the art or by processes analogous to those described in the Schemes and Examples herein using appropriate isotopically-enriched reagents and/or intermediates.

Unless expressly stated to the contrary in a particular context, any of the various cyclic rings and ring systems described herein may be attached to the rest of the compound at any ring atom (i.e., any carbon atom or any heteroatom) provided that a stable compound results.

Unless expressly stated to the contrary, all ranges cited herein are inclusive. For example, a heteroaromatic ring described as containing from " 1 to 4 heteroatoms" means the ring can contain 1, 2, 3 or 4 heteroatoms. It is also to be understood that any range cited herein includes within its scope all of the sub-ranges within that range. Thus, for example, a heterocyclic ring described as containing from " 1 to 4 heteroatoms" is intended to include as aspects thereof, heterocyclic rings containing 2 to 4 heteroatoms, 3 or 4 heteroatoms, 1 to 3 heteroatoms, 2 or 3 heteroatoms, 1 or 2 heteroatoms, 1 heteroatom, 2 heteroatoms, 3

heteroatoms, and 4 heteroatoms. Similarly, Ci-Ce when used with a chain, for example an alkyl chain, means that the chain can contain 1, 2, 3, 4, 5 or 6 carbon atoms. It also includes all ranges contained therein including C1-C5, C1-C4, C1-C3, Ci-C ₂ , C2-C6, C3-C6, C4-C6, C5-C6, and all other possible combinations.

When any variable (e.g., RA or RB) occurs more than one time in any constituent or in Formula I or in any other formula depicting and describing compounds of the present invention, its definition on each occurrence is independent of its definition at every other occurrence. Also, combinations of substituents and/or variables are permissible only if such combinations result in stable compounds.

A "stable" compound is a compound which can be prepared and isolated and whose structure and properties remain or can be caused to remain essentially unchanged for a period of time sufficient to allow use of the compound for the purposes described herein (e.g., therapeutic administration to a subject). The compounds of the present invention are limited to stable compounds embraced by Formula I.

The compounds of the present invention may have one or more asymmetric centers. Accordingly, compounds of the invention can occur as mixtures of stereoisomers, or as individual diastereomers, or enantiomers. All isomeric forms of these compounds, whether individually or in mixtures, are within the scope of the present invention.

The term "compound" refers to the compound and, in certain embodiments, to the extent they are stable, any hydrate or solvate thereof. A hydrate is the compound complexed with water, and a solvate is the compound complexed with an organic solvent.

As indicated above, the compounds of the present invention can be employed in the form of pharmaceutically acceptable salts. The term "pharmaceutically acceptable salt" refers to a salt which possesses the effectiveness of the parent compound and which is not biologically or otherwise undesirable (e.g., is neither toxic nor otherwise deleterious to the recipient thereof).

As set forth above, the present invention includes pharmaceutical compositions comprising a compound of Formula I of the present invention, optionally one or more other active components (e.g., a β-lactam antibiotic), and a pharmaceutically acceptable carrier. The characteristics of the carrier will depend on the route of administration. By "pharmaceutically acceptable" is meant that the ingredients of the pharmaceutical composition must be compatible with each other, do not interfere with the effectiveness of the active ingredient(s), and are not deleterious (e.g., toxic) to the recipient thereof. Thus, compositions according to the invention may, in addition to the inhibitor, contain diluents, fillers, salts, buffers, stabilizers, solubilizers, and other materials well known in the art.

Also as set forth above, the present invention includes a method for treating a bacterial infection which comprises administering to a subject in need of such treatment a therapeutically effective amount of a compound of Formula I, or a pharmaceutically acceptable salt thereof, optionally in combination with a β-lactam antibiotic and/or a DHP inhibitor. The term "subject" (or, alternatively, "patient") as used herein refers to an animal, preferably a mammal, most preferably a human, who has been the object of treatment, observation or experiment. The term "administration" and variants thereof (e.g., "administering" a compound) in reference to a compound of Formula I mean providing the compound, or a pharmaceutically acceptable salt thereof, to the individual in need of treatment. When a compound or a salt thereof is provided in combination with one or more other active agents (e.g., a carbapenem antibiotic or a DHP inhibitor or both), "administration" and its variants are each understood to include provision of the compound or its salt and the other agents at the same time or at different times. When the agents of a combination are administered at the same time, they can be administered together in a single composition or they can be administered separately. It is understood that a "combination" of active agents can be a single composition containing all of the active agents or multiple compositions each containing one or more of the active agents. In the case of two active agents a combination can be either a single composition comprising both agents or two separate compositions each comprising one of the agents; in the case of three active agents a combination can be either a single composition comprising all three agents, three separate compositions each comprising one of the agents, or two compositions one of which comprises two of the agents and the other comprises the third agent; and so forth.

The compositions and combinations of the present invention are suitably administered in effective amounts. The term "effective amount" means the amount of active compound sufficient to inhibit β-lactamase and thereby elicit the response being sought (i.e., an "inhibition effective amount") in a cell, tissue, system, animal or human. In one embodiment, the effective amount is a "therapeutically effective amount" for the alleviation of the symptoms of the disease or condition being treated (e.g., the healing of conditions associated with bacterial infection, and/or bacterial drug resistance). In another embodiment, the effective amount is a "prophylactically effective amount" for prophylaxis of the symptoms of the disease or condition being prevented. When the active compound (i.e., active ingredient) is administered as the salt, references to the amount of active ingredient are to the free acid or free base form of the compound.

The administration of a composition of the present invention is suitably parenteral, oral, sublingual, transdermal, topical, intranasal, intratracheal, intraocular, or intrarectal, wherein the composition is suitably formulated for administration by the selected route using formulation methods well known in the art, including, for example, the methods for preparing and administering formulations described in chapters 39, 41, 42, 44 and 45 in

Remington - The Science and Practice of Pharmacy, 21 ^st edition, 2006. In one embodiment, compounds of the invention are administered intravenously in a hospital setting. In another embodiment, administration is oral in the form of a tablet or capsule or the like. When administered systemically, a therapeutic composition is for example, suitably administered at a sufficient dosage to attain a blood level of inhibitor of at least about 1 microgram/mL, and in additional embodiment at least about 10 micrograms/mL, and at least about 25 micrograms/mL. For localized administration, much lower concentrations than this may be effective, and much higher concentrations may be tolerated.

Intravenous administration of a compound of the invention can be conducted by reconstituting a powdered form of the compound with an acceptable solvent. Suitable solvents include, for example, saline solutions (e.g., 0.9% Sodium Chloride Injection) and sterile water (e.g., Sterile Water for Injection, Bacteriostatic Water for Injection with methylparaben and propylparaben, or Bacteriostatic Water for Injection with 0.9% benzyl alcohol). The powdered form of the compound can be obtained by gamma- irradiation of the compound or by

lyophilization of a solution of the compound, after which the powder can be stored (e.g., in a sealed vial) at or below room temperature until it is reconstituted. The concentration of the compound in the reconstituted IV solution can be, for example, in a range of from about 0.1 mg/mL to about 20 mg/mL.

The present invention also includes a method for inhibiting bacterial growth which comprises administering to a bacterial cell culture, or to a bacterially infected cell culture, tissue, or organism, an inhibition effective amount of a compound of Formula I. Additional embodiments of the invention include the bacterial growth inhibiting method just described, wherein the compound of the present invention employed therein is a compound of one of the embodiments, sub-embodiments or classes described above. The compound may optionally be used in the form of a pharmaceutically acceptable salt in these embodiments. The method can involve administration of a compound of Formula I to an experimental cell culture in vitro to prevent the growth of β-lactam resistant bacteria. The method can alternatively involve administration of a compound of Formula I to an animal, including a human, to prevent the growth of β-lactam resistant bacteria in vivo. In these cases the compound of Formula I is typically co-administered with a β-lactam antibiotic.

Compounds of the invention can be employed for the treatment, prophylaxis or inhibition of bacterial growth or infections due to bacteria that are resistant to β-lactam antibiotics. More particularly, the bacteria can be metallo^-lactamase positive strains that are highly resistant to β-lactam antibiotics. The terms "slightly resistant" and "highly resistant" are well-understood by those of ordinary skill in the art (see, e.g., Payne et al, Antimicrobial Agents and Chemotherapy 38:767-772 (1994); Hanaki et al, Antimicrobial Agents and Chemotherapy 30: 11.20-1 1.26 (1995)). For the purposes of this invention, bacterial strains which are highly resistant to imipenem are those against which the MIC of imipenem is >16 μg/mL, and bacterial strains which are slightly resistant to imipenem are those against which the MIC of imipenem is >4 μg/mL.

Compounds of the invention can be used in combination with antibiotic agents for the treatment of infections caused by Class Β-β-lactamase producing strains, in addition to those infections which are subsumed within the antibacterial spectrum of the antibiotic agent.

Examples of class B-metallo^-lactamase producing bacteria are Pseudomonas aeruginosa, Pseudomonas putida, Enterobacter cloacae, Klebsiella pneumoniae, Klebsiella oxytoca, Escherichia coli, Serratia marcescens, Enterobacter aerogenes, Enterobacter asburiae, Citrobacter freundii, Proteus mirabilis, Morganella morganii, Providencia rettgeri, and Acinetobacter baumannii.

It is generally advantageous to use a compound of Formula I in admixture or conjunction with a carbapenem, penicillin, cephalosporin, or other β-lactam antibiotic, or a prodrug thereof. It is advantageous to use a compound of Formula I in combination with one or more β-lactam antibiotics because of the class B β-lactamase inhibitory properties of the compounds. It is also advantageous to use a compound of Formula I in combination with one or more Class A, C, and D β-lactamase inhibitors to further limit β-lactam susceptability. As already noted, the compound of Formula I and the β-lactam antibiotic can be administered separately (at the same time or as different times) or in the form of a single composition containing both active ingredients.

Carbapenems, penicillins, cephalosporins and other β-lactam antibiotics suitable for use in the present invention include both those known to show instability to or to be otherwise susceptible to class Β-β-lactamases.

When the compounds of Formula I are combined with a carbapenem antibiotic, a dehydropeptidase (DHP) inhibitor can also be combined. Many carbapenems are susceptible to attack by a renal enzyme known as DHP. This attack or degradation may reduce the efficacy of the carbapenem antibacterial agent. Inhibitors of DHP and their use with carbapenems are disclosed in, e.g., U.S. Patent Nos. 4,539,208; 4,616,038; 4,880,793; and 5,071,843. A preferred DHP inhibitor is 7-(L-2-amino-2-carboxyethylthio)-2-(2,2-dimethylcyclopropane carboxamide)- 2-heptenoic acid or a pharmaceutically acceptable salt thereof.

Carbapenems suitable for co-administration with compounds of the present invention include imipenem, ertapenem, meropenem, biapenem, (4R, 5S, 6S)-3-[3S, 5S)-5-(3- carboxyphenyl-carbamoyl)pyrrolidin-3-ylthio]-6-(lR)-l-hydrox yethyl]-4-methyl-7-oxo-l- azabicyclo[3.2.0]hept-2-ene-2-carboxylic acid, (IS, 5R, 6S)-2-(4-(2-(((carbamoylmethyl)-l,4- diazoniabicyclo[2.2.2]oct-l-yl)-ethyl(l,8-naphthosultam)meth yl)-6-[l(R)-hydroxyethyl]-l- methylcarbapen-2-em-3-carboxylate chloride, BMS181 139 ([4R-[4a^^(R*)]]-4-[2- [(aminoiminomethyl)amino]ethyl]-3-[(2-cyanoethyl)thio]-6-(l- hydroxyethyl)-7-oxo-l- azabicyclo[3.2.0]hept-2-ene-2-carboxylic acid), B02727 ([4R-3 [3S*,5S*(R*)], 4α,5β,6β^*)]]- 6-(l-hydroxyethyl)-3-[[5-[l-hydroxy-3-(methylamino)propyl]-3 -pyrrolidinyl]thio]-4-methyl-7- oxo-l-azabicyclo[3.2.0] hept-2-ene-2-carboxylic acid monohydrochloride), E1010 ((1R, 5S, 6S)- 6-[l(R)-hydroxymethyl]-2-[2(S)-[l(R)-hydroxy-l-[pyrrolidin-3 (R)-yl] methyl]pyrrolidin-4(S)- ylsulfanyl]-l -methyl- l-carba-2-penem-3-carboxylic acid hydrochloride) and S4661 ((1R,5S,6S)- 2-[(3S,5S)-5-(sulfamoylaminomethyl) pyrrolidin-3-yl]thio-6-[(lR)-l-hydroxyethyl]-l- methylcarbapen-2-em-3-carboxylic acid), (l S,5R,6S)-l-methyl-2- {7-[4-(aminocarbonylmethyl)- l,4-diazoniabicyclo(2.2.2)octan-lyl]-methyl-fluoren-9-on-3-y l}-6-(lR-hydroxyethyl)-carbapen- 2-em-3 carboxylate chloride.

Penicillins suitable for co-administration with compounds of the present invention include benzylpenicillin, phenoxymethylpenicillin, carbenicillin, azidocillin, propicillin, ampicillin, amoxicillin, epicillin, ticarcillin, cyclacillin, pirbenicillin, azlocillin, mezlocillin, sulbenicillin, piperacillin, and other known penicillins. The penicillins may be used in the form of pro-drugs thereof; for example as in vivo hydro lysable esters, for example the acetoxymethyl, pivaloyloxymethyl, a-ethoxycarbonyloxy-ethyl and phthalidyl esters of ampicillin,

benzylpenicillin and amoxicillin; as aldehyde or ketone adducts of penicillins containing a 6-a- aminoacetamido side chain (for example hetacillin, metampicillin and analogous derivatives of amoxicillin); and as esters of carbenicillin and ticarcillin, for example the phenyl and indanyl a- esters.

Cephalosporins suitable for co-administration with compound of the present invention include cefatrizine, cephaloridine, cephalothin, cefazolin, cephalexin, cephacetrile, cephapirin, cephamandole nafate, cephradine, 4-hydroxycephalexin, cephaloglycin,

cefoperazone, cefsulodin, ceftazidime, cefuroxime, cefmetazole, cefotaxime, ceftriaxone, and other known cephalosporins, all of which may be used in the form of pro-drugs thereof.

β-Lactam antibiotics other than penicillins and cephalosporins that may be coadministered with compounds of the present invention include aztreonam, latamoxef

(MOXALACTAM), and other known β-lactam antibiotics such as carbapenems like imipenem, ertapenem, meropenem or (4R, 5S, 6S)-3-[(3S,5S)-5-(3-carboxyphenylcarbamoyl)pyrrolidin-3- ylthio]-6-(lR)-l-hydroxyethyl]-4-methyl-7-oxo-l-azabicyclo[3 .2.0]hept-2-ene-2-carboxylic acid, all of which may be used in the form of pro-drugs thereof.

In one embodiment, the antibiotic co-administered with a compound of the present invention is selected from the group consisting of imipenem, ertapenem, meropenem and (4R, 5 S, 6S)-3 -[(3 S,5 S)-5 -(3 -carboxyphenylcarbamoyl)pyrrolidin-3 -ylthio] -6-( 1 R)- 1 - hydroxyethyl]-4-methyl-7-oxo-l-azabicyclo[3.2.0]hept-2-ene-2 -carboxylic acid. In another embodiment, the antibiotic co-administered with a compound of the present invention is selected from the group of penicillins consisting of ampicillin, amoxicillin, carbenicillin, piperacillin, azlocillin, mezlocillin, and ticarcillin. Such penicillins can optionally be used in the form of their pharmaceutically acceptable salts, for example their sodium salts. Ampicillin or amoxicillin can alternatively be employed in the form of fine particles of the zwitterionic form (generally as ampicillin trihydrate or amoxicillin trihydrate) for use in an injectable or infusable suspension. In an aspect of this embodiment, the penicillin coadministered with a compound of the present invention is amoxicillin, optionally in the form of its sodium salt or the trihydrate.

In another embodiment, the antibiotic co-administered with a compound of the present invention is selected from the group of cephalosporins consisting of cefotaxime, ceftriaxone and ceftazidime, which are optionally used in the form of their pharmaceutically acceptable salts, for example their sodium salts.

When co-administered with a β-lactam antibiotic, the combination of the compound of the invention and the antibiotic can provide a synergistic effect. The terms

"synergistic effect" and "synergy" indicate that the effect produced when two or more drugs are co-administered is greater than would be predicted based on the effect produced when the compounds are administered individually. While not wishing to be bound by theory, it is believed that the compounds of the present invention are β-lactamase inhibitors that act to prevent degradation of β-lactam antibiotics, thereby enhancing their efficacy and producing a synergistic effect.

Abbreviations employed herein include the following: acac = acetylacetonate; ACN = acetonitrile; AIBN = 2,2-azobisisobutyronitrile; BISPI = 4,4,4',4',5,5,5',5'-octamethyl- 2,2'-bi(l,3,2-dioxaborolane); BLI = β-lactamase inhibitor; Bn = benzyl; BOC (or Boc) = tert- butyloxycarbonyl; Boc anhydride = B0C2O = di-tert-butyl dicarbonate; BOC-ON = 2-(tert- butoxycarbonyloxyamino)-2-phenyl acetonitrile; BOC-OSN = ^~ N-tert- butoxycarbonyloxy)succinimide; BOP = benzotriazol-l-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; BSA = bovine serum albumin; CBZ (or Cbz) = carbobenzoxy

(alternatively, benzyloxycarbonyl); CH ₃ CN = acetonitrile; COD = cyclooctadieneyl; DBU = 1,8- diazabicyclo[5.4.0]undec-7-ene; DCC = dicyclohexyl carbodiimide; DCE = 1,2-dichloroethane; DCM = dichloromethane; DIBAL-H = diisobutylaluminum hydride; DIPEA =

diisopropylethylamine (or Hunig's base); DMA = dimethylacetamide; DMAC = N,N- dimethylacetamide; DMAP = 4-dimethylaminopyridine or Ν,Ν-dimethylaminopyridine; DME = 1,2-dimethoxyethane; DMF = Ν,Ν-dimethylformamide; DMSO = dimethyl sulfoxide; EDC = 1- ethyl-3-(3-dimethylaminopropyl) carbodiimide; DSC = differential scanning calorimetry; EA = EtOAc = ethyl acetate; Et = ethyl; EtOH = ethanol; hex = hexane; HMDS =

hexamethyldisilazide; HOBT = 1 -hydroxy benzotriazole; HOPO = 2-hydroxypyridine-N-oxide; HPLC = high-performance liquid chromatography; IPA = isopropyl alcohol; IP Ac = isopropyl acetate; i-Pr = isopropyl; LC/MS = liquid chromatography/mass spectrometry; mCPBA = meta- chloroperoxybenzoic acid; Me = methyl; MeCN = acetonitrile; MHBII = Mueller Hinton Broth type II; MIC = minimum inhibitory concentration; MPLC = medium pressure liquid

chromatography; MSA = methanesulfonic acid; NMO = N-methylmorpholine-N-oxide; NMP = N-methyl pyrrolidinone; PCy3 Pd G2 = Chloro[(tricyclohexylphosphine)-2-(2'- aminobiphenyl)]palladium(II); Pd(dppf)C12 · DCM = [1,1 '-

Bis(diphenylphosphino)ferrocene]dichloropalladium(II), complex with dichloromethane; PE = petroleum ether; PG = protective group; Ph = phenyl; Pd(DTBPF)Ci ₂ = [l, l '-Bis(di-tert- butylphosphino)ferrocene]dichloropalladium(II); RT = rt = room temperature; SEM-C1 = 2- (Trimethylsilyl)ethoxymethyl chloride; SFC = supercritical fluid chromatography; SiliaMetS® DMT (Si-DMT) is the silica bound equivalent of 2,4,6-trimercaptotriazine (trithiocyanuric acid). It is a versatile metal scavenger for a variety of metals including Cd, Co, Ni, Pd, Pt, Rh, and Ru under a wide range of conditions and the preferred metal scavenger for ruthenium catalysts; SPhos-Pd-G2 = 2nd Generation SPhos Precatalyst, Chloro(2-dicyclohexylphosphino-2',6'- dimethoxy-l, -biphenyl)[2-(2'-amino-l, -biphenyl)]palladium(II); SM = starting material; TBAF = tetrabutylammonium fluoride; TEA = triethylamine; TFA = trifluoroacetic acid; TFE =2,2,2-trifluoroethaonol; THF = tetrahydrofuran; TLC = thin layer chromatography; TNS-N3 = azidotrimethylsilane; TPAP = Tetrapropylammonium perruthenate; TSB = trypticase soy broth; TsOH = p-toluenesulfonic acid; XPhos-Pd-2G or XPHOS Pd G2 precatalyst = Chloro(2- dicyclohexylphosphino-2',4',6'-triisopropyl- 1 , 1 '-biphenyl)[2-(2'-amino- 1, 1'- biphenyl)]palladium(II), X-Phos aminobiphenyl palladium chloride precatalyst; XRPD = X-ray powder diffraction.

The compounds of the present invention can be readily prepared according to the following reaction schemes and examples, or modifications thereof, using readily available starting materials, reagents and conventional synthesis procedures. In these reactions, it is also possible to make use of variants which are themselves known to those of ordinary skill in this art, but are not mentioned in greater detail. Furthermore, other methods for preparing compounds of the invention will be readily apparent to the person of ordinary skill in the art in light of the following reaction schemes and examples. Unless otherwise indicated, all variables are as defined above.

Scheme I.

A6a

Route 1

A10 A11 A9

A10a A11a A9

As outlined in Scheme I, 2-bromo-6-fluoro-benzonitrile Al is reacted with benzylmercaptan in the presence of strong base, such as sodium hydride, to form sulfide A2. The nitrile in A2 is reacted with trimethylsilylazide in the presence of dibutyltin oxide to afford the tetrazole A3. Paramethoxy-benzylchloride (PMBC1) is reacted with A3 under phase transfer conditions (base: potassium carbonate and phase transfer agent: tetrabutylammonium chloride in chloroform/water) to yield a positional mixture of N-protected tetrazoles A4 and A5. This mixture of N-substituted tetrazoles can be reacted with sulfuryl chloride or N-chlorosuccinimide in aqueous acetic acid followed by treatment with ammonium hydroxide solution to afford a mixture of sulfonamides A6 and A7. The sulfonamide can optionally be protected as the corresponding Bis-para-methoxybenzyl sulfonamides A6a and A7a. Per Route 1, the PMB protecting group is removed with strong acid (TFA or HC1) to yield 3-bromo-2-(tetrazol-5- yl)benzenesulfonamide A8. The bromo group is A8 is replaced under C-C, C-N, or C-0 coupling conditions by reacting with an organoboronate, organotin, organozinc, or organocopper reagent in the presence of a catalyst, usually a palladium catalyst, to afford the 3 -substituted 2- (tetrazol-5-yl)benzenesulfonamide A9. Alternatively, according to Route 2 the order of the last two steps may be switched; the mixture of bromo sulfonamides A6 and A7 is subjected to C-C, C-N, or C-0 coupling conditions by reacting with an organoboronate, organotin, organozinc, or organocopper reagent in the presence of a catalyst, usually a palladium catalyst, to afford the coupled PMB protected tetrazole isomers A10 and All. Final PMB protective group removal under acidic conditions such as by using TFA in the presence of a carbocation scavenger, such as anisole or triethylsilane, provides target compounds A9. When the organoboronate, organotin, organozinc, or organocopper reagent contains an acid labile protecting group (like tert- butoxycarbonyl) concurrent removal of this protecting group occurs in the final acidic removal of the PMB groups. This can be done in one step, or in stepwise fashion by treatment with TFA at room temperature to remove a group such as tert-butoxycarbonyl, then heating with TFA and anisole or thioanisole to remove the PMB group. Similarly, according to Route 3, the is-para- methoxybenzyl sulfonamides A6a and A7a may be employed as in Route 2, sometimes providing improved coupling yields compared to A6 and A7. Other positional isomers may be available starting with other bromo isomers of Al. Moreover, the bromo sulfonamides, including PMB protected tetrazole positional isomers may be separated by chromatography and each individual isomer may be used in place of the isomer mixture with similar results. The R group in A10, All, AlOa, Alia or A9 may be further modified. For example, when the R group contains an amine functional group, reductive alkylation reactions with aldehydes or ketones will provide amine containing examples. Alternatively, when the R group contains an amine functional group it may be converted to amide, sulfonamide, or urea containing analogs by, for example, coupling with acids, sulfonyl chlorides, or isocyanates, respectively. Or when the R group contains an aldehyde or ketone group, reductive amination with amines will also provide substituted amine containing examples.

Scheme II:

A10a A11a ^A9

According to Scheme 2 analogs A9 may also be prepared from boronic acid or boronic ester precursors. Intermediates A6a and A7a may be converted to the corresponding boronic acids and boronic esters in a number of ways, for example, by coupling with 5,5,5',5'- tetramethyl-2,2'-bi(l,3,2-dioxaborinane) or other similar reagents using palladium catalysis. This affords the boronic esters A12 and A13 or their corresponding boronic acids. The boronic esters or boronic acids may be coupled with halide or triflate reagents according to Route 4 to provide AlOa and Alia, which can be deprotected as previously described in Scheme 1. Scheme III:

A24 A25 A9a

There are numerous methods for incorporation of substitution at the C-6 position of A9 to provide analogs A9a. One general method is outlined in Scheme 3. According to the Scheme, commercially available aryl fluoride A14 can be converted to the carboxylic acid A15 by treatment with LDA, followed by dry ice. The carboxylic acid functionality can be transformed to the corresponding nitrile A16 in numerous ways known to the chemist. One approach involves conversion to the acid chloride, for example using oxalyl chloride, followed by treatment with ammonium hydroxide to afford the carboxamide, and finally, dehydration, for example using trichloro-1, 3, 5-triazine, to give the nitrile A16. Nucleophilic aromatic substitution of the fluoride using benzyl mercaptan and a base such as sodium hydride provides the sulfide A17. The nitrile present in A17 can be converted to the tetrazole A18 using one of several methods, for example by treatment with trimethylsilyl azide and dibutyltin oxide.

Conversion of the benzyl sulfide to the sulfonyl chloride can be accomplished in several ways, for example, by treatment with NCS in acetic acid. Treatment with ammonium hydroxide then affords the sulfonamide A19. Concommittant protection of the tetrazole and sulfonamide to afford positional isomer mixture A20 and A21 can be achieved by treatment with excess oipara- methoxybenzyl chloride in the presence of a base, such as potassium carbonate, and Nal and tetrabutyl ammonium chloride as catalysts. Selective coupling at the iodo substituted position of A20 and A21 can be achieved with one equivalent of boronic acid or boronic ester reagents in the presence of palladium catalysts, affording bromides A22 and A23. Introduction of functionality at the C-6 position of A22 and A23 can be achieved in numberous ways, for example by using Suzuki (Pd mediated coupling of boronic acids and esters), Negishi (transition metal mediated coupling of organozincates), or Sonogashira coupling (palladium mediated coupling of alkynes) conditions. One generally useful method for introduction of alkyl substitution is shown in Scheme 3, wherein reductive Nickel coupling of A22 and A23 with alkyl iodides or bromides is accomplished to afford A24 and A25 using nickel(II) iodide, bathophenanthroline and manganese (Biswas, Soumik; Weix, Daniel J. J. Am. Chem. Soc. 2013, 135, 16192-16197). Removal of the ara-methoxybenzyl protective groups is achieved under acidic conditions as described in Scheme 1 to provide analogs A9a.

REFERENCE EXAMPLE 1

3-Bromo-2-(l-(4-methoxybenzyl)(lH-tetrazol-5-yl))benzenes ulfonamide and 3-bromo-2-(2-(4- methoxybenzyl)(lH-tetrazol-5- l benzenesulfonamide

Step A: 2-(Benzylthio)-6-bromobenzonitrile

To a mixture of 2-bromo-6-fluorobenzonitrile (10 g, 50.0 mmol) and benzyl mercaptan (5.87 mL, 50.0 mmol) in 1,4-dioxane (100 mL) was added NaH (2.40 g, 60.0 mmol) at 0°C, and the resulting solution was slowly warmed to room temperature and stirred for 2 hr, then it was heated at 60°C for 1.5 hr. The mixture was cooled to rt, diluted with ethyl acetate (20 mL), washed with IN hydrochloric acid (20 mL) followed by addition of brine. The organic layer was dried over MgSC^, filtered and was evaporated under reduced pressure to provide 2- (benzylthio)-6-bromobenzonitrile.

Step B: 5-(2-(Benzylthio)-6-bromophenyl)-lH-tetrazole To a solution of 2-(benzylthio)-6-bromobenzonitrile, 10.5 g, 34.5 mmol) and dibutyltin oxide (1.72 g, 6.90 mmol) in toluene (75 mL) was added TMS-N ₃ (9.16 mL, 69.0 mmol), and resulting mixture was heated at 105°C for 12 hr. The reaction mixture was cooled to rt, filtered, and the precipitate was collected. The filtrate was concentrated and diluted with sat. a ₂ C0 ₃ (30 mL), 2N NaOH (5 mL) and subsequently transferred to a separatory funnel, and washed with ethyl acetate (100 mL). The aqueous layer was acidified by 6N HC1 to pH~l, and the white precipitate was collected by filtration. The combined solids were dried under vacuum to afford 5-(2-(benzylthio)-6-bromophenyl)-lH-tetrazole, which was used in the next step without further purification.

Step C: 5-(2-(Benzylthio)-6-bromophenyl)-l-(4-methoxybenzyl)-lH-tetr azole and 5-(2-

(benzylthio)-6-bromophenyl)-2-(4-methoxybenzyl)-lH-tetraz ole

To a solution of 5-(2-(benzylthio)-6-bromophenyl)-lH-tetrazole in a mixture of chloroform and water (6 mL and 8 mL, respectively) were added potassium carbonate (1.544 g, 1 1.17 mmol), tetrabutylammonium chloride (0.31 1 g, 1.12 mmol) followed by a solution of 1- (chloromethyl)-4-methoxybenzene (1.14 mL, 8.38 mmol) in 2 mL of CHC1 ₃ at 15°C. The resulting mixture was slowly warm to rt, and heated at 50°C for 3 hr. The reaction mixture was cooled to rt, and transferred to a sep. funnel. The organic layer was separated, dried over MgS0 ₄ , filtered and purified using 5 to 80% ethyl acetate in hexanes to provide a mixture of 5- (2-(benzylthio)-6-bromophenyl)-l-(4-methoxybenzyl)-lH-tetraz ole and 5-(2-(benzylthio)-6- bromophenyl)-2-(4-methoxybenzyl)- lH-tetrazole.

Step D: 3-Bromo-2-(l-(4-methoxybenzyl)-lH-tetrazol-5-yl)benzenesulfo namide and 3- bromo-2-(2-(4-methoxybenzyl)-lH-tetrazol-5-yl)benzenesulfona mide To a solution of the mixture of 5-(2-(benzylthio)-6-bromophenyl)-l-(4- methoxybenzyl)- lH-tetrazole and 5-(2-(benzylthio)-6-bromophenyl)-2-(4-methoxybenzyl)- 1H- tetrazole in DCM (40 mL) was added water (0.251 mL, 13.9 mmol) followed by acetic acid (0.796 ml, 13.91 mmol). The resulting mixture was cooled to 0°C, then a solution of sulfuryl chloride (1.131 mL, 13.91 mmol) in DCM (2 mL) was slowly added. The reaction mixture was slowly warmed to rt, and stirred for 4 hr, and then evaporated to dryness. To this residue was added THF (5 mL) and then a mixture of aqueous ammonium hydroxide and THF (20 mL each) at O°C. The reaction mixture was slowly warmed to rt and stirred for 1.5 hr. The resulting solution was diluted with ethyl acetate (100 mL), washed with water (50 mL) and brine (50 mL). The organic layer was dried over MgS0 ₄ , filtered and purified by column chromatography on silica gel eluted with 10 to 90% ethyl acetate in hexanes to provide mixture of 3-bromo-2-(l-(4- methoxybenzyl)- lH-tetrazol-5-yl)benzenesulfonamide and 3-bromo-2-(2-(4-methoxybenzyl)- 1 H-tetrazol-5 -y l)benzenesulfonamide.

The isomer mixture 3-bromo-2-(l-(4-methoxybenzyl)-lH-tetrazol-5- yl)benzenesulfonamide and 3-bromo-2-(2-(4-methoxybenzyl)-lH-tetrazol-5- yl)benzenesulfonamide may be separated to single isomers employing SFC (35% MeOH/C02 on DEAP column, flow rate 70 mL/min). The individual isomers or the mixture may be used as intermediates in the the below examples with similar results.

REFERENCE EXAMPLE 2

4-Bromo-3-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)pyridine- 2-sulfonamide and 4-Bromo-3-(l- (4-methoxybenzyl)-lH-tetrazol-5-yl)pyridine-2-sulfonamide

Step A: 4-Amino-2-((2-(trimethylsilyl)ethyl)thio)nicotinonitrile

A mixture of 2-chloro-3-iodopyridin-4-amine (5000 mg, 20 mmol) and copper(i) cyanide (2800 mg, 31 mmol) in DMF (15 ml) was heated to 135°C for 30 minutes in a microwave reactor. LC showed complete reaction. The dark brown suspension was poured into 200 mL of DCM to ppt the copper salt. The suspension was filtered through a pad of celite. The filtrate was washed with ammonium hydroxide, dried over sodium sulfate, and concentrated down on a rotavapor. LC/MS [M+FLJ+: 154.

To the resulting DMSO solution was added 2-(trimethylsilyl)ethanethiol (4200 mg, 31 mmol) and potassium carbonate (5400 mg, 39 mmol). The mixture was purged three times was nitrogen, and heated to 50°C overnight. LC showed the reaction was very clean. The reaction was diluted with water, and extracted with EtOAc. The extraction was dried over sodium sulfate, filtered and concentrated, and the resulting yellow oil was used in the next step without further purification. LC/MS [M+H]+: 252.

Step B : 4-Bromo-2-((2-(trimethylsilyl)ethyl)thio)nicotinonitrile

To a solution of 4-amino-2-((2-(trimethylsilyl)ethyl)thio)nicotinonitrile (4.9 g, 19 mmol) in acetonitrile (100 mL) was added copper(II) bromide (8.7 g, 39 mmol) and /er/-butyl nitrite (4.0 g, 39 mmol). The reaction was allowed to stir at 0°C then warmed up naturally as the ice bath melted and reached room temperature, and then stirred at room temperature over the weekend. LC showed formation of the desired product. The reaction was diluted with EtOAc, washed with NH ₄ OH and brine, and separated. The crude solution was dried over sodium sulfate, filtered and concentrated to give a brown oil. The oil was loaded onto a 80G ISCO column, and separated by MPLC with hexane and EtOAc. The product eluted at about 8% EtOAc. It was a waxy solid. LC/MS [M-CN]: 288.

Step C: 4-Bromo-2-((2-(trimethylsilyl)ethyl)sulfonyl)nicotinonitrile

To a solution of 4-bromo-2-((2-(trimethylsilyl)ethyl)thio)nicotinonitrile (3.0 g, 9.5 mmol) in DCM (50 ml) was added m-CPBA (7.0 g, 28 mmol) at 0°C. The mixture was allowed to stir for 16 hr. LC showed a clean reaction. Excess m-CPBA was quenched with a ₂ S ₂ 0 ₃ , and the crude material was extracted with DCM. The DCM solution was dried over sodium sulfate, filtered and concentrated. The residue was adsorbed onto silica gel, and purified by MPLC with a 80G ISCO column with hexane and EtOAc. LC/MS [M+H]+: 349.

Step D: 4-Bromo-3-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-2-((2-

(trimethylsilyl)ethyl)sulfonyl)pyridine and 4-bromo-3 -( 1 -(4-methoxybenzyl)- 1 Η- tetrazol-5-yl)-2-((2-(trimethylsilyl)ethyl)sulfonyl)pyridine

A mixture of 4-bromo-2-((2-(trimethylsilyl)ethyl)sulfonyl)nicotinonitrile (2.5 g, 7.2 mmol), azidotrimethylsilane (1.66 g, 14.4 mmol), and dibutylstannanone (0.54 g, 2.2 mmol) in toluene (50 mL) was heated to 1 15°C for 24 hours. LC showed a complete reaction. LC/MS [M+H]+: 392. The solvent was removed, and the dark residue was dissolved in acetonitrile (50 mL). To the solution was added Hunig's base (2.9 g, 22 mmol) and 1 -(chloromethyl)-4- methoxybenzene (2.3 g, 14.4 mmol). The mixture was allowed to stir for 72 hours. LC showed a complete reaction. The reaction was diluted with EtOAc, washed with water, and the separated organic layer was dried over sodium sulfate, filtered, and concentrated. The resulting dark residue was loaded onto an 80G ISCO column, and purified by MPLC with hexane and EtOAc. LC/MS [M+H]+: 512.

Step E: 4-Bromo-3-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)pyridine-2-s ulfonamide and 4- bromo-3-(l -(4-methoxybenzyl)- lH-tetrazol-5-yl)pyridine-2-sulfonamide

To a solution of a mixture of 4-bromo-3-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-

2-((2-(trimethylsilyl)ethyl)sulfonyl)pyridine and 4-bromo-3-(l-(4-methoxybenzyl)-lH-tetrazol- 5-yl)pyridine-2-sulfonamide (2.5 g, 4.9 mmol) in THF (10 mL) was added TBAF (20 mL, 20 mmol), and the mixture was allowed to stir at 50°C for 16 hours. LC showed disappearance of all starting material. The reaction was cooled, and to the reaction was added sodium acetate (4.0 g, 49 mmol) in 10 mL water and (aminooxy)sulfonic acid (5.5 g, 49 mmol). The mixture was allowed to stir at RT for 24 hours. LC showed a good reaction. It was diluted with water, extracted with DCM twice. The extractions were combined, dried over sodium sulfate, and concentrated. The residue was loaded onto a 80G silica column, and purified by MPLC with DCM and MeOH system to afford a mixture of 4-bromo-3-(2-(4-methoxybenzyl)-2H-tetrazol-5- yl)pyridine-2-sulfonamide and 4-bromo-3-(l-(4-methoxybenzyl)-lH-tetrazol-5-yl)pyridine-2- sulfonamide. LC/MS [M+H]+: 427.

REFERENCE EXAMPLE 3

2-((Benzyloxy)methyl)-5-(tributylstannyl)-2H-tetrazole

Step A: 2-((Benzyloxy)methyl)-2H-tetrazole

[lH]-tetrazole (1 g, 14.27 mmol) and K ₂ CO ₃ (2.96 g, 21.41 mmol) were dissolved in DMF (15 ml) and cooled to 0°C, then ((chloromethoxy)methyl)benzene (2.382 ml, 17.13 mmol) was added. The reaction was stirred for 30 mins before warming up to RT and stirred for 16 hrs. The reaction was poured into water and extracted with ether. The ether layer was washed with water, brine, dried over sodium sulfate and concentrated. The residue was absorbed onto silica gel and purified by MPLC with ETOAc and hexane to yield a colorless oil. ^- MR (500 MHz, CDC13) δ ppm 8.62 (s, lH), 7.42-7.36 (m,5H), 6.00 (s, 2H), 4.70 (s, 2H).

Step B: 2-((Benzyloxy)methyl)-5-(tributylstannyl)-2H-tetrazole

2-((Benzyloxy)methyl)-2H-tetrazole (l.Og, 5.26 mmol) and TMEDA (1.603 ml, 10.62 mmol) were dissolved in ethyl ether (15 mL) and cooled to -78°C, then n-BuLi (2.313 mL, 5.78 mmol) was added. The reaction was stirred for 0.5 hr, then cannulated to a solution of tributyltin chloride (1.426 ml, 5.26 mmol) in ether (15 ml) at -78°C. After stirring for 45 mins, the reaction was quenched with saturated NH ₄ CI solution and extracted with ether. The organic layer was washed with brine, dried over a2S0 ₄ , and concentrated. The residue was absorbed onto silica gel and purified by MPLC with 0-15% ETOAc/hexane to yield an oil. ¾-NMR (500 MHz, CDC13) δ ppm 7.40-7.33 (m,5H), 6.01(s, 2H), 4.68 (s, 2H), 1.67-1.61 (m,6H), 1.42-1.33 (m, 6H), 1.30-1.26 (m, 6H), 0.92 (t, J=7.25Hz, 9H).

REFERENCE EXAMPLE 4

tert-Butyl (3-(4-(4,4,5,5-tetramethy -l,3,2-dioxaborolan-2-yl)phenyl)propyl)carbamate

Step A: tert-Butyl (3-(4-chlorophenyl)propyl)carbamate

A 40 niL reaction vial was charged with 3-(4-chlorophenyl)propan-l-amine (150 mg, 0.884 mmol), BOC-Anhydride (0.226 ml, 0.973 mmol), DMF (3 mL) and triethylamine (0.370 mL, 2.65 mmol). The reaction was allowed to stir at room temp for 30 minutes. The reaction was diluted with ethyl acetate and washed with water three times. The organic layer was extracted out and concentrated. The residue was purified by normal phase ISCO on a 12 g column eluted with 0% to 100% ethyl acetate in hexane. The pure fractions were concentrated to afford tert-butyl (3-(4-chlorophenyl)propyl)carbamate. LC-MS: calculated for C14H2 ₀ CI O2 269.12 observed m/e: 214.21 (M - t-butyl) ⁺ .

Step B: tert-Butyl (3-(4-(4,4,5,5-tetramethyl-l,3,2-dioxaborolan-2- yl)phenyl)propyl)carbamate

A 40 mL reaction vial was charged with tert-butyl (3-(4- chlorophenyl)propyl)carbamate (182 mg, 0.675 mmol)), potassium acetate (199 mg, 2.024 mmol) and 4,4,4',4',5,5,5',5'-octamethyl-2,2'-bi(l,3,2-dioxaborolane) (343 mg, 1.349 mmol)) and 2nd generation x-phos precatalyst (53.1 mg, 0.067 mmol). The vial was capped via a red sure seal, and the vial was degassed via vacuum/nitrogen flushes three times (line with needle from manifold). Then, dioxane (6 ml) was syringed in, and again, the vial was degassed via vacuum/nitrogen flushes (3 times). After stirring at room temp for 10 minutes, the vial was heated at 80°C via an oil bath for 18 hr. The excess catalyst was filtered off, and the solution was concentrated. The residue was purified by normal phase ISCO on a 24 g column eluted with 0% to 100% ethyl acetate in hexane. The pure fractions were concentrated to afford tert-butyl (3-(4-(4,4,5,5-tetramethyl-l,3,2-dioxaborolan-2-yl)phenyl)pr opyl)carbamate. LC-MS: calculated for C ₂₀ H ₃₂ B O ₄ 361.283 observed m/e: 384.48 (M+Na) ⁺ . 1H NMR δ (ppm) (MeOH): 7.63 (d, 2H), 7.18 (d, 2H), 3.03 (t, 2H), 2.62 (t, 2H), 1.72-1.79 (m, 2H), 1.42 (s,9H), 1.32 (s, 12H).

The following Reference Examples 5-7 were prepared by the method described in Reference Example 4 substituting the appropriate amine starting material:

REFERENCE EXAMPLE 8

3-bromo-N,N-bis(4-methoxybenzyl)-2-(l-(4-methoxybenzyl)-l H-tetrazol-5- yl)benzenesulfonamide and 3 -bromo-N,N-bis(4-methoxybenzyl)-2-(2-(4-methoxybi tetrazol-5-yl)benzenesulfonamide

To a mixture of 3-Bromo-2-(l-(4-methoxybenzyl)(lH-tetrazol-5- yl))benzenesulfonamide and 3-bromo-2-(2-(4-methoxybenzyl)(lH-tetrazol-5- yl))benzenesulfonamide isomers (3.00 g, 7.07 mmol), l-(chloromethyl)-4-methoxybenzene (2.436 g, 15.56 mmol), in butanone at room temperature, was added potassium carbonate (3.91 g, 28.3 mmol) and sodium iodide (2.332 g, 15.56 mmol). The reaction mixture was stirred overnight under N ₂ at 80°C. LC-MS showed completion of the reaction. The reaction was filtered and the cake was washed with EtOAc. The filtrates were evaporated, and the crude product was purified by column chromatography (EtOAc/hexanes 0-100%) to afford the title compounds. LC/MS [M+H]+: 664, 666.

REFERENCE EXAMPLE 9

3 -(5, 5 -dimethyl- 1 ,3 ,2-dioxaborinan-2-yl)-N,N-bis(4-methoxybenzyl)-2-( 1 -(4-methoxybenzyl)- lH-tetrazol-5-yl)benzenesulfonamide and 3-(5,5-dimethyl-l,3,2-dioxaborinan-2-yl)-N,N-bis(4- methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)benze nesulfonamide

To a reaction vessel was added an isomeric mixture of 3-bromo-N,N-bis(4- methoxybenzyl)-2-(l-(4-methoxybenzyl)-lH-tetrazol-5-yl)benze nesulfonamide and 3-bromo- N,N-bis(4-methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol- 5-yl)benzenesulfonamide (3.23 g, 4.86 mmol), 5,5,5',5'-tetramethyl-2,2'-bi(l,3,2-dioxaborinane) (3.29 g, 14.6 mmol), PCy3 Pd G2 (0.287 g, 0.486 mmol), and potassium acetate (1.431 g, 14.58 mmol). Then anhydrous acetonitrile (new bottle, 25 mL) was added to this flask. Nitrogen was bubbled through this mixture for 10 min, then the mixture was heated at 85°C for 24 hr. The mixture was cooled to room temperature. 1 M NaOH was added to the reaction mixture. The mixture was extracted with EtOAc. The organic phase was concentrated under reduced pressure. The residue was purified by column chromatography on silica gel, eluting with 0-80%hexane/EtOAc to give the product, which was contaminated by about 1/3 of de-Br side product.

REFERENCE EXAMPLE 10

5-chloro-2-(l-(4-methoxybenzyl)-lH-tetrazol-5-yl)-4'-meth yl-[l, l'-biphenyl]-3-sulfonamide and 5-chloro-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-4'-methyl- [l,r-biphenyl]-3-sulfonamide

Step A: (3-bromo-4-(l-(4-methoxybenzyl)-lH-tetrazol-5-yl)-5-sulfamoy lphenyl)boronic acid and (3-bromo-4-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-5-sulfamoy lphenyl)boronic acid

(l,5-cyclooctadiene)(methoxy)iridium(I) dimer (0.312 g, 0.471 mmol) and BISPIN (4.79 g, 18.9 mmol) were dissolved in 3 mL THF and added to a 15 mL pressure tube containing a 2 mL THF solution of 3,4,7, 8-tetramethyl-l,10-phenanthroline (0.223 g, 0.943 mmol). Finally, a 1 mL THF solution containing an isomeric mixture of 3-bromo-2-(l-(4- methoxybenzyl)- lH-tetrazol-5-yl)benzenesulfonamide and 3-bromo-2-(2-(4-methoxybenzyl)- lH-tetrazol-5-yl)benzenesulfonamide (4.00 g, 9.43 mmol) was added to the pressure tube via pipette and the reaction vessel was sealed and heated in an oil bath at 80°C for 16 hr. The reaction mixture was concentrated under reduced pressure. The crude product was purified by reverse phase HPLC, eluting with 10% to 100% MeCN in water.

Step B: 3-bromo-5-chloro-2-(l-(4-methoxybenzyl)-lH-tetrazol-5-yl)ben zenesulfonamide and 3-bromo-5-chloro-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)ben zenesulfonamide

To a solution of (3-bromo-4-(l-(4-methoxybenzyl)-lH-tetrazol-5-yl)-5- sulfamoylphenyl)boronic acid and (3-bromo-4-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-5- sulfamoylphenyl)boronic acid (2.7 g, 5.8 mmol) in MeCN (57.7 mL) was added N-chloro succinimide (0.770 g, 5.77 mmol) and copper (I) chloride (0.571 g, 5.77 mmol). The reaction mixture was heated at 65 °C for 6 hr. The reaction mixture was diluted with water and extracted twice with ethyl acetate. The combined organic layers were washed with brine, dried over anhydrous Na ₂ S0 ₄ , filtered, and concentrated. The crude product was purified by MPLC (ISCO 120g column, eluting with 0% to 100% EtOAc in hexane gradient.

Step C: 5-chloro-2-(l-(4-methoxybenzyl)-lH-tetrazol-5-yl)-4'-methyl- [l,l'-biphenyl]-3- sulfonamide and 5-chloro-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-4'-methyl- [l,l'-biphenyl]-3- sulfonamide

A 40 dram reaction vial was charged with p-tolylboronic acid (0.363 g, 2.67 mmol) and the isomer mixture 3-bromo-5-chloro-2-(l-(4-methoxybenzyl)-lH-tetrazol-5- yl)benzenesulfonamide and 3-bromo-5-chloro-2-(2-(4-methoxybenzyl)-2H-tetrazol-5- yl)benzenesulfonamide (1.36 g, 2.96 mmol). EtOH (29.6 niL) and 1 M potassium phosphate (8.89 mL, 8.89 mmol) were added and the reaction mixture was sparged with 2 for 10 min. To this mixture was added l, l'-Bis(di-tert-butylphosphino)ferrocene palladium dichloride (0.193 g, 0.296 mmol) and then the reaction mixture was heated to 80°C for 1 hr in a microwave apparatus. The reaction mixture was diluted with water and extracted with ethyl acetate. The organic phase was washed with brine, dried over anhydrous Na ₂ S0 ₄ , filtered, and concentrated. The crude residue was purified by MPLC (ISCO 80g column, eluted with 0% to 100% EtOAc in Hexane gradient) to afford the title compounds (isomer mixture). LC/MS (M+H) ⁺ = 470.3, 472.3 (3 : 1 ratio).

REFERENCE EXAMPLE 11

tert-butyl 3-hydroxy-3-(4-(4,4,5,5-tetramethyl-l,3,2-dioxaborolan-2-yl) phenyl)azetidine-l- carboxylate

Step A: tert-butyl 3-(4-bromophenyl)-3-hydroxyazetidine-l-carboxylate

To a solution of 1 ,4-dibromobenzene (5.37 g, 22.8 mmol) in THF (15 mL) at - 78°C under 2 was added N-butyl lithium (7.01 mL, 17.5 mmol) dropwise. The reaction mixture was stirred for 40 minutes. Then the resulting mixture was added to a pre-cooled -78°C solution of l-Boc-3-azetidinone (3.00 g, 17.5 mmol) in 20 mL THF. The mixture was stirred at -78°C for 20 minutes and was warmed up to rt by removing the dry-ice acetone bath. Aqueous NH4CI was added and the mixture was extracted with EtOAc four times. The combined organic layers were dried over anhydrous Na ₂ S0 ₄ , filtered, and concentrated to give a viscous residue. To the residue was added ether, followed by hexane. Collection of the resulting white solid by filtration to remove the organic solvents gave the title compound.

Step B: tert-butyl 3-hydroxy-3-(4-(4,4,5,5-tetramethyl-l,3,2-dioxaborolan-2- yl)phenyl)azetidine- 1 -carboxylate

A dried round bottom flask was charged with tert-butyl 3-(4-bromophenyl)-3- hydroxyazetidine-1 -carboxylate (1.00 g, 3.05 mmol), potassium acetate (0.897 g, 9.14 mmol), l,r-Bis(diphenylphosphino)ferrocene-palladium(II)dichloride dichloromethane complex (0.124 g, 0.152 mmol) and Bis(pinacolato)diboron (1.16 g, 4.57 mmol). DMSO (8 mL) was added and the reaction mixture was degassed with N ₂ , three times. The mixture was heated at 80°C for 90 minutes. The reaction mixture was allowed to cool to room temperature (over about 90 minutes). The reaction mixture was diluted with water and extracted with EtOAc. The organic layer was dried over anhydrous Na ₂ S0 ₄ , filtered, and concentrated under reduced pressure. The crude material was dissovled in DCM and purified by MPLC chromatography, RediSep Column: Silica 24g, to give desired compound. LC/MS [M+H] ⁺ = 376.

REFERENCE EXAMPLE 12

tert-butyl 4-(4-(4,4,5,5-tetramethyl-l,3,2-dioxaborolan-2-yl)phenoxy)pi peridine-l-carboxylate

In a reaction vessel, /er/-butyl 4-(4-bromophenoxy)piperidine-l-carboxylate and

Bis(pinacolato)diboron (285 mg, 1.12 mmol) were combined, followed by addition of potassium acetate (110 mg, 1.123 mmol) and XPHOS PD G2 (22 mg, 0.028 mmol). This mixture was then evacuated and backfilled with 2 (3 times). Then dry, degassed dioxane (2807 μΐ) was added to this flask. This mixture was then heated at 1 10°C for 12 hr. The mixture was cooled, water was added and the mixture was extracted with EtOAc twice. The combined organic fractions were washed with brine, dried (anhydrous Na ₂ S0 ₄ ), filtered and the solvent was evaporated under reduced pressure. The residue was purified by column chromatography on silica gel, eluting with hexane/EtOAc (0-100% gradient) to give the title compound. LC/MS [M+H] ⁺ = 404.

REFERENCE EXAMPLE 13

6-bromo-3 -iodo-2-( 1 -(4-methoxybenzyl)- lH-tetrazol-5-yl)benzenesulfonamide and 6-bromo-3 - iodo-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)benzenesulfonam ide

Step A: 3-bromo-2-fluoro-6-iodobenzoic acid Into a 2000-mL 3 -necked round-bottom flask purged and maintained with an inert atmosphere of nitrogen was placed a solution of (i-Pr) ₂ NH (40.4 g, 400.00 mmol, 1.20 equiv) in tetrahydrofuran (400 mL). This was followed by the addition of n-butyl lithium (146 mL, 1.10 equiv) dropwise with stirring at -20°C over 30 min. To this was added a solution of l-bromo-2- fluoro-4-iodobenzene (100 g, 332.34 mmol, 1.00 equiv) in tetrahydrofuran (600 mL) dropwise with stirring at -78°C. The resulting solution was stirred for 90 min at -78°C. The reaction mixture was then poured into 1.5 L of dry ice. The resulting mixture was concentrated under vacuum. The residue was diluted with 2000 mL of aq. sodium hydroxide (4 M), then washed with 2x800 mL of ether. The aq. solution was adjusted to pH 2 with HCl (2 M), then extracted with 3x800 mL of ethyl acetate. The organic layers were combined, washed with 3x500 mL of water, dried and concentrated under vacuum to afford the title compound.

Step B: 3-bromo-2-fluoro-6-iodobenzoyl chloride

Into a 3000-mL round-bottom flask was placed 3-bromo-2-fluoro-6-iodobenzoic acid (235 g, 681.35 mmol, 1.00 equiv) and thionyl chloride (1175 mL). The resulting solution was stirred for 2 hr at 80°C in an oil bath. The resulting mixture was cooled and concentrated under vacuum to afford the title compound.

Step C: 3-bromo-2-fluoro-6-iodobenzamide

Into a 10000-mL 4-necked round-bottom flask was placed a solution of NH ₄ OH (840 g) in tetrahydrofuran (2000 mL). This was followed by the addition of a solution of 3- bromo-2-fluoro-6-iodobenzoyl chloride (223 g, 614 mmol, 1.00 equiv) in tetrahydrofuran (2460 mL) dropwise with stirring at 0°C. The resulting solution was stirred for 60 min at room temperature. The resulting mixture was concentrated under vacuum. The solids were collected by filtration to afford the title compound.

Step D: 3-bromo-2-fluoro-6-iodobenzonitrile

Into a 10000-mL 4-necked round-bottom flask was placed a solution of 3-bromo-

2-fluoro-6-iodobenzamide (223 g, 648 mmol, 1.00 equiv) in N,N-dimethylformamide (4460 mL), trichloro-l,3,5-triazine (840 g, 4.56 mol, 7.00 equiv). The resulting solution was stirred overnight at room temperature. The reaction mixture was poured into 10 L of aq. sodium bicarbonate. The solids were collected by filtration to afford the title compound.

Step E: 2-(benzylsulfanyl)-3-bromo-6-iodobenzonitrile

Into a 5000-mL 4-necked round-bottom flask purged and maintained with an inert atmosphere of nitrogen was placed a solution of sodium hydride (14.8 g, 617 mmol, 1.20 equiv) in 1,4-dioxane (1000 mL). This was followed by the addition of a solution of phenylmethanethiol (38.1 g, 306.76 mmol, 1.00 equiv) in 1,4-dioxane (100 mL) dropwise with stirring at 0°C over 20 min. To this was added a solution of 3-bromo-2-fluoro-6-iodobenzonitrile (100 g, 306.84 mmol, 1.00 equiv) in 1,4-dioxane (400 mL) dropwise with stirring at 0°C. The resulting solution was stirred for 60 min at room temperature and for an additional 60 min at 60°C. The reaction was then quenched by the addition of 750 mL of HCl (1 M). The resulting solution was diluted with 3 L of water, then extracted with 3x1 L of ethyl acetate. The organic layers were combined, dried and concentrated under vacuum. The residue was applied onto a silica gel column and eluted with ethyl acetate/petroleum ether (1 :4) to afford the title compound.

Step F: 5-[2-(benzylsulfanyl)-3-bromo-6-iodophenyl]-lH-l,2,3,4-tetra zole

Into a 3000-mL 4-necked round-bottom flask was placed a solution of 2- (benzylsulfanyl)-3-bromo-6-iodobenzonitrile (54.0 g, 126 mmol, 1.00 equiv) in toluene (750 mL), TMSN ₃ (43.4 g, 3.00 equiv) and dibutyltin oxide (6.3 g, 0.20 equiv). The resulting solution was stirred for 48 hr at 105°C in an oil bath. The reaction mixture was cooled to r.t. The resulting solution was diluted with 3 L of aq. sodium hydroxide, then extracted with ethyl acetate. The aqueous layer was adjusted to pH 3 with HCl (2 M), then extracted with 2x1 L of ethyl acetate. The organic layers were combined, washed with 2x1 L of water, dried over anhydrous sodium sulfate and concentrated under vacuum to provide the title compound.

Step G: 5-[2-(benzylsulfanyl)-3-bromo-6-iodophenyl]-l-[(4-methoxyphe nyl)methyl]-lH- 1,2,3,4-tetrazole and 5-[2-(benzylsulfanyl)-3-bromo-6-iodophenyl]-2-[(4- methoxyphenyl)methyl]-2H-l,2,3,4-tetrazole

Into a 3000-mL 3 -necked round-bottom flask purged and maintained with an inert atmosphere of nitrogen was placed a solution of 5-[2-(benzylsulfanyl)-3-bromo-6-iodophenyl]- lH-l,2,3,4-tetrazole (84.4 g, 178 mmol, 1.00 equiv) in chloroform (700 mL), a solution of potassium carbonate (49.0 g, 355 mmol, 2.00 equiv) in water (520 mL), and

tetrabutylammonium chloride (10.2 g, 0.20 equiv). This was followed by the addition oipara- methoxybenzyl chloride (42.2 g, 1.50 equiv) dropwise with stirring at 15°C. The resulting solution was stirred for 180 min at 50°C in an oil bath. The reaction mixture was cooled to r.t. The resulting solution was diluted with 200 mL of water, then extracted with 2x200 mL of dichloromethane. The organic layers were combined, dried over sodium sulfate and

concentrated under vacuum. The residue was applied onto a silica gel column and eluted with ethyl acetate/petroleum ether (1 :2). This resulted in the title compound as a mixture of two isomers.

Step H: 6-bromo-3-iodo-2-(l-(4-methoxybenzyl)-lH-tetrazol-5-yl)benze ne-l-sulfonyl chloride and 6-bromo-3-iodo-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)benze ne-l-sulfonyl chloride

Into a 2000-mL 4-necked round-bottom flask purged and maintained with an inert atmosphere of nitrogen was placed mixture of 5-[2-(benzylsulfanyl)-3-bromo-6-iodophenyl]-l- [(4-methoxyphenyl)methyl]-lH-l,2,3,4-tetrazole and 5-[2-(benzylsulfanyl)-3-bromo-6- iodophenyl]-2-[(4-methoxyphenyl)methyl]-2H-l,2,3,4-tetrazole (50.0 g, 84.3 mmol, 1.00 equiv, 60%), dichloromethane (750 mL), AcOH (12.7 g, 211 mmol, 2.50 equivalents), and water (3.8 g, 2.5 equiv). This was followed by the addition of SO2CI2 (28.3 g, 2.50 equivalents) dropwise with stirring at 0°C. The resulting solution was stirred for 60 min at room temperature. The resulting mixture was concentrated under vacuum to afford the title compound isomer mixture. Step I: 6-bromo-3-iodo-2-(l-(4-methoxybenzyl)-lH-tetrazol-5-yl)benze nesulfonamide and 6-bromo-3-iodo-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)benze nesulfonamide

Into a 2000-mL 4-necked round-bottom flask purged and maintained with an inert atmosphere of nitrogen was placed a solution of 6-bromo-3-iodo-2-(l-(4-methoxybenzyl)-lH- tetrazol-5-yl)benzene-l-sulfonyl chloride and 6-bromo-3-iodo-2-(2-(4-methoxybenzyl)-2H- tetrazol-5-yl)benzene-l-sulfonyl chloride (isomer mixture, 50.0 g, 52.7 mmol, 1.00 equiv, 60%) in tetrahydrofuran (300 mL) and a solution of ΝΗ ₄ ΟΗ (200 mL) in tetrahydrofuran (200 mL). The resulting solution was stirred for 60 min at room temperature. The resulting solution was extracted with 3x150 mL of ethyl acetate. The organic layers were combined, dried over anhydrous sodium sulfate and concentrated under vacuum. The crude product was purified with Flash-Prep-HPLC under the following conditions: Column, CI 8 silica gel; mobile phase, H ₂ 0: MeCN = 25 increasing to H20: MeCN = 55 within 30 min; Detector, UV 210 nm, to afford the title compound.

H-NMR (DMSO-d6, 300MHz, ppm): δ 3.727-3.748 (3H, d), 5.001-5.068 (0.78H, m), 5.428- 5.477 (0.75H, m), 5.941 (0.5H, m), 6.823-6.958 (2H, m), 7.148-7.363 (2H, m), 7.732-7.864 (1.6H, m), 7.993-8.117 (3H, m).

REFERENCE EXAMPLE 14

tert-butyl 3 -(4-(4,4,5,5-tetramethyl- 1 ,3 ,2-dioxaborolan-2-yl)phenyl)pyrrolidine- 1 -carboxylate

Step A: tert-butyl 3-(4-chlorophenyl)pyrrolidine-l-carboxylate

In 50 ml RB flask, Boc-Anhydride (0.792 mL, 3.41 mmol) was added to 3-(4- chlorophenyl)pyrrolidine, HCl (500 mg, 2.27 mmol) and TEA (0.48 ml, 3.4 mmol) in DCM (20 mL) then stirred at RT overnight. The reaction was poured into IN HCl and extracted with more DCM (20 ml). The DCM was dried over Na ₂ S0 ₄ , filtered and concentrated. The residue was purified by MPLC ISCO Combi-flash on ISCO Redi-Sep 40g column, eluting with 0-50% EtOAc/hexane to give the title compound. LC-MS [M+l] ⁺ : 282.

Step B: tert-butyl 3-(4-(4,4,5,5-tetramethyl-l,3,2-dioxaborolan-2-yl)phenyl)pyr rolidine-l- carboxylate

To a 25 mL microwave vial was added tert-butyl 3-(4-chlorophenyl)pyrrolidine- 1-carboxylate (270 mg, 0.95 mmol), potassium acetate (280 mg, 2.8 mmol), 4,4,4',4',5,5,5',5'- octamethyl-2,2'-bi(l,3,2-dioxaborolane) (480 mg, 1.9 mmol), 2nd generation XPHOS precatalyst (149 mg, 0.19 mmol) and dioxane (5 ml). The vial was capped and degassed via

vacuum/nitrogen flushes (3 times). After stirring at room temp for 10 minutes, the vial was microwaved at 70°C for 3 hrs. The reaction was filtered and concentrated. The residue was purified by MPLC ISCO Combi-flash on ISCO Redi-Sep 40g column, eluting with 0-50% EtOAc/hexane to give a colorless solid. LC-MS [M+l : 374.

REFERENCE EXAMPLE 15

tert-butyl 4-(4-(4,4,5,5-tetramethyl- 1 ,3 ,2-dioxaborolan-2-yl)phenyl)piperidine- 1 -carboxylate

Step A: tert-butyl 4-(4-bromophenyl)-4-hydroxypiperidine-l -carboxylate

A solution of 1 ,4-dibromobenzene (35.5 g, 150 mmol) in THF (250 mL) at -78°C was treated with n-BuLi (2.5 M, 60 mL, 150 mmol) and stirred for 1 hr, followed by N-Boc-4- piperidone (10.0 g, 50 mmol) in THF (20 mL). After 1 hr the cooling bath was removed and the reaction mixture was stirred for 16 hr at 20°C. The mixture was diluted with saturated aqueous NH ₄ C1, extracted with ethyl acetate, and the combined organic layers were washed with 0.1 N HCl, brine, dried over anhydrous Na ₂ S0 ₄ and concentrated to get the crude product, which was purified by silica gel (PE: EA=10: 1) to obtain the title compound. ^X H NMR (300 MHz, CDC13) δ: 7.48 (d, Jl = 6.9 Hz, J2 = 1.8 Hz, 2H), 7.34 (d, Jl = 6.9 Hz, J2 = 1.8 Hz, 2H), 4.02 (brs, 2H), 3.21 (bit, J = 12.3 Hz, 2H), 1.91 (m, 2H), 1.61 - 1.71 (m, 3H), 1.47 (s, 9H).

Step B: 4-(4-bromophenyl)-l,2,3,6-tetrahydropyridine

The mixture of tert-butyl 4-(4-bromophenyl)-4-hydroxypiperidine-l-carboxylate (2.0 g, 14 mmol) in acetic acid (1 mL) and concentrated HC1 (10 mL) was heated at 100°C for 16 hr. The reaction mixture was cooled down and washed with EA. The aqueous layer was basified by saturated NaHCCh solution and the solid K2CO3 to pH 8. Then the mixture was extracted with EA, dried and concentrated to obtain the title compound. ^X H NMR (300 MHz, CDC13) δ: 7.44 (d, J = 8.7 Hz, 2H), 7.24 (d, J = 9.0 Hz, 2H), 6.12 (s, 1H), 4.70 (brs, 1H), 3.51 (d, J = 3.0 Hz, 2H), 3.10 (t, J = 5.7 Hz, 2H), 2.42 (t, J = 1.5 Hz, 2H).

Step C: tert-butyl 4-(4-bromophenyl)-5,6-dihydropyridine-l(2H)-carboxylate

An ice-cooled mixture of 4-(4-bromophenyl)- 1,2,3, 6-tetrahydropyridine (1.3 g, 5.46 mmol) in 1,4-dioxane (4 mL) and IN NaOH (6 mL) was were added a solution of B0C ₂ O (1.2 g, 5.46 mmol) in 1,4-dioxane (4 mL) and the mixture was stirred for 2 hr at room

temperature and concentrated to remove the dioxane, extracted with EA. The combined organic layer was washed with 0.1 N HC1, water and brine, dried over anhydrous a ₂ S04, concentrated to obtain the title compound. ¾ NMR (300 MHz, CDC13) δ: 7.43 (d, J = 8.7 Hz, 2H), 7.23 (d, J = 8.4 Hz, 2H), 6.04 (brs, 1H), 4.06 - 4.10 (m, 2H), 3.62 (m, 2H), 2.49 (m, 2H), 1.48 (s, 9H). Step D: tert-butyl 4-(4-(4,4,5,5-tetramethyl-l,3,2-dioxaborolan-2-yl)phenyl)-5, 6- dihydropyridine- 1 (2H)-carboxylate

To the solution of tert-butyl 4-(4-bromophenyl)-5,6-dihydropyridine-l(2H)- carboxylate (1.4 g, 4.1 mmol) in DMSO (30 mL) was added bis(pinacolato)- diboron (1.6 g, 6.2 mmol), Pd(PPh ₃ ) ₂ Ci ₂ (0.35 g) and KOAc (1.2 g, 12.3 mmol). The reaction mixture was heated at 100°C for 16 hr under N ₂ . The reaction mixture was cooled down and filtered, diluted with water (400 mL), and extracted with DCM (200 mL x 3). The combined organic phases were washed with water, brine, dried and concentrated. The crude product was purified by silica gel to obtain the title compound. ¾ NMR (300 MHz, CDC13) δ: 7.78 (d, J = 8.4 Hz, 2H), 7.37 (d, J = 8.4 Hz, 2H), 6.10 (s, 1H), 4.08 (s, 2H), 3.63 (m, 2H), 2.54 (m, 2H), 1.50 (s, 9H), 1.36 (s, 12H). Step E: tert-butyl 4-(4-(4,4,5,5-tetramethyl-l,3,2-dioxaborolan-2-yl)phenyl)pip eridine-l- carboxylate

To the solution of tert-butyl 4-(4-(4,4,5,5-tetramethyl-l,3,2-dioxaborolan-2- yl)phenyl)-5,6-dihydropyridine-l(2H)-carboxylate (6.0 g, 15.6 mmol) in methanol (150 mL) was added Pd/C (10 %, 0.6 g). The reaction mixture was stirred at room temperature under hydrogen gas for 16 hr. The Pd/C was filtered off and the filtrate was concentrated to obtain the title compound. ^X H NMR (300 MHz, CDC13) δ: 7.75 (d, J = 7.2 Hz, 2H), 7.21 (d, J = 6.9 Hz, 2H), 4.25 (s, 2H), 2.61-2.82 (m, 3H), 1.60-1.83 (m, 4H), 1.47 (s, 9H), 1.33 (s, 12H).

REFERENCE EXAMPLE 16

2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-3-(piperidin-4-yl)b enzenesulfonamide and 2-(l-(4- methoxybenzyl)-lH-tetrazol-5-yl)-3-(piperidin-4-yl)benzenesu lfonamide

Step A: tert-butyl 4-(2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-3- sulfamoylphenyl)piperidine- 1 -carboxylate and tert-butyl 4-(2-( 1 -(4-methoxybenzyl)- lH-tetrazol- 5-yl)-3-sulfamoylphenyl)piperidine-l-carboxylate

To a mixture of 3-Bromo-2-(l-(4-methoxybenzyl)(lH-tetrazol-5- yl))benzenesulfonamide and 3-bromo-2-(2-(4-methoxybenzyl)(lH-tetrazol-5- yl))benzenesulfonamide (60 mg, 0.141 mmol), tert-butyl 4-iodopiperidine-l-carboxylate (88 mg, 0.283 mmol), pyridine (0.057 mL, 0.707 mmol), nickel chloride dimethoxyethane adduct (6.21 mg, 0.028 mmol), zinc (55.5 mg, 0.849 mmol), and ligand A 2,2':6',2"-terpyridine (19.79 mg, 0.085 mmol) (or ligand B 4,4',4"-tri-tert-butyl-2,2':6',2"-terpyridine) in a ₂ filled microwave reaction vial was added DMA (1 mL). The vial was capped, and the reaction was heated to 100°C for 1 hr in a microwave. The excess catalyst was filtered off and the solution was concentrated. The residue was purified by reverse phase HPLC column

(acetonitrile/water/0.05% TFA system) eluted with 20% to 70% MeCN in water. The pure fractions were concentrated to afford the product. LC-MS: calculated for C25H32N605S 528.62 observed m/e: 529.45 (M+H) ⁺ .

Step B: 2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-3-(piperidin-4-yl)b enzenesulfonamide and 2-(l -(4-methoxybenzyl)- lH-tetrazol-5-yl)-3-(piperidin-4-yl)benzenesulfonamide

The product from Step A was dissolved in CH ₂ CI ₂ (1 mL) and TFA (1 mL). The reaction was stirred at room temperature for 20 min, then was concentrated to give crude TFA salt which was used for the next step without any purification. REFERENCE EXAMPLE 17

tert-butyl 5-(4,4,5,5-tetramethyl-l,3,2-dioxaborolan-2-yl)isoindoline-2 -carboxylate

Commercially available tert-butyl 5-bromoisoindoline-2-carboxylate (i.e., Matric Scientific, catalog #74109) (20 g, 0.0671 mol), 4,4,4',4',5,5,5',5'-octamethyl-2,2'-bi(l,3,2- dioxaborolane) (17 g, 0.0671 mol), KAc (8.5 g, 0.087 mol) and PdCfedppf (1.8 g, 0.00221 mol) in 200 mL 1,4-dioxane was heated to 80°C overnight. The mixture was cooled, water was added, the mixture was extacted with EA, dried and concentrated. The residue was purified by chromatography on silica gel to afford the title compound. ¹ HNMR (300MHz,DMSO)5: 1.2-1.3 (s, 12H), 1.4-1.5 (s, 9H), 4.5-4.6 (s, 4H), 7.2-7.3(m,lH), 7.5-7.6 (M,2H); LC-MS: m/z=246 (M+l-100) ⁺ .

REFERENCE EXAMPLE 18

2-(2-(4-Methoxybenzyl)-2H-tetrazol-5-yl)-3-(4-oxocyclohexyl) benzenesulfonamide

Step A: 2-(2-(4-Methoxybenzyl)-2H-tetrazol-5-yl)-3-(l,4-dioxaspiro[4 .5]dec-7-en-8- yl)benzenesulfonamide

4,4,5, 5-Tetramethyl-2-(l,4-dioxaspiro[4.5]dec-7-en-8-yl)-l,3,2-dio xaborolane (3.76 g, 14.1 mmol), 3-bromo-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)benzenesulfo namide (5.00 g, 11.8 mmol), Na ₂ C0 ₃ (2.498 g, 23.57 mmol), and PdC12(dppf) (0.862 g, 1.18 mmol) were placed in a reaction vessel, and 1,4-dioxane (58.9 mL) and water (19.64 mL) were added). N2 was bubbled through the mixture for 20 min. The reaction vessel was sealed and the mixture heated at 95°C overnight. The reaction mixture was diluted with EtOAc and washed with water. The organic layer was separated, concentrated and the resulting residue was purified by column chromatography (0-90% EtOAc/Hexane) to give the title compound. LC-MS 484 (M+l).

Step B: 2-(2-(4-Methoxybenzyl)-2H-tetrazol-5-yl)-3-(l,4-dioxaspiro[4 .5]decan-8- yl)benzenesulfonamide A flask was charged with 2-(2-(4-Methoxybenzyl)-2H-tetrazol-5-yl)-3-(l,4- dioxaspiro[4.5]dec-7-en-8-yl)benzenesulfonamide (4.00 g, 8.27 mmol), dissolved in MeOH (40 mL) and DCM (40 mL). Palladium hydroxide on carbon (2846 mg, 4.05 mmol) was added under N ₂ . The reaction was stirred under an atmosphere of ¾ for 3 hr. The reaction mixture was filtered through a pad of celite and the filtrate was concentrated to give the title compound. LC-MS 486 (M+l) ⁺ .

Step C: 2-(2-(4-Methoxybenzyl)-2H-tetrazol-5-yl)-3-(4- oxocyclohexyl)benzenesulfonamide

2-(2-(4-Methoxybenzyl)-2H-tetrazol-5-yl)-3-(l,4-dioxaspiro[4 .5]decan-8- yl)benzenesulfonamide (3.56 g, 7.33 mmol) was dissolved in THF (70 mL) and treated with 2N HC1 (5 mL). The reaction mixture was stirred at rt for 4 hr. LC-MS showed that the reaction was not completed yet. An additional amount of 2N HC1 (10 mL) was added and stirred at rt overnight. The reaction mixture was diluted with EtOAc and washed with saturated aHC0 ₃ aqueous solution. The organic layer was separated and wahsed with brine, dried ( a ₂ S0 ₄ ), filtered and concentrated. The residue was purified by column chromatography (0-100% EtOAc/Hexane) to give the title compound.

REFERENCE EXAMPLE 19

(4-iodopiperidin- 1 -yl)( 1 -phenylcyclopropyl)methanone

Step A: 4-iodopiperidine, TFA salt

To a solution of tert-butyl 4-iodopiperidine- 1 -carboxylate (3.02 g, 9,72 mmol) in C¾C (10 mL) was added TFA (10 mL). The reaction was stirred at room temperature for 30 min, then was concentrated to give crude TFA salt which was used for the next step without any purification.

Step B: (4-iodopiperidin- l-yl)(l-phenylcyclopropyl)methanone

To 4-iodopiperidine, TFA salt from Step A in CH2CI2 (14 mL) was added 1- phenylcyclopropanecarboxylic acid (1.928 g, 11.66 mmol), HATU (4.806 g, 12.64 mmol) and DIEA (3.40 mL, 38.88 mmol). The mixture was stirred at room temperature for 30 min and the solvent was concentrated. The residue was purified by normal phase ISCO on a 120 g column eluting with 0% to 50% ethyl acetate in hexane. The pure fractions were concentrated to afford product. LC-MS: calculated for C15H18I O 355.21 observed m/e: 355.94 (M+H) ⁺ .

REFERENCE EXAMPLE 20

5-(piperidin-4-yl)-l,3,4-thiadiazol-2-amine

Into a 2000-mL round-bottom flask, was placed piperidine-4-carboxylic acid (50 g, 387 mmol, 1.00 equiv), aminothiourea (70.5 g, 774 mmol, 2.00 equiv), and hydrogen chloride (750 mL, 2.00 equiv, 10 M). The reaction mixture was heated to reflux overnight in an oil bath, and then concentrated under vacuum. The residue was diluted with 100 mL of water at 0°C. The pH of the solution was adjusted to 10-1 1 with saturated NaOH. The resulting mixture was stirred for 30 min. The solid was collected by filtration. The filter cake was washed with 2x200 mL of ice/water. The crude product was purified by re-crystallization from 200 mL of ethanol.

LC/MS (ES, m/z): 185 [M+l] ; H-NMR (CDC13, ppm): δ 5.136 (s, 2H), 3.11 1 (m, 3H), 2.783 (m, 2H), 2.088 (m, 2H), 1.708 (m, 2H).

REFERENCE EXAMPLE 21

3 -(piperidin-4-yl)pyridine dihydrochloride

Step A: trifluoro-N-phenyl-N-(trifluoromethylsulfonyl)methanesulfona mide

A solution of aniline (80 g, 0.86 mol) and NEt ₃ (191 g, 1.89 mol) in dry CH ₂ C1 ₂ (2 L) was added Tf ₂ 0 (507 g, 1.8 mol) dropwise at 78°C, maintained at this temperature for about 1 hr, then warmed to room temperature and allowed to stir overnight. The CH2CI2 was removed under reduced pressure and the residue was washed by 1 (500 mLx3) to obtain the title compound.

Step B : 1 -(tert-butoxycarbonyl)- 1 ,2,3 ,6-tetrahydropyridin-4-yltrifluoromethanesulfonate Di-iso-propylamine (6.06 g, 0.06 mol) dissolved in dry THF (100 mL), cooled to 78°C under N ₂ , w-BuLi (24 mL, 0.06 mol) was added dropwise, and the reaction mixture was stirred at 78°C for 1 hr. tert-butyl 4-oxopiperidine-l-carboxylate (10 g,0.05 mol) in 50 mL THF was added dropwise at 78°C, then trifluoro-N-phenyl-N- (trifluoromethylsulfonyl)methanesulfonamide (19.8 g, 0.055 mol) in 50 mL THF was added dropwise at 78°C and maintained at this temperature for about 1 hr after which it was allowed to be warmed to room temperature overnight. The reaction mixture was quenched with NH ₄ C1 (aq) with vigorously stirred. The aqueous was extracted with EtOAc (100 mL*3) and the combined organic extracts was dried, concentrated in vacuum and the residue was purified on silica gel (PE:EA=10: 1) to give the product.

Step C: tert-butyl 5,6-dihydro-4-(pyridin-3-yl)pyridine-l(2H)-carboxylate

3-pyridylboronic acid (8.9 g, 0.072 mol), l-(tert-butoxycarbonyl)-l,2,3,6- tetrahydropyridin-4-yltrifluoromethanesulfonate (20 g, 0.06 mol) and K2CO ₃ (24.8 g, 0.18) was dissolved in toluene (500 mL) and water (80 mL). The mixture was degassed and Pd (PPh ₃ ) ₄ (3.5 g, 3 mmol) was added in. The mixture was then heated to reflux for 2 hr with vigorous stirring. The reaction was cooled to room temperature and concentrated under reduced pressure. The residue was partitioned between DCM and saturated aHCOs; the aqueous was extracted with DCM (20 mLx3) and the combined organic extracts were dried. The solvent was removed under reduced pressure and the residue was purified on silica gel (PE:EA=5: 1) to obtain product. LC-MS: m/e =261 (M+H) ⁺ .

Step D: tert-butyl 4-(pyridin-3-yl)piperidine-l-carboxylate

tert-butyl 5,6-dihydro-4-(pyridin-3-yl)pyridine-l(2H)-carboxylate (51 g, 196 mmol) was dissolved in methanol (1000 mL), and Pd(OH)2(9.5 g, 9.8 mmol, 15%) was added in. The mixture was stirred under ¾ (0.35Mpa) at room temperature for 8 hr. After evaporation of the solvent, the residue was purified by column chromatography on silica gel (PE:EA=2: 1) to give the product. LC-MS: m/e =261 (M+H) ⁺ .

Step E: 3-(piperidin-4-yl)pyridine dihydrochloride

tert-butyl 4-(pyridin-3-yl)piperidine-l-carboxylate (12 g, 45.8 mmol) was dissolved in the dioxane (100 mL) then HC1 gas was introduced. White precipitates was collected and recrystallized to afford the product. LC-MS: m/e =163 (M+H) ⁺ ; 1HNMR (DMSO, 300 MHz): δ 9.5 (s, 2H), 8.84 (s, 2H), 8.5 (m, 1H), 8.1 (m, 1H), 3.37 (m, 2H), 3.33 (m, 1H), 3.19 (s, 1H), 2.5 (m, 4H). REFERENCE EXAMPLE 22

2-(piperid -3 -yl)pyridine hydrochloride

Step A: methyl 2-(pyridin-2-yl)acetate

To a stirred solution of 2-(pyridin-2-yl)acetic acid (245 g, 1.41 mol) in methanol

(2.5 L) was added thionyl chloride (206 mL, 2.83 mol) drop wise over a period of 45 min at 0°C. The resulting reaction mixture was allowed to come to room temperature and stirred for 16 hr. After completion of the reaction (TLC), the reaction mixture was concentrated under reduced pressure to get the crude compound. The crude compound was dissolved in ethyl acetate (2.5 L) and washed with saturated sodium carbonate solution. The organic layer was dried over sodium sulphate and concentrated under reduced pressure to afford the crude title compound.

Step B: methyl 4-cyano-2-(pyridin-2-yl)butanoate

To a stirred solution of methyl 2-(pyridin-2-yl)acetate (190 g, 1.260 mol) in 1,4- dioxane (1.9 L) was added Triton-B (Benzyl Trimethyl ammonium hydroxide) (46 mL, 0.252 mol) at room temperature and stirred for 10 min. Acrylonitrile (49.7 mL, 0.760 mol) was dissolved in 1,4-dioxane (0.9 L) and was added drop wise over period of 30 minutes. The resulting reaction mixture was stirred for 16 hr at room temperature. The reaction progress was monitored by TLC. After completion of the reaction (TLC), the reaction mixture was concentrated under reduced pressure to afford the crude title compound. Purification by column chromatography was by using (100-200 silica gels) using 15 % ethyl acetate and pet. ether as the eluent afforded pure compound.

Step C: 3-(pyridin-2-yl)piperidin-2-one

To a stirred solution of methyl 4-cyano-2-(pyridin-2-yl)butanoate (60 g, 0.292 mol) in methanol (600 mL) was added Raney Ni (30 g) and Aq. ammonia (10 mL) at room temperature. The resulting reaction mixture was hydrogenated in a par shaker vessel at 60 psi for 16 hr. The reaction progress was monitored by TLC. After completion of reaction (TLC), the reaction mixture was filtered through celite bed and the bed was washed with methanol (600 mL) and the filtrate was concentrated under reduced pressure to afford the crude compound (50 g). Purification: The crude compound was triturated with diethyl ether (2 X 100 mL) and to afford pure compound. Step D: tert-butyl 3-(pyridin-2-yl)piperidine-l-carboxylate

To a stirred solution of 3-(pyridin-2-yl)piperidin-2-one (60 g, 0.340 mol) in THF (430 mL) was added sodium borohydride (38.5 g, 1.019 mol) and BF ₃ Et ₂ 0 (86 mL, 0.686 mol) at 0°C. The resulting reaction mixture was allowed to come to room temperature and stirred for 16 hr. The reaction progress was monitored by TLC. After completion of the reaction (TLC), the reaction mixture was quenched with cone. HC1 (175 mL) and heated to 90°C for 1 hr and then cooled to 0°C. The reaction mixture was basified with 10 NaOH solution (200 mL) and BOC anhydride (93.34 mL, 0.406 mol) was added and the reaction stirred for 1 hr. After completion of reaction (TLC), the reaction mixture was diluted with water (1 L) and extracted into ethyl acetate (2 X 1 L). The organic layer was dried over sodium sulphate and concentrated under reduced pressure to obtain the crude compound (80 g). Purification: Crude was obtained which was purified by column chromatography by using (100-200 silica gels) using 10 % ethyl acetate and pet ether as the eluent to afford pure compound.

Step E: 2-(piperidin-3-yl)pyridine hydrochloride

To a stirred solution of tert-butyl 3-(pyridin-2-yl)piperidine-l-carboxylate (80 g,

0.306 mol) in dioxane (80 mL) was added HC1 in 1,4-dioxane (500 mL, 3 M solution) drop wise over a period of 15 minutes at 0°C. The resulting reaction mixture was allowed to come to room temperature and stirred for 16 hr. After completion of the reaction (TLC), the reaction mixture was concentrated under reduced pressure to afford the crude compound. Purification: The crude compound was washed with diethyl ether (2 X 250 mL) and dried under vaccum to afford the title compound. LC-MS: 99.56 %, (m/z = 163.1, [M+H] ⁺ ).

REFERENCE EXAMPLE 23

3-(piperidin-4-yl)-5,6,7,8-tetrahydroimidazo[l,2-a]pyridine hydrochloride

Step A: tert-butyl 4-(2-ethoxy-2-oxoethylidene)piperidine-l-carboxylate

To a stirred suspention of sodium hydride (60.2 g, 2.509 mol) in tetrahydrofuran (2.0 L) was added diethyl ethoxymethylphosphonate (309.1 g, 1.380 mol) drop wise under nitrogen atmosphere at 0 °C and stirred for 1 h. Tert-butyl 4-oxopiperidine-l-carboxylate (250 g, 1.254 mol) in tetrahydrofuran (2.0 L) was added drop wise to above reaction mixture at 0°C and stirred at same temperature for 1 hr. After the completion of reaction (TLC), reaction mixture was quenched in ice cold water (1.0 L) and extracted with ethyl acetate (2 x 1.5 L). The combined organic layer was washed with brine (500 mL) and dried over sodium sulfate. The solvent was evaporated under reduced pressure to afford title compound.

Step B: tert-butyl 4-(2-ethoxy-2-oxoethyl)piperidine-l -carboxylate

To a stirred solution of tert-butyl 4-(2-ethoxy-2-oxoethylidene)piperidine-l- carboxylate (120 g, 0.446 mol) in methanol (1.0 L), 10% Pd/C (45 g) was added portion wise under nitrogen atmosphere at room temperature. The reaction mixture was hydrogenated under hydrogen atmosphere at 60 psi for 2 hr. The reaction progress was monitored by TLC method [(silica gel plate 60 F254 from Merck), 25 % ethyl acetate in pet ether, using 254 nm UV light to visualize the spots]. Rf values of starting material and product were 0.4 and 0.35 respectively. After the completion of the reaction (TLC), the reaction mixture was filtered through celite bed and washed the bed with excess methanol. Filtrate was concentrated under reduced pressure to afford title compound.

Step C: /er/-butyl 4-(l-bromo-2-ethoxy-2-oxoethyl)piperidine-l -carboxylate

To a stirred solution of LiHMDS (389.5 g, 2.029 mol) in tetrahydrofuran (2.0 L) was added tert-butyl 4-(2-ethoxy-2-oxoethyl)piperidine- 1 -carboxylate (250 g, 0.922 mol) in

tetrahydrofuran (200 mL) drop wise under nitrogen atmosphere at -78°C over a period of 1 hr. Trimethylsilyl chloride (314.5 g, 2.894 mol) was added drop wise to the above reaction mixture at -78°C over a period of 2 hr and followed by drop wise addition of bromine (186 g, 1.162 mol) at the same temperature over a period of 45 minutes. After the completion of the reaction (TLC), the reaction mixture was quenched in saturated sodium bicarbonate solution (1.0 L) and extracted with ethyl acetate (2 x 1.5 L). The combined organic layer was washed with brine (500 mL) and dried over sodium sulfate. The solvent was evaporated under reduced pressure to afford title compound. Step D: tert-butyl 4-(l-bromo-2-hydroxyethyl)piperidine-l -carboxylate

To a stirred solution of /er/-butyl 4-(l-bromo-2-ethoxy-2-oxoethyl)piperidine-l- carboxylate (250 g, 0.716 mol) in tetrahydrofuran (2.5 L) was added sodium borohydride (136.1 g, 3.581 mol) portion wise at 0°C. Methanol (600 mL) was added drop wise to above reaction mixture at 0°C. The reaction mixture was allowed to stir at room temperature for 16 hr. After the completion of reaction (TLC), the reaction mixture was concentrated under reduced pressure to afford the residue. The residue was diluted with water (1.0 L) and extracted with ethyl acetate (2 x 1.5 L). The combined organic layer was washed with brine (500 mL) and dried over sodium sulfate. The solvent was evaporated under reduced pressure to afford the crude compound. The crude compound was adsorbed on 500 g of 100-200 silica gel, which was loaded over a pre-packed column with silica gel [200 mm x 120 cm width and height of column, loaded with 3.0 kg of 100- 200 silica gel]. Elution started with 20% ethyl acetate/pet. ether and finished with 30 % ethyl acetate/pet. ether to afford the title compound.

Step E: tert-butyl 4-( 1 -bromo-2-oxoethyl)piperidine- 1 -carboxylate

To a stirred solution of tert-butyl 4-(l-bromo-2-hydroxyethyl)piperidine-l- carboxylate (200 g, 0.653 mol) in dichloromethane (2.0 L) was added Dess-martin periodinane (304.8 g, 0.718 mol) at 0°C. The resulting reaction mixture was allowed to stir at room temperature for 16 hr. After the completion of the reaction (TLC), the reaction mixture was quenched in saturated sodium bicarbonate solution (1.0 L) and extracted with dichloromethane (2 x 1.5 L). The combined organic layer was washed with brine (500 mL) and dried over sodium sulfate. The solvent was evaporated under reduced pressure to afford the title compound.

Step F: tert-butyl 4-(imidazo[l,2-a]pyridin-3-yl)piperidine-l -carboxylate

To a stirred solution of tert-butyl 4-(l-bromo-2-oxoethyl)piperidine-l -carboxylate

(175 g, 0.571 mol) in ethanol (1.5 L) was added 2-amino pyridine (75.26 g, 0.8 mol) at room temperature. The resulting reaction mixture was refluxed for 16 hr. After completion of the reaction (TLC), the reaction mixture was evaporated under reduced pressure to afford the crude title compound. The crude compound was adsorbed on 400 g of 100-200 silica gel, which was loaded over a pre-packed column with silica gel [120 mm x 90 cm width and height of column, loaded with 2.5 kg of 100-200 silica gel]. Elution started with 1% methanol/dichloromethane and finished with 3 % ethyl methanol/dichloromethane to afford the pure title compound.

Step G: tert-butyl 4-(5,6,7,8-tetrahydroimidazo[l,2-a]pyridin-3-yl)piperidine-l -carboxylate

To a stirred solution of tert-butyl 4-(imidazo[l,2-a]pyridin-3-yl)piperidine-l- carboxylate (60 g, 0.199 mol) in acetic acid (600 mL) was added 10% Pd/C (20 g) portion wise under nitrogen atmosphere at room temperature. The reaction mixture was hydrogenated under hydrogen atmosphere at 40 psi for 6 hr. After completion of the reaction (TLC), the reaction mixture was filtered through celite bed and the bed was washed with methanol. Filtrate was evaporated under reduced pressure to afford crude compound. The crude product was washed with 10% methyl tertiary butyl ether in pet. ether (500 mL) and dried under vacuum to afford the title compound.

Step H: 3-(piperidin-4-yl)-5,6,7,8-tetrahydroimidazo[l,2-a]pyridine hydrochloride To a stirred solution of tert-butyl 4-(5,6,7,8-tetrahydroimidazo[l,2-a]pyridin-3- yl)piperidine-l-carboxylate (50 g, 0.164 mol) in 1,4-dioxane (500 mL) was added drop wise HC1 in 1,4-dioxane solution (500 mL, 3M solution) over a period of 45 minutes at 0°C. The resulting reaction mixture was allowed to stir at room temperature for 16 hr. The reaction mixture was concentrated under reduced pressure to afford the crude compound. Purification: The above crude compound was washed with MTBE (2 X 100 mL) and dried under vacuum to afford the title compound. LC/MS: 98.85 %, (m/z = 206.0 [(M-HC1)+H] ⁺ .

REFERENCE EXAMPLE 24

3-bromo-N,N-bis(4-methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-t etrazol-5-yl)-6- (trifluoromethyl)benzenesulfonamide and 3-bromo-N,N-bis(4-methoxybenzyl)-2-(l-(4- methoxybenzyl)-lH-tetrazol-5-yl)-6-(trifluoromethyl)benzenes ulfonamide

Step A: 6-bromo-2-fluoro-3-(trifluoromethyl)benzoic acid

Into a 10000-mL 4-necked round-bottom flask purged and maintained with an inert atmosphere of nitrogen, was placed tetrahydrofuran (5000 mL), NH(i-Pr) ₂ (249 g, 1.20 equiv). This was followed by the addition of n-BuLi (905 mL, 1.10 equiv) dropwise with stirring in 30 min at -70°C. The resulting solution was stirred for 0.5 hr at -30°C. To this was added 4-bromo-2-fluoro- l-(trifluoromethyl)benzene (500 g, 2.06 mol, 1.00 equiv) dropwise with stirring at -78°C in 2 hr. The resulting solution was stirred for 2 hr at -78°C. The reaction was then poured into 1000 g of C02(s) at -70°C. The pH value of the solution was adjusted to 3 with hydrogen chloride (2N) (1.5 mol/L). The resulting solution was extracted with 3x2000 mL of ethyl acetate and the organic layers combined and dried over anhydrous sodium sulfate and concentrated under vacuum. This resulted in 301 g (50%) of 6-bromo-2-fluoro-3-(trifluoromethyl)benzoic acid as a white solid. Step B: 6-bromo-2-fluoro-3-(trifluoromethyl)benzoyl chloride

Into a 10000-mL 4-necked round-bottom flask purged and maintained with an inert atmosphere of nitrogen, was placed 6-bromo-2-fluoro-3-(trifluoromethyl)benzoic acid (560 g, 1.95 mol, 1.00 equiv), tetrahydrofuran (5600 mL), COCl ₂ (374 g), N,N-dimethylformamide (2 g). The resulting solution was stirred for 12 hr at 25°C. The resulting mixture was concentrated under vacuum to afford crude 6-bromo-2-fluoro-3-(trifluoromethyl)benzoyl chloride.

Step C: 6-bromo-2-fluoro-3-(trifluoromethyl)benzamide

Into a 10000-mL 4-necked round-bottom flask, was placed NH ₄ OH (837 mL), tetrahydrofuran (4000 mL). This was followed by the addition of 6-bromo-2-fluoro-3-

(trifluoromethyl)benzoyl chloride (600 g, 1.96 mol, 1.00 equiv) dropwise with stirring at 0°C. The resulting solution was stirred for 2 hr at 0°C. The resulting mixture was concentrated under vacuum to afford 6-bromo-2-fluoro-3-(trifluoromethyl)benzamide.

Step D: 6-bromo-2-fluoro-3-(trifluoromethyl)benzonitrile

Into a 10000-mL 4-necked round-bottom flask, was placed 6-bromo-2-fluoro-3-

(trifluoromethyl)benzamide (400 g, 1.40 mol, 1.00 equiv), trichloro-l,3,5-triazine (1807 g, 9.80 mol, 7.00 equiv), N,N-dimethylformamide (4000 mL). The resulting solution was stirred for 12 hr at 25°C. The reaction was then quenched by pouring into 10000 mL of water/ice. The solids were collected by filtration and dried in an oven under reduced pressure to afford the title compound. Step E: 2-(benzylsulfanyl)-6-bromo-3-(trifluoromethyl)benzonitrile

Into a 10000-mL 4-necked round-bottom flask purged and maintained with an inert atmosphere of nitrogen, was placed 6-bromo-2-fluoro-3-(trifluoromethyl)benzonitrile (300 g, 1.12 mol, 1.00 equiv), 1,4-dioxane (3000 mL). To the above was added sodium hydride (138 g, 5.75 mol, 1.20 equiv) at 0°C. This was followed by the addition of BnSH (138 g) dropwise with stirring at 0°C. The resulting solution was stirred for 2 hr at 25°C. The reaction was then quenched by pouring into 1000 mL of water/ice. The resulting solution was extracted with 3x1000 mL of ethyl acetate and the organic layers combined and concentrated under vacuum to afford the title compound.

Step F: 5-[2-(benzylsulfanyl)-6-bromo-3-(trifluoromethyl)phenyl]-lH- l,2,3,4-tetrazole

Into a 3000-mL 4-necked round-bottom flask purged and maintained with an inert atmosphere of nitrogen, was placed 2-(benzylsulfanyl)-6-bromo-3-(trifluoromethyl)benzonitrile (100 g, 269 mmol, 1.00 equiv), toluene (1000 mL), azidotrimethylsilane (77.5 g, 673 mmol, 2.50 equiv), Bu ₂ SnS0 ₂ (13.4 g). The resulting solution was stirred for 48 hr at 100°C. The resulting mixture was concentrated under vacuum providing the title compound.

Step G: 3-bromo-2-(lH-l,2,3,4-tetrazol-5-yl)-6-(trifluoromethyl)benz ene-l-sulfonyl chloride

Into a 3000-mL 4-necked round-bottom flask purged and maintained with an inert atmosphere of nitrogen, was placed 5-[2-(benzylsulfanyl)-6-bromo-3-(trifluoromethyl)phenyl]-lH- 1,2,3,4-tetrazole (240 g, 577.99 mmol, 1.00 equiv), AcOH (200 mL), water (200 mL). To the above was added NCS (160 g) in portions at RT. The resulting solution was stirred for 12 hr at 25°C. The resulting mixture was concentrated under vacuum to afford the title compound.

Step H: 3-bromo-2-(lH-l,2,3,4-tetrazol-5-yl)-6-(trifluoromethyl)benz ene-l-sulfonamide

Into a 5000-mL 4-necked round-bottom flask, was placed 3-bromo-2-(lH-l,2,3,4- tetrazol-5-yl)-6-(trifluoromethyl)benzene-l-sulfonyl chloride (200 g, 511 mmol, 1.00 equiv), ΝΗ ₄ ΟΗ (1200 mL), tetrahydrofuran (2000 mL). The resulting solution was stirred for 1 hr at 25°C. The resulting mixture was concentrated under vacuum to furnish the title compound.

Step I: 3 -bromo-N,N-bis [(4-methoxyphenyl)methyl]-2- [ 1 - [(4-methoxyphenyl)methyl] - 1H- l,2,3,4-tetrazol-5-yl]-6-(trifluoromethyl)benzene-l-sulfonam ide, and 3-bromo-N,N-bis[(4- methoxyphenyl)methyl]-2-[2-[(4-methoxyphenyl)methyl]-2H-l,2, 3,4-tetrazol-5-yl]-6- (trifluoromethyl)benzene- 1 -sulfonamide

Into a 10000-mL 4-necked round-bottom flask purged and maintained with an inert atmosphere of nitrogen, was placed 3-bromo-2-(lH-l,2,3,4-tetrazol-5-yl)-6- (trifluoromethyl)benzene-l -sulfonamide (230 g, 618.08 mmol, 1.00 equiv), potassium carbonate (276 g, 2.00 mol, 3.23 equiv), Nal (18.4 g), Bu ₄ NCl (34.0 g, 122 mmol, 0.20 equiv), chloroform (3800 mL, 1.00 equiv), l-(chloromethyl)-4-methoxybenzene (380 g, 2.43 mol, 3.93 equiv), water (2550 mL). The resulting solution was stirred for 12 hr at 55°C. The aqueous phase was extracted with 2x1000 mL of DCM. The mixture was dried over anhydrous sodium sulfate and concentrated under vacuum. The residue was applied onto a silica gel column with ethyl acetate/hexane (1 : 10). Purification afforded 3 -bromo-N,N-bis [(4-methoxyphenyl)methyl] -2- [ 1 -[(4- methoxyphenyl)methyl]-lH-l,2,3,4-tetrazol-5-yl]-6-(trifluoro methyl)benzene-l-sulfonamide, and 3 -bromo-N,N-bis [(4-methoxyphenyl)methyl] -2- [2- [(4-methoxyphenyl)methyl] -2H- 1 ,2,3 ,4-tetrazol- 5-yl]-6-(trifluoromethyl)benzene-l -sulfonamide.

LC-MS: (ES, m/z): 732 [Μ+Η] +.

H-NMR: (CDC13, 300Hz, ppm): δ 3.763 (9H, s), 3.820-3.872 (2H, d, J= 15.6), 4.402-4.454 (2H, d, J=15.6), 5.154-5.203 (1H, d, J= 14.7), 5.560-5.609 (lH,d, J= 14.7), 6.702-6.763 (6H, m), 6.912- 6.941 (4H, m), 7.109-7.138 (2H, m), 7.839-7.854 (2H, m). REFERENCE EXAMPLE 25

(3-[bis[(4-methoxyphenyl)methyl]sulfamoyl]-2-[l-[(4-metho xyphenyl)methyl]-lH-l,2,3,4-tetrazol- 5-yl]-4-(trifluoromethyl)phenyl)boronic acid and (3-[bis[(4-methoxyphenyl)methyl]sulfamoyl]-2- [2-[(4-methoxyphenyl)methyl]-2H-l,2,3,44etrazol-5-yl]-4-(tri fluoromethyl)phenyl)boronic acid

Into a 1 L 4-necked round-bottom flask purged and maintained with an inert atmosphere of nitrogen, was placed a mixture of 3-bromo-N,N-bis[(4-methoxyphenyl)methyl]-2- [ 1 -[(4-methoxyphenyl)methyl]- 1H- 1 ,2,3 ,4-tetrazol-5-yl]-6-(trifluoromethyl)benzene- 1 - sulfonamide and 3-bromo-N,N-bis[(4-methoxyphenyl)methyl]-2-[2-[(4-methoxyphe nyl)methyl]- 2H-l,2,3,4-tetrazol-5-yl]-6-(trifluoromethyl)benzene-l-sulfo namide (REFERENCE EXAMPLE 24, 120 g, 163.81 mmol, 1.00 equiv), 1,4-dioxane (360 mL), 2-(5,5-dimethyl-l,3,2- dioxaborinan-2-yl)-5,5-dimethyl-l,3,2-dioxaborinane (111 g, 491 mmol, 3.00 equiv), KOAc (80.3 g, 818 mmol, 5.00 equiv), 2-2-[chloro(triphenyl- ^A 5- phosphanylidene)palladio]phenylaniline (9.4 g, 16.42 mmol, 0.10 equiv). The resulting solution was stirred for 6 hr at 60°C. The resulting solution was diluted with 500 mL of CH ₃ CN. The solids were filtered out. The filtrate was concentrated under vacuum. The crude product was purified by Flash-Prep-HPLC with the following conditions (CombiFlash-1): Column, CI 8 silica gel; mobile phase, CH ₃ CN/H ₂ 0=1:2 increasing to CH ₃ CN/H ₂ 0=2: 1 within 25 min, and then CH ₃ CN/H ₂ 0=2: 1 within 25 min, and then CH ₃ CN/H ₂ O=l:0 within 10 min; Detector, UV 210 nm. This afforded (3-[bis[(4-methoxyphenyl)methyl]sulfamoyl]-2-[l-[(4- methoxyphenyl)methyl]-lH-l,2,3,4-tetrazol-5-yl]-4-(trifluoro methyl)phenyl)boronic acid and (3- [bis[(4-methoxyphenyl)methyl]sulfamoyl]-2-[2-[(4-methoxyphen yl)methyl]-2H-l,2,3,4-tetrazol- 5-yl]-4-(trifluoromethyl)phenyl)boronic acid.

LC-MS: (ES, m/z): 698 [M+H]+

H-NMR: (300MHz, DMSO, ppm): δ 3.616-3.860 (11H, m), 3.860 (0.855H, s), 4.459-4.511 (1.492H, m),5.172 (1.335H, s) , 5.877 (0.403H, s), 6.733-6.827 (10H, m), 7.199-7.306 (2 H, 8.456 (1.2H, m). REFERENCE EXAMPLE 26

2-( 1 -(4-methoxybenzyl)- lH-tetrazol-5-yl)-4'-(piperidin-4-yl)- [1,1 '-biphenyl] -3 -sulfonamide and 2- (2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-4'-(piperidin-4-yl)-[ l,r-biphenyl]-3-sulfonamide

Step A: tert-butyl 4-(2'-(l-(4-methoxybenzyl)-lH-tetrazol-5-yl)-3'-sulfamoyl-[l ,l'- biphenyl]-4-yl)piperidine- 1 -carboxylate and tert-butyl 4-(2'-(2-(4-methoxybenzyl)-2H-tetrazol-5- yl)-3'-sulfamoyl-[l,r-biphenyl]-4-yl)piperidine-l-carboxylat e: tert-Butyl 4-(4-(4,4,5,5-tetramethyl- 1, 3, 2-dioxaborolan-2-yl)phenyl)piperidine-l -carboxylate (3.29 g, 8.49 mmol), 3-bromo-2-(l-(4- methoxybenzyl)-lH-tetrazol-5-yl)benzenesulfonamide (and the PMB tetrazole isomer, 3 g, 7.07 mmol), Na ₂ C0 ₃ (1.499 g, 14.14 mmol), PdCl ₂ (dppf) (0.517 g, 0.707 mmol) was placed in a reaction vessel, and to this was added 1,4-Dioxane (35.4 mL) and water (11.8 mL). N ₂ was bubbled through the mixture for 20 min. The mixture was then heated at 95°C overnight. The reaction mixture was diluted with EtOAc and washed with water. The organic layer was concentrated and the crude product was purified by column chromatography (0% EtOAc/hexane to 100% EtOAc/Hexane gradient) to give the product. LC/MS (M+H) ⁺ : 605.5.

Step B : 2-( 1 -(4-methoxybenzyl)- lH-tetrazol-5-yl)-4'-(piperidin-4-yl)-[ 1 , 1 '-biphenyl]-3- sulfonamide and 2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-4'-(piperidin-4-yl) -[l,l'-biphenyl]-3- sulfonamide: tert-Butyl 4-(2'-( 1 -(4-methoxybenzyl)- lH-tetrazol-5-yl)-3 '-sulfamoyl-[ 1 , 1 '-biphenyl]-

4- yl)piperidine- 1 -carboxylate and tert-butyl 4-(2'-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-3'- sulfamoyl-[l,l'-biphenyl]-4-yl)piperidine-l-carboxylate (2.95 g, 4.88 mmol) was dissolved in DCM (20 mL) and then treated with TFA (10 mL). The reaction mixture was stirred at RT for 2 hr. The mixture was concentrated and co-evaporated with DCM and toluene to afford the title compound as a mixture of two isomers.

REFERENCE EXAMPLE 27

3-(2-bromobenzo[d]thiazol-4-yl)-N,N-bis(4-methoxybenzyl)- 2-(l-(4-methoxybenzyl)-lH-tetrazol-

5- yl)benzenesulfonamide and 3-(2-bromobenzo[d]thiazol-4-yl)-N,N-bis(4-methoxybenzyl)-2-( 2-(4- methoxybenzyl)-2H-tetrazol-5-yl)benzenesulfonamide

Step A: 3-(2-aminobenzo[if|thiazol-4-yl)-N,N-bis(4-methoxybenzyl)-2- (l-(4- methoxybenzyl)- lH-tetrazol-5-yl)benzenesulfonamide and 3 -(2-aminobenzo[<i]thiazol-4-yl)-N,N- bis(4-methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl )benzenesulfonamide:

4-Bromobenzo[d]thiazol-2-amine (600 mg, 2.62 mmol), a mixture of (3-(N,N-bis(4- methoxybenzyl)sulfamoyl)-2-(l-(4-methoxybenzyl)-lH-tetrazol- 5-yl)phenyl)boronic acid and (3- (N,N-bis(4-methoxybenzyl)sulfamoyl)-2-(2-(4-methoxybenzyl)-2 H-tetrazol-5-yl)phenyl)boronic acid (2473 mg, 3.93 mmol), 2nd Generation Xphos Precatalyst (309 mg, 0.393 mmol), CS2CO ₃ (2560 mg, 7.86 mmol) was placed in a reaction vessel, and 1,4-Dioxane (1.40E+04 μΐ) and Water (3492 μΐ) were added. 2 was bubbled through the mixture for 20 min. The mixture was then heated at 85°C for 20 hr. The crude product was directly loaded onto a silica gel column and purified by column chromatography (100% EtOAc to 20% MeOH/EtOAc gradient). LC/MS (M+H) ⁺ : 734.

Step B : 3 -(2-bromobenzo [d]thiazol-4-yl)-N,N-bis(4-methoxybenzyl)-2-( 1 -(4- methoxybenzyl)-lH-tetrazol-5-yl)benzenesulfonamide and 3-(2-bromobenzo[d]thiazol-4-yl)-N,N- bis(4-methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl )benzenesulfonamide:

The isomer mixture from Step A (1.56 g, 2.126 mmol) was added portionwise to a solution of Copper(II) Bromide (0.570 g, 2.55 mmol) and Tert-Butyl Nitrite (0.351 g, 3.40 mmol) in

Acetonitrile (7.87 mL) at rt under N ₂ . The mixture was stirred for 30 min. The mixture was diluted with IN HQ solution and extracted with EtOAc. After concentration of the organic extract, the crude product was purified by column chromatography (100% hexane to 50% EtOAc/Hexane gradient) to give the title compound. LC/MS (M+H) ⁺ : 797, 799.

REFERENCE EXAMPLE 28

3-(6-bromopyridin-3-yl)-N,N-bis(4-methoxybenzyl)-2-(2-(4-met hoxybenzyl)-2H-tetrazol-5- yl)benzenesulfonamide and 3-(6-bromopyridin-3-yl)-N,N-bis(4-methoxybenzyl)-2-(l-(4- methoxybenzyl)-lH-tetrazol-5-yl)benzenesulfonamide

Step A: 3-(6-aminopyridin-3-yl)-N,N-bis(4-methoxybenzyl)-2-(2-(4-met hoxybenzyl)-2H- tetrazol-5-yl)benzenesulfonamide and 3 -(6-aminopyridin-3 -yl)-N,N-bis(4-methoxybenzyl)-2-( 1 -(4- methoxybenzyl)-lH-tetrazol-5-yl)benzenesulfonamide:

To a mixture of 5-(4,4,5,5-tetramethyl-l,3,2-dioxaborolan-2-yl)pyridin-2-ami ne

(6.64 g, 30.2 mmol), and a mixture of 3-bromo-N,N-bis(4-methoxybenzyl)-2-(l-(4- methoxybenzyl)- lH-tetrazol-5-yl)benzenesulfonamide and 3-bromo-N,N-bis(4-methoxybenzyl)- 2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)benzenesulfonamide (10.0 g, 15.1 mmol) and a ₂ C0 ₃ (4.80 g, 45.2 mmol) in 1,4,-dioxane (100 mL) and water (25 mL) was added Pd(dppf)Cl ₂ (0.17 g, 0.15 mmol) and the mixture was stirred at 80°C overnight. The resulting mixture was filtered, the filtrate was concentrated in vacuo, the residue was diluted with water and extracted with EtOAc (100 mL x 3), the combined organic phase was dried over anhydrous sodium sulfate, filtered and the filtrate was concentrated in vacuo, the residue was purified with column purification procedure (PE: EA=1 : 1) to give the title compound. MS (ESI): m/z (M+H)+ 678.2 Step B: 3-(6-bromopyridin-3-yl)-N,N-bis(4-methoxybenzyl)-2-(2-(4-met hoxybenzyl)-2H- tetrazol-5-yl)benzenesulfonamide and 3 -(6-bromopyridin-3 -yl)-N,N-bis(4-methoxybenzyl)-2-( 1 -(4- methoxybenzyl)-lH-tetrazol-5-yl)benzenesulfonamide:

To a solution of 3-(6-aminopyridin-3-yl)-N,N-bis(4-methoxybenzyl)-2-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)benzenesulfonamide and 3-(6-aminopyridin-3-yl)-N,N-bis(4- methoxybenzyl)-2-(l-(4-methoxybenzyl)-lH-tetrazol-5-yl)benze nesulfonamide (5.0 g, 7.5 mmol) and benzyltrimethylammonium bromide (7.72 g, 33.7 mmol) in dibromomethane (75 mL) was added tert-butylnitrite (7.72 g, 75.0 mmol) at room temperature. The mixture was stirred at room temperature overnight. The resulting mixture was concentrated in vacuo, the residue was diluted with water and extracted with DCM (50 mL * 3), the combined organic phase was dried over anhydrous sodium sulfate, filtered and the filtrate was concentrated in vacuo, the residue was purified with column purification procedure (PE: EA=30: 1) to give the title compound.

1HNMR HL00386-012-1 (CDC1 ₃ , 400MHz): δ 8.15 (d, J = 7.6 Hz, 1H), 7.68-7.69 (m, 2H), 7.49 (d, J = 8.0 Hz, 1H), 6.97-7.14 (m, 6H), 6.65-6.74 (m, 8H), 5.46 (d, J = 15.2 Hz, 1H), 4.90 (d, J = 15.2 Hz, 1H), 4.15 (d, J = 15.2 Hz, 2H), 3.96 (d, J = 15.2 Hz, 2H ), 3.74-3.81 (m, 9H). MS (ESI): m/z (M+H)+ 741.1, 743.1.

REFERENCE EXAMPLE 29

6-bromo-3-iodo-N,N-bis(4-methoxybenzyl)-2-(l-(4-methoxybenzy l)-lH-tetrazol-5- yl)benzenesulfonamide and 6-bromo-3-iodo-N,N-bis(4-methoxybenzyl)-2-(2-(4-methoxyb(

-tetrazol-5-yl)benzenesulfonamide

Step A: 3-bromo-2-fluoro-6-iodobenzoic acid

Into a 5000-mL 4-necked round-bottom flask purged and maintained with an inert atmosphere of nitrogen, was placed bis(propan-2-yl)amine (121.2 g, 1.20 mol, 1.20 equiv), tetrahydrofuran (1000 mL). This was followed by the addition of butyllithium (440 mL, 1.10 equiv, 2.5 Ν) dropwise with stirring at -78°C in 20 min. 60 min later, to this was added a solution of l-bromo-2-fluoro-4-iodobenzene (300 g, 997 mmol, 1.00 equiv) in tetrahydrofuran (2000 mL) dropwise with stirring at -78°C in 30 min. The resulting solution was stirred for 2 hr at -78°C in a liquid nitrogen bath. The reaction progress was monitored by LCMS. The reaction was then quenched by pouring into 5000 g of dry ice. After stirring for 2 hours, the resulting mixture was concentrated under vacuum. The residue was dissolved in 3000 mL of 4Ν sodium hydroxide. The resulting solution was extracted with 2x1000 mL of ether and the aqueous layers combined. The pH value of the solution was adjusted to 2-3 with hydrogen chloride (1 mmol/L). The resulting solution was extracted with 4x1000 mL of ethyl acetate and the organic layers combined and dried over anhydrous sodium sulfate and concentrated under vacuum. The crude product was purified by re-crystallization from Hexane.

Step B: 3-bromo-2-fluoro-6-iodobenzoyl

Into a 5000-mL 3 -necked round-bottom flask purged and maintained with an inert atmosphere of nitrogen, was placed 3-bromo-2-fluoro-6-iodobenzoic acid (273 g, 791.52 mmol, 1.00 equiv), tetrahydrofuran (2730 mL), Ν,Ν-dimethylformamide (27.3 mL). This was followed by the addition of (COCl) ₂ (1 10.9 g, 1.10 equiv) dropwise with stirring at 20°C in 20 min. The resulting solution was stirred for 1 hr at room temperature. The reaction progress was monitored by LCMS. The resulting mixture was concentrated under vacuum.

Step C: 3-bromo-2-fluoro-6-iodobenzamide

Into a 5000-mL 4-necked round-bottom flask purged and maintained with an inert atmosphere of nitrogen, was placed NH ₄ OH (1200 g). This was followed by the addition of a solution of 3-bromo-2-fluoro-6-iodobenzoyl chloride (280 g, 771 mmol, 1.00 equiv) in tetrahydrofuran (2800 mL) dropwise with stirring at 0°C in 30 min. The resulting solution was stirred for 1 hr at room temperature. The reaction progress was monitored by LCMS. The resulting mixture was concentrated under vacuum. The solids were collected by filtration, washed with H ₂ 0 to afford the title compound.

Step D: 3-bromo-2-fluoro-6-iodobenzonitrile

Into a 10000-mL 4-necked round-bottom flask purged and maintained with an inert atmosphere of nitrogen, was placed 3-bromo-2-fluoro-6-iodobenzamide (270 g, 785.07 mmol, 1.00 equiv), N,N-dimethylformamide (5400 mL). This was followed by the addition of trichloro-l,3,5-triazine (1014 g, 5.50 mol, 7.00 equiv), in portions at 0°C. The resulting solution was stirred for 2 hr at room temperature. The reaction progress was monitored by LCMS. The reaction was then quenched by the addition of 15000 mL of sodium bicarbonate aq. The solids were collected by filtration to afford the title compound.

Step E: 2-(benzylsulfanyl)-3-bromo-6-iodobenzonitrile

Into a 5000-mL 4-necked round-bottom flask purged and maintained with an inert atmosphere of nitrogen, was placed sodium hydride (34 g, 852 mmol, 1.20 equiv, 60%), 1,4- dioxane (700 mL). This was followed by the addition of a solution of phenylmethanethiol (88.7 g, 714.15 mmol, 1.00 equiv) in 1,4-dioxane (950 mL) dropwise with stirring at 10°C in 15 min. 30 min later, to this was added a solution of 3-bromo-2-fluoro-6-iodobenzonitrile (230 g, 705.73 mmol, 1.00 equiv) in 1,4-dioxane (1800 mL) dropwise with stirring at 10°C. The resulting solution was stirred for 2 hr at room temperature. The reaction progress was monitored by LCMS. The reaction was then quenched by pouring into 5000 mL of water/ice. The resulting solution was extracted with 5x1000 mL of ethyl acetate and the organic layers combined. The resulting mixture was washed with 2x1000 mL of water and 2x1000 mL of sodium bicarbonate and 2x1000 mL of sodium chloride. The mixture was dried over anhydrous sodium sulfate and concentrated under vacuum. The crude product was purified by re-crystallization from ether to afford the title compound.

Step F: 5-[2-(benzylsulfanyl)-3-bromo-6-iodophenyl]-lH-l,2,3,4-tetra zole

Into a 2000-mL 4-necked round-bottom flask, was placed 2-(benzylsulfanyl)-3- bromo-6-iodobenzonitrile (66 g, 153.45 mmol, 1.00 equiv), toluene (660 mL),

azidotrimethylsilane (44.2 g, 383.65 mmol, 2.50 equiv), dibutylstannanone (7.7 g, 30.93 mmol, 0.20 equiv). The resulting solution was stirred for 48 hr at 105°C in an oil bath. The reaction progress was monitored by LCMS. The reaction mixture was cooled to room temperature. The resulting mixture was concentrated under vacuum. The residue was purified by silica gel column with tetrahydrofuran:PE (100: 1) to afford the title compound.

Step G: 6-bromo-3-iodo-2-(lH-l,2,3,4-tetrazol-5-yl)benzene-l-sulfony l chloride

Into a 2000-mL 3 -necked round-bottom flask purged and maintained with an inert atmosphere of nitrogen, was placed 5-[2-(benzylsulfanyl)-3-bromo-6-iodophenyl]-lH-l,2,3,4- tetrazole (1 15.6 g, 244.33 mmol, 1.00 equiv), acetic acid (1 156 mL), water(l 15.6 mL), NCS (81.74 g, 612.15 mmol, 2.50 equiv). The resulting solution was stirred overnight at room temperature in an ice/salt bath. The reaction progress was monitored by LCMS. The resulting mixture was concentrated under vacuum to afford the title compound.

Step H: 6-bromo-3-iodo-2-(lH-l,2,3,4-tetrazol-5-yl)benzene-l-sulfona mide

Into a 3000-mL 4-necked round-bottom flask purged and maintained with an inert atmosphere of nitrogen, was placed ΝΗ ₄ ΟΗ (1180 mL), tetrahydrofuran (290 mL). This was followed by the addition of a solution of 6-bromo-3-iodo-2-(lH-l,2,3,4-tetrazol-5-yl)benzene-l- sulfonyl chloride (1 18 g, 262.54 mmol, 1.00 equiv) in tetrahydrofuran (300 mL) dropwise with stirring at 0°C. The resulting solution was stirred for 2 hr at 0-25°C in an ice/salt bath (slowly warming to RT). The reaction progress was monitored by LCMS. The resulting mixture was concentrated under vacuum. The resulting solution was diluted with 500 mL of ether. After stirring for 30 min, the solids were collected by filtration to afford the title compound.

Step I: 6-bromo-3-iodo-N,N-bis[(4-methoxyphenyl)methyl]-2-[l-[(4- methoxyphenyl)methyl] - 1 H- 1 ,2,3 ,4-tetrazol-5-yl]benzene- 1 -sulfonamide and 6-bromo-3 -iodo- N,N-bis[(4-methoxyphenyl)methyl]-2-[2-[(4-methoxyphenyl)meth yl]-2H-l,2,3,4-tetrazol-5- yljbenzene- 1 -sulfonamide Into a 3000-mL 4-necked round-bottom flask purged and maintained with an inert atmosphere of nitrogen, was placed 6-bromo-3-iodo-2-(lH-l,2,3,4-tetrazol-5-yl)benzene-l- sulfonamide (105 g, 244.17 mmol, 1.00 equiv), chloroform (1050 mL), potassium carbonate (168.9 g, 1.22 mol, 5.00 equiv), water (525 mL), Nal (1 1 g, 0.30 equiv), tetrabutyl(chloro)amine (20.4 g, 73.40 mmol, 0.30 equiv), l-(chloromethyl)-4-methoxybenzene (230 g, 1.47 mol, 6.00 equiv). The resulting solution was stirred overnight at 50°C in an oil bath. The reaction progress was monitored by LCMS. The reaction mixture was cooled to room temperature. The resulting solution was extracted with 2x1000 mL of dichloromethane and the organic layers combined and dried over anhydrous sodium sulfate and concentrated under vacuum to afford the title compounds.

LC-MS: (ES, m/z): 790 [M+H] ⁺

H-NMR: (300MHz, CDC1 ₃ , ppm): δ 7.956-7.928 (m, 0.5H), 7.852-7.824 (m, 1H), 7.656-7.612 (m, 1.5H), 7.323-7.282 (m, 1.5H), 7.195-7.224 (m, 2H), 6.944-6.908 (m, 6H), 6.822-6.760 (m, 9H), 5.791 (m, 1H), 5.570-5.521 (m, 1H), 5.149-5.100 (m, 1H), 4.769-4.718 (m, 2H), 4.232- 4.221 (m, 2H), 3.900-3.848 (m, 2H), 3.789-3.742 (m, 14H).

REFERENCE EXAMPLE 30

tert-butyl 4- -iodoethyl)piperidine- 1 -carboxylate

Step A : tert-butyl 4-(2-hydroxyethyl)piperidine- 1 -carboxylate

To a stirred solution of l-(tert-butoxycarbonyl)piperidine-4-carboxylic acid (2.00 g, 8.72 mmol) in THF (20 mL), a solution of borane (1 M) in THF (8.72 mL) was added dropwise at 0°C. The resulting mixture was stirred for 6 hr at ambient temperature and then quenched with water (20 mL), extracted with EtOAc (2 x 40 mL). The combined organic layers were washed with brine (2 x 30 mL), dried over anhydrous Na ₂ S0 ₄ and concentrated under reduced pressure to afford tert-butyl 4-(hydroxymethyl)piperidine- 1 -carboxylate which was used in the next step directly. LCMS (ESI) calc'd for Ci ₂ H ₂₃ 03 [M + H] ⁺ : 230, found 230.

Step B : tert-butyl 4-(2-iodoethyl)piperidine- 1 -carboxylate

To a stirred mixture of tert-butyl 4-(hydroxymethyl)piperidine- 1 -carboxylate (1.80 g, 8.36 mmol), triphenylphosphine (2.63 g, 10.0 mmol) and lH-imidazole (0.68 g, 10.03 mmol) in THF (30 mL) was added dropwise a solution of I ₂ (2.55 g, 10.03 mmol) in THF (10 mL) at 0°C. The resulting mixture was stirred 12 hr at ambient temperature and then quenched with water (50 mL), extracted with EtOAc (3 x 50 mL). The combined organic layers were washed with a ₂ S0 ₃ (aq.) (2 x 50 mL), dried over anhydrous Na ₂ S0 ₄ and concentrated under vacuum. The residue was purified by silica gel chromatography, eluted with EtOAc/PE (1/5). The combined organic fractions were concentrated under reduced pressure to afford tert-butyl 4- (iodomethyl)piperidine-l -carboxylate: LCMS (ESI) calc'd for: C11H2 ₀ INO2 [M + H] ⁺ : 326, found 326; 'H NMR (400 MHz, CDC1 ₃ ): δ 4.10-4.07 (m, 2H), 3.23-3.19 (m, 2H), 2.73-2.66 (m, 2H), 1.80-1.75 (m, 2H), 1.67-1.58 (m, 3H), 1.57 (s, 9H), 1.15-1.08 (m, 2H).

REFERENCE EXAMPLES 31A, 3 IB

(R)-tert-butyl 3 -amino-3-(4-bromophenyl)pyrrolidine-l -carboxylate and (5)-tert-butyl 3-amino- 3 -(4-bromophenyl)pyrrolidin - 1 -carboxylate

Step A : Synthesis of tert-butyl 3 -(4-bromophenyl)-3 -hydroxypyrrolidine- 1 -carboxylate

To a stirred solution of l-bromo-4-iodobenzene (20.00 g, 70.70 mmol) in THF

(320 mL) was added dropwise w-butyllithium (30 mL, 75 mmol, 2.5 M in THF) at -78°C. After the resulting mixture was stirred at -78°C for 1 hr, a solution of tert-butyl 3-oxopyrrolidine-l- carboxylate (19.64 g, 0.1 1 mol) in THF (20 mL) was added dropwise. The resulting mixture was stirred at -78°C for 2 hr and then it was quenched with water (50 mL), diluted with water (200 mL) and extracted with EtOAc (3 x 200 mL). The combined organic layers were washed with brine (3 x 100 mL), dried over anhydrous Na ₂ S0 ₄ and concentrated under vacuum. The residue was purified by silica gel column chromatography, eluted with EtOAc/PE (1/1) to afford tert- butyl 3-(4-bromophenyl)-3-hydroxypyrrolidine-l-carboxylate: LCMS (ESI) calc'd for

Ci ₅ H ₂ oBrN0 ₃ [M -56 : 268, 270 (1 : 1), found: 268, 270 (1 : 1); 'H NMR (300 MHz, DMSO- d ₆ ): δ 7.52 (d, J= 6.6 Hz, 2H), 7.46 (d, J= 6.6 Hz, 2H), 3.62-3.39 (m, 3H), 2.25-2.01 (m, 3H), 1.42(s,9H).

Step B : Synthesis of tert-butyl 3-(4-bromophenyl)-3-(2-chloroacetamido)pyrrolidine-l- carboxylate

To a stirred mixture of tert-butyl 3 -(4-bromophenyl)-3 -hydroxypyrrolidine- 1- carboxylate (5.00 g, 14.61 mmol) in 2-chloroacetonitrile (55 g, 0.73 mmol) was added dropwise sulfuric acid (3 mL, 14.61 mmol) at 0°C. The resulting mixture was stirred for 1 hr at ambient temperature and then concentrated under vacuum. The residue was added to the ice/water and the pH of the solution was adjusted to 8 with saturated a ₂ C0 ₃ . Methanol (10 mL) and di-tert- butyl dicarbonate (4.78 g, 21.92 mmol) were added to the mixture. The resulting mixture was stirred for 1 hr and then extracted with EtOAc (3 x 100 mL). The combined organic phases were dried over anhydrous a ₂ S0 ₄ , concentrated under vacuum. The residue was purified by silica gel column chromatography, eluted with EtOAc/PE (1/2) to afford 1.50 g (25%) of tert-butyl 3- (4-bromophenyl)-3-(2-chloroacetamido) pyrrolidine- 1-carboxylate as a yellow solid: LCMS (ESI) calc'd for Ci ₇ H ₂₂ BrClN ₂ 0 ₃ [M -56 : 363, found: 363.

Step C: Synthesis of (R)-tert-butyl 3 -amino-3-(4-bromophenyl)pyrrolidine- 1-carboxylate and (5)-/er/-butyl 3 -amino-3-(4-bromophenyl)pyrrolidine- 1-carboxylate

To a stirred mixture of tert-butyl 3-(4-bromophenyl)-3-(2-chloroacetamido) pyrrolidine- 1-carboxylate (1.50 g, 3.59 mmol) in EtOH (10 mL) were added thiourea (2.73 g, 35.90 mmol), acetic acid (0.43 g, 7.18 mmol) at ambient temperature. The resulting mixture was stirred at 120°C for 6 hr and then concentrated under vacuum. The residue was diluted with DCM (20 mL). The solids were filtered out and the filtrate was concentrated. The residue was purified by silica gel column chromatography, eluted with EtOAC/PE(5/l) to afford 0.30 g (25%) of tert-butyl 3 -amino-3-(4-bromophenyl)pyrrolidine- 1-carboxylate as a brown oil. The product was purified by Chiral-Prep-HPLC with the following conditions: Column, Chiralpak IA, 2 x 25 cm, 5 μιη; Mobile phase: Hex and ethanol (hold 40.0% ethanol in 30 min); Detector: UV 254/220 nm. The collected fractions were concentrated to afford (R)-tert-butyl 3-amino-3- (4-bromophenyl)pyrrolidine- 1-carboxylate (faster eluting, stereochemistry arbitrarily assigned): LCMS (ESI) calc'd for C ₁₅ H ₂₁ BrN ₂ 0 ₂ [M + H] ⁺ : 341, 343 (1 : 1), found: 341, 343 (1 : 1); ^X H NMR (300 MHz, CDC1 ₃ ): δ 7.50 (d, J= 8.7 Hz, 2H), 7.33 (d, J= 8.4 Hz, 2H), 3.85-7.51 (m, 4H), 2.28-2.25 (br, 2H), 1.46 (s, 9H) and (5)-tert-butyl 3-amino-3-(4-bromophenyl)pyrrolidine- 1-carboxylate as a yellow solid (slower eluting, stereochemistry arbitrarily assigned): LCMS (ESI) calc'd for Ci ₅ H ₂₁ BrN ₂ 0 ₂ [M + H] ⁺ : 341, 343 (1 : 1), found: 341, 343 (1 : 1); ^X H NMR (300 MHz, CDC1 ₃ ): δ 7.49 (d, J= 6.4 Hz, 2H), 7.32 (d, J= 7.8 Hz, 2H), 3.78-3.52 (m, 4H), 2.26-2.21 (m, 2H), 1.46 (s, 9H). REFERENCE EXAMPLE 32

-butyl 3-(3'-(N,N-bis(4-methoxybenzyl)sulfamoyl)-4'-bromo-2'-(2-(4- methoxybi

tetrazol-5-yl)biphenyl-4-yl)azetidine- 1 -carboxylate

Step A : Synthesis of tert-butyl 3 -(4-bromophenyl)azetidine- 1 -carboxylate

To a stirred solution of (4-bromophenyl)boronic acid (2.13 g, 10.60 mmol) in 2- Propanol (20 mL) was added tert-butyl-3-iodoazetidine-l -carboxylate (2.00 g, 7.06 mmol) at ambient temperature. To the mixture was added (lS,25)-2-aminocyclohexanol (0.08 g, 0.71 mmol), nickel (II) iodide (0.22 g, 0.71 mmol) and sodium bis(trimethylsilyl)amide (7.06 mL, 1.0 mol/L) under nitrogen. After the resulting mixture was stirred for 30 min at ambient temperature, it was irradiated with microwave radiation at 80°C for 1 hr. The reaction was quenched with water (25 mL), extracted with EtOAc (3 x 150 mL). The combined organic layers were washed with brine (2 x 100 mL), dried over anhydrous Na ₂ S0 ₄ and concentrated under vacuum. The residue was purified by silica gel chromatography, eluted with EtOAc/PE (1/10) to afford the title compound: LCMS (ESI) calc'd for Ci ₄ H ₁₈ BrN0 ₂ [M + H] ⁺ : 312, 314 (1 : 1), found 312, 314 (1 : 1);

Step B: Synthesis of tert-butyl 3-(4-(4,4,5,5-tetramethyl-l,3,2-dioxaborolan-2- yl)phenyl)azetidine- 1 -carboxylate

To a stirred mixture of 4,4,4',4',5,5,5',5'-octamethyl-2,2'-bi(l,3,2-dioxaborolane) (3.40 g, 13.45 mmol) and potassium acetate (3.30 g, 33.60 mmol) in DMF (35 mL) were added tert-butyl-3-(4-bromophenyl)azetidine-l -carboxylate (3.50 g, 11.20 mmol) and Pd(dppf)Ci2 adduct CH2CI2 (0.92 g, 1.12 mmol) at ambient temperature under nitrogen. The resulting mixture was degassed for two times under nitrogen and then stirred at 110°C for 16 hr. The reaction was quenched with water (25 mL) and extracted with EtOAc (2 x 150 mL). The combined organic layers were washed with brine (2 x 100 mL), dried over anhydrous Na ₂ S0 ₄ and concentrated under vacuum. The residue was purified by silica gel chromatography, eluted with EtOAc/PE (1/10) to afford the title compound: LCMS (ESI) calc'd for C ₂ oH ₃ oN0 ₄ [M + H] ⁺ : 360, found 360; Step C : Synthesis of tert-butyl 3-(3'-(N,N-bis(4-methoxybenzyl)sulfamoyl)-4'-bromo-2'- (2-(4-methoxybenzyl)-2H-tetrazol-5-yl)biphenyl-4-yl)azetidin e-l-carboxylate

A degassed solution of 6-bromo-3-iodo-N,N-bis -(4-methoxybenzyl)-2-(l-(4- methoxybenzyl)-lH-tetrazol-5-yl)benzenesulfonamide (1.60 g, 3.20 mmol), tert-butyl 3-(4- (4,4,5,5-tetramethyl-l,3,2-dioxaborolan-2-yl)phenyl)azetidin e-l-carboxylate (1.30 g, 3.50 mmol), Na ₂ C0 ₃ (1.00 g, 9.50 mmol) and Pd(PPh ₃ ) ₄ (0.37 g, 0.32 mmol) in 1,4-dioxane (50 mL) and water (5 mL) was stirred at 80°C for 16 hr under nitrogen. The resulting mixture was cooled down to ambient temperature and filtered. The filtrate was concentrated under vacuum. The residue was purified by silica gel chromatography, eluted with EtOAC/PE (1/2) to afford the title compound: LCMS (ESI) calc'd for C45H47N6O7S [M + H] ⁺ : 895, 897 (1 : 1), found 895, 897 (1 : 1); ^X H NMR (400 MHz, CDC1 ₃ ): δ 8.08-8.00 (m, 1H), 7.43 (d, J= 8.4 Hz, 2H), 7.07 (d, J= 8.0 Hz, 1H), 7.02 (d, J= 8.8 Hz, 3H), 6.88-6.80 (m, 9H), 6.79-6.71 (m, 2H), 5.19-5.15 (m, 1H), 4.92- 4.88 (m, 1H), 4.82 (d, J= 9.2 Hz, 1H), 4.34-4.30 (m, 2H), 4.14-4.10 (m, 1H), 3.99-3.91 (m, 2H), 3.89-3.80 (m, 2H), 3.78 (s, 9H), 3.70-3.60 (m, 1H), 1.49 (s, 9H).

REFERENCE EXAMPLE 33

tert-butyl (( 1 r,4r)-4-(iodomethyl)cyclohexyl)methylcarbamate

BocHN — ' I

Step A : Synthesis of tert-butyl ((lr,4r)-4-(hydroxymethyl)cyclohexyl)methylcarbamate

Borane (7.77 mL, 15.5 mmol) was added dropwise to a stirred solution of (lr,4r)- 4-(((tert-butoxycarbonyl)amino)methyl)cyclohexanecarboxylic acid (2.0 g, 7.77 mmol) in THF (20 ml) at 0°C. After the reaction mixture was stirred for 6 hr at ambient temperature, it was quenched with water (20 mL) and extracted with EtOAc (2 x 40 mL). The combined organic layers were washed brine (2 x 30 mL), dried over anhydrous Na ₂ S0 ₄ and concentrated under vacuum to afford the title compound: ^X H NMR (400 MHz, CDC1 ₃ ) δ 4.60-4.50 (brs, 1H), 3.46 (d, J= 6.4 Hz, 2H), 3.01-2.98 (m, 2H), 1.90-1.82 (m, 4H), 1.81-1.80 (m, 1H ), 1.46 (brs, 9H), 1.45- 1.42 (m, 2H), 1.02-097(m, 4H).

Step B : Synthesis of tert-butyl ((lr,4r)-4-(iodomethyl)cyclohexyl)methylcarbamate

L (2.253 g, 8.88 mmol) in 10 mlTHF was added dropwise to a stirred mixture of tert-butyl (((lr,4r)-4-(hydroxymethyl)cyclohexyl)methyl)carbamate (1.8 g, 7.40 mmol), triphenylphosphine (2.328 g, 8.88 mmol) andlH-imidazole (0.604 g, 8.88 mmol) in THF (30 ml) at 0°C. The reaction mixture was stirred 12 hr at ambient temperature and then quenched with water (50 mL) and extracted with EtOAc (3 x 50 mL). The combined organic layers were washed with a ₂ S0 ₃ (aq.) ( 2 x 50 mL), dried over anhydrous Na ₂ S0 ₄ and concentrated under vacuum. The residue was purified by silica gel chromatography, eluted with EtOAc/PE (1/5) to give the title compound: ^X H NMR (400 MHz, CDC1 ₃ ) δ 4.70-4.60 (m, 1H), 3.10 (dd, J= 6.4 Hz, 2H), 2.99 (dd, J= 6.4 Hz, 2H), 1.94-1.92 (m, 2H), 1.80-1.78 (m, 2H), 1.45 (brs, 9H ), 1.42-1.39 (m, 2H), 1.04-0.97 (m,4H).

REFERENCE EXAMPLE 34

tert-butyl (4-(iodomethyl)cyclohexyl)methylcarbamate

BocHN — ' I

Step A: Synthesis of tert-butyl (4-(iodomethyl)cyclohexyl)methylcarbamate

Borane (7.77 mL, 15.5 mmol) was added dropwise to a stirred solution of 4- (((/er/-butoxycarbonyl)amino)methyl)cyclohexanecarboxylic acid (2.0 g, 7.77 mmol) in THF (20 ml) at 0°C. To the reaction mixture was stirred for 6 hr at ambient temperature and then quenched with water (20 mL) and extracted with EtOAc (2 x 40 mL). The combined organic layers were washed brine (2 x 30 mL), dried over anhydrous Na ₂ S0 ₄ and concentrated under vacuum to afford the title compound: ^X H NMR (400 MHz, CDC1 ₃ ) δ 4.70-4.60 (brs, 1H), 3.47 (dd, J= 6.0 Hz, 2H), 3.01-2.98 (m, 2H), 1.90-1.80 (m, 4H), 1.71-1.69 (m, 1H ), 1.46 (brs, 9H), 1.43-1.40 (m, 2H), 1.02-0.97 (m, 4H).

Step B : Synthesis of tert-butyl (4-(iodomethyl)cyclohexyl)methylcarbamate

I ₂ (2.253 g, 8.88 mmol) in 10 mlTHF was added dropwise to a stirred mixture of tert-butyl (((lr,4r)-4-(hydroxymethyl)cyclohexyl)methyl)carbamate (1.8 g, 7.40 mmol), triphenylphosphine (2.328 g, 8.88 mmol) andlH-imidazole (0.604 g, 8.88 mmol) in THF (30 ml) at 0°C. The reaction mixture was stirred 12 hr at ambient temperature and then quenched with water (50 mL) and extracted with EtOAc (3 x 50 mL). The combined organic layers were washed with Na ₂ S03 (aq.) (2 x 50 mL), dried over anhydrous Na ₂ S0 ₄ and concentrated under vacuum. The residue was purified by silica gel chromatography, eluted with EtOAc/PE (1/5) to give the title compound: ^X H NMR (400 MHz, CDC1 ₃ ) δ 4.70 - 4.60 (brs, 1H), 3.10 (dd, J= 6.4 Hz, 2H), 2.99 (dd, J= 6.4 Hz, 2H), 1.94 - 1.92 (m, 2H), 1.80 - 1.78 (m, 2H), 1.45 (brs, 9H), 1.42 - 1.40 (m, 2H), 1.04 - 0.97 (m, 4H).

REFERENCE EXAMPLE 35

tert-butyl ( 1 s,4s)-4-(iodomethyl)cyclohexylcarbamate

BocHN-

I

Step A: Synthesis of tert-butyl (ls,4s)-4-(hydroxymethyl)cyclohexylcarbamate

Borane (8.22 niL, 16.4 mmol) was added dropwise to a stirred solution of (ls,4s)- 4-((ter?-butoxycarbonyl)amino)cyclohexanecarboxylic acid (2.0 g, 8.22 mmol) in THF (20 ml) at 0°C. After the reaction mixture was stirred for 6 hr at room temperature, it was quenched with water (20 mL) and extracted with EtOAc (2 x 40 mL). The combined organic layers were washed brine (2 x 30 mL), dried over anhydrous Na ₂ S0 ₄ and concentrated under vacuum to afford the title compound which was used in the next step directly.

Step B: Synthesis of tert-butyl (ls,4s)-4-(iodomethyl)cyclohexylcarbamate

(2.125 g, 8.37 mmol) in 10 ml THF) was added dropwise to a stirred mixture of tert-butyl ((ls,4s)-4-(hydroxymethyl)cyclohexyl)carbamate (1.6 g, 6.98 mmol),

triphenylphosphine (2.196 g, 8.37 mmol) and IH-imidazole (0.570 g, 8.37 mmol) in THF (30 ml) at 0°C. The resulting mixture was stirred 12 hr at ambient temperature and then quenched with water (50 mL) and extracted with ethyl acacate (3 x 50 mL). The combined organic layers was washed with a ₂ S0 ₃ (aq.) (2 x 50 mL), dried over anhydrous Na ₂ S0 ₄ and concentrated under vacuum. The residue was purified by silica gel chromatography, eluted with EtOAc/PE (1/5) to the title compound: ¾ NMR (400 MHz, CDC1 ₃ ) δ 4.70 - 4.60 (brs, 1H), 3.80 - 3.70 (brs, 1H), 3.40 - 3.30 (m, 1H), 3.16 (dd, J= 6.0Hz, 1H), 1.98-1.80 (m, 1H), 1.80-1.70 (m, 2H), 1.60 - 1.50 (m, 4H ), 1.47 (brs, 9H), 1.34 - 1.30 (m, 2H).

REFERENCE EXAMPLE 36

ter/-butyl 4- -iodoethyl)cyclohexylcarbamate

Synthesis of /er/-butyl 4-(2-hydroxyethyl)cyclohexylcarbamate Borane (7.77 mL, 15.5 mmol) was added dropwise to a stirred solution of 2-(4-

((tert-butoxycarbonyl)amino)cyclohexyl)acetic acid (2.0 g, 7.8 mmol) in THF (20 mL) at 0°C. The resulting mixture was stirred for 6 hr at room temperature and then quenched with water (20 mL) and extracted with EtOAC (2 x 40 mL). The combined organic layers was washed brine ( 2 x 30 mL), dried over anhydrous sodium sulfate and filtered. The filtrate was concentrated under vacuum to afford the title compound, which was used in the next step directly.

Step B: Synthesis of tert-butyl (4-(2-iodoethyl)cyclohexyl)carbamate

(2.128 g, 8.38 mmol)( in 10 mlTHF) was added dropwise to a stirred mixture of tert-butyl (4-(2-hydroxyethyl)cyclohexyl)carbamate (1.7 g, 6.99 mmol), triphenylphosphine (2.199 g, 8.38 mmol) and lH-imidazole (0.571 g, 8.38 mmol) in THF (30 ml) at 0°C. The reaction mixture was stirred 12 hr at ambient temperature and then quenched with water (50 mL) and extracted with ethyl acetate (3 x 50 mL). The combined organic layers were washed with a ₂ S0 ₃ (aq.) (2 x 50 mL), dried over anhydrous sodium sulfate and concentrated under vacuum. The residue was purified by silica gel chromatography, eluted with EtOAc/petroleum ether (1/5) to give the title compound: ^X H NMR (400 MHz, CDC1 ₃ ) δ 4.40-4.30 (brs, 1H), 3.40-3.30 (brs, 1H), 3.24-3.20 (m, 2H), 2.08-1.95 (m, 2H), 1.84-1.73 (m, 4H ), 1.70-1.1.60 (m, 2H), 1.47 (brs, 9H), 1.40-1.30 (m,lH), 1.10-0.90 (m, 2H).

REFERENCE EXAMPLE 37

N,N-bis(4-methoxybenzyl)-2-(l-(4-methoxybenzyl)-lH-tetrazol- 5-yl)-3-(4-oxocyclohexyl)-6-

(trifluoromethyl)benzenesulfonamide

Step A: 4'-hydroxy-N,N-bis(4-methoxybenzyl)-2-(l -(4-methoxybenzyl)- lH-tetrazol-5-yl)-

4-(trifluoromethyl)-2',3',4',5'-tetrahydro-[l, r-biphenyl]-3-sulfonamide

The title compound was prepared by coupling of 3-bromo-N,N-bis(4- methoxybenzyl)-2-(l -(4-methoxybenzyl)- lH-tetrazol-5-y l)-6-

(trifluoromethyl)benzenesulfonamide and 4-(4,4,5,5-tetramethyl-l,3,2-dioxaborolan-2- yl)cyclohex-3-en-l-ol in an analogous fashion as shown in step A of REFERENCE EXAMPLE 18. LC/MS: Cal'd mass: 749.25; Observed mass 750.62 (M+H)+.

Step B : 3 -(4-hydroxycyclohexyl)-N,N-bis(4-methoxybenzyl)-2-( 1 -(4-methoxybenzyl)- lH-tetrazol-5-yl)-6-(trifluoromethyl)benzenesulfonamide

4'-hydroxy-N,N-bis(4-methoxybenzyl)-2-(l-(4-methoxybenzyl)-l H-tetrazol-5- yl)-4-(trifluoromethyl)-2',3',4',5'-tetrahydro-[l,r-biphenyl ]-3-sulfonamide (2.45 g, 3.27 mmol) was stirred with palladium hydroxide on carbon (2.29 g, 3.27 mmol) under H ₂ (balloon) overnight. The reaction mixture was filtered and concentrated to give the title compound. LC/MS: Cal'd mass: 751.27; Observed mass 752.59 (M+H)+.

Step C: N,N-bis(4-methoxybenzyl)-2-(l-(4-methoxybenzyl)-lH-tetrazol- 5-yl)-3-(4- oxocyclohexyl)-6-(trifluoromethyl)benzenesulfonamide

To a solution of 3-(4-hydroxycyclohexyl)-N,N-bis(4-methoxybenzyl)-2-(l-(4- methoxybenzyl)-lH-tetrazol-5-yl)-6-(trifluoromethyl)benzenes ulfonamide (200 mg, 0.266 mmol) in CH2CI2 (2660 μΐ), was added NMO (46.7 mg, 0.399 mmol) and 4A molecular sieves (160 mg). Stirred at rt under N ₂ for 0.5 hr, then added TPAP (9.35 mg, 0.027 mmol). The mixture was stirred at rt under N2 for 1.5 hr. LC-MS showed the completion of the reaction. Filtered and filtrates were concentrated and purified by column chromatography (100% hexane to 70% EtOAc/Hexane) to give the title compound. LC/MS: Cal'd mass: 749.25; Observed mass 750.57 (M+H)+.

REFERENCE EXAMPLE 38

3-(2-(6-Amino-5-(methoxymethyl)pyridin-3-yl)ethyl)-N,N-bis(4 -methoxybenzyl)-2-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)-6-(trifluoromethyl)benzenes ulfonamide and 3 -(2-(6-amino-5- (methoxymethyl)pyridin-3-yl)ethyl)-N,N-bis(4-methoxybenzyl)- 2-(l-(4-methoxybenzyl)-lH-

3-((6-Amino-5-(hydroxymethyl)pyridin-3-yl)ethynyl)-N,N-bis(4 - methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-6- (trifluoromethyl)benzenesulfonamide and 3-((6-amino-5-(hydroxymethyl)pyridin-3-yl)ethynyl)- N,N-bis(4-methoxybenzyl)-2-( 1 -(4-methoxybenzyl)- 1 H-tetrazol-5-yl)-6- (trifluoromethyl)benzenesulfonamide (100 mg, 0.124 mmol) was taken into Ethanol (1244 μΐ) and iodomethane (46.7 μΐ, 0.746 mmol) was added and stirred for 16 hr under a nitrogen atmosphere. The solution was filtered and concentrated under reduced pressure and used without further purification. LC/MS [M+H] ⁺ : 818.55.

REFERENCE EXAMPLE 39

3-(2-(5-Amino-6-(aminomethyl)pyridin-3-yl)ethyl)-N,N-bis( 4-methoxybenzyl)-2-(l-(4- methoxybenzyl)- lH-tetrazol-5-yl)-6-(trifluoromethyl)benzenesulfonamide and 3-(2-(5-amino-6- (aminomethyl)pyridin-3-yl)ethyl)-N,N-bis(4-methoxybenzyl)-2- (2-(4-methoxybenzyl)-2H- tetrazol-5- -6-(trifluoromethyl)benzenesulfonamide

Step A: 3-((6-Cyano-5-nitropyridin-3-yl)ethynyl)-N,N-bis(4-methoxybe nzyl)-2-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)-6-(trifluoromethyl)benzenes ulfonamide and 3-((6-cyano-5- nitropyridin-3 -yl)ethynyl)-N,N-bis(4-methoxybenzyl)-2-( 1 -(4-methoxybenzyl)- 1 H-tetrazol-5 - yl)-6-(trifluoromethyl)benzenesulfonamide

To a solution of 3-ethynyl-N,N-bis(4-methoxybenzyl)-2-(2-(4-methoxybenzyl)- 2H-tetrazol-5-yl)-6-(trifluoromethyl)benzenesulfonamide and 3 -ethynyl-N,N-bis(4- methoxybenzyl)-2-(l -(4-methoxybenzyl)- 1 H-tetrazol-5 -yl)-6- (trifluoromethyl)benzenesulfonamide (200 mg, 0.295 mmol) and 5-bromo-3-nitropicolinonitrile (100 mg, 0.439 mmol) was treated following the procedure from 3-((6-Amino-5- (hydroxymethyl)pyridin-3-yl)ethynyl)-N,N-bis(4-methoxybenzyl )-2-(2-(4-methoxybenzyl)-2H- tetrazol-5-yl)-6-(trifluoromethyl)benzenesulfonamide and 3-((6-amino-5- (hydroxymethyl)pyridin-3 -yl)ethynyl)-N,N-bis(4-methoxybenzyl)-2-( 1 -(4-methoxybenzyl)- 1H- tetrazol-5-yl)-6-(trifluoromethyl)benzenesulfonamide above using Pd(PPh ₃ ) ₄ , TEA, and Cul in THF and stirring for 4 hr at 80°C. LC/MS [M+H] ⁺ : 825.61.

Step B : 3 -(2-(5-Amino-6-(aminomethyl)pyridin-3 -yl)ethyl)-N,N-bis(4-methoxybenzyl)-2-

(l-(4-methoxybenzyl)-lH-tetrazol-5-yl)-6-(trifluoromethyl )benzenesulfonamide and 3-(2-(5- amino-6-(aminomethyl)pyridin-3-yl)ethyl)-N,N-bis(4-methoxybe nzyl)-2-(2-(4-methoxybenzyl)- 2H-tetrazol-5-yl)-6-(trifluoromethyl)benzenesulfonamide

A mixture of 3-((6-cyano-5-nitropyridin-3-yl)ethynyl)-N,N-bis(4- methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-6-

(trifluoromethyl)benzenesulfonamide and 3 -((6-cyano-5-nitropyridin-3 -yl)ethynyl)-N,N-bis(4- methoxybenzyl)-2-(l -(4-methoxybenzyl)- lH-tetrazol-5-yl)-6-

(trifluoromethyl)benzenesulfonamide (243 mg, 0.295 mmol) and platinum(IV) oxide (0.475 mmol) in AcOH (5 niL) was stirred under a hydrogen atmosphere for 16 hr. The solution was filtered through celite and then concentrated and the title compounds and used without further purification. LC/MS [M+H] ⁺ : 803.

REFERENCE EXAMPLE 40

5-(3-(N,N-Bis(4-methoxybenzyl)sulfamoyl)-2-(l-(4-methoxyb enzyl)-lH-tetrazol-5-yl)-4- (trifluoromethyl)phenyl)quinoline 1-oxide and 5-(3-(N,N-bis(4-methoxybenzyl)sulfamoyl)-2-(2- (4-methoxybenzyl)-2H-tetrazol-5-yl)-4-(trifluoromethyl)pheny l)quinoline 1-oxide

N,N-Bis(4-methoxybenzyl)-2-( 1 -(4-methoxybenzyl)- 1 H-tetrazol-5-yl)-3 - (quinolin-5-yl)-6-(trifluoromethyl)benzenesulfonamide and N,N-bis(4-methoxybenzyl)-2-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)-3-(quinolin-5-yl)-6-(triflu oromethyl)benzenesulfonamide (300 mg, 0.384 mmol) was dissolved in dichloromethane (10 mL) and mCPBA (172 mg, 0.768 mmol) was added and stirred for 3 hr. The solution was diluted with EtOAc (50 mL) and washed with IN NaOH (10 mL), dried over MgSC^, and concentrated under reduced pressure. Purified by silica gel chromatography to isolate the title compounds. LC/MS [M+H] ⁺ : 797.33.

REFERENCE EXAMPLE 41

3-(Isoquinolin-5-yl)-N,N-bis(4-methoxybenzyl)-2-(l -(4-methoxybenzyl)- lH-tetrazol-5-yl)-6- (trifluoromethyl)benzenesulfonamide and 3-(isoquinolin-5-yl)-N,N-bis(4-methoxybenzyl)-2-(2- (4-methoxybenzyl)-2H-tetrazol-5-yl)-6-(trifluoromethyl)benze nesulfonamide

A microwave vial was charged with 3-bromo-N,N-bis(4-methoxybenzyl)-2-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)-6-(trifluoromethyl)benzenes ulfonamide and 3-bromo-N,N- bis(4-methoxybenzyl)-2-(l-(4-methoxybenzyl)-lH-tetrazol-5-yl )-6-(trifluoromethyl) benzenesulfonamide (1000 mg, 1.365 mmol) and isoquinolin-5-ylboronic acid (283 mg, 1.638 mmol), Na ₂ C0 ₃ (723 mg, 6.83 mmol) and PdCl ₂ (dppf)-CH ₂ Cl ₂ Adduct (1 11 mg, 0.137 mmol). The vial was sealed, degassed, and filled with Dioxane (4095 μΚ) and Water (1365 μΚ). The resulting mixture was heated at 175°C for 15 min in the microwave. The solution was filtered and concentrated and loaded onto a Teledyne ISCO gold silica 120g column. Fractions containing product were combined and concentrated. LC/MS [M+H] ⁺ : 781.42.

REFERENCE EXAMPLE 42

5-(3 -(N,N-Bis(4-methoxybenzyl)sulfamoyl)-2-( 1 -(4-methoxybenzyl)- lH-tetrazol-5-yl)-4- (trifluoromethyl)phenyl)isoquinoline 2-oxide and 5-(3-(N,N-bis(4-methoxybenzyl)sulfamoyl)-2- -(4-methoxybenzyl)-2H-tetrazol-5-yl)-4-(trifluoromethyl)phen yl)isoquinoline 2-oxide

3-(Isoquinolin-5-yl)-N,N-bis(4-methoxybenzyl)-2-(l -(4-methoxybenzyl)- 1H- tetrazol-5-yl)-6-(trifluoromethyl)benzenesulfonamide and 3-(isoquinolin-5-yl)-N,N-bis(4- methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-6-

(trifluoromethyl)benzenesulfonamide (120 mg, 0.154 mmol) was dissolved in CH ₂ C1 ₂ (2 mL) and mCPBA (68.9 mg, 0.307 mmol) was added and stirred for 3 hr. The solution was diluted with EtOAc (50 mL) and washed with IN NaOH (10 mL), dried (MgS0 ₄ ), and concentrated under reduced pressure. LC/MS [M+H] ⁺ : 797.42. REFERENCE EXAMPLE 43

N,N-Bis(4-methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetraz ol-5-yl)-3-(l,2,3,4- tetrahydroisoquinolin-5-yl)-6-(trifluoromethyl)benzenesulfon amide and N,N-bis(4- methoxybenzyl)-2-(l-(4-methoxybenzyl)-lH-tetrazol-5-yl)-3-(l ,2,3,4-tetrahydroisoquinolin-5- yl)-6-(trifluoromethyl)benzenesulfonamide

3-(Isoquinolin-5-yl)-N,N-bis(4-methoxybenzyl)-2-(l-(4-methox ybenzyl)-lH- tetrazol-5-yl)-6-(trifluoromethyl)benzenesulfonamide and 3-(isoquinolin-5-yl)-N,N-bis(4- methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-6-(t rifluoromethyl)

benzenesulfonamide (370 mg, 0.413 mmol) and platinum(IV) oxide (46.9 mg, 0.207 mmol) in AcOH (20 niL) was stirred under 50 psi of hydrogen for 16 hr. The catalyst was filtered off and the filtrate was concentrated and used without further purification to isolate the title compounds. LC/MS [M+H] ⁺ : 785.57.

REFERENCE EXAMPLE 44

N,N-Bis(4-methoxybenzyl)-2-(l-(4-methoxybenzyl)-lH-tetraz ol-5-yl)-3-(l,2,3,4- tetrahydroquinolin-5-yl)-6-(trifluoromethyl)benzenesulfonami de and N,N-bis(4-methoxybenzyl)-

2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-3-(l,2,3,4-tetra hydroquinolin-5-yl)-6-

(trifluoromethyl)benzenesulfonamide

To a solution of N,N-bis(4-methoxybenzyl)-2-(l-(4-methoxybenzyl)-lH-tetrazol-

5-yl)-3-(quinolin-5-yl)-6-(trifluoromethyl)benzenesulfona mide and N,N-bis(4-methoxybenzyl)- 2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-3-(quinolin-5-yl)-6 -(trifluoromethyl)

benzenesulfonamide (100 mg, 0.1 12 mmol) was combined with platinum(IV) oxide in AcOH under 50 psi of hydrogen according to the immediately preceding Reference Example 43 to yield N,N-bis(4-methoxybenzyl)-2-(l-(4-methoxybenzyl)-lH-tetrazol- 5-yl)-3-(l,2,3,4- tetrahydroquinolin-5-yl)-6-(trifluoromethyl)benzenesulfonami de and N,N-bis(4-methoxybenzyl)- 2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-3-(l,2,3,4-tetrahyd roquinolin-5-yl)-6- (trifluoromethyl)benzenesulfonamide.

REFERENCE EXAMPLE 45

N,N-Bis(4-methoxybenzyl)-2-(l-(4-methoxybenzyl)-lH-tetraz ol-5-yl)-3-(5,6,7,8- tetrahydroquinolin-5-yl)benzenesulfonamide and N,N-bis(4-methoxybenzyl)-2-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)-3-(5,6,7,8-tetrahydroquinol in-5-yl)benzenesulfonamide

Step A: 3-(7,8-Dihydroquinolin-5-yl)-N,N-bis(4-methoxybenzyl)-2-(l-( 4- methoxybenzyl)-lH-tetrazol-5-yl)benzenesulfonamide and 3-(7,8-dihydroquinolin-5-yl)-N,N- bis(4-methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl )benzenesulfonamide

To a mixture of (3-(N,N-bis(4-methoxybenzyl)sulfamoyl)-2-(l-(4- methoxybenzyl)-lH-tetrazol-5-yl)phenyl)boronic acid and (3-(N,N-bis(4- methoxybenzyl)sulfamoyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol- 5-yl)phenyl)boronic acid (1.5 g, 2.383 mmol) and 7,8-dihydroquinolin-5-yl trifluoromethanesulfonate (0.998 g, 3.57 mmol), a solution of 7, 8-dihydroquinolin-5-yl trifluoromethanesulfonate (0.998 g, 3.57 mmol), l,l'-bis(di- tert-butylphosphino) ferrocene palladium dichloride (0.078 g, 0.1 19 mmol), (3-(N,N-bis(4- methoxybenzyl)sulfamoyl)-2-(l-(4-methoxybenzyl)-lH-tetrazol- 5-yl)phenyl)boronic acid (1.5 g, 2.4 mmol) and Potassium Carbonate (9.53 mmol) in THF (50 mL) was stirred at rt for two days. The mixture was diluted with EtOAc, washed with brine, dried over MgSC^, and concentrated. The residue was purified by ISCO column (0-50% EtOAc in hexane). LC/MS [M+H] ⁺ : 715.65. Step B: N,N-Bis(4-methoxybenzyl)-2-(l-(4-methoxybenzyl)-lH-tetrazol- 5-yl)-3-(5,6,7,8- tetrahydroquinolin-5-yl)benzenesulfonamide and N,N-bis(4-methoxybenzyl)-2-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)-3-(5,6,7,8-tetrahydroquinol in-5-yl)benzenesulfonamide

A solution of 3-(7,8-dihydroquinolin-5-yl)-N,N-bis(4-methoxybenzyl)-2-(l-( 4- methoxybenzyl)- lH-tetrazol-5-yl)benzenesulfonamide and 3-(7,8-dihydroquinolin-5-yl)-N,N- bis(4-methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl )benzenesulfonamide (120 mg, 0.168 mmol) in a mixture solvent of DCM (20 mL) and MeOH (20 mL) was hydrogenated under ¾ atomosphere of a balloon at rt overnight. The catalyst was filtered off through a celite pad. The filtration was concentrated. LC/MS [M+H] ⁺ : 717.70.

REFERENCE EXAMPLE 46

5-(3-(N,N-Bis(4-methoxybenzyl)sulfamoyl)-2-(2-(4-methoxyb enzyl)-2H-tetrazol-5-yl)-4- (trifluoromethyl)phenyl)-2,2-dimethyl-l,2,3,4-tetrahydroisoq uinolin-2-ium and 5-(3-(N,N-bis(4- methoxybenzyl)sulfamoyl)-2-(l-(4-methoxybenzyl)-lH-tetrazol- 5-yl)-4- (trifluoromethyl)phenyl)-2,2-dimethyl- 1 ,2,3 ,4-tetrahydroisoquinolin-2-ium

N,N-bis(4-methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol- 5-yl)-3-(l,2,3,4- tetrahydroisoquinolin-5-yl)-6-(trifluoromethyl)benzenesulfon amide and N,N-bis(4- methoxybenzyl)-2-(l-(4-methoxybenzyl)-lH-tetrazol-5-yl)-3-(l ,2,3,4-tetrahydroisoquinolin-5- yl)-6-(trifluoromethyl)benzenesulfonamide (100 mg, 0.127 mmol) in Ethanol (1274 μΕ) was treated with lodomethane (7.17 μΐ, 0.1 15 mmol) and K ₂ CO ₃ (38.7 mg, 0.280 mmol) and stirred overnight at room temperature. The reaction mixture was filtered and concentrated under reduced pressure. LC/MS [M+H] ⁺ : 813.48.

REFERENCE EXAMPLE 47

N,N-Bis(4-methoxybenzyl)-2-( 1 -(4-methoxybenzyl)- lH-tetrazol-5-yl)-3 -(3 -oxo-2,3 - dihydrobenzofuran-7-yl)benzenesulfonamide and N,N-bis(4-methoxybenzyl)-2-(2-(4- methoxybenzyl)-2H etrazol-5-yl)-3-(3-oxo-2,3-dihydrobenzofuran-7-yl)benzenesul fonamide

A mixture of N,N-bis(4-methoxybenzyl)-2-( 1 -(4-methoxybenzyl)- lH-tetrazol-5 - yl)-3-(4,4,5,5-tetramethyl-l,3,2-dioxaborolan-2-yl)benzenesu lfonamide and N,N-bis(4- methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-3-(4 ,4,5,5-tetramethyl- 1,3,2- dioxaborolan-2-yl)benzenesulfonamide (1200 mg, 1.686 mmol) with 7-bromobenzofuran-3(2H)- one (395 mg, 1.855 mmol), Na ₂ C0 ₃ (894 mg, 8.43 mmol) and Pd dppf ₂ CH ₂ C1 ₂ adduct

(catalytic) was sealed in a microwave vial, degassed, and filled with Dioxane (4216 μΐ,) and Water (1405 μΐ _^ ). Then the mixture was heated at 120°C for 40 min, concentrated and purified by MPLC. LC/MS [M+H] ⁺ : 718.36.

REFERENCE EXAMPLE 48

3-(3-Hydroxy-2,3-dihydrobenzofuran-7-yl)-N,N-bis(4-methoxybe nzyl)-2-(l-(4-methoxybenzyl)- lH-tetrazol-5-yl)benzenesulfonamide and 3-(3-hydroxy-2,3-dihydrobenzofuran-7-yl)-N,N-bis(4- methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)benze nesulfonamide

To a mixture of N,N-bis(4-methoxybenzyl)-2-( 1 -(4-methoxybenzyl)- lH-tetrazol-

5-yl)-3-(3-oxo-2,3-dihydrobenzofuran-7-yl)benzenesulfonam ide and N,N-bis(4-methoxybenzyl)-

2- (2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-3-(3-oxo-2,3-dihydrob enzofuran-7- yl)benzenesulfonamide (1000 mg, 1.393 mmol) was dissolved in THF (4644 μί) and sodium borohydride (105 mg, 2.79 mmol) was added to the solution and the reaction was stirred under nitrogen for 16 hr. Water (10 mL) was added slowly to the reaction mixture. The aqueous was extracted with EtOAc (3 x 30 mL). Organic was dried and concentrated and used without further purification to yield title compounds. LC/MS [M+H] ⁺ : 720.42.

REFERENCE EXAMPLE 49

3 - (5, 6-Diaminopyridin-3-yl)-N,N-bis(4-methoxybenzyl)-2-(l -(4-methoxybenzyl)- lH-tetrazol-5- yl)benzenesulfonamide and 3-(5,6-diaminopyridin-3-yl)-N,N-bis(4-methoxybenzyl)-2-(2-(4 - methoxybenzyl)-2H-tetrazol-5-yl)benzenesulfonamide

Step A: 3-(6-Amino-5-nitropyridin-3-yl)-N,N-bis(4-methoxybenzyl)-2-( l-(4- methoxybenzyl)-lH-tetrazol-5-yl)benzenesulfonamide and 3-(6-amino-5-nitropyridin-3-yl)-N,N- bis(4-methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl )benzenesulfonamide To a mixture of N,N-bis(4-methoxybenzyl)-2-(l-(4-methoxybenzyl)-lH-tetrazol- 5-yl)-3-(4,4,5,5-tetramethyl-l,3,2-dioxaborolan-2-yl)benzene sulfonamide and NN-bis^- methoxybenzyl^-^-^-methoxybenzyl^H-tetrazol-S-yl)-^^

dioxaborolan-2-yl)benzenesulfonamide (300 mg, 0.422 mmol) and 5-iodo-3-nitro-pyridin-2- amine (134 mg, 0.506 mmol) was added Na ₂ C0 ₃ (223 mg, 2.108 mmol) and PdCl ₂ (dppf)-

CH ₂ CI ₂ Adduct (34.4 mg, 0.042 mmol). The vial was sealed, degassed, and filled with Dioxane (3162 μΚ) and Water (1054 μΚ). Then the sample was microwaved at 120°C for 40 minutes. The solution was filtered through celite and the material was taken into EtOAc (20 mL) and washed with water (10 mL), brine (10 mL), and dried (MgS0 ₄ ). LC/MS [M+H] ⁺ : 723.50. Step B: 3-(5,6-Diaminopyridin-3-yl)-N,N-bis(4-methoxybenzyl)-2-(l-(4 -methoxybenzyl)- lH-tetrazol-5-yl)benzenesulfonamide and 3-(5,6-diaminopyridin-3-yl)-N,N-bis(4- methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)benze nesulfonamide

3-(6-Amino-5-nitropyridin-3-yl)-N,N-bis(4-methoxybenzyl)-2-( l-(4- methoxybenzyl)-lH-tetrazol-5-yl)benzenesulfonamide and 3-(6-amino-5-nitropyridin-3-yl)-N,N- bis(4-methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl )benzenesulfonamide

(305 mg, 0.422 mmol) was dissolved in ethyl acetate (5 mL) and Pd-C (13.5 mg, 0.127 mmol) was introduced into the system as well as HQ (4M, 0.5 mL) in dioxanes. The system was degassed three times then a balloon of hydrogen was added. The solution was stirred 4 hr and then filtered through celite. The resulting solution was concentrated to isolate the title compounds. LC/MS [M+H] ⁺ : 693.47.

REFERENCE EXAMPLE 50

3 -(2-(4-Guanidinocyclohexyl)ethyl)-N,N-bis(4-methoxybenzyl)-2 -( 1 -(4-methoxybenzyl)- 1H- tetrazol-5-yl)-6-(trifluoromethyl)benzenesulfonamide and 3-(2-(4-guanidinocyclohexyl)ethyl)- N,N-bis(4-methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol- 5-yl)-6- (trifluoromethyl)benzenesulfonamide

Step A: 4-((/er/-Butoxycarbonyl)amino)cyclohex- 1 -en- 1 -yl trifluoromethanesulfonate tert-Butyl (4-oxocyclohexyl)carbamate (5.00 g, 23.4 mmol) was dissolved in tetrahydrofuran (234 ml) at -78°C. Lithium bis(trimethylsilyl)amide (58.6 mL, 58.6 mmol) was added and stirred for 15 min before the addition of 2-[N,N-bis(trifluoromethanesulfonyl)amino]- 5-chloropyridine (1 1.1 g, 28.1 mmol) suspended in 30 mL THF in a dry ice/acetone bath. Upon addition of the material, the solution went from an opaque suspension to a clear yellow solution. The solution was stirred for 30 min. Water (100 mL) was added to quench the reaction. The solution was then concentrated under reduced pressure. After the concentration, hexanes (300 mL) was added causeing a percipitate to form and was filtered off. The solid was advanced to the next step.

Step B: tert-Butyl (4-((3-(N,N-bis(4-methoxybenzyl)sulfamoyl)-2-(l-(4-methoxybe nzyl)- lH-tetrazol-5-yl)-4-(trifluoromethyl)phenyl)ethynyl)cyclohex -3-en- 1 -yl)carbamate and tert-butyl (4-((3-(N,N-bis(4-methoxybenzyl)sulfamoyl)-2-(2-(4-methoxybe nzyl)-2H-tetrazol-5-yl)-4- (trifluoromethyl)phenyl)ethynyl)cyclohex-3 -en- 1 -yl)carbamate

To a solution of 3-ethynyl-N,N-bis(4-methoxybenzyl)-2-(2-(4-methoxybenzyl)- 2H-tetrazol-5-yl)-6-(trifluoromethyl)benzenesulfonamide and 3-ethynyl-N,N-bis(4- methoxybenzyl)-2-( 1 -(4-methoxybenzyl)- lH-tetrazol-5-yl)-6- (trifluoromethyl)benzenesulfonamide (400 mg, 0.590 mmol) was added 4-((tert- butoxycarbonyl)amino)cyclohex-l-en-l-yl trifluoromethanesulfonate (306 mg, 0.885 mmol), Pd tetrakis (136 mg, 0.118 mmol)), triethylamine (165 μΐ, 1.180 mmol)) and copper(I) iodide (1 1.24 mg, 0.059 mmol) in Dioxane (1.18E+04 μί<) and the resulting mixture was stirred for overnight at 80°C under nitrogen atmosphere. Additional reagents added in the same amount as before with the exception of 3 equiv ethynyl-TMS. The reaction was quenched by brine, extracted with ethyl acetate (3 x 30 mL). The combined organic layers were washed with brine (1 x 30 mL), dried over anhydrous Na ₂ S0 ₄ , filtered and concentrated under reduced pressure to give a residue,which was purified by a silica gel column, eluting with EtOAc:Hex (0-100%) to afford the title compounds. LC/MS [M+H] ⁺ : 873.65.

Step C: tert-Butyl (4-(3-(N,N-bis(4-methoxybenzyl)sulfamoyl)-2-(l-(4-methoxyben zyl)- lH-tetrazol-5-yl)-4-(trifluoromethyl)phenethyl)cyclohexyl)ca rbamate and tert-butyl (4-(3-(N,N- bis(4-methoxybenzyl)sulfamoyl)-2-(2-(4-methoxybenzyl)-2H-tet razol-5-yl)-4- (trifluoromethyl)phenethyl)cyclohexyl)carbamate

To a solution of tert-butyl (4-((3-(N,N-bis(4-methoxybenzyl)sulfamoyl)-2-(l-(4- methoxybenzyl)-lH-tetrazol-5-yl)-4-(trifluoromethyl)phenyl)e thynyl)cyclohex-3-en-l- yl)carbamate and tert-butyl (4-((3-(N,N-bis(4-methoxybenzyl)sulfamoyl)-2-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)-4-(trifluoromethyl)phenyl)e thynyl)cyclohex-3-en-l- yl)carbamate (278 mg, 0.318 mmol) in Acetic Acid (10 niL) was added platinum (IV) oxide (36.2 mg, 0.159 mmol). The solution was degassed and Hydrogen was introduced into the system. When the reaction had proceeded to completion by HPLC-MS the mixture was filtered and concentrated to afford the title compounds. LC/MS [M+H] ⁺ : 880.2.

Step D: 3-(2-(4-Aminocyclohexyl)ethyl)-N,N-bis(4-methoxybenzyl)-2-(l -(4- methoxybenzyl)- lH-tetrazol-5-yl)-6-(trifluoromethyl)benzenesulfonamide and 3-(2-(4- aminocyclohexyl)ethyl)-N,N-bis(4-methoxybenzyl)-2-(2-(4-meth oxybenzyl)-2H-tetrazol-5-yl)-6- (trifluoromethyl)benzenesulfonamide

To a solution tert-butyl (4-(3-(N,N-bis(4-methoxybenzyl)sulfamoyl)-2-(l-(4- methoxybenzyl)- lH-tetrazol-5-yl)-4-(trifluoromethyl)phenethyl)cyclohexyl)ca rbamate and tert- butyl (4-(3-(N,N-bis(4-methoxybenzyl)sulfamoyl)-2-(2-(4-methoxyben zyl)-2H-tetrazol-5-yl)-4- (trifluoromethyl)phenethyl)cyclohexyl)carbamate (280 mg, 0.319 mmol) was added TFA (0.245 mL, 3.19 mmol) at 0°C. The solution was slowly warmed to room temperature. After 3 hr, the reaction was at completion for the title compound. The solution was concentrated and toluene (3 x 25 mL) was added and concentrated to isolate the title compounds. LC/MS [M+H] ⁺ : 779.76. Step E: 3 -(2-(4-Guanidinocyclohexyl)ethyl)-N,N-bis(4-methoxybenzyl)-2 -( 1 -(4- methoxybenzyl)- lH-tetrazol-5-yl)-6-(trifluoromethyl)benzenesulfonamide and 3-(2-(4- guanidinocyclohexyl)ethyl)-N,N-bis(4-methoxybenzyl)-2-(2-(4- methoxybenzyl)-2H-tetrazol-5- yl)-6-(trifluoromethyl)benzenesulfonamide

3-(2-(4-Aminocyclohexyl)ethyl)-N,N-bis(4-methoxybenzyl)-2-(l -(4- methoxybenzyl)- lH-tetrazol-5-yl)-6-(trifluoromethyl)benzenesulfonamide and 3-(2-(4- aminocyclohexyl)ethyl)-N,N-bis(4-methoxybenzyl)-2-(2-(4-meth oxybenzyl)-2H-tetrazol-5-yl)-6- (trifluoromethyl)benzenesulfonamide (140 mg, 0.180 mmol) in DMF (3595 μ was treated with lH-pyrazole-l-carboxami dine hydrochloride (42.2 mg, 0.288 mmol) and DIEA (157 μί, 0.899 mmol). The solution was stirred at room temperature under a nitrogen atmosphere for 16 hr. The material was added to EtOAc (50 mL) and washed with brine (2 x 15 mL) and dried with magnesium sulfate. The solution was filtered and concentrated to isolate the title compound and used in the next step without further purification. [M+H] ⁺ : 821.83. REFERENCE EXAMPLE 51

N,N-Bis(4-methoxybenzyl)-2-(l-(4-methoxybenzyl)-lH-tetraz ol-5-yl)-3-(l-oxoisoindolin-4-yl)- 6-(trifluoromethyl)benzenesulfonamide and N,N-bis(4-methoxybenzyl)-2-(2-(4-methoxybenzyl)- 2H-tetrazol-5- -3 -( 1 -oxoisoindolin-4-yl)-6-(trifluoromethyl)benzenesulfonamide

A microwave vial was charged with 3-bromo-N,N-bis(4-methoxybenzyl)-2-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)-6-(trifluoromethyl)benzenes ulfonamide and 3 -bromo-N,N- bis(4-methoxybenzyl)-2-(l-(4-methoxybenzyl)-lH-tetrazol-5-yl )-6-

(trifluoromethyl)benzenesulfonamide (300 mg, 0.410 mmol) and 4-(4,4,5,5-tetramethyl-l,3,2- dioxaborolan-2-yl)isoindolin-l-one (170 mg, 0.655 mmol) and Toluene (3723 μΚ):ΕίΟΗ (372 μί) and 4-(4,4,5,5-tetramethyl-l,3,2-dioxaborolan-2-yl)isoindolin-l- one (170 mg, 0.655 mmol) was added. The solution was degassed and Pd(Ph ₃ P) ₄ (47.3 mg, 0.041 mmol), Lithium Chloride (1.736 mg, 0.041 mmol) and lastly Pd(Ph ₃ P) ₄ (47.3 mg, 0.041 mmol) was added. The solution was degassed for another 20 min. and then was heated to 70°C overnight. EtOAc (60 mL) was added to the mixture and then it was washed with water (30 mL), brine (30 mL), dried (MgS0 ₄ ) and concentrated under reduced pressure. LC/MS [Μ+Η] : 785.75.

REFERENCE EXAMPLE 52

8-Amino-4-(3-(N,N-bis(4-methoxybenzyl)sulfamoyl)-2-(l-(4- methoxybenzyl)-lH-tetrazol-5-yl)- 4-(trifluoromethyl)phenyl)quinoline-2-carboxylic acid and 8-amino-4-(3-(N,N-bis(4- methoxybenzyl)sulfamoyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol- 5-yl)-4- (trifluoromethyl)phenyl)quinoline-2-carboxylic acid

A microwave vial was charged with 3-bromo-N,N-bis(4-methoxybenzyl)-2-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)-6-(trifluoromethyl)benzenes ulfonamide and 3-bromo-N,N- bis(4-methoxybenzyl)-2-(l-(4-methoxybenzyl)-lH-tetrazol-5-yl )-6- (trifluoromethyl)benzenesulfonamide (750 mg, 1.024 mmol) and methyl 8-amino-4-(4,4,5,5- tetramethyl-l,3,2-dioxaborolan-2-yl)quinoline-2-carboxylate (403 mg, 1.229 mmol), a2C0 ₃ (543 mg, 5.12 mmol) and PdCl ₂ (dppf)-CH ₂ Cl ₂ Adduct (84 mg, 0.102 mmol). The vial was sealed, degassed, and filled with Dioxane (7678 μΐ,) and Water (2559 μΐ,). The resulting mixture was heated overnight at 90°C. To the reaction was added more a ₂ C0 ₃ (543 mg, 5.12 mmol), PdCl ₂ (dppf)-CH ₂ Cl ₂ Adduct (84 mg, 0.102 mmol), and methyl 8-amino-4-(4,4,5,5- tetramethyl-l,3,2-dioxaborolan-2-yl)quinoline-2-carboxylate (403 mg, 1.229 mmol). The reaction mixture was degassed and heated to 90°C overnight. The reaction mixture was filtered over celite to removed palladium. The filtrate was diluted with EtOAc and washed with water. The organic layer was dried over anhydrous MgS0 ₄ , filtered, concentrated and purified by silica gel column chromatography (RediSep gold column, 42 g) using (15-100)% EtOAc/Hexanes over 20 min, then 100%EtOAc for 10 min to afford the title compounds. LC/MS [M+H] ⁺ : 840.75.

REFERENCE EXAMPLE 53

5-(3 -(N,N-Bis(4-methoxybenzyl)sulfamoyl)-2-( 1 -(4-methoxybenzyl)- lH-tetrazol-5-yl)-4- (trifluoromethyl)phenyl)-N,N-bis(4-methoxybenzyl)picolinamid e and 5-(3-(N,N-bis(4- methoxybenzyl)sulfamoyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol- 5-yl)-4- (trifluoromethyl)phenyl)-N,N-bis(4-methoxybenzyl)picolinamid e

Step A: 5-(3-(N,N-Bis(4-methoxybenzyl)sulfamoyl)-2-(l-(4-methoxybenz yl)-lH-tetrazol- 5-yl)-4-(trifluoromethyl)phenyl)picolinic acid and 5-(3-(N,N-bis(4-methoxybenzyl)sulfamoyl)-2- (2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-4-(trifluoromethyl)ph enyl)picolinic acid

A microwave vial was charged with 3-bromo-N,N-bis(4-methoxybenzyl)-2-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)-6-(trifluoromethyl)benzenes ulfonamide and 3 -bromo-N,N- bis(4-methoxybenzyl)-2-(l -(4-methoxybenzyl)- lH-tetrazol-5-yl)-6-(trifluoromethyl) benzenesulfonamide (500 mg, 0.683 mmol) and ethyl 5-(4,4,5,5-tetramethyl-l,3,2-dioxaborolan- 2-yl)picolinate (300 mg, 1.083 mmol), Na ₂ C0 ₃ (362 mg, 3.41 mmol) and PdC12(dppf)- CH2C12Adduct (55.7 mg, 0.068 mmol). The vial was sealed, degassed, and filled with Dioxane (2048 μί) and Water (683 μί). The resulting mixture was heated overnight at 90°C. The reaction mixture was filtered over celite to removed palladium. The filtrate was diluted with EtOAc and washed with water. The organic layer was dried over anhydrous MgS0 ₄ , filtered, concentrated and purified by silica gel column chromatography (RediSep gold column, 80 g) using (15-100)% EtOAc/Hexanes over 20 min, then 100%EtOAc for 10 min. LC/MS [M+H] ⁺ : 775.72.

Step B : 5-(3 -(N,N-Bis(4-methoxybenzyl)sulfamoyl)-2-( 1 -(4-methoxybenzyl)- lH-tetrazol-

5-yl)-4-(trifluoromethyl)phenyl)-N,N-bis(4-methoxybenzyl) picolinamide and 5-(3-(N,N-bis(4- methoxybenzyl)sulfamoyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol- 5-yl)-4- (trifluoromethyl)phenyl)-N,N-bis(4-methoxybenzyl)picolinamid e

5 -(3 -(N,N-bis(4-methoxybenzyl)sulfamoyl)-2-( 1 -(4-methoxybenzyl)- lH-tetrazol-

5-yl)-4-(trifluoromethyl)phenyl)picolinic acid and 5-(3-(N,N-bis(4-methoxybenzyl)sulfamoyl)-2- (2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-4-(trifluoromethyl)ph enyl)picolinic acid (22.4 mg, 0.029 mmol) was dissolved in DMF (1 mL) and EDC (19.40 mg, 0.101 mmol), l-hydroxy-7- azabenzotriazole (3.94 mg, 0.029 mmol), and DIPEA (0.025 mL, 0.145 mmol) were added. The solution was stirred for 5 minutes before the addition of bis(4-methoxybenzyl)amine (18.60 mg, 0.072 mmol). The solution was stirred at for 16 hr. The solution is added to EtOAc (20 mL) and washed with water (3 x 5 mL) and brine (2 x 5 mL). Then the organic is dried, concentrated and purified by silica gel chromatography to isolate the title compounds. LC/MS [M+H] ⁺ : 1014.94.

REFERENCE EXAMPLE 54

7-(3-(N,N-Bis(4-methoxybenzyl)sulfamoyl)-2-(l -(4-methoxybenzyl)- lH-tetrazol-5-yl)-4-

(trifluoromethyl)phenyl)-N,N-bis(4-methoxybenzyl)- lH-indole-2-carboxamide and 7-(3-(N,N- bis(4-methoxybenzyl)sulfamoyl)-2-(2-(4-methoxybenzyl)-2H-tet razol-5-yl)-4- (trifluoromethyl)phenyl)-N,N-bis(4-methoxybenzyl)-lH-indole- 2-carboxamide

Step A: Ethyl 7-(3-(N,N-bis(4-methoxybenzyl)sulfamoyl)-2-(l-(4-methoxybenz yl)-lH- tetrazol-5-yl)-4-(trifluoromethyl)phenyl)-lH-indole-2-carbox ylate and ethyl 7-(3-(N,N-bis(4- methoxybenzyl)sulfamoyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol- 5-yl)-4- (trifluoromethyl)phenyl)-lH-indole-2-carboxylate A microwave vial was charged with 3-bromo-N,N-bis(4-methoxybenzyl)-2-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)-6-(trifluoromethyl)benzenes ulfonamide and 3 -bromo-N,N- bis(4-methoxybenzyl)-2-(l-(4-methoxybenzyl)-lH-tetrazol-5-yl )-6-(trifluoromethyl) benzenesulfonamide (500 mg, 0.683 mmol) and ethyl 7-(4,4,5,5-tetramethyl-l,3,2-dioxaborolan- 2-yl)-lH-indole-2-carboxylate (300 mg, 0.952 mmol), [l, l'-Bis(Diphenylphosphino)

Ferrocene]Dichloropalladium(Ii) (49.9 mg, 0.068 mmol) and sodium carbonate (2.05 mmol) in Toluene (5688 μΚ) and Ethanol (1138 μΚ) and was heated at 90°C for 17 hr. The mixture was filtered through a celite pad. The filtrate was concentrated, and the residue was purified by MPLC (0-100% EtOAc in Hexane). LC/MS [M+H] ⁺ : 841.76.

Step B: 7-(3-(N,N-Bis(4-methoxybenzyl)sulfamoyl)-2-(l-(4-methoxybenz yl)-lH-tetrazol- 5-yl)-4-(trifluoromethyl)phenyl)-lH-indole-2-carboxylic acid and 7-(3-(N,N-bis(4- methoxybenzyl)sulfamoyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol- 5-yl)-4- (trifluoromethyl)phenyl)- lH-indole-2-carboxylic acid

Ethyl 7-(3-(N,N-bis(4-methoxybenzyl)sulfamoyl)-2-(l-(4-methoxybenz yl)-lH- tetrazol-5-yl)-4-(trifluoromethyl)phenyl)-lH-indole-2-carbox ylate and ethyl 7-(3-(N,N-bis(4- methoxybenzyl)sulfamo3yl)-2-(2-(4-methoxybenzyl)-2H-tetrazol -5-yl)-4- (trifluoromethyl)phenyl)-lH-indole-2-carboxylate (187 mg, 0.222 mmol) was dissolved in dioxane (2224 μL):water (2224 μΕ) and LiOH (53.3 mg, 2.224 mmol) was added to the system and stirred for 16 hr. The solution was added to EtOAc (50 mL) and washed with brine (3 x 15 mL) and concentrated. The title compounds were used without further purification. LC/MS [M+H] ⁺ : 813.68.

Step C: 7-(3-(N,N-Bis(4-methoxybenzyl)sulfamoyl)-2-(l-(4-methoxybenz yl)-lH-tetrazol- 5-yl)-4-(trifluoromethyl)phenyl)-N,N-bis(4-methoxybenzyl)-lH -indole-2-carboxamide and 7-(3- (N,N-bis(4-methoxybenzyl)sulfamoyl)-2-(2-(4-methoxybenzyl)-2 H-tetrazol-5-yl)-4- (trifluoromethyl)phenyl)-N,N-bis(4-methoxybenzyl)-lH-indole- 2-carboxamide

7-(3 -(N,N-Bis(4-methoxybenzyl)sulfamoyl)-2-( 1 -(4-methoxybenzyl)- lH-tetrazol- 5-yl)-4-(trifluoromethyl)phenyl)-lH-indole-2-carboxylic acid and 7-(3-(N,N-bis(4- methoxybenzyl)sulfamoyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol- 5-yl)-4- (trifluoromethyl)phenyl)-lH-indole-2-carboxylic acid (90 mg, 0.11 1 mmol) was dissolved in DMF (1 mL) and EDC (53.1 mg, 0.277 mmol), l-Hydroxy-7-Azabenzotriazole (1.507 mg, 0.01 1 mmol), and Hunig's Base (0.077 mL, 0.443 mmol) were added. This was stirred for 5 mins before the addition of Bis(4-Methoxybenzyl)Amine (85 mg, 0.332 mmol). The solution was stirred overnight. An additional equiv of amine, EDC, and Hunig's base was added and the mixture was stirred over the weekend. The reaction mixture was diluted with EtOAc (40 mL) and extracted with water (2 x 20 mL) brine (2 x 20 mL) dried (MgS0 ₄ ) and concentrated. Used crude in next step. LC/MS [M+H] ⁺ : 1052.96.

REFERENCE EXAMPLE 55

6-Cyclopropyl-N,N-bis(4-methoxybenzyl)-2-(l-(4-methoxybenzyl )-lH-tetrazol-5-yl)-3- (quinolin-5-yl)benzenesulfonamide and 6-cyclopropyl-N,N-bis(4-methoxybenzyl)-2-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)-3-(quinolin-5-yl)benzenesul fonamide

A mixture of N,N-bis(4-methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol- 5- yl)-3-(quinolin-5-yl)-6-(trifluoromethyl)benzenesulfonamide and 6-bromo-N,N-bis(4- methoxybenzyl)-2-(l-(4-methoxybenzyl)-lH-tetrazol-5-yl)-3-(q uinolin-5-yl)benzenesulfonamide (described above, 200 mg, 0.253 mmol), 2-cyclopropyl-4,4,5,5-tetramethyl-l,3,2-dioxaborolane (63.7 mg, 0.379 mmol) and PdCl ₂ (dppf)-CH ₂ Cl ₂ Adduct (20.63 mg, 0.025 mmol) was sealed in a microwave vial, degassed, and filled with Dioxane (758 μί) and Water (253 μί). The resulting mixture was heated overnight at 90°C. The reaction mixture was filtered over celite to remove the palladium. The filtrate was diluted with MeOH and loaded onto 3x SCX (20 g) ion exchange columns. The material was washed with MeOH. Next, the columns were washed with IN N¾ in MeOH until the red band on the cartidge was fully eluted to afford the title compound after removal of the volatiles. LC/MS [M+H] ⁺ : 753.47.

REFERENCE EXAMPLE 56

6-(2-Hydroxyethyl)-N,N-bis(4-methoxybenzyl)-2-(l-(4-methoxyb enzyl)-lH-tetrazol-5-yl)-3- (quinolin-5-yl)benzenesulfonamide and 6-(2-hydroxyethyl)-N,N-bis(4-methoxybenzyl)-2-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)-3-(quinolin-5-yl)benzenesul fonamide

Step A: tert-Butyl 2-(2-(N,N-bis(4-methoxybenzyl)sulfamoyl)-3 -( 1 -(4- methoxybenzyl)tetrazolidin-5-yl)-4-(quinolin-5-yl)phenyl)ace tate and tert-butyl 2-(2-(N,N-bis(4- methoxybenzyl)sulfamoyl)-3-(2-(4-methoxybenzyl)-2H-tetrazol- 5-yl)-4-(quinolin-5- yl)phenyl)acetate

N,N-Bis(4-methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol- 5-yl)-3-

(quinolin-5-yl)-6-(trifluoromethyl)benzenesulfonamide and 6-bromo-N,N-bis(4-methoxybenzyl)- 2-(l-(4-methoxybenzyl)-lH-tetrazol-5-yl)-3-(quinolin-5-yl)be nzenesulfonamide (100 mg, 0.126 mmol) and second generation SPHOS (9.10 mg, 0.013 mmol) was placed in a microwave tube, and added anhydrous THF (421 μΐ). The tube was sealed and nitrogen was used to degas for 10 min. (2-(tert-butoxy)-2-oxoethyl)zinc(II) chloride (1010 μΐ, 0.505 mmol) was then added to the solution and the resulting mixture was heated at 50°C for 16 hr. The reaction was quenched with a saturated NH ₄ C1 solution. The reaction mixture was extracted with EtOAc (60 mL). Organic washed with brine (15 mL), dried ( a ₂ S04), filtered and concentrated. The reaction mixture was purified by silca gel chromatography to isolate the title compounds. LC/MS [M+H] ⁺ : 827.46. Step B: 6-(2-Hydroxyethyl)-N,N-bis(4-methoxybenzyl)-2-(l-(4-methoxyb enzyl)-lH- tetrazol-5-yl)-3-(quinolin-5-yl)benzenesulfonamide and 6-(2-hydroxyethyl)-N,N-bis(4- methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-3-(q uinolin-5-yl)benzenesulfonamide tert-Butyl 2-(2-(N,N-bis(4-methoxybenzyl)sulfamoyl)-3 -( 1 -(4- methoxybenzyl)tetrazolidin-5-yl)-4-(quinolin-5-yl)phenyl)ace tate and tert-butyl 2-(2-(N,N-bis(4- methoxybenzyl)sulfamoyl)-3-(2-(4-methoxybenzyl)-2H-tetrazol- 5-yl)-4-(quinolin-5- yl)phenyl)acetate (522 mg, 0.631 mmol) was dissolved in tetrahydrofuran (6312 μΚ) at 0°C where upon lithium aluminum hydride 1 M in diethyl ether (947 μί, 1.894 mmol) was added to the solution. The solution stirred for 16 hr and was cooled to 0°C and the reaction was quenched with water (100 μΐ,, 5.55 mmol) and NaOH (1578 μΐ,, 3.16 mmol)). The resulting solution was stirred for 30 minutes where a white suspension formed. The suspension was filtered. The solution was concentrated and the oil was purified by silica MPLC to isolate the title compounds LC/MS [M+H] ⁺ : 757.46.

REFERENCE EXAMPLE 57

3-(2-Aminobenzo[i/]thiazol-4-yl)-6-bromo-N,N-bis(4-methox ybenzyl)-2-(l-(4-methoxybenzyl)- lH-tetrazol-5-yl)benzenesulfonamide and 3-(2-aminobenzo[if|thiazol-4-yl)-6-bromo-N,N-bis(4- methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)benze nesulfonamide

Step A: (2-Aminobenzo[if|thiazol-4-yl)boronic acid

In the reaction vessel 4-bromobenzo[<i]thiazol-2-amine (10 g, 43.6 mmol) and bispinacolatodiboron (33.3 g, 131 mmol) were combined, followed by potassium acetate (12.85 g, 131 mmol) and PCy3 Pd G2 (2.58 g, 4.36 mmol). Then dry dioxane (400 ml) was added to this flask. This mixture was degassed and then heated at 80°C for 72 hr. The solution was filtered, and the filtrate was concentrated under reduced pressure. The residue was dissolved in EtOAc (400 mL), and extracted with 2N HQ (2x150 ml). The aqueous was concentrated under reduced pressure. The crude material was dissolved in 3: 1 CHC13:i-PrOH, dried over MgS0 ₄ . The MgS0 ₄ was filtered off and the filtrate was concentrated. The material was used without further purification. LC/MS [M+H] ⁺ : 195

Step B : 3 -(2-Aminobenzo [<i]thiazol-4-yl)-6-bromo-N,N-bis(4-methoxybenzyl)-2-( 1 -(4- methoxybenzyl)- lH-tetrazol-5-yl)benzenesulfonamide and 3-(2-aminobenzo[<i]thiazol-4-yi)-6- bromo-N,N-bis(4-methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tet razol-5- yl)benzenesulfonamide

Starting with a solution of 6-bromo-3-iodo-2-(l-(4-methoxybenzyl)-lH-tetrazol- 5-yl)benzenesulfonamide and 6-bromo-3-iodo-N,N-bis(4-methoxybenzyl)-2-(2-(4- methoxybenzyl)tetrazolidin-5-yl)benzenesulfonamide (7.3 g, 9.24 mmol) and (2- aminobenzo[i/]thiazol-4-yl)boronic acid (1.971 g, 10.16 mmol) the title compounds were prepared in an analogous fashion as described for 6-Bromo-N,N-bis(4-methoxybenzyl)-2-(l-(4- methoxybenzyl)- lH-tetrazol-5-yl)-3 -(quinolin-5-yl)benzenesulfonamide and 6-bromo-N,N- bis(4-methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl )-3-(quinolin-5- yl)benzenesulfonamide. LC/MS [M+H] ⁺ : 812, 814.

REFERENCE EXAMPLE 58

3-(2-Aminobenzo[i/]thiazol-4-yl)-6-(2-hydroxyethyl)-N,N-b is(4-methoxybenzyl)-2-(l-(4- methoxybenzyl)- lH-tetrazol-5-yl)benzenesulfonamide and 3-(2-aminobenzo[i/]thiazol-4-yl)-6- (2 -hydroxy ethyl)-N,N-bis(4-methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-te trazol-5- yl)benzenesulfonamide

Step A: tert-Butyl N-[4-[3-[bis[(4-methoxyphenyl)methyl]sulfamoyl]-4-bromo-2-[2 -[(4- methoxyphenyl)methyl]tetrazol-5 -yl]phenyl] -1,3 -benzothiazol-2-yl] -N-tert-butoxycarbonyl- carbamate and tert-butyl N-[4-[3-[bis[(4-methoxyphenyl)methyl]sulfamoyl]-4-bromo-2-[l -[(4- methoxyphenyl)methyl]tetrazol-5 -yl]phenyl] -1,3 -benzothiazol-2-yl] -N-tert-butoxycarbonyl- carbamate

To 3-(2-aminobenzo[if|thiazol-4-yl)-6-bromo-N,N-bis(4-methoxybe nzyl)-2-(l-(4- methoxybenzyl)- lH-tetrazol-5-yl)benzenesulfonamide and 3-(2-aminobenzo[i/]thiazol-4-yl)-6- bromo-N,N-bis(4-methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tet razol-5- yl)benzenesulfonamide (2.6 g, 3.2 mmol) was dissolved in DCM (16 mL). Then DMAP (0.039 g, 0.320 mmol) was added to the system followed by the addition of BOC-Anhydride (1.63 mL, 7.04 mmol). The solution was stirred for 16 hr. The resulting solution was taken into EtOAc (100 mL) and washed with brine (30 mL), dried over magnesium sulfate and concentrated to isolate the title compounds. LC/MS [M+H] ⁺ : 1012, 1014.

Step B: tert-Butyl 2-(2-(N,N-bis(4-methoxybenzyl)sulfamoyl)-4-(2-((/ert- butoxycarbonyl)amino)benzo[i/]thiazol-4-yl)-3-(l-(4-methoxyb enzyl)-lH-tetrazol-5- yl)phenyl)acetate and tert-butyl 2-(2-(N,N-bis(4-methoxybenzyl)sulfamoyl)-4-(2-((/ert- butoxycarbonyl)amino)benzo[i/]thiazol-4-yl)-3-(2-(4-methoxyb enzyl)-2H-tetrazol-5- yl)phenyl)acetate To a solution of tert-Butyl N-[4-[3-[bis[(4-methoxyphenyl)methyl]sulfamoyl]-4- bromo-2-[2-[(4-methoxyphenyl)methyl]tetrazol-5-yl]phenyl]-l, 3-benzothiazol-2-yl]-N-tert- butoxycarbonyl-carbamate and tert-butyl N-[4-[3-[bis[(4-methoxyphenyl)methyl]sulfamoyl]-4- bromo-2-[l-[(4-methoxyphenyl)methyl]tetrazol-5-yl]phenyl]-l, 3-benzothiazol-2-yl]-N-tert- butoxycarbonyl-carbamate (1.3 g, 1.3 mmol) and 2nd Gen SPHOS (0.185 g, 0.257 mmol) was placed in a microwave tube, and anhydrous THF (4.3 mL) was added. The tube was sealed and 2 was bubbled through for 10 min. (2-(tert-butoxy)-2-oxoethyl)zinc(II) chloride (12.8 mL, 6.42 mmol) was then added. The resulting mixture was heated at 60°C for overnight. A mixture of di boc, mono boc, and no boc material was identified by LC-MS. LC/MS [M+H] ⁺ : 948.81.

Step C: tert-Butyl 2-(4-(2-aminobenzo[if|thiazol-4-yl)-2-(N,N-bis(4- methoxybenzyl)sulfamoyl)-3-(l -(4-methoxybenzyl)- lH-tetrazol-5-yl)phenyl)acetate and tert- butyl 2-(4-(2-aminobenzo[if|thiazol-4-yl)-2-(N,N-bis(4-methoxybenz yl)sulfamoyl)-3-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)phenyl)acetate

To a solution of tert-butyl 2-(2-(N,N-bis(4-methoxybenzyl)sulfamoyl)-4-(2-((/ert- butoxycarbonyl)amino)benzo[i/]thiazol-4-yl)-3-(l -(4-methoxybenzyl)- lH-tetrazol-5- yl)phenyl)acetate and tert-butyl 2-(2-(N,N-bis(4-methoxybenzyl)sulfamoyl)-4-(2-((/ert- butoxycarbonyl)amino)benzo[i/]thiazol-4-yl)-3-(2-(4-methoxyb enzyl)-2H-tetrazol-5- yl)phenyl)acetate (900 mg, 0.949 mmol was dissolved in DCM (9493 μΐ) and TFA (293 μΐ, 3.80 mmol) was added to the system. The reaction was stirred for 16 hr. The solution was concentrated to yield the title compound and used without further purification. LC/MS [M+H] ⁺ : 848.85.

Step D: 3-(2-Aminobenzo[if|thiazol-4-yl)-6-(2-hydroxyethyl)-N,N-bis( 4-methoxybenzyl)- 2-(l-(4-methoxybenzyl)-lH-tetrazol-5-yl)benzenesulfonamide and 3-(2-aminobenzo[i/]thiazol-4- yl)-6-(2-hydroxyethyl)-N,N-bis(4-methoxybenzyl)-2-(2-(4-meth oxybenzyl)-2H-tetrazol-5- yl)benzenesulfonamide

tert-Butyl 2-(4-(2-aminobenzo[if|thiazol-4-yl)-2-(N,N-bis(4- methoxybenzyl)sulfamoyl)-3-(l -(4-methoxybenzyl)- lH-tetrazol-5-yl)phenyl)acetate and tert- butyl 2-(4-(2-aminobenzo[if|thiazol-4-yl)-2-(N,N-bis(4-methoxybenz yl)sulfamoyl)-3-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)phenyl)acetate (717 mg, 0.846 mmol) was dissolved in Tetrahydrofuran (8455 μΓ) at 0°C where LAH 1 M in diethyl ether (1268 iL, 2.54 mmol) was added to the solution. The solution stirred overnight. The solution was cooled to 0°C and the reaction was quenched with Water (15.23 iL, 0.846 mmol) and Sodium Hydroxide (5.92 mmol)). The resulting solution was stirred for 30 mins where a white suspension formed. The suspension was filtered. The solution was concentrated and the oil was loaded onto a teledyne isco silica 24 g column eluting with EtOAC:Ethanol (3: 1): Hexanes from 10-70% over 20 min. LC/MS [M+H] ⁺ : 778.66.

REFERENCE EXAMPLE 59

6-( 1 -Fluoro-2-hydroxyethyl)-N,N-bis(4-methoxybenzyl)-2-( 1 -(4-methoxybenzyl)- lH-tetrazol-5- yl)-3-(2-((4-methoxybenzyl)amino)benzo[i/]thiazol-4-yl)benze nesulfonamide and 6-(l -fluoro-2- hydroxyethyl)-N,N-bis(4-methoxybenzyl)-2-(2-(4-methoxybenzyl )-2H-tetrazol-5-yl)-3-(2-((4- methoxybenzyl)amino)benzo[if|thiazol-4-yl)benzenesulfonamide

Step A: 3-(2-(Bis(4-methoxybenzyl)amino)benzo[i/]thiazol-4-yl)-6-bro mo-N,N-bis(4- methoxybenzyl)-2-(l -(4-methoxybenzyl)- lH-tetrazol-5-yl)benzenesulfonamide and 3-(2-(bis(4- methoxybenzyl)amino)benzo[if|thiazol-4-yl)-6-bromo-N,N-bis(4 -methoxybenzyl)-2-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)benzenesulfonamide

3-(2-Aminobenzo[if|thiazol-4-yl)-6-bromo-N,N-bis(4-methoxybe nzyl)-2-(l-(4- methoxybenzyl)- lH-tetrazol-5-yl)benzenesulfonamide and 3-(2-aminobenzo[i/]thiazol-4-yl)-6- bromo-N,N-bis(4-methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tet razol-5- yl)benzenesulfonamide (1.6 g, 1.97 mmol) was dissolved into 2-butanone (9.84 mL). This was followed by the addition of 4-methoxybenzyl chloride (0.587 mL, 4.33 mmol), Nal (0.649 g, 4.33 mmol), and K2CO ₃ (1.088 g, 7.87 mmol). The reaction was heated to 80°C under an atmosphere of nitrogen for 16 hr. The solution was filtered to remove the inorganics. The resulting solution was taken into to EtOAc (60 mL) and washed with water (2 x 20 mL), brine (20 mL), dried (MgSC^), and concentrated under reduced pressure resulting in an oil. The oil was loaded onto a silica column to yield the title compound. LC/MS [M+H] ⁺ : 1054.92.

Step B: tert-Butyl 2-(4-(2-(bis(4-methoxybenzyl)amino)benzo[i/]thiazol-4-yl)-2- (N,N- bis(4-methoxybenzyl)sulfamoyl)-3-(l -(4-methoxybenzyl)- lH-tetrazol-5-yl)phenyl)acetate and tert-butyl 2-(4-(2-(bis(4-methoxybenzyl)amino)benzo[i/]thiazol-4-yl)-2- (N,N-bis(4- methoxybenzyl)sulfamoyl)-3-(2-(4-methoxybenzyl)-2H-tetrazol- 5-yl)phenyl)acetate

To a solution of 3-(2-(bis(4-methoxybenzyl)amino)benzo[i/]thiazol-4-yl)-6- bromo-N,N-bis(4-methoxybenzyl)-2-(l-(4-methoxybenzyl)-lH-tet razol-5- yl)benzenesulfonamide and 3-(2-(bis(4-methoxybenzyl)amino)benzo[i/]thiazol-4-yl)-6-bro mo- N,N-bis(4-methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol- 5-yl)benzenesulfonamide and (2-(tert-butoxy)-2-oxoethyl)zinc(II) chloride (6852 μΐ, 3.43 mmol) were reacted in an analogous fashion to that described for tert-Butyl 2-(2-(N,N-bis(4-methoxybenzyl)sulfamoyl)-4-(2-((teri- butoxycarbonyl)amino)benzo[i/]thiazol-4-yl)-3-(l-(4-methoxyb enzyl)-lH-tetrazol-5- yl)phenyl)acetate and tert-butyl 2-(2-(N,N-bis(4-methoxybenzyl)sulfamoyl)-4-(2-((tert- butoxycarbonyl)amino)benzo[i/]thiazol-4-yl)-3-(2-(4-methoxyb enzyl)-2H-tetrazol-5- yl)phenyl)acetate to isolate the title compounds. LC/MS [M+H] ⁺ : 1089.04.

Step C: tert-Butyl 2-(2-(N,N-bis(4-methoxybenzyl)sulfamoyl)-3-(l-(4-methoxybenz yl)- lH-tetrazol-5-yl)-4-(2-((4-methoxybenzyl)amino)benzo[i/]thia zol-4-yl)phenyl)-2-fluoroacetate and tert-butyl 2-(2-(N,N-bis(4-methoxybenzyl)sulfamoyl)-3-(2-(4-methoxybenz yl)-2H-tetrazol-

5- yl)-4-(2-((4-methoxybenzyl)amino)benzo[i/]thiazol-4-yl)pheny l)-2-fluoroacetate

To a solution of tert-butyl 2-(2-(N,N-bis(4-methoxybenzyl)sulfamoyl)-4-(2-((tert- butoxycarbonyl)amino)benzo[i/]thiazol-4-yl)-3-(l-(4-methoxyb enzyl)-lH-tetrazol-5- yl)phenyl)acetate and tert-butyl 2-(2-(N,N-bis(4-methoxybenzyl)sulfamoyl)-4-(2-((tert- butoxycarbonyl)amino)benzo[i/]thiazol-4-yl)-3-(2-(4-methoxyb enzyl)-2H-tetrazol-5- yl)phenyl)acetate (655 mg, 0.602 mmol) was dissolved in THF (10 mL) and chilled to -78°C and 2 M LDA (1.204 mL, 2.407 mmol) was added to the system. After an hour Ν- fluorobenzenesulfonimide (569 mg, 1.806 mmol) was added and the mixture was stirred under a nitrogen atmosphere for 16 hr. Upon completion, the solution was poured into brine (20 mL) and EtOAc (3 x 30 mL) was used to extract the aqueous. The organic was dried and purified on silica to isolate the title compounds. LC/MS [M+H] ⁺ : 986.88.

Step D: 6-( 1 -Fluoro-2-hydroxyethyl)-N,N-bis(4-methoxybenzyl)-2-( 1 -(4-methoxybenzyl)- lH-tetrazol-5-yl)-3-(2-((4-methoxybenzyl)amino)benzo[i/]thia zol-4-yl)benzenesulfonamide and

6- (l-fluoro-2-hydroxyethyl)-N,N-bis(4-methoxybenzyl)-2-(2-(4-m ethoxybenzyl)-2H-tetrazol-5- yl)-3-(2-((4-methoxybenzyl)amino)benzo[i/]thiazol-4-yl)benze nesulfonamide

To a solution of tert-butyl 2-(2-(N,N-bis(4-methoxybenzyl)sulfamoyl)-3-(l-(4- methoxybenzyl)-lH-tetrazol-5-yl)-4-(2-((4-methoxybenzyl)amin o)benzo[if|thiazol-4-yl)phenyl)- 2-fluoroacetate and tert-butyl 2-(2-(N,N-bis(4-methoxybenzyl)sulfamoyl)-3-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)-4-(2-((4-methoxybenzyl)amin o)benzo[(i]thiazol-4-yl)phenyl)-

2- fluoroacetate (131 mg, 0.133 mmol) was treated in an analogous fashion as described for 3-(2- Aminobenzo[i/]thiazol-4-yl)-6-(2-hydroxyethyl)-N,N-bis(4-met hoxybenzyl)-2-(l-(4- methoxybenzyl)-lH-tetrazol-5-yl)benzenesulfonamide and 3-(2-aminobenzo[i/]thiazol-4-yl)-6- (2 -hydroxy ethyl)-N,N-bis(4-methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-te trazol-5- yl)benzenesulfonamide to isolate the title compounds. LC/MS [M+H] ⁺ : 916.79.

REFERENCE EXAMPLE 60

3- (2-Aminobenzo[i/]thiazol-4-yl)-6-(3-hydroxypropyl)-2-(l-(4-m ethoxybenzyl)-lH-tetrazol-5- yl)benzenesulfonamide and 3-(2-aminobenzo[if|thiazol-4-yl)-6-(3-hydroxypropyl)-2-(2-(4 - methoxybenzyl)-2H-tetrazol-5-yl)benzenesulfonamide

Step A: Ethyl 3-(2-(N,N-bis(4-methoxybenzyl)sulfamoyl)-4-(2-((tert- butoxycarbonyl)amino)benzo[d]thiazol-4-yl)-3-(l-(4-methoxybe nzyl)-lH-tetrazol-5- yl)phenyl)propanoate and ethyl 3-(2-(N,N-bis(4-methoxybenzyl)sulfamoyl)-4-(2-((tert- butoxycarbonyl)amino)benzo[d]thiazol-4-yl)-3-(2-(4-methoxybe nzyl)-2H-tetrazol-5- yl)phenyl)propanoate

To a solution of tert-butyl -[4-[3-[bis[(4-methoxyphenyl)methyl]sulfamoyl]-4- bromo-2-[2-[(4-methoxyphenyl)methyl]tetrazol-5-yl]phenyl]-l, 3-benzothiazol-2-yl]-N-tert- butoxycarbonyl-carbamate and tert-butyl N- [4- [3 - [bis [(4-methoxyphenyl)methyl] sulfamoyl] -4- bromo-2-[l-[(4-methoxyphenyl)methyl]tetrazol-5-yl]phenyl]-l, 3-benzothiazol-2-yl]-N-tert- butoxycarbonyl-carbamate, (1000 mg, 0.987 mmol) and (3-ethoxy-3-oxopropyl)zinc(II) bromide (9872 μΐ, 4.94 mmol) were reacted in an analogous fashion to that described for tert-Butyl 2-(2- (N,N-bis(4-methoxybenzyl)sulfamoyl)-4-(2-((tert-butoxycarbon yl)amino)benzo[i/]thiazol-4-yl)- 3-(l-(4-methoxybenzyl)-lH-tetrazol-5-yl)phenyl)acetate and tert-butyl 2-(2-(N,N-bis(4- methoxybenzyl)sulfamoyl)-4-(2-((ter?-butoxycarbonyl)amino)be nzo[if|thiazol-4-yl)-3-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)phenyl)acetate to afford the title compounds. LC/MS [Μ+Η] : 934.9.

Step B: Ethyl 3-(4-(2-aminobenzo[d]thiazol-4-yl)-3-(l-(4-methoxybenzyl)-lH -tetrazol-5- yl)-2-sulfamoylphenyl)propanoate and ethyl 3-(4-(2-aminobenzo[d]thiazol-4-yl)-3-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)-2-sulfamoylphenyl)propanoat e

To a solution from ethyl 3-(2-(N,N-bis(4-methoxybenzyl)sulfamoyl)-4-(2-((tert- butoxycarbonyl)amino)benzo[d]thiazol-4-yl)-3-(l-(4-methoxybe nzyl)-lH-tetrazol-5- yl)phenyl)propanoate and ethyl 3-(2-(N,N-bis(4-methoxybenzyl)sulfamoyl)-4-(2-((tert- butoxycarbonyl)amino)benzo[d]thiazol-4-yl)-3-(2-(4-methoxybe nzyl)-2H-tetrazol-5- yl)phenyl)propanoate (1021 mg, 0.987 mmol) was dissolved in DCM (20 mL) and TFA (1.521 mL, 19.74 mmol) was added to the system. The solution was stirred for 16 hr. The solution was concentrated and used without further purification to isolate the title compounds. LC/MS

[M+H] ⁺ : 594.50.

Step C: 3-(2-Aminobenzo[d]thiazol-4-yl)-6-(3-hydroxypropyl)-2-(l-(4- methoxybenzyl)- lH-tetrazol-5-yl)benzenesulfonamide and 3-(2-aminobenzo[d]thiazol-4-yl)-6-(3-hydroxypropyl)-

2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)benzenesulfonamid e

To a solution of ethyl 3-(4-(2-aminobenzo[d]thiazol-4-yl)-3-(l-(4- methoxybenzyl)-lH-tetrazol-5-yl)-2-sulfamoylphenyl)propanoat e and ethyl 3-(4-(2- aminobenzo[d]thiazol-4-yl)-3-(2-(4-methoxybenzyl)-2H-tetrazo l-5-yl)-2- sulfamoylphenyl)propanoate (586 mg, 0.987 mmol) was treated in an analogous fashion as described for 3-(2-Aminobenzo[i/]thiazol-4-yl)-6-(2-hydroxyethyl)-N,N-bis( 4-methoxybenzyl)-

2- (l-(4-methoxybenzyl)-lH-tetrazol-5-yl)benzenesulfonamide and 3-(2-aminobenzo[i/]thiazol-4- yl)-6-(2-hydroxyethyl)-N,N-bis(4-methoxybenzyl)-2-(2-(4-meth oxybenzyl)-2H-tetrazol-5- yl)benzenesulfonamide to isolate the title compounds. LC/MS [M+H] ⁺ : 552.58.

REFERENCE EXAMPLE 61

3- (2-Aminobenzo[d]thiazol-4-yl)-6-(5-hydroxypentyl)-2-(l-(4-me thoxybenzyl)-lH-tetrazol-5- yl)benzenesulfonamide and 3-(2-aminobenzo[d]thiazol-4-yl)-6-(5-hydroxypentyl)-2-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)benzenesulfonamide

Step A: Ethyl 5-(2-( ,N-bis(4-methoxybenzyl)sulfamoyl)-4-(2-((tert- butoxycarbonyl)amino)benzo[d]thiazol-4-yl)-3-(l-(4-methoxybe nzyl)-lH-tetrazol-5- yl)phenyl)pentanoate and ethyl 5-(2-(N,N-bis(4-methoxybenzyl)sulfamoyl)-4-(2-((tert- butoxycarbonyl)amino)benzo[d]thiazol-4-yl)-3-(2-(4-methoxybe nzyl)-2H-tetrazol-5- yl)phenyl)pentanoate

To a solution of tert-butyl N-[4-[3-[bis[(4-methoxyphenyl)methyl]sulfamoyl]-4- bromo-2-[2-[(4-methoxyphenyl)methyl]tetrazol-5-yl]phenyl]-l, 3-benzothiazol-2-yl]-N-tert- butoxycarbonyl-carbamate and tert-butyl N-[4-[3-[bis[(4-methoxyphenyl)methyl]sulfamoyl]-4- bromo-2-[l-[(4-methoxyphenyl)methyl]tetrazol-5-yl]phenyl]-l, 3-benzothiazol-2-yl]-N-tert- butoxycarbonyl-carbamate (1000 mg, 0.987 mmol) and (5-ethoxy-5-oxopentyl)zinc(II) bromide (9872 μΐ, 4.94 mmol) were reacted in an analogous fashion to that described for tert-Butyl 2-(2- (N,N-bis(4-methoxybenzyl)sulfamoyl)-4-(2-((tert-butoxycarbon yl)amino)benzo[i/]thiazol-4-yl)- 3-(l-(4-methoxybenzyl)-lH-tetrazol-5-yl)phenyl)acetate and tert-butyl 2-(2-(N,N-bis(4- methoxybenzyl)sulfamoyl)-4-(2-((ter?-butoxycarbonyl)amino)be nzo[if|thiazol-4-yl)-3-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)phenyl)acetate to afford the title compounds. LC/MS [M+H] ⁺ : 962.89.

Step B: Ethyl 5-(4-(2-aminobenzo[d]thiazol-4-yl)-3-(l-(4-methoxybenzyl)-lH -tetrazol-5- yl)-2-sulfamoylphenyl)pentanoate and ethyl 5-(4-(2-aminobenzo[d]thiazol-4-yl)-3-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)-2-sulfamoylphenyl)pentanoat e

To a solution of ethyl 5-(2-(N,N-bis(4-methoxybenzyl)sulfamoyl)-4-(2-((tert- butoxycarbonyl)amino)benzo[d]thiazol-4-yl)-3-(l-(4-methoxybe nzyl)-lH-tetrazol-5- yl)phenyl)pentanoate and ethyl 5-(2-(N,N-bis(4-methoxybenzyl)sulfamoyl)-4-(2-((tert- butoxycarbonyl)amino)benzo[d]thiazol-4-yl)-3-(2-(4-methoxybe nzyl)-2H-tetrazol-5- yl)phenyl)pentanoate (597 mg, 0.620 mmol) was treated in an analogous fashion as described for the synthesis of tert-Butyl 2-(4-(2-aminobenzo[d]thiazol-4-yl)-2-(N,N-bis(4- methoxybenzyl)sulfamoyl)-3 -( 1 -(4-methoxybenzyl)- 1 H-tetrazol-5-yl)phenyl)acetate and tert- butyl 2-(4-(2-aminobenzo[d]thiazol-4-yl)-2-(N,N-bis(4-methoxybenzy l)sulfamoyl)-3-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)phenyl)acetate to isolate title compounds. LC/MS [M+H] : 742.64.

Step C: 3-(2-Aminobenzo[d]thiazol-4-yl)-6-(5-hydroxypentyl)-2-(l-(4- methoxybenzyl)- lH-tetrazol-5-yl)benzenesulfonamide and 3-(2-aminobenzo[d]thiazol-4-yl)-6-(5-hydroxypentyl)- 2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)benzenesulfonamide

To a solution of ethyl 5-(4-(2-aminobenzo[d]thiazol-4-yl)-3-(l-(4- methoxybenzyl)-lH-tetrazol-5-yl)-2-sulfamoylphenyl)pentanoat e and ethyl 5-(4-(2- aminobenzo[d]thiazol-4-yl)-3-(2-(4-methoxybenzyl)-2H-tetrazo l-5-yl)-2- sulfamoylphenyl)pentanoate (460 mg, 0.620 mmol) was treated in an analogous fashion as described for 3-(2-Aminobenzo[i/]thiazol-4-yl)-6-(2-hydroxyethyl)-N,N-bis( 4-methoxybenzyl)- 2-(l-(4-methoxybenzyl)-lH-tetrazol-5-yl)benzenesulfonamide and 3-(2-aminobenzo[i/]thiazol-4- yl)-6-(2-hydroxyethyl)-N,N-bis(4-methoxybenzyl)-2-(2-(4-meth oxybenzyl)-2H-tetrazol-5- yl)benzenesulfonamide to isolate the title compounds. LC/MS [M+H] ⁺ : 580.52.

REFERENCE EXAMPLE 62

3-(2-Aminobenzo[d]thiazol-4-yl)-6-(cyclobutylmethyl)-N-(4 -methoxybenzyl)-2-(l-(4- methoxybenzyl)-lH-tetrazol-5-yl)benzenesulfonamide and 3-(2-aminobenzo[d]thiazol-4-yl)-6-

(cyclobutylmethyl)-N-(4-methoxybenzyl)-2-(2-(4-methoxyben zyl)-2H-tetrazol-5- yl)benzenesulfonamide

Step A: tert-Butyl (4-(3-(N,N-bis(4-methoxybenzyl)sulfamoyl)-4-(cyclobutylmethy l)-2-

(l-(4-methoxybenzyl)-lH-tetrazol-5-yl)phenyl)benzo[d]thia zol-2-yl)carbamate and tert-butyl (4- (3-(N,N-bis(4-methoxybenzyl)sulfamoyl)-4-(cyclobutylmethyl)- 2-(2-(4-methoxybenzyl)-2H- tetrazol-5-yl)phenyl)benzo[d]thiazol-2-yl)carbamate

To a solution of tert-butyl N-[4-[3-[bis[(4-methoxyphenyl)methyl]sulfamoyl]-4- bromo-2-[2-[(4-methoxyphenyl)methyl]tetrazol-5-yl]phenyl]-l, 3-benzothiazol-2-yl]-N-tert- butoxycarbonyl-carbamate and tert-butyl N-[4-[3-[bis[(4-methoxyphenyl)methyl]sulfamoyl]-4- bromo-2-[l-[(4-methoxyphenyl)methyl]tetrazol-5-yl]phenyl]-l, 3-benzothiazol-2-yl]-N-tert- butoxycarbonyl-carbamate (200 mg, 0.197 mmol) and 0.5 M (cyclobutylmethyl)zinc(il) chloride (1974 μΐ, 0.987 mmol) in diethyl ether were reacted in an analogous fashion to that described for tert-Butyl 2-(2-(N,N-bis(4-methoxybenzyl)sulfamoyl)-4-(2-((tert-butoxyc arbonyl)amino) benzo[i/]thiazol-4-yl)-3-(l-(4-methoxybenzyl)-lH-tetrazol-5- yl)phenyl)acetate and tert-butyl 2- (2-(N,N-bis(4-methoxybenzyl)sulfamoyl)-4-(2-((ter?-butoxycar bonyl)amino)benzo[(i]thiazol-4- yl)-3-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)phenyl)acetate to afford the title compounds.

LC/MS [M+H] ⁺ : 902.86.

Step B: 3-(2-Aminobenzo[d]thiazol-4-yl)-6-(cyclobutylmethyl)-N-(4-me thoxybenzyl)-2- (l-(4-methoxybenzyl)-lH-tetrazol-5-yl)benzenesulfonamide and 3-(2-aminobenzo[d]thiazol-4- yl)-6-(cyclobutylmethyl)-N-(4-methoxybenzyl)-2-(2-(4-methoxy benzyl)-2H-tetrazol-5- yl)benzenesulfonamide

To a solution of tert-butyl (4-(3-( ,N-bis(4-methoxybenzyl)sulfamoyl)-4- (cyclobutylmethyl)-2-( 1 -(4-methoxybenzyl)- 1 H-tetrazol-5-yl)phenyl)benzo[d]thiazol-2- yl)carbamate and tert-butyl (4-(3-( ,N-bis(4-methoxybenzyl)sulfamoyl)-4-(cyclobutylmethyl)-2- (2-(4-methoxybenzyl)-2H-tetrazol-5-yl)phenyl)benzo[d]thiazol -2-yl)carbamate (170 mg, 0.188 mmol) was treated in an analogous fashion to that described for the synthesis of tert-Butyl 2-(4- (2-aminobenzo[d]thiazol-4-yl)-2-( ,N-bis(4-methoxybenzyl)sulfamoyl)-3-(l-(4- methoxybenzyl)-lH-tetrazol-5-yl)phenyl)acetate and tert-butyl 2-(4-(2-aminobenzo[d]thiazol-4- yl)-2-(N,N-bis(4-methoxybenzyl)sulfamoyl)-3-(2-(4-methoxyben zyl)-2H-tetrazol-5- yl)phenyl)acetate to afford the title compounds. LC/MS [M+H] ⁺ : 682.63.

REFERENCE EXAMPLE 63

3-(2-Aminobenzo[d]thiazol-4-yl)-6-(2-aminothiazol-5-yl)-2 -(l -(4-methoxybenzyl)- lH-tetrazol- 5-yl)benzenesulfonamide and 3-(2-aminobenzo[d]thiazol-4-yl)-6-(2-aminothiazol-5-yl)-2-(2 -(4- methoxybenzyl)-2H-tetrazol-5-yl)benzenesulfonamide

Step A: tert-Butyl (4-(3-(N,N-bis(4-methoxybenzyl)sulfamoyl)-4-(2-((tert- butoxycarbonyl)amino)thiazol-5-yl)-2-( 1 -(4-methoxybenzyl)- 1 H-tetrazol-5 - yl)phenyl)benzo[d]thiazol-2-yl)carbamate and tert-butyl (4-(3-(N,N-bis(4- methoxybenzyl)sulfamoyl)-4-(2-((tert-butoxycarbonyl)amino)th iazol-5-yl)-2-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)phenyl)benzo[d]thiazol-2-yl) carbamate

To a solution of tert-butyl N-[4-[3-[bis[(4-methoxyphenyl)methyl]sulfamoyl]-4- bromo-2-[2-[(4-methoxyphenyl)methyl]tetrazol-5-yl]phenyl]-l, 3-benzothiazol-2-yl]-N-tert- butoxycarbonyl-carbamate and tert-butyl N- [4- [3 - [bis [(4-methoxyphenyl)methyl] sulfamoyl] -4- bromo-2-[l-[(4-methoxyphenyl)methyl]tetrazol-5-yl]phenyl]-l, 3-benzothiazol-2-yl]-N-tert- butoxycarbonyl-carbamate (327 mg, 0.323 mmol) and tert-butyl (5-(4,4,5,5-tetramethyl-l,3,2- dioxaborolan-2-yl)thiazol-2-yl)carbamate (211 mg, 0.646 mmol) was treated as described for the synthesis of 6-Bromo-N,N-bis(4-methoxybenzyl)-2-(l-(4-methoxybenzyl)-lH-t etrazol-5-yl)-3- (quinolin-5-yl)benzenesulfonamide compound with 6-bromo-N,N-bis(4-methoxybenzyl)-2-(2- (4-methoxybenzyl)-2H-tetrazol-5-yl)-3-(quinolin-5-yl)benzene sulfonamide to afford the title compound. LC/MS [M+H] ⁺ : 1032.92.

Step B : 3 -(2-Aminobenzo[d]thiazol-4-yl)-6-(2-aminothiazol-5-yl)-2-( 1 -(4- methoxybenzyl)-lH-tetrazol-5-yl)benzenesulfonamide and 3-(2-aminobenzo[d]thiazol-4-yl)-6- (2-aminothiazol-5-yl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-y l)benzenesulfonamide

To a solution of tert-butyl (4-(3-( ,N-bis(4-methoxybenzyl)sulfamoyl)-4-(2- ((tert-butoxycarbonyl)amino)thiazol-5 -yl)-2-( 1 -(4-methoxybenzyl)- 1 H-tetrazol-5- yl)phenyl)benzo[d]thiazol-2-yl)carbamate and tert-butyl (4-(3-(N,N-bis(4- methoxybenzyl)sulfamoyl)-4-(2-((tert-butoxycarbonyl)amino)th iazol-5-yl)-2-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)phenyl)benzo[d]thiazol-2-yl) carbamate (120 mg, 0.116 mmol) was treated in an analogous fashion to that described for the synthesis of tert-Butyl 2-(4-(2- aminobenzo[d]thiazol-4-yl)-2-( ,N-bis(4-methoxybenzyl)sulfamoyl)-3-(l-(4-methoxybenzyl)- lH-tetrazol-5-yl)phenyl)acetate and tert-butyl 2-(4-(2-aminobenzo[d]thiazol-4-yl)-2-(N,N-bis(4- methoxybenzyl)sulfamoyl)-3 -(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)phenyl)acetate to afford the title compounds. LC/MS [M+H] ⁺ : 592.47.

REFERENCE EXAMPLE 64

3-(2-Aminobenzo[d]thiazol-4-yl)-2-(l -(4-methoxybenzyl)- lH-tetrazol-5-yl)-6- neopentylbenzenesulfonamide and 3-(2-aminobenzo[d]thiazol-4-yl)-2-(2-(4-methoxybenzyl)- 2H-tetrazol-5-yl)-6-neopentylbenzenesulfonamide

The title compounds were prepared in an analogous fashion to that described for 3-(2-Aminobenzo[d]thiazol-4-yl)-6-(cyclobutylmethyl)-N-(4-me thoxybenzyl)-2-(l-(4- methoxybenzyl)-lH-tetrazol-5-yl)benzenesulfonamide and 3-(2-aminobenzo[d]thiazol-4-yl)-6- (cyclobutylmethyl)-N-(4-methoxybenzyl)-2-(2-(4-methoxybenzyl )-2H-tetrazol-5- yl)benzenesulfonamide

Starting from tert-butyl N-[4-[3-[bis[(4-methoxyphenyl)methyl]sulfamoyl]-4- bromo-2-[2-[(4-methoxyphenyl)methyl]tetrazol-5-yl]phenyl]-l, 3-benzothiazol-2-yl]-N-tert- butoxycarbonyl-carbamate and tert-butyl N-[4-[3-[bis[(4-methoxyphenyl)methyl]sulfamoyl]-4- bromo-2-[l-[(4-methoxyphenyl)methyl]tetrazol-5-yl]phenyl]-l, 3-benzothiazol-2-yl]-N-tert- butoxycarbonyl-carbamate and 0.5 M Neopentylzinc Bromide (2369 μΐ, 1.185 mmol). LC/MS [M+H] ⁺ : 564.57.

REFERENCE EXAMPLE 65

3-(4-(2-Aminobenzo[d]thiazol-4-yl)-3-(l-(4-methoxybenzyl) -lH-tetrazol-5-yl)-2- sulfamoylphenyl)propanoic acid and 3-(4-(2-aminobenzo[d]thiazol-4-yl)-3-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)-2-sulfamoylphenyl)propanoic acid

Step A: 3-(2-(N,N-Bis(4-methoxybenzyl)sulfamoyl)-4-(2-((tert- butoxycarbonyl)amino)benzo[d]thiazol-4-yl)-3-(l-(4-methoxybe nzyl)-lH-tetrazol-5- yl)phenyl)propanoic acid and 3-(2-(N,N-bis(4-methoxybenzyl)sulfamoyl)-4-(2-((tert- butoxycarbonyl)amino)benzo[d]thiazol-4-yl)-3-(2-(4-methoxybe nzyl)-2H-tetrazol-5- yl)phenyl)propanoic acid

To a solution of ethyl 3-(2-(N,N-bis(4-methoxybenzyl)sulfamoyl)-4-(2-((tert- butoxycarbonyl)amino)benzo[d]thiazol-4-yl)-3-(l-(4-methoxybe nzyl)-lH-tetrazol-5- yl)phenyl)propanoate and ethyl 3-(2-(N,N-bis(4-methoxybenzyl)sulfamoyl)-4-(2-((tert- butoxycarbonyl)amino)benzo[d]thiazol-4-yl)-3-(2-(4-methoxybe nzyl)-2H-tetrazol-5- yl)phenyl)propanoate (220 mg, 0.236 mmol) was dissolved in dioxane (2355 μl):water (2355 μΐ) and LiOH (28.2 mg, 1.178 mmol) was added to the system. The solution was stirred for 16 hr. The solution was then added to EtOAc (60 mL) and washed with brine (2 x 20 mL). The organic was dried and used without further purification to isolate the title compounds. LC/MS [M+H] ⁺ : 906.91

Step B : 3 -(4-(2-Aminobenzo [d]thiazol-4-yl)-3 -( 1 -(4-methoxybenzyl)- 1 H-tetrazol-5-yl)-2- sulfamoylphenyl)propanoic acid and 3-(4-(2-aminobenzo[d]thiazol-4-yl)-3-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)-2-sulfamoylphenyl)propanoic acid

To a solution of 3-(2-(N,N-Bis(4-methoxybenzyl)sulfamoyl)-4-(2-((tert- butoxycarbonyl)amino)benzo[d]thiazol-4-yl)-3-(l-(4-methoxybe nzyl)-lH-tetrazol-5- yl)phenyl)propanoic acid and 3-(2-(N,N-bis(4-methoxybenzyl)sulfamoyl)-4-(2-((tert- butoxycarbonyl)amino)benzo[d]thiazol-4-yl)-3-(2-(4-methoxybe nzyl)-2H-tetrazol-5- yl)phenyl)propanoic acid (100 mg, 0.1 10 mmol) was treated in the same fashion as described for the synthesis of tert-Butyl 2-(4-(2-aminobenzo[d]thiazol-4-yl)-2-(N,N-bis(4- methoxybenzyl)sulfamoyl)-3 -( 1 -(4-methoxybenzyl)- 1 H-tetrazol-5-yl)phenyl)acetate and tert- butyl 2-(4-(2-aminobenzo[d]thiazol-4-yl)-2-(N,N-bis(4-methoxybenzy l)sulfamoyl)-3-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)phenyl)acetate to afford the title compounds. LC/MS [M+H] ⁺ : 566.44.

REFERENCE EXAMPLE 66

3-(4-(2-Aminobenzo[d]thiazol-4-yl)-3-(l-(4-methoxybenzyl)-lH -tetrazol-5-yl)-2- sulfamoylphenyl)-N-(4-methoxybenzyl)propanamide and 3 -(4-(2-aminobenzo[d]thiazol-4-yl)-3 - (2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-2-sulfamoylphenyl)-N- (4-methoxybenzyl)propanamide

Step A: tert-Butyl (4-(4-(3-(bis(4-methoxybenzyl)amino)-3-oxopropyl)-3-(N,N-bis (4- methoxybenzyl)sulfamoyl)-2-(l-(4-methoxybenzyl)-lH-tetrazol- 5-yl)phenyl)benzo[d]thiazol-2- yl)carbamate and with tert-butyl (4-(4-(3-(bis(4-methoxybenzyl)amino)-3-oxopropyl)-3-(N,N- bis(4-methoxybenzyl)sulfamoyl)-2-(2-(4-methoxybenzyl)-2H-tet razol-5- yl)phenyl)benzo[d]thiazol-2-yl)carbamate

To a solution of 3-(2-(N,N-bis(4-methoxybenzyl)sulfamoyl)-4-(2-((tert- butoxycarbonyl)amino)benzo[d]thiazol-4-yl)-3 -( 1 -(4-methoxybenzyl)- 1 H-tetrazol-5 - yl)phenyl)propanoic acid and 3-(2-(N,N-bis(4-methoxybenzyl)sulfamoyl)-4-(2-((tert- butoxycarbonyl)amino)benzo[d]thiazol-4-yl)-3-(2-(4-methoxybe nzyl)-2H-tetrazol-5- yl)phenyl)propanoic acid (100 mg, 0.110 mmol) was dissolved in DMF (3 mL) and EDC (52.9 mg, 0.276 mmol), HOAT (1.502 mg, 0.011 mmol), and DIPEA (0.077 mL, 0.441 mmol) was added. This was stirred for 5 minutes before the addition of bis(4-methoxybenzyl)amine (85 mg, 0.331 mmol). The solution was stirred under an atmosphere of nitrogen for 16 hr. The solution was diluted with EtOAc (40 mL) and extracted with water (2 x 20 mL), brine (2 x 20 mL), dried (MgS0 ₄ ) and concentrated. The reaction mixture was used without further purification to isolate the title compounds. LC/MS [M+H] ⁺ : 1146.24.

Step B : 3 -(4-(2-Aminobenzo [d]thiazol-4-yl)-3 -( 1 -(4-methoxybenzyl)- 1 H-tetrazol-5-yl)-2- sulfamoylphenyl)-N-(4-methoxybenzyl)propanamide and 3 -(4-(2-aminobenzo[d]thiazol-4-yl)-3 - (2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-2-sulfamoylphenyl)-N- (4-methoxybenzyl)propanamide

To a solution of tert-butyl (4-(4-(3-(bis(4-methoxybenzyl)amino)-3-oxopropyl)-3- (N,N-bis(4-methoxybenzyl)sulfamoyl)-2-(l-(4-methoxybenzyl)-l H-tetrazol-5- yl)phenyl)benzo[d]thiazol-2-yl)carbamate compound with tert-butyl (4-(4-(3-(bis(4- methoxybenzyl)amino)-3-oxopropyl)-3-( ,N-bis(4-methoxybenzyl)sulfamoyl)-2-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)phenyl)benzo[d]thiazol-2-yl) carbamate (126 mg, 0.110 mmol) was treated in the same fashion as described for the synthesis of tert-Butyl 2-(4-(2- aminobenzo[d]thiazol-4-yl)-2-( ,N-bis(4-methoxybenzyl)sulfamoyl)-3-(l -(4-methoxybenzyl)- lH-tetrazol-5-yl)phenyl)acetate and tert-butyl 2-(4-(2-aminobenzo[d]thiazol-4-yl)-2-(N,N-bis(4- methoxybenzyl)sulfamoyl)-3 -(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)phenyl)acetate to afford the title compounds. LC/MS [M+H] ⁺ : 685.63.

REFERENCE EXAMPLE 67

tert-Butyl (4-(3-(N,N-bis(4-methoxybenzyl)sulfamoyl)-4-ethynyl-2-(l-(4- methoxybenzyl)-lH- tetrazol-5-yl)phenyl)benzo[d]thiazol-2-yl)carbamate and tert-butyl (4-(3-(N,N-bis(4- methoxybenzyl)sulfamoyl)-4-ethynyl-2-(2-(4-methoxybenzyl)-2H -tetrazol-5- yl)phenyl)benzo[d]thiazol-2-yl)carbamate

Step A: 3-(2-Aminobenzo[d]thiazol-4-yl)-N,N-bis(4-methoxybenzyl)-2-( l-(4- methoxybenzyl)- lH-tetrazol-5-yl)-6-((trimethylsilyl)ethynyl)benzenesulfonam ide and 3-(2- aminobenzo[d]thiazol-4-yl)-N,N-bis(4-methoxybenzyl)-2-(2-(4- methoxybenzyl)-2H-tetrazol-5- yl)-6-((trimethylsilyl)ethynyl)benzenesulfonamide

To a solution of 3-(2-aminobenzo[d]thiazol-4-yl)-6-bromo-N,N-bis(4- methoxybenzyl)-2-(l-(4-methoxybenzyl)-lH-tetrazol-5-yl)benze nesulfonamide and 3-(2- aminobenzo[d]thiazol-4-yl)-6-bromo-N,N-bis(4-methoxybenzyl)- 2-(2-(4-methoxybenzyl)-2H- tetrazol-5-yl)benzenesulfonamide (3.5 g, 4.31 mmol) was treated as in the synthesis of N,N- bis(4-methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl )-3- ((trimethylsilyl)ethynyl)benzenesulfonamide and N,N-bis(4-methoxybenzyl)-2-( 1 -(4- methoxybenzyl)-lH-tetrazol-5-yl)-3-((trimethylsilyl)ethynyl) benzenesulfonamide to afford the title compounds. LC/MS [M+H] ⁺ : 830.72.

Step B : 3 -(2-Aminobenzo [d]thiazol-4-yl)-6-ethynyl-N,N-bis(4-methoxybenzyl)-2-( 1 -(4- methoxybenzyl)-lH-tetrazol-5-yl)benzenesulfonamide and 3-(2-aminobenzo[d]thiazol-4-yl)-6- ethynyl-N,N-bis(4-methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-t etrazol-5- yl)benzenesulfonamide

To a solution of 3-(2-aminobenzo[d]thiazol-4-yl)-N,N-bis(4-methoxybenzyl)-2- ( 1 -(4-methoxybenzyl)- lH-tetrazol-5-yl)-6-((trimethylsilyl)ethynyl)benzenesulfonam ide and 3 - (2-aminobenzo[d]thiazol-4-yl)-N,N-bis(4-methoxybenzyl)-2-(2- (4-methoxybenzyl)-2H-tetrazol- 5-yl)-6-((trimethylsilyl)ethynyl)benzenesulfonamide (3.1 g, 3.73 mmol) in THF was stirred with TBAF (2 equivalents) at room temperature for 1 hr. The mixture was diluted with ether (100 mL), washed with brine (3 x 25 mL), dried over MgS0 ₄ and concentrated to give the title compound.

Step C: tert-Butyl (4-(3-( ,N-bis(4-methoxybenzyl)sulfamoyl)-4-ethynyl-2-(l-(4- methoxybenzyl)-lH-tetrazol-5-yl)phenyl)benzo[d]thiazol-2-yl) carbamate and tert-butyl (4-(3-

(N,N-bis(4-methoxybenzyl)sulfamoyl)-4-ethynyl-2-(2-(4-met hoxybenzyl)-2H-tetrazol-5- yl)phenyl)benzo[d]thiazol-2-yl)carbamate

To a solution of 3-(2-aminobenzo[d]thiazol-4-yl)-6-ethynyl-N,N-bis(4- methoxybenzyl)-2-(l-(4-methoxybenzyl)-lH-tetrazol-5-yl)benze nesulfonamide and 3-(2- aminobenzo[d]thiazol-4-yl)-6-ethynyl-N,N-bis(4-methoxybenzyl )-2-(2-(4-methoxybenzyl)-2H- tetrazol-5-yl)benzenesulfonamide was treated as in the synthesis of tert-Butyl N- [4- [3 -[bis [(4- methoxyphenyl)methyl]sulfamoyl]-4-bromo-2-[2-[(4-methoxyphen yl)methyl]tetrazol-5- yl]phenyl]-l,3-benzothiazol-2-yl]-N-tert-butoxycarbonyl-carb amate and tert-butyl N-[4-[3- [bis[(4-methoxyphenyl)methyl]sulfamoyl]-4-bromo-2-[l-[(4-met hoxyphenyl)methyl]tetrazol-5- yl]phenyl]-l,3-benzothiazol-2-yl]-N-tert-butoxycarbonyl-carb amate to provide the title compounds. LC/MS [M+H] ⁺ : 858.71.

REFERENCE EXAMPLE 68

tert-Butyl 4-(2-(N,N-bis(4-methoxybenzyl)sulfamoyl)-4-(2-((tert- butoxycarbonyl)amino)benzo[d]thiazol-4-yl)-3-(l-(4-methoxybe nzyl)-lH-tetrazol-5- yl)phenethyl)piperidine-l-carboxylate and tert-butyl 4-(2-(N,N-bis(4- methoxybenzyl)sulfamoyl)-4-(2-((tert-butoxycarbonyl)amino)be nzo[d]thiazol-4-yl)-3-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)phenethyl)piperidine-l-carbo xylate

Step A: tert-Butyl 4-((2-(N,N-bis(4-methoxybenzyl)sulfamoyl)-4-(2-((tert- butoxycarbonyl)amino)benzo[d]thiazol-4-yl)-3-(l-(4-methoxybe nzyl)-lH-tetrazol-5- yl)phenyl)ethynyl)-3,6-dihydropyridine-l(2H)-carboxylate and tert-butyl 4-((2-(N,N-bis(4- methoxybenzyl)sulfamoyl)-4-(2-((tert-butoxycarbonyl)amino)be nzo[d]thiazol-4-yl)-3-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)phenyl)ethynyl)-3,6-dihydrop yridine-l(2H)-carboxylate

To a solution of tert-butyl (4-(3-( ,N-bis(4-methoxybenzyl)sulfamoyl)-4-ethynyl- 2-( 1 -(4-methoxybenzyl)- 1 H-tetrazol-5-yl)phenyl)benzo[d]thiazol-2-yl)carbamate and tert-butyl (4-(3-CN,N-bis(4-methoxybenzyl)sulfamoyl)-4-ethynyl-2-(2-(4- methoxybenzyl)-2H-tetrazol-5- yl)phenyl)benzo[d]thiazol-2-yl)carbamate (0.4 g, 0.466 mmol) and tert-butyl 4-bromo-5,6- dihydropyridine-l(2H)-carboxylate (0.183 g, 0.699 mmol) was treated as in the synthesis of 3- ((6-Amino-5-(hydroxymethyl)pyridin-3-yl)ethynyl)-N,N-bis(4-m ethoxybenzyl)-2-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)benzenesulfonamide and 3-((6-amino-5- (hydroxymethyl)pyridin-3 -yl)ethynyl)-N,N-bis(4-methoxybenzyl)-2-( 1 -(4-methoxybenzyl)- 1 H- tetrazol-5-yl)benzenesulfonamide to provide the title compounds. LC/MS [M+H] ⁺ : 1039.96. Step B: tert-Butyl 4-(2-(N,N-bis(4-methoxybenzyl)sulfamoyl)-4-(2-((tert- butoxycarbonyl)amino)benzo[d]thiazol-4-yl)-3-(l-(4-methoxybe nzyl)-lH-tetrazol-5- yl)phenethyl)piperidine-l-carboxylate and tert-butyl 4-(2-(N,N-bis(4- methoxybenzyl)sulfamoyl)-4-(2-((tert-butoxycarbonyl)amino)be nzo[d]thiazol-4-yl)-3-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)phenethyl)piperidine-l-carbo xylate

To a solution of tert-butyl 4-((2-(N,N-bis(4-methoxybenzyl)sulfamoyl)-4-(2- ((tert-butoxycarbonyl)amino)benzo[d]thiazol-4-yl)-3-(l-(4-me thoxybenzyl)-lH-tetrazol-5- yl)phenyl)ethynyl)-3,6-dihydropyridine-l(2H)-carboxylate and tert-butyl 4-((2-(N,N-bis(4- methoxybenzyl)sulfamoyl)-4-(2-((tert-butoxycarbonyl)amino)be nzo[d]thiazol-4-yl)-3-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)phenyl)ethynyl)-3,6-dihydrop yridine-l(2H)-carboxylate (0.090 g, 0.087 mmol) are treated as in the synthesis of 3-(2-(6-Amino-5- (hydroxymethyl)pyridin-3-yl)ethyl)-N,N-bis(4-methoxybenzyl)- 2-(2-(4-methoxybenzyl)-2H- tetrazol-5-yl)-6-(trifluoromethyl)benzenesulfonamide and 3-(2-(6-amino-5- (hydroxymethyl)pyridin-3-yl)ethyl)-N,N-bis(4-methoxybenzyl)- 2-(2-(4-methoxybenzyl)-2H- tetrazol-5-yl)-6-(trifluoromethyl)benzenesulfonamide to isolate the title compounds.

REFERENCE EXAMPLE 69

tert-Butyl (4-(3-(N,N-bis(4-methoxybenzyl)sulfamoyl)-4-(2-(4-((tert- butoxycarbonyl)amino)cyclohexyl)ethyl)-2-(l-(4-methoxybenzyl )-lH-tetrazol-5- yl)phenyl)benzo[d]thiazol-2-yl)carbamate and tert-butyl (4-(3-(N,N-bis(4- methoxybenzyl)sulfamoyl)-4-(2-(4-((tert-butoxycarbonyl)amino )cyclohexyl)ethyl)-2-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)phenyl)benzo[d]thiazol-2-yl) carbamate

Step A: tert-Butyl (4-(3-( ,N-bis(4-methoxybenzyl)sulfamoyl)-4-((4-((tert- butoxycarbonyl)amino)cyclohex- 1 -en- 1 -yl)ethynyl)-2-( 1 -(4-methoxybenzyl)- 1 H-tetrazol-5- yl)phenyl)benzo[d]thiazol-2-yl)carbamate and tert-butyl (4-(3-(N,N-bis(4- methoxybenzyl)sulfamoyl)-4-((4-((tert-butoxycarbonyl)amino)c yclohex- 1 -en- 1 -yl)ethynyl)-2-(2- (4-methoxybenzyl)-2H-tetrazol-5-yl)phenyl)benzo[d]thiazol-2- yl)carbamate

To a solution of tert-butyl (4-(3-( ,N-bis(4-methoxybenzyl)sulfamoyl)-4-ethynyl- 2-( 1 -(4-methoxybenzyl)- 1 H-tetrazol-5-yl)phenyl)benzo[d]thiazol-2-yl)carbamate and tert-butyl (4-(3-( ,N-bis(4-methoxybenzyl)sulfamoyl)-4-ethynyl-2-(2-(4-methoxyb enzyl)-2H-tetrazol-5- yl)phenyl)benzo[d]thiazol-2-yl)carbamate (0.2 g, 0.233 mmol) was added 4-((tert- butoxycarbonyl)amino)cyclohex- 1 -en- 1-yl trifluoromethanesulfonate (0.121 g, 0.350 mmol) and was treated as in the synthesis of 3-((6-Amino-5-(hydroxymethyl)pyridin-3-yl)ethynyl)-N,N- bis(4-methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl )benzenesulfonamide and 3-((6- amino-5-(hydroxymethyl)pyridin-3-yl)ethynyl)-N,N-bis(4-metho xybenzyl)-2-(l-(4- methoxybenzyl)-lH-tetrazol-5-yl)benzenesulfonamide to provide the title compounds. LC/MS [M+H] ⁺ : 1054.05.

Step B : tert-Butyl (4-(3 -( ,N-bis(4-methoxybenzyl)sulfamoyl)-4-(2-(4-((tert- butoxycarbonyl)amino)cyclohexyl)ethyl)-2-(l-(4-methoxybenzyl )-lH-tetrazol-5- yl)phenyl)benzo[d]thiazol-2-yl)carbamate and tert-butyl (4-(3-(N,N-bis(4- methoxybenzyl)sulfamoyl)-4-(2-(4-((tert-butoxycarbonyl)amino )cyclohexyl)ethyl)-2-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)phenyl)benzo[d]thiazol-2-yl) carbamate

A solution of tert-butyl (4-(3-(N,N-bis(4-methoxybenzyl)sulfamoyl)-4-((4-((tert- butoxycarbonyl)amino)cyclohex- 1 -en- 1 -yl)ethynyl)-2-( 1 -(4-methoxybenzyl)- 1 H-tetrazol-5- yl)phenyl)benzo[d]thiazol-2-yl)carbamate and tert-butyl (4-(3-(N,N-bis(4- methoxybenzyl)sulfamoyl)-4-((4-((tert-butoxycarbonyl)amino)c yclohex- 1 -en- 1 -yl)ethynyl)-2-(2- (4-methoxybenzyl)-2H-tetrazol-5-yl)phenyl)benzo[d]thiazol-2- yl)carbamate (0.090 g, 0.085 mmol) was treated as in the synthesis of 3-(2-(6-Amino-5-(hydroxymethyl)pyridin-3-yl)ethyl)- N,N-bis(4-methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol- 5-yl)-6- (trifluoromethyl)benzenesulfonamide and 3 -(2-(6-amino-5-(hydroxymethyl)pyridin-3 -yl)ethyl)- N,N-bis(4-methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol- 5-yl)-6- (trifluoromethyl)benzenesulfonamide to isolate the title compounds. LC/MS [M+H] ⁺ : 1060.03.

REFERENCE EXAMPLE 70

3,6-Bis(5-hydroxypentyl)-N,N-bis(4-methoxybenzyl)-2-(l-(4-me thoxybenzyl)-lH-tetrazol-5- yl)benzenesulfonamide and 3,6-bis(5-hydroxypentyl)-N,N-bis(4-methoxybenzyl)-2-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)benzenesulfonamide

Step A: Diethyl 5,5'-(2-(N,N-bis(4-methoxybenzyl)sulfamoyl)-3-(l-(4-methoxyb enzyl)- lH-tetrazol-5-yl)-l,4-phenylene)dipentanoate and diethyl 5,5'-(2-(N,N-bis(4- methoxybenzyl)sulfamoyl)-3-(2-(4-methoxybenzyl)-2H-tetrazol- 5-yl)-l,4- phenylene)dipentanoate

To a solution of 6-bromo-3-iodo-N,N-bis(4-methoxybenzyl)-2-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)benzenesulfonamide and 6-bromo-3-iodo-N,N-bis(4- methoxybenzyl)-2-(l-(4-methoxybenzyl)-lH-tetrazol-5-yl)benze nesulfonamide was added 0.5 M 5-ethoxy-oxopentylzinc bromide (1.27E+04 μΐ, 6.33 mmol) and treated in an analogous fashion as in the synthesis of tert-Butyl 2-(2-(N,N-bis(4-methoxybenzyl)sulfamoyl)-3-(l-(4- methoxybenzyl)tetrazolidin-5-yl)-4-(quinolin-5-yl)phenyl)ace tate and tert-butyl 2-(2-(N,N-bis(4- methoxybenzyl)sulfamoyl)-3-(2-(4-methoxybenzyl)-2H-tetrazol- 5-yl)-4-(quinolin-5- yl)phenyl)acetate to provide the title compounds. LC/MS [M+H] ⁺ : 842.75.

Step B: 3,6-Bis(5-hydroxypentyl)-N,N-bis(4-methoxybenzyl)-2-(l-(4-me thoxybenzyl)- lH-tetrazol-5-yl)benzenesulfonamide and 3,6-bis(5-hydroxypentyl)-N,N-bis(4-methoxybenzyl)- 2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)benzenesulfonamide

To the solution of diethyl 5,5'-(2-(N,N-bis(4-methoxybenzyl)sulfamoyl)-3-(l-(4- methoxybenzyl)-lH-tetrazol-5-yl)-l,4-phenylene)dipentanoate and diethyl 5,5'-(2-(N,N-bis(4- methoxybenzyl)sulfamoyl)-3-(2-(4-methoxybenzyl)-2H-tetrazol- 5-yl)-l,4- phenylene)dipentanoate (210 mg, 0.249 mmol) in THF (10 mL) was added DIBAL-H (2.494 mL, 2.494 mmol). The solution was stirred for 2 hr and the reaction was quenched with HC1 (1.871 mL, 3.74 mmol) and then concentrated under reduced pressure to yield the title compound. LC/MS [M+H] ⁺ : 758.7

REFERENCE EXAMPLE 71

3,6-Bis(6-hydroxyhexyl)-N,N-bis(4-methoxybenzyl)-2-(l-(4- methoxybenzyl)-lH-tetrazol-5- yl)benzenesulfonamide and 3,6-bis(6-hydroxyhexyl)-N,N-bis(4-methoxybenzyl)-2-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)benzenesulfonamide

Step A: Di-tert-butyl 6,6'-(2-(N,N-bis(4-methoxybenzyl)sulfamoyl)-3-(l-(4- methoxybenzyl)-lH-tetrazol-5-yl)-l,4-phenylene)dihexanoate and di-tert-butyl 6,6'-(2-(N,N- bis(4-methoxybenzyl)sulfamoyl)-3-(2-(4-methoxybenzyl)-2H-tet razol-5-yl)-l,4- phenylene)dihexanoate

To a solution of 6-bromo-3-iodo-N,N-bis(4-methoxybenzyl)-2-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)benzenesulfonamide and 6-bromo-3-iodo-N,N-bis(4- methoxybenzyl)-2-(l-(4-methoxybenzyl)-lH-tetrazol-5-yl)benze nesulfonamide (500 mg, 0.670 mmol) was added 0.5 M (6-(tert-butoxy)-6-oxohexyl)zinc(II) bromide (13.400 mL, 6.70 mmol) in diethyl ether and was treated in an analogous fashion as in the synthesis of tert-Butyl 2-(2- (N,N-bis(4-methoxybenzyl)sulfamoyl)-3-(l-(4-methoxybenzyl)te trazolidin-5-yl)-4-(quinolin-5- yl)phenyl)acetate and tert-butyl 2-(2-(N,N-bis(4-methoxybenzyl)sulfamoyl)-3-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)-4-(quinolin-5-yl)phenyl)ace tate to provide the title compounds. LC/MS [M+H] ⁺ : 927.03.

Step B : 3 ,6-Bis(6-hydroxyhexyl)-N,N-bis(4-methoxybenzyl)-2-( 1 -(4-methoxybenzyl)-

1 H-tetrazol-5-yl)benzenesulfonamide and 3 ,6-bis(6-hydroxyhexyl)-N,N-bis(4-methoxybenzyl)- 2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)benzenesulfonamide

To a solution of di-tert-butyl 6,6'-(2-(N,N-bis(4-methoxybenzyl)sulfamoyl)-3-(l- (4-methoxybenzyl)-lH-tetrazol-5-yl)-l,4-phenylene)dihexanoat e and di-tert-butyl 6,6'-(2-(N,N- bis(4-methoxybenzyl)sulfamoyl)-3-(2-(4-methoxybenzyl)-2H-tet razol-5-yl)-l,4- phenylene)dihexanoate (412 mg, 0.445 mmol) was treated in the same fashion as in the synthesis of 6-(2-Hydroxyethyl)-N,N-bis(4-methoxybenzyl)-2-( 1 -(4-methoxybenzyl)- 1 H-tetrazol-5-yl)-3- (quinolin-5-yl)benzenesulfonamide and 6-(2-hydroxyethyl)-N,N-bis(4-methoxybenzyl)-2-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)-3-(quinolin-5-yl)benzenesul fonamide to provide the title compound. LC/MS [M+H] ⁺ : 786.83.

EXAMPLE 1

4'-Methyl-2-(lH-tetrazol-5-yl)-[l,l'-biphenyl]-3-sulfonamide

To a solution of 3-bromo-2-(l-(4-methoxybenzyl)-lH-tetrazol-5- yl)benzenesulfonamide and 3-bromo-2-(2-(4-methoxybenzyl)-lH-tetrazol-5- yl)benzenesulfonamide (250 mg, 0.589 mmol) in a mixture of DME (4 mL) and water (1 mL) was added bis(tri-tert-butylphosphine)palladium(0) (30.1 mg, 0.059 mmol), p-tolylboronic acid (96 mg, 0.707 mmol) and a ₂ C0 ₃ (74.9 mg, 0.707 mmol) at rt. The resulting mixture was degassed and heated at 97°C for 12 hr. The reaction mixture was cooled to rt, diluted with ethyl acetate (20 mL), washed with IN HQ (10 mL) followed by brine (10 mL). The organic layer was dried over MgS0 ₄ , filtered and concentrated to dryness to give crude products which were taken to the next step without further purification. To this crude product was added anisole (0.102 mL, 0.932 mmol) followed by TFA (3 mL) and the resulting mixture was stirred at room temperature for 12 hr. The reaction mixture was concentrated to dryness and purified by reverse phase CI 8 column using 0 to 90% water (0.05% TFA) in acetonitrile (0.05% TFA). LC/MS (M+Na) ⁺ : 338.2.

EXAMPLES 2-18

Parallel synthesis of 4'-substituted 2-(lH-tetrazol-5-yl)-[l,l'-biphenyl]-3-sulfonamides

Step A: Palladium catalyzed C-C coupling of arylbromide and boronic acids or boronic esters (such as pinacol esters).

Into 2 dram vials were added substituted boronic acid or esters (commercially available, known from the literature, or prepared as described herein) and l, l'-bis(di-tert- butylphosphino) ferrocene palladium chloride (2.480 mg, 3.80 μιηοΐ) and 254 μΐ, of 1 N degassed aq. K3PO4 solution. In a glove box under a dry nitrogen atomosphere, 1.5 mL of a solution of the mixture of isomers 3-bromo-2-(l-(4-methoxybenzyl)-lH-tetrazol-5- yl)benzenesulfonamide and 3-bromo-2-(2-(4-methoxybenzyl)-lH-tetrazol-5- yl)benzenesulfonamide from Reference Example 1 (25 mg, 0.063 mmol) in EtOH were added into each vial. The vials were capped and heated at 70°C with stirring for 20 hr. After the vials were cooled to room temperature, the solvent was removed in a GeneVac. Into each residue was added 600 μϊ _^ of H ₂ 0 and 2 mL of EtOAc. The organic layers were transferred into 2 dram vials. The organic solvent was removed in GeneVac to afford the crude intermediates which were deprotected without further purification in the subsequent step.

Step B: Removal of the p-methoxybenzyl (PMB) protecting group by hydrogenation

The residues from Step A were dissolved in 1.5 mL of EtOH. Into each vial was added 20 mg of 10% Pd/C and 250 mg of ammonium formate (250.0 mg, 3.96 mmol). The vials were sealed and heated at 55°C under stirring. The pressure was released periodically by unscrewing the cap. After 5 hr, the reactions were monitored by UPLC. The reaction only partially proceeded. Another aliquot of ammonium formate (250.0 mg, 3.96 mmol) was added and the vial heated at 55°C for another 5 hrs. The mixtures were cooled to room temperature and filtered through filters. The filtrates were concentrated in a GeneVac. The residues were dissolved in DMSO. Each crude mixture was filtered into a 96-well tray and purified with HPLC to afford Examples 2-18.

EXAMPLES 19-30

Parallel synthesis of 3 -substituted 2-(lH-tetrazol-5-yl)benzenesulfonamides

Step A: Palladium catalyzed C-C coupling of arylbromide and boronic acids or boronic esters (such as pinacol esters).

Into 2 dram vials were added substituted boronic acids or esters (commercially available, or prepared as described herein, 0.071 mmol) and l,l'-bis(di-?ert-butylphosphino) ferrocene palladium chloride (3.07 mg, 4.7 μιηοΐ) and 189 μΐ, of 1 N degassed aq. K3PO4 solution. In glove box, 1.3 mL of solution of the mixture of isomeric 3-bromo-2-(l-(4- methoxybenzyl)- lH-tetrazol-5-yl)benzenesulfonamide and 3-bromo-2-(2-(4-methoxybenzyl)- lH-tetrazol-5-yl)benzenesulfonamide from Reference Example 1 (20 mg, 0.047 mmol) in EtOH were added into each vial. The vials were capped and heated at 70°C with stirring for 20 hr

(overnight). After the vials were cooled down to room temperature, the solvent was removed in GeneVac. Into each residue was added 600 μϊ _^ of H ₂ 0 and 2 mL of EtOAc. The organic layers were transferred into 2 dram vials. The organic solvent was removed in GeneVac to afford the crude intermediates.

Step B: Removal of the p-methoxybenzyl (PMB) protecting group under acidic conditions.

Into each vial was added a solution of anisole (21 mg) in TFA (600 μί). The vials were heated at 45 °C for 16 hr. The solvent was removed in a GeneVac. The residues were dissolved in 1.3 mL of DMSO. Each crude mixture was filtered into a 96-well tray and purified by HPLC to afford the following Examples. Boronic acids and boronic esters were obtained from commercial sources, are known in the literature, or were prepared as described herein. Note that in some instances the boronic acid used in Step A contains an amine group. In these cases, the reagent is typically obtained with a tert-butoxycarbonyl protective group on the amine moiety, which is concurrently removed under the final PMB deprotection step (Step B) with TFA and anisole.

EXAMPLE 31

4'-piperidin-4-yl-2-(lH- ide, hydrochloride salt

Step A: tert-butyl 4-(2'-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-3'-sulfamoyl-[l ,l'- biphenyl]-4-yl)piperidine- 1 -carboxylate and tert-butyl 4-(2'-( 1 -(4-methoxybenzyl)- lH-tetrazol- 5 -yl)-3 '-sulfamoyl-[ 1 , 1 '-biphenyl] -4-yl)piperidine- 1 -carboxylate

To the isomer mixture 3-Bromo-2-(l-(4-methoxybenzyl)(lH-tetrazol-5- yl))benzenesulfonamide and 3-bromo-2-(2-(4-methoxybenzyl)(lH-tetrazol-5- yl))benzenesulfonamide (200 mg, 0.471 mmol), tert-butyl 4-(4-(4,4,5,5-tetramethyl-l,3,2- dioxaborolan-2-yl)phenyl)piperidine-l -carboxylate (274 mg, 0.707 mmol), l,l'-Bis(di-tert- butylphosphino)ferrocene palladium dichloride (46.1 mg, 0.071 mmol) and ethanol (5 mL) was added aqueous potassium phosphate (1.414 mL, 1.414 mmol). The closed vial was evacuated by vacuum and flushed with 2 three times, and then stirred at 90°C overnight. The solution was filtered and partitioned between H2O and EtOAc. The organic layer was separated from aqueous, dried over Na ₂ S0 ₄ , filtered, and evaporated to dryness. The crude product as an isomer mixture was used directly in the next reaction. LC/MS [M+H] ⁺ 605.6.

Step B: 4'-piperidin-4-yl-2-(lH-tetrazol-5-yl)biphenyl-3-sulfonamide , hydrochloride salt

TFA (3631 μΐ,, 47.1 mmol) was added into a mixture of tert-butyl 4-(2'-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)-3'-sulfamoyl-[l,r-biphenyl] -4-yl)piperidine-l-carboxylate and tert-butyl 4-(2'-(l-(4-methoxybenzyl)-lH-tetrazol-5-yl)-3'-sulfamoyl-[l , -biphenyl]-4- yl)piperidine-l-carboxylate (285 mg, 0.471 mmol) and thioanisole (1115 μί, 9.43 mmol). The mixture was stirred at RT overnight. The reaction mixture was heated to 45°C for ~4 hr to drive to completion, then was stirred at RT overnight. The reaction mixture was concentrated, then trituated with hexane. The hexane was removed. The residue was evaporated, and purified by reverse phase HPLC. To a sample of 19 mg of the purified product was added water (5 mL). To this stirred suspension was added HC1 (IN, -450 uL) dropwise, during which the solids dissolved and the solution turned clear. The solution was freeze-dried using a lyophilizer to obtain the HC1 salt. LC/MS [M+H] ⁺ 385.

EXAMPLE 32

4-(3 '-Sulfamoyl-2'-(2H-tetr eridine- 1 -carboximidamide

Step A: 4-(2'-(2-(4-Methoxybenzyl)-2H-tetrazol-5-yl)-3'-sulfamoyl-[l ,l'-biphenyl]-4- yl)piperidine- 1 -carboximidamide

4-(2'-(2-(4-Methoxybenzyl)-2H-tetrazol-5-yl)-3'-sulfamoyl-[l ,l'-biphenyl]-4- yl)piperidine- 1 -carboximidamide 2,2,2-trifluoroacetate (0.384 g, 0.62 mmol) in THF (6.20 mL) was treated with lH-pyrazole-l-carboxamidine hydrochloride (0.273 g, 1.86 mmol) and DIEA (1.08 mL, 6.20 mmol). The reaction mixture was stirred at rt under 2 overnight. The mixture was concentrated and purified by reverse phase HPLC (0-55% CH3CN/water with 0.1% FA). The correct fractions were combined and concentrated to give the crude title compound, which was used directly in the next step. LC-MS 547 (M+l) ⁺ ;

Step B : 4-(3 '-Sulfamoy l-2'-(2H-tetrazol-5-y 1)- [1, 1 '-biphenyl] -4-yl)piperidine- 1 - carboximidamide

4-(2'-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-3'-sulfamoyl-[l , l'-biphenyl]-4- yl)piperidine- 1 -carboximidamide (339 mg, 0.62 mmol) was treated with TFA at 80°C for 3 hr. The reaction mixture was concentrated and the crude product was purified by reverse phase HPLC (5-55% CH ₃ CN/water with 0.1% FA). The correct fractions were combined, concentrated and converted to HC1 salt and then lypholized. LC-MS 427 (M+l) ⁺ .

EXAMPLE 33

l, l-dimethyl-4-(3'-sulfamoyl-2'-(lH-tetrazol-5-yl)-[l, r-biphenyl]-4-yl)piperidin-l-ium 2,2,2- trifluoroacetate

Step A: 4-(4-Bromophenyl)- 1 , 1 -dimethylpiperidin- 1 -ium

In acetone (20 mL), 4-(4-bromophenyl)-l-methylpiperidine (500 mg, 1.967 mmol) was dissolved, and Mel (160 μί, 2.56 mmol) was added dropwise. The mixture was stirred at rt for 2.5 hr. LC-MS showed the reaction was complete. The mixture was filtered and the solid was washed with acetone and collected.

Step B : 4-(3 '-(N,N-bis(4-methoxybenzyl)sulfamoyl)-2'-(2-(4-methoxybenzyl )-2H-tetrazol- 5-yl)- [1, 1 '-biphenyl] -4-yl)- 1 , 1 -dimethylpiperidin- 1 -ium

4-(4-Bromophenyl)-l, l-dimethylpiperidin-l-ium (93 mg, 0.344 mmol), 3-(5,5- dimethyl- 1 ,3 ,2-dioxaborinan-2-yl)-N,N-bis(4-methoxybenzyl)-2-(2-(4-metho xybenzyl)-2H- tetrazol-5-yl)benzenesulfonamide (200 mg, 0.287 mmol), a ₂ C0 ₃ (60.8 mg, 0.573 mmol), and PdC dppf) (20.98 mg, 0.029 mmol) was placed in a reaction vessel, to which 1,4-dioxane (1433 μί) and water (478 μί) was added. 2 was bubbled through for 20 min. The reaction mixture was heated at 95°C overnight. The reaction mixture was diluted with EtOAc and filtered. The filtrates were concentrated and the residue was purified by Gilson (30-100% CH ₃ CN/water with 0.05% TFA) to give the title compound. LC-MS 773 (M) ⁺ ; Step C: l,l-dimethyl-4-(3'-sulfamoyl-2'-(lH-tetrazol-5-yl)-[l, l'-biphenyl]-4-yl)piperidin- 1-ium

4-(3'-(N,N-bis(4-methoxybenzyl)sulfamoyl)-2'-(2-(4-methoxybe nzyl)-2H- tetrazol-5-yl)-[l,r-biphenyl]-4-yl)-l, l-dimethylpiperidin-l-ium (30 mg, 0.039 mmol) was heated in TFA for 2 hr. The mixture was concentrated and purified with Gilson (2-40%

CHsCN/water with 0.1%TFA). The correct fractions were combined, concentrated and lypholized. LC-MS 413 (M) ⁺ .

EXAMPLES 34-49

Parallel synthesis of 3 -substituted 2-(lH-tetrazol-5-yl)benzenesulfonamides

Step A: Palladium catalyzed C-C coupling of arylbromides and substituted tin reagents.

A mixture of 3-bromo-2-(l-(4-methoxybenzyl)-2H-tetrazol-5- yl)benzenesulfonamide and 3-bromo-2-(2-(4-methoxybenzyl)-2H-tetrazol-5- yl)benzenesulfonamide from Reference Example 1 (15 mg, 0.035 mmol), substituted tin reagents (0.07 mmol), and (RuPhos)palladium (II) phenthylamine chloride catalyst (2.5 mg, 0.0035 mmol) were mixed into a 1-dram vial. Under dry nitrogen atmosphere, THF (300 μΐ) was added into the vial and the reaction was agitated at 75°C for 16 hours. The solvent was removed under reduced pressure to afford the intermediates.

Step B: Removal of the p-methoxybenzyl (PMB) protecting group under acidic conditions

TFA (545 μΐ, 7.07 mmol) was added to each vial. The vials were heated to 65°C for 16 hours. LC/MS showed formation of the desired products. Solvent was removed under reduced pressure. To each vial, 1 mL DMSO was added and filtered into a 96-well plate. The crude products were purified by HPLC to afford Examples 35-50.

Ex. Structure Name Calc'd LC/MS

No. Mass m/e

[M+H]+ [M+H] ⁺

EXAMPLES 50-110

Parallel synthesis of 3 -substituted 2-(lH-tetrazol-5-yl)benzenesulfonamides

Step A: Palladium catalyzed C-C coupling of arylbromide and boronic acids or boronic esters (such as pinacol esters).

A mixture of 3-bromo-2-(l-(4-methoxybenzyl)-2H-tetrazol-5- yl)benzenesulfonamide and 3-bromo-2-(2-(4-methoxybenzyl)-2H-tetrazol-5- yl)benzenesulfonamide from Reference Example 1 (30 mg, 0.071 mmol), substituted boronic acids or esters (0.142 mmol), potassium phosphate (0.212 mL IN solution, 0.212 mmol), 1, 1'- bis(di-tert-butylphosphino) ferrocene palladium chloride (4.61 mg, 7.07 μιηοΐ) were mixed into a 1-dram vial, and under dry nitrogen atmosphere, EtOH (1 mL) was added into the vial under 2 and the reaction was agitated at 70-75°C for 16 hours. Crude LC/MS showed formation of the desired intermediate. Solvent was removed under reduced pressure. To each vial, 1.5 mL DCM was added along with 0.4 mL water, with shaking for 15 min. The organic layer was collected and solvent was removed under reduced pressure.

Step B: Removal of the p-methoxybenzyl (PMB) protecting group under acidic conditions.

To each vial from Step A, TFA (0.545 mL, 7.07 mmol), anisole (7.72 μΐ, 0.071 mmol) was added and agitated at 60°C for 12 hours. Crude LC/MS showed formation of the desired products. The solvent were removed under reduced pressure. To each vial, 1 mL DMSO was added and filtered into a 96-well plate. These crude materials were purified by HPLC to afford Examples 51-1 10.

Ex. Structure Name Calc'd LC/MS

No. Mass m/e

[M+H] ⁺ [M+H] ⁺

-130

Step A: Palladium catalyzed C-C coupling of arylbromide and boronic acids or boronic esters (such as pinacol esters).

A mixture of 3-bromo-2-(l-(4-methoxybenzyl)-2H-tetrazol-5- yl)benzenesulfonamide and 3-bromo-2-(2-(4-methoxybenzyl)-2H-tetrazol-5- yl)benzenesulfonamide from Reference Example 1 (30 mg, 0.071 mmol), commercially available or known boronic acids (0.071 mmol) and XPhos-Pd-2G precatalyst (2.23 mg, 2.83 μιηοΐ) were weighed into a 1 dram vial and taken into the glove box. THF (1 mL) and 1 M potassium phosphate (0.25 mL, 0.250 mmol) were added and the mixture was stirred at 65°C for 4 days. The organic solvents were removed under reduced pressure.

Step B: Removal of the p-methoxybenzyl (PMB) protecting group under acidic conditions.

To remove the PMB protecting group, TFA (1 mL) and anisole (0.031 mL, 0.283 mmol) were added to the intermediates from Step A and the mixtures were stirred at 65 °C for 3 hours. The mixtures were allowed to cool and concentrated under reduced pressure. To each vial, 1 mL DMSO was added and the mixtures were filtered into a 96-well plate. These crude materials and others prepared in the same way were purified by mass directed reverse phase HPLC to afford Examples 1 11-130.

Ex. Structure Name Calc'd LC/MS

No. Mass m/e

[M+H] ⁺ [M+H] ⁺

EXAMPLES 131-139

Parallel synthesis of 3 -substituted 2-(lH-tetrazol-5-yl)benzenesulfonamides

Step A: Palladium catalyzed C-C coupling of arylboronic ester with bromides.

An isomeric mixture of 3-(5,5-dimethyl-l,3,2-dioxaborinan-2-yl)-N,N-bis(4- methoxybenzyl)-2-(l-(4-methoxybenzyl)-lH-tetrazol-5-yl)benze nesulfonamide and 3-(5,5- dimethyl- 1 ,3 ,2-dioxaborinan-2-yl)-N,N-bis(4-methoxybenzyl)-2-(2-(4-metho xybenzyl)-2H- tetrazol-5-yl)benzenesulfonamide, Reference Example 9, (30 mg, 0.043 mmol), were combined with commercially available or known aryl or heteroaryl bromides (0.065 mmol), sodium carbonate (9.12 mg, 0.086 mmol) and PdCl ₂ (dppf)-CH ₂ Cl2 adduct (5.27 mg, 6.45 μιηοΐ) in a 1 dram vial and taken into the glove box. Acetonitrile (1 mL) and water (0.1 mL) were added and the mixture stirred at 95°C for 18 hours. The mixtures were allowed to cool and the solvent was removed under reduced pressure. 1 mL DCM and 1 mL saturated ammoinium chloride were added and the mixtures stirred for 5 minutes. The aqeuous layer was removed by pipette and the remaning organic phases were concentrated under reduced pressure.

Step B: Removal of the p-methoxybenzyl (PMB) protecting group under acidic conditions.

To each vial from Step A was added TFA (1 mL) and anisole (0.019 mL, 0.172 mmol) and the mixtures were stirred at 50°C for 3 hours. The vials were allowed to cool and the volatile organics were removed under reduced pressure. DMSO (1 mL) was added and the mixtures were filtered through a 96 well 0.4 micron filter plate. These crude materials and others made in the same way were purified by HPLC to afford Examples 131-139.

EXAMPLES 140-144

Parallel synthesis of 3 -substituted 2-(lH-tetrazol-5-yl)benzenesulfonamides

Step A: Palladium catalyzed C-C coupling of alkyl, vinyl and aryl-BF ₃ salts with 3- bromo-N,N-bis(4-methoxybenzyl)-2-(l-(4-methoxybenzyl)-lH-tet razol-5- yl)benzenesulfonamide and 3 -bromo-N,N-bis(4-methoxybenzyl)-2-(2-(4-methoxybi tetrazol-5-yl)benzenesulfonamide.

3 -Bromo-N,N-bis(4-methoxybenzyl)-2-( 1 -(4-methoxybenzyl)- lH-tetrazol-5- yl)benzenesulfonamide and 3 -bromo-N,N-bis(4-methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H- tetrazol-5-yl)benzenesulfonamide (40 mg, 0.060 mmol), cesium carbonate (58.8 mg, 0.181 mmol), commercially available alkyl, vinyl and aryl-BF ₃ ^~ salts (0.060 mmol) and chloro[(di(l- adamantyl)-N-butylphosphine)-2-(2-aminobiphenyl)]palladium(I I) (4.02 mg, 6.02 μιηοΐ) were weighed into a 1 dram vial and taken into the glove box. Toluene (1 mL) and water (0.1 mL) were added and the mixtures were stirred at 110° C for 18 hours. The mixtures were allowed to cool and the organics were removed under reduced pressure.

Step B: Removal of the / methoxybenzyl (PMB) protecting group under acidic conditions.

To remove the PMB protecting groups TFA (1 mL) and anisole (0.026 mL, 0.241 mmol) were added and the mixtures were stirred at 55°C for 3 hours. The mixtures were allowed to cool and concentrated under reduced pressure. DMSO (1 mL) was added and the mixtures were filtered through a (96 well) 0.4 micron filter plate. These crude materials and others made in the same way were purified by HPLC to afford Examples 140-144. -148

Step A: Palladium catalyzed C-C coupling of arylbromide with substituted acetylenes.

In the reaction vessel, a mixture of isomeric 3-bromo-2-(l-(4-methoxybenzyl)- lH-tetrazol-5-yl)benzenesulfonamide and 3-bromo-2-(2-(4-methoxybenzyl)-lH-tetrazol-5- yl)benzenesulfonamide from Reference Example 1 (30 mg, 0.071 mmol) and alkynes were combined, followed by cesium carbonate (69.1 mg, 0.212 mmol), and XPhos-Pd-2G precatalyst (5.56 mg, 7.07 μιηοΐ). This mixture was then evacuated and backfilled with 2 (3 times). Then dry, degassed acetonitrile (700 μΐ) was added to this flask. This mixture was stirred at 90°C for 16 hours. Crude LC/MS showed formation of the desired intermediates.

Step B: Removal of the p-methoxybenzyl (PMB) protecting group under acidic conditions

To each vial, TFA (0.7 mL) was added and agitated at 65°C for 16 hours. The solvent was removed and to each vial, siliaMetS DMT (Vendor: Silicycle, Cat. No.: R79030B) resin (40 mg) was added followed by addition of 1.1 mL of DMSO with shaking for 12 hours. The crude was filtered into a 96-well plate and purified by HPLC to yield Examples 145-148.

Ex. Structure Name Calc'd LC/MS No. Mass m/e

[M+H] ⁺ [M+H] ⁺

145 3 -(3 -morpholin-2-ylprop- 1 - 349.0 349.1 yn-l-yl)-2-(2H-tetrazol-5- yl)benzenesulfonamide

146 3 - [3 -(4-oxopiperidin- 1 - 361.0 361.1 yl)prop- 1 -yn- 1 -yl] -2-(2H- tetrazol-5-

yl)benzenesulfonamide

EXAMPLES 149- 166

Step A: Palladium catalyzed C-C coupling of alkyl, aryl or heteroaryl zinc bromides.

To a 40 mL vial was added 1040 mg of a mixture of isomeric 3-bromo-2-(l-(4- methoxybenzyl)- lH-tetrazol-5-yl)benzenesulfonamide and 3-bromo-2-(2-(4-methoxybenzyl)- lH-tetrazol-5-yl)benzenesulfonamide from Reference Example 1 (enough for 13 reactions each having 80 mg, 0.189 mmol) and 136 mg of SPhos-Pd-G2 precatalyst (enough for 13 reactions each having (5.44 mg, 7.54 μηιοι)). The vial was taken into the glove box. Then 3.64 mL of

THF was added. 0.26 mL of this solution was added to each of 13 x 1 dram vials. Commercially available alkyl, aryl or heteroaryl zinc bromides were added to the vials which were then stirred at 55°C for 18 hours. The mixtures were allowed to cool and then 1 mL of saturated ammonium chloride solution and 1 mL of DCM were added. The mixtures were stirred for 20 minutes. The layers were separated and the organic phases were concentrated under reduced pressure. Step B: Removal of the p-methoxybenzyl (PMB) protecting group under acidic conditions.

The intermediates from Step A were treated with anisole (0.082 mL, 0.754 mmol) and TFA (0.5 mL). The mixtures were stirred uncapped for 2 hours at 65°C. The mixtures were allowed to cool and the volatile organics were removed under reduced pressure. 1 mL DMSO was added to each vial and the mixtures filtered through a (96 well) 0.4 micron filter plate. These crude materials (and others prepared in the same fashion) were purified by mass directed reverse phase HPLC to afford Examples 149-166.

EXAMPLE 167

3-isobutyl-2-(2H-tetrazol-5-yl)benzenesulfonamide

Step A: 3-Isobutyl-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)benzenesu lfonamide

3-Bromo-2-(l-(4-methoxybenzyl)-lH-tetrazol-5-yl)benzenesulfo namide (200 mg, 0.471 mmol) and 2nd generation SPHOS precatalyst (34.0 mg, 0.0470 mmol) was placed in a microwave tube, to which anhydrous THF (471 μί) was added. The tube was sealed and N ₂ was bubbled through for 10 min. Isobutyl zinc(II) bromide (3771 μί, 1.886 mmol) was then added. The resulting mixture was heated at 50°C for 3 hr. After being cooled to rt, the reaction was quenched with a saturated NH ₄ C1 solution. The resulting mixture was extracted with EtOAC, and the organic layers were separated, washed with brine, dried (Na ₂ S0 ₄ ), filtered and concentrated. The crude product was purified by column chromatography (0-80%

EtOAc/Hexane) to give the title compound. LC-MS 402 (M+l) ⁺ .

Step B: 3-Isobutyl-2-(2H-tetrazol-5-yl)benzenesulfonamide

3-Isobutyl-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)benzenesu lfonamide (50 mg, 0.125 mmol) was heated at 80°C in TFA (2 mL). The reaction mixture was concentrated and the residue was purified with Gilson 5-65% CH ₃ CN/water with 0.1 % FA. The correct fractions were combined, concentrated and lypholized to give the title compound. LC-MS 282 (M+l) ⁺ .

EXAMPLE 168

3-(4-Aminocyclohex -2-(2H-tetrazol-5-yl)benzenesulfonamide

Step A: 3-(4-Aminocyclohexyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5- yl)benzenesulfonamide

To a microwave tube was added 2-(2-(4-Methoxybenzyl)-2H-tetrazol-5-yl)-3-(4- oxocyclohexyl)benzenesulfonamide (400 mg, 0.906 mmol), NaCNBH ₄ (159 mg, 2.54 mmol), ammonium acetate (908 mg, 11.8 mmol), magnesium sulfate (600 mg, 4.98 mmol) and MeOH (6 mL). The tube was sealed and heated at 80°C overnight. The reaction mixture was cooled and filtered, and the filtration cake was washed with MeOH. The filtrates were concentrated and partitioned between EtOAc and a small amount of water. The EtOAc layer was washed with brine, dried ( a ₂ S0 ₄ ), filtered and concentrated to give the tiltle compound. LC-MS 443 (M+l) ⁺ .

Step B: 3-(4-Aminocyclohexyl)-2-(2H-tetrazol-5-yl)benzenesulfonamide

3-(4-Aminocyclohexyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5- yl)benzenesulfonamide (100 mg, 0.226 mmol) was heated in TFA for 2 h at 80 °C. The mixture was concentrated and the residue was purified with Gilson (2-40% CH ₃ CN/water with 0.1% TFA). The product was concentrated and lypholized from CH ₃ CN/water. LC-MS 323 (M+l) ⁺ .

EXAMPLE 169

3-(4-(methylsulfonamido)cyclohexyl)-2-(2H-tetrazol-5-yl)benz enesulfonamide

Step A: 2-(2-(4-Methoxybenzyl)-2H-tetrazol-5-yl)-3-(4- (methylsulfonamido)cyclohexyl)benzenesulfonamide

3-(4-Aminocyclohexyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5- yl)benzenesulfonamide (140 mg, 0.316 mmol) was dissolved in DCM (1.6 mL), cooled to -78°C and treated with TEA (132 μΕ, 0.949 mmol), follwed by dropwise addition of methanesulfonyl chloride (29.4 μΕ, 0.380 mmol) in DCM (0.5 mL). The mixture was stirred at this temperature for 40 min. LC-MS showed most of the starting material was consumed and the desired product was the major product. The reaction was quenched by adding water (2 mL). The mixture was allowed to warm up to rt and extracted with DCM. The organics were washed with sat. aHC03 solution, concentrated and the residue was purified by column chromatography (0-100%

EtOAC/hexane) to give the tiltle compoound. LC-MS 521(M+1) ⁺ .

Step B: 3-(4-(Methylsulfonamido)cyclohexyl)-2-(2H-tetrazol-5-yl)benz enesulfonamide

2-(2-(4-Methoxybenzyl)-2H-tetrazol-5-yl)-3-(4-

(methylsulfonamido)cyclohexyl)benzenesulfonamide (81 mg, 0.16 mmol) was heated in TFA (2 mL) in the presence of anisole (85 μΐ, 0.778 mmol) at 60°C overnight. The reaction mixture was concentrated and purified with Gilson (2-40% CH ₃ CN/water with 0.1% TFA) to give the title compound.

EXAMPLE 170

3-(4-(piperazin-l-yl)cyclohexyl)-2-(2H-tetrazol-5-yl)benzene sulfonamide

Step A: 2-(2-(4-Methoxybenzyl)-2H-tetrazol-5-yl)-3-(4-(piperazin-l- yl)cyclohexyl)benzenesulfonamide

To a solution of 2-(2-(4-Methoxybenzyl)-2H-tetrazol-5-yl)-3-(4- oxocyclohexyl)benzenesulfonamide (150 mg, 0.340 mmol) and tert-butyl piperazine-1- carboxylate (69.6 mg, 0.374 mmol) in THF (1.1 mL) was added titanium(IV) isopropoxide (151 μΐ,, 0.510 mmol). The mixture was stirred at rt under 2 overnight. Sodium cyanoborohydride (64.1 mg, 1.02 mmol) was added in one portion and stirring was continued for 2 hr. The reaction was quenched with water and extracted with EtOAc. Purification by column chromatography (0 - 90% EtOAc/Hexane) gave the title compound. LC-MS 612 (M+l) ⁺ .

Step B: 3-(4-(Piperazin-l-yl)cyclohexyl)-2-(2H-tetrazol-5-yl)benzene sulfonamide

tert-Butyl 2-(2-(4-Methoxybenzyl)-2H-tetrazol-5-yl)-3-(4-(piperazin-l- yl)cyclohexyl)benzenesulfonamide_(60 mg, 0.098 mmol) wsa treated with TFA (1 mL) in DCM (1 mL). After the reaction was stirred at rt for 1 hr, LC-MS indicated that the Boc protecting was removed. The reaction mixture was concentrated and co-evaporated with toluene 3 times. The resulting residue was taken up in TFA (2 mL) and heated at 80°C for 1.5 hr, and then concentrated to remove the excess of TFA. The crude product was purified with gilson (1- 40%CH3CN/water with 0.1% TFA), and lypholized to give the title compound. LC-MS 392 (M+l) ⁺ .

EXAMPLE 171

3-(4-hydroxycyclohex -2-(2H-tetrazol-5-yl)benzenesulfonamide

Step A: 3-(4-Hydroxycyclohexyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5 - yl)benzenesulfonamide 2- (2-(4-Methoxybenzyl)-2H-tetrazol-5-yl)-3-(4- oxocyclohexyl)benzenesulfonamide (500 mg, 1.132 mmol) was suspended in MeOH (10 mL). Under 2 and at 0°C NaBH ₄ (42.8 mg, 1.132 mmol) was added. The mixture was stirred at 0°C for 2 hr, and then quenched with NH ₄ C1 aqueous solution. The mixture was filtered and the filtrates were concentrated to remove MeOH. The residue was partitioned between EtOAc and water. The organic phase was separated, washed with brine, dried (Na ₂ S0 ₄ ) and concentrated to give the title compound. LC-MS 444 (M+l) ⁺ .

Step B: 3-(4-Hydroxycyclohexyl)-2-(2H-tetrazol-5-yl)benzenesulfonami de

3- (4-Hydroxycyclohexyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5- yl)benzenesulfonamide (100 mg, 0.225 mmol) was heated in TFA (2 mL) for 2 hr at 80°C. The reaction mixture was then concentrated to remove the excess of TFA. The residue was dissolved in THF (2 mL) and treated with saturated a ₂ C0 ₃ aqueous solution (2 mL). After being stirred at rt for 2 hr, the reaction mixture was extracted with EtOAc. The organic layeres were combined, dried (Na ₂ S04) and concentrated. The residue was purified with Gilson (2-35% CHsCN/water with 0.1% TFA) and the desired fractions were combined, lypholized (freezed without concentration) to give the title compound. LC-MS 324 (M+l) ⁺ .

EXAMPLE 172

3-(l-(methylsulfonyl)piperidin-4-yl)-2-(2H-tetrazol-5-yl)ben zenesulfonamide

ethyl 4-(3-sulfamoyl-2-(2H-tetrazol-5-yl)phenyl)piperidine-l-carbo xylate

To a 1-dram vial with methanesulfonyl chloride (5.35 mg, 0.047 mmol) was added isomer mixture 2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-3-(piperidin-4- yl)benzenesulfonamide and 2-(3-(4-methoxybenzyl)-2H-tetrazol-5-yl)-3-(piperidin-4- yl)benzenesulfonamide (20 mg, 0.047 mmol) in DMF (1.5 mL) followed by DIEA (0.033 mL, 0.187 mmol). The vial was agitated for 16 hr at 25°C. The solvent was removed and residue was dissolved in 1 mL TFA and agitated at 65°C for 12 hours. The solvent was removed and 1.5 mL DMSO was added, and the mixture was filtered and purified by reverse phase HPLC.

LC/MS [M+H] ⁺ 387. EXAMPLE 173

To a 1-dram vial with isomer mixture 2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)- 3-(piperidin-4-yl)benzenesulfonamide and 2-(3-(4-methoxybenzyl)-2H-tetrazol-5-yl)-3- (piperidin-4-yl)benzenesulfonamide (Reference Example 16, 20 mg, 0.047 mmol) was added ethyl chloroformate (15.2 mg, 0.140 mmol) in DMF (1.5 mL) followed by addition of DIEA (0.033 mL, 0.187 mmol). The vial was agitated for 16 hr at 25°C. The solvent was removed and residue was dissolved in 1 mL TFA and agitated at 65°C for 12 hours. The solvent was removed and 1.5 mL DMSO was added. The mixture was filtered and purified by reverse phase HPLC. LC/MS [M+H] ⁺ 381.

EXAMPLE 174

N-ethyl-4-(3-sulfamoyl-2-(2H-tetrazol-5-yl)phenyl)piperidine -l-carboxamide

To a 1-drum vial with an isomer mixture of 2-(2-(4-methoxybenzyl)-2H-tetrazol- 5-yl)-3-(piperidin-4-yl)benzenesulfonamide and 2-(3-(4-methoxybenzyl)-2H-tetrazol-5-yl)-3-

(piperidin-4-yl)benzenesulfonamide (20 mg, 0.047 mmol) was added isocyanatoethane (3.32 mg, 0.047 mmol) in DMF (1.5 mL) followed by addition of DIEA (0.033 mL, 0.187 mmol). The vial was agitated for 16 hr at 25°C. The crude intermediate material was purified by reverse phase HPLC. The solvent was removed and residue was dissolved in 1 mL TFA and agitated at 65°C for 12 hours. The solvent was removed and 1.5 mL DMSO was added. The mixture was filtered and purified by reverse phase HPLC. LC/MS [M+H] ⁺ 380.

EXAMPLE 175

3-(piperidin-3-yl)-2-(2H-tetrazol-5-yl)benzenesulfonamide

Step A: To a mixture of 3-bromo-2-(2-(4-methoxybenzyl)-2H-tetrazol-5- yl)benzenesulfonamide (1.00 g, 2.36 mmol), tert-butyl 3-iodopiperidine-l-carboxylate (1.47 g, 4.71 mmol), pyridine (0.953 mL, 11.8 mmol), nickel chloride dimethoxyethane adduct (0.104 g, 0.471 mmol), zinc (0.925 g, 14.1 mmol), and ligand A 2,2':6',2"-terpyridine (0.330 g, 1.414 mmol) (or ligand B 4,4',4"-tri-tert-butyl-2,2':6',2"-terpyridine) in an ₂ filled microwave reaction vial was added DMA (8 mL). The vial was capped, and the reaction was heated to 100°C for 2 hr in a microwave. The excess catalyst was filtered off and the solution was concentrated. The crude material was used for the next step.

Step B: The crude from Step A was dissolved in (¾(¾ (4 mL) and TFA (2 mL). The reaction was stirred at room temperature for 20 min; the resulting suspension was filtered, washed with small ammount of MeOH. Then the solution was passed through Varian Bond Elut SCX ion exchange cartridge, washed with MeOH to get rid of most of the impurities from the previous step, and the desired product was eluted from the cartridge with 2 M NEUOH/MeOH, and concentrated to get 2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-3-(piperidin-3- yl)benzenesulfonamide. LC-MS: calculated for C2 ₀ H24 ₆ O ₃ S 428.51 observed m/e: 429.41 (M+H) ⁺ .

Step C: 10 mg of the product from Step B was dissolved in 1 mL of TFA, and was heated to 65°C for 16 hr. The reaction was concentrated and purified by reverse phase HPLC column (acetonitrile/water/0.05% TFA system) eluted with 2% to 30% MeCN in water. The pure fractions were concentrated to afford product. LC-MS: calculated for C12H16N602S 308.36 observed m/e: 309.30 (M+H) ⁺ ; 1H MR δ (ppm) (CD30D): 8.08-8.12 (d, 1H), 7.75-7.85 (m, 2H), 3.35-3.30 (m, 2H) 3.17 (t, 1H), 2.8-2.9 (m, 2H), 1.8-1.9 (m, 2H), 1.6-1.7 (m, 2H).

EXAMPLE 176

3 -( 1 -( 1 -phenylcyclopropanecarbonyl)piperidin-4-yl)-2-(2H-tetrazol-5 -yl)benzenesulfonamide

The title compound was prepared using Reference Example 19, 3-bromo-2-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)benzenesulfonamide and Ligand B (see below) in an analogous fashion to 3-(piperidin-3-yl)-2-(2H-tetrazol-5-yl)benzenesulfonamide. LC/MS [M+H] ⁺ 453.34.

EXAMPLE 177

3-(l-(cyclopropanecarbonyl)piperidin-3-yl)-2-(2H-tetrazol-5- yl)benzenesulfonamide

Step A: To a solution of 2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-3-(piperidin-3- yl)benzenesulfonamide (20 mg, 0.047 mmol) in 1 mL of (¾(¾ was added

cyclopropanecarbonyl chloride (7.32 mg, 0.070 mmol) and TEA (0.065 mL, 0.467 mmol), stirred at rt for 1 hr. The reaction solution was concentrated and purified by reverse phase HPLC column (acetonitrile/water/0.05% TFA system) and eluted with 10% to 60% MeCN in water. The pure fractions were concentrated to afford the desired product. LC-MS: calculated for C24H ₂ 8 ₆ 0 ₄ S 496.58 observed m/e: 497.47 (M+H) ⁺ ;

Step B: The resulting product from Step A was dissolved in 1 mL of TFA, and was heated to 65°C for 16 hr. The reaction was concentrated and purified by reverse phase HPLC column (acetonitrile/water/0.05% TFA system) and eluted with 2% to 30% MeCN in water. The pure fractions were concentrated to afford product. LC-MS: calculated for C16H20N6O3S 376.43 observed m/e: 377.39 (M+H) ⁺ ; 1H MR δ (ppm) (CD30D): 8.17-8.19 (d, 1H), 7.73-7.75 (m,

2H), 4.65-4.68 (m, 1H), 4.30-4.34 (m, 1H), 2.89-2.92 (m, 1H), 2.39-2.43 (m, 1H), 2.22-2.26 (m, 1H), 1.92-1.95 (m, 1H), 1.81-1.86 (m, 1H), 1.77-1.81 (m, 2H), 1.45-1.49 (m, 1H), 0.84-0.89 (m, 2H), 0.82-0.84 (m, 2H).

EXAMPLE 178

3-(5,6,7,8-tetrahydroimidazo[l,5-a]pyridin-7-yl)-2-(2H-tetra zol-5-yl)benzenesulfonamide

Step A: 2-(2-(4-Methoxybenzyl)-2H-tetrazol-5-yl)-3-(5,6,7,8-tetrahyd roimidazo[l,5- a]pyridin-7-yl)benzenesulfonamide

3-(Imidazo[l,5-a]pyridin-7-yl)-2-(2-(4-methoxybenzyl)-2H-tet razol-5- yl)benzenesulfonamide (121 mg, 0.262 mmol) was dissolved in MeOH (2.6 niL), to which was added 2 drops of cone. HC1, then Pd-C (120 mg). The reaction head space was vacuumed and filled with H ₂ two times. The mixture was stirred at rt under H ₂ for 48 hr. LC-MS showed the conversion was complete. The reaction mixture was filtered and the filtrates were concentrated to give the title compound, which was used directly in the next step.

Step B: 3-(5,6,7,8-Tetrahydroimidazo[l,5-a]pyridin-7-yl)-2-(2H-tetra zol-5- yl)benzenesulfonamide

2-(l-(4-Methoxybenzyl)-lH-tetrazol-5-yl)-3-(5,6,7,8-tetrahyd roimidazo[l,5- a]pyridin-7-yl)benzenesulfonamide (122 mg, 0.262 mmol) was heated in TFA (3 mL) at 80°C for 2 hr. LC-MS showed the reaction was completed. The mixture was then concentrated and the residue was purified with Gilson (5%-40% CH3CN/water with 0.1% FA). The correct fractions were combined, concentrated and lypholized to give the title compound. LC-MS 346 (M+l) ⁺ .

EXAMPLE 179

2-(2H-tetrazol-5- -3-(p-tolyloxy)benzenesulfonamide

Step A: 2-(p-tolyloxy)-6-((2-(trimethylsilyl)ethyl)thio)benzonitrile

To a solution of 2-fluoro-6-(p-tolyloxy)benzonitrile (0.5 g, 2.2 mmol) and potassium carbonate (0.608 g, 4.40 mmol) in DMF (30 mL) was added 2- (trimethylsilyl)ethanethiol (0.355 g, 2.64 mmol) and the resulting mixture was stirred at room temperature overnight. The reaction mixture was filtered. The filtrate was diluted with EtOAc, and washed with water and brine. The organic layer was dried over anhydrous MgS0 ₄ , filtered, and concentrated. The residue was purified by silica gel column chromatography using 0-30% EtOAc/Hexanes as mobile phase to afford the title compound. LC-MS (IE, m/z): 342.18

[M+l]+.

Step B : 2-(p-tolyloxy)-6-((2-(trimethylsilyl)ethyl)sulfonyl)benzonit rile

To a solution of 2-(p-tolyloxy)-6-((2-(trimethylsilyl)ethyl)thio)benzonitrile (0.44 g, 1.288 mmol) in DCM (8.6 mL) at 0°C was added mCPBA (0.778 g, 4.51 mmol) and the mixture was stirred at room temperature overnight. Sat. a ₂ S ₂ C>3 was added to the mixture and stirred for 10 min, followed by sat. aHC0 ₃ . After separation of layers, aqueous layer was extracted with DCM. The combined organic layer was dried over anhydrous a ₂ S0 ₄ , filtered and concentrated to get the title compound. LC-MS (IE, m/z): 374.26 [M+l]+.

Step C: 5-(2-(p-tolyloxy)-6-((2-(trimethylsilyl)ethyl)sulfonyl)pheny l)-2H-tetrazole

To a solution of 2-(p-tolyloxy)-6-((2-(trimethylsilyl)ethyl)sulfonyl)benzonit rile (200 mg, 0.535 mmol) in toluene (4.5 mL) was added azidotrimethyltin (551 mg, 2.68 mmol) and the resulting mixture was heated overnight at 100°C. Solid precipitate was filtered, and washed with hexanes. The filtrate was purified by silica gel column chromatography using 0- 10% MeOH/DCM (containing 0.2%> AcOH additive) as solvent system to afford the title compound. LC-MS (IE, m/z): 417.19 [M+l]+.

Step D: 2-(2H-tetrazol-5-yl)-3-(p-tolyloxy)benzenesulfonamide

To a solution of 5-(2-(p-tolyloxy)-6-((2-(trimethylsilyl)ethyl)sulfonyl)pheny l)- lH-tetrazole (120 mg, 0.288 mmol) in THF (5761 μΓ) was added TBAF in THF (1440 μΐ, 1.440 mmol). The resulting solution was degassed with N ₂ , stirred at 40°C for 2 hr, and checked by LCMS for completion of the first step conversion. Then sodium acetate (236 mg, 2.88 mmol) in 2.5 mL water was added, followed by addition of hydroxylamine-O-sulfonic acid (326 mg, 2.88 mmol). The resulting solution was stirred at rt overnight. The mixture was partitioned between EtOAc (50 mL) and saturated aHC0 ₃ . The organic phase was washed with NaHCC twice, dried over Na ₂ S0 ₄ , and concentrated. The residue was purified by silica gel column

chromatography using 0-10% MeOH/DCM and 0.5% AcOH as mobile phase to give the title compound. LC-MS (IE, m/z): 332.34 [M+l]+.

EXAMPLE 180

4'-(pyrrolidin-3-yl)-2-(lH-tetrazol-5-yl)-[l, l'-biphenyl]-3-sulfonamide

Step A: tert-butyl 3-(2'-(l-(4-methoxybenzyl)-lH-tetrazol-5-yl)-3'-sulfamoyl-[l ,l'- biphenyl]-4-yl)pyrrolidine-l-carboxylate

In a 25 niL microwave tube, 3-bromo-2-(l-(4-methoxybenzyl)-lH-tetrazol-5- yl)benzenesulfonamide (300 mg, 0.71 mmol), tert-butyl 3-(4-(4,4,5,5-tetramethyl-l,3,2- dioxaborolan-2-yl)phenyl)pyrrolidine-l-carboxylate (Reference Example 14, 530mg,

1.41 mmol), 1 , 1 '-bis(diphenylphosphino)ferrocene-palladium(II)dichloride dichloromethane complex (115 mg, 0.14 mmol) and K ₂ CO ₃ (390 mg, 2.83 mmol) were dissolved in a mixture of EtOH:water (10:1.4ml) then degassed and sealed under nitrogen. The mixture was microwaved for 2 hr at 120°C. The reaction was cooled, filtered and concentrated then the residue was purified by MPLC ISCO Combi-flash on ISCO Redi-Sep 40g column, eluting with

5%MeOH:CH ₂ Cl ₂ . LC-MS [M+H] ⁺ : 591.

Step B: 4'-(pyrrolidin-3-yl)-2-(lH-tetrazol-5-yl)-[l,l'-biphenyl]-3- sulfonamide

In a 50 mL round botomed flask under N ₂ , tert-butyl 3-(2'-(l-(4-methoxybenzyl)- lH-tetrazol-5-yl)-3'-sulfamoyl-[l,l'-biphenyl]-4-yl)pyrrolid ine-l-carboxylate (200 mg, 0.34 mmol) was stirred in DCM:TFA (6 mL) for 0.5 hour. The reaction was concentrated and the residue was taken up with DCM then washed with sat'd aHC03, brine, dried over a ₂ S0 ₄ , filtered and concentrated to give 2-(l-(4-methoxybenzyl)-lH-tetrazol-5-yl)-4'-(pyrrolidin-3-yl )- [l,l'-biphenyl] -3 -sulfonamide. LC-MS [M+H] ⁺ : 491.

Step C: 4'-(pyrrolidin-3-yl)-2-(lH-tetrazol-5-yl)-[l,l'-biphenyl]-3- sulfonamide

2-(l-(4-methoxybenzyl)-lH-tetrazol-5-yl)-4'-(pyrrolidin-3-yl )-[l,l'-biphenyl]-3- sulfonamide was redissolved in thioanisole (3 ml):TFA (3 mL) and heated to 65°C overnight. LC-MS showed some starting material was present. The reaction was heated at 80°C for another 2 hr. The reaction was concentrated and the residue was purified by reverse phase HPLC with ACN and water buffered with 0.05% TFA to afford 4'-(pyrrolidin-3-yl)-2-(lH-tetrazol-5-yl)- [l,l'-biphenyl] -3 -sulfonamide. LC-MS [M+l] ⁺ : 371.3.

EXAMPLE 181

4-(4-(Hydroxymethyl)phenyl)-3-(lH-tetrazol-5-yl)pyridine-2-s ulfonamide

Step A: 2-Chloro-4-(4-(hydroxymethyl)phenyl)nicotinonitrile

To a 100 mL RB flask charged with (4-bromophenyl)methanol (1000 mg, 5.4 mmol), 2-chloro-4-(4,4,5,5-tetramethyl-l,3,2-dioxaborolan-2-yl)nico tinonitrile (2100 mg, 8.02 mmol), and a stir bar was added Pd(DTBPF)Cl ₂ (523 mg, 0.802 mmol), K ₃ P0 ₄ (1.0 M, 10.7 ml, 10.7 mmol), and EtOH (50 ml). The mixture was purged three times with nitrogen, and heated to 60°C for 18 hours. LC showed good reaction. The reaction was diluted with EtOAc, washed with water, and separated. The crude solution was dried over sodium sulfate, filtered and concentrated. The resulting residue was adsorbed onto silica gel, and purified by MPLC with hexane and EtOAc. 2-Chloro-4-(4-(hydroxymethyl)phenyl)nicotinonitrile was isolated as a white solid. LC/MS [M+H] ⁺ : 245.

Step B : 4-(4-(Hydroxymethyl)phenyl)-2-((2-(trimethylsilyl)ethyl)thio )nicotinonitrile

To a flask charged with 2-chloro-4-(4-(hydroxymethyl)phenyl)nicotinonitrile (400 mg, 1.64 mmol) and a stir bar was added 2-(trimethylsilyl)ethanethiol (329 mg, 2.45 mmol), K ₂ C0 ₃ (452 mg, 3.27 mmol), and DMF (20 ml). The mixture was heated to 50°C for 16 hours. LC showed complete and clean reaction. The reaction was diluted with EtOAc, washed with water and brine, and separated. The crude solution was dried over sodium sulfate, filtered and concentrated to give 4-(4-(hydroxymethyl)phenyl)-2-((2-(trimethylsilyl)ethyl)thio )nicotinonitrile as a light yellow solid which was used in the next step without further purification. LC/MS

[M+H] ⁺ : 343.

Step C: 4-(4-(Hydroxymethyl)phenyl)-2-((2-(trimethylsilyl)ethyl)sulf onyl)nicotinonitrile

To a solution of 4-(4-(hydroxymethyl)phenyl)-2-((2- (trimethylsilyl)ethyl)thio)nicotinonitrile (560 mg, 1.64 mmol) in DCM was added m-CPBA (1100 mg, 4.90 mmol). The mixture was allowed to stir for 72 hours. LC showed good reaction. The reaction was diluted with DCM, and quenched with a2S203. The DCM layer was separated, dried over sodium sulfate, and concentrated. The resulting oil was adsorbed onto silica gel, and purified by MPLC with hexanes and EtOAc. The product was a white solid. LC/MS [M+H] ⁺ : 375.

Step D: (4-(3-(lH-Tetrazol-5-yl)-2-((2-(trimethylsilyl)ethyl)sulfony l)pyridin-4- yl)phenyl)methanol

To a flask charged with 4-(4-(hydroxymethyl)phenyl)-2-((2- (trimethylsilyl)ethyl)sulfonyl)nicotinonitrile (240 mg, 0.64 mmol) and a stir bar was added dibutyltin oxide (48 mg, 0.19 mmol), azidotrimethylsilane (220 mg, 1.9 mmol), and toluene (5 ml). The mixture was heated to 100°C for 16 hours. LC/MS suggested little starting material was left, and the reaction was fairly clean. The solvent was removed under vacuum, and the brown residue was used in the next step without further purification. LC/MS [M+H] ⁺ : 418.0. Step E: 4-(4-(Hydroxymethyl)phenyl)-3-(lH-tetrazol-5-yl)pyridine-2-s ulfonamide

To a 100 mL RB flask charged with (4-(3-(2H-tetrazol-5-yl)-2-((2- (trimethylsilyl)ethyl)sulfonyl)pyridin-4-yl)phenyl)methanol (200 mg, 0.48 mmol) and a stir bar was added THF (10 ml) and TBAF (1.4 ml, 1.4 mmol). The mixture was allowed to stir at 55°C for 24 hours. LC showed all starting material was gone. The reaction was cooled, and added aq. sodium acetate (390 mg, 4.8 mmol) in 5 mL of water and hydroxylamine-O-sulfonic acid (540 mg, 4.8 mmol). The mixture was allowed to age for 24 hours at RT. LC/MS showed formation of the desired product. THF was removed on a rotavapor, and the resulting aqueous solution was filtered. The solution was purified on a CI 8 reverse phase HPLC. The product eluted at about 20% eerie ammonium nitrate and was isolated as a light yellow solid. LC/MS [M+H] : 333.2.

EXAMPLE 182

Methyl 4-(2-sulfamoyl-3-(lH-tetraz -5-yl)pyridin-4-yl)benzoate

Step A: Methyl 4-(2-chloro-3-cyanopyridin-4-yl)benzoate

To a 100 RB flask was added methyl 4-bromobenzoate (1000 mg, 4.6 mmol), 2- chloro-4-(4,4,5,5-tetramethyl-l,3,2-dioxaborolan-2-yl)nicoti nonitrile (1230 mg, 4.6 mmol), Pd(DTBPF)Cl ₂ (300 mg, 0.46 mmol), K ₃ P0 ₄ (1.0 M, 9.30 ml, 9.30 mmol), EtOH (20 ml), and a stir bar. The mixture was sealed with a condensor, and purged three times with nitrogen. It was then heated to 60°C for 5 hours. TLC and LC showed very good reaction. The reaction was diluted with EtOAc, washed with water and brine, dried over sodium sulfate, filtered and concentrated to give a brown oil. The oil was dissolved in DCM (30 mL) and adsorbed onto silica gel, and purified by MPLC with hexanes and EtOAc. Methyl 4-(2-chloro-3-cyanopyridin- 4-yl)benzoate eluted at about 40% EtOAc and was isolated as a white solid. LC/MS [M+H] ⁺ : 273.

Step B: Methyl 4-(3-cyano-2-((2-(trimethylsilyl)ethyl)thio)pyridin-4-yl)ben zoate

A mixture of methyl 4-(2-chloro-3-cyanopyridin-4-yl)benzoate (600 mg, 2.2 mmol), 2-(trimethylsilyl)-ethanethiol (380 mg, 2.9 mmol), and K2CO ₃ (460 mg, 3.3 mmol) in DMF (10 ml) was allowed to stir at RT overnight. TLC and LC showed a clean reaction. The reaction was diluted with EtOAc (50 mL), washed with water and brine, and separated. The crude solution was dried over sodium sulfate, filtered and concentrated to give methyl 4-(3- cyano-2-((2-(trimethylsilyl)ethyl)thio)pyridin-4-yl)benzoate as a yellow oil. The material was used in the next step without purification. LC/MS [M+H] ⁺ : 371.

Step C: Methyl 4-(3-cyano-2-((2-(trimethylsilyl)ethyl)sulfonyl)pyridin-4-yl )benzoate

To a solution of methyl 4-(3-cyano-2-((2-(trimethylsilyl)ethyl)thio)pyridin-4- yl)benzoate (800 mg, 2.16 mmol) in CH ₂ C1 ₂ (40 mL) was added m-CPBA (1452 mg, 6.48 mmol). The reaction was allowed to stir at RT for 2 hours. The reaction was quenched with aq a ₂ S203 solution. The mixture was stirred for 1 hour, diluted with DCM, and separated. The solution was dried over sodium sulfate, filtered and concentrated to give a sticky oil, which was then injected onto a 40G ISCO column and purified by MPLC with hexanes and EtOAc gradient system. LC/MS [M+H] ⁺ : 403.

Step D: methyl 4-(3-(lH-tetrazol-5-yl)-2-((2-

(trimethylsilyl)ethyl)sulfonyl)pyridin-4-yl)benzoateTo a solution of methyl 4-(3-cyano-2-((2- (trimethylsilyl)ethyl)sulfonyl)pyridin-4-yl)benzoate (800 mg, 2.0 mmol) in toluene (10 mL) was added dibutyltin oxide (99 mg, 0.40 mmol) and azidotrimethylsilane (460 mg, 4.0 mmol). The mixture was allowed to reflux for 16 hours. LC showed complete and clean reaction. The solvent was removed under reduced pressure, and the residue was dissolved in DCM and injected onto a 40G ISCO column. The product was purified by MPLC eluted with a DCM and MeOH gradient. Methyl 4-(3-(lH-tetrazol-5-yl)-2-((2-(trimethylsilyl)ethyl)thio)pyr idin-4- yl)benzoate eluted at about 4% MeOH. LC/MS [M+H] ⁺ : 446.

Step E: Methyl 4-(2-sulfamoyl-3-(lH-tetrazol-5-yl)pyridin-4-yl)benzoate

To a THF solution of methyl 4-(3-(lH-tetrazol-5-yl)-2-((2- (trimethylsilyl)ethyl)sulfonyl)pyridin-4-yl)benzoate (100 mg, 0.22 mmol) was added TBAF (0.45 ml, 0.45 mmol) and CsF (170 mg, 1.12 mmol). The mixture was allowed to stir at 60°C for 3 hours. At that point, LC showed most of thestarting material was gone. The reaction was cooled, and added an aq. solution of sodium acetate (180 mg, 2.2 mmol), followed by addition of hydroxylamine-O-sulfonic acid (250 mg, 2.2 mmol). The mixture was allowed to stir at RT for 16 hours. LC showed good and clean reaction. The reaction was filtered and purified by HPLC eluted with a gradient of ACN and water containing 0.05% TFA. LC/MS [M+H] ⁺ : 360.9.

EXAMPLE 183

4- (2-Sulfamoyl-3-(lH-tetrazol-5-yl)pyridin-4-yl)benzamide and 4-(2-Sulfamoyl-3-(lH-tetrazol-

5- yl)pyridin-4-yl)benzoic acid

Step A: 4-(3-(lH-Tetrazol-5-yl)-2-((2-(trimethylsilyl)ethyl)sulfonyl )pyridin-4-yl)benzoic acid

To a 20 mL microwave tube charged with methyl 4-(3-(lH-tetrazol-5-yl)-2-((2- (trimethylsilyl)ethyl)sulfonyl)pyridin-4-yl)benzoate from Example 182, Steps A-D (100 mg, 0.224 mmol) and a stir bar was added ammonium hydroxide (5 ml, 36 mmol) and MeOH (1 ml). The tube was sealed and heated to 140°C for 30 minutes. LC/MS showed formation of both the amide and acid in about 1 : 1 ratio. The reaction was transferred into a RB flask, and the volatiles were removed under reduced pressure. The resulting foam was used directly in the next step. LC/MS [M+H] ⁺ : 43 1, 432.

Step B: 4-(2-Sulfamoyl-3-(lH-tetrazol-5-yl)pyridin-4-yl)benzoic acid

To a solution of a crude mixture of 4-(3-(lH-tetrazol-5-yl)-2-((2- (trimethylsilyl)ethyl)sulfonyl)pyridin-4-yl)benzamide and 4-(3-(lH-tetrazol-5-yl)-2-((2- (trimethylsilyl)ethyl)sulfonyl)pyridin-4-yl)benzoic acid in THF (5 mL) was added cesium fluoride (176 mg, 1.2 mmol) and TBAF (0.46 mL, 0.46 mmol). The mixture was heated to 60°C for 2 hours. Most of the starting material was still there, so another 10 eq. of TBAF was added to the reaction, and the reaction was allowed to reflux overnight. LC/MS suggested complete consumption of the starting materials at that point. The reaction was cooled to rt, and an aq. solution of sodium acetate (190 mg, 2.3 mmol) was added, followed by addition of

(aminooxy)sulfonic acid (260 mg, 2.3 mmol). The reaction was allowed to stir at rt. LC/MS showed formation of the desired products within 1 hour. The reaction was allowed to age overnight, the solvent removed in vacuo and the residue purified by reverse phase HPLC eluted with water and acetonitrile containing 0.05% TFA to afford the amide and 4-(2-sulfamoyl-3- (lH-tetrazol-5-yl)pyridin-4-yl)benzoic acid. LC/MS [M+H] ⁺ : 346.9.

EXAMPLE 184

4-(2-Sulfamoyl-3 -( 1 H-tetrazol-5 -yl)pyridin-4-yl)benzamide

To a solution of 4-(2-sulfamoyl-3-(lH-tetrazol-5-yl)pyridin-4-yl)benzoic acid from Example 183 (29 mg, 0.084 mmol), N,N-diisopropylethylamine (0.12 ml, 0.67 mmol) and HATU (47.8 mg, 0.13 mmol) in DMF (5 ml) was added ammonium chloride (134 mg, 2.51 mmol). The reaction mixture was stirred under a dry nitrogen atmosphere at room temperature for 16 hours. The reaction mixture was concentrated under vacuum and purified by reverse phase HPLC eluted with ACN and H ₂ 0 containing 0.05% TFA to afford 4-(2-sulfamoyl-3-(lH- tetrazol-5-yl)pyridin-4-yl)benzamide. LC/MS [M+H] ⁺ : 346.1.

EXAMPLE 185

N-Cyclopropyl-4-(2-sulfamoyl-3- -tetrazol-5-yl)pyridin-4-yl)benzamide

N-cyclopropyl-4-(2-sulfamoyl-3-(lH-tetrazol-5-yl)pyridin-4-y l)benzamide was prepared by the method described in Example 184 substituting cyclopropylamine HC1 for ammonium chloride. LC/MS [M+H] ⁺ : 386.1.

EXAMPLE 186

4-(2-Sulfamoyl-3-(lH-tetrazol-5-yl)pyridin-4-yl)-N-(tetrahyd ro-2H-pyran-4-yl)benzamide

4-(2-sulfamoyl-3-(lH-tetrazol-5-yl)pyridin-4-yl)-N-(tetrahyd ro-2H-pyran-4- yl)benzamide was prepared by the method described in Example 184 substituting 4-amino- tetrahydro-2H-pyran HC1 for ammonium chloride. LC/MS [M+H] ⁺ : 430.1.

EXAMPLE 187

4-(4-(Tetrahydro-2H-pyran-4-yl)phenyl)-3-(lH-tetrazol-5-yl)p yridine-2-sulfonamide

Step A: 4-(4-(Tetrahydro-2H-pyran-4-yl)phenyl)-2-((2- (trimethylsilyl)ethyl)sulfonyl)nicotinonitrile

To a 5 mL microwave tube charged with a stir bar was added 4-bromo-2-((2- (trimethylsilyl)ethyl)sulfonyl)nicotinonitrile (45 mg, 0.13 mmol), (4-(tetrahydro-2H-pyran-4- yl)phenyl)boronic acid (40 mg, 0.19 mmol), Pd(DTBPF)Cl ₂ (17 mg, 0.026 mmol), K ₃ P0 ₄ (1 M, 0.39 mL), and EtOH (1.5 mL). The mixture was sealed, purged with nitrogen, and then heated to 60°C for 1 hour. LC showed complete and clean reaction. The reaction was diluted with EtOAc, washed with brine, and separated. The crude solution was dried over sodium sulfate, and concentrated. The residue was adsorbed onto silica gel, and purified by MPLC with eluted with hexane and EtOAc on a 24G ISCO column. 4-(4-(Tetrahydro-2H-pyran-4-yl)phenyl)-2-((2- (trimethylsilyl)ethyl)sulfonyl)nicotinonitrile was isolated as a white solid. LC/MS [M+H] ⁺ : 429.

Step B: 4-(4-(Tetrahydro-2H-pyran-4-yl)phenyl)-3-(lH-tetrazol-5-yl)- 2-((2- (trimethylsilyl)ethyl)sulfonyl)pyridine

To a 20 mL microwave tube charged with 4-(4-(tetrahydro-2H-pyran-4- yl)phenyl)-2-((2-(trimethylsilyl)ethyl)sulfonyl)nicotinonitr ile (50 mg, 0.12 mmol) and a stir bar was added azidotrimethylsilane (40 mg, 0.35 mmol), dibutylstannanone (8.7 mg, 0.035 mmol), and toluene (2 ml). The mixture was sealed and heated to 115°C for 16 hours. LC showed complete reaction. The solvent was removed under vacuum, and the residue was dissolved in DCM and loaded onto a 24G ISCO column. The product was eluted with hexane and EtOAc with a gradient of MeOH and eluted at about 10% MeOH. LC/MS [M+H] ⁺ : 472. Step C: 4-(4-(Tetrahydro-2H-pyran-4-yl)phenyl)-3-(lH-tetrazol-5-yl)p yridine-2- sulfonamide

To a solution of 4-(4-(tetrahydro-2H-pyran-4-yl)phenyl)-3-(2H-tetrazol-5-yl)- 2- ((2-(trimethylsilyl)ethyl)sulfonyl)pyridine (20 mg, 0.042 mmol) in THF (1 niL) was added TBAF (0.21 niL, 0.21 mmol). The mixture was heated to 65°C for 1 hour. LC showed all starting material was gone. The reaction was cooled, and aq. NaOAc (35 mg, 0.42 mmol) and hydroxylamne-O-sulfonic acid (48 mg, 0.42 mmol) was added. The mixture was allowed to stir at rt for 16 hours. LC showed formation of the desired product. The product was isolated by HPLC eluted with ACN and water (containing 0.05% TFA). LC showed the product contained some TBAF, so it was passed through a negative ion-exchange resin column with water. 4-(4- (Tetrahydro-2H-pyran-4-yl)phenyl)-3-(lH-tetrazol-5-yl)pyridi ne-2-sulfonamide was isolated. LC/MS [M+H] ⁺ : 387.1.

EXAMPLE 188

2-(4-(Hydroxymethyl)phenyl)-3-(lH-tetrazol-5-yl)pyridine-4-s ulfonamide

Step A: 2-Chloro-4-((2-(trimethylsilyl)ethyl)thio)nicotinonitrile

To a solution of 2-chloro-4-iodonicotinonitrile (2.0 g, 7.6 mmol) and K2CO ₃ (1.57 g, 1 1.34 mmol) in DMF (7 mL) was added 2-(trimethylsilyl)ethanethiol (1.21 mL, 7.56 mmol) under dry 2 atmosphere at room temperature. The mixture was stirred at the room temperature for 16 hours. The crude UPLC did not show the desired peak but the TLC indicated complete consumption of starting material. The reaction mixture was concentrated under vacuo. The crude was adsorbed onto silica gel, and loaded onto silica gel column and eluted with hexane and ethyl acetate to give 2-chloro-4-((2-(trimethylsilyl)ethyl)thio)nicotinonitrile. LC/MS [M+H] ⁺ : 271.

Step B: 2-Chloro-4-((2-(trimethylsilyl)ethyl)sulfonyl)nicotinonitril e

To a solution of 2-chloro-4-((2-(trimethylsilyl)ethyl)thio)nicotinonitrile (900 mg, 3.32 mmol) in DCM (20 mL) was added mCPBA (2.0, 11.63 mmol) under dry 2 atmosphere at room temperature. The mixture was stirred for 16 hours at room temperature. The TLC in 20:80 EtOAc:Hex indicated complete consumption of starting material. To that mixture, sat. a ₂ S ₂ 0 ₃ was added and stirred for 15 minutes and then sat. NaHC0 ₃ was added and stirred for another 15 minutes. The organic was extracted with DCM (3x), dried over a ₂ S04, filtered and

concentrated to give 2-chloro-4-((2-(trimethylsilyl)ethyl)sulfonyl)nicotinonitril e which was used without purification. LC/MS [M+H] ⁺ : 302.

Step C: 2-(4-(Hydroxymethyl)phenyl)-4-((2-(trimethylsilyl)ethyl)sulf onyl)nicotinonitrile

A solution of 2-chloro-4-((2-(trimethylsilyl)ethyl)sulfonyl)nicotinonitril e (300 mg, 0.99 mmol), (4-(hydroxymethyl)phenyl)boronic acid (527 mg, 3.47 mmol),, aminobiphenyl palladium chloride precatalyst (XPhos-Pd-G2; 78 mg, 0.10 mmol) and potassium phosphate tribasic (735 mg, 3.46 mmol) dissolved in 3 mL of water was purged with dry N ₂ . The mixture was heated at 60°C for 16 hours. The crude UPLC showed the desired peak at 1.28 ppm,

375m/e. The reaction mixture was filtered through a packed celite pad and washed with EtOAc. The filtrate was concentrated in vacuo to dryness. The crude material was adsorbed onto silica gel and purified by MPLC eluted with hexane and ethyl acetate to give 2-(4- (hydroxymethyl)phenyl)-4-((2-(trimethylsilyl)ethyl)sulfonyl) nicotinonitrile. LC/MS [M+H] ⁺ : 375.

Step D: (4-(3-(lH-Tetrazol-5-yl)-4-((2-(trimethylsilyl)ethyl)sulfony l)pyridin-2- yl)phenyl)methanol

A solution of 2-(4-(hydroxymethyl)phenyl)-4-((2- (trimethylsilyl)ethyl)sulfonyl)nicotinonitrile (100 mg, 0.27 mmol) and azidotrimethyltin (275 mg, 1.34 mmol) in THF (4 mL) was purged several times with dry nitrogen. The mixture was heated in a microwave at 140°C for 30 minutes. The crude UPLC indicated a desired peak at 1.18ppm, 418m/z. Very small amount of starting material still remained at 1.29ppm, 375m/z. The mixture was concentrated in vacuo. The crude was purified by silica gel column eluted with hexane and ethyl acetate as solvent to give (4-(3-(lH-tetrazol-5-yl)-4-((2- (trimethylsilyl)ethyl)sulfonyl)pyridin-2-yl)phenyl)methanol. LC/MS [M+H] ⁺ : 418.

Step E: 2-(4-(Hydroxymethyl)phenyl)-3-(lH-tetrazol-5-yl)pyridine-4-s ulfonamide

A solution of (4-(3-(lH-tetrazol-5-yl)-4-((2-(trimethylsilyl)ethyl)sulfony l)pyridin- 2-yl)phenyl)methanol (20 mg, 0.048 mmol) and tetrabutylammonium fluoride (0.144 ml, 0.144 mmol) in THF (3 ml) was heated at 70°C for 3 hours. The sulfinic acid peak was observed at 0.79ppm, 317m/z. Sodium acetate (19.65 mg, 0.239 mmol) dissolved in water (0.1 12 ml, 6.23 mmol) and hydroxylamine-o-sulfonic acid (27.1 mg, 0.239 mmol) were added and stirred at 70°C for 16 hours. The reaction mixture was filtered and concentrated. The crude product was purified by HPLC and eluted with a gradient of ACN and H ₂ 0 buffered with 0.05 TFA. After removing the solvent in vacuo, the compound was dissolved in H ₂ 0/acetone and eluted via a packed resin column (Dowex 50wx8, 100-200 mesh, ion-exchange resin) which was activated with IN NaOH and neutralized to pH~7 with H ₂ 0. The eluted water was concentrated and dried under lyophilizer to give 2-(4-(hydroxymethyl)phenyl)-3-(lH-tetrazol-5-yl)pyridine-4- sulfonamide. LC/MS [M+H] ⁺ : 333.1.

EXAMPLE 189

5-(4-(Hydroxymethyl)phenyl)-4-(lH-tetrazol-5-yl)pyridine-3-s ulfonamide

Step A: 3-Chloro-5-(4-(hydroxymethyl)phenyl)isonicotinonitrile

A solution of 3,5-dichloro-4-pyridinecarbonitrile (2.27 g, 13.12 mmol), 4- (hydroxymethyl)phenylboronic acid (1.99 g, 13.12 mmol), potassium phosphate tribasic (19.68 ml, 19.68 mmol) dissolved in water (17 mL) and XPhos (1.032 g, 1.312 mmol) in THF (100 ml) was flashed with N ₂ . The mixture was heated at 60°C under dry N ₂ for 4 hours. The reaction mixture was allowed to stir for a total of 24 hours. The reaction mixture was filtered and concentrated under vacuum. The crude product was purified on a silica gel column, RediSep Column, eluted with hexane and ethyl acetate to afford 3-chloro-5-(4- (hydroxymethyl)phenyl)isonicotinonitrile. LC/MS [M+H] ⁺ : 245.

Step B : 3 -(4-(Hydroxymethyl)phenyl)-5-((2-(trimethylsilyl)ethyl)thio) isonicotinonitrile

To a solution of 3-chloro-5-(4-(hydroxymethyl)phenyl)isonicotinonitrile (1.1 g,

4.50 mmol) and potassium carbonate (0.746 g, 5.39 mmol) in DMF (25 mL) was added 2- (trimethylsilyl)ethanethiol (1.1 mL, 6.87 mmol) at room temperature under N ₂ . The reaction mixture was stirred for 3 hours. The crude UPLC indicated starting material still remained. The mixture was allowed to stir for a total of 24 hours. The crude UPLC indicated complete consumption of starting material. The reaction was diluted with EtOAc and washed with H ₂ 0. The organic layer was concentrated under vacuum and purified on a silica gel column eluted with hexane and ethyl acetate to give 3-(4-(hydroxymethyl)phenyl)-5-((2- (trimethylsilyl)ethyl)thio)isonicotinonitrile. LC/MS [M+H] ⁺ : 343. Step C: 3-(4-(Hydroxymethyl)phenyl)-5-((2- (trimethylsilyl)ethyl)sulfonyl)isonicotinonitrile

A solution of 3-(4-(hydroxymethyl)phenyl)-5-((2- (trimethylsilyl)ethyl)thio)isonicotinonitrile (1.4 g, 4.09 mmol) and mCPBA (2.47 g, 14.31 mmol) in DCM (40 ml) was stirred at room temperature under 2 for 16 hours. The TLC indicated complete consumption of starting material. To a reaction mixture, sat. Na ₂ S ₂ 0 ₃ was added and stirred for 15 minutes and then sat. NaHCC was added and stirred for another 15 more minutes. The organic layer was extracted with DCM (4x), dried over a ₂ S0 ₄ , filtered and concentrated. The crude was purified on a silica gel column eluted with hexane and ethyl acetate to afford 3- (4-(hydroxymethyl)phenyl)-5-((2-(trimethylsilyl)ethyl)sulfon yl)isonicotinonitrile. LC/MS

[M+H] ⁺ : 375.

Step D: (4-(4-(lH-Tetrazol-5-yl)-5-((2-(trimethylsilyl)ethyl)sulfony l)pyridin-3- yl)phenyl)methanol

A solution of 3-(4-(hydroxymethyl)phenyl)-5-((2- (trimethylsilyl)ethyl)sulfonyl)isonicotinonitrile (200 mg, 0.53 mmol) and azidotrimethyltin (550 mg, 2.67 mmol) in THF (4 ml) was microwaved at 140°C for 30 minutes. The crude reaction mixture was injected directly onto a HPLC and eluted with a gradient of ACN and H2O buffered with 0.05% TFA to afford (4-(4-(lH-tetrazol-5-yl)-5-((2-(trimethylsilyl)ethyl)sulfony l)pyridin-3- yl)phenyl)methanol. LC/MS [M+H] ⁺ : 418.

Step E: 5 -(4-(Hydroxymethyl)phenyl)-4-(lH-tetrazol-5-yl)pyridine-3 -sulfonamide

A solution of (4-(4-(lH-tetrazol-5-yl)-5-((2-(trimethylsilyl)ethyl)sulfony l)pyridin- 3-yl)phenyl)methanol (180 mg, 0.43 mmol) and tetrabutylammonium fluoride (1.29 ml, 1.29 mmol) in THF (5 ml) was heated at 68°C for 2 hours. The mixture was allowed to stir for total of 17 hours. A solution of sodium acetate (177 mg, 2.16 mmol) in water (1.01 mL, 56.0 mmol) and hydroxylamine-o-sulfonic acid (244 mg, 2.16 mmol) were added sequentially, and the mixture was stirred for 2 more hours. The reaction mixture was injected directly into HPLC and was eluted with a gradient of ACN and H ₂ 0 buffering with 0.05% TFA. The ^X H-NMR showed strong peaks of tetrabutyl ammonium salt. The compound was dissolved in H2O and a minimum amount of acetone was added. The crude solution was placed on a packed resin column (Dowex 50wx8, 100-200 mesh, ion-exchange resin) which was activated with IN NaOH and neutralized to pH~7 with H2O to give 5-(4-(hydroxymethyl)phenyl)-4-(lH-tetrazol-5-yl)pyridine-3- sulfonamide. LC/MS [M+H] ⁺ : 333.1. EXAMPLE 190

3-(lH-Tetrazol-5-yl)-4-(p-tolyl)pyridine-2-sulfonamide

Step A: 2-Chloro-4-(p-tolyl)nicotinonitrile

A microwave vial containing 2-chloro-3-cyanopyridine-4-boronic acid pinacol ester (2 g, 7.56 mmol), 4-bromotoluene (1.94 g, 1 1.34 mmol), freshly prepared aqueous 1 M of potassium phosphate tribasic (11.34 ml, 11.34 mmol) and 1 , l'-bis(di-tert- butylphosphino)ferrocene palladium dichloride (0.49 g, 0.76 mmol) in EtOH (40 ml) was purged with 2 (3x). The mixture was stirred at 55°C for 12 hours. The crude UPLC indicated the desired product. The reaction mixture was diluted with EtOAc and washed with H2O and brine. The organic was dried over Na ₂ S0 ₄ , filtered and concentrated under vacuum. The crude was purified by Silica gel column with hexane and ethyl acetate to give the desired compound.

LC/MS [M+H] ⁺ : 229.

Step B : 4-(p-Tolyl)-2-((2-(trimethylsilyl)ethyl)thio)nicotinonitrile

To a solution of 2-chloro-4-(p-tolyl)nicotinonitrile (907 mg, 3.97 mmol) and potassium carbonate (l . lg, 7.93 mmol) in DMF (10 mL) was added 2-(trimethylsilyl)ethanethiol (0.57 ml, 3.57 mmol) at room temperature under dry N ₂ . The mixture was stirred for 60 hours. The reaction mixture was poured into a separatory funnel containing H2O and the organic layer was extracted with EtOAc (3x). The combined extracts were dried over Na ₂ S0 ₄ , filtered and the solution was evaporated to dryness under reduced pressure. The crude 1H-NMR showed 4-(p- tolyl)-2-((2-(trimethylsilyl)ethyl)thio)nicotinonitrile with small amount of impurities so the crude product was used without further purification in the next step. LC/MS [M+H] ⁺ : 327.

Step C: 4-(p-Tolyl)-2-((2-(trimethylsilyl)ethyl)sulfonyl)nicotinonit rile

To a solution of 4-(p-tolyl)-2-((2-(trimethylsilyl)ethyl)thio)nicotinonitrile (2.3 g crude, 7.04 mmol) in DCM (40 mL) was added mCPBA (4.25 g, 24.7 mmol) at 0°C. The reaction was slowly brought to room temperature and stirred for 1-1/2 hours. To the reaction mixture, sat. a ₂ S0 ₃ was added and stirred for 20 minutes and then sat. aHC0 ₃ was added. After stirring for 20 minutes, the organic layer was extracted with DCM (3x), dried over NaS0 ₄ , filtered and concentrated. The crude product was used in the next step without further purification. LC/MS [M+H] ⁺ : 359.

Step D: 3-(lH-Tetrazol-5-yl)-4-( 7-tolyl)-2-((2-(trimethylsilyl)ethyl)sulfonyl)pyridine

A solution of 4-(p-tolyl)-2-((2-(trimethylsilyl)ethyl)sulfonyl)nicotinonit rile (1.0 g, 2.79 mmol) and tributyltin azide (1.53 ml, 5.58 mmol) in THF (25 ml) was refluxed overnight. The crude UPLC showed a very small amount of the desired product. The reaction mixture was transferred into a microwave vial and it was microwaved at 140°C for 4 hours. The reaction mixture was concentrated under vacuum. The crude reaction was dissolved in DMSO and purified by HPLC eluted with a gradient of ACN and H ₂ 0 buffered with 0.05% TFA to give 3- (lH-tetrazol-5-yl)-4-(p-tolyl)-2-((2-(trimethylsilyl)ethyl)s ulfonyl)pyridine. LC/MS [M+H] ⁺ : 403.

Step E: 3-(lH-Tetrazol-5-yl)-4-(p-tolyl)pyridine-2-sulfonamide

To a solution of 3-(lH-tetrazol-5-yl)-4-(p-tolyl)-2-((2- (trimethylsilyl)ethyl)sulfonyl)pyridine (400 mg, 1.0 mmol) in THF (10 ml) was added tetrabutylammonium fluoride (2.99 ml, 2.99 mmol). The mixture was refluxed for 1 hr and cooled to room temperature. A solution of sodium acetate (409 mg, 4.98 mmol) in water (2.33 ml, 129 mmol) and aminooxysulfonic acid (563 mg, 4.98 mmol) were added sequentially, and the mixture was stirred for 2 hours. The crude UPLC indicated starting material mostly remained. Another 3 eq. of tetrabutylammonium fluoride (3.0mL) was added and reaction was allowed to stir overnight The crude UPLC indicated that most of starting material was consumed. The reaction was evaporated under vacuum and the crude was dissolved in H ₂ 0 and purified by HPLC eluted with a gradient of ACN and H ₂ 0 buffered with 0.05% TFA. The ^X H- NMR showed a large amount of tBu-ammonium salt. The organic layer was eluted via a column cartridge containing activated Dowex 50Wx8 100-200 mesh, Ion-exchange resin charged with IN NaOH and then neutralized with water. The water was removed under vacuum and dried under lyophilizer to give 3-(lH-tetrazol-5-yl)-4-(p-tolyl)pyridine-2-sulfonamide as a white solid compound. LC/MS [M+H] ⁺ : 317.2.

EXAMPLE 191

(±)-4-(4-(cis-4-Methyl-2-oxooxazolidin-5-yl)phenyl)-3-(lH-t etrazol-5-yl)pyridine-2- sulfonamide

Step A: General method via Pd-coupling from Br-intermediate:

A solution of the mixture of 4-bromo-3-(2-(4-methoxybenzyl)-2H-tetrazol-5- yl)pyridine-2-sulfonamide and 4-bromo-3-(l-(4-methoxybenzyl)-lH-tetrazol-5-yl)pyridine-2- sulfonamide from Reference Example 2 (60 mg, 0.14 mmol), (±)-cis-4-methyl-5-(4-(4,4,5,5- tetramethyl-l,3,2-dioxaborolan-2-yl)phenyl)oxazolidin-2-one (64 mg, 0.21 mmol),

Pd(DTBPF)Cl ₂ (9.2 mg, 0.014 mmol), and K ₃ P0 ₄ (1 M, 0.42 mL, 0.42 mmol) in EtOH (2 mL) was heated to 70°C for 24 hours. LC showed formation of the desired product, along with a small amount of starting material left. The reaction was cooled, and extracted three times with EtOAc. The extractions were combined, and concentrated. The residue was dissolved in anisole (0.1 mL) and TFA (1 mL), and the solution was heated to 45°C for 16 hours. LC showed good reaction. The solvents were removed, and the residue was purified by reverse phase HPLC with ACN and water with (0.05% TFA). LC/MS [M+H] ⁺ : 402.2.

EXAMPLES 192-198

The following Examples 192-198 were prepared according to the general procedure described above for Example 191, using boronic acids or boronic esters that are commercially available, known, or prepared as described herein. Note that in some instances the boronic acid or boronic ester contains an amine group. In these cases, the amine moiety is typically protected with a tert-butoxycarbonyl group, which is concurrently removed under the final PMB deprotection step (Step B) with TFA and anisole. Alternatively, a Boc protected amine may be de-protected by treatedment with TFA at room temperature, followed by de- protection of the PMB group with heating as described.

Ex. Structure Name Calc'd LC/MS

No. Mass m/e

[M+H] [M+H] ⁺

+

EXAMPLES 199-215

Parallel synthesis of 4-substituted 3-(lH-tetrazol-5-yl)pyridine-2-sulfonamides Step A Step B

Step A: Palladium catalyzed C-C coupling of pyridyl bromide and boronic acids or boronic esters such as pinicol esters.

Boronic acids or esters (commercially available, known, or prepared as described herein, 0.235 mmol) and Chloro[(di(l-adamantyl)-N-butylphosphine)-2-(2- aminobiphenyl)]palladium(II) (7.86 mg, 0.012 mmol) were added into a microwave vial and under N ₂ . Then a mixture of 4-Bromo-3-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)pyridine-2- sulfonamide and 4-Bromo-3-(l-(4-methoxybenzyl)-lH-tetrazol-5-yl)pyridine-2-s ulfonamide (50 mg, 0.118 mmol) in THF (1 mL) was added into the vial under 2 followed by 1.0 M potassium phosphate (0.470 mL, 0.470 mmol) and the reaction was agitated at 110°C for 16 hours. Solvent was removed under reduced pressure. To each vial, 1.5 mL DCM was added along with 0.4 mL water, with shaking for 15 min. The organic layer was collected and solvent was removed under reduced pressure.

Step B: Removal of the p-methoxybenzyl (PMB) protecting group under acidic conditions.

To each vial from Step A, TFA (0.545 mL, 7.07 mmol), anisole (7.72 μΐ, 0.071 mmol) was added and agitated at 60°C for 12 hours. LC/MS showed formation of the desired products. The solvent were removed under reduced pressure. To each vial, 1 mL DMSO was added followed by addition of SiliaMetS® DMT to remove the Pd catalyst. The mixtures were shaken for 6 hours and filterered into a 96-well plate. These crude materials were purified by HPLC to afford Examples 199-215.

Ex. Structure Name Calc'd LC/MS

No. Mass m/e

EXAMPLES 216-244

Parallel synthesis of aminopyridinyl examples:

Step A: Coupling of commercially available or known amines with 4-Bromo-3-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)pyridine-2-sulfonamide and 4-Bromo-3-(l-(4-methoxybenzyl)- lH-tetrazol-5-yl)pyridine-2-sulfonamide

A mixture of 4-Bromo-3-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)pyridine-2- sulfonamide and 4-Bromo-3-(l-(4-methoxybenzyl)-lH-tetrazol-5-yl)pyridine-2-s ulfonamide (30 mg, 0.071 mmol) was combined with potassium carbonate (58.5 mg, 0.423 mmol) and commercially available or known primary or secondary amines (0.071 mmol) in a microwave vial with DMF (1 mL). The mixture was stirred at 150°C for 1 hour. The mixtures were concentrated under reduced pressure.

Step B: Removal of the PMB protective group under acidic conditions

To the intermediates produced in Step A was added TFA (0.5 mL) and Anisole (0.031 mL, 0.282 mmol) and the mixtures were stirred at 65°C for 3 hours. The mixtures were allowed to cool and were then concentrated under reduced pressure. DMSO (1 mL) was added to each vial and the mixtures were filtered through a (96 well) 0.4 micron filter plate.

Purification by mass directed reverse phase HPLC afforded Examples 216-244. 4-[4-(l- 354 354 hydroxyethyl)piperidin- 1 -yl] - 3-(lH-tetrazol-5-yl)pyridine-

244 2-sulfonamide

EXAMPLE 245

4-(3 ,9-diazaspiro[5.5 ]undecan-3 -yl)-3 -(2H-tetrazol-5-yl)pyridine-2-sulfonamide

Step A: tert-butyl 9-(3-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-2-sulfamoylpyrid in-4-yl)-

3,9-diazaspiro[5.5]undecane-3-carboxylate and tert-butyl 9-(3-(l-(4-methoxybenzyl)-lH- tetrazol-5-yl)-2-sulfamoylpyridin-4-yl)-3,9-diazaspiro[5.5]u ndecane-3-carboxylate

The mixture of tert-butyl 3,9-diazaspiro[5.5]undecane-3-carboxylate hydrochloride (29.3 mg, 0.101 mmol), 4-Bromo-3-(2-(4-methoxybenzyl)-2H-tetrazol-5- yl)pyridine-2-sulfonamide and 4-Bromo-3 -( 1 -(4-methoxybenzyl)- lH-tetrazol-5-yl)pyridine-2- sulfonamide (33 mg, 0.078 mmol), and K ₂ C0 ₃ (42.9 mg, 0.310 mmol) in DMF (1 mL) was heated at 140°C overnight. The mixture was partitioned between EtOAc (50 mL) and sat.

NaHCCh, the organic phase was washed with NaHCCh twice, dried over a2S0 ₄ , concentrated and the residue was purified on preparative TLC (1000MU) using 10%MeOH/DCM as developing solvents to give the residue which was then further purified on preparative TLC (1000MU) using EtOAc as developing solvent to the title compound.

Step B : 4-(3 ,9-diazaspiro [5.5]undecan-3 -yl)-3 -(2H-tetrazol-5-yl)pyridine-2-sulfonamide

To the solution of tert-butyl 9-(3-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-2- sulfamoylpyridin-4-yl)-3,9-diazaspiro[5.5]undecane-3-carboxy late and tert-butyl 9-(3-(l-(4- methoxybenzyl)-lH-tetrazol-5-yl)-2-sulfamoylpyridin-4-yl)-3, 9-diazaspiro[5.5]undecane-3- carboxylate (37 mg, 0.062 mmol) in CH ₂ CI ₂ (2 mL) was added TFA (2 mL, 26.0 mmol), and the resulting solution was stirred at rt for 1 hr, and then was concentrated; to the resulting residue was added triisopropylsilane (98 mg, 0.62 mmol) and TFA (2 mL, 26.0 mmol). The solution was then transfered to a sealed tube and heated at 80°C for 1 hr. After removing the volatiles, the residue was dissolved in acetonitrile/water and purified by reverse phase HPLC using 5-40% acetonitrile (0.1%formic acid) over 10 min to give the title compound. LC/MS [M+H] ⁺ 379.

EXAMPLE 246

4-(lH-benzo[d]imidazol-l- -3-(2H-tetrazol-5-yl)pyridine-2-sulfonamide

Step A: l-(3-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-2-((2- (trimethylsilyl)ethyl)sulfonyl)pyridin-4-yl)-lH-benzo[d]imid azole

To a microwave vial was charged 4-bromo-3-(l-(4-methoxybenzyl)-lH-tetrazol- 5-yl)-2-((2-(trimethylsilyl)ethyl)sulfonyl)pyridine (300 mg, 0.588 mmol), lH-benzo[d] imidazole (83 mg, 0.705 mmol), Pd ₂ (dba) ₃ (53.8 mg, 0.059 mmol), Xantphos (68.0 mg, 0.118 mmol), and potassium carbonate (244 mg, 1.76 mmol). The vial was sealed, degassed, and filled with dioxane (2938 μΐ). The reaction mixture was heated at 90°C overnight, and was diluted with water, and extracted with EtOAc. The organic layer was washed with brine, dried, and evaporated to give the crude product, which was purified by silica gel column chromatography (0-10% MeOH/DCM) to give the title compound. LC-MS (IE, m/z): 548.7 [M+l]+.

Step B: 4-(lH-benzo[d]imidazol-l-yl)-3-(2-(4-methoxybenzyl)-2H-tetra zol-5-yl)pyridine- 2 -sulfonamide

In a glove box to the solution of l-(3-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-2- ((2-(trimethylsilyl)ethyl)sulfonyl)pyridin-4-yl)-lH-benzo[d] imidazole (150 mg, 0.274 mmol) in THF (5.5 mL) was added TBAF (1.4 mL, 1 M in THF, 1.4 mmol). The resulting solution was stirred at rt for 2 hr, and checked by LCMS for completion of the first step conversion. Sodium acetate (225 mg, 2.74 mmol) in 2 mL of water was then added followed by addition of hydroxylamine-O-sulfonic acid (310 mg, 2.74 mmol). The resulting solution was stirred at rt overnight in the glove box. The mixture was partitined between EtOAc (50 mL) and sat.

aHC03. The organic phase was washed with NaHCC twice, and dried over Na ₂ S0 ₄ , concentrated and the resiude was purified by silica gel chromatography using 10% MeOH/DCM as mobile phase to afford the title compound.

LC-MS (IE, m/z): 463.28 [M+l] ⁺ . Step C: 4-(lH-benzo[d]imidazol-l-yl)-3-(2H-tetrazol-5-yl)pyridine-2- sulfonamide

To a solution of 4-(lH-benzo[d]imidazol-l-yl)-3-(2-(4-methoxybenzyl)-2H- tetrazol-5-yl)pyridine-2-sulfonamide (100 mg, 0.216 mmol) in DCM (3 mL) was added thioanisole (0.512 ml, 4.32 mmol) and TFA (1.666 mL, 21.62 mmol). The resulting solution was heated at 80°C for 1.5 hr. After removing the volatile, the residue was purified by reverse phase HPLC using DMSO to load sample and 5-40% acetonitrile/water (0.1% formic acid additive) as mobile phase to afford the title compound. LC-MS (IE, m/z): 343.22 [M+l] ⁺ .

EXAMPLE 247

3-(Imidazo[l,5-a]pyridin-7-yl)-2-(2H-tetrazol-5-yl)benzenesu lfonamide

Step A: 3-(Imidazo[l,5-a]pyridin-7-yl)-2-(2-(4-methoxybenzyl)-2H-tet razol-5- yl)benzenesulfonamide

In a reaction vessel, 7-bromoimidazo[l,5-a]pyridine (200 mg, 1.02 mmol) and bispinacolatodiboron (773 mg, 3.05 mmol) were combined, followed by potassium acetate (299 mg, 3.05 mmol) and PCy3 Pd G2 (59.9 mg, 0.102 mmol). Then dry dioxane (5 mL) was added to this flask. This mixture was degassed and then heated at 80°C for 12 hr. The reaction was cooled to rt, then to the reaction was added 3-bromo-2-(2-(4-methoxybenzyl)-2H-tetrazol-5- yl)benzenesulfonamide (431 mg, 1.02 mmol), (83 mg, 0.102 mmol), and K ₂ CO ₃ (842 mg, 6.09 mmol) dissolved in 1.2 ml of water. ₂ was bubbled through for 10 min. The mixture was then heated at 85°C overnight. The mixture was cooled, diluted with

EtOAc, and washed with water. The combined organic fractions were separated and the solvent was evaporated under reduced pressure. The residue was purified by column chromatography on silica gel (80 g), eluting with 0-5% MeOH/EtOAc to give the title compound. LC-MS 462 (M+l) ⁺ .

Step B: 3-(Imidazo[l,5-a]pyridin-7-yl)-2-(2H-tetrazol-5-yl)benzenesu lfonamide

3-(Imidazo[l,5-a]pyridin-7-yl)-2-(2-(4-methoxybenzyl)-2H-tet razol-5- yl)benzenesulfonamide was heated at 80°C in TFA for 3 hr. The mixture was then cooled and concentrated to remove the excess of TFA. The residue was dissolved in ΟΗ ₃ ΟΝ/Η ₂ 0/ΜεΟΗ and purified by reverse phase HPLC, eluting with 5-40% CH ₃ CN/H ₂ 0 with 0.1 % formic acid. The correct fractions were combined, concentrated and lypholized. LC-MS 342 (M+l) ⁺ .

EXAMPLE 248

3-(5-Methylpyrazin-2- -2-(2H-tetrazol-5-yl)benzenesulfonamide

Step A: N,N-bis(4-Methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol- 5-yl)-3 -(5- methylpyrazin-2-yl)benzenesulfonamide

To a reaction vessel, was added 3-bromo-N,N-bis(4-methoxybenzyl)-2-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)benzenesulfonamide (200 mg, 0.301 mmol), 5,5,5',5'- tetramethyl-2,2'-bi(l,3,2-dioxaborinane) (204 mg, 0.903 mmol), PCy3 Pd G2 (17.8 mg, 0.030 mmol), and potassium acetate (89 mg, 0.90 mmol). Then amhydrous CH ₃ CN (1.5 mL) was added to this flask. The mixture was sealed and degassed for 10 min. This mixture was then heated at 85°C for 24 hr. LC-MS analysis indicated the formation of the desired boronic ester. After cooling to rt, to this reaction mixture, was added 2-bromo-5-methylpyrazine (78 mg, 0.451 mmol), PdCl ₂ (dppf) (22.02 mg, 0.030 mmol), and Na ₂ C0 ₃ (63.8 mg, 0.602 mmol) dissolved in water (0.4 mL). The reaction mixture was degassed for 10 min and heated at 95°C overnight. The mixture was cooled, water was added and the mixture was extracted with EtOAc. The combined organic fractions were washed with brine, dried (Na ₂ S0 ₄ ), filtered and the solvent was evaporated under reduced pressure. The residue was purified by column chromatography on silica gel, eluting with EtOAc/Hexanes (0-100%) to give the title compound. LC-MS 678 (M+l) ⁺ .

Step B: 3-(5-Methylpyrazin-2-yl)-2-(2H-tetrazol-5-yl)benzenesulfonam ide

N,N-bis(4-methoxybenzyl)-2-(l-(4-methoxybenzyl)-lH-tetrazol- 5-yl)-3-(5- methylpyrazin-2-yl)benzenesulfonamide (78 mg, 0.12 mmol) was treated with TFA (2 mL) and Anisole (12.57 μί, 0.115 mmol). After heating at 60°C for 3 hr, LC-MS analysis showed completion of the reaction. The reaction mixture was concentrated and the residue was purified by reverse phase HPLC (5-60% CH ₃ CN/water with 0.1 % TFA). The correct fractions were combined, concentrated, and lypholized to give the title compound. LC-MS 318 (M+l) ⁺ . EXAMPLE 249

4'-(5-(Aminomethyl)-l,2,4-o l,r-biphenyl]-3-sulfonamide

Step A: 4'-Cyano-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-[l,l'-biph enyl]-3- sulfonamide

To a reaction vessel was added 3-bromo-2-(2-(4-methoxybenzyl)-2H-tetrazol-5- yl)benzenesulfonamide (2.00 g, 4.71 mmol), 4-(4,4,5,5-tetramethyl-l,3,2-dioxaborolan-2- yl)benzonitrile (1.296 g, 5.66 mmol), PdCl ₂ (dppf) (0.345 g, 0.471 mmol), and a ₂ C0 ₃ (0.999 g, 9.43 mmol) followed by 1,4-dioxane (23.57 mL) and water (7.86 mL). The mixture was degassed for 10 min and then heated at 90°C overnight. After cooled to rt, the mixture was filtered through a pad of celite. The filtrates were concentrated and the residue was purified by column chromatography (0 - 70% EtOAc/Hexane) to give the title compound. LC-MS 447 (M+l) ⁺ ;

Step B : N-Hydroxy-2'-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-3 '-sulfamoyl-[ 1,1'- biphenyl]-4-carboximidamide

4'-Cyano-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-[l,l'-biph enyl]-3- sulfonamide (3 g, 6.72 mmol) and hydroxylamine (8.24 mL, 134 mmol) in EtOH (20 mL) was heated at 80°C overnight. The mixture was cooled and the excess solvents and reagent were removed under the reduced pressure to give the title compound, which was used directly in the next step. LC-MS 480 (M+l) ⁺ .

Step C: tert-butyl ((3-(2'-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-3'-sulfamoyl- [l,l'- biphenyl]-4-yl)- 1 ,2,4-oxadiazol-5-yl)methyl)carbamate

2-((tert-Butoxycarbonyl)amino)acetic acid (65.8 mg, 0.375 mmol) in CH2CI2 (3.1 mL) was treated with di( ¹ H-imidazol-l-yl)methanone (60.9 mg, 0.375 mmol). The mixture was stirred at rt under 2 for 30 min before N-hydroxy-2'-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-3'- sulfamoyl-[l,l'-biphenyl]-4-carboximidamide (150 mg, 0.313 mmol) was added. The resulting mixture was stired at rt under 2 overnight and then concentrated. The residue was heated at 110°C in toluene for 8 hr. LC-MS showed the desired mass. The mixture was concentrated and the residue was purified by column chromatography to give the title compound. LC-MS 619 (M+l) ⁺ .

Step D: 4'-(5-(Aminomethyl)-l,2,4-oxadiazol-3-yl)-2-(2H-tetrazol-5-y l)-[l,l'-biphenyl]-3- sulfonamide

tert-butyl ((3-(2'-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-3'-sulfamoyl- [l,l'- biphenyl]-4-yl)-l,2,4-oxadiazol-5-yl)methyl)carbamate (129 mg, 0.209 mmol) was treated with TFA at rt until LC-MS indicated the Boc group was removed. The reaction was concentrated under the reduced pressure and co-evaporated with toluene 3 times. Then the resulting residue was heated in TFA at 80°C for 3 hr before the reaction mixture was cooled and concentrated. The crude product was purified by Gilson (5%-40%ACN/water with 0.1% TFA). The correct fractions were combined, concentrated, converted to HQ salt and lypholized to give the title compound. LC-MS 399 (M+l) ⁺ .

EXAMPLE 250

4'-(5-(pyrrolidin-3-yl)-l,2,4-oxadiazol-3-yl)-2-(2H-tetrazol -5-yl)-[l,l'-biphenyl]-3-sulfonamide

The title compound was prepared in a similar fashion to the synthesis of 4'-(5- (Aminomethyl)- 1 ,2,4-oxadiazol-3 -yl)-2-(2H-tetrazol-5 -yl)- [ 1 , 1 '-biphenyl]-3 -sulfonamide from l-Boc-pyrrolidine-3-carboxylic acid and N-hydroxy-2'-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)- 3'-sulfamoyl-[l,l'-biphenyl]-4-carboximidamide. LC-MS 439 (M+l) ⁺ .

EXAMPLE 251

(5)-4'-(5-( 1 -hydroxyethyl)- 1 ,2,4-oxadiazol-3 -yl)-2-(2H-tetrazol-5-yl)-[ 1 , 1 '-biphenyl]-3- sulfonamide

Step A: (5)-4'-(5-(l-hydroxyethyl)-l,2,4-oxadiazol-3-yl)-2-(2-(4-met hoxybenzyl)-2H- tetrazol-5-yl)-[l,l'-biphenyl]-3-sulfonamide

L-(+)-lactic acid (28.2 mg, 0.313 mmol) was combined with EDC (90 mg, 0.469 mmol), HOBt (86 mg, 0.563 mmol), and -hydroxy-2'-(l-(4-methoxybenzyl)-lH-tetrazol-5-yl)- 3'-sulfamoyl-[l,l'-biphenyl]-4-carboximidamide (150 mg, 0.313 mmol), then DCM (1.6 mL) was added and then TEA (131 μΐ, 0.938 mmol). The mixture was stirred at rt for 16 hr. After being diluted with EtOAc, the reaction mixture was washed with water, sat. NaHCC solution and brine, dried (Na ₂ S0 ₄ ) and concentrated to give an oil, which was dissolved in pyridine (1.5 mL) and heated at 80°C overnight. The reaction mixture was concentrated and the residue was purified with column chromatography to give the title compound. LC-MS 534 (M+l) ⁺ .

Step B : (5)-4'-(5 -( 1 -hydroxy ethyl)- 1 ,2,4-oxadiazol-3 -yl)-2-(2H-tetrazol-5 -yl)- [ 1 , 1 '-biphenyl]-3 - sulfonamide

(5)-4'-(5-(l-hydroxyethyl)-l,2,4-oxadiazol-3-yl)-2-(2-(4-met hoxybenzyl)-2H- tetrazol-5-yl)-[l,l'-biphenyl]-3-sulfonamide (100 mg, 0.187 mmol) was heated in TFA for 3 hr before it was concentrated. The crude product was purified by reverse phase HPLC (5-60% acetonitrile/water with 0.1 %FA) and the correct fractions were combined, concentrated and lypholized to give the title compound. LC-MS 414 (M+l) ⁺ .

EXAMPLE 252

4,5-Dimethyl-2-(2H-tetr sulfonamide

Step A: 2-(2-((Benzyloxy)methyl)-2H-tetrazol-5-yl)-4,5-dimethylbenze nesulfonamide

A mixture of 2-((benzyloxy)methyl)-5-(tributylstannyl)-2H-tetrazole (109 mg, 0.227 mmol), 2-bromo-4,5-dimethylbenzenesulfonamide (50 mg, 0.189 mmol), tetrakis(triphenylphosphine)palladium(0) (10.94 mg, 9.46 μιηοΐ) and copper(I) iodide (3.61 mg, 0.019 mmol) in toluene (1 ml) was refluxed at 1 10°C for 4 hr. The reaction was filtered through celite and concentrated then purified by mass directed reverse phase HPLC with ACN and water with 0.05% TFA. LC/MS [M+H] ⁺ :374.

Step B: 4,5-Dimethyl-2-(2H-tetrazol-5-yl)benzenesulfonamide

A mixture of 2-(2-((benzyloxy)methyl)-2H-tetrazol-5-yl)-4,5- dimethylbenzenesulfonamide (16 mg, 0.043 mmol) and HCl (14 μΐ, 0.084 mmol) in methanol (1 ml) was heated at 65°C for 2 hr. LC/MS showed incomplete hydrolysis of BOM group. Another 0.3 ml of 6N HCl was added and heating continued for another 3 hr. The reaction was concentrated and purified by mass directed reverse phase hplc with ACN and water with 0.05% TFA. LC/MS [M+H] ⁺ :254.1.

EXAMPLE 253

4-Methoxy-2-(2H-tetrazol-5-yl)benzenesulfonamide

Step A: 2-(2-((Benzyloxy)methyl)-2H-tetrazol-yl)-4-methoxybenzenesul fonamide

2-((Benzyloxy)methyl)-5-(tributylstannyl)-2H-tetrazole from Reference Example 3 (180 mg, 0.376 mmol), 2-bromo-4-methoxybenzenesulfonamide (50 mg, 0.188 mmol) and chloro(2-dicyclohexylphosphino-2',6'-di-i-propoxy-l, l'-biphenyl)[2-(2- aminoethylphenyl)]palladium(II) methyl-t-butylether adduct (15.35 mg, 0.019 mmol) were dissolved in THF (376 μΐ) and heated to 80°C overnight. The reaction was filtered and concentrated and the residue was purified by mass directed reverse phase HPLC with ACN and water with 0.05% TFA. LC/MS [M+H] ⁺ :376.

Step B: 4-Methoxy-2-(2H-tetrazol-5-yl)benzenesulfonamide

2-(2-((Benzyloxy)methyl)-2H-tetrazol-5-yl)-4-methoxybenzenes ulfonamide (20 mg, 0.053 mmol) was dissolved in MeOH (1 ml) then HCl (0.018 ml, 0.107 mmol) was added and the reaction heated to 65°C. The reaction was monitored with LC/MS until no starting material was left. The reaction was concentrated and the residue was purified by reverse phase hplc with ACN and water with with 0.05% TFA. LC/MS [M+H] ⁺ :256.2. EXAMPLE 254

4-Hydroxy-2-(2H-tetrazol-yl)benzenesulfonamide

4-Methoxy-2-(2H-tetrazol-5-yl)benzenesulfonamide from Example 148 (6.6 mg, 0.026 mmol) was dissolved in DCM (5 ml) then cooled to 0°C and BBr ₃ (0.259 mL, 1 M, 0.259 mmol) was added. The reaction was then warmed up to RT and stirred for 18 hr. The reaction was quenched with water and concentrated. The residue purified by reverse phase HPLC with ACN and water with 0.05% TFA to afford 4-hydroxy-2-(2H-tetrazol-yl)benzenesulfonamide. LC/MS [M+H] ⁺ :242.1.

EXAMPLE 255

Methyl 3-sulfamoyl-4-(2H-tetrazol-5-yl)benzoate

Step A: Methyl 4-(2-((benzyloxy)methyl)-2H-tetrazol-5-yl)-3-sulfamoylbenzoa te

2-((Benzyloxy)methyl)-5-(tributylstannyl)-2H-tetrazole from Reference Example 3 (384 mg, 0.801 mmol), methyl 4-chloro-3-sulfamoylbenzoate (100 mg, 0.401 mmol) and chloro(2-dicyclohexylphosphino-2',6'-di-i-propoxy-l,l'-biphe nyl)[2-(2- aminoethylphenyl)]palladium(ii) methyl-t-butylether adduct (32.7 mg, 0.040 mmol) in THF (0.8 mL) was heated at 80°C overnight. The reaction was filtered and concentrated. The residue was absorbed onto silica gel and purified by MPLC with 5% methanol in methylene chloride.

LC/MS [M+H] ⁺ :404.

Step B: Methyl 3-sulfamoyl-4-(2H-tetrazol-5-yl)benzoate

Methyl 4-(2-((benzyloxy)methyl)-2H-tetrazol-5-yl)-3-sulfamoylbenzoa te (149 mg, 0.369 mmol) was dissolved in MeOH (2 ml) then HC1 (0.185 ml, 0.739 mmol) was added and the reaction was heated to 65 °C overnight. The reaction was concentrated and the residue purified by reverse phase HPLC with ACN and water with 0.05% TFA to afford the title compound. ^X H-NMR (500 MHz, CD30D) δ ppm 8.81 (s,lH), 8.38 (d, J=8 Ηζ,ΙΗ), 7.93 (d, J=8 Ηζ,ΙΗ) 4.01 (s, 3H); LC/MS [M+H] ⁺ :284.1.

EXAMPLE 256

2-(lH-Tetrazol-5-yl)-3-(trifluoromethyl)benzenesulfonamid e

Step A: 2-(Trifluoromethyl)-6-((2-(trimethylsilyl)ethyl)thio)benzoni trile

To a solution of 2-fluoro-6-(trifluoromethyl)benzonitrile (1.0 g, 5.29 mmol) and K ₂ C0 ₃ (1.46 g, 10.58 mmol) in DMF (5 mL) was added 2-(trimethylsilyl)ethanethiol (1.01 ml, 6.35 mmol). The mixture was stirred at room temperature for 4 hours. The TLC indicated complete consumption of starting material. The mixture was filtered and evaporated to dryness in vacuo. The crude was adsorbed onto silica gel, and purified by hexane and ethyl acetate to afford the desired compound. LC/MS [M+H] ⁺ :304.

Step B : 2-(Trifluoromethyl)-6-((2-(trimethylsilyl)ethyl)sulfonyl)ben zonitrile

To a solution of 2-(trifluoromethyl)-6-((2-(trimethylsilyl)ethyl)thio)benzoni trile (400 mg, 1.32 mmol) in DCM (10 ml) was added mCPBA (796 mg, 4.61 mmol). The mixture was stirred at room temperature for 3 hours. The TLC indicated complete consumption of starting material. Sat. a ₂ S ₂ 03 was added to the mixture and stirred for 10 minutes, then sat. aHC03 was added. The organic was extracted with DCM (3x), dried over Na ₂ S0 ₄ , filtered and concentrated. The crude 2-(trifluoromethyl)-6-((2-(trimethylsilyl)ethyl)sulfonyl)ben zonitrile was used without further purification in the next step. ^X H-NMR (CDCI3): δ 0.098 (s, 9H), 0.98- 1.01 ppm (m, 2H), 3.41-3.44 ppm (m, 2H), 8.0 (dd, J= 7.8 Hz, 1H), 8.13 (d, J= 7.8 Hz, 1H), 8.45 (d,

J= 7.8 Hz, 1H).

Step C: 5-(2-(Trifluoromethyl)-6-((2-(trimethylsilyl)ethyl)sulfonyl) phenyl)-lH-tetrazole

A solution of 2-(trifluoromethyl)-6-((2-(trimethylsilyl)ethyl)sulfonyl)ben zonitrile (350 mg, 1.04 mmol), azidotrimethylsilane (0.28 ml, 2.09 mmol) and dibutyltin oxide (78 mg, 0.31 mmol) was heated at 110°C overnight. The crude was concentrated and purified by HPLC with ACN and H ₂ 0 with buffering with 0.05 TFA to give the desired compound. LC/MS

[M+H] ⁺ :379.

Step D: 2-(lH-Tetrazol-5-yl)-3-(trifluoromethyl)benzenesulfonamide A solution of 5-(2-(trifluoromethyl)-6-((2-(trimethylsilyl)ethyl)sulfonyl) phenyl)- lH-tetrazole (301 mg, 0.80 mmol) and tetrabutylammonium fluoride (7.95 ml, 7.95 mmol) in THF (8 ml) was heated at 60°C for 16 hr. To that reaction mixture, sodium acetate (652 mg, 7.95 mmol) dissolved in water (3.73 ml, 207 mmol) followed by hydroxylamine-o-sulfonic acid (899 mg, 7.95 mmol) were added and stirred overnight. The reaction mixture was concentrated under vacuum and purified by HPLC with ACN and H ₂ 0 buffered with 0.05% TFA to give the desired compound. LC/MS [M+H] ⁺ :294.2.

EXAMPLE 257

3-Methoxy-2-(lH-tetrazol-5-yl)benzenesulfonamide

Step A: 2-Methoxy-6-((2-(trimethylsilyl)ethyl)thio)benzonitrile

To a solution of 2-fluoro-6-methoxybenzonitrile (1.0 g, 6.62 mmol) and potassium carbonate (1.83 g, 13.23 mmol) in DMF (5 ml) was added 2-

(trimethylsilyl)ethanethiol (1.27 ml, 7.94 mmol). The mixture was stirred at room temprature for 4 hours. The TLC indicated complete consumption of starting material. The mixture was filtered and the filtrate was concentrated under vacuum. The crude was adsorbed onto silica gel, and purified by silica gel column with hexane and ethyl acetate to give 2-methoxy-6-((2- (trimethylsilyl)ethyl)thio)benzonitrile. LC/MS [M+H] ⁺ :266.

Step B : 2-Methoxy-6-((2-(trimethylsilyl)ethyl)sulfonyl)benzonitrile

A solution of 2-methoxy-6-((2-(trimethylsilyl)ethyl)thio)benzonitrile (200 mg, 0.75 mmol) and mCPBA (455 mg, 2.64 mmol) in DCM (5 ml) was stirred at room temprature for 2 hr. The TLC indicated complete consumption of starting material. Sat. a ₂ S ₂ 0 ₃ was added to the mixture and stirred for 10 minutes and then sat. aHC0 ₃ was added. After stirring for another 10 minutes, organic was extracted with DCM (3x), dried over Na ₂ S0 ₄ , filtered and the filtrate was concentrated to dryness in vacuo. The crude 2-methoxy-6-((2- (trimethylsilyl)ethyl)sulfonyl)benzonitrile was taken as is for the next step. LC/MS [M+H] ⁺ :298. Step C: 5-(2-Methoxy-6-((2-(trimethylsilyl)ethyl)sulfonyl)phenyl)- lH-tetrazole

A solution of 2-methoxy-6-((2-(trimethylsilyl)ethyl)sulfonyl)benzonitrile (120 mg, 0.40 mmol), azidotrimethylsilane (0.11 ml, 0.81 mmol) and dibutyltin oxide (50.2 mg, 0.20 mmol) in toluene (5 ml) was heated at 110°C for 2 days. The reaction mixture was concentrated under vacuum. The crude was dissolved in DMSO and purified by HPLC with ACN and H ₂ 0 buffering with 0.05 % TFA to give the desired compound. LC/MS [M+H] ⁺ :341.

Step D: 3-Methoxy-2-(lH-tetrazol-5-yl)benzenesulfonamide

A solution of 5-(2-methoxy-6-((2-(trimethylsilyl)ethyl)sulfonyl)phenyl)-lH - tetrazole (103 mg, 0.30 mmol) and tetrabutylammonium fluoride (3.03 ml, 3.03 mmol) was heated at 60°C overnight. The crude reaction mixture was concentrated and dissolved in DMF and purified by HPLC with ACN and H ₂ 0 buffered with 0.05% TFA to afford 3-methoxy-2- (lH-tetrazol-5-yl)benzenesulfonamide. LC/MS [M+H] ⁺ :256.1.

EXAMPLE 258

3-(6-(Hydroxymethyl)pyridin-3-yl)-2-(l -tetrazol-5-yl)benzenesulfonamide

Step A: 3-(6-(Hydroxymethyl)pyridin-3-yl)-2-(l-(4-methoxybenzyl)-lH- tetrazol-5- yl)benzenesulfonamide and 2-(l-(3-chloro-4-methoxybenzyl)-lH-tetrazol-5-yl)-3- (6-(hydroxymethyl)pyridin-3-yl)benzenesulfonamide

A solution of mixture of 3-bromo-2-(l-(4-methoxybenzyl)-lH-tetrazol-5- yl)benzenesulfonamide (600 mg, 1.41 mmol) and 3-bromo-2-(l-(3-chloro-4-methoxybenzyl)- lH-tetrazol-5-yl)benzenesulfonamide, potassium phosphate tribasic (4.24 ml, 4.24 mmol), 1,1'- bis(di-/er/-butylphosphino)ferrocene palladium dichloride (184 mg, 0.28 mmol) and 6- (hydroxymethyl)pyridine-3-boronic acid (281 mg, 1.84 mmol) in ethanol (3 mL) was purged with N ₂ . The mixture was heated at 95°C for 16 hours. The mixture was filtered and concentrated under vacuum. The crude residue was adsorbed onto silica gel, and purified by column chromatograph on silica gel with hexane and ethyl acetate to give a mixture of 3-(6- (hydroxymethyl)pyridin-3 -yl)-2-( 1 -(4-methoxybenzyl)- lH-tetrazol-5-yl)benzenesulfonamide and 2-(l-(3-chloro-4-methoxybenzyl)-lH-tetrazol-5-yl)-3-(6-(hydr oxymethyl)pyridin-3- yl)benzenesulfonamide. LC/MS [M+H] ⁺ :453.

Step B : 3 -(6-(Hydroxymethyl)pyridin-3 -yl)-2-( lH-tetrazol-5-yl)benzenesulfonamide

A solution of a mixture 3-(6-(hydroxymethyl)pyridin-3-yl)-2-(l-(4- methoxybenzyl)-lH-tetrazol-5-yl)benzenesulfonamide (140mg, 0.31 mmol) and 2-(l-(3-chloro- 4-methoxybenzyl)-lH-tetrazol-5-yl)-3-(6-(hydroxymethyl)pyrid in-3-yl)benzenesulfonamide, trifluoroacetic acid (3.9 mL, 51.1 mmol) and anisole (67.6 μϊ _^ , 0.62 mmol) was heated at room temperature for 5 hours. The crude UPLC indicated only starting material remained. The temperature was increased to 40°C and stirred for 16 hours. A small desired peak was observed on crude UPLC. The temperature was increased to 80°C and stirred for another 6 hours. The crude UPLC indicated most of the starting material was consumed. The reaction mixture was filtered and removal of the solvent furnished a residue that was purified by Reverse HPLC with ACN and H ₂ 0 containing 0.16% formic acid to give 3-(6-(hydroxymethyl)pyridin-3-yl)-2-(lH- tetrazol-5-yl)benzenesulfonamide. LC/MS [M+H] ⁺ :333.1.

EXAMPLE 259

4-Bromo-4'-(piperidin-4-yl)-2-(l -tetrazol-5-yl)-[l,r-biphenyl]-3-sulfonamide

Step A: tert-Butyl 4-(4'-bromo-2'-cyano-3'-fluoro-[l,r-biphenyl]-4-yl)piperidin e-l- carboxylate

40 mL reaction vials were charged with 3-bromo-2-fluoro-6-iodobenzonitrile (4.2 g, 12.89 mmol), tert-butyl 4-(4-(4,4,5,5-tetramethyl-l,3,2-dioxaborolan-2-yl)phenyl)pip eridine- 1-carboxylate (4.99 g, 12.89 mmol), potassium carbonate (5.34 g, 38.7 mmol) and l, l'-Bis(di- tert-butylphosphino)ferrocene palladium (2.105 g, 2.58 mmol). The vials were capped via a red sure seal pressure release cap, and the vials were degassed via vacuum/nitrogen flushes three times (via line with needle through manifold). Then, dioxane (8 mL) was added via syringe to each vial. Again, the vials were degassed via vacuum/nitrogen flushes three times (via line with needle through manifold). After stirring at room temp for 10 minutes, the vials were heated at 70°C via an oil bath for 18 hr. Contents from the vials were then combined. After diluting with ethyl acetate, the organic solvent was filtered to remove excess catalyst, and the solvent was concentrated. The residue was purified by normal phase ISCO on a 120 g column eluted with 0% to 100% ethyl acetate in hexane. The pure fractions were concentrated to afford tert-butyl 4- (4'-bromo-2'-cyano-3'-fluoro-[l,r-biphenyl]-4-yl)piperidine- l-carboxylate (1.44g, 24.3%). LC- MS: calculated for C ₂ 3H24BrF ₂ 02 458.1 ; observed m/e (M+H) ⁺ : 459.4. Step B: tert-Butyl 4-(4'-bromo-2'-cyano-3'-((2-(trimethylsilyl)ethyl)thio)-[l, l'-biphenyl]-

4-yl)piperidine- 1 -carboxylate

To a round bottom containing tert-butyl 4-(4'-bromo-2'-cyano-3'-fluoro-[l,r- biphenyl]-4-yl)piperidine-l -carboxylate (1.41 g, 3.07 mmol) was added potassium carbonate (0.636 g, 4.60 mmol), followed by a solution of 2-(trimethylsilyl)ethanethiol (0.309 g, 2.302 mmol) in DMF (15 ml). The reaction stirred at room temp for 7 hr. The reaction was diluted with ethyl acetate and washed with water and brine (3 times). The organic was extracted out and concentrated. The residue was purified by normal phase ISCO on a 40g column eluted with 0% to 30% ethyl acetate in hexane. The pure fractions were concentrated to afford tert-butyl 4-(4'- bromo-2'-cyano-3 '-((2-(trimethylsilyl)ethyl)thio)-[ 1 , 1 '-biphenyl]-4-yl)piperidine- 1 -carboxylate (540 mg, 29.1%). LC-MS: calculated for CzsHsvBr zOzSSi 572.2 observed m/e (M+H) ⁺ : 573.5. Step C: tert-Butyl 4-(4'-bromo-2'-cyano-3'-((2-(trimethylsilyl)ethyl)sulfonyl)- [l, l'- biphenyl]-4-yl)piperidine-l -carboxylate

To a round bottom flask containing tert-butyl 4-(4'-bromo-2'-cyano-3'-((2- (trimethylsilyl)ethyl)thio)-[l,r-biphenyl]-4-yl)piperidine-l -carboxylate (540 mg, 0.941 mmol) was added DCM (20 mL), followed by mCPBA (487 mg, 2.82 mmol). The reaction needed 7 hours to complete. The reaction was quenched with a ₂ S ₂ 0 ₃ (saturated aqueous solution) and diluted with ethyl acetate. The organic layer was extracted out and concentrated. The residue was purified by normal phase ISCO on a 40g column eluted with 0% to 100% ethyl acetate in hexane. The pure fractions were concentrated to afford tert-butyl 4-(4'-bromo-2'-cyano-3'-((2- (trimethylsilyl)ethyl)sulfonyl)-[ 1 , 1 '-biphenyl]-4-yl)piperidine- 1 -carboxylate (418 mg, 73.3%). LC-MS: calculated for C ₂₈ H ₃₇ Br ₂ 0 ₄ SSi 606.1 ; observed m/e (M+H) ⁺ : 607.4.

Step D: tert-Butyl 4-(4'-bromo-2'-(lH-tetrazol-5-yl)-3'-((2-(trimethylsilyl)eth yl)sulfonyl)-

[1, 1 '-biphenyl]-4-yl)piperidine- 1 -carboxylate

A 40 mL reaction vial was charged with tert-butyl 4-(4'-bromo-2'-cyano-3'-((2-

(trimethylsilyl)ethyl)sulfonyl)-[l,r-biphenyl]-4-yl)piper idine-l-carboxylate (15 mg, 0.025 mmol), azidotrimethyltin (25.5 mg, 0.124 mmol) and toluene (2 mL). The vial was capped via a red sure seal cap, and the vial was heated at 100°C via an oil bath for 10 hr. The crude was dissolved in acetonitrile (1.5 mL) and washed with hexane to remove the tin impurity.

Purification by reverse phase HPLC column (acetonitrile/water/0.05% TFA system) eluted with 10% to 100% MeCN in water. The solution was concentrated to afford tert-butyl 4-(4'-bromo-2'- (lH-tetrazol-5-yl)-3'-((2-(trimethylsilyl)ethyl)sulfonyl)-[l ,r-biphenyl]-4-yl)piperidine-l- carboxylate (7 mg, 43.6%). LC-MS: calculated for C ₂₈ H ₃₈ Br ₅ 0 ₄ SSi 647.2; observed m/e (M+H) ⁺ : 648.4.

Step E: 4-Bromo-4'-(piperidin-4-yl)-2-(lH-tetrazol-5-yl)-[l, -biphenyl]-3-sulfonamide

To a 40 mL reaction vial containing tert-butyl 4-(4'-bromo-2'-(lH-tetrazol-5-yl)- 3 '-((2-(trimethylsilyl)ethyl)sulfonyl)-[l,r-biphenyl]-4-yl)pi peridine-l -carboxylate (10 mg, 0.015 mmol) was added THF (500 μΚ) and TBAF (0.077 mL, 0.077 mmol). The vial was capped, and the reaction was heated at 40°C via an oil bath for 6 hr. LCMS showed a good profile. Then, a solution of sodium acetate (25.3 mg, 0.308 mmol) in water (500 μί) was added to the reaction, which was then followed by addition of hydroxylamine-o-sulfonic acid (34.9 mg, 0.308 mmol). The vial was capped, and the reaction stirred at room temp for 3 hr. The reaction was concentrated. To the vial was added DCM (1000 μΚ), followed by a mixture of TFA (1 mL, 12.98 mmol) and anisole (0.034 mL, 0.308 mmol). The reaction was allowed to stir at room temp for 1 hr and then concentrated. The crude was dissolved in a 1 mL: 1 mL acetonitrile:water mix, and the solution was acidified with 0.5 mL TFA. Purification by reverse phase HPLC column (acetonitrile/water/0.05% TFA system) eluted with 0% to 20% MeCN in water. The solution was concentrated to afford 4-bromo-4'-(piperidin-4-yl)-2-(lH-tetrazol-5-yl)-[l,r- biphenyl]-3-sulfonamide as the TFA salt (5 mg, 56.3%). LC-MS: calculated for Ci ₈ H ₁₉ Br ₆ 02S 464.1 observed m/e (M+H) ⁺ : 465.3. 'H NMR δ (ppm) (MeOH): 8.13 (d, 1H), 7.49 (d, 1H), 7.145(d, 2H), 7.01 (d, 2H), 3.42-3.49 (m, 2H), 3.04-3.15 (m, 2H), 2.81-2.90 (m, 1H), 1.96-2.04 (m, 2H), 1.76-1.83 (m, 2H).

EXAMPLE 260

4'-(Piperidin-4-yl)-4-propyl-2-(l -tetrazol-5-yl)-[l,r-biphenyl]-3-sulfonamide

Step A: tert-Butyl 4-(2'-cyano-4'-propyl-3'-((2-(trimethylsilyl)ethyl)sulfonyl) -[l,l'- biphenyl] -4-yl)piperidine- 1 -carboxylate

A 40 mL reaction vial was charged with 4-bromo-4'-(piperidin-4-yl)-2-(lH- tetrazol-5-yl)-[l,l'-biphenyl]-3-sulfonamide (100 mg, 0.165 mmol), and Chloro(2- dicyclohexylphosphino-2',6'-diisopropoxy- 1 , 1 '-biphenyl) [2-(2 '-amino- 1, 1 '- biphenyl)]palladium(II) [Aldrich] (51.3 mg, 0.066 mmol). The vial was capped via a red sure seal and degassed three times with vacuum/nitrogen (line with needle connected to manifold). Then, DMA (2 mL), THF (1 mL) and propylzinc(II) bromide (0.991 ml, 0.495 mmol) were added via syringe. Again, the vial was degassed three times with vacuum/nitrogen (line with needle connected to manifold). After stirring at room temp for 10 minutes, the reaction was allowed to stir at 80°C via an oil bath for 5 hr. The reaction was diluted with ethyl acetate and quenched with NH ₄ C1 (sat. aq.). The organic layer was extracted out and concentrated. The residue was purified by normal phase ISCO on a 24g column eluted with 0% to 100% ethyl acetate in hexane. The pure fractions were concentrated to afford product (24 mg, 25.6%). LC- MS: calculated for C ₃ 1H44N2O4SS1 568.8; observed m/e (M+H) ⁺ : 569.6.

Step B: tert-Butyl 4-(4'-propyl-2'-(lH-tetrazol-5-yl)-3'-((2-(trimethylsilyl)et hyl)sulfonyl)-

[1, 1 '-biphenyl]-4-yl)piperidine- 1 -carboxylate

To a 40 mL reaction vial containing tert-butyl 4-(2'-cyano-4'-propyl-3'-((2- (trimethylsilyl)ethyl)sulfonyl)-[l,r-biphenyl]-4-yl)piperidi ne-l-carboxylate (24 mg, 0.042 mmol) was added azidotrimethyltin (43.4 mg, 0.211 mmol) and toluene (1.5 mL). The vial was capped via a red sure seal cap, and the vial was heated at 100°C via an oil bath for 10 hr to completion of the reaction. The crude was dissolved in acetonitrile (1.5 mL), washed with hexane to remove the tin. The acetonitrile layer was extracted and diluted with water (1.5 mL). The reaction was purified by reverse phase HPLC column (acetonitrile/water/0.05% TFA system) and eluted with 0% to 100% MeCN in water. The solution was concentrated to afford tert-butyl 4-(4'-propyl-2'-(lH-tetrazol-5-yl)-3'-((2-(trimethylsilyl)et hyl)sulfonyl)-[l, l'-biphenyl]- 4-yl)piperidine-l -carboxylate (15 mg, 58.1%). LC-MS: calculated for C ₃ 1H45N5O4SS1 611.871 observed m/e: 612.65 (M+H) ⁺ .

Step C: 4'-(Piperidin-4-yl)-4-propyl-2-(lH-tetrazol-5-yl)-[l,r-biphe nyl]-3-sulfonamide

To a vial containing tert-butyl 4-(4'-propyl-2'-(lH-tetrazol-5-yl)-3'-((2-

(trimethylsilyl)ethyl)sulfonyl)-[l,r-biphenyl]-4-yl)piper idine-l-carboxylate (15 mg, 0.025 mmol) was added THF (2 mL) and TBAF (0.074 mL, 0.074 mmol). The vial was capped, and the reaction was heated at 40°C via an oil bath for 2 hr. Then, a solution of sodium acetate (40.2 mg, 0.490 mmol) in water (2 mL) was added, followed by addition of hydroxylamine-o-sulfonic acid (55.4 mg, 0.490 mmol). The reaction was stirred at room temp overnight, and was then concentrated. Purification by reverse phase HPLC column (acetonitrile/water/0.05% TFA system) eluted with 0% to 100% MeCN in water. The major fraction was concentrated to afford tert-butyl 4-(4'-propyl-3 '-sulfamoyl-2'-( 1 H-tetrazol-5 -yl)- [ 1 , 1 '-biphenyl] -4-yl)piperidine- 1 - carboxylate (3.5mg, 27.1%). LC-MS: calculated for C21H2 _{6 6} O2S 526.535 observed m/e (M+H) ⁺ : 527.5 (Rt 1.34 / 2 min).

Step D: 4'-(piperidin-4-yl)-4-propyl-2-(lH-tetrazol-5-yl)-[ 1 , 1 '-biphenyl] -3 -sulfonamide

To a vial containing tert-butyl 4-(4'-propyl-3'-sulfamoyl-2'-(lH-tetrazol-5-yl)- [l,l'-biphenyl]-4-yl)piperidine-l -carboxylate (3.5 mg, 6.65 μιηοΐ) was added DCM (1000 μΚ), followed by a mixture of TFA (1 mL, 12.98 mmol) and anisole (0.015 mL, 0.133 mmol). The reaction was allowed to stir at room temp for 2 hr and then concentrated. The reaction was purified by reverse phase HPLC column (acetonitrile/water/0.05% TFA system) and eluted with 0% to 20% MeCN in water. The solution was concentrated to afford 4'-(piperidin-4-yl)-4- propyl-2-(lH-tetrazol-5-yl)-[l,l'-biphenyl]-3-sulfonamide as the TFA salt (2.7 mg, 75%). LC- MS: calculated for C ₂ iH ₂₆ N ₆ 0 ₂ S: 426; observed m/e (M+H) ⁺ : 427.4; 1H NMR δ (ppm) (MeOH): 7.74 (d, 1H), 7.60 (d, 1H), 7.175 (d, 2H), 7.03 (d, 2H), 3.46-3.52 (m, 2H), 3.17-3.28 (m, 2H), 3.10-3.14 (m, 2H), 2.84-2.92 (m, 1H), 2.02-2.08 (m, 2H), 1.77-1.90 (m, 4H), 1.10 (t, 3H).

EXAMPLES 261-262

The following Examples 261-262 were prepared according to the general procedure described in Example 260 above:

EXAMPLE 263

4-chloro-4'-methyl-2-(2H-tetrazol-5-yl)-[l,l'-biphenyl]-3-su lfonamide

Step A: 3-chloro-6-iodo-2-((2-(trimethylsilyl)ethyl)thio)benzonitril e

To a solution of 3-chloro-2-fluoro-6-iodobenzonitrile (0.500 g, 1.78 mmol) and K ₂ C0 ₃ (0.491 g, 3.55 mmol) in DMF (3 mL) was added 2-(trimethylsilyl)ethanethiol (0.341 mL, 2.13 mmol), and the resulting mixture was stirred at room temperature overnight. The reaction mixture was filtered, the filtrate was diluted with EtOAc and washed with water (twice) and then with brine. The organic layer was dried over anhydrous MgS0 ₄ , filtered, concentrated and purified by silica gel column chromatography using (0-15)% EtOAc/Hexanes as mobile phase to afford the title compound.

Step B: 3-chloro-6-iodo-2-((2-(trimethylsilyl)ethyl)sulfonyl)benzoni trile

To a solution of 3-chloro-6-iodo-2-((2-(trimethylsilyl)ethyl)thio)benzonitril e (0.43 g, 1.1 mmol) in DCM (7.24 mL) at 0°C was added 3-chlroroperoxybenzoic acid (0.656 g, 3.80 mmol) and the mixture was stirred at room temperature overnight. Saturated a ₂ S ₂ C>3 was added to the mixture and it was stirred for 10 min. Then saturated aHC03 was added. After separation of layers, the aqueous layer was extracted with DCM (3x), the combined organic layers were dried over anhydrous a2S0 ₄ , filtered, and concentrated to get the title compound. Step C: 4-chloro-4'-methyl-3-((2-(trimethylsilyl)ethyl)sulfonyl)-[l, l'-biphenyl]-2- carbonitrile

3-Chloro-6-iodo-2-((2-(trimethylsilyl)ethyl)sulfonyl)benzoni trile (300 mg, 0.701 mmol), p-tolylboronic acid (95 mg, 0.70 mmol), Na ₂ C0 ₃ (149 mg, 1.40 mmol) and PdCl ₂ (dppf)- CH2CI2 adduct (57.3 mg, 0.070 mmol) were combined in dioxane (4.5 mL) and water (1.5 mL) in a microwave vial. The mixture was degassed with nitrogen and the resulting mixture was heated overnight at 90°C. The reaction mixture was filtered over celite to removed palladium. The filtrate was diluted with EtOAc and washed with water. The organic layer was dried over anhydrous MgS0 ₄ , filtered, concentrated and purified by silica gel column chromatography (RediSep gold column, 40g) using (0-25)% EtOAc/Hexanes gradient as the mobile phase to afford the title compound.

Step D: 5-(4-chloro-4'-methyl-3-((2-(trimethylsilyl)ethyl)sulfonyl)- [l, l'-biphenyl]-2-yl)- 2H-tetrazole To a solution of 4-chloro-4'-methyl-3-((2-(trimethylsilyl)ethyl)sulfonyl)-[l, r- biphenyl]-2-carbonitrile (157 mg, 0.401 mmol) in toluene (3 mL) in a microwave vial was added azidotrimethyltin (412 mg, 2.00 mmol) and the resulting mixture was heated overnight at 100°C. The precipitated solid was filtered and washed with hexanes. Purification of the solid was by silica gel column chromatography (24g RediSep gold column) using (40-100)%

EtOAc/Hexanes gradient (containing 1 ml AcOH per 500 mL of solvent) to afford the title compound. LC/MS [M+H] ⁺ 435, 437.

Step E: 4-chloro-4'-methyl-2-(2H-tetrazol-5-yl)-[l, l'-biphenyl]-3-sulfonamide

To a solution of 5-(4-chloro-4'-methyl-3-((2-(trimethylsilyl)ethyl)sulfonyl)- [l, l'- biphenyl]-2-yl)-2H-tetrazole (1 15 mg, 0.264 mmol) in THF (4.5 mL) was added TBAF in THF (1.322 mL, 1.322 mmol) and the resulting solution was stirred at 40°C for 2 hr. Sodium acetate (217 mg, 2.64 mmol) in 2 mL of water was added followed by addition of hydroxy lamine-O- sulfonic acid (299 mg, 2.64 mmol) and the resulting solution was stirred at rt overnight. The mixture was partitioned between EtOAc (50 mL) and saturated aHC0 ₃ , the organic phase was washed with NaHCCh twice, dried over anhydrous a2S0 ₄ , concentrated, and the residue was purified by silica gel column chromatography (RediSep gold, 24g column), eluting with 2.5% MeOH/DCM (containing 0.2 mL of acetic acid per 100 mL of solvent) to give the title compound. LC/MS [M+H] ⁺ 350.

EXAMPLE 264

3-(6-aminopyridin-3-yl)-6-bromo-2-(2H-tetrazol-5-yl)benzenes ulfonamide

Step A: 3-(6-aminopyridin-3-yl)-6-bromo-2-(2-(4-methoxybenzyl)-2H-te trazol-5- yl)benzenesulfonamide

A microwave vial was charged with 6-bromo-3-iodo-2-(2-(4-methoxybenzyl)-2H- tetrazol-5-yl)benzenesulfonamide (1.0 g, 1.8 mmol), (6-aminopyridin-3-yl)boronic acid hydrochloride (0.697 g, 4.00 mmol), Na ₂ C0 ₃ (0.578 g, 5.45 mmol) and PdCl ₂ (dppf)-CH ₂ Cl ₂ adduct (0.223 g, 0.273 mmol). The vial was sealed, degassed, and filled with dioxane (9.09 mL) and water (3.03 mL). The resulting mixture was heated overnight at 90°C. The reaction mixture was filtered over celite to remove palladium. The filtrate was diluted with EtOAc and washed with water. The organic layer was dried over anhydrous MgSO_i, filtered, and concentrated. The crude mixture was purified by silica gel column chromatography using 0-10% MeOH/DCM as mobile phase to afford the title compound. LC-MS (IE, m/z): 518.3 [M+2] ⁺ .

Step B: 3-(6-aminopyridin-3-yl)-6-bromo-2-(2H-tetrazol-5-yl)benzenes ulfonamide

To a solution of 3-(6-aminopyridin-3-yl)-6-bromo-2-(2-(4-methoxybenzyl)-2H- tetrazol-5-yl)benzenesulfonamide (430 mg, 0.833 mmol) in DCM (4.2 mL) was added anisole (0.9 mL, 8.33 mmol) and TFA (6.4 mL, 83 mmol) at rt. The resulting mixture was heated at 80°C for 1 hr. After removing the volatile the residue was purified by reverse phase HPLC using DMSO to load sample and 5-45 % acetonitrile/water (0.1% formic acid as additive) as mobile phase to afford the title compound. LC-MS (IE, m/z): 397.99 [M+2] ⁺ .

EXAMPLE 265

3-(6-aminopyridin-3-yl)-2-(2H-tetrazol-5-yl)-6-(trifluoromet hyl)benzenesulfonamide

Step A: 3-(6-aminopyridin-3-yl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5 -yl)-6- (trifluoromethyl)benzenesulfonamide

To a microwave vial was added (l, 10-phenanthroline)(trifluoromethyl)copper(I) (242 mg, 0.775 mmol), 3-(6-aminopyridin-3-yl)-6-bromo-2-(2-(4-methoxybenzyl)-2H-te trazol- 5-yl)benzenesulfonamide (Step A, 200 mg, 0.387 mmol) and copper(I) iodide (148 mg, 0.775 mmol). The vial was sealed, flushed with N ₂ , and DMF (2.6 mL) was added. This resulting mixture was then heated at 80°C overnight. The reaction mixture was cooled, filtered through celite, and rinsed with EtOAc. The filtrate was evaporated and the residue was purified by silica gel chromatograph, eluting with 0-10% MeOH/DCM to give the title compound. LC-MS (IE, m/z): 506.4 [M+l] ⁺ .

Step B: 3-(6-aminopyridin-3-yl)-2-(2H-tetrazol-5-yl)-6- (trifluoromethyl)benzenesulfonamide To a solution of 3-(6-aminopyridin-3-yl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5 - yl)-6-(trifluoromethyl)benzenesulfonamide (200 mg, 0.396 mmol) in DCM (2.0 mL) was added TFA (3.0 mL, 39.6 mmol) and anisole (0.43 mL, 3.96 mmol). The resulting mixture was heated at 80°C for 1 hr. After removing the volatile the residue was purified by reverse phase HPLC using DMSO to load sample and 5-60% acetonitrile/water (0.1% formic acid as additive) as mobile phase to afford the title compound. LC-MS (IE, m/z): 386.23 [M+l] ⁺ .

EXAMPLES 266-274

The following compounds were prepared in an analogous fashion to Examples 264 (3-(6-aminopyridin-3-yl)-6-bromo-2-(2H-tetrazol-5-yl)benzene sulfonamide) and 265 (3-(6- aminopyridin-3-yl)-2-(2H-tetrazol-5-yl)-6-(trifluoromethyl)b enzenesulfonamide) starting from 6-bromo-3-iodo-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)benze nesulfonamide (Reference

Example 13) and the corresponding boronic acids or esters (commercially available, known, or prepared as described herein) listed below.

EXAMPLE 275

6-cyclopropyl-3-(quinolin-4-yl)-2-(2H-tetrazol-5-yl)benzenes ulfonamide

Step A: 6-bromo-3-iodo-N,N-bis(4-methoxybenzyl)-2-(2-(4-methoxybenzy l)-2H-tetrazol- 5 -yl)benzenesulfonamide

To a mixture of 6-bromo-3-iodo-2-(l-(4-methoxybenzyl)-lH-tetrazol-5- yl)benzenesulfonamide (Reference Example 13) 3200 mg, 5.82 mmol), l-(chloromethyl)-4- methoxybenzene (2004 mg, 12.80 mmol) in 2-butanone (29 mL) at rt, 1 -(chloromethyl)-4- methoxybenzene (2004 mg, 12.80 mmol) was added, followed by potassium carbonate (3215 mg, 23.27 mmol) and sodium iodide (1918 mg, 12.80 mmol). The reaction was stirred under nitrogen overnight at 80°C and monitored by LCMS. The reaction mixture was then filtered, and rinsed by EtOAc. The combined organic layer was evaporated, and the crude product was purified by silica gel column chromatography with EtO Ac/Hex (0-100%) as eluent to give the title compound. LC-MS (IE, m/z): 792.6 [M+2] ⁺ .

Step B: 6-bromo-N,N-bis(4-methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-t etrazol-5-yl)-3- (quinolin-4-yl)benzenesulfonamide

A microwave vial was charged with 6-bromo-3-iodo-N,N-bis(4-methoxybenzyl)- 2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)benzenesulfonamide (1.00 g, 1.27 mmol), quinolin-4- ylboronic acid (0.481 g, 2.78 mmol), PdCl ₂ (dppf)-CH ₂ Cl ₂ adduct (0.103 g, 0.127 mmol) and sodium carbonate (0.402 g, 3.80 mmol). The vial was sealed, degassed, and filled with dioxane (6.33 mL) and water (2.1 1 mL). The resulting mixture was heated overnight at 90°C. The reaction mixture was filtered over celite to removed palladium. The filtrate was diluted with EtOAc and washed with water. The organic layer was dried over anhydrous MgS04, filtered, concentrated and purified by silica gel column chromatography using 15-60% EtOAc/Hexanes as mobile phase to afford the title compound. LC-MS (IE, m/z): 793.60[M+2] ⁺ .

Step C: 6-cyclopropyl-N,N-bis(4-methoxybenzyl)-2-(2-(4-methoxybenzyl )-2H-tetrazol-5- yl)-3-(quinolin-4-yl)benzenesulfonamide

A microwave vial was charged with 6-bromo-N,N-bis(4-methoxybenzyl)-2-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)-3-(quinolin-4-yl)benzenesul fonamide (0.228 g, 0.288 mmol), and chloro(2-dicyclohexylphosphino-2',6'-dimethoxy-l, l'-biphenyl)[2-(2- aminoethylphenyl)]palladium(II) - methyl-t-butyl ether adduct (0.022 g, 0.029 mmol). The vial was sealed, degassed, and filled with THF (2.88 mL) and cyclopropylzinc(II) bromide (1.728 mL, 0.5 M in THF, 0.864 mmol). The resulting mixture was heated overnight at 60°C. The reaction mixture was filtered over celite to removed palladium. The filtrate was concentrated and purified by silica gel column chromatography using 0-100% EtOAc/Hexanes as mobile phase to afford the title compound. LC-MS (IE, m/z): 753.2 [M+l .

Step D: 6-cyclopropyl-3-(quinolin-4-yl)-2-(2H-tetrazol-5-yl)benzenes ulfonamide

To a solution of 6-cyclopropyl-N,N-bis(4-methoxybenzyl)-2-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)-3-(quinolin-4-yl)benzenesul fonamide (100 mg, 0.133 mmol) in DCM (2.6 mL) was added TFA (1.0 mL, 13.28 mmol) and anisole (0.29 μί, 2.66 mmol). The resulting mixture was heated at 80°C for 1 hr. After removing the volatile the residue was purified by reverse phase HPLC using DMSO to load sample and 5-70% acetonitrile/water (0.1% formic acid as additive) as mobile phase to afford the title compound. LC-MS (IE, m/z): 393.18 [M+l .

EXAMPLE 276

4-chloro-4'-(piperidin-4-yl)-2-(2H-tetrazol-5-yl)-[ l, -biphenyl]-3-sulfonamide

Step A: 3-chloro-6-iodo-2-((2-(trimethylsilyl)ethyl)thio)benzonitril e

To a solution of 3-chloro-2-fluoro-6-iodobenzonitrile (2.00 g, 7.1 1 mmol) and potassium carbonate (1.964 g, 14.21 mmol) in DMF (12 mL) was added 2-(trimethylsilyl) ethanethiol (1.25 mL, 7.82 mmol), and the resulting mixture was stirred at room temperature overnight. The reaction mixture was filtered. The filtrate was diluted with EtOAc, washed with water and brine. The organic layer was dried over MgS04, filtered, and concentrated. The residue was purified by silica gel column chromatography using 0- 15%EtOAc/Hexanes as mobile phase to afford the title compound. ^X H NMR (500 MHz, CDC1 ₃ ), δ 7.76 (d, J= 8.5 Hz, 1H), 7.31 (d, J = 8.5 Hz, 1H), 3.08-3.04 (m, 2H), 0.88-0.84 (m, 2H), 0.00 (s, 9H).

Step B: 3-chloro-6-iodo-2-((2-(trimethylsilyl)ethyl)sulfonyl)benzoni trile

To a solution of 3-chloro-6-iodo-2-((2-(trimethylsilyl)ethyl)thio)benzonitril e (0.88 g, 2.2 mmol) in DCM (14.82 mL) at 0°C, was added mCPBA (1.34 g, 7.78 mmol), and the mixture was stirred at room temperature overnight. Saturated a2S203 solution was added to the mixture to quench the reaction, and saturated aHC03 was then added. After separation of layers, the aqueous layer was extracted with DCM. The combined organic layer was dried over anhydrous a2S04, filtered and concentrated to get the title compound. ^X H NMR (500 MHz,

CDC1 ₃ ), δ 8.10 (d, J = 8.6 Hz, 1H), 7.40 (d, J = 8.6 Hz, 1H), 3.36-3.32 (m, 2H), 0.96-0.92 (m, 2H), 0.00 (s, 9H).

Step C: tert-butyl 4-(4'-chloro-2'-cyano-3'-((2-(trimethylsilyl)ethyl)sulfonyl) -[l , l'- biphenyl]-4-yl)piperidine- 1 -carboxylate 3-Chloro-6-iodo-2-((2-(trimethylsilyl)ethyl)sulfonyl)benzoni trile (160 mg, 0.374 mmol), (4-(l-(tert-butoxycarbonyl)piperidin-4-yl)phenyl)boronic acid (114 mg, 0.374 mmol), sodium carbonate (79 mg, 0.748 mmol) and PdCl ₂ (dppf)-CH ₂ Cl ₂ adduct (30.5 mg, 0.037 mmol) were combined in dioxane (4.5 mL) and water (1.5 mL) in a microwave vial. The vial was sealed, degassed, and the resulting mixture was heated overnight at 90°C. The reaction mixture was filtered over celite to removed palladium. The filtrate was diluted with EtOAc and washed with water. The organic layer was dried over anhydrous MgS04, filtered, and concentrated.

The residue was purified by silica gel column chromatography using 0-25% EtOAc/Hexanes as mobile phase to afford the title compound. LC-MS (IE, m/z): 561.35 [M] ⁺ .

Step D: tert-butyl 4-(4'-chloro-2'-(2H-tetrazol-5-yl)-3'-((2-(trimethylsilyl)et hyl)sulfonyl)-

[1, 1 '-biphenyl] -4-yl)piperidine- 1 -carboxylate

To a solution of tert-butyl 4-(4'-chloro-2'-cyano-3'-((2- (trimethylsilyl)ethyl)sulfonyl)-[l,r-biphenyl]-4-yl)piperidi ne-l-carboxylate (290 mg, 0.517 mmol) in toluene (4.3 mL) in a microwave vial was added azidotrimethyltin (532 mg, 2.58 mmol) and the resulting mixture was heated overnight at 100°C. Solid precipitate was filtered, and washed with hexanes. The filtrate was concentrated, and purified by silica gel column chromatography using 40-100% EtOAc/Hexanes (containing 0.2% AcOH as additive) as solvent system to afford the title compound. LC-MS (IE, m/z): 604.37 [M] ⁺ .

Step E: tert-butyl 4-(4'-chloro-3 '-sulfamoyl-2'-(2H-tetrazol-5-yl)-[ 1, 1 '-biphenyl] -4- yl)piperidine-l -carboxylate

To a solution of tert-butyl 4-(4'-chloro-2'-(lH-tetrazol-5-yl)-3'-((2- (trimethylsilyl)ethyl)sulfonyl)-[l,r-biphenyl]-4-yl)piperidi ne-l-carboxylate (200 mg, 0.331 mmol) in THF (6.6 mL) was added TBAF in THF (1.66 mL, 1M in THF, 1.66 mmol). The resulting solution was bubbled with N ₂ , stirred at 40 °C for 2 hr, and checked by LCMS for completion of the first step conversion. Then sodium acetate (272 mg, 3.31 mmol) in 2.5 mL water was added, followed by addition of hydroxylamine-O-sulfonic acid (374 mg, 3.31 mmol). The resulting solution was stirred at rt overnight. The mixture was partitioned between EtOAc (50 mL) and sat. aHC0 ₃ . The organic phase was washed with aHC03, dried over a2S04, and concentrated. The residue was purified by silica gel column chromatography using 0-15% MeOH/DCM (containing 0.2% AcOH as additive) as mobile phase to give the title compound. LC-MS (IE, m/z): 519.46 [M] ⁺ .

Step F: 4-chloro-4'-(piperidin-4-yl)-2-(2H-tetrazol-5-yl)-[l,r-biphe nyl]-3-sulfonamide To a solution of tert-butyl 4-(4'-chloro-3'-sulfamoyl-2'-(2H-tetrazol-5-yl)-[l, r- biphenyl]-4-yl)piperidine-l-carboxylate (70 mg, 0.135 mmol) in DCM (2.7 mL) was added anisole (0.6 mL, 5.39 mmol) and TFA (1.0 mL, 13.49 mmol) at rt. The resulting mixture was stirred at rt for 1 hr. After removing the volatile the residue was purified by reverse phase HPLC using DMSO to load sample and 5-40% acetonitrile/water (0.1% formic acid as additive) as mobile phase to afford the title compound. LC-MS (IE, m/z): 419.14 [M] ⁺ .

EXAMPLE 277

5-(4-Bromophenyl)-4-(2H-tetrazol-5-yl)pyridazine-3-sulfonami de

Step A: 5-(4-Bromophenyl)-3-hydroxypyridazine-4-carbonitrile

2-(4-Bromophenyl)-2-oxoacetaldehyde (10.7 g, 50.2 mmol) and

cyanoacetohydrazide (4.98 g, 50.2 mmol) were dissolved in EtOH (67.0 mL) and stirred overnight at rt. The reaction was filtered and concentrated to afford 5-(4-bromophenyl)-3- hydroxypyridazine-4-carbonitrile. LC-MS: calculated for CnH ₆ Br ₃ 0 275.0; observed m/e (M+H) ⁺ : 275.9.

Step B: 5-(4-Bromophenyl)-3-chloropyridazine-4-carbonitrile

5-(4-Bromophenyl)-3-hydroxypyridazine-4-carbonitrile (1.00 g, 3.62 mmol) was dissolved in dioxane (36.2 mL) and POCI ₃ (0.405 mL, 4.35 mmol) was added. The reaction was heated to reflux overnight. The solution was poured into water at 0°C and 5-(4-bromophenyl)-3- chloropyridazine-4-carbonitrile was collected as a solid. LC-MS: calculated for CnHsBrCl s 292.9; observed m/e (M+H) ⁺ : 294.0.

Step C: 5-(4-Bromophenyl)-3-((2-(trimethylsilyl)ethyl)thio)pyridazin e-4-carbonitrile

5-(4-Bromophenyl)-3-chloropyridazine-4-carbonitrile (2.50 g, 8.49 mmol) was dissolved in DMF (42.4 mL). K ₂ C0 ₃ (2.346 g, 16.98 mmol) and 2-(trimethylsilyl)ethanethiol (1.03 g, 7.64 mmol) were added and the reaction was stirrred overnight at rt. The reaction was diluted with EtOAc and water. The organic phase was washed with water (x2) and brine, then dried over anhydrous a ₂ S04, filtered, and concentrated. The residue was purified by MPLC on a 40g silica column eluting with 0% to 35% EtOAc in Hexane to afford 5-(4-bromophenyl)-3- ((2-(trimethylsilyl)ethyl)thio)pyridazine-4-carbonitrile. LC-MS: calculated for C^HisBr sSSi 393.0; observed m/e (M+H) ⁺ : 394.2. 'H NMR δ (ppm) (MeOH): 9.09 (s, 1H), 7.67 (d, 2H), 7.57 (d, 2H), 3.42-3.37 (m, 2H), 1.04-0.99 (m, 2H), 0.00 (s, 9H).

Step E: 5-(4-Bromophenyl)-3-((2-(trimethylsilyl)ethyl)sulfonyl)pyrid azine-4-carbonitrile

5-(4-Bromophenyl)-3-((2-(trimethylsilyl)ethyl)thio)pyridazin e-4-carbonitrile (85 mg, 0.217 mmol) was dissolved in DCM (2.17 mL). mCPBA (97 mg, 0.43 mmol) was added and the reaction was stirred overnight at rt. The reaction was diluted with EtOAc and sat.

a ₂ S203. The aqueous phase was extracted with EtOAc (x2) and the combined extracts were washed with brine, dried over a ₂ S0 ₄ , filtered, and concentrated. The residue was purified by MPLC on a 40g silica column eluted with 0% to 40% EtOAc in Hexane to give 5-(4- bromophenyl)-3-((2-(trimethylsilyl)ethyl)sulfonyl)pyridazine -4-carbonitrile. LC-MS: calculated for Ci ₆ H ₁₈ BrN ₃ 0 ₂ SSi 423.0; observed m/e (M+H) ⁺ : 424.2.

Step F: 5-(4-Bromophenyl)-4-(2H-tetrazol-5-yl)-3-((2- (trimethylsilyl)ethyl)sulfonyl)pyridazine

5-(4-Bromophenyl)-3-((2-(trimethylsilyl)ethyl)sulfonyl)pyrid azine-4-carbonitrile (60 mg, 0.141 mmol) was dissolved in toluene (1414 μΕ). Dibutyltin oxide (10.6 mg, 0.042 mmol) and azidotrimethylsilane (56.3 μΐ, 0.424 mmol) were added and the reaction was heated to 100°C for 5 hr. The reaction mixture was concentrated and partitioned between

hexane/acetonitrile. The MeCN layer was collected and dilute with water, then purified by revesre phase HPLC on a C18 column eluted with 10% to 100% MeCN in water. The combined fractions were concentrated to provide 5-(4-bromophenyl)-4-(2H-tetrazol-5-yl)-3-((2- (trimethylsilyl)ethyl)sulfonyl)pyridazine as a white solid. LC-MS: calculated for

Ci ₆ Hi ₉ BrN ₆ 02SSi 468.0; observed m/e (M+H) ⁺ : 469.26.

Step G: 5-(4-Bromophenyl)-4-(2H-tetrazol-5-yl)pyridazine-3-sulfonami de

5-(4-Bromophenyl)-4-(2H-tetrazol-5-yl)-3-((2- (trimethylsilyl)ethyl)sulfonyl)pyridazine (10 mg, 0.021 mmol) was dissolved in THF (500 μί). TBAF (64.2 μΐ _^ , 0.064 mmol) was added and the reaction heated to 55°C overnight. Sodium acetate (17.6 mg, 0.214 mmol) in water (500 μί) and hydroxylamine-0 -sulfonic acid (24.2 mg, 0.214 mmol) were added and the reaction was stirred at rt overnight. The crude reaction mixture was concentrated and purified by revese phase HPLC on a CI 8 column eluted with 0% to 80% MeCN in water. A significant amount of TBAF was determined to be present by NMR. The oil was dissolved in TFA (1 mL) then repurified by reverse phase HPLC on a C18 column eluted with 0% to 80% MeCN in water. The combined fractions were lyopholized to provide 5 -(4- bromophenyl)-4-(2H-tetrazol-5-yl)pyridazine-3 -sulfonamide. LC-MS: calculated for

CiiH ₈ Br 70 ₂ S 383.0 observed m/e (M+H) ⁺ : 384.11. 1H NMR δ (ppm) (MeOH): 9.55 (s, 7.51 (d, 2H), 7.11 (d, 2H).

EXAMPLE 278

3-(5-chloro-2-(methylsulfonyl)-lH-benzo[d]imidazol-6-yl)-2-( 2H-tetrazol-5- yl)benzenesulfonamide

Step A: 6-chloro-5-iodo-2-(methylsulfonyl)-l-((2-(trimethylsilyl)eth oxy)methyl)-lH- benzo[if| imidazole

To a suspension of 6-chloro-5-iodo-2-(methylsulfonyl)-lH-benzo[d]imidazole

(5.042 g, 14.14 mmol) in DCM (100 mL) at 0°C was added TEA (2.96 mL, 21.21 mmol), and SEM-C1 (2.76 mL, 15.55 mmol) dropwise. The resulting solution was stirred from 0°C for 1 hr. The reaction mixture was partitioned between water (200 mL) and DCM (100 mL), the aqueous phase was extracted with DCM (200 mL), and the combined organic phase was dried over anhydrous Na ₂ S0 ₄ , concentrated and the residue was purified on silica gel column using EtOAc/hexane as eluting solvents to give the title compound. LC/MS: (M+l) : 487.17.

Step B: 6-chloro-2-(methylsulfonyl)-5-(4,4,5,5-tetramethyl-l,3,2-dio xaborolan-2-yl)-l- ((2-(trimethylsilyl)ethoxy)methyl)-lH-benzo[d]imidazole

A mixture of potassium acetate (4.02 g, 40.9 mmol), bis(pinacolato)diboron (4.16 g, 16.4 mmol), and 6-chloro-5-iodo-2-(methylsulfonyl)-l-((2-(trimethylsilyl)eth oxy)methyl)-lH- benzo[d]imidazole (6.64 g, 13.6 mmol) in dioxane (100 mL) was degassed with ₂ for 1 hr before addition of PdCl ₂ (dppf)-CH ₂ Cl ₂ adduct (0.557 g, 0.682 mmol). The resulting mixture was heated at 100°C overnight. After filtration through celite, the filtrate was concentrated and the residue was partitioned between DCM (200 mL) and water (200 mL), the aqueous phase was extracted with DCM (200 mL) and the combined organic phase was dried over Na ₂ S0 ₄ , concentrated and the residue was purified on silica gel column using EtOAc/hexane as eluting solvents to give the title compound. LC/MS: (M+l) ⁺ : 487.37 Step C: 3-(5-chloro-2-(methylsulfonyl)-l-((2-(trimethylsilyl)ethoxy) methyl)-lH- benzo[d]imidazol-6-yl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5- yl)benzenesulfonamide

To a mixture of 6-chloro-2-(methylsulfonyl)-5-(4,4,5,5-tetramethyl-l,3,2- dioxaborolan-2-yl)-l-((2-(trimethylsilyl)ethoxy)methyl)-lH-b enzo[d]imidazole (1.149 g, 2.359 mmol) and 3-bromo-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)benzenesulfo namide (0.77 g, 1.8 mmol) in dioxane (10 mL) was added Na ₂ C0 ₃ (2.72 mL, 5.44 mmol) and PdC dppfyCF^C . adduct (0.148 g, 0.182 mmol). After being flushed with N ₂ , the mixture was heated in microwave at 140°C for 30 min. After filtration through celite, the filtrate was concentrated and the residue was purified on silica gel column using EtOAc/hexane as eluting solvents to give the title compound. LC/MS: (M+l) ⁺ :704.36.

Step D: 3-(5-chloro-2-(methylsulfonyl)-lH-benzo[if|imidazol-6-yl)-2- (2H-tetrazol-5- yl)benzenesulfonamide

To a mixture of S-^-chloro^^methylsulfonyrt-l-^- ^rimethylsily^ethoxy^ethyi iH-benzo^imM^

5-yl)benzenesulfonamide (70 mg, 0.099 mmol) and triisopropylsilane (157 mg, 0.994 mmol) was added trifluoroacetic acid (2 mL, 26.0 mmol). The resulting solution was heated at 80°C for 3 hr. After removing the volatile materials the residue was purified by reverse phase HPLC using acetonitrile (0.05%TFA)/water (0.05%TFA) as mobile phase to give the title compound.

LC/MS: (M+l) ⁺ : 454.25.

EXAMPLE 279

3-(5-chloro-2-methoxy-lH-benzo[d]imidazol-6-yl)-2-(2H-tetraz ol-5-yl)benzenesulfonamide

Step A: 3-(5-chloro-2-methoxy-l-((2-(trimethylsilyl)ethoxy)methyl)-l H- benzo[if|imidazol-6-yl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5 -yl)benzenesulfonamide

3 -(5-chloro-2-(methylsulfonyl)- 1 -((2-(trimethylsilyl)ethoxy)methyl)- 1H- benzo[d]imidazol-6-yl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5- yl)benzenesulfonamide

(described above, 70 mg, 0.099 mmol) in 7 N ammonia/MeOH (2 mL) was heated at 80°C for 2 hr. After concentration the residue was purified by preparative TLC using EtOAc/hexane as developing solvents to give the title compound. LC/MS: (M+l) ⁺ : 656.63.

Step B: 3-(5-chloro-2-methoxy-lH-benzo[d]imidazol-6-yl)-2-(2H-tetraz ol-5- yl)benzenesulfonamide

The solution of 3 -(5-chloro-2-methoxy- 1 -((2-(trimethylsilyl)ethoxy)methyl)- 1H- benzo[d]imidazol-6-yl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5- yl)benzenesulfonamide (65 mg, 0.099 mmol) and triisopropylsilane (100 mg, 0.631 mmol) in trifluoroacetic acid (2 mL) was heated at 80°C for 0.5 hr. After removing the volatile materials the residue was purified on reverse phase HPLC using acetonitrile (0.05%TFA)/water(0.05%TFA) as mobile phase to give the title compound. LC/MS: (M+l) ⁺ : 406.41.

EXAMPLE 280

3-(l-(aminomethyl)isoqu 5-yl)benzenesulfonamide

Step A: (l-cyanoisoquinolin-6-yl)boronic acid

A mixture of 4,4,4',4',5,5,5',5'-octamethyl-2,2'-bi(l,3,2-dioxaborolane) (2.83 g,

11.2 mmol), 6-bromoisoquinoline-l-carbonitrile (2.00 g, 8.58 mmol), and potassium acetate (2.53 g, 25.7 mmol) in dioxane (20 mL) was degassed for 30 min before addition of

PdCl ₂ (dppf)-CH ₂ Cl ₂ adduct (0.701 g, 0.858 mmol). The resulting mixture was heated at 100°C overnight. After cooling to rt the mixture was filtered through celite, the filtrate was concentrated and the residue was partitioned between 0. IN NaOH (200 mL) and DCM (200 mL). The alkaline phase was extracted with DCM twice. The alkaline phase was then acidified by 2N HC1 to pH 5 and extracted with 30% isopropanol/DCM three times. The combined isopropanol/DCM phase was dried over Na ₂ S0 ₄ , concentrated to give (l-cyanoisoquinolin-6- yl)boronic acid. LC/MS: (M+l) ⁺ : 199.10.

Step B: 3-(l-cyanoisoquinolin-6-yl)-2-(2-(4-methoxybenzyl)-2H-tetraz ol-5- yl)benzenesulfonamide

A mixture of 3-bromo-2-(2-(4-methoxybenzyl)-2H-tetrazol-5- yl)benzenesulfonamide (2.97 g, 7.00 mmol), (l-cyanoisoquinolin-6-yl)boronic acid (1.66 g, 8.40 mmol), and aqueous a ₂ C0 ₃ (10.50 mL, 21.00 mmol) in dioxane (40 mL) was bubbled with N ₂ for 1 hr before addition of PdCl ₂ (dppf)-CH ₂ Cl ₂ adduct (0.572 g, 0.700 mmol). The mixture was heated at 90°C overnight. After cooling to rt the mixture was filtered through celite, the filtrate was concentrated and the residue was purified on silica gel column using EtOAc/hexane as eluting solvents to give the title compound. LC/MS: (M+l) ⁺ : 498.65.

Step C: 3-(l-(aminomethyl)isoquinolin-6-yl)-2-(2-(4-methoxybenzyl)-2 H-tetrazol-5- yl)benzenesulfonamide

To a solution of 3-(l-cyanoisoquinolin-6-yl)-2-(2-(4-methoxybenzyl)-2H-tetraz ol- 5-yl)benzenesulfonamide (1.58 g, 3.18 mmol) in toluene (20 mL) and CH ₂ C1 ₂ (40 mL) at -78°C was added DIBAL-H in THF (15.88 mL, 15.88 mmol) dropwise. The resulting solution was stirred at -78°C for 2 hr, and quenched by addition of MeOH (5 mL) dropwise, followed by addition of 20 mL of saturated Na ₂ S0 ₄ solution; the mixture was then stirred at rt for 0.5 hr. The mixture was filtered and the filtrate was concentrated and the residue was purified on reverse phase HPLC using acetonitrile (0.1% formic acid)/water (0.1% formic acid) as mobile phase to give the title compound. LC/MS: (M+l) ⁺ : 502.57.

Step D: 3-(l-(aminomethyl)isoquinolin-6-yl)-2-(2H-tetrazol-5-yl)benz enesulfonamide

To a solution of 3-(l-(aminomethyl)isoquinolin-6-yl)-2-(2-(4-methoxybenzyl)- 2H-tetrazol-5-yl)benzenesulfonamide (45 mg, 0.090 mmol) in trifluoroacetic acid (3 mL) was added anisole (0.078 mL, 0.718 mmol), and the resulting solution was heated at 80°C for 2 hr. After removing the volatile materials the residue was purified on reverse phase HPLC using acetonitrile (0.1%TFA)/ water (0. l%formic acid) as mobile phase to give 3-(l-

(aminomethyl)isoquinolin-6-yl)-2-(2H-tetrazol-5-yl)benzen esulfonamide. LC/MS: (M+l) ⁺ : 382.45.

EXAMPLE 281

6-(3-sulfamoyl-2-( noline-l-carboxamide

Step A: 6-(2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-3-sulfamoylpheny l)isoquinoline-l- carboxamide The solution of 3-(l-cyanoisoquinolin-6-yl)-2-(2-(4-methoxybenzyl)-2H-tetraz ol- 5-yl)benzenesulfonamide (76 mg, 0.15 mmol) and cerium(IV) oxide (131 mg, 0.764 mmol) in dioxane (1 niL) and water (1 mL) was heated at 100°C for 2 days. After filtration the filtrate was concentrated and the residue was purified on reverse phase HPLC using acetonitrile (0.1%TFA) /water (0.1%formic acid) as mobile phase to give the title compound. LC/MS: (M+l) ⁺ : 516.59. Step B: 6-(3-sulfamoyl-2-(2H-tetrazol-5-yl)phenyl)isoquinoline-l-car boxamide

The solution of 6-(2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-3- sulfamoylphenyl)isoquinoline-l-carboxamide (34 mg, 0.066 mmol) and triisopropylsilane (41.8 mg, 0.264 mmol) in TFA (3 mL, 38.9 mmol) was heated at 80°C for 1 hr. After concentration the residue was purified by reverse phase HPLC using 5-40% acetonitrile (0.1% formic acid) gradient over 10 min to give the title compound. LC/MS: (M+l) ⁺ : 396.45.

EXAMPLE 282

4'-(3-amino-4-hydroxypiperidin-4-yl)-2-(2H-tetrazol-5-yl)-[l ,r-biphenyl]-3-sulfonamide dihydrochloride (trans, racemate)

Step A: tert-butyl 4-(4-chlorophenyl)-5,6-dihydropyridine-l(2H)-carboxylate

The mixture of tert-butyl 4-(((trifluoromethyl)sulfonyl)oxy)-5,6-dihydropyridine- l(2H)-carboxylate (5.00 g, 15.09 mmol), (4-chlorophenyl)boronic acid (2.360 g, 15.09 mmol) and aqueous a ₂ C0 ₃ (22.64 mL, 45.3 mmol) in dioxane (100 mL) was degassed by 2 for 1 hr before addition of PdC dppf) (0.552 g, 0.755 mmol). The resulting mixture was heated at

100°C overnight. After filtration through celite, the filtrate was concentrated and the residue was purified on silica gel column using EtOAc/hexane as eluting solvents to give the title compound. LC/MS: (M-56+l) ⁺ : 238.12 (100%); 240.08 (30%).

Step B: tert-butyl 6-(4-chlorophenyl)-7-oxa-3-azabicyclo[4.1.0]heptane-3-carbox ylate

To the solution of tert-butyl 4-(4-chlorophenyl)-5,6-dihydropyridine-l(2H)- carboxylate (2.15 g, 7.32 mmol) in DCM (100 mL) at 0°C was added mCPBA (2.53 g, 1 1.0 mmol) and the resulting solution was stirred from 0°C to rt overnight. The mixture was partitioned between DCM and 10% K^CCVwater, the organic phase was washed with

10%K ₂ CO ₃ /water, dried over Na ₂ S0 ₄ , concentrated, and the residue was purified on silica gel column using EtOAC/hexane as eluting solvents to give the title compound. LC/MS: (M- 56+l) ⁺ : 254.18(100%), 256.15(30%).

Step C: tert-butyl 3-azido-4-(4-chlorophenyl)-4-hydroxypiperidine-l-carboxylate (trans, racemate)

To the solution of tert-butyl 6-(4-chlorophenyl)-7-oxa-3- azabicyclo[4.1.0]heptane-3-carboxylate (1.59 g, 5.13 mmol) in DMSO (20 mL) was added sodium azide (1.67 g, 25.7 mmol) and the resulting mixture was heated at 100 °C under 2 overnight. After cooling to rt the mixture was partitioned between EtOAc and water, the organic phase was washed with water, brine, dried over Na ₂ S0 ₄ , concentrated, and the residue was purified on silica gel column using EtOAc/hexane as eluting solvents to give the title compound (trans, racemate). LC/MS: (M+l) ⁺ : 353.30 (100%), 355.08 (30%).

Step D: tert-butyl 3-amino-4-(4-chlorophenyl)-4-hydroxypiperidine-l-carboxylate (trans, racemate)

To the solution of tert-butyl 3-azido-4-(4-chlorophenyl)-4-hydroxypiperidine-l- carboxylate (trans, racemate, 0.74 g, 2.1 mmol) in THF (20 mL) was added L1AIH ₄ (5.03 mL, 5.03 mmol) at 0°C, the resulting solution was stirred at 0°C for 4 hr. The reaction was quenched with water, the mixture was treated with a ₂ S0 ₄ , filtered and washed with DCM; the filtrate was concentrated to give crude title compound (trans, racemate). LC/MS: (M+l) ⁺ : 327.27(100%), 329.22 (30%).

Step E: tert-butyl 3-((tert-butoxycarbonyl)amino)-4-(4-chlorophenyl)-4- hydroxypiperidine- 1 -carboxylate (trans, racemate)

To the solution of tert-butyl 3-amino-4-(4-chlorophenyl)-4-hydroxypiperidine-l- carboxylate (trans, racemate, 700 mg, 2.14 mmol) and Boc ₂ 0 (0.597 mL, 2.57 mmol) in DCM

(20 mL) was added triethylamine (0.597 mL, 4.28 mmol). The resulting solution was stirred at rt overnight. After concentration the residue was purified by preparative TLC using EtOAc/hexane as developing solvents to give the title compound (trans, racemate). LC/MS: (M+l) ⁺ : 427.38

(100%), 429.31(30%).

Step F: tert-butyl 3-((tert-butoxycarbonyl)amino)-4-hydroxy-4-(4-(4,4,5,5-tetra methyl-

1 ,3 ,2-dioxaborolan-2-yl)phenyl)piperidine- 1 -carboxylate (trans, racemate)

The mixture of potassium acetate (252 mg, 2.57 mmol), tert-butyl 3-((tert- butoxycarbonyl)amino)-4-(4-chlorophenyl)-4-hydroxypiperidine - 1 -carboxylate (trans, racemate, 366 mg, 0.857 mmol), and bis(pinacolato)diboron (435 mg, 1.72 mmol) in dioxane (10 mL) was degassed with 2 by vacuum/^ three times before addition of 2nd generation xphos precatalyst (135 mg, 0.171 mmol). The resulting mixture was further degassed by vacuum/^ three times and heated at 70°C overnight under N ₂ . After filtration through celite, the filtrate was concentrated and the residue was purified on silica gel column using EtOAc/hexane as eluting solvents to give the title compound (trans, racemate). LC/MS: (M+l) ⁺ : 519.47.

Step G: tert-butyl 3-((tert-butoxycarbonyl)amino)-4-hydroxy-4-(2'-(2-(4-methoxy benzyl)-

2H-tetrazol-5-yl)-3 '-sulfamoyl-[ 1 , 1 '-biphenyl]-4-yl)piperidine- 1 -carboxylate (trans, racemate)

A mixture of tert-butyl 3-((tert-butoxycarbonyl)amino)-4-hydroxy-4-(4-(4,4,5,5- tetramethyl-l,3,2-dioxaborolan-2-yl)phenyl)piperidine-l-carb oxylate (trans, racemate, 690 mg, 1.331 mmol), 3-bromo-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)benzenesulfo namide (1129 mg, 2.66 mmol), and K ₂ CO ₃ (552 mg, 3.99 mmol) in dioxane (7 mL) and water (2 mL) was degassed by vacuum/ 2 three times before addition of PdC dppf) (195 mg, 0.266 mmol). The resulting mixture was further degassed by vacuum/^ three times, then heated at 90°C for 2 days. After filiation through celite, the filtrate was concentrated and the residue was purified on silica gel column using EtOAc/hexane as eluting solvents to give the residue which was further purified on reverse phase HPLC using acetonitrile (0.1% formic acid)/water (0.1% formic acid) as mobile phase to give the title compound (trans, racemate). LC/MS: (M+l) ⁺ : 736.86.

Step H: 4'-(3-amino-4-hydroxypiperidin-4-yl)-2-(2-(4-methoxybenzyl)- 2H-tetrazol-5-yl)- [Ι, Γ-biphenyl] -3 -sulfonamide (trans, racemate)

To a solution of tert-butyl 3-((tert-butoxycarbonyl)amino)-4-hydroxy-4-(2'-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)-3 '-sulfamoyl-[ 1 , 1 '-biphenyl]-4-yl)piperidine- 1 -carboxylate (trans, racemate) (215 mg, 0.292 mmol) in DCM (2 mL) was added trifluoroacetic acid (2 mL, 26.0 mmol) and the resulting solution was stirred at rt for 1 hr. After concentraion the residue was purified on reverse phase HPLC using acetonitrile (0.1% formic acid)/water (0.1% formic acid) as mobile phase to give the title compound (trans, racemate). LC/MS: (M+l) ⁺ : 536.44. Step I: 4'-(3-amino-4-hydroxypiperidin-4-yl)-2-(2H-tetrazol-5-yl)-[l ,r-biphenyl]-3- sulfonamide dihydrochloride (trans, racemate)

To a solution of 4'-(3-amino-4-hydroxypiperidin-4-yl)-2-(2-(4-methoxybenzyl)- 2H-tetrazol-5-yl)-[l, l'-biphenyl]-3 -sulfonamide (trans, racemate, 126 mg, 0.235 mmol) in trifluoroacetic acid (3 mL, 38.9 mmol) was added anisole (0.103 mL, 0.941 mmol), and the resulting solution was heated at 80°C for 1 hr. After concentration, the residue was purified on reverse phase HPLC using acetonitrile (0.1% formic acid)/water (0.1% formic acid) as mobile phase to give the residue which was dissolved in MeOH (10 mL) and treated with HC1 (1.25 M in ethanol) (0.226 mL, 0.282 mmol) at 0°C; the resulting solution was stirred at 0°C for 10 min before concentration. The residue was lyophilized from acetonitrile/water to give 4'-(3-amino-4- hydroxypiperidin-4-yl)-2-(2H-tetrazol-5-yl)-[l, l '-biphenyl]-3-sulfonamide dihydrochloride (trans, racemate). LC/MS: (M+l) ⁺ : 416.29.

EXAMPLE 283

4'-(4-aminopiperidin-4-yl)-2-( -tetrazol-5-yl)-[l,r-biphenyl]-3-sulfonamide dihydrochloride

Step A: tert-butyl 4-(4-chlorophenyl)-4-hydroxypiperidine-l-carboxylate

To a solution of tert-butyl 4-oxopiperidine-l-carboxylate (2.06 g, 10.3 mmol) in

THF (20 mL) was added lanthanum trichloride lithium chloride complex in THF (17.23 mL, 10.34 mmol) and the resulting solution was stirred at rt for 1 hr. The solution was cooled to 0°C and was treated with 4-chlorophenylmagnesium bromide (12.41 mL, 12.41 mmol) dropwise. The resulting solution was stirred at rt for 2 hr. The reaction was quenched with saturated NH ₄ C1 solution, and partitioned between EtO Ac/brine. The organic phase was dried over a2S0 ₄ , concentrated, and the residue was purified on silica gel column using EtOAc/hexane as eluting solvents to give the title compound. LC/MS: (M+l) ⁺ : 312.23 (100%), 314.21(30%).

Step B: 4-(4-chlorophenyl)piperidin-4-ol

To the solution of tert-butyl 4-(4-chlorophenyl)-4-hydroxypiperidine-l- carboxylate (2.83 g, 9.08 mmol) in CH ₂ CI ₂ (20 mL) was added trifluoroacetic acid (7.0 mL, 91 mmol) and the resulting solution was stirred at rt for 2 hr. The reaction solution was concentrated to give 4-(4-chlorophenyl)piperidin-4-ol. LC/MS: (M+l) ⁺ : 212.16 (100%), 214.1 1(30%).

Step C: benzyl 4-(4-chlorophenyl)-4-hydroxypiperidine-l -carboxylate

To the solution of 4-(4-chlorophenyl)piperidin-4-ol (1.92 g, 9.08 mmol) in

CH ₂ C1 ₂ (30 mL) was added triethylamine (5.06 mL, 36.3 mmol) and Cbz-Cl (1.30 mL, 9.08 mmol) at 0°C; the resulting solution was stirred at 0°C for 1 hr. The reaction was quenched by addition of water, the mixture was partitioned between DCM and saturated aHC0 ₃ , the aqueous phase was extracted with DCM three times, the combined organic phases were dried over a ₂ S0 ₄ , concentrated and the residue was purified on silica gel column using

EtOAc/hexane as eluting solvents to give the title compound. LC/MS: (M+l) ⁺ : 346.24 (100%), 348.23 (30%).

Step D: tert-butyl 4-(2-chloroacetamido)-4-(4-chlorophenyl)piperidine-l-carboxy late

To a solution of benzyl 4-(4-chlorophenyl)-4-hydroxypiperidine-l-carboxylate

(2.23 g, 6.45 mmol) in chloroacetonitrile (20 mL, 315 mmol) at 0°C was added H ₂ S0 ₄ (5.16 mL, 97 mmol) and the resulting solution was stirred at rt for 2 hr. The reaction mixture was poured into ice water/K ₂ C03, the aqueous phase was extracted with DCM three times, the organic phase was dried over Na ₂ S0 ₄ , concentrated and the residue was suspended in DCM (100 mL) and saturated NaHC0 ₃ (100 mL). To this solution was added Boc ₂ 0 (1.50 mL, 6.45 mmol) in DCM (10 mL), and the resulting mixture was stirred at rt overnight. The mixture was extracted with DCM three times, the combined organic phase was dried over Na ₂ S0 ₄ , concentrated and the residue was purified by silica gel column chromatography using EtOAc/hexane as eluting solvents to give the title compound. LC/MS: (M+l) ⁺ : 331.38(100%), 333.38(70%).

Step E: tert-butyl 4-amino-4-(4-chlorophenyl)piperidine- 1 -carboxylate

To a solution of tert-butyl 4-(2-chloroacetamido)-4-(4-chlorophenyl)piperidine- 1 - carboxylate (0.715 g, 1.85 mmol) in ethanol (20 mL) was added thiourea (1.405 g, 18.46 mmol). The resulting mixture was heated at 120°C for 2.5 hr. After filtration the filtrate was concentrated and the residue was suspended in DCM (100 mL) and filtered. The filtrate was concentrated to give the title compound. LC/MS: (M+l) ⁺ : 311.20 (100%), 313.18 (30%).

Step F: tert-butyl 4-((tert-butoxycarbonyl)amino)-4-(4-chlorophenyl)piperidine- 1 - carboxylate

To the solution of tert-butyl 4-amino-4-(4-chlorophenyl)piperidine-l -carboxylate (574 mg, 1.85 mmol) in CH ₂ C1 ₂ (20 mL) was added Boc ₂ 0 (0.515 mL, 2.22 mmol) in DCM (5 mL) and triethylamine (0.515 mL, 3.69 mmol). The resulting solution was stirred at rt over the weekend. Additional Boc ₂ 0 (0.515 mL, 2.22 mmol) and triethylamine (0.25 mL) were added and the resulting mixture was heated at reflux for 1 hr. After concentration, the residue was purified on silica gel column using EtOAc/hexane as eluting solvents to give the title compound. LC/MS: (M+l) ⁺ : 411.29 (100%), 413.27 (30%).

Step G: tert-butyl 4-((tert-butoxycarbonyl)amino)-4-(4-(4,4,5,5-tetramethyl-l,3 ,2- dioxaborolan-2-yl)phenyl)piperidine- 1 -carboxylate The mixture of potassium acetate (221 mg, 2.249 mmol), tert-butyl 4-((tert- butoxycarbonyl)amino)-4-(4-chlorophenyl)piperidine-l-carboxy late (308 mg, 0.750 mmol), and bis(pinacolato)diboron (381 mg, 1.50 mmol) in dioxane (10 mL) was degassed with 2 by vacuum/N2 three times before addition of 2nd generation xphos precatalyst (1 18 mg, 0.150 mmol). The resulting mixture was further degassed by vacuum/^ three times and heated at 70°C overnight under N ₂ . After filtration through celite, the filtrate was concentrated and the residue was purified on reverse phase HPLC using acetonitrile (0.1% formic)/water (0.1% formic acid) to give tert-butyl 4-((tert-butoxycarbonyl)amino)-4-(4-(4,4,5,5-tetramethyl-l,3 ,2- dioxaborolan-2-yl)phenyl)piperidine-l-carboxylate. LC/MS: (M+l) ⁺ : 503.44.

Step H: tert-butyl 4-((tert-butoxycarbonyl)amino)-4-(2'-(2-(4-methoxybenzyl)-2H - tetrazol-5 -yl)-3 '-sulfamoyl- [1, 1 '-biphenyl]-4-yl)piperidine- 1 -carboxylate

The mixture of tert-butyl 4-((tert-butoxycarbonyl)amino)-4-(4-(4,4,5,5- tetramethyl-l,3,2-dioxaborolan-2-yl)phenyl)piperidine-l-carb oxylate (242 mg, 0.482 mmol), 3- bromo-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)benzenesulfona mide (286 mg, 0.674 mmol), and K2CO3 (200 mg, 1.45 mmol) in dioxane (7 mL) and water (2 mL) was degassed by vacuum/N2 three times before addition of PdC dppf) (70.5 mg, 0.096 mmol). The resulting mixture was further degassed by vacuum/^ three times, then heated at 90°C for 2 days. After filiation through celite, the filtrate was concentrated and the residue was purified on silica gel column using EtOAc/hexane as eluting solvents to give the title compound. LC/MS: (M+l) ⁺ : 720.44.

Step I: 4'-(4-aminopiperidin-4-yl)-2-(2-(4-methoxybenzyl)-2H-tetrazo l-5-yl)-[l,r- biphenyl]-3 -sulfonamide

To the solution of tert-butyl 4-((/er/-butoxycarbonyl)amino)-4-(2'-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)-3'-sulfamoyl-[l,r-biphenyl] -4-yl)piperidine-l -carboxylate (125 mg, 0.174 mmol) in DCM (2 mL) was added trifluoroacetic acid (2 mL, 26.0 mmol) and the resulting solution was stirred at rt for 1 hr. After concentration the residue was purified by reverse phase HPLC using acetonitrile (0.1% formic acid)/water (0.1% formic acid) to give the title compound. LC/MS: (M+l) ⁺ : 520.60.

Step J: 4'-(4-aminopiperidin-4-yl)-2-(2H-tetrazol-5-yl)-[ 1 , 1 '-biphenyl] -3 -sulfonamide dihydrochloride

To the solution of 4'-(4-aminopiperidin-4-yl)-2-(2-(4-methoxybenzyl)-2H- tetrazol-5-yl)-[l, l'-biphenyl]-3-sulfonamide (70 mg, 0.135 mmol) in trifluoroacetic acid (2 mL, 26.0 mmol) was added anisole (0.059 mL, 0.539 mmol), and the resulting solution was heated at 80°C for 1 hr. After concentration, the residue was purified on reverse phase HPLC using acetonitrile (0.1% formic acid)/water (0.1% formic acid) as mobile phase to give the pure product which was dissolved in MeOH (10 mL) and treated with HC1 in ethanol (1.25 N) (0.216 mL, 0.269 mmol); after concentration, the residue was lyophilized from acetonitrile/water to give 4'-(4-aminopiperidin-4-yl)-2-(2H-tetrazol-5-yl)-[l,r-bipheny l]-3-sulfonamide dihydrochloride. LC/MS: (M+l) ⁺ : 400.22.

EXAMPLES 284 and 285

4'-(3-hydroxypyrrolidin-3-yl)-2-(2H-tetrazol-5-yl)-[l, l'-biphenyl]-3-sulfonamide and 4'-(2,5- dihydr -lH-pyrrol-3-yl)-2-(2H-tetrazol-5-yl)-[l, l'-biphenyl] -3 -sulfonamide

Step A: tert-butyl 3-(4-chlorophenyl)-3-hydroxypyrrolidine-l-carboxylate

To a solution of tert-butyl 3-oxopyrrolidine-l-carboxylate (4.86 g, 26.2 mmol) in THF (40 mL) was added lanthanum trichloride lithium chloride complex in THF (43.7 mL, 26.2 mmol) and the resulting solution was stirred at rt for 1 hr. The solution was cooled to 0°C and was treated with 4-chlorophenylmagnesium bromide (31.5 mL, 31.5 mmol) dropwise. The resulting solution was stirred at rt for 2 hr. The reaction was quenched by sat. NH ₄ C1 solution, and partitioned between EtO Ac/brine. The organic phase was dried over Na ₂ S0 ₄ , concentrated, and the residue was purified on silica gel column using EtOAc/hexane as eluting solvents to give the title compound. LC/MS: (M+l) ⁺ : 298 (100%), 300 (30%).

Step B: tert-butyl 3-hydroxy-3-(4-(4,4,5,5-tetramethyl-l,3,2-dioxaborolan-2- yl)phenyl)pyrrolidine- 1 -carboxylate

A mixture of potassium acetate (513 mg, 5.23 mmol), tert-butyl 3-(4- chlorophenyl)-3-hydroxypyrrolidine-l -carboxylate (519 mg, 1.74 mmol), and

bis(pinacolato)diboron (885 mg, 3.49 mmol) in dioxane (10 mL) was degassed with 2 by vacuum/N2 three times before addition of 2nd generation xphos precatalyst (274 mg, 0.349 mmol). The resulting mixture was further degassed by vacuum/N2 three times and heated at 70°C overnight under N ₂ . After filtration through celite, the filtrate was concentrated and the residue was purified on silica gel column using EtOAc/hexane as eluting solvents to give the title compound. LC/MS: (M+l) ⁺ : 390.52.

Step C: tert-butyl 3-hydroxy-3-(2'-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-3'-su lfamoyl-

[1,1 '-biphenyl] -4-yl)pyrrolidine- 1 -carboxylate

The mixture of tert-butyl 3-hydroxy-3-(4-(4,4,5,5-tetramethyl-l,3,2- dioxaborolan-2-yl)phenyl)pyrrolidine-l -carboxylate (0.568 g, 1.46 mmol), 3-bromo-2-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)benzenesulfonamide (0.619 g, 1.46 mmol), and a ₂ C0 ₃ (2.2 mL, 4.38 mmol) in dioxane (10 mL) was degassed by vacuum/^ three times before addition of PdC dppf) (0.214 g, 0.292 mmol). The resulting mixture was further degassed by vacuum/^ three times, then heated at 90°C for 2 days. After filtration through celite, the filtrate was concentrated and the residue was purified on silica gel column using EtOAc/hexane as eluting solvents to give the title compound. LC/MS: (M+l) ⁺ : 607.29.

Step D: 4'-(3-hydroxypyrrolidin-3-yl)-2-(2-(4-methoxybenzyl)-2H-tetr azol-5-yl)-[l, l'- biphenyl]-3-sulfonamide 2,2,2-trifluoroacetate

To a solution of tert-butyl 3-hydroxy-3-(2'-(2-(4-methoxybenzyl)-2H-tetrazol-5- yl)-3'-sulfamoyl-[l, l'-biphenyl]-4-yl)pyrrolidine-l -carboxylate (330 mg, 0.544 mmol) in DCM (3 mL) was added trifluoroacetic acid (3 mL, 38.9 mmol). The resulting solution was stirred at rt for 1 hr then the reaction solution was concentrated to give the title compound. LC/MS:

(M+l)+: 507.25.

Step E: 4'-(3-hydroxypyrrolidin-3-yl)-2-(2H-tetrazol-5-yl)-[l, l'-biphenyl]-3-sulfonamide and

4'-(2,5-dihydro-lH-pyrrol-3-yl)-2-(2H-tetrazol-5-yl)-[l, l'-biphenyl]-3-sulfonamide

To a solution of 4'-(3-hydroxypyrrolidin-3-yl)-2-(2-(4-methoxybenzyl)-2H- tetrazol-5-yl)-[l, l'-biphenyl]-3-sulfonamide 2,2,2-trifluoroacetate (200 mg, 0.322 mmol) in trifluoroacetic acid (2 mL) was added anisole (0.141 mL, 1.29 mmol) and the resulting solution was heated at 80°C for 0.5 hr. After concentration, the residue was purified on reverse phase HPLC using acetonitrile (0.1% formic acid)/water (0.1% formic acid) as mobile phase to give 4'- (3-hydroxypyrrolidin-3-yl)-2-(2H-tetrazol-5-yl)-[l, l '-biphenyl]-3-sulfonamide. LC/MS:

(M+l) ⁺ : 387.15, and 4'-(2,5-dihydro-lH-pyrrol-3-yl)-2-(2H-tetrazol-5-yl)-[l, l '-biphenyl]-3- sulfonamide. LC/MS: (M+l) ⁺ : 369.15.

EXAMPLE 286

3-(2-(aminomethyl)quinolin-6-yl)-2-(2H-tetrazol-5-yl)benzene sulfonamide

Step A: (2-cyanoquinolin-6-yl)boronic acid

A mixture of 4,4,4',4',5,5,5',5'-octamethyl-2,2'-bi(l,3,2-dioxaborolane) (2.86 g, 1 1.3 mmol), 6-bromoquinoline-2-carbonitrile (2.02 g, 8.67 mmol), and potassium acetate (2.55 g, 26.0 mmol) in dioxane (20 mL) was degassed for 30 min before addition of PdC dppf)- CH2CI2 adduct (0.708 g, 0.867 mmol). The resulting mixture was heated at 100°C overnight. After cooling to rt the mixture was filtered through celite, the filtrate was concentrated, and the residue was partitioned between 0. IN NaOH (200 mL) and DCM (200 mL). The alkaline phase was extracted with DCM twice. The alkaline phase was then acidified by 2N HC1 to pH 5, extracted with 30% isopropanol/DCM (3x150 mL). The combined isopropanol/DCM phases were dried over Na ₂ S0 ₄ , concentrated to give (2-cyanoquinolin-6-yl)boronic acid as a crude product which was used in next step directly without further purification. LC/MS:

(M+l) ⁺ : 199.1 1.

Step B: 3-(2-cyanoquinolin-6-yl)-2-(2-(4-methoxybenzyl)-2H-tetrazol- 5- yl)benzenesulfonamide

The mixture of 3-bromo-2-(2-(4-methoxybenzyl)-2H-tetrazol-5- yl)benzenesulfonamide (1.73 g, 4.07 mmol), (2-cyanoquinolin-6-yl)boronic acid (1.68 g, 5.09 mmol), and a ₂ C0 ₃ (7.64 mL, 15.3 mmol) in dioxane (40 mL) was bubbled with 2 for 1 hr before addition of PdCl ₂ (dppf)-CH ₂ Cl ₂ adduct (0.416 g, 0.509 mmol). The mixture was heated at 90°C overnight. After cooled to rt the mixture was filtered through celite, the filtrate was concentrated and the residue was purified by silica gel column using EtOAc/hexane as eluting solvents to give the title compound. LC/MS: (M+l) ⁺ : 498.25.

Step C: 3-(2-(aminomethyl)quinolin-6-yl)-2-(2-(4-methoxybenzyl)-2H-t etrazol-5- yl)benzenesulfonamide

To the solution of 3-(2-cyanoquinolin-6-yl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-

5-yl)benzenesulfonamide (0.43 g, 0.864 mmol) in CH ₂ C1 ₂ (20 mL) and MeOH (20 mL) was added B0C2O (0.221 mL, 0.951 mmol) and Raney nickel (0.074 g, 0.864 mmol). The resulting mixture was subjected to hydrogenation at 50 psi at rt overnight. After filtration through celite under _¾ the filtrate was concentrated and the residue was dissolved in DCM (5 mL) and the resulting solution was treated with trifluoroacetic acid (5 mL) at rt for 1 hr. The reaction solution was concentrated to give 3-(2-(aminomethyl)quinolin-6-yl)-2-(2-(4-methoxybenzyl)-2H-t etrazol- 5-yl)benzenesulfonamide. LC/MS: (M+l) ⁺ : 502.18.

Step D: 3-(2-(aminomethyl)quinolin-6-yl)-2-(2H-tetrazol-5-yl)benzene sulfonamide

To the solution of 3-(2-(aminomethyl)quinolin-6-yl)-2-(2-(4-methoxybenzyl)-2H- tetrazol-5-yl)benzenesulfonamide (227 mg, 0.453 mmol) in trifluoroacetic acid (2 mL, 26.0 mmol) was added anisole (0.198 mL, 1.81 mmol), and the resulting solution was heated at 80°C for 1 hr. After concentration, the residue was purified on reverse phase HPLC using acetonitrile (0.1% formic acid)/water (0.1% formic acid) as mobile phase to give 3-(2- (aminomethyl)quinolin-6-yl)-2-(2H-tetrazol-5-yl)benzenesulfo namide. LC/MS: (M+l) ⁺ : 382.20.

EXAMPLE 287

6-(3-sulfamoyl-2-( -tetrazol-5-yl)phenyl)quinoline-2-carboxylic acid

Step A: 6-(2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-3-sulfamoylpheny l)quinoline-2- carboxylic acid and 6-(2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-3-sulfamoylpheny l)quinoline- 2-carboxamide

The solution of 3-(2-cyanoquinolin-6-yl)-2-(2-(4-methoxybenzyl)-2H-tetrazol- 5- yl)benzenesulfonamide (90 mg, 0.181 mmol) in dioxane (2 mL) and water (2 mL) was added H ₂ 0 ₂ (0.032 ml, 0.362 mmol) and NaOH (IN, 0.362 mL, 0.362 mmol). The resulting mixture was heated at 70°C overnight. After acidified to pH 4, the mixture was extracted with 30% isopropanol/CHCi ₃ three times, the combined organic phase was dried over Na ₂ S0 ₄ ,

concentrated and the residue was purified on reverse phase HPLC using acetonitrile (0.1% formic acid)/water (0.1% formic acid) to give the title compound. LC/MS: (M+l) ⁺ : 517.20, and 6-(2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-3-sulfamoylpheny l)quinoline-2-carboxamide. LC/MS: (M+l) ⁺ : 516.21.

Step B: 6-(3-sulfamoyl-2-(2H-tetrazol-5-yl)phenyl)quinoline-2 -carboxylic acid

To the solution of 6-(2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-3- sulfamoylphenyl)quinoline-2-carboxylic acid (20 mg, 0.039 mmol) in trifluoroacetic acid (3 mL, 38.9 mmol) was added anisole (0.017 mL, 0.155 mmol), the resulting solution was heated 80°C for 1 hr. After concentration, the residue was purified on reverse phase HPLC using acetonitrile (0.1% formic acid) /water (0.1% formic acid) to give 6-(3-sulfamoyl-2-(2H-tetrazol-5- yl)phenyl)quinoline-2-carboxylic acid. LC/MS: (M+l) ⁺ : 397. 13.

EXAMPLE 288

6-(3-sulfamoyl-2-(2H-tetrazol-5-yl)phenyl)quinoline-2-carbox amide

To a solution of 6-(2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-3- sulfamoylphenyl)quinoline-2-carboxamide (22 mg, 0.043 mmol) in trifuoroacetic acid (3 mL, 38.9 mmol) was added anisole (0.019 mL, 0.171 mmol) and the resulting solution was heated 80°C for 1 hr. After concentration, the residue was purified on reverse phase HPLC using acetonitrile (0.1% formic acid)/ water (0.1% formic acid) over 1 min to give 6-(3-sulfamoyl-2- (2H-tetrazol-5-yl)phenyl)quinoline-2-carboxamide. LC/MS: (M+l) ⁺ :396.15.

EXAMPLE 289

5-Chloro-3-(3-oxo-2,3-dihydro-lH-isoindol-5-yl)-2-(2H-tetraz ol-5-yl)benzenesulfonamide

Step A: (3-Bromo-4-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-5-sulfamoy lphenyl)boronic acid

(l,5-Cyclooctadiene)(methoxy)iridium(i) dimer (39.1 mg, 0.059 mmol) and bis(pinacolato)diboron (449 mg, 1.768 mmol) were dissolved in 3 mL THF and added to a 15 mL pressure tube containing a 2 mL THF solution of 3,4,7,8-tetramethyl-l,10-phenanthroline (27.8 mg, 0.118 mmol). Finally, a 1 mL THF solution containing 3-bromo-2-(l-(4- methoxybenzyl)( lH-tetrazol-5-yl))benzenesulfonamide and 3 -bromo-2-(2-(4- methoxybenzyl)(lH-tetrazol-5-yl))benzenesulfonamide (500 mg, 1.178 mmol) was added to the pressure tube via pipette and the reaction vessel was sealed and heated in an oil bath at 80°C for 16 hr. The reaction was dark red. The reaction mixture was concentrated and purified by reverse phase HPLC with C-18 column, eluted with 10% to 100% MeCN in water with 0.05% TFA. The solution was lyopholized to provide (3-bromo-4-(2-(4-methoxybenzyl)-2H-tetrazol-5- yl)-5-sulfamoylphenyl)boronic acid. LC-MS: calculated for CisHisBBr sOsS 469.0 observed m/e (M+H) ⁺ : 470.2.

Step B: 3-Bromo-5-chloro-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)ben zenesulfonamide

(3-Bromo-4-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-5-sulfamoy lphenyl)boronic acid (2.7 g, 5.77 mmol) was dissolved in ACN (57.7 ml), to which was added NCS (0.770 g, 5.77 mmol) and copper(I) chloride (0.571 g, 5.77 mmol), and then heated to 65°C for 6 hr. The reaction was diluted with water and EtOAc. The aqueous phase was extracted with EtOAc (x2) and the combined extracts were washed with brine, dried over Na ₂ S0 ₄ , filtered, and

concentrated. The residue was purified by MPLC on a 120g slica column eluted with 0% to 100% EtOAc in Hexane. The major UV active material was collected (only major PMB regioisomer) to provide the target compound. LC-MS: calculated for CisHnBrCl sOsS 457.0 observed m/e (M+H) ⁺ : 457.9; ¾ NMR δ (ppm) (MeOH): 8.15 (s, 1H), 8.01 (s, 1H), 7.12 (d, 2H), 6.77 (d, 2H), 5.53 (d, 1H), 5.27 (d, 1H), 3.75 (s, 3H).

Step C: 5-Chloro-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-3-(3-oxois oindolin-5- yl)benzenesulfonamide

A reaction vial was charged with 6-(4,4,5,5-tetramethyl-l,3,2-dioxaborolan-2- yl)isoindolin-l-one (73.2 mg, 0.283 mmol) and 3-bromo-5-chloro-2-(2-(4-methoxybenzyl)-2H- tetrazol-5-yl)benzenesulfonamide (144 mg, 0.314 mmol). EtOH (3139 μΐ) and potassium phosphate tribasic (942 μΐ, 0.942 mmol) were added and the reaction mixture was sparged with N ₂ for 10 min. l, l'-bis(di-tert-butylphosphino)ferrocene palladium dichloride (20.46 mg, 0.031 mmol) was added and the reaction was heated to 100°C for 1 hr in a microwave. The crude reaction mixture was diltued with EtOAc and water. The aqueous phase was extracted with EtOAc (x2) and the combined organic extracts were washed with brine, dried over Na ₂ S0 ₄ , filtered, and concentrated. The residue was purified by reverse phase HPLC on a CI 8 column eluted with 5% to 90% MeCN in water with 0.05% TFA. The solution was concentrated to provide 5 -chloro-2-(2-(4-methoxybenzyl)-2H-tetrazol-5 -yl)-3 -(3 -oxoisoindolin-5 - yl)benzenesulfonamide. LC-MS: calculated for C ₂₃ H ₁₉ C1N ₆ 0 ₄ S 510.09; observed m/e (M+H) ⁺ : 511.3. Step D: 5-Chloro-3-(3-oxo-2,3-dihydro-lH-isoindol-5-yl)-2-(2H-tetraz ol-5- yl)benzenesulfonamide

5-chloro-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-3-(3-oxois oindolin-5- yl)benzenesulfonamide (45 mg, 0.088 mmol) was dissolved in TFA (1 120 μΐ, 14.53 mmol) and Anisole (28.9 μΐ, 0.264 mmol) was added. The reaction was heated to 45°C overnight then concentrated in vacuo. The residue was purified by reverse phase HPLC on a C ₁₈ column and eluted with 0% to 70% MeCN in water with 0.05% TFA. The solution was lyopholized to provide 5-chloro-3-(3-oxo-2,3-dihydro-lH-isoindol-5-yl)-2-(2H-tetraz ol-5- yl)benzenesulfonamide. LC-MS: calculated for 390.03 observed m/e: 391.26 (M+H) ⁺ ; 'H NMR δ (ppm) (MeOH): 8.15 (s, 1H), 7.79 (s, 1H), 7.49 (s, 1H), 7.40 (d, 1H), 7.19 (d, 1H), 4.36 (s, 3H).

EXAMPLE 290

4'-Methyl-5-(l-oxoisoindolin-5-yl)-2-(2H-tetrazol-5-yl)-[l, l'-biphenyl]-3-sulfonamide

Step A: 2-(2-(4-Methoxybenzyl)-2H-tetrazol-5-yl)-4'-methyl-[l, l'-biphenyl]-3- sulfonamide

A reaction flask was charged with 4,4,5, 5-tetramethyl-2-(p-tolyl)-l, 3,2- dioxaborolane (1928 mg, 8.84 mmol) and a mixture of 3-bromo-2-(l-(4-methoxybenzyl)(lH- tetrazol-5-yl))benzenesulfonamide and 3-bromo-2-(2-(4-methoxybenzyl)(lH-tetrazol-5- yl))benzenesulfonamide (3000 mg, 7.07 mmol). EtOH (23.6 mL) and potassium phosphate tribasic (21.21 ml, 21.21 mmol) were added and the reaction mixture was sparged with 2 for 10 min. l,l'-bis(di-tert-butylphosphino)ferrocene palladium dichloride (461 mg, 0.707 mmol) was added and the reaction heated to 100°C for 18 hr. The crude reaction mixture was diluted with water and EtOAc. The organic was washed with brine, dried over Na ₂ S0 ₄ , filter, and concentrated. The oil was purified by MPLC on a 120 g silica eluted with 0% to 20% MeOH in DCM. The major UV active material was collected to provide 2-(2-(4-methoxybenzyl)-2H- tetrazol-5-yl)-4'-methyl-[l,l'-biphenyl]-3-sulfonamide. LC-MS: calculated for C22H21 5O ₃ S 435.1 ; observed m/e (M+H) ⁺ : 436.6.

Ste B: (6-(2-(4-Methoxybenzyl)-2H-tetrazol-5-yl)-4'-methyl-5-sulfam oyl-[l,l'- biphenyl]-3-yl)boronic acid

(l,5-Cyclooctadiene)(methoxy)iridium(i) dimer (38.1 mg, 0.057 mmol) and

BISPIN (292 mg, 1.148 mmol) were dissolved in 3 mL THF and added to a 15 mL pressure tube containing a 2 mL THF solution of 3,4,7,8-tetramethyl-l, 10-phenanthroline (27.1 mg, 0.115 mmol). Finally, a 1 mL THF solution containing 2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-4'- methyl-[l, l'-biphenyl]-3 -sulfonamide (250 mg, 0.574 mmol) was added to the pressure tube via pipette and the reaction vessel was sealed and heated in an oil bath at 80°C for 3.5 hr. The reaction was concentrated en vacuo then purified by reverse phase HPLC on a CI 8 column eluted with 10% to 100% MeCN in water with 0.05% TFA. The major UV active material was collected and lyopholized to provide (6-(l-(and 2-)(4-methoxybenzyl)-2H-tetrazol-5-yl)-4'- methyl-5-sulfamoyl-[l, l'-biphenyl]-3-yl)boronic acid. LC-MS: calculated for C22H22BN5O5S 479.1 ; observed m/e: 480.3 (M+H) ⁺ ;

Step C : 4'-Methyl-5 -( 1 -oxoisoindolin-5-yl)-2-(2H-tetrazol-5-yl)- [ 1 , 1 '-biphenyl] -3 - sulfonamide

(6-( 1 - (and 2-)(4-methoxybenzyl)-2H-tetrazol-5 -yl)-4'-methyl-5-sulfamoyl- [ 1 , 1 '- biphenyl]-3-yl)boronic acid (40 mg, 0.083 mmol) and 6-bromoisoindolin-l-one (19.47 mg, 0.092 mmol) was suspended in ethanol (835 μΐ) and potassium phosphate tribasic (250 μΐ, 0.250 mmol). The reaction mixture was sparged with 2 for 5 min. 1 , l'-bis(di-tert- butylphosphino)ferrocene palladium dichloride (5.44 mg, 8.35 μιηοΐ) was added and the reaction mixture micro waved at 1 10°C for 90 min. The crude reaction mixture was diluted with EtOAc and water. The aqueous phase was extract with EtOAc (x2), then the combined extracts were washed with brine, dried over Na ₂ S0 ₄ , filtered, and concentrated. The reaction mixture was purified by reverse phase HPLC on a Cis column and then eluted with 10% to 100% MeCN in water. The major UV active material was lyopholized to provide a white solid that was utilized directly in the deprotection. LC-MS: calculated for C ₃ oH ₂ 6N60 ₄ S 566.2; observed m/e: 467.5 (M+H) ⁺ . The resulting solid was dissolved in TFA and heated to 45°C overnight, then concentrated. The residue was purified by reverse phase HPLC on a Cis column eluted with 0% to 80% MeCN in water. The major UV active material was lyopholized to provide 4'-methyl-5- (l-oxoisoindolin-5-yl)-2-(2H-tetrazol-5-yl)-[l, l'-biphenyl]-3-sulfonamide. LC-MS: calculated for C ₂₂ H ₁₈ N ₆ 0 ₃ S 446.1 ; observed m/e: 447.4 (M+H) ⁺ ; 1H NMR δ (ppm) (DMSO): 8.72 (s, 1H), 8.44 (s, 1H), 8.16 (s, 1H), 8.12 (d, 1H), 8.05 (s, 1H), 7.77 (d, 1H), 7.60 (s, 2H), 7.11-7.05 (m, 4H), 4.48 (s, 2H), 2.27 (s, 3H).

EXAMPLES 291-296

Parallel synthesis of 5 -substituted 4'-methyl-2-(lH-tetrazol-5-yl)-[l,r-biphenyl]-3-sulfonamides

Palladium catalyzed C-C coupling of arylbromide and boronic acids or boronic

Into a mixture of boronic acid (commercially available, known, or prepared as described herein, 10.9 mg, 0.080 mmol) and 1 , 1 '-bis(di-tert-butylphosphino) ferrocene palladium dichloride (2.08 mg, 3.19 μιηοΐ) in vials were added a solution of isomeric mixture 5-chloro-2- (l-(4-methoxybenzyl)-lH-tetrazol-5-yl)-4'-methyl-[l, l'-biphenyl] -3 -sulfonamide and 5-chloro-2- (2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-4'-methyl-[l, l'-biphenyl] -3 -sulfonamide (25 mg, 0.053 mmol) in 2 mL of EtOH and 0.5 mL of THF, followed by a 1.0 M solution of potassium phosphate (0.213 mL, 0.213 mmol). The mixtures were heated at 70°C for 18 hr. The solvent was removed under reduced pressure. Into the residue in each vial was added 800 of water and 2.4 mL of ethyl acetate. The organic layers were transferred into 2 dram vials and the solvent was removed under reduced pressure.

Step B: Removal of the p-methoxybenzyl (PMB) protecting group under acidic conditions.

Into the residues were added a mixture of TFA (0.6 mL, 0.053 mmol) and anisole (58 mg) in 0.4 mL of DCM. The mixtures were heated at 50°C for 20 hr. After cooling to room temperature, the solvent was removed under reduced pressure. The residue was dissolved in 1.4 mL of DMSO. The crude solution was filtered through a filter plate. These crude materials were purified by HPLC to afford Examples 291-296.

Ex. Structure Name Calc'd LC/MS No. Mass m/e

[M+H] ⁺ [M+H] ⁺

291 4'-methyl-5-( 1 -methyl- 1H- 396 396 pyrazol-4-yl)-2-(2H-tetrazol- 5-yl)-[l,l'-biphenyl]-3- sulfonamide

292 5 -(6-hydroxypyridin-3 -yl)-4'- 409 409 methyl-2-(2H-tetrazol-5-yl)- [1,1 '-biphenyl] -3 -sulfonamide

293 O ⁰ 4'-methyl-5-(pyridin-3-yl)-2- 393 393

N _{¾ N} *«^NH ₂

(2H-tetrazol-5-yl)-[l,l'- biphenyl] -3 -sulfonamide

294 5-(isoindolin-5-yl)-4'-methyl- 433 433

2-(2H-tetrazol-5-yl)-[l,l'- biphenyl] -3 -sulfonamide

295 4"-methyl-5'-sulfamoyl-4'- 435 435

(2H-tetrazol-5-yl)-[l,l':3', r- terphenyl] -3 -carboxamide 296 4"-methyl-5'-sulfamoyl-4'- 435 435

(2H-tetrazol-5-yl)-[l, l':3',l"- terphenyl]-4-carboxamide

EXAMPLE 297

3-Sulfamoy -2-(2H-tetrazol-5-yl)benzoic acid

Step A: 3-Cyano-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)benzenesulfo namide

The mixture of 3-bromo-2-(l-(4-methoxybenzyl)(lH-tetrazol-5- yl))benzenesulfonamide and 3-bromo-2-(2-(4-methoxybenzyl)(lH-tetrazol-5- yl))benzenesulfonamide amide (650 mg, 1.532 mmol) was dissolved in DMA (7660 μί). Zinc cyanide (360 mg, 3.06 mmol) was added and the reaction was sparged with ₂ for 5 min.

Tetrakis(triphenylphosphine)palladium(0) (354 mg, 0.306 mmol) was added and the reaction mixture was heated to 1 10°C overnight. The crude reaction mixture was diluted with water and EtOAc. The aqueaus phase was extracted with EtOAc (x2) and the combined extracts were washed with brine, dried over Na ₂ S0 ₄ , filtered, and concentrated. The residue was purified by MPLC on a 80g silica column eluted with 10% to 100% EtOAc in hexane. The solution was concentrated to provide 3-cyano-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)benzenesulfo namide. LC-MS: calculated for CigHM gOsSCzsHss gOsS 370.1 ; observed m/e: 371.3 (M+H) ⁺ (Rt 0.9 / 2 min).

Step B: 3-Sulfamoyl-2-(2H-tetrazol-5-yl)benzoic acid

3-cyano-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)benzenesulfo namide (50 mg, 0.135 mmol) was dissolved in dioxane (675 μΐ), MeOH (675 μΐ), and NaOH (225 μΐ, 1.350 mmol) was added. The reaction mixture was then heated to 90°C overnight. TFA (104 μΐ, 1.350 mmol) was added and the reaction was concentrate to provide a white solid. The white solid was dissolved in 2 mL TFA and heated to 45°C overnight then concentrated. The residue was purified by reverse phase HPLC with Phenomenex Polar-RP column eluted with 0% to 50% MeCN in water. The major UV active material was lyopholized to provide 3-sulfamoyl-2-(2H- tetrazol-5-yl)benzoic acid. LC-MS: calculated for C ₈ H7 5O4S 269.0; observed m/e: 270.2 (M) ⁺ ; 'H NMR δ (ppm) (MeOH): 8.38-8.35 (m, 2H), 7.89 (t, 1H).

EXAMPLE 298

3-(6-Aminopyridin-3-yl)-2-(lH-tetrazol-5-yl)benzene sulfonamide, TFA salt

Step A: 3-(6-Aminopyridin-3-yl)-l-(and 2-)(4-methoxybenzyl)-2-(lH-tetrazol-5- yl)benzene sulfonamide

A 20 mL microwave reaction vial was charged with a mixture of 3-bromo-2-(l- (4-methoxybenzyl)(lH-tetrazol-5-yl))benzenesulfonamide and 3-bromo-2-(2-(4- methoxybenzyl)(lH-tetrazol-5-yl))benzenesulfonamide (200 mg, 0.471 mmol), (6-aminopyridin- 3-yl)boronic acid hydrochloride (164 mg, 0.943 mmol), l, l'-Bis(di-tert- butylphosphino)ferrocene palladium (38.5 mg, 0.047 mmol), potassium carbonate (saturated aqueous solution, 3 mL, 0.471 mmol) and ethanol (8 mL). The vial was capped, and the reaction was heated to 120°C for 20 minutes in a microwave. The excess catalyst was filtered off and the reaction was concentrated. The residue was purified by normal phase ISCO on a 24g column eluted with 0% to 100% ethyl acetate in hexane. The pure fractions were concentrated to afford a mixture of 3-(6-aminopyridin-3-yl)-l-(and 2-)(4-methoxybenzyl)-2-(lH-tetrazol-5- yl)benzene sulfonamide. LC-MS: calculated for C2 ₀ H1 ₉ N7O ₃ S 437.5; observed m/e: 438.4 (M+H) ⁺ .

Step B: 3-(6-Aminopyridin-3-yl)-2-(lH-tetrazol-5-yl)benzene sulfonamide, TFA salt

The residue was dissolved in TFA (2 mL) and anisole (198 mg, 1.829 mmol) and heated to 45°C via an oil bath for 18 hr. The reaction mixture was purified by reverse phase HPLC column (acetonitrile/water/0.05% TFA system) and eluted with 0% to 20% MeCN in water. The solution was concentrated to afford 3-(6-aminopyridin-3-yl)-2-(lH-tetrazol-5- yl)benzene sulfonamide, TFA salt. LC-MS: calculated for C12H11 7O2S 317.3; observed m/e: 318.3 (M+H) ⁺ ; ^l H NMR δ (ppm) (MeOH): 8.27 (d, 1H), 7.89 (t, 1H), 7.8 (d, 1H), 7.63 (d, 1H), 7.52-7.56 (m, 1H), 6.87 (d, 1H). EXAMPLES 299-316

The following Examples 299-316 were prepared from the mixture of 3-bromo-2- (l-(and 2-)(4-methoxybenzyl)-2H-tetrazol-5-yl)benzenesulfonamide and the appropriate substituted aryl or heteroaryl boronic acid esters (from commercially available sources or prepared as described herein) according to the method described in Example 298 (except that boronic esters are used in place of the boronic acid).

sulfonamide

EXAMPLES 317-319

The following Examples 317-319 were prepared from the mixture of 3 -bromo-2- (l-(and 2-)(4-methoxybenzyl)-2H-tetrazol-5-yl)benzenesulfonamide and the appropriate substituted aryl or heteroaryl boronic acids (from commercially available sources or prepared as described herein) according to the method described in Example 298.

EXAMPLE 320

3 -(2-(Piperazin- 1 -yl)pyrimidin-5 -yl)-2-( -tetrazol-5 -yl)benzenesulfonamide

Step A: 3-(2-(Piperazin-l-yl)pyrimidin-5-yl)-2-(l-(and 2-)2-(4-methoxybenzyl)-2H- tetrazol-5-yl)benzenesulfonamide

A microwave reaction vial was charged with tert-butyl 4-(5-(4,4,5,5-tetramethyl- l,3,2-dioxaborolan-2-yl)pyrimidin-2-yl)piperazine-l-carboxyl ate (259 mg, 0.663 mmol) and a mixture of 3-bromo-2-(l-(4-methoxybenzyl)(lH-tetrazol-5-yl))benzenesulf onamide and 3- bromo-2-(2-(4-methoxybenzyl)(lH-tetrazol-5-yl))benzenesulfon amide (225 mg, 0.530 mmol). EtOH (5303 μΐ) and potassium phospate tribasic (1 M aq. solution, 1591 μί, 1.591 mmol) were added and the reaction mixture was sparged with 2 for 10 min. 1, l'-bis(di-tert- butylphosphino)ferrocene palladium dichloride (34.6 mg, 0.053 mmol) was added and the reaction vessel was sealed and heated to 100°C for 1 hr in a microwave. The crude reaction mixture was diluted with water and EtOAc. The organic was washed with brine, dried over Na ₂ S0 ₄ , filtered and concentrated. The residue was purified by reverse phase HPLC on a C18 column eluted with 5% to 90% MeCN in water with 0.05% TFA. The solution was concentrated to provide a mixture of 3-(2-(piperazin-l-yl)pyrimidin-5-yl)-2-(l-(and 2-)2-(4-methoxybenzyl)- 2H-tetrazol-5-yl)benzenesulfonamide. LC-MS: calculated for C2 ₈ H _{33 9} O5S 607.2; observed m/e: 608.6 (M+H) ⁺ ;

Step B: 3-(2-(Piperazin-l-yl)pyrimidin-5-yl)-2-(2H-tetrazol-5-yl)ben zenesulfonamide

The mixture of 3-(2-(piperazin-l-yl)pyrimidin-5-yl)-2-(l-(and 2-)2-(4- methoxybenzyl)-2H-tetrazol-5-yl)benzenesulfonamide was dissolved in TFA (2 mL) and anisole (200 μί) and heated to 45°C overnight. Purification by reverse phase HPLC with Phenomenex Polar RP column eluted with 0% to 80% MeCN in water. The solution was lyopholized to provide the title compound. LC-MS: calculated for C15H17 ₉ O2S 387.4; observed m/e: 387.4 (M+H) ⁺ ; 'H NMR δ (ppm) (DMSO): 8.75 (br s, 1H), 8.05-8.03 (m, 1H), 7.98 (s, 2H), 7.81 (br s, 1H), 7.70-7.69 (m, 1H), 3.90 (t, 2H), 3.17 (t, 2H). EXAMPLES 321-326

The following Examples 321-326 were prepared from the mixture of 3-bromo-2- ( 1 -(4-methoxybenzyl)( lH-tetrazol-5 -yl))benzenesulfonamide and 3 -bromo-2-(2-(4- methoxybenzyl)(lH-tetrazol-5-yl))benzenesulfonamide and the appropriate substituted aryl boronic acid esters (from commercially available sources or prepared as described herein) according to the method described in Example 320.

EXAMPLE 327

4'-((Dimethylamino)methyl)-2-(lH-tetrazol-5-yl)-[l,r-bipheny l]-3-sulfonamide, TFA salt

Step A: 4'-((Dimethylamino)methyl)-2-(l-(and 2-)(4-methoxybenzyl)-2-(lH-tetrazol-5- y 1)- [ 1 , 1 '-bipheny 1] -3 -sulfonamide

A 40 mL reaction vial was charged with the mixture of 3-bromo-2-(l-(4- methoxybenzyl)(lH-tetrazol-5-yl))benzenesulfonamide and 3-bromo-2-(2-(4- methoxybenzyl)(lH-tetrazol-5-yl))benzenesulfonamide (35 mg, 0.082 mmol), (4- ((dimethylamino)methyl)phenyl)boronic acid (44.3 mg, 0.247 mmol), potassium phosphate (52.5 mg, 0.247 mmol), diacetoxypalladium (5.56 mg, 0.025 mmol) and SPhos-Pd-G2 (20.32 mg, 0.049 mmol). The vial was capped via a red sure-seal cap, and the reaction was degassed via vacuum/nitrogen flushes (line with needle from manifold). THF (4 mL) was added via syringe, and again, the reaction was degassed via vacuum/nitrogen flushes. The reaction stirred at room temp for 15 minutes, and was then heated at 90°C via an oil bath for 18 hours. The excess catalyst was filtered off and the reaction was concentrated, and then purified by reverse phase HPLC column (acetonitrile/water/0.05% TFA system) and eluted with 5% to 100% MeCN in water. The solution was concentrated to afford product. LC-MS: calculated for C24H2 _{6 6} O ₃ S 478.6; observed m/e: 479.2 (M+H) ⁺ (Rt 0.79 / 2 min).

Step B : 4'-((Dimethylamino)methyl)-2-( lH-tetrazol-5 -yl)-[ 1 , 1 '-biphenyl] -3 -sulfonamide,

TFA salt

The residue was dissolved in TFA (500 μί) and anisole (7.23 mg, 0.067 mmol) and heated to 45°C for 18 hr. The reaction mixture was purified by reverse phase HPLC column (acetonitrile/water/0.05% TFA system) and eluted with 0% to 20% MeCN in water. The solution was concentrated to afford 4'-((dimethylamino)methyl)-2-(lH-tetrazol-5-yl)-[l,l'- biphenyl]-3-sulfonamide,TFA salt. LC-MS: calculated for C1 ₆ H1 ₈ N ₆ O2S 358.4; observed m/e: 359.3 (M+H) ⁺ ; ¾ NMR δ (ppm) (MeOH): 8.24 (d, 1H), 7.88 (t, 1H), 7.78 (d, 1H), 7.40 (d, 2H), 7.22 (d, 2H), 4.26 (s, 2H), 2.80 (s, 6H).

EXAMPLES 328-396

Parallel synthesis of 4'-(aminomethyl)-2-(lH-tetrazol-5-yl)-[l,r-biphenyl]-3-sulfo namides by reductive amination reaction

Step A: Reductive animation of the isomer mixture 4'-formyl-2-(l-(4-methoxybenzyl)- lH-tetrazol-5-yl)-[l,l'-biphenyl]-3-sulfonamide and 4'-formyl-2-(2-(4-methoxybenzyl)-2H- tetrazol-5-yl)-[l,l'-biphenyl]-3-sulfonamide (Reference Example 13) with primary and secondary amines

4'-formyl-2-( 1 -(4-methoxybenzyl)- lH-tetrazol-5-yl)-[ 1 , 1 '-biphenyl]-3 - sulfonamide and 4'-formyl-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-[l,l'-bip henyl]-3- sulfonamide (Reference Example 13) (25 mg, 0.056 mmol) and commercially available primary and secondary amines (0.111 mmol) in MeOH (0.5 mL) and tetrahydrofuran (0.5 mL) were treated with acetic acid (0.016 mL, 0.278 mmol). An excess of polymer supported sodium cyanaoborohydride was added and the mixtures were stirred for 18 hours. The mixtures were filtered and the filtrates were concentrated.

Step B: Removal of the PMB protective group under acidic conditions

To remove the PMB protecting group the residues from Step A were each dissolved in TFA (0.5 mL) and treated with Anisole (0.018 mL, 0.167 mmol). The mixtures were stirred at 50°C for 18 hours. The mixtures were concentrated under reduced pressure. DMSO (1 mL) was added to each crude product and the mixtures were filtered through a 0.4 micron filter. Purification by mass directed reverse phase HPLC afforded Examples 330-398.

Ex. Structure Name Calc'd. LC/MS

No. MW m/e

[M+H] ⁺ (M+H) ⁺

EXAMPLE 397

4'-(Ethoxymethyl)-2-(lH-tetrazol-5-yl)-[l,r-biphenyl]-3-sulf onamide

Step A: 4'-(Ethoxymethyl)- l-(and 2-)(4-methoxybenzyl)-2-(lH-tetrazol-5-yl)-[l,l'- biphenyl] -3 -sulfonamide

A 4 mL microwave reaction vial was charged with the mixture of 3-bromo-2-(l- (4-methoxybenzyl)(lH-tetrazol-5-yl))benzenesulfonamide and 3-bromo-2-(2-(4- methoxybenzyl)(lH-tetrazol-5-yl))benzenesulfonamide (150 mg, 0.354 mmol), (4- (chloromethyl)phenyl)boronic acid (120 mg, 0.707 mmol), 1 , l'-Bis(di-tert- butylphosphino)ferrocene palladium (28.9 mg, 0.035 mmol), potassium carbonate (saturated aqueous solution, 1.5 ml, 0.354 mmol) and ethanol (3 mL). The vial was capped, and heated in a microwave at 120°C for 20 minutes. The excess catalyst was filtered off, and the solution was concentrated and then purified by reverse phase HPLC column (acetonitrile/water/0.05% TFA system) eluted with 10% to 100% MeCN in water. The solution was concentrated to afford product. LC-MS: calculated for C ₂ 4H ₂ 5 50 ₄ S 479.5; observed m/e: 480.4 (M+H) ⁺ .

Step B: 4'-(Ethoxymethyl)-2-(lH-tetrazol-5-yl)-[l,l'-biphenyl]-3-sul fonamide

The residue was dissolved in TFA (1.5 uL) and anisole (108 mg, 1.001 mmol) and heated to 45°C for 18 hr. The reaction mixture was purified by reverse phase HPLC column (acetonitrile/water/0.05% TFA system) and eluted with 0% to 20% MeCN in water. The solution was concentrated to afford product. LC-MS: calculated for C1 ₆ H17 5O ₃ S 359.4; observed m/e: 360.3 (M+H) ⁺ ; ¾ NMR δ (ppm) (MeOH): 8.2 (d, 1H), 7.84 (t, 1H), 7.76 (d, 1H), 7.25 (d, 2H), 7.06 (d, 2H), 4.45 (s, 2H), 3.51 (q, 2H), 1.19 (t, 3H).

EXAMPLE 398

3-(5-Methylpyridin-2-yl)-2-(lH-tetrazol-5-yl)benzenesulfonam ide, TFA salt

Step A: 3-(5-Methylpyridin-2-yl)-2-(l-(4-methoxybenzyl)(lH-tetrazol- 5- yl))benzenesulfonamide and 3-(5-methylpyridin-2-yl)-2-(2-(4- methoxybenzyl)(lH-tetrazol-5-yl))benzenesulfonamide

A 40 mL reaction vial was charged with the mixture of 3-bromo-2-(l-(4- methoxybenzyl)(lH-tetrazol-5-yl))benzenesulfonamide and 3-bromo-2-(2-(4- methoxybenzyl)(lH-tetrazol-5-yl))benzenesulfonamide (50 mg, 0.118 mmol), and RuPhos precatalyst (18.31 mg, 0.024 mmol). The vial was capped via a red sure seal and degassed three times with vacuum/nitrogen (line with needle connected to manifold). Then, DMA (3 mL), THF (1.5 mL) and (5-methylpyridin-2-yl)zinc(II) bromide (0.471 ml, 0.236 mmol) were syringed into the vial. Again, the vial was degassed three times with vacuum/nitrogen (line with needle connected to manifold). After stirring at room temp for 10 minutes, the reaction was allowed to stir at 80°C via an oil bath for 18 hours. The reaction was diluted with ethyl acetate and quenched with NH ₄ C1 (saturated aqueous solution). The organic layer was extracted out and concentrated. The residue was purified by normal phase ISCO on a 4g column eluted with 0% to 100% ethyl acetate in hexane. The pure fractions were concentrated to afford product. LC-MS: calculated for C ₂ iH ₂ oN ₆ 0 ₃ S 436.5; observed m/e: 437.3 (M+H) ⁺ (Rt 0.96 / 2 min).

Step B: 3-(5-Methylpyridin-2-yl)-2-(lH-tetrazol-5-yl)benzenesulfonam ide, TFA salt

The residue was dissolved in TFA (800 uL) and anisole (9.29 mg, 0.086 mmol) and heated to 45°C for 18 hr. Purification by reverse phase HPLC column

(acetonitrile/water/0.05% TFA system) eluted with 0% to 20% MeCN in water. The solution was concentrated to afford 3-(5-methylpyridin-2-yl)-2-(lH-tetrazol-5-yl)benzenesulfonam ide, TFA salt. LC-MS: calculated for Ci ₃ H ₁₂ N ₆ 0 ₂ 316.3; observed m/e: 317.2 (M+H) ⁺ (Rt 0.32 / 2 min); 1H NMR δ (ppm) (MeOH): 8.27-8.32 (m, 2H), 7.87-7.95 (m, 2H), 7.67 (d, 1H), 7.22 (d, 1H), 2.33 (s, 3H). EXAMPLE 399

l-(lH-tetrazol-5-yl)naphthalene-2-sulfonamide

Step A: 2-((2-(trimethylsilyl)ethyl)thio)-l-naphthonitrile

A solution of n-butyllithium (2.5M in Hexane) (2.74 ml, 6.8 mmol) was added drop wise to a solution of 2,2,6,6-tetramethylpiperidine (1.15 ml, 6.8 mmol) in THF (5mL) while maintaining the temperature at 0°C. After 30 minutes of stirring, the reaction mixture was cooled to -78°C and a solution of 1-naphthonitrile (1 g, 6.53 mmol) in THF (3 mL) was added drop wise. The resulting dark solution was maintained at -78°C and stirred for 2 hours. A solution of iodine (1.74 g, 6.8 mmol) in THF (3 mL) was added drop wise and stirred at -78°C for 2 hours, then allowed to warm to room temperature overnight. The reaction mixtue was quenched with ¾0 and resulting mixture was extracted with EtOAc. The combined organic extracts were dried over Na ₂ S0 ₄ , filtered and concentrated. The resulting crude, 2-iodo-l- naphthonitrile (1.7 g, 6.1 mmol) and potassium carbonate (1.01 g, 7.3 mmol) were dissolved in DMF (10 ml). To that mixture, 2-(trimethylsilyl)ethanethiol (1.46 ml, 9.1 mmol) was added and stirred at room temperature under 2 overnight. The reaction mixture was washed with water and organic was extracted with EtOAc. The combined organic layer was dried over Na ₂ S0 ₄ , filtered and concentrated under vacuum. The crude was purfied by MPLC with hexanes and EtOAc to give desired compound. ¾ NMR (MeOD): δ 0.1 lppm (s, 9H), 1.03ppm (m, 2H), 3.28ppm (m, 2H), 7.61ppm (dd, J= 8.2 Hz, 1H), 7.64ppm (d, J= 8.8 Hz, 1H), 7.73ppm (d, J = 7.1 Hz, 1H), 7.98ppm (d, J= 8.2Hz, 1H), 8.03ppm (d, J= 8.8Hz, 1H), 8.09ppm, (d, J= 8.5Hz, 1H).

Step B: 2-((2-(trimethylsilyl)ethyl)sulfonyl)- 1-naphthonitrile

To a solution of 2-((2-(trimethylsilyl)ethyl)thio)- 1-naphthonitrile (1.35 g, 4.7 mmol) in DCM (50 ml) was added 3-chloroperoxybenzoic acid (2.9 g, 16.6 mmol). The mixture was stirred at room temperature under ₂ for 4 hours. The TLC indicated complete consumption of starting material. To a reaction mixture, sat. a ₂ S ₂ 03 was added and stirred for 15 minutes and then sat. aHC03 was added stirred for another 15 more minutes. The organic was extracted with DCM, dried over NaS0 ₄ , filtered and concentrated under vacuum. The crude was purfied by MPLC with hexanes and EtOAc to give desired compound. ^X H NMR (MeOD): δ 0.06ppm (9 H, s), 0.96ppm (2 H, m), 3.48ppm (2 H, m), 7.90ppm (ddd, J= 8.2 Hz, 1H), 7.96ppm (ddd, J= 8.5 Hz, 1H), 8.20 (d, J= 8.7, 1 H), 8.23ppm (d, J= 8.2 Hz, 1H), 8.46ppm (d, J= 8.2Hz, 1H), 8.49ppm (d, J= 8.7Hz, 1H).

Step C: 5-(2-((2-(trimethylsilyl)ethyl)sulfonyl)naphthalen-l-yl)-lH- tetrazole

A solution of 2-((2-(trimethylsilyl)ethyl)sulfonyl)-l-naphthonitrile (113 mg, 0.36 mmol) and azidotrimethyltin (370 mg, 1.78 mmol) in toluene (3 ml) was microwaved at 140°C for 1 hour. The reaction mixture was filtered and concentrated. The crude was dissolved in water/ACN and purified by HPLC with ACN and water with 0.05% TFA to afford the desired compound. LC-MS [M+l] ⁺ : 361.

Step D: l-(lH-tetrazol-5-yl)naphthalene-2-sulfonamide

To a solution of 5-(2-((2-(trimethylsilyl)ethyl)sulfonyl)naphthalen-l-yl)-lH- tetrazole (50 mg, 0.139 mmol) in THF (5 ml) was added tetrabutylammonium fluoride (0.42 ml, 0.42 mmol). The mixture was stirred for 16 hours at room temperature under N ₂ . A solution of sodium acetate (57 mg, 0.69 mmol) in water (0.32 ml, 18 mmol) and hydroxylamine-o-sulfonic acid (78 mg, 0.69 mmol) were added sequentially, and the mixture was allowed to stir at room temperature for 3 hours. The solvent was removed under vacuum and the crude was dissolved in water/ACN and purified by HPLC with ACN and water with 0.05% TFA to give desire compound as ammonium salt. The compound was dissolved in H ₂ 0 and acetone (minimum amount) and ran through a packed resin column (Dowex 50wx8, 100-200 mesh, ion-exchange resin, cas# 11 119-67-8) which was washed with IN NaOH and neutralized to pH~7) to give pure compound. LC-MS [M+H] ⁺ : 276.1.

EXAMPLE 400

3 -( 1 -aminoisoquinolin-7-yl)-2-( lH-tetrazol-5 -yl)benzenesulfonamide

3-(5,5-dimethyl-l,3,2-dioxaborinan-2-yl)-N,N-bis(4-methoxybe nzyl)-2-(l-(4- methoxybenzyl)-lH-tetrazol-5-yl)benzenesulfonamide (80 mg, 0.12 mmol), Chloro[(Di(l- Adamantyl)-N-Butylphosphine)-2-(2-Aminobiphenyl)]Palladium(I I) (7.7 mg, 0.011 mmol), Cesium Carbonate (1 12 mg, 0.344 mmol) and 7-Bromoisoquinolin- 1 -Amine (25.6 mg, 0.115 mmol) were weighed into a 1 dram vial and taken into the glove box. Toluene (1 mL) and Water (0.1 mL) were added and the mixture stirred at 110°C for 18 hours. The organics were removed in the genevac under reduced pressure.

To remove the PMB protecting group, TFA (1 mL) and Anisole (0.050 mL, 0.459 mmol) was added to the residue and the mixture stirred at 65°C for 2.5 hours. The mixture was allowed to cool, and the volatile organics were removed in the genenvac undder reduced pressure. The crude product was purified using mass directed reverse phase HPLC. LC-MS [M+H] ⁺ : 368.

EXAMPLES 401-415

Examples 401-415 in the following table were prepared in the same fashion as described for 3-(l-amino-7-isoquinolyl)-2-(lH-tetrazol-5-yl)benzenesulfona mide (EXAMPLE 400) above starting from 3-(5,5-dimethyl-l,3,2-dioxaborinan-2-yl)-N,N-bis(4-methoxybe nzyl)-2- (l-(4-methoxybenzyl)-lH-tetrazol-5-yl)benzenesulfonamide and heteroaryl bromides

(commercially available, known, or prepared as described herein).

412 3-(4-amino-7-quinolyl)-2-(lH- 368 368 tetrazol-5-yl)benzenesulfonamide

413 N=N 3 -isothiazolo[3 ,4-b]pyridin-3 -yl-2- 360 360

(lH-tetrazol-5- yl)benzenesulfonamide

414 N=N 3-isothiazolo[4,3 -b]pyridin-3 -yl-2- 360 360

S T /// NH ₂ (lH-tetrazol-5- yl)benzenesulfonamide

415 3-(8-amino-5-isoquinolyl)-2-(lH- 368 368 tetrazol-5-yl)benzenesulfonamide

N^ _j jjJ L^

EXAMPLES 416-419

Parallel synthesis of 3 -substituted 2-(lH-tetrazol-5-yl)benzenesulfonamides

Step A

Step A: Palladium catalyzed C-C coupling of arylboronic ester with bromides.

An isomeric mixture of 3-(5,5-dimethyl-l,3,2-dioxaborinan-2-yl)-N,N-bis(4- methoxybenzyl)-2-(l-(4-methoxybenzyl)-lH-tetrazol-5-yl)benze nesulfonamide and 3-(5,5- dimethyl- 1 ,3 ,2-dioxaborinan-2-yl)-N,N-bis(4-methoxybenzyl)-2-(2-(4-metho xybenzyl)-2H- tetrazol-5-yl)benzenesulfonamide, Reference Example 9, (80 mg, 0.12 mmol), were combined with commercially available or known aryl or heteroaryl bromides (0.138 mmol), cesium carbonate (1 12 mg, 0.344 mmol) and 2nd Generation Xphos Precatalyst (13.5 mg, 17 μιηοΐ) in a 1 dram vial and taken into the glove box. Dioxane (0.8 mL) and water (0.2 mL) were added and the mixture stirred at 85°C for 18 hours. Then 2 mL DCM and 1 mL saturated ammonium chloride was added and the mixtures were stirred for 5 minutes. The aqeuous layer was removed by pipette and the remaning organics concentrated under reduced pressure in the genevac.

Step B: Removal of the p-methoxybenzyl (PMB) protecting group under acidic conditions.

To each vial from Step A was added Anisole (0.125 ml, 1.15 mmol) and TFA (1 mL) and the mixture stirred at 60°C for 4 hours. The mixture was allowed to cool and the volatile organics removed in the genevac. DMSO (1 mL) was added and the mixtures were filtered through a 96 well 0.4 micron filter plate. These crude materials and others made in the same way were purified by mass directed reverse phase HPLC to afford Examples 416-419.

5 -yl)benzenesulfonamide

EXAMPLE 420

3-(2-Aminoquinazolin-7-yl)-2-(lH-tetrazol-5-yl)benzenesulfon amide

Step A: 3-(2-Aminoquinazolin-7-yl)-N,N-bis(4-methoxybenzyl)-2-(l-(4- methoxybenzyl)- lH-tetrazol-5-yl)benzenesulfonamide and 3-(2-aminoquinazolin-7-yl)-N,N-bis(4- methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)benze nesulfonamide

A mixture of 3-(5,5-dimethyl-l,3,2-dioxaborinan-2-yl)-N,N-bis(4- methoxybenzyl)-2-(l-(4-methoxybenzyl)-lH-tetrazol-5-yl)benze nesulfonamide and 3-(5,5- dimethyl- 1 ,3 ,2-dioxaborinan-2-yl)-N,N-bis(4-methoxybenzyl)-2-(2-(4-metho xybenzyl)-2H- tetrazol-5-yl)benzenesulfonamide (200 mg, 0.287 mmol), 7-bromoquinazolin-2-amine (96 mg, 0.430 mmol), cesium carbonate (280 mg, 0.860 mmol), Xphos Pd G2 (33.8 mg, 0.043 mmol) were placed in a microwave tube. Dioxane (2294 μΐ) and water (573 μΐ) were added to this tube. After degassing, the reaction mixture was heated at 85°C overnight. The reaction mixture was purified by column chromatography (0-10% MeOH/EtOAc) to afford the title compounds. LC/MS (M+l) ⁺ = 729.5.

Step B: 3-(2-Aminoquinazolin-7-yl)-2-(lH-tetrazol-5-yl)benzenesulfon amide

3-(2-Aminoquinazolin-7-yl)-N,N-bis(4-methoxybenzyl)-2-(l-(4- methoxybenzyl)- lH-tetrazol-5-yl)benzenesulfonamide and 3-(2-aminoquinazolin-7-yl)-N,N-bis(4- methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)benze nesulfonamide (133 mg, 0.182 mmol) was heated in TFA at 60°C for 2 hr. After cooling, the reaction mixture was concentrated and purified with Gilson (2-40% CHsCN/water with 0.1% TFA). The correct fractions were combined, concentrated and lypholized to give 3-(2-aminoquinazolin-7-yl)-2-(lH-tetrazol-5- yl)benzenesulfonamide. LC/MS (M+l) ⁺ = 369.3.

EXAMPLE 421

3-(2-Bromobenzo[d]thiazol-4-yl)-2-(lH-tetrazol-5-yl)benzenes ulfonamide

Step A: 3-(2-aminobenzo[d]thiazol-4-yl)-N,N-bis(4-methoxybenzyl)-2-( l-(4- methoxybenzyl)-lH-tetrazol-5-yl)benzenesulfonamide and 3-(2-aminobenzo[d]thiazol-4-yl)- N,N-bis(4-methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol- 5-yl)benzenesulfonamide

4-Bromobenzo[d]thiazol-2-amine (600 mg, 2.62 mmol), (3-(N,N-bis(4- methoxybenzyl)sulfamoyl)-2-( 1 -(4-methoxybenzyl)- lH-tetrazol-5-yl)phenyl)boronic acid and (3-(N,N-bis(4-methoxybenzyl)sulfamoyl)-2-(2-(4-methoxybenzyl )-2H-tetrazol-5- yl)phenyl)boronic acid (2473 mg, 3.93 mmol), 2nd Generation Xphos Precatalyst (309 mg, 0.393 mmol), CS2CO3 (2560 mg, 7.86 mmol) was placed in a reaction vessel, 1,4-Dioxane (1.40E+04 μΐ,) and Water (3492 μΐ,) were added. The reaction mixture was degassed for 20 min and heated at 85°C for 20 hr. LC-MS showed the completion of the reaction. After cooling, the reaction mixture was directly loaded onto a silica gel column, eluting with 0-20% MeOH/EtOAc to give the title compounds. LC/MS (M+l) ⁺ = 734.4

Step B: 3-(2-Bromobenzo[d]thiazol-4-yl)-N,N-bis(4-methoxybenzyl)-2-( l-(4- methoxybenzyl)-lH-tetrazol-5-yl)benzenesulfonamide and 3-(2-bromobenzo[d]thiazol-4-yl)- N,N-bis(4-methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol- 5-yl)benzenesulfonamide

3-(2-Aminobenzo[d]thiazol-4-yl)-N,N-bis(4-methoxybenzyl)-2-( l-(4- methoxybenzyl)-lH-tetrazol-5-yl)benzenesulfonamide and 3-(2-aminobenzo[d]thiazol-4-yl)- N,N-bis(4-methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol- 5-yl)benzenesulfonamide (1.56 g, 2.13 mmol) was added portionwise to a black solution of Copper(II) Bromide (0.570 g, 2.55 mmol) and Tert-Butyl Nitrite (0.351 g, 3.40 mmol) in acetonitrile (7.87 mL) at room temperature under N ₂ . The mixture was stirred for 30 min and then diluted with IN HQ and extracted with EtOAc. The organics were separated and purified by column chromatography (0-50%

EtOAc/Hexane) to give the title compounds. LC/MS (M+l) ⁺ = 797.6, 799.6

Step C: 3-(2-Bromobenzo[if|thiazol-4-yl)-2-(lH-tetrazol-5-yl)benzene sulfonamide

3-(2-Bromobenzo[if|thiazol-4-yl)-N,N-bis(4-methoxybenzyl)-2- (l-(4- methoxybenzyl)-lH-tetrazol-5-yl)benzenesulfonamide (100 mg, 0.125 mmol) was heated in TFA (2 mL) at 60°C for 3 hr. The reaction mixture was concentrated and the residue was purified with Gilson (5-70% CHsCN/water) with 0.1% TFA. The correct fractions were combined, concentrated and lypholized to give 3-(2-bromobenzo[<f]thiazol-4-yl)-2-(lH-tetrazol-5- yl)benzenesulfonamide. LC/MS (M+l) ⁺ = 437.2

EXAMPLE 422

3 -(Benzo [< Jthiazol-4-yl)-2-( lH-tetrazol-5 -yl)benzenesulfonamide

Step A: 3-(Benzo[d]thiazol-4-yl)-N,N-bis(4-methoxybenzyl)-2-(l-(4-me thoxybenzyl)-lH- tetrazol-5-yl)benzenesulfonamide and 3-(Benzo[d]thiazol-4-yl)-N,N-bis(4-methoxybenzyl)-2-(2- (4-methoxybenzyl)-2H-tetrazol-5-yl)benzenesulfonamide

3-(2-Bromobenzo[if|thiazol-4-yl)-N,N-bis(4-methoxybenzyl)-2- (l-(4- methoxybenzyl)- lH-tetrazol-5-yl)benzenesulfonamide and 3-(2-bromobenzo[<i]thiazol-4-yi)- N,N-bis(4-methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol- 5-yl)benzenesulfonamide (43 mg, 0.054 mmol) was hydrogenated with a ballon in the presence of Pd(OH) ₂ (37.8 mg, 0.054 mmol) at room temperaure overnight. Another 15 mg of Pd(OH)2 was added, and hydrogenation was continued for 5 hr until LC-MS showed the completion of the reaction. The reaction mixture was filtered and concentrated to give the title compounds. LC/MS (M+l) ⁺ = 719.8. Step B: 3-(Benzo[<f|thiazol-4-yl)-2-(lH-tetrazol-5-yl)benzenesulf onamide

3-(Benzo[if|thiazol-4-yl)-N,N-bis(4-methoxybenzyl)-2-(l-(4-m ethoxybenzyl)-lH- tetrazol-5-yl)benzenesulfonamide and 3-(benzo[<f|thiazol-4-yl)-N,N-bis(4-methoxybenzyl)-2-(2- (4-methoxybenzyl)-2H-tetrazol-5-yl)benzenesulfonamide (37 mg, 0.051 mmol) was heated in TFA (2 mL) at 60°C for 2 hr. The mixture was concentarted and purified with Gilson (3-80% CHsCN/water with 0.1% TFA). The correct fractions were combined, concentrated and lypholized to give 3-(benzo[<f|thiazol-4-yl)-2-(lH-tetrazol-5-yl)benzenesulf onamide. LC/MS (M+l)+ = 359.3.

EXAMPLE 423

3-(2-amino-l,3-benzothiazol-4-yl)-2-(2H-tetrazol-5-yl)-6-(tr ifluoromethyl)benzenesulfonamide

Step A: 3-(2-aminobenzo[d]thiazol-4-yl)-N,N-bis(4-methoxybenzyl)-2-( l-(4- methoxybenzyl)-lH-tetrazol-5-yl)-6-(trifluoromethyl)benzenes ulfonamide: To the reaction mixture of (3-[bis[(4-methoxyphenyl)methyl]sulfamoyl]-2-[l-[(4-methoxyp henyl)methyl]-lH- l,2,3,4-tetrazol-5-yl]-4-(trifluoromethyl)phenyl)boronic acid and (3-[bis[(4- methoxyphenyl)methyl]sulfamoyl]-2-[2-[(4-methoxyphenyl)methy l]-2H-l,2,3,4-tetrazol-5-yl]-4- (trifluoromethyl)phenyl)boronic acid (4.00 g, 5.73 mmol) was added 4-bromobenzo[<i]thiazol-2- amine (1708 mg, 7.46 mmol), PdCl ₂ (dppf) (420 mg, 0.573 mmol), and a ₂ C0 ₃ (1216 mg, 11.47 mmol) in water (1.43E+04 μΐ). Then 3.5 mL of dioxane was added. The reaction mixture was degassed for 20 min. The reaction mixture was sealed and heated at 85°C overnight. After removal of the solvent under reduced pressure, the crude reaction mixture was purified by column chromatography (100% hexane to 50% EtOAc/Hexane gradient) on a 330 g ISCO column to give the title compound as an tetrazole para-methoxybenzyl isomer mixture. LC-MS [M+H] ⁺ : 802.7.

Step B: 3-(2-amino-l,3-benzothiazol-4-yl)-2-(2H-tetrazol-5-yl)-6-

(trifluoromethyl)benzenesulfonamide: 3-(2-aminobenzo[d]thiazol-4-yl)-N,N-bis(4- methoxybenzyl)-2-( 1 -(4-methoxybenzyl)- lH-tetrazol-5-yl)-6-

(trifluoromethyl)benzenesulfonamide and its para-methoxybenzyl regioisomer (664 mg, 0.828 mmol) was heated in TFA (5 mL) at 60°C for 2 hr. LC-MS showed the reaction was complete. The mixture was concentrated and purified using a Gilson HPLC (3-75% CH3CN/water) with 0.1% TFA. The correct fractions were combined and concentrated. The resulting TFA salt was neutralized with a sex ion exchange cartridge. Lyophilization gave the title compound. LC-MS [M+H] ⁺ : 442.3.

EXAMPLE 424

3-(2-aminothiazol-5-yl)-6-bromo-2-(2H-tetrazol-5-yl)benzenes ulfonamide

Step A: 3-(2-aminothiazol-5-yl)-6-bromo-N.N-bis(4-methoxybenzyl)-2-( 2-(4- methoxybenzyl)-2H-tetrazol-5-yl)benzenesulfonamide

A microwave vial was charged with 6-bromo-3-iodo-N,N-bis(4-methoxybenzyl)- 2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)benzenesulfonamide (0.2 g, 0.253 mmol), 5-(4,4,5,5- tetramethyl- 1, 3, 2-dioxaborolan-2-yl)thiazol-2-amine hydrochloride (0.266 g, 1.012 mmol), potassium carbonate (0.210 g, 1.518 mmol) and PdCl ₂ (dppf)-CH ₂ Cl ₂ adduct (0.083 g, 0.101 mmol). The vial was sealed, degassed, and filled with dioxane (1.26 mL) and water (0.42 mL). The resulting mixture was heated overnight at 90°C. The reaction mixture was filtered over celite to removed palladium. The filtrate was diluted with EtO Ac and washed with water. The organic layer was dried over anhydrous MgS0 ₄ , filtered, concentrated and purified by silica gel column chromatography using 0-10% MeOH/DCM as mobile phase to afford the title compound. LC-MS (IE, m/z): 764.38 [M+2] ⁺ .

Step B: 3-(2-aminothiazol-5-yl)-6-bromo-2-(2H-tetrazol-5-yl)benzenes ulfonamide

To a solution of 3-(2-aminothiazol-5-yl)-6-bromo-N,N-bis(4-methoxybenzyl)-2-

(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)benzenesulfonamide (80 mg, 0.105 mmol) in DCM (0.52 mL) was added anisole (1 14 pL, 1.049 mmol) and TFA (808 μί, 10.49 mmol) at rt. The resulting mixture was heated at 80°C for 1 hr. After removing the volatile the residue was purified by reverse phase HPLC using DMSO to load sample and 5-45 % acetonitrile/water (0.1% formic acid as additive) as mobile phase over 10 min to give the title compound. LC-MS

(IE, m/z): 404.01 [M+2] ⁺ .

EXAMPLE 425

N-((4'-bromo-3'-sulfamoyl-2'-(2H-tetrazol-5-yl)-rL -biphenyl1-4-yl)methyl)formimidamide

Step A: fert-butyl 4'-bromo-2'- 2- 4-methoxybenzylV2H-tetrazol-5-ylV3'-sulfamoyl-riJ'- biphenyl1-4-yl)methyl)carbamate

A microwave vial was charged with 6-bromo-3-iodo-2-(2-(4-methoxybenzyl)- 2H-tetrazol-5-yl)benzenesulfonamide (0.4 g, 0.727 mmol), (4-(((tert- butoxycarbonyl)amino)methyl)phenyl)boronic acid (0.402 g, 1.600 mmol), Na ₂ C03 (0.231 g, 2.181 mmol) and PdCl2(dppf)-CH2Cl2 adduct (0.089 g, 0.109 mmol). The vial was sealed, degassed, and filled with dioxane (3.64 mL) and water (1.21 mL). The resulting mixture was heated overnight at 80°C. The reaction mixture was filtered over celite to removed palladium. The filtrate was evaporated and the residue was purified by silica gel chromatograph eluting with 0-10% MeOH/DCM to give the title compound.

Step B: 4'-(aminomethyl)-4-bromo-2-(2-(4-methoxybenzyl)-2H-tetrazol- 5-yl)-r 1 , 1 '- biphenyll-3 -sulfonamide

To the solution of tert-butyl ((4'-bromo-2'-(2-(4-methoxybenzyl)-2H-tetrazol-5- yl)-3'-sulfamoyl-[l, l'-biphenyl]-4-yl)methyl)carbamate (580 mg, 0.921 mmol) in DCM (18 mL) was added anisole (2.0 mL, 18.43 mmol) and TFA (7.1 mL, 92 mmol) at rt. The resulting mixture was stirred at rt for 1 hr. After removing the volatile the residue was purified by ion exchange column (load sample and rinse with MeOH, rinse out product with 2 M NH ₃ in MeOH) to give the product as a free amine. LC-MS (IE, m/z): 531.11 [M+2] . Step C: N-((4'-bromo-2'-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-3'-su lfamoyl-ri .l'- biphenyll-4-yl)methyl)formimidamide

4'-(aminomethyl)-4-bromo-2-( 1 -(4-methoxybenzyl)- 1 H-tetrazol-5 -yl)- [ 1, 1'- biphenyl]-3 -sulfonamide (80 mg, 0.151 mmol) in DMF (1.5 mL) was treated with ethyl formimidate hydrochloride (19.87 mg, 0.181 mmol) and DIPEA (106 μί, 0.604 mmol) at 0°C. The reaction mixture was stirred at rt overnight. LC-MS showed the reaction was not completed.

More reagents were added with 20 mg ethyl formimidate hydrochloride and 0.1 mL of DIPEA.

After stirring once more overnight, the reaction mixture was concentrated and purified with reverse phase HPLC eluting with 5-70% CH3CN/water with 0.1% TFA to afford the title compound. LC-MS (IE, m/z): 558.28 [M+2] ⁺ .

Step D: N-((4'-bromo-3'-sulfamoyl-2'-(2H-tetrazol-5-vn-ri . l'-biphenyl1-4- yl)methyl)formimidamide

To the solution of N-((4'-bromo-2'-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-3'- sulfamoyl-[l, l'-biphenyl]-4-yl)methyl)formimidamide (20 mg, 0.036 mmol) in DCM (0.72 mL) was added anisole (78 μί, 0.719 mmol) and TFA (277 μί, 3.59 mmol) at rt. The resulting mixture was heated at 80°C for 2 hr. After removing the volatile the residue was purified by reverse phase HPLC eluting with 5-40 % acetonitrile/water (0.1% formic acid) to give the title product. LC-MS (IE, m/z): 438.32 [M+2] ⁺ .

EXAMPLE 426

3-(6-((2-hydroxyethyl)amino)pyridin-3-yl)-2-(2H-tetrazol-5-y l)benzenesulfonamide

Step A: 3-(6-((2-hvdroxyethyl)amino)pyridin-3-yl)-N,N-bis(4-methoxyb enzyl)-2-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)benzenesulfonamide

In a MW vial, 2-aminoethanol (12 μΕ, 0.202 mmol), 3-(6-bromopyridin-3-yl)- N,N-bis(4-methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol- 5-yl)benzenesulfonamide (100 mg, 0.135 mmol), Cs ₂ C0 ₃ (88 mg, 0.270 mmol) and bis((2-isobutyrylcyclohex-l-en-l- yl)oxy)copper (21.47 mg, 0.054 mmol) were suspended in DMF (1.3 mL). The vial was sealed, and degassed with N ₂ . The reaction mixture was heated at 100°C for 24 hr. After filtration through celite, the filtrate was concentrated and the residue was purified on silica gel column using 0-15% MeOH/DCM to give the title compound. LC-MS (IE, m/z): 722.99 [M+l] ⁺ .

Step B: 3-(6-((2-hvdroxyethyl)amino)pyridin-3-yl)-2-(2H-tetrazol-5- vDbenzenesulfonamide

To a solution of 3-(6-((2-hydroxyethyl)amino)pyridin-3-yl)-N,N-bis(4- methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)benze nesulfonamide (80 mg, 0.11 1 mmol) in DCM (554 μΓ) was added anisole (120 μί, 1.108 mmol) and TFA (854 μί, 11.08 mmol) at rt. The resulting mixture was heated at 80°C for 1 hr. After removing the volatile the residue was purified by reverse phase HPLC using DMSO to load sample and 5-60 %

acetonitrile/water (0.1% TFA as additive) as mobile phase over 10 min to give the title compound. LC-MS (IE, m/z): 362.31 [M+l] ⁺ .

EXAMPLE 427

3-(2-(6-aminopyridin-3-yl)ethyl)-2-(2H-tetrazol-5-yl)benzene sulfonamide

Step A: 3-bromo-N.N-bis(4-methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-t etrazol-5- vDbenzenesulfonamide

To a solution of 3-bromo-2-(2-(4-methoxybenzyl)-2H-tetrazol-5- yl)benzenesulfonamide (20.0 g, 47.1 mmol) in acetone (300 mL) were added PMB-C1 (16.2 g, 104 mmol), KI (17.2 g, 104 mmol) and K ₂ CO ₃ (26.1 g, 188 mmol). The resultant mixture was stirred for 3 hr at 70°C. The mixture was concentrated in vacuo and 400 mL of water was added. The mixture was extracted with ethyl acetate (100 mL x 3). The organic layer was dried over anhydrous sodium sulfate, filtered and the filtrate was concentrated in vacuo to give the crude product. The crude product was purified by silica gel chromatography (20 % EtOAc in petroleum ether) to give the title compound. MS (ESI): m/z (M+H) ⁺ 663.9, 665.9.

Step B: N,N-bis(4-methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol- 5-yl)-3- vinylbenzenesulfonamide

To a solution of 3-bromo-N,N-bis(4-methoxybenzyl)-2-(2-(4-methoxybenzyl)- 2H-tetrazol-5-yl)benzenesulfonamide (10.0 g, 15.1 mmol) in dioxane/water (120/12 mL) were added potassium vinyltrifluroborate (4.03 g, 30.2 mmol), a ₂ C03 (3.19 g, 30.1 mmol) and Pd(dppf)Cl ₂ (2.20 g, 3.01 mmol) under nitrogen atmosphere. The mixture was stirred for overnight at 110°C. The mixture was filtered and the filtrate was concentrated in vacuo, the residue was purified by silica gel chromatography (30 % EtOAc in petroleum ether) to give the title compound. MS (ESI): m/z (M+H) ⁺ 612.1. Step C: teit-butyl (E)-(5-(3 -CN.N-bisC 4-methoxybenzyl)sulfamoyl)-2-( 2-Γ4- methoxybenzyl -2H-tetrazol-5-yl styryl pyridin-2-yl carbamate

In the reaction vessel tert-butyl (5-bromopyridin-2-yl)carbamate (0.035 g, 0.128 mmol), and ,N-bis(4-methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5 -yl)-3- vinylbenzenesulfonamide (0.094 g, 0.154 mmol) were combined, followed by tBu ₃ P HBF ₄

(0.015 g, 0.051 mmol), Pd ₂ (dba) ₃ (0.012 g, 0.013 mmol) and dicyclohexylmethylamine (0.041 ml, 0.192 mmol). This mixture was then evacuated and backfilled with N ₂ (3 times). Then dry, degassed dioxane (1.28 mL) was added to this flask. This mixture was stirred at 100°C overnight. The mixture was cooled, filtered and the solvent was evaporated under reduced pressure. The residue was purified by silica gel chromatography eluting with 0-100%

EtOAc/hexan to give the title compound. LC-MS (IE, m/z): 804.31 [M+l] ⁺ .

Step D: 3-(2-(6-aminopyridin-3-yl)ethyl)-2-(2H-tetrazol-5-yl)benzene sulfonamide

To a solution of tert-butyl (5-(3-( ,N-bis(4-methoxybenzyl)sulfamoyl)-2-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)phenethyl)pyridin-2-yl)carba mate (50 mg, 0.062 mmol) in DCM (310 μΐ was added anisole (67 μί, 0.620 mmol) and TFA (478 μΐ, 6.20 mmol) at rt. The resulting mixture was heated at 80°C for 1 hr. After removing the volatile the residue was purified by reverse phase HPLC using DMSO to load sample and 5-55 % acetonitrile/water (0.1% TFA as additive) as mobile phase over 10 min to give the title compound. LC-MS (IE, m/z): 346.12 [M+l] ⁺ .

EXAMPLE 428

3-(2-amino-lH-benzor(i1imidazol-7-yl)-2-(2H-tetrazol-5-yl)be nzenesulfonamide

Step A: 3-(2-amino-lH-benzord1imidazol-7-yl)-N,N-bis(4-methoxybenzyl )-2-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)benzenesulfonamide A microwave vial was charged with cesium carbonate (0.280 g, 0.860 mmol), 2nd generation XPhos precatalyst (0.045 g, 0.057 mmol), 7-chloro-lH-benzo[d]imidazol-2- amine (0.072 g, 0.430 mmol) and 3-(5,5-dimethyl-l,3,2-dioxaborinan-2-yl)-N,N-bis(4- methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)benze nesulfonamide (0.2 g, 0.287 mmol). The vial was sealed, degassed, and filled with dioxane (1.529 ml) and water (0.382 ml). The resulting mixture was heated overnight at 80°C. The reaction mixture was filtered over celite to removed palladium. The filtrate was concentrated and the residue was purified by silica gel column chromatography using 0-10% MeOH/DCM as mobile phase to afford the title product. MS (ESI): m/z (M+H) ⁺ 717.48. Step B: 3-(2-amino-lH-benzord1imidazol-7-yl)-2-(2H-tetrazol-5-yl)ben zenesulfonamide

To the solution of 3-(2-amino-lH-benzo[d]imidazol-7-yl)-N,N-bis(4- methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)benze nesulfonamide (200 mg, 0.279 mmol) in DCM (1.4 mL) was added anisole (303 μΐ, 2.79 mmol) and TFA (2150 μΐ, 27.9 mmol) at rt. The resulting mixture was stirred at 80°C for 1 hr. After removing the volatile the residue was purified by reverse phase HPLC (5-35% ACN/water, 0.1% TFA as additive) to give the title compound. MS (ESI): m/z (M+H) ⁺ 357.31

EXAMPLE 429

EXAMPLE 429 was prepared in an analogous fashion to EXAMPLE 428, 3-(2- amino-lH-benzo[i/]imidazol-7-yl)-2-(2H-tetrazol-5-yl)benzene sulfonamide, starting from 3-(5,5- dimethyl- 1,3, 2-dioxaborinan-2-yl)-N,N-bis(4-methoxybenzyl)-2-(2-(4-methox ybenzyl)-2H- tetrazol-5- l)benzenesulfonamide and corresponding halides listed below.

yl)benzenesulfonamide

EXAMPLE 430

3.6-bisr4-(4-piperidyl)phenyll-2-(2H-tetrazol-5-yl)benzenesu lfonamide

Step A: di-tert-butyl 4.4'-(2'-(N.N-bis(4-methoxybenzyl)su^

methoxybenzyl)-2H-tetrazol-5-yl)-| ^" l .r:4'. l"-terphenyll-4.4"-diyl)bis(piperidine-l-carboxylate)

A microwave vial was charged with 6-bromo-3-iodo-N,N-bis(4-methoxybenzyl)- 2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)benzenesulfonamide (0.5 g, 0.633 mmol), tert-butyl 4- (4-(4,4,5,5-tetramethyl-l,3,2-dioxaborolan-2-yl)phenyl)piper idine-l-carboxylate (0.294 g, 0.759 mmol), PdCl ₂ (dppf)-CH ₂ Cl ₂ adduct (0.052 g, 0.063 mmol) and sodium carbonate (0.201 g, 1.898 mmol). The vial was sealed, degassed, and filled with dioxane (3.37 mL) and water (0.84 mL). The resulting mixture was heated overnight at 70°C. The reaction mixture was filtered over celite to removed palladium. The filtrate was diluted with EtOAc and washed with water. The organic layer was dried over anhydrous MgS0 ₄ , filtered, concentrated and purified by silica gel column chromatography using 0-100% EtOAc/Hexanes as mobile phase to afford the title product. LC-MS (IE, m/z): 1 105.6 [M+l .

Step B: 3,6-bisr4-(4-piperidyl)phenyl1-2-(2H-tetrazol-5-yl)benzenesu lfonamide

To the solution of di-tert-butyl 4,4'-(2'-(N,N-bis(4-methoxybenzyl)sulfamoyl)-3'- (2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-[l, :4', l"-terphenyl]-4,4"-diyl)bis(piperidine-l- carboxylate) (200 mg, 0.181 mmol) in DCM (3.6 mL) was added anisole (394 μί, 3.62 mmol) and TFA (1.4 mL, 18.11 mmol) at 0°C. The resulting mixture was heated at rt for 1 hr. After completely removing the volatile, the residue was redissolved in DCM (3.6 mL). Anisole (394 μί, 3.62 mmol) and TFA (1.4 mL, 18.11 mmol) were added, and the reaction mixture was heated at 80°C for 1 hr. After removing the volatile the residue was purified (DMSO loading) on reverse phase HPLC using 5-70 % acetonitrile/water (0.1% formic acid) as eluent over 10 min to give the title compound. LC-MS (IE, m/z): 544.49 [M+l] ⁺ . EXAMPLES 431 and 432

431 (fast eluting isomer): 3-( ^' 2-( ^' ( ^' lr,4s -4-aminocvclohexyl ethyl -2-( ^' 2H-tetrazol-5-yl -6- (trifluoromethyl)benzenesulfonamide

432 (slow eluting isomer): 3-(2-((ls.4r)-4-aminocyclohexyl)ethyl)-2-(2H-tetrazol-5-yl)- 6- (trifluoromethyl)benzenesulfonamide

Fast eluting isomer Slow eluting isomer

Step A: tert-butyl (4-(3-rN.N-bis(4-methoxybenzyl)sulfamoyl)-2-(2-(4-methoxyben zyD-

2H-tetrazol-5-yl)-4-(trifluoromethyl)phenethyl)cvclohexyl )carbamate

A microwave vial was charged with nickel(II) idodide (25.6 mg, 0.082 mmol), manganese (90 mg, 1.638 mmol), tert-butyl (4-(2-iodoethyl)cyclohexyl)carbamate (289 mg, 0.819 mmol), bathophenanthroline (27.2 mg, 0.082 mmol) and 3-bromo-N,N-bis(4- methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-6-

(trifluoromethyl)benzenesulfonamide (400 mg, 0.546 mmol). The vial was sealed, purged with N ₂ for 10 min, and filled with DMA (3640 μΐ). The resulting mixture was purged with N ₂ for another 10 min and heated overnight at 80°C. The reaction mixture was filtered over celite to remove metal. The filtrate was concentrated and purified by silica gel column chromatography using 0-100% EtOAc/hexane as mobile phase to afford the title compound. LC-MS (IE, m/z):

Step B: 431 (fast eluting isomer): 3-(2-((lr,4s)-4-aminocvclohexyl)ethyl)-2-(2H-tetrazol- 5-yl)-6-(trifluoromethyl)benzenesulfonamide

432 (slow eluting isomer): 3-(2-((ls,4r)-4-aminocvclohexyl)ethyl)-2-(2H-tetrazol-5-yl)- 6-(trifluoromethyl)benzenesulfonamide

To tert-butyl (4-(3-( ,N-bis(4-methoxybenzyl)sulfamoyl)-2-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)-4-(trifluoromethyl)phenethy l)cyclohexyl)carbamate (330 mg, 0.375 mmol) was added anisole (204 μΕ, 1.877 mmol) and TFA (2.9 mL, 37.5 mmol) at rt (neat TFA, no solvent). The resulting mixture was stirred at rt for 2 hr. After removing the volatile the residue was passed through SCX ion exchange column to remove debromide side product from the coupling reaction. To the free amine was added anisole (204 μΐ _^ , 1.877 mmol) and TFA (2.9 mL, 37.5 mmol) at rt (neat TFA, no solvent). The resulting mixture was heated at 80°C for 2 hr. After removing the volatile the residue was purified (DMSO loading) on reverse phase HPLC using 5-40 % acetonitrile/water (0.1% NH40H as additive) to give the title compounds. 431 LC-MS (IE, m/z): 419.40 [M+l] ⁺ . 432 LC-MS (IE, m/z): 419.43 [M+l] ⁺ .

EXAMPLE 433

4'-(azetidin-3-yl)-2-(2H-tetrazol-5-yl)-4-(trifluoromethyl)- [l,r-biphenyl]-3-sulfonamide

Step A: 4'-(azetidin-3-yl)-N,N-bis(4-methoxybenzyl)-2-(2-(4-methoxyb enzyl)-2H- tetrazol-5-yl)-4-(trifluoromethyl)-[l.r-biphenyll-3-sulfonam ide

The mixture of 2nd generation PCy3 precatalyst (81 mg, 0.137 mmol), potassium acetate (402 mg, 4.10 mmol), 3-bromo-N,N-bis(4-methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H- tetrazol-5-yl)-6-(trifluoromethyl)benzenesulfonamide (1000 mg, 1.365 mmol) and 5,5,5',5'- tetramethyl-2,2'-bi(l,3,2-dioxaborinane) (925 mg, 4.10 mmol) in dioxane (6.8 mL) was degassed with N2. The resulting mixture was heated at 75°C for 6 hr. LCMS indicated complete coversion to boronic acid. 3-(4-chlorophenyl)azetidine (343 mg, 2.048 mmol), potassium carbonate (943 mg, 6.83 mmol) and 2nd generation XPhos precatalyst (161 mg, 0.205 mmol) were added followed by 2 mL water. The reaction mixture was degassed with 2 and heated at 90°C overnight. After cooling to rt the mixture was filtered through celite, the filtrate was concentrated and the residue was purified by silica gel column chromatography using 0-10%

MeOH/DCM (with NH3 as additive) as mobile phase to afford the title compound. LC-MS (IE,

Step B: 4'-(azetidin-3-yl)-2-(2H-tetrazol-5-yl)-4-(trifluoromethyl)- rLr-biphenyl1-3- sulfonamide

To a solution of 4'-(azetidin-3-yl)-N,N-bis(4-methoxybenzyl)-2-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)-4-(trifluoromethyl)-[l,r-bi phenyl]-3-sulfonamide (90 mg, 0.1 15 mmol) in DCM (573 μΐ was added anisole (125 μΐ, 1.147 mmol) and TFA (883 μΐ, 1 1.47 mmol) at rt. The resulting mixture was stirred at 80°C for 1 hr to remove the PMB protection. After removing the volatile the residue was purified by reverse phase HPLC using DMSO to load sample and 5-55 % acetonitrile/water (0.1% TFA as additive) as mobile phase over 10 min to give the final product. LC-MS (IE, m/z): 425.42 [M+l] ⁺ .

EXAMPLE 434

3 -(3 '-sulfamoyl-2'-(2H-tetrazol-5-yl)-4'-(trifluoromethyl)- [1, 1 '-biphenyl]-4-yl)azetidine- 1 - carboximidamide

Step A: tert-butyl 4-(4'-chloro-3'-sulfamoyl-2'-(2H-tetrazol-5-yl)-r 1 , 1 '-biphenyll-4- vDpiperidine- 1 -carboxylate

4'-(azetidin-3 -yl)-N,N-bis(4-methoxybenzyl)-2-( 1 -(4-methoxybenzyl)- 1 H- tetrazol-5-yl)-4-(trifluoromethyl)-[l,r-biphenyl]-3-sulfonam ide (60 mg, 0.076 mmol) in DMF (1.5 mL) was treated with lH-pyrazole-1 -carboxamidine hydrochloride (17.93 mg, 0.122 mmol) and DIPEA (66.8 μΐ, 0.382 mmol). The reaction mixture was stirred at rt overnight. LC-MS showed the reaction was not completed. More reagents were added with lH-pyrazole-1- carboxamidine hydrochloride (17.93 mg, 0.122 mmol) and DIPEA (66.8 μΐ, 0.382 mmol). After once more overnight, the reaction mixture was purified with reverse phase HPLC (10-90% MeCN/water as gradient) to afford the titlecompound. LC-MS (IE, m/z): 827.69 [M+l] ⁺ .

Step B: 4-chloro-4'-(piperidin-4-yl)-2-(2H-tetrazol-5-yl)-r 1 , 1 '-biphenyll -3 -sulfonamide

To the solution of 3-(2'-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-3'-(N-(4- methoxybenzyl)sulfamoyl)-4'-(trifluoromethyl)-[l,r-biphenyl] -4-yl)azetidine-l- carboximidamide (30 mg, 0.042 mmol) in DCM (212 μΕ) was added anisole (46.1 μΐ, 0.424 mmol) and TFA (327 μΐ, 4.24 mmol) at rt. The resulting mixture was stirred at 80°C for 1 hr. After removing the volatile the residue was purified by reverse phase HPLC (5-60% ACN/water, 0.1% TFA as additive) to give the title compound. LC-MS (IE, m/z): 467.39 [M+l] ⁺ . EXAMPLE 435

1 , 1 -dimethyl-3 -(3 '-sulfamoyl-2'-(2H-tetrazol-5 -yl)-4'-(trifluoromethyl)- [1,1 '-biphei

yl)azetidin- 1 -ium

Step A: 3- 3'-(N,N-bis 4-methoxybenzvnsulfamoylV2'- 2- 4-methoxybenzylV2H- tetrazol-5-yl)-4'-(trifluoromethyl)- [1.1 '-biphenyl] -4-yl)- 1.1 -dimethylazetidin- 1 -ium

To the solution of 4'-(azetidin-3-yl)-N,N-bis(4-methoxybenzyl)-2-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)-4-(trifluoromethyl)-[l,r-bi phenyl] -3 -sulfonamide (60 mg, 0.076 mmol) in acetone (2 ml) was added K ₂ C0 ₃ (63.4 mg, 0.459 mmol) and Mel (0.029 ml, 0.459 mmol). The resulting mixture was stirred at rt overnight. After concentration the residue was purified on reverse phase HPLC using 40-100% acetonitrile/water (0.05% TFA) to give the title compound. LC-MS (IE, m/z): 813.64 [M] ⁺ .

Step B: 1.1 -dimethyl-3 -(3 '-sulfamoyl-2'-(2H-tetrazol-5 -yl)-4'-(trifluoromethyl)-[ 1.1'- biphenyl1-4-yl)azetidin- 1 -ium

To the solution of 3-(2'-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-3'-(N-(4- methoxybenzyl)sulfamoyl)-4'-(trifluoromethyl)- [1,1 '-biphenyl] -4-yl)- 1 , 1 -dimethylazetidin- 1 -ium (20 mg, 0.029 mmol) in DCM (144 μΐ was added anisole (31.3 μΐ, 0.288 mmol) and TFA (222 μί, 2.88 mmol) at rt. The resulting mixture was stirred at 80°C for 1 hr. After removing the volatile the residue was purified by reverse phase HPLC (5-50% ACN/water, 0.1% TFA as additive) to give the title compound. LC-MS (IE, m/z): 453.36 [M] ⁺ .

EXAMPLE 436

4'-(4-aminopiperidin-4-yl)-2-(2H-tetrazol-5-yl)-4-(trifluoro methyl)-[l,r-biphenyl]-3- sulfonamide

Step A: tert-butyl 4-amino-4-( ^' 3'-nS[,N-bis( ^' 4-methoxybenzyl sulfamoyl -2'-( ^' 2-( ^' 4- methoxybenzyl -2H-tetrazol-5-yl -4'-( ^' trifluoromethyl -r 1 , 1 '-biphenyl1-4-yl piperidine- 1 - carboxylate

The mixture of 5,5,5',5'-tetramethyl-2,2'-bi(l,3,2-dioxaborinane) (370 mg, 1.638 mmol), 3-bromo-N,N-bis(4-methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-t etrazol-5-yl)-6- (trifluoromethyl)benzenesulfonamide (400 mg, 0.546 mmol), PCy3 2nd generation precatalyst (32.2 mg, 0.055 mmol) and potassium acetate (161 mg, 1.638 mmol) in dioxane (5.5 mL) was degassed with N ₂ . The resulting mixture was heated at 75°C for 6 hr. LCMS indicated complete conversion to boronic acid. Tert-butyl 4-amino-4-(4-bromophenyl)piperidine-l -carboxylate (which can be prepared in an analogous fashion as described for tert-butyl 4-amino-4-(4- chlorophenyl)piperidine-l -carboxylate in Example 283, Steps A-F; 233 mg, 0.655 mmol), Pd(dppf)Cl2 (44.6 mg, 0.055 mmol), and potassium carbonate (377 mg, 2.73 mmol) were added followed by 1.5 mL water. The reaction mixture was degassed with N ₂ and heated at 90°C overnight. After cooling to rt, the mixture was filtered through celite, the filtrate was concentrated and the residue was purified by silica gel column chromatography using 0-10% MeOH/DCM as mobile phase to give the title compound. LC-MS (IE, m/z): 928.74 [M+l] ⁺ .

Step B: 4'-(4-aminopiperidin-4-yl)-N-(4-methoxybenzyl)-2-(2-(4-metho xybenzyl)-2H- tetrazol-5-yl)-4-(trifluoromethyl)-rLr-biphenyl1-3-sulfonami de

To the solution of tert-butyl 4-amino-4-(3'-(N,N-bis(4- methoxybenzyl)sulfamoyl)-2'-(2-(4-methoxybenzyl)-2H-tetrazol -5-yl)-4'-(trifluoromethyl)-[l,r- biphenyl]-4-yl)piperidine-l -carboxylate (100 mg, 0.108 mmol) in DCM (539 μΚ) was added anisole (117 μί, 1.078 mmol) and TFA (830 μί, 10.78 mmol) at rt. After 2 hr the reaction mixture was treated with ion exchange column (load sample and rinse with MeOH, rinse out product with 2 M NH ₃ in MeOH) to give the title compound. LC-MS (IE, m/z): 708.52 [M+l] ⁺ . Step C: 4'-(4-aminopiperidin-4-yl)-2-(2H-tetrazol-5-yl)-4-(trifluoro methyl)-rLr- biphenyll-3 -sulfonamide

To the solution of 4'-(4-aminopiperidin-4-yl)-N-(4-methoxybenzyl)-2-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)-4-(trifluoromethyl)-[l,r-bi phenyl] -3 -sulfonamide (153 mg, 0.216 mmol) in DCM (1.1 mL) was added anisole (234 μί, 2.155 mmol) and TFA (2.5 μί, 32.3 mmol) at rt. The resulting mixture was stirred at 80°C for 1 hr. After removing the volatile the residue was purified by reverse phase HPLC (DMSO loading sample; 5-35% ACN/water, 0.1% TFA as additive) to give the title compound. LC-MS (IE, m/z): 468.32 [M+l .

EXAMPLE 437

4'-(4-amino-l-(iminomethyl)piperidin-4-yl)-2-(2H-tetrazol-5- yl)-4-(trifluoromethyl)-[l,r- biphenyl]-3-sulfonamide

Step A: 4'-(4-amino-l-(iminomethyl)piperidin-4-yl)-N.N-bis(4-methoxy benzyl)-2-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)-4-(trifluoromethyl)-rL -biphenyl1-3-sulfonamide

4'-(4-aminopiperidin-4-yl)-N-(4-methoxybenzyl)-2-( 1 -(4-methoxybenzyl)- 1 H- tetrazol-5-yl)-4-(trifluoromethyl)-[l,r-biphenyl]-3-sulfonam ide (30 mg, 0.042 mmol) in DMF (424 μΕ) was treated with ethyl formimidate hydrochloride (5.57 mg, 0.051 mmol) and DIPEA (29.6 μί, 0.170 mmol) at rt. After overnight LC-MS showed the reaction was not completed. Additional reagents with ethyl formimidate hydrochloride (5.57 mg, 0.051 mmol) and DIPEA (29.6 μί, 0.170 mmol) were added and the reaction was monitored carefully by LCMS. The reaction was complete in another 7 hr, and purified by reverse phase HPLC (10-90%

MeCN/water as gradient, 0.1% TFA as additive) to give the title compound. LC-MS (IE, m/z): 735.64 [M+l] ⁺ .

Step B: 4'-(4-amino-l-(iminomethyl)piperidin-4-yl)-2-(2H-tetrazol-5- yl)-4-

(trifluoromethyl)-[ 1.1 '-biphenyl]-3 -sulfonamide

To the solution of 4'-(4-amino- 1 -(iminomethyl)piperidin-4-yl)-N-(4- methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-4-(t rifluoromethyl)-[l,r-biphenyl]- 3-sulfonamide (15 mg, 0.020 mmol) in DCM (102 μΐ was added anisole (22.19 μΐ, 0.204 mmol) and TFA (157 μϊ _^ , 2.041 mmol) at rt. The resulting mixture was stirred at 80°C for 1 hr. After removing the volatile the residue was purified by reverse phase HPLC (5-50% ACN/water, 0.1% TFA as additive) to give the title compound. LC-MS (IE, m/z): 495.47 [M+l] ⁺ . EXAMPLE 438

4-amino-4-(3'-sulfamoyl-2'-(2H-tetrazol-5-yl)-4'-(trifluorom ethyl)-[l,r-biphenyl]-4- yl)piperidine- 1 -carboximidamide

Step A: 4-amino-4-(3'-(N.N-bis(4-methoxyberizyl)sulfamoyl)-2'-(2-(4- methoxybenzy

2H-tetrazol-5-yl)-4'-(trifluoromethyl)-r 1 J'-biphenvi ^" |-4-yl)piperidine- 1 -carboximidamide

4'-(4-aminopiperidin-4-yl)-N-(4-methoxybenzyl)-2-( 1 -(4-methoxybenzyl)- 1 H- tetrazol-5-yl)-4-(trifluoromethyl)-[l,r-biphenyl]-3-sulfonam ide (30 mg, 0.042 mmol) in DMF (848 μ was treated with lH-pyrazole-l-carboxamidine hydrochloride (9.94 mg, 0.068 mmol) and DIPEA (37.0 μί, 0.212 mmol). After overnight LC-MS showed the reaction was not completed. More reagents were added with lH-pyrazole-l-carboxamidine hydrochloride (9.94 mg, 0.068 mmol) and DIPEA (37.0 μί, 0.212 mmol). After once more overnight the reaction mixture was purified with reverse phase HPLC (10-90% MeCN/water as gradient, 0.1% TFA as additive) to give the title compound. LC-MS (IE, m/z): 750.68 [M+l] ⁺ . Step B: 4-amino-4-(3'-sulfamoyl-2'-(2H-tetrazol-5-yl)-4'-(trifluorom ethyl)-rLr- biphenyl1-4-yl)piperidine- 1 -carboximidamide

To the solution of 4-amino-4-(2'-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-3'-(N- (4-methoxybenzyl)sulfamoyl)-4'-(trifluoromethyl)-[l,r-biphen yl]-4-yl)piperidine-l- carboximidamide (15 mg, 0.020 mmol) in DCM (100 μί) was added anisole (21 μί, 0.200 mmol) and TFA (154 μΕ, 2.001 mmol) at rt. The resulting mixture was stirred at 80°C for 1 hr. After removing the volatile the residue was purified by reverse phase HPLC (5-50% ACN/water, 0.1% TFA as additive) to give the title compound. LC-MS (IE, m/z): 510.44 [M+l] ⁺ .

EXAMPLE 439

4'-(aminomethyl)-2-(2H-tetrazol-5-yl)-4-(trifluoromethyl)-[l ,r-biphenyl]-3-sulfonamide

Step A: tert-butyl ((3'-(NJv[-bis(4-methoxybenzyl)sulfamoyl)-2'-(2-(4-m

2H-tetrazol-5-yl)-4'-(trifluoromethyl)-[l J'-biphenyll-4-yl)methyl)carbamate

A microwave vial was charged with 3-bromo-N,N-bis(4-methoxybenzyl)-2-(2- (4-methoxybenzyl)-2H-tetrazol-5-yl)-6-(trifluoromethyl)benze nesulfonamide (0.4 g, 0.546 mmol), (4-(((tert-butoxycarbonyl)amino)methyl)phenyl)boronic acid (0.151 g, 0.601 mmol), a2C03 (0.174 g, 1.638 mmol) and PdCl ₂ (dppf)-CH2Cl2 adduct (0.067 g, 0.082 mmol). The vial was sealed, degassed, and filled with dioxane (2.91 mL) and water (0.728 mL). The resulting mixture was heated overnight at 80°C. The reaction mixture was filtered over celite to remove palladium. The filtrate was diluted with EtOAc and washed with water. The organic layer was dried over anhydrous MgS0 ₄ , filtered, concentrated and purified by silica gel column chromatography using 0-100% EtOAc/Hexanes as mobile phase to give the title compound. LC- MS (IE, m/z): 859.58 [M+l .

Step B: 4'-(aminomethyl)-N-(4-methoxybenzyl)-2-(2-(4-methoxybenzyl)- 2H-tetrazol-5- yl)-4-(trifluoromethyl)- [ 1.1 '-biphenyl]-3 -sulfonamide

To the solution of tert-butyl ((3'-( ,N-bis(4-methoxybenzyl)sulfamoyl)-2'-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)-4'-(trifluoromethyl)-[l,r-b iphenyl]-4-yl)methyl)carbamate (490 mg, 0.570 mmol) in DCM (2.8 mL) was added anisole (620 μΐ, 5.70 mmol) and TFA (4.4 mL, 57.0 mmol) at rt. The resulting mixture was stirred at rt for 1 hr. After removing the volatile the residue was purified by ion exchange column (load sample and rinse with MeOH, rinse out product with 2 M NH ₃ in MeOH) to give the title product as a free amine. LC-MS (IE, m/z): 639.40 [M+l] ⁺ .

Step C: 4'-(aminomethyl)-2-(2H-tetrazol-5-yl)-4-(trifluoromethyl)-rL r-biphenyl1-3- sulfonamide

To the solution of 4'-(aminomethyl)-N-(4-methoxybenzyl)-2-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)-4-(trifluoromethyl)-[l,r-bi phenyl] -3 -sulfonamide (80 mg, 0.125 mmol) in DCM (626 μΐ was added anisole (136 μΐ, 1.253 mmol) and TFA (965 μΐ, 12.53 mmol) at rt. The resulting mixture was stirred at 80°C for 1 hr. After removing the volatile the residue was purified by reverse phase HPLC (5-60% ACN/water, 0.1% TFA as additive) to give the title compound. LC-MS (IE, m/z): 399.22 [M+l .

EXAMPLE 440

4'-(guanidinomethyl)-2-(2H-tetrazol-5-yl)-4-(trifluoromethyl )-[l,r-biphenyl]-3-sulfonamide

Step A: 4'-(guanidinomethyl)-N-(4-methoxybenzyl)-2-(2-(4-methoxybenz yl)-2H-tetrazol-

5-yl)-4-(trifluoromethyl)-r 1.1 '-biphenyll -3 -sulfonamide

4'-(aminomethyl)-N-(4-methoxybenzyl)-2-( 1 -(4-methoxybenzyl)- 1 H-tetrazol-5 - yl)-4-(trifluoromethyl)-[l,l'-biphenyl] -3 -sulfonamide (0009) (60 mg, 0.094 mmol) in DMF

(1879 μΐ) was treated with IH-pyrazole-l-carboxamidine hydrochloride (22.03 mg, 0.150 mmol) and DIPEA (82 μΐ, 0.470 mmol). After stirring overnight LC-MS showed that the reaction was not completed. More reagents were added with IH-pyrazole-l-carboxamidine hydrochloride (22.03 mg, 0.150 mmol) and DIPEA (82 μΐ, 0.470 mmol). After once more overnight the reaction mixture was purified with reverse phase HPLC (10-90% MeCN/water as gradient, 0.1% TFA as additive) to give the title compound. LC-MS (IE, m/z): 681.49 [M+l] ⁺ .

Step B: 4'-(guanidinomethyl)-2-(2H-tetrazol-5-yl)-4-(trifluoromethyl )-r 1 , 1 '-biphenyll -3- sulfonamide

To the solution of 4'-(guanidinomethyl)-N-(4-methoxybenzyl)-2-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)-4-(trifluoromethyl)-[l,r-bi phenyl]-3-sulfonamide (50 mg, 0.073 mmol) in DCM (367 μΓ) was added anisole (80 μί, 0.735 mmol) and TFA (566 μί, 7.35 mmol) at rt. The resulting mixture was stirred at 80°C for 1 hr. After removing the volatile the residue was purified by reverse phase HPLC (5-60% ACN/water, 0.1% TFA as additive) to give the title compound. LC-MS (IE, m/z): 441.32 [M+l] ⁺ . EXAMPLES 441-447

The following compounds were prepared in an analogous fashion to EXAMPLES 433-440 starting from 3-bromo-N,N-bis(4-methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-t etrazol- 5-yl)-6-(trifluoromethyl)benzenesulfonamide and corresponding coupling partners as listed below. As quite a few different sets of conditions were used for EXAMPLES 441-447 depending on structural feature (amine, non-amine, amidine, guanidine, quaternary amine etc.), the method will be listed for the followin analogs.

EXAMPLE 448

-sulfamoyl-2'-(2H4etrazol-5-yl)-4'-(trifluoromethyl)-[l,r-bi phenyl]-4-yl)acetamide

Step A: 2-(3'-nS[,N-bis( ^' 4-methoxybenzyl sulfamoyl -2'-( ^' 2-( ^' 4-methoxybenzyl -2H- tetrazol-5-yl -4'-( ^' trifluoromethyl -ri J'-biphenyl1-4-yl acetamide

The mixture of 4,4,4',4',5,5,5',5'-octamethyl-2,2'-bi(l,3,2-dioxaborolane) (125 mg, 0.491 mmol), 2-(4-bromophenyl)acetimidamide (87 mg, 0.410 mmol), PCy3 2nd generation precatalyst (16.12 mg, 0.027 mmol) and potassium acetate (107 mg, 1.092 mmol) in dioxane (2.7 mL) was degassed with N2. The resulting mixture was heated at 100°C for overnight. LCMS indicated complete coversion to boronic acid. 3-bromo-N,N-bis(4-methoxybenzyl)-2-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)-6-(trifluoromethyl)benzenes ulfonamide (200 mg, 0.273 mmol), Pd(dppf)Cl2 (22.30 mg, 0.027 mmol), and sodium carbonate (116 mg, 1.092 mmol) were added followed by 1.0 mL water. The reaction mixture was degassed with 2 and heated at 90°C overnight. After cooling to rt the mixture was filtered through celite, the filtrate was concentrated and the residue was purified by silica gel column chromatography using 0-10% MeOH/DCM as mobile phase to give the title compound. LC-MS (IE, m/z): 787.70 [M+l] ⁺ .

Step B: 2-(3'-sulfamoyl-2'-(2H-tetrazol-5-yl)-4'-(trifluoromethyl)-r 1.1 '-biphenvH-4- yPacetamide

To the solution of 2-(3'-( ,N-bis(4-methoxybenzyl)sulfamoyl)-2'-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)-4'-(trifluoromethyl)-[ 1 , 1 '-biphenyl]-4-yl)acetimidamide (100 mg, 0.127 mmol) in DCM (636 μΐ was added anisole (138 μί, 1.273 mmol) and TFA (980 μΐ, 12.73 mmol) at rt. The resulting mixture was stirred at 80°C for 1 hr. After removing the volatile the residue was purified by reverse phase HPLC (5-60% ACN/water, 0.1% TFA as additive) to give the title compound.

LC-MS (IE, m/z): 427.28 [M+l . EXAMPLE 449

-sulfamoyl-2'-(2H etrazol-5-yl)-4'-(trifluoromethyl)-[l,r-biphenyl]-4-yl)propa namide

The title compound was prepared in an analogous fashion to 2-(3'-sulfamoyl-2'- (2H-tetrazol-5-yl)-4'-(trifluoromethyl)-[l,r-biphenyl]-4-yl) acetamide starting from 3-bromo- N,N-bis(4-methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol- 5-yl)-6- (trifluoromethyl)benzenesulfonamide and 3-(4-chlorophenyl)propanimidamide. LC-MS (IE, m/z): 441.33 [M+l] ⁺ .

EXAMPLE 450

3-(4-(4-(hydroxymethyl)phenyl)piperidin-l-yl)-2-(2H-tetrazol -5-yl)-6- (trifluoromethyl)benzenesulfonamide

Step A: tert-butyl 4-(4-(hydroxymethyl)phenyl)piperidine- 1 -carboxylate

To a solution of tert-butyl 4-(4-(hydroxymethyl)phenyl)piperidine-l -carboxylate (1000 mg, 3.43 mmol) in DCM (17 mL) was added anisole (1.9 mL, 17.16 mmol) and TFA (26 mL, 343 mmol) at rt. The resulting mixture was stirred at rt for 1 hr to remove Boc protection. After removing the volatile the residue was purified by SCX ion exchange column to give the desired product.

Step B: 3 -(4-(4-(hvdroxymethyl)phenyl)piperidin- 1 -yl)-N,N-bis(4-methoxybenzyl)-2-(2-

(4-methoxybenzyl)-2H-tetrazol-5-yl)-6-(trifluoromethyl)be nzenesulfonamide

To 3-bromo-N,N-bis(4-methoxybenzyl)-2-(l-(4-methoxybenzyl)-lH-t etrazol-5- yl)-6-(trifluoromethyl)benzenesulfonamide (1000 mg, 1.365 mmol), potassium carbonate (1 132 mg, 8.19 mmol) and (4-(piperidin-4-yl)phenyl)methanol (522 mg, 2.73 mmol) in a microwave vial was added DMF (4.5 mL). The mixture was MW at 140°C for 3 hr. LCMS indicated a complete reaction. The mixtures were diuted with water, extracted with EtOAc (2X), washed with brine, dried(MgS0 ₄ ), and concentrated. The residue was purified by column

chromatography (0-100 EtOAc/hex) to give the title compound. LC-MS (IE, m/z): 843.77

Step C: 3-(4-(4-(hvdroxymethyl)phenyl)piperidin-l-yl)-2-(2H-tetrazol -5-yl)-6-

(trifluoromethyl)benzenesulfonamide

To the solution of 3-(4-(4-(hydroxymethyl)phenyl)piperidin-l-yl)-N,N-bis(4- methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-6- (trifluoromethyl)benzenesulfonamide (50 mg, 0.059 mmol) in DCM (297 μΚ) was added anisole (64 μΕ, 0.593 mmol) and TFA (457 μί, 5.93 mmol) at rt. The resulting mixture was stirred at 80°C for 1 hr. After removing the volatile the residue was purified by reverse phase HPLC (5- 60% ACN/water, 0.1% TFA as additive) to give the title compound. LC-MS (IE, m/z): 483.41 [M+l] ⁺ .

EXAMPLE 451

6-(((ls,4s)-4-aminocyclohexyl)methyl)-3-(quinolin-4-yl)-2-(2 H-tetrazol-5- yl)benzenesulfonamide

H ₂

Step A: 6-bromo-N,N-bis(4-methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-t etrazol-5-yl)-3- (quinolin-4-yl)benzenesulfonamide

A microwave vial was charged with 6-bromo-3-iodo-N,N-bis(4-methoxybenzyl)- 2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)benzenesulfonamide (0030 and 0125) (1 g, 1.265 mmol), quinolin-4-ylboronic acid (0.656 g, 3.80 mmol), PdCl2(dppf)-CH2Cl2 adduct (0.155 g, 0.190 mmol) and sodium carbonate (0.536 g, 5.06 mmol). The vial was sealed, degassed, and filled with dioxane (6.33 mL) and water (2.1 1 mL). The resulting mixture was heated overnight at 90°C. The reaction mixture was filtered over celite to removed palladium. The filtrate was diluted with EtOAc and washed with water. The organic layer was dried over anhydrous MgS0 ₄ , filtered, concentrated and purified by silica gel column chromatography using 0-100% EtOAc/Hexanes as mobile phase to give the desired product. LC-MS (IE, m/z): 793.2 [M+2] ⁺ . Step B: 6-(((ls,4s -4-aminocvclohexyl methyl -N-(4-methoxybenzyl -2-(2-(4- methoxybenzyl -2H-tetrazol-5-yl -3-(quinolin-4-yl benzenesulfonamide

A microwave vial was charged with tert-butyl ((lr,4r)-4- (bromomethyl)cyclohexyl)carbamate (prepared in an analogous fashion to that described for tert- butyl (ls,4s)-4-(iodomethyl)cyclohexylcarbamate, Reference Example 35, except starting from (lr,4r)-4-((tert-butoxycarbonyl)amino)cyclohexanecarboxylic acid; 55.4 mg, 0.189 mmol), nickel(II) iodide (5.92 mg, 0.019 mmol), manganese (20.82 mg, 0.379 mmol),

bathophenanthroline (6.30 mg, 0.019 mmol) and 6-bromo-N,N-bis(4-methoxybenzyl)-2-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)-3-(quinolin-4-yl)benzenesul fonamide (100 mg, 0.126 mmol). The vial was sealed, purged with 2 for 10 min, and filled with DMA (1.3 mL). The resulting mixture was purged with 2 for another 10 min and heated overnight at 80°C. The reaction mixture was filtered over celite to remove metal. The filtrate was treated with TFA (0.973 mL, 12.63 mmol) and anisole (0.069 mL, 0.632 mmol) in DCM (2 mL) to remove the Boc group, and the title compound as a free amine was obtained by passing through an ion exchange column. LC-MS (IE, m/z): 704.42 [M+l] ⁺ . Step C: 6-(((ls,4s)-4-aminocvclohexyl)methyl)-3-(quinolin-4-yl)-2-(2 H-tetrazol-5- vDbenzenesulfonamide

To a solution of 6-(((lr,4r)-4-aminocyclohexyl)methyl)-N-(4-methoxybenzyl)-2- (2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-3-(quinolin-4-yl)benz enesulfonamide (89 mg, 0.126 mmol) in DCM (632 μΐ was added anisole (138 μΐ, 1.264 mmol) and TFA (974 μΐ, 12.64 mmol) at rt. The resulting mixture was heated at 80°C for 1 hr. After removing the volatile the residue was purified by reverse phase HPLC using DMSO to load sample and 5-35 % acetonitrile/water (0.1% TFA as additive) as mobile phase over 10 min to give the title compound. LC-MS (IE, m/z): 464.38 [M+l] ⁺ .

EXAMPLE 452

6-(2-(piperidin-4-yl)ethyl)-3-(quinolin-4-yl)-2-(2H-tetrazol -5-yl)benzenesulfonamide

The title compound was prepared in an analogous fashion to 6-(((ls,4s)-4- aminocyclohexyl)methyl)-3-(quinolin-4-yl)-2-(2H-tetrazol-5-y l)benzenesulfonamide using 6- bromo-N,N-bis(4-methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tet razol-5-yl)-3-(quinolin-4- yl)benzenesulfonamide and tert-butyl 4-(2-iodoethyl)piperidine-l-carboxylate. LC-MS (IE, m/z): 441.33 [M+l] ⁺ .

EXAMPLE 453

6-(2-cyanoethyl)-3-(quinolin-4-yl)-2-(2H-tetrazol-5-yl)benze nesulfonamide

Step A: 6-(2-cvanoethyl -N-(4-methoxybenzyl -2-(2-(4-methoxybenzyl -2H-tetrazol-5- yl)-3-(quinolin-4-yl)benzenesulfonamide

A microwave vial was charged with 6-bromo-N,N-bis(4-methoxybenzyl)-2-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)-3-(quinolin-4-yl)benzenesul fonamide (0.12 g, 0.152 mmol), and t-Bu-XPhos 1st generation precatalyst (0.021 g, 0.030 mmol). The vial was sealed, degased, and filled with THF (1.516 ml) and (2-cyanoethyl)zinc(II) bromide (1.213 ml, 0.606 mmol). The resulting mixture was heated overnight at 60°C. The reaction mixture was filtered over celite to remove palladium. The filtrate was concentrated and purified by silica gel column

chromatography using (20-80)% EtOAc/Hexanes as mobile phase to give the desired product. LC-MS (IE, m/z): 766.25 [M+l] ⁺ . Step B: 6-(2-cvanoethyl)-3-(quinolin-4-yl)-2-(2H-tetrazol-5-yl)benze nesulfonamide To the solution of 6-(2-cyanoethyl)-N,N-bis(4-methoxybenzyl)-2-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)-3-(quinolin-4-yl)benzenesul fonamide (80 mg, 0.104 mmol) in DCM (2089 μΐ) was added TFA (805 μΐ, 10.45 mmol) and anisole (227 μΐ, 2.089 mmol), and the reaction mixture was heated at 80°C for 1 hr. After removing the volatile the residue was purified (DMSO loading) on reverse phase HPLC using 5-70 % acetonitrile/water (0.1% formic acid) over 10 min to give the title compound. LC-MS (IE, m/z): 406.28 [M+l] ⁺ .

EXAMPLE 454

6-cyclohexyl-3-(quinolin-4-yl)-2-(2H-tetrazol-5-yl)benzenesu lfonamide

6-cyclohexyl-3 -(quinolin-4-yl)-2-(2H-tetrazol-5 -vDbenzenesulfonamide was prepared in an analogous fashion to 6-(2-cyanoethyl)-3-(quinolin-4-yl)-2-(2H-tetrazol-5- yl)benzenesulfonamide using 6-bromo-N,N-bis(4-methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H tetrazol-5-yl)-3-(quinolin-4-yl)benzenesulfonamide and cyclohexylzinc(II) bromide. LC-MS (IE, m/z): 435.32 [M+l] ⁺ .

EXAMPLE 455

4-(((ls,4s)-4-aminocyclohexyl)methyl)-4'-(piperidin-4-yl)-2- (2H-tetrazol-5-yl)-[ 1 , 1 '-biphenyl]

3 -sulfonamide

H ₂

Step A: tert-butyl 4-(3'-( ,N-bis(4-methoxybenzyl)sulfamoyl)-4'-bromo-2'-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)-[ 1.1 '-biphenyll-4-yl)piperidine- 1 -carboxylate A thick- wall flask was charged with tert-butyl 4-(4-(4,4,5,5-tetramethyl- 1,3,2- dioxaborolan-2-yl)phenyl)piperidine-l-carboxylate (4.04 g, 10.44 mmol), 6-bromo-3-iodo-N,N- bis(4-methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl )benzenesulfonamide (5.5 g, 6.96 mmol), sodium carbonate (2.212 g, 20.87 mmol) and

tetrakis(triphenylphosphine)palladium(0) (0.402 g, 0.348 mmol). The vial was degassed, sealed, and filled with dioxane (20.87 ml) and water (6.96 ml). The resulting mixture was heated for 16 hr at 80°C. The reaction mixture was filtered over celite to remove palladium. The filtrate was diluted with EtOAc and washed with water. The organic layer was dried over anhydrous MgS04, filtered, concentrated. The residue was purified by silica gel column chromatography using 0-100% EtOAc/Hexanes as mobile phase to give the title compound. LC-MS (IE, m/z): 925.75 [M+2] ⁺ .

Step B: tert-butyl 4-(3 '-(N.N-bisC 4-methoxybenzyl)sulfamoyl)-4'-( (( 1 s .4s)-4-( (tert- butoxycarbonyl)amino)cvclohexyl)methyl)-2'-(2-(4-methoxybenz yl)-2H-tetrazol-5-yl)-rU'- biphenyl1-4-yl)piperidine- 1 -carboxylate

A microwave vial was charged with tert-butyl ((lr,4r)-4-

(bromomethyl)cyclohexyl)carbamate (47.4 mg, 0.162 mmol), nickel(II) iodide (5.07 mg, 0.016 mmol), manganese (17.84 mg, 0.325 mmol), bathophenanthroline (5.40 mg, 0.016 mmol) and tert-butyl 4-(3'-(N,N-bis(4-methoxybenzyl)sulfamoyl)-4'-bromo-2'-(2-(4- methoxybenzyl)-2H- tetrazol-5-yl)-[l, l'-biphenyl]-4-yl)piperidine-l-carboxylate (100 mg, 0.108 mmol). The vial was sealed, purged with 2 for 10 min, and filled with DMA (1.3 mL). The resulting mixture was purged with 2 for another 10 min and heated overnight at 70°C. The reaction mixture was filtered over celite to removed metal. The filtrate was concentrated and purified by silica gel chromatography (0-100% EtOAc/hexane as gradient) to afford the title compound. LC-MS (IE, m/z): 1056.87 [M+l] ⁺ . Step C: 4-(((ls,4s)-4-aminocvclohexyl)methyl)-4'-(piperidin-4-yl)-2- (2H-tetrazol-5-yl)-

[1.1 '-biphenyl] -3 -sulfonamide

To tert-butyl 4-(3'-(N,N-bis(4-methoxybenzyl)sulfamoyl)-4'-(((lr,4r)-4-((t ert- butoxycarbonyl)amino)cyclohexyl)methyl)-2'-(2-(4-methoxybenz yl)-2H-tetrazol-5-yl)-[l, - biphenyl]-4-yl)piperidine-l -carboxylate (90 mg, 0.085 mmol) was added anisole (93 μί, 0.852 mmol) and TFA (656 μί, 8.52 mmol) at rt. The resulting mixture was stirred at rt for 1 hr to remove both Boc and both PMB protection. After removing the volatile the residue was purified by reverse phase HPLC using DMSO to load sample and 5-60 % acetonitrile/water (0.1% TFA as additive) as mobile phase over 10 min to separate the desired product from debromide side- product from the coupling reaction. To a solution of the desired product in DCM (426 μΐ,) was added anisole (93 μΐ,, 0.852 mmol) and TFA (656 μΐ,, 8.52 mmol) at rt. The resulting mixture was stirred at 80°C for 1 hr to remove the final PMB protection. After removing the volatile the residue was purified by reverse phase HPLC using DMSO to load sample and 5-40 % acetonitrile/water (0.1% TFA as additive) as mobile phase over 10 min to give the final product. LC-MS (IE, m/z): 496.61 [M+l] ⁺ .

EXAMPLE 456

4'-(piperidin-4-yl)-4-( iperidin-4-ylmethyl)-2-(2H-tetrazol-5-yl)-[l,r-biphenyl]-3-s ulfonamide

Step A: tert-butyl 4-(3 '-(N.N-bis(4-methoxybenzyl)sulfamoyl)-4'-(( 1 -(tert- butoxycarbonyl)piperidin-4-yl)methyl)-2'-(2-(4-methoxybenzyl )-2H-tetrazol-5-yl)-r 1, 1'- biphenyll-4-yl)piperidine- 1 -carboxylate

A microwave vial was charged with bathophenanthroline (27.0 mg, 0.081 mmol), tert-butyl 4-(iodomethyl)piperidine- 1 -carboxylate (Synnovator) (528 mg, 1.62 mmol), nickel(II) iodide (50.7 mg, 0.162 mmol), tert-butyl 4-(3'-(N,N-bis(4-methoxybenzyl)sulfamoyl)-4'-bromo- 2'-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-[ 1 , 1 '-biphenyl]-4-yl)piperidine- 1 -carboxylate (500 mg, 0.541 mmol) and manganese (89 mg, 1.624 mmol). The vial was sealed, purged with 2 for 10 min, and filled with DMAc (2.2 mL). The reaction mixture was purged with 2 for 10 min, and benzonitrile (1 1 μΐ _^ , 0.108 mmol) (added 0.1 mL stock solution, which was prepared by dissolving 0.22 mL benzonitrile in 2 mL DMAc), and TMSC1 (14 μί, 0.108 mmol) (added 0.1 mL stock solution, which was prepared by dissolving 0.27 mL benzonitrile in 2 mL DMAc). The resulting mixture was purged with 2 for another 10 min, and heated for 1 hr at 40°C. The reaction mixture was directly purified by silica gel column chromatography using 0-100%

EtOAc/hexane as mobile phase (isostatic at 20% and 40% for a while, removed debromide side- product, which came out first) to afford the title product. LC-MS (IE, m/z): 1043.10 [M+l] ⁺ . Step B: 4'-( ^' piperidin-4-yl -4-( ^' piperidin-4-ylmethyl -2-( ^' 2H-tetrazol-5 -vD- Γ 1, 1 '-biphenvH -

3 -sulfonamide

To tert-butyl 4-(3'-(N,N-bis(4-methoxybenzyl)sulfamoyl)-4'-((l-(tert- butoxycarbonyl)piperidin-4-yl)methyl)-2'-(2-(4-methoxybenzyl )-2H-tetrazol-5-yl)-[ 1 , 1 '- biphenyl]-4-yl)piperidine-l-carboxylate (1950 mg, 1.871 mmol) was added anisole (2.0 mL,

18.71 mmol) and TFA (14 mL, 187 mmol) (neat TFA, no DCM) at rt. The resulting mixture was stirred at rt for 1 hr to remove both Boc and both PMB protection. After removing the volatile the residue was purified by reverse phase HPLC using DMSO to load sample and 5-55% acetonitrile/water (0.1% TFA as additive) as mobile phase over 10 min to separate the desired product from side products. To a solution of the desired mono-PMB product in DCM (19 mL) was added anisole (2.0 mL, 18.71 mmol) and TFA (14 mL, 187 mmol) at rt. The resulting mixture was stirred at 80°C for 1 h to remove the final PMB protection. After removing the volatile the residue was purified by reverse phase HPLC using DMSO to load sample and 5-40% acetonitrile/water (0.1% TFA as additive) as mobile phase over 10 min to give the title compound. LC-MS (IE, m/z): 482.56 [M+l] ⁺ .

EXAMPLE 457

4-(((lr,4r)-4-(aminomethyl)cyclohexyl)methyl)-4'-(piperidin- 4-yl)-2-(2H-tetrazol-5-yl)-[l,r- biphenyl]-3-sulfonamide

NH ₂

Step A: tert-butyl (((lr.4r)-4-(iodomethyl)cyclohexyl)methyl)carbamate

Triphenylphosphine (701 mg, 2.67 mmol) and tert-butyl (((lr,4r)-4- (hydroxymethyl)cyclohexyl)methyl)carbamate (500 mg, 2.055 mmol) in acetonitrile (2.5 ml) and diethyl ether (7.5 ml) were added imidazole (182 mg, 2.67 mmol) at 0°C, and then stirred at room temperature for 15 minutes. tert-Butyl (((lr,4r)-4- (hydroxymethyl)cyclohexyl)methyl)carbamate (500 mg, 2.055 mmol) in the same solvent system (2 mL) was added dropwise at 0°C. After finished, the solution was stirred at rt overnight. The reaction mixture was evaporated, and added DCM (5 mL). The suspension was filtered and evaporated to get the crude product. The crude was purified by column chromatography on silica gel, eluting with 0-10% MeOH/DCM (254 nm has weak absorption, out early) to give the desired product. LC-MS (IE, m/z): 354.32 [M+l] ⁺ .

Step B: tert-butyl 4-(3'-(TS[.N-bis(4-methoxybenzyl)sulfamoyl)-4'-(((lr.4r)-4-( ((tert- butoxycarbonyl)amino)methyl)cvclohexyl)methyl)-2'-(2-(4-meth oxybenzyl)-2H-tetrazol-5-yl)- Γ 1.1 '-biphenyll -4-yl)piperidine- 1 -carboxylate

A microwave vial was charged with 4,5-diazafluoren-9-one (2.96 mg, 0.016 mmol), manganese (17.84 mg, 0.325 mmol), pyridine (1.751 μΐ, 0.022 mmol), tert-butyl

(((lr,4r)-4-(iodomethyl)cyclohexyl)methyl)carbamate (76 mg, 0.216 mmol), tert-butyl 4-(3'- (N,N-bis(4-methoxybenzyl)sulfamoyl)-4'-bromo-2'-(2-(4-methox ybenzyl)-2H-tetrazol-5-yl)- [l, l'-biphenyl]-4-yl)piperidine-l -carboxylate (100 mg, 0.108 mmol) and nickel(II) iodide (5.07 mg, 0.016 mmol). The vial was sealed, purged with 2 for 10 min, and filled with DMA (1.3 mL). The resulting mixture was purged with 2 for another 10 min and heated overnight at 70°C. The reaction mixture was filtered over celite to remove metal. The filtrate was concentrated and purified by silica gel chromatography (0-100% EtOAc/hexane as gradient) to afford the title compound. LC-MS (IE, m/z): 1071.00 [M+l .

Step C: 4-(((lr,4r)-4-(aminomethyl)cvclohexyl)methyl)-4'-(piperidin- 4-yl)-2-(2H-tetrazol- 5 -vD- Γ L 1 '-biphenyll -3 -sulfonamide

To tert-butyl 4-(3'-(N,N-bis(4-methoxybenzyl)sulfamoyl)-4'-(((lr,4r)-4-((( tert- butoxycarbonyl)amino)methyl)cyclohexyl)methyl)-2'-(2-(4-meth oxybenzyl)-2H-tetrazol-5-yl)- [l, l'-biphenyl]-4-yl)piperidine-l -carboxylate (140 mg, 0.131 mmol) was added anisole (143 μί, 1.308 mmol) and TFA (1.0 mL, 13.08 mmol) at rt. The resulting mixture was stirred at rt for 1 hr to remove both Boc and both PMB protection. After removing the volatile the residue was purified by reverse phase HPLC using DMSO to load sample and 5-60 % acetonitrile/water (0.1% TFA as additive) as mobile phase over 10 min to separate the desired product from the debromide side-product from the coupling reaction. To a solution of the desired mono-PMB product in DCM (1.3 mL) was added anisole (143 μί, 1.308 mmol) and TFA (1.0 mL, 13.08 mmol) at rt. The resulting mixture was stirred at 80°C for 1 hr to remove the final PMB protection. After removing the volatile the residue was purified by reverse phase HPLC using DMSO to load sample and 5-40 % acetonitrile/water (0.1% TFA as additive) as mobile phase over 10 min to give the final product. LC-MS (IE, m/z): 510.3 [M+l f.

EXAMPLES 458-469

The following compounds were prepared in an analogous fashion to EXAMPLES 455-457 starting from tert-butyl 4-(3'-(N,N-bis(4-methoxybenzyl)sulfamoyl)-4'-bromo-2'-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)-[ 1 , 1 '-biphenyl]-4-yl)piperidine- 1 -carboxylate and corresponding halides as coupling partners as listed below. As there is evolution of Ni reductive coupling conditions, the method will be listed for the following analogs, which is similar either to Example 456 or 457. Although many halides are commercially available, some were prepared. For the latter ones they were prepared following the condition shown in Step A of Exam le 457.

tetrazol-5 -yl)- [1,1 '-biphenyl] -3 -sulfonamide

EXAMPLE 470

4'-( 1 -(azetidin-3 -ylmethyl)piperidin-4-yl)-4-(piperidin-4-ylmethyl)-2-(2H-tet razol-5 -yl)-[ 1,1'- biphenyl]-3-sulfonamide

Step A: benzyl 4-( ^' ( ^' 3-( ^' N,N-bis( ^' 4-methoxybenzyl sulfamoyl -4'-( ^' l -(tert- butoxycarbonyl piperidin-4-yl -2-(2-(4-methoxybenzyl -2H etrazol-5-yl -riJ'-biphenyl1-4- yl)methyl)piperidine- 1 -carboxylate

A microwave vial was charged with bathophenanthroline (27.0 mg, 0.081 mmol), benzyl 4-(iodomethyl)piperidine- 1 -carboxylate (583 mg, 1.624 mmol), nickel(II) iodide (50.7 mg, 0.162 mmol), tert-butyl 4-(3'-( ,N-bis(4-methoxybenzyl)sulfamoyl)-4'-bromo-2'-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)-[l,l'-biphenyl]-4-yl)piperi dine-l -carboxylate (500 mg, 0.541 mmol) and manganese (89 mg, 1.624 mmol). The vial was sealed, purged with 2 for 10 min, and filled with DMAc (2.2 mL), purged with 2 for 10 min, and then benzonitrile (11 μί, 0.108 mmol) (added 0.1 mL stock solution, which was prepared by dissolving 0.22 mL benzonitrile in 2 mL DMAc), and TMSC1 (14 μί, 0.108 mmol) (added 0.1 mL stock solution, which was prepared by dissolving 0.27 mL benzonitrile in 2 mL DMAc). The resulting mixture was purged with 2 for another 10 min, and heated for 1 hr at 40° C. The reaction mixture was directly purified by silica gel column chromatography using 0-100% EtOAc/hexane as mobile phase (isostatic at 20% and 40% for a while, removed some des-Br product, which came out first) to afford the title product. LC-MS (IE, m/z): 1077.1 1 [M+l .

Step B: benzyl 4-((2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-3-(N-(4- methoxybenzyl)sulfamoyl)-4'-(piperidin-4-yl)-rLr-biphenyl1-4 -yl)methyl)piperidine-l- carboxylate

To the solution of benzyl 4-((3-( ,N-bis(4-methoxybenzyl)sulfamoyl)-4'-(l-(tert- butoxycarbonyl)piperidin-4-yl)-2-(2-(4-methoxybenzyl)-2H-tet razol-5-yl)-[l, l'-biphenyl]-4- yl)methyl)piperidine- 1 -carboxylate (220 mg, 0.204 mmol) in DCM (2.0 mL) was added anisole (222 μΕ, 2.044 mmol) and TFA (1.6 mL, 20.44 mmol) at rt. The resulting mixture was stirred at rt for 1 hr. After removing the volatile the residue was purified by SCX ion exchange column (load sample and rinse with MeOH, rinse out product with 2 M NH3 in MeOH) to give the desired product as a free amine. LC-MS (IE, m/z): 856.91 [M+l] ⁺ .

Step C: benzyl 4-((4'-(l-((l-(ter?-butoxycarbonyl azetidin-3-yl methyl piperidin-4-yl -2-

(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-3-(N-(4-methoxyben zyl)sulfamoyl)-[l.r-biphenyll-4- vDmethyDpiperidine- 1 -carboxylate

To benzyl 4-((2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-4'-(piperidin-4 -yl)-3- sulfamoyl-[l,l'-biphenyl]-4-yl)methyl)piperidine-l-carboxyla te (80 mg, 0.109 mmol) and tert- butyl 3-formylazetidine-l -carboxylate (30.2 mg, 0.163 mmol) in DCM (1.1 mL) was added acetic acid (37 μΐ,, 0.652 mmol) and, after 5 min sodium triacetoxyborohydride (92 mg, 0.435 mmol). After being stirred at rt for 1 hr, the reaction mixture was purified by silica gel column chromatography (0-10% MeOH/DCM as eluent) to afford the title compound.

LC-MS (IE, m/z): 1026.29 [M+l .

Step D: 4'-(l-(azetidin-3-ylmethyl)piperidin-4-yl)-4-(piperidin-4-yl methyl)-2-(2H- tetrazol-5-yl)-[ 1.1 '-biphenyll-3-sulfonamide

To the solution benzyl 4-((4'-(l-((l-(tert-butoxycarbonyl)azetidin-3- yl)methyl)piperidin-4-yl)-2-(2-(4-methoxybenzyl)-2H-tetrazol -5-yl)-3-(N-(4- methoxybenzyl)sulfamoyl)-[l,r-biphenyl]-4-yl)methyl)piperidi ne-l -carboxylate (100 mg, 0.098 mmol) in MeOH (2 mL) was added Pd-C (10.38 mg, 0.098 mmol). The reaction mixture was stiired under ¾ atmosphere with a ¾ balloon for 2 hr. After filtration through celite, the filtrate was concentrated. To the solution of this residue in DCM (975 μί) was added anisole (106 μί, 0.975 mmol) and TFA (751 μΐ _^ , 9.75 mmol) at rt. The resulting mixture was stirred at rt for 1 hr. After removing the volatile the residue was purified by SCX ion exchange column (load sample and rinse with MeOH, rinse out product with 2 M ΝΗ ₃ in MeOH) to give a free amine. The free amine was then treated with anisole (106 μϊ _^ , 0.975 mmol) and TFA (751 μϊ _^ , 9.75 mmol) at 80°C for 1 hr. After removing the volatile the residue was purified by reverse phase HPLC using DMSO to load sample and 3-30 % acetonitrile/water (0.1% TFA as additive) as mobile phase over 10 min to give the title compound. LC-MS (IE, m/z): 551.87 [M+l] ⁺ .

EXAMPLE 471

4-((l-(azetidin-3-ylmethyl)piperidin-4-yl)methyl)-4'-(piperi din-4-yl)-2-(2H-tetrazol-5-yl)-[l,r- biphenyl]-3-sulfonamide

Step A: tert-butyl 4-(2'-( ^' 2-( ^' 4-methoxybenzyl -2H-tetrazol-5-yl -3'-( ^' N-( ^' 4- methoxybenzyl sulfamoyl -4'-( ^' piperidin-4-ylmethyl -r 1 , r-biphenyl1-4-yl piperidine- 1 - carboxylate

To the solution of benzyl 4-((3-( ,N-bis(4-methoxybenzyl)sulfamoyl)-4'-(l-(tert- butoxycarbonyl)piperidin-4-yl)-2-(2-(4-methoxybenzyl)-2H-tet razol-5-yl)-[l, l'-biphenyl]-4- yl)methyl)piperidine- 1 -carboxylate (220 mg, 0.204 mmol) in MeOH (2044 μΐ) was added Pd-C (218 mg, 0.204 mmol) and equipped with ¾ balloon at rt. The resulting mixture was stirred at rt for 1 hr. After removing the volatile, the residue was purified by SCX ion exchange column (load sample and rinse with MeOH, rinse out product with 2 M NH ₃ in MeOH) to give the title product as a free amine. LC-MS (IE, m/z): 943.38 [M+l .

Step B: tert-butyl 4-(4'-((l-((l-(tert-butoxycarbonyl)azetidin-3-yl)methyl)pipe ridin-4- yl)methyl)-2'-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-3'-(N-( 4-methoxybenzyl)sulfamoyl)-r 1.1 '- biphenyl1-4-yl)piperidine- 1 -carboxylate

To tert-butyl 4-(3'-(N,N-bis(4-methoxybenzyl)sulfamoyl)-2'-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)-4'-(piperidin-4-ylmethyl)-[ l , 1 '-biphenyl]-4-yl)piperidine- 1 - carboxylate (80 mg, 0.085 mmol) and tert-butyl 3 -formylazetidine-1 -carboxylate (23.59 mg, 0.127 mmol) in DCM (0.9 mL) was added acetic acid (29 μΐ _^ , 0.509 mmol) and, after 5 min sodium triacetoxyborohydride (72.0 mg, 0.340 mmol). After being stirred at rt for 1 hr, the reaction mixture was purified by silica gel column chromatography (0-10% MeOH/DCM) to give the title compound. LC-MS (IE, m/z): 1 112.44 [M+l] ⁺ .

Step C: 4'-(l-(azetidin-3-ylmethyl)piperidin-4-yl)-4-(piperidin-4-yl methyl)-2-(2H- tetrazol-5-yl)-[ 1.1 '-biphenyl]-3 -sulfonamide

To the solution of tert-butyl 4-(4'-((l-((l-(tert-butoxycarbonyl)azetidin-3- yl)methyl)piperidin-4-yl)methyl)-2'-(2-(4-methoxybenzyl)-2H- tetrazol-5-yl)-3'-( -(4- methoxybenzyl)sulfamoyl)-[l,r-biphenyl]-4-yl)piperidine-l-ca rboxylate (50 mg, 0.050 mmol) in DCM (504 μΐ was added anisole (55 μΐ, 0.504 mmol) and TFA (390 μί, 5.04 mmol) at rt. The resulting mixture was stirred at rt for 1 hr. After removing the volatile the residue was treated with anisole (55 μί, 0.504 mmol) and TFA (390 μί, 5.04 mmol) at 80°C for 1 hr. After removing the volatile the residue was purified by reverse phase HPLC using DMSO to load sample and 3-30 % acetonitrile/water (0.1% TFA as additive) as mobile phase over 10 min to give the title compound.

LC-MS (IE, m/z): 551.86 [M+l .

EXAMPLE 472

4-(4'-(2-(4-guanidinocyclohexyl)ethyl)-3'-sulfamoyl-2'-(2H-t etrazol-5-yl)-[ 1 , 1 '-biphenyl]-4- yl)piperidine- 1 -carboximidamide

Step A: 4-(4'-(2-(4-guanidinocvclohexyl)ethyl)-2'-(2-(4-methoxybenzy l)-2H-tetrazol-5- yl)-3'-sulfamoyl-[l.r-biphenyll-4-yl)piperidine-l -carboximidamide

To a solution of 4-(2-(4-aminocyclohexyl)ethyl)-2-(l -(4-methoxybenzyl)- 1H- tetrazol-5-yl)-4'-(piperidin-4-yl)-[l,r-biphenyl]-3-sulfonam ide (Intermediate of Example 38) (30 mg, 0.048 mmol) in DMF (953 μΚ) was added lH-pyrazole-l-carboxamidine hydrochloride (41.9 mg, 0.286 mmol) and DIPEA (100 μϊ _^ , 0.572 mmol). The reaction mixture was stirred at rt overnight, and purified by reverse phase HPLC (10-80% MeCN/water as gradient, 0.1% TFA as additive) to afford the title compound.

Steps B: 4-(4'-(2-(4-guanidinocvclohexyl)ethyl)-3'-sulfamoyl-2'-(2H-t etrazol-5-yl)-rLr- biphenyl1-4-yl)piperidine- 1 -carboximidamide

To a solution of 4-(4'-(2-(4-guanidinocyclohexyl)ethyl)-2'-(2-(4-methoxybenzy l)- 2H-tetrazol-5-yl)-3'-sulfamoyl-[l,r-biphenyl]-4-yl)piperidin e-l-carboximidamide (25 mg, 0.035 mmol) in DCM (175 μΐ was added anisole (38 μΐ, 0.350 mmol) and TFA (270 μΐ, 3.50 mmol) at rt. The resulting mixture was stirred at 80°C for 1 hr to remove the final PMB protection. After removing the volatile the residue was purified by reverse phase HPLC using DMSO to load sample and 5-40 % acetonitrile/water (0.1% TFA as additive) as mobile phase over 10 min to give the title compound. LC-MS (IE, m/z): 594.8 [M+lf.

EXAMPLE 473

4'-(piperidin-4-yl)-2-(2H-tetrazol-5-yl)-4-(3,3,3-trifluorop ropyl)-[l,r-biphenyl]-3-sulfonamide

Step A: tert-butyl 4-(3'-rN.N-bis(4-methoxybenzyl)sulfamoyl)-2'-(2-(4-methoxybe nzyl)-

2H-tetrazol-5-yl)-4'-(3,3,3-trifluoropropyl)-[Lr-biphenyl 1-4-yl)piperidine-l-carboxylate

A microwave vial was charged with potassium trifluoro(3,3,3- trifluoropropyl)borate (0.066 g, 0.325 mmol), chloro[(di(l-adamantyl)-N-butylphosphine)-2-(2- aminobiphenyl)]palladium(II) (0.022 g, 0.032 mmol), and tert-butyl 4-(3'-(N,N-bis(4- methoxybenzyl)sulfamoyl)-4'-bromo-2'-(2-(4-methoxybenzyl)-2H -tetrazol-5-yl)-[l, -biphenyl]- 4-yl)piperidine-l-carboxylate (0.1 g, 0.108 mmol). The vial was sealed and purged with N2, and dioxane (0.87 mL) and water (0.22 mL) were added. The resulting mixture was heated overnight at 100°C. The reaction mixture was filtered over celite to remove palladium. The filtrate was concentrated and purified by silica gel column chromatography using 0-100% EtOAc/Hexanes as mobile phase to afford the title compound.

LC-MS (IE, m/z): 941.97 [M+lf.

Steps B: 4'-(piperidin-4-yl -2-(2H-tetrazol-5-yl -4-(3.3.3-trifluoropropyl -ri.r-biphenyl1- 3 -sulfonamide

To tert-butyl 4-(3'-(N,N-bis(4-methoxybenzyl)sulfamoyl)-2'-(2-(4- methoxybenzyl)-2H-tetrazol-5 -yl)-4'-(3 ,3 ,3 -trifluoropropyl)- [1, 1 '-biphenyl] -4-yl)piperidine- 1 - carboxylate (80 mg, 0.085 mmol) was added anisole (93 μί, 0.850 mmol) and TFA (655 μί, 8.50 mmol) at rt. The resulting mixture was stirred at rt for 2 hr to remove both Boc and PMB protection. After removing the volatile the residue was purified by reverse phase HPLC using DMSO to load sample and 5-60 % acetonitrile/water (0.1% TFA as additive) as mobile phase over 10 min to separate the desired product from des-Br product (from the coupling reaction). To a solution of the desired product in DCM (425 μΚ) was added anisole (93 μΐ _^ , 0.850 mmol) and TFA (655 μϊ _^ , 8.50 mmol) at rt. The resulting mixture was stirred at 80°C for 1 hr to remove the final PMB protection. After removing the volatile the residue was purified by reverse phase HPLC using DMSO to load sample and 5-40 % acetonitrile/water (0.1% TFA as additive) as mobile phase over 10 min to give the title compound. LC-MS (IE, m/z): 481.36 [M+l] ⁺ .

EXAMPLES 474-481

Parallel synthesis of 3-aryl- or 3-heteroaryl-2-(lH-tetrazol-5-yl)-6- (trifluoromethyl)benzenesulfonamides

Step A

Step A: Suzuki coupling of a mixture of (3-[bis[(4-methoxyphenyl)methyl]sulfamoyl]-2-

[l-[(4-methoxyphenyl)methyl]-lH-l,2,3,4-tetrazol-5-yl]-4- (trifluoromethyl)phenyl)boronic acid and (3-[bis[(4-methoxyphenyl)methyl]sulfamoyl]-2-[2-[(4-methoxyp henyl)methyl]-2H- 1,2,3,4- tetrazol-5-yl]-4-(trifluoromethyl)phenyl)boronic acid with aryl and heteroaryl halides:

A solution of (3-[bis[(4-methoxyphenyl)methyl]sulfamoyl]-2-[l-[(4-methoxyp henyl)methyl]- lH-l,2,3,4-tetrazol-5-yl]-4-(trifluoromethyl)phenyl)boronic acid and (3-[bis[(4- methoxyphenyl)methyl]sulfamoyl]-2-[2-[(4-methoxyphenyl)methy l]-2H-l,2,3,4-tetrazol-5-yl]-4- (trifluoromethyl)phenyl)boronic acid (80 mg, 0.104 mmol) and 2nd Generation Xphos

Precatalyst (12.33 mg, 0.016 mmol) in 1.2 mL of dioxane was added to 1 dram vials containing commercially available or known aryl or heteroaryl bromides (0.125 mmol). Then Cesium Carbonate (0.209 ml, 0.313 mmol) was added and the mixtures were stirred at 85°C for 18 hr. The mixtures were allowed to cool. DCM (1 mL) and water (1 mL) was added and the mixtures were stirred for 5 minutes. The aqeuous layer was removed by pipette and the remaning organics concentrated under reduced pressure in the genevac. Step B: Removal of the paramethoxybenzyl protective groups:

Anisole (0.1 14 mL, 1.045 mmol) and TFA (1 mL) were added to the residues and the mixtures were stirred at 60°C for 4 hr. The mixtures were allowed to cool and the volatile organics were removed in the genevac under reduced pressure. DMSO (1 mL) was added to the residues and the mixtures were puridied using mass directed reverse phase HPLC to afford the examples in the Table below.

EXAMPLE 482

4-(3-Sulfamoyl-2-(lH-tetrazol-5-yl)-4-(trifluoromethyl)pheny l)benzo[(i]thiazole-2-

Step A: 3-(2-Bromobenzo[d]thiazol-4-yl)-N,N-bis(4-methoxybenzyl)-2-( l-(4- methoxybenzyl)- lH-tetrazol-5-yl)-6-(trifluoromethyl)benzenesulfonamide and 3-(2- bromobenzo[(i]thiazol-4-yl)-N,N-bis(4-methoxybenzyl)-2-(2-(4 -methoxybenzyl)-2H-tetrazol-5- yl)-6-(trifluoromethyl)benzenesulfonamide

3-(2-Bromobenzo[if|thiazol-4-yl)-N,N-bis(4-methoxybenzyl)-2- (l-(4- methoxybenzyl)- lH-tetrazol-5-yl)-6-(trifluoromethyl)benzenesulfonamide and 3-(2- bromobenzo[(i]thiazol-4-yl)-N,N-bis(4-methoxybenzyl)-2-(2-(4 -methoxybenzyl)-2H-tetrazol-5- yl)-6-(trifluoromethyl)benzenesulfonamide was prepared in an analogous way to that of 3-(2- bromobenzo[(flthiazol-4-yl)-N,N-bis(4-methoxybenzyl)-2-(l-(4 -methoxybenzyl)-lH-tetrazol-5- yl)benzenesulfonamide and 3-(2-bromobenzo[fi?]thiazol-4-yl)-N,N-bis(4-methoxybenzyl)-2 -(2- (4-methoxybenzyl)-2H-tetrazol-5-yl)benzenesulfonamide. LC/MS (M+l) ⁺ = 866, 868.

Step B : 3 -(2-Cyanobenzo[d]thiazol-4-yl)-N,N-bis(4-methoxybenzyl)-2-( 1 -(4- methoxybenzyl)-lH-tetrazol-5-yl)-6-(trifluoromethyl)benzenes ulfonamide and 3-(2- cyanobenzo[i/]thiazol-4-yl)-N,N-bis(4-methoxybenzyl)-2-(2-(4 -methoxybenzyl)-2H-tetrazol-5- yl)-6-(trifluoromethyl)benzenesulfonamide

3-(2-Bromobenzo[if|thiazol-4-yl)-N,N-bis(4-methoxybenzyl)-2- (l-(4- methoxybenzyl)- lH-tetrazol-5-yl)-6-(trifluoromethyl)benzenesulfonamide and 3-(2- bromobenzo[(i]thiazol-4-yl)-N,N-bis(4-methoxybenzyl)-2-(2-(4 -methoxybenzyl)-2H-tetrazol-5- yl)-6-(trifluoromethyl)benzenesulfonamide (285 mg, 0.329 mmol) was dissolved in pyridine (329 μΚ), and Copper(I) Cyanide (59.0 mg, 0.658 mmol) was added. The mixture was heated at 100°C for 2 hr. LC-MS showed the reaction was completed. The reaction mixture was concentrated to remove pyridine and the residue was purified by column chromatography (0- 55% EtOAc/Hexane) to give the title compounds. LC/MS (M+l)+ = 812.8

Step C: 4-(3 -(N,N-bis(4-methoxybenzyl)sulfamoyl)-2-( 1 -(4-methoxybenzyl)- lH-tetrazol-

5-yl)-4-(trifluoromethyl)phenyl)benzo[d]thiazole-2-carbox imidamide and 4-(3-(N,N-bis(4- methoxybenzyl)sulfamoyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol- 5-yl)-4- (trifluoromethyl)phenyl)benzo[d]thiazole-2-carboximidamide

3-(2-Cyanobenzo[i/]thiazol-4-yl)-N,N-bis(4-methoxybenzyl)-2- (l-(4- methoxybenzyl)- lH-tetrazol-5-yl)-6-(trifluoromethyl)benzenesulfonamide and 3-(2- cyanobenzo[i/]thiazol-4-yl)-N,N-bis(4-methoxybenzyl)-2-(2-(4 -methoxybenzyl)-2H-tetrazol-5- yl)-6-(trifluoromethyl)benzenesulfonamide (98 mg, 0.12 mmol) was suspended in MeOH ( 1 mL) and THF (0.5 mL) was added to aid the solubility. Then Sodium Methoxide (2.61 mg, 0.012 mmol) was added at room temperature. The mixture was stirred at room temperature for 1 hr. Ammonium Chloride (12.9 mg, 0.241 mmol) was then added and the mixture was stirred at room temperature for about 36 hr. LC-MS showed that the desired product was the major product. The reaction mixture was directly loaded onto a 40 g ESCO column and eluted with 0- 10%MeOH/EtOAC. The correct fractions were combined and concentrated to give the title compounds. LC/MS (M+l) ⁺ = 830.05.

Step D: 4-(3-Sulfamoyl-2-(lH-tetrazol-5-yl)-4-(trifluoromethyl)pheny l)benzo[(i]thiazole- 2-carboximidamide 4-(3 -(N,N-bis(4-methoxybenzyl)sulfamoyl)-2-( 1 -(4-methoxybenzyl)- lH-tetrazol- 5-yl)-4-(trifluoromethyl)phenyl)benzo[(i]thiazole-2-carboxim idamide and 4-(3-(N,N-bis(4- methoxybenzyl)sulfamoyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol- 5-yl)-4- (trifluoromethyl)phenyl)benzo[(i]thiazole-2-carboximidamide (48 mg, 0.058 mmol) was heated in TFA (2 mL) at 60°C for 2 hr. The reaction was concentrated to remove TFA and the residue was purified with Gilson (3-80% CH ₃ CN/water with 0.1% TFA). The correct fractions were combined, concentrated and lypholized from CHsCN/water to give 4-(3-Sulfamoyl-2-(lH- tetrazol-5-yl)-4-(trifluoromethyl)phenyl)benzo[(i]thiazole-2 -carboximidamide. LC/MS (M+l) ⁺ = 469.5

EXAMPLE 483

3-(2-Cyanobenzo[d]thiazol-4-yl)-2- -tetrazol-5-yl)-6-(trifluoromethyl)benzenesulfonamide

3 -(2-Cyanobenzo[i/]thiazol-4-yl)-N,N-bis(4-methoxybenzyl)-2-( 1 -(4- methoxybenzyl)- lH-tetrazol-5-yl)-6-(trifluoromethyl)benzenesulfonamide and 3-(2- cyanobenzo[i/]thiazol-4-yl)-N,N-bis(4-methoxybenzyl)-2-(2-(4 -methoxybenzyl)-2H-tetrazol-5- yl)-6-(trifluoromethyl)benzenesulfonamide (65 mg, 0.080 mmol) was heated in TFA (2 mL) for 2 hr. The reaction was concentrated and the residue was purified with Gilson (3-90%

CHsCN/water with 0.1 % TFA). The correct fractions were concentrated and lypholized to give 3-(2-cyanobenzo[i/]thiazol-4-yl)-2-(lH-tetrazol-5-yl)-6-(tri fluoromethyl)benzenesulfonamide. LC/MS (M+l) ⁺ = 452.3.

EXAMPLE 484

3-(Imidazo[l,2-a]pyridin-6-yl)-2-(lH-tetrazol-5-yl)-6-(trifl uoromethyl)benzenesulfonamide

Step A: 3-(Imidazo[l,2-a]pyridin-6-yl)-N,N-bis(4-methoxybenzyl)-2-(l -(4- methoxybenzyl)-lH-tetrazol-5-yl)-6-(trifluoromethyl)benzenes ulfonamide and 3-(imidazo[l,2- a]pyridin-6-yl)-N,N-bis(4-methoxybenzyl)-2-(2-(4-methoxybenz yl)-2H-tetrazol-5-yl)-6- (trifluoromethyl)benzenesulfonamide

3 -(Imidazo [ 1 ,2-a]pyridin-6-yl)-N,N-bis(4-methoxybenzyl)-2-( 1 -(4- methoxybenzyl)-lH-tetrazol-5-yl)-6-(trifluoromethyl)benzenes ulfonamide and 3 -(imidazo [1,2- a]pyridin-6-yl)-N,N-bis(4-methoxybenzyl)-2-(2-(4-methoxybenz yl)-2H-tetrazol-5-yl)-6- (trifluoromethyl)benzenesulfonamide was synthesized in an analogous way to that of 3- (Imidazo[ 1 ,5-a]pyridin-7-yl)-N,N-bis(4-methoxybenzyl)-2-( 1 -(4-methoxybenzyl)- lH-tetrazol-5- yl)-6-(trifluoromethyl)benzenesulfonamide and 3-(imidazo[l,5-a]pyridin-7-yl)-N,N-bis(4- methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-6- (trifluoromethyl)benzenesulfonamide. LC/MS (M+l) ⁺ = 770.5.

Step B: 3 -(Imidazo [1, 2-a]pyridin-6-yl)-2-(lH-tetrazol-5-yl)-6-

(trifluoromethyl)benzenesulfonamide

3 -(Imidazo [ 1 ,2-a]pyridin-6-yl)-N,N-bis(4-methoxybenzyl)-2-( 1 -(4- methoxybenzyl)-lH-tetrazol-5-yl)-6-(trifluoromethyl)benzenes ulfonamide and 3-(imidazo[l,2- a]pyridin-6-yl)-N,N-bis(4-methoxybenzyl)-2-(2-(4-methoxybenz yl)-2H-tetrazol-5-yl)-6- (trifluoromethyl)benzenesulfonamide (609 mg, 0.791 mmol) were heated at 60°C in TFA for 2 hr. After cooling, the reaction mixture was concentrated and purified with Gilson (2-55% CHsCN/water with 0.1% TFA). The correct fractions were combined, concentrated and lypholized to give 3-(imidazo[l,2-a]pyridin-6-yl)-2-(lH-tetrazol-5-yl)-6- (trifluoromethyl)benzenesulfonamide. LC/MS (M+l) ⁺ = 410.2

EXAMPLE 485

3-(Imidazo[l,5-a]pyridin-8-yl)-2-(l -tetrazol-5-yl)-6-(trifluoromethyl)benzenesulfonamide

3-(Imidazo[l,5-a]pyridin-8-yl)-2-(lH-tetrazol-5-yl)-6- (trifluoromethyl)benzenesulfonamide was prepared in an analogous way to that of 3- (imidazo[l,2-a]pyridin-6-yl)-2-(lH-tetrazol-5-yl)-6-(trifluo romethyl)benzenesulfonamide (immediately above). LC/MS (M+l) ⁺ = 410.4.

EXAMPLE 486

3-(Quinolin-5-yl)-2-(2 ethyl)benzenesulfonamide

Step A: 6-Bromo-N,N-bis(4-methoxybenzyl)-2-(l-(4-methoxybenzyl)-lH-t etrazol-5-yl)- 3-(quinolin-5-yl)benzenesulfonamide compound with 6-bromo-N,N-bis(4-methoxybenzyl)-2-(2- (4-methoxybenzyl)-2H-tetrazol-5-yl)-3-(quinolin-5-yl)benzene sulfonamide

A microwave vial was charged with 6-bromo-3-iodo-N,N-bis(4-methoxybenzyl)- 2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)benzenesulfonamide and 6-bromo-3-iodo-N,N-bis(4- methoxybenzyl)-2-(l-(4-methoxybenzyl)-lH-tetrazol-5-yl)benze nesulfonamide (1.24 g, 1.569 mmol), quinoline-5-boronic acid (0.271 g, 1.569 mmol), sodium carbonate (0.333 g, 3.14 mmol) and PdCl ₂ (dppf)-CH ₂ Cl ₂ adduct (0.128 g, 0.157 mmol). The vial was sealed, degassed, and filled with dioxane (4.71 ml) and water (1.569 ml) and degassed with nitrogen. The resulting mixture was heated at 90°C for 16 hr. The reaction mixture was filtered over celite and diluted with ethyl acetate (50 mL) and washed with water (2 x 15 mL). The organic layer was dried over anhydrous magnesium sulfate, filtered, concentrated and purified by silica gel column chromatography and the title compounds was isolated very light yellow colored foam. LC/MS [M+H] ⁺ : 791, 793.

Step B: N,N-Bis(4-methoxybenzyl)-2-(l-(4-methoxybenzyl)-lH-tetrazol- 5-yl)-3- (quinolin-5-yl)-6-(trifluoromethyl)benzenesulfonamide compound with N,N-bis(4- methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-3-(q uinolin-5-yl)-6-

(trifluoromethyl)benzenesulfonamide

To a microwave vial was added "Trifluoromethylator" (79 mg, 0.253 mmol), 6- bromo-N,N-bis(4-methoxybenzyl)-2-(l-(4-methoxybenzyl)-lH-tet razol-5-yl)-3-(quinolin-5- yl)benzenesulfonamide compound with 6-bromo-N,N-bis(4-methoxybenzyl)-2-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)-3-(quinolin-5-yl)benzenesul fonamide (100 mg, 0.126 mmol),

Cul (48.1 mg, 0.253 mmol), and DMF (1263 μΐ). The vial was sealed, degassed with N ₂ , and heated at 80°C for 16 hr. The reaction mixture was added to EtOAc (20 mL) and filtered through celite. The organic was washed with brine (10 mL) and the residue loaded was purified with silica gel chromatography to give the title compounds. LC/MS [M+H] ⁺ : 781.71.

Step C: 3-(Quinolin-5-yl)-2-(2H-tetrazol-5-yl)-6-(trifluoromethyl)be nzenesulfonamide

To the solution of N,N-bis(4-methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H- tetrazol-5-yl)-3-(quinolin-5-yl)-6-(trifluoromethyl)benzenes ulfonamide and N,N-bis(4- methoxybenzyl)-2-(l-(4-methoxybenzyl)-lH-tetrazol-5-yl)-3-(q uinolin-5-yl)-6- (trifluoromethyl)benzenesulfonamide (40 mg, 0.051 mmol) in DCM (1.5 mL) was added TFA (0.395 mL, 5.12 mmol) and anisole (0.056 mL, 0.512 mmol. The reaction mixture was heated at 80°C for 1 hr. After removing the volatile the residue was purified by HPLC and then lyophilized to give the title compound. LC/MS [M+H] ⁺ : 421.08.

EXAMPLES 487-492

Parallel synthesis of 3-alkyl- or 3-cycloalkyl-2-(lH-tetrazol-5-yl)-6- (trifluoromethyl)benzenesulfonamides

Step A

Step A: Negishi coupling of 3-bromo-N,N-bis(4-methoxybenzyl)-2-(l-(4- methoxybenzyl)- lH-tetrazol-5-yl)-6-(trifluoromethyl)benzenesulfonamide and 3-bromo-N,N- bis(4-methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl )-6-

(trifluoromethyl)benzenesulfonamide with commercially available alkyl and cycloalkyl zinc reagents:

In a glove box, a mixture of 3-bromo-N,N-bis(4-methoxybenzyl)-2-(l-(4- methoxybenzyl)- lH-tetrazol-5-yl)-6-(trifluoromethyl)benzenesulfonamide and 3-bromo-N,N- bis(4-methoxybenzyl)-2-(l-(4-methoxybenzyl)-2H-tetrazol-5-yl )-6-

(trifluoromethyl)benzenesulfonamide (80 mg, 0.109 mmol)) and G2 SPhos precatalyst (3.15 mg, 4.37 μηιοΐ)) in 2 mL of THF was combined withcommercially available alkyl and cycloalkyl zincate reagents (0.437 mmol) and stirred at 55°C for 18 hours. The mixtures were allowed to cool. Saturated ammonium chloride solution (1 mL) and DCM (1 mL) were added. The mixtures were stirred for 20 minutes. The organics layers were separated and the volatile organics removed under reduced pressure in the genevac.

Step B: Removal of the ara-methoxybenzyl protective groups:

The mixtures from Step A were treated with Anisole (0.048 mL, 0.44 mmol) and TFA (0.5 mL). The mixtures were stirred uncapped for 2 hr at 65°C. The mixtures were allowed to cool and the volatile organics removed under reduced pressure in the genevac. DMSO (1 mL) was added and the mixtures were filtered through a MTP (96 well) 0.4 micron filter plate and the filtrates were purified by mass directed reverse phase HPLC to afford the compounds in the Table below.

490 3 -cyclopentyl-2-( lH-tetrazol-5 -yl)-6- 362 362

(trifluoromethyl)benzenesulfonamide

491 3-cyclohexyl-2-(lH-tetrazol-5-yl)-6- 376 376

(trifluoromethyl)benzenesulfonamide

492 N=N 3 -cyclobutyl-2-( lH-tetrazol-5 -yl)-6- 348 348

(trifluoromethyl)benzenesulfonamide

EXAMPLE 493

3-(l,2,3,4-Tetrahydroquinolin-4-yl)- -(lH4etrazol-5-yl)-6-(trifluoromethyl)benzenesulfonamide

Step A: 6-Bromo-2-(l-(4-methoxybenzyl)-lH-tetrazol-5-yl)-3-(quinolin -4- yl)benzenesulfonamide

Quinolin-4-ylboronic acid (0.629 g, 3.64 mmol), 6-bromo-3-iodo-2-(l-(4- methoxybenzyl)-lH-tetrazol-5-yl)benzenesulfonamide (lg, 1.818 mmol), a ₂ C0 ₃ (0.385 g, 3.64 mmol), PdCi ₂ (dppf) (0.133 g, 0.182 mmol) was placed in a reaction vessell, and 1,4-dioxane (9.09 ml) and water (3.03 ml) were added. The reaction was sealed, degassed for 20 min and then heated at 85°C overnight. After cooling to room temperature, the reaction mixture was diluted with EtOAc and washed with water. The organic phase was separated and concentrated. The resulting residue was purified by column chromatography (0% to 90% EtOAc/Hexane) to give 6-bromo-2-(l-(4-methoxybenzyl)-lH-tetrazol-5-yl)-3-(quinolin -4-yl)benzenesulfonamide. Ste B: 2-(l-(4-Methoxybenzyl)-lH-tetrazol-5-yl)-3-(quinolin-4-yl)-6 - (trifluoromethyl)benzenesulfonamide

A mixture of 6-bromo-2-(l-(4-methoxybenzyl)-lH-tetrazol-5-yl)-3-(quinolin -4- yl)benzenesulfonamide (0.43 g, 0.780 mmol), trifluoromethlator (0.488 g, 1.560 mmol), and Copper(I) Iodide (0.297 g, 1.560 mmol) in DMF (8 mL) was degassed and heated at 80°C overnight. LC-MS analysis suggested that the stating material was consumed and the desired product was formed. The reaction mixture was cooled to room temperature and then loaded onto a silica gel column eluting with 0-100% EtOAc/hexane to give 2-(l-(4-methoxybenzyl)-lH- tetrazol-5-yl)-3-(quinolin-4-yl)-6-(trifluoromethyl)benzenes ulfonamide.

Step C: 2-(l-(4-Methoxybenzyl)-lH-tetrazol-5-yl)-3-(l,2,3,4-tetrahyd roquinolin-4-yl)-6- (trifluoromethyl)benzenesulfonamide

2-(l-(4-Methoxybenzyl)-lH-tetrazol-5-yl)-3-(quinolin-4-yl)-6 - (trifluoromethyl)benzenesulfonamide (167 mg, 0.309 mmol) was stirred with Pd(OH) ₂ (217 mg, 0.309 mmol) under H ₂ atmosphere (ballon) at room temperature for 36 hr. The reaction mixture was then filtered. The filtrates were concentrated and the residue purified by column chromatography (0-100% EtOAc/Hexane) to give 2-(l-(4-methoxybenzyl)-lH-tetrazol-5-yl)-3- ( 1 ,2,3 ,4-tetrahydroquinolin-4-yl)-6-(trifluoromethyl)benzenesulfon amide.

Step D : 3 -( 1 ,2,3 ,4-Tetrahydroquinolin-4-yl)-2-( lH-tetrazol-5 -yl)-6-

(trifluoromethyl)benzenesulfonamide

2-(l-(4-Methoxybenzyl)-lH-tetrazol-5-yl)-3-(l,2,3,4-tetrahyd roquinolin-4-yl)-6- (trifluoromethyl)benzenesulfonamide (40 mg, 0.073 mmol) was heated in neat TFA (2 mL) at 80°C for 3 hr. The reaction was concentrated and purified with reverse phase HPLC eluted with 3-90% CH ₃ CN/water with 0.1% TFA to give 3-(l,2,3,4-tetrahydroquinolin-4-yl)-2-(lH-tetrazol- 5-yl)-6-(trifluoromethyl)benzenesulfonamide. LC/MS (M+l)+ = 425.3

EXAMPLE 494

3-(5,6,7,8-Tetrahydroimidazo[l,5-a]pyridin-7-yl)-2-(lH-tetra zol-5-yl)-6- (trifluoromethyl)benzenesulfonamide

Step A: 3-(Imidazo[l,5-a]pyridin-7-yl)-N,N-bis(4-methoxybenzyl)-2-(l -(4- methoxybenzyl)-lH-tetrazol-5-yl)-6-(trifluoromethyl)benzenes ulfonamide and 3-(imidazo[l,5- a]pyridin-7-yl)-N,N-bis(4-methoxybenzyl)-2-(2-(4-methoxybenz yl)-2H-tetrazol-5-yl)-6- (trifluoromethyl)benzenesulfonamide

In a reaction vessel, 7-bromoimidazo[l,5-a]pyridine (200 mg, 1.015 mmol) and bispinacolatodiboron (773 mg, 3.05 mmol) were combined, followed by potassium acetate (299 mg, 3.05 mmol) and PCy3 Pd G2 (59.9 mg, 0.102 mmol). Then anhydrous dioxane (5075 μΐ) was added to this flask. This mixture was degassed and then heated at 80°C for 12 hr. LC-MS analysis showed the desired mass. After cooled to rt, to this reaction mixture, was added a mixture of 3-bromo-N,N-bis(4-methoxybenzyl)-2-(l-(4-methoxybenzyl)-lH-t etrazol-5-yl)-6- (trifluoromethyl)benzenesulfonamide and 3-bromo-N,N-bis(4-methoxybenzyl)-2-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)-6-(trifluoromethyl)benzenes ulfonamide (744 mg, 1.015 mmol), PdCl ₂ (dppf)-CH ₂ Cl ₂ Adduct (83 mg, 0.102 mmol), and K ₂ C0 ₃ (842 mg, 6.09 mmol) dissolved in water (1.2 mL). The mixture was degassed for 10 min, and then heated at 85°C overnight. After cooled to room temperature, the reaction mixture was diluted with EtOAc, washed with water. The organic layer was separated and evaporated under the reduced pressure. The residue was purified by column chromatography on silica gel (80 g), eluting with 0 to 5% MeOH/EtOAc to give the title compounds. LC/MS (M+l) ⁺ : 770.7.

Step B: 3-(5,6,7,8-Tetrahydroimidazo[l,5-a]pyridin-7-yl)-2-(lH-tetra zol-5-yl)-6- (trifluoromethyl)benzenesulfonamide

3 -(Imidazo [ 1 ,5-a]pyridin-7-yl)-N,N-bis(4-methoxybenzyl)-2-( 1 -(4- methoxybenzyl)-lH-tetrazol-5-yl)-6-(trifluoromethyl)benzenes ulfonamide and 3 -(imidazo [1,5- a]pyridin-7-yl)-N,N-bis(4-methoxybenzyl)-2-(2-(4-methoxybenz yl)-2H-tetrazol-5-yl)-6- (trifluoromethyl)benzenesulfonamide (240 mg, 0.312 mmol) was dissolved in MeOH (3118 μΐ), to which, was added 2 drops of cone. HCl followed by Pd-C (120 mg). The reaction head space was vacuumed and filled with H a couple of times. The mixture was stirred at room

temperature under H ₂ for 48 hr before it was filtered. The filtrates were concentrated to give a crude partially hydrogenated product. LC/MS (M+l) ⁺ = 772.7. The crude product was heated in TFA (2 mL) at 60°C for 2 hr to remove protecting group and then concentrtaed to afford an oil. LC/MS (M+l) ⁺ = 412.3. This crude oil was dissolved in EtOH/DCM (1/1, 3 mL) with TFA (3 mL) and Platinum(IV) Oxide (41.25 mg, 0.181 mmol) was added. The hydrogenation was carried out using a par shaker (40 psi) at room temeprature for 6 hr. LC-MS showed the completion of the reaction. The reaction mixture was filtered and the filtrates were concentrated, the resulting residue was purified with Gilson (2-50%CH ₃ CN/water with 0.1%TFA). The product was neutralized with a SCX cartridge and lypholized to afford 3-(5,6,7,8- Tetrahydroimidazo[l,5-a]pyridin-7-yl)-2-(lH-tetrazol-5-yl)-6 - (trifluoromethyl)benzenesulfonamide. LC/MS (M+l) ⁺ = 414.3.

EXAMPLE 495 and 496

3-((cis 4-hydroxycyclohexyl)-2-(lH-tetrazol-5-yl)-6-(trifluoromethyl )benzenesulfonamide and 3-((trans 4-hydroxycyclohexyl)-2-(lH-tetrazol-5-yl)-6-(trifluoromethyl )benzenesulfonamide

Step A: 4-Bromo-4'-hydroxy-2-(l-(4-methoxybenzyl)-lH-tetrazol-5-yl)- 2',3',4',5'- tetrahydro-[l, l'-biphenyl] -3 -sulfonamide and 4-bromo-4'-hydroxy-2-(2-(4-methoxybenzyl)-2H- tetrazol-5-yl)-2',3',4',5'-tetrahydro-[l, -biphenyl]-3-sulfonamide

4-Bromo-4'-hydroxy-2-(l-(4-methoxybenzyl)-lH-tetrazol-5-yl)- 2',3',4',5'- tetrahydro-[l, l'-biphenyl] -3 -sulfonamide and 4-bromo-4'-hydroxy-2-(2-(4-methoxybenzyl)-2H- tetrazol-5-yl)-2',3',4',5'-tetrahydro-[l, -biphenyl]-3-sulfonamide were prepared in an analogous way to that of 3-(2-Aminoquinazolin-7-yl)-N,N-bis(4-methoxybenzyl)-2-(l-(4- methoxybenzyl)- lH-tetrazol-5-yl)benzenesulfonamide and 3 -(2-aminoquinazolin-7-yl)-N,N-bis(4- methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)benze nesulfonamide (Step A).

LC/MS (M+l) ⁺ = 520.0, 522.0.

Step B: 4'-Hydroxy-2-(l-(4-methoxybenzyl)-lH-tetrazol-5-yl)-4-(trifl uoromethyl)- 2',3',4',5'-tetrahydro-[l,r-biphenyl]-3-sulfonamide and 4'-hydroxy-2-(2-(4-methoxybenzyl)-2H- tetrazol-5-yl)-4-(trifluoromethyl)-2',3',4',5'-tetrahydro-[l ,r-biphenyl]-3-sulfonamide

Trifluoromethyl(l, 10-Phenanthroline)Copper (1.29 g, 4.11 mmol), 4-bromo-4'- hydroxy-2-(l-(4-methoxybenzyl)-lH-tetrazol-5-yl)-2',3',4',5' -tetrahydro-[l, l'-biphenyl]-3- sulfonamide and 4-bromo-4'-hydroxy-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)- 2',3',4',5'- tetrahydro-[l, l'-biphenyl] -3 -sulfonamide (1.07 g, 2.06 mmol), Copper(I) Iodide (0.783 g, 4.11 mmol) and DMF (20.56 mL) were added to a microwave vial. The reaction mixture was sealed, degassed, and heated at 80°C overnight. After cooling to room temperature, the reaction mixture was loaded onto a silica gel column, eluting with 0-80% EtOAc/hexanes, to give the title compounds. LC/MS (M+l) ⁺ = 510.2

Step C: 3-(4-Hydroxycyclohexyl)-2-(l-(4-methoxybenzyl)-lH-tetrazol-5 -yl)-6- (trifluoromethyl)benzenesulfonamide and 3-(4-hydroxycyclohexyl)-2-(2-(4-methoxybenzyl)-2H- tetrazol-5-yl)-6-(trifluoromethyl)benzenesulfonamide

4'-hydroxy-2-( 1 -(4-methoxybenzyl)- lH-tetrazol-5-yl)-4-(trifruoromethyl)- 2',3',4',5'-tetrahydro-[l, -biphenyl]-3-sulfonamide and 4'-hydroxy-2-(2-(4-methoxybenzyl)-2H- tetrazol-5-yl)-4-(trifluoromethyl)-2',3',4',5'-tetrahydro-[l ,r-biphenyl]-3-sulfonamide

(447 mg, 0.877 mmol) was dissolved in MeOH (2 mL) and Palladium Hydroxide on Carbon (616 mg, 0.877 mmol) was added. The mixture was stired under hydogen atmosphere overnight. The mixture was then filtered and the filtrates were concentrated to give the crude 3-(4- hydroxycyclohexyl)-2-(l-(4-methoxybenzyl)-lH-tetrazol-5-yl)- 6-

(trifluoromethyl)benzenesulfonamide and 3-(4-hydroxycyclohexyl)-2-(2-(4-methoxybenzyl)-2H- tetrazol-5-yl)-6-(trifluoromethyl)benzenesulfonamide. LC/MS (M+l) ⁺ = 512.1.

Step D: 3-((cis 4-Hydroxycyclohexyl)-2-(lH-tetrazol-5-yl)-6-

(trifluoromethyl)benzenesulfonamide and 3-((trans 4-hydroxycyclohexyl)-2-(lH-tetrazol-5-yl)- 6-(trifluoromethyl)benzenesulfonamide

The crude 3 -(4-hydroxycyclohexyl)-2-( 1 -(4-methoxybenzyl)- lH-tetrazol-5-yl)-6- (trifluoromethyl)benzenesulfonamide and 3-(4-hydroxycyclohexyl)-2-(2-(4-methoxybenzyl)-2H- tetrazol-5-yl)-6-(trifluoromethyl)benzenesulfonamide was treated with TFA at 80°C for 3 hr. The reaction was concentrated after cooled to room temperature and the residue was purified with Gilson (3-100% CH ₃ CN/water with 0.1% TFA) to give the product as a mixture of trans/cis isomers, which were separated by SFC chiral separations (IC column, 15% MeOH with 0.1% NH ₄ OH/C0 ₂ ). LC/MS (M+l) ⁺ = 392.1.

EXAMPLE 497

3-(4-Amino-4-(aminomethyl)cyclohexyl)-2-(lH-tetrazol-5-yl)-6 - (trifluoromethyl)benzenesulfonamide

Step A: 4'-Hydroxy-N,N-bis(4-methoxybenzyl)-2-(l-(4-methoxybenzyl)-l H-tetrazol-5- yl)-4-(trifluoromethyl)-2',3 ',4',5'-tetrahydro-[ 1 , 1 '-biphenyl]-3 -sulfonamide and 4'-hydroxy-N,N- bis(4-methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl )-4-(trifluoromethyl)-2',3',4',5'- tetrahydro- [1, 1 '-biphenyl] -3 -sulfonamide

4-(4,4,5,5-tetramethyl-l,3,2-dioxaborolan-2-yl)cyclohex-3-en ol (1.2 g, 5.4 mmol), 3-bromo-N,N-bis(4-methoxybenzyl)-2-(l-(4-methoxybenzyl)-lH-t etrazol-5-yl)-6- (trifluoromethyl)benzenesulfonamide and 3-bromo-N,N-bis(4-methoxybenzyl)-2-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)-6-(trifluoromethyl)benzenes ulfonamide (2.5 g, 3.4 mmol), sodium carbonate (0.723 g, 6.83 mmol), PdCi ₂ (dppf) (0.250 g, 0.341 mmol) were placed in a reaction vessel. Dioxane (25.6 mL) and water (8.53 mL) were added. The reaction mixture was degassed for 20 min and then heated at 85°C overnight. LC-MS showed the reaction was completed. The reaction was then diluted with water and extracted with EtOAc. The organics were combined, washed with brine, separated and concentrated and the residue was purified by column chromatography (0-100% EtOAc/Hexane) to give the title compounds. LC/MS (M+l) ⁺ = 750.6

Step B : 3 -(4-Hydroxycyclohexyl)-N,N-bis(4-methoxybenzyl)-2-( 1 -(4-methoxybenzyl)- lH-tetrazol-5-yl)-6-(trifluoromethyl)benzenesulfonamide and 3 -(4-hydroxycyclohexyl)-N,N- bis(4-methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl )-6- (trifluoromethyl)benzenesulfonamide

4'-Hydroxy-N,N-bis(4-methoxybenzyl)-2-(l -(4-methoxybenzyl)- lH-tetrazol-5- yl)-4-(trifluoromethyl)-2',3 ',4',5'-tetrahydro-[ 1 , 1 '-biphenyl]-3 -sulfonamide and 4'-hydroxy-N,N- bis(4-methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl )-4-(trifluoromethyl)-2',3',4',5'- tetrahydro-[l, l'-biphenyl] -3 -sulfonamide (2.45 g, 3.27 mmol) was stired with Palladium

Hydroxide on Carbon (2.29 g, 3.27 mmol) under ¾ (balloon) overnight. The reaction mixture was filtered and the filtrates were concentrated to give the title compounds.

Step C: N,N-bis(4-Methoxybenzyl)-2-(l -(4-methoxybenzyl)- lH-tetrazol-5-yl)-3 -(4- oxocyclohexyl)-6-(trifluoromethyl)benzenesulfonamide and N,N-bis(4-methoxybenzyl)-2-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)-3-(4-oxocyclohexyl)-6-(trif luoromethyl)benzenesulfonamide

ΝΜΟ (467 mg, 3.99 mmol) and 4A molecular sieves (160 mg) were added to a solution of 3-(4-hydroxycyclohexyl)-N,N-bis(4-methoxybenzyl)-2-(l-(4-met hoxybenzyl)-lH- tetrazol-5-yl)-6-(trifluoromethyl)benzenesulfonamide and 3-(4-hydroxycyclohexyl)-N,N-bis(4- methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-6- (trifluoromethyl)benzenesulfonamide (2000 mg, 2.66 mmol) in (¾(¾ (26 niL). The mixture was stirred at room temperature under 2 for 0.5 hr, then TPAP (93 mg, 0.27 mmol) was added. The mixture was continued to stir at room temperature under 2 for 1.5 hr, and then filtered. The filtrates were concentrated and the residue was purified by column chromatography (100% hexane to 70% EtOAc/Hexane) to give the title compounds. LC-MS (M+l) ⁺ = 750.6

Step D: 3-(4-Amino-4-cyanocyclohexyl)-N,N-bis(4-methoxybenzyl)-2-(l- (4- methoxybenzyl)- lH-tetrazol-5-yl)-6-(trifluoromethyl)benzenesulfonamide and 3-(4-amino-4- cyanocyclohexyl)-N,N-bis(4-methoxybenzyl)-2-(2-(4-methoxyben zyl)-2H-tetrazol-5-yl)-6- (trifluoromethyl)benzenesulfonamide

N,N-bis(4-Methoxybenzyl)-2-( 1 -(4-methoxybenzyl)- lH-tetrazol-5-yl)-3 -(4- oxocyclohexyl)-6-(trifluoromethyl)benzenesulfonamide and N,N-bis(4-methoxybenzyl)-2-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)-3-(4-oxocyclohexyl)-6-(trif luoromethyl)benzenesulfonamide (300 mg, 0.400 mmol) in cone ΝΗ ₄ ΟΗ/ΜεΟΗ (1/1, 3 mL) was treated with KCN (52.1 mg, 0.800 mmol) and Ammonium Chloride (86 mg, 1.6 mmol). The mixture was heated in a sealed reaction vessel overnight. After cooling to rt, the reaction mixture was partitioned between

EtOAc and water. The organic layer was separated and concentrated. The residue was purified by column chromatography (0-80% EtOAc/Hexane) to give the title compounds. LC/MS (M+1) ^"1 = 776.6.

Step E: 3 -(4-Amino-4-(aminomethyl)cyclohexyl)-N,N-bis(4-methoxybenzyl )-2-( 1 -(4- methoxybenzyl)-lH-tetrazol-5-yl)-6-(trifluoromethyl)benzenes ulfonamide and 3-(4-amino-4-

(aminomethyl)cyclohexyl)-N,N-bis(4-methoxybenzyl)-2-(2-(4 -methoxybenzyl)-2H-tetrazol-5- yl)-6-(trifluoromethyl)benzenesulfonamide

3 -(4-Amino-4-cyanocyclohexyl)-N,N-bis(4-methoxybenzyl)-2-( 1 -(4- methoxybenzyl)- lH-tetrazol-5-yl)-6-(trifluoromethyl)benzenesulfonamide and 3-(4-amino-4- cyanocyclohexyl)-N,N-bis(4-methoxybenzyl)-2-(2-(4-methoxyben zyl)-2H-tetrazol-5-yl)-6-

(trifluoromethyl)benzenesulfonamide (222 mg, 0.286 mmol) was dissolved in acetic acid (1.5 mL), EtOH (1 mL), and DCM (2 mL). PlatinumOV) Oxide (38 mg, 0.167 mmol) was added.

The mixture was hydrogenated using a par shaker (40 psi) overnight. LC-MS showed the completion of the reaction. The reaction mixture was filtered and the filtrates were concentrated to give the crude title compounds, which were used directly in the next step. LC/MS (M+l) ⁺ =

780.7. Step F: 3-(4-Amino-4-(aminomethyl)cyclohexyl)-2-(lH-tetrazol-5-yl)-6 - (trifluoromethyl)benzenesulfonamide

3 -(4-Amino-4-(aminomethyl)cyclohexyl)-N,N-bis(4-methoxybenzyl )-2-( 1 -(4- methoxybenzyl)- lH-tetrazol-5-yl)-6-(trifluoromethyl)benzenesulfonamide and 3-(4-amino-4- (aminomethyl)cyclohexyl)-N,N-bis(4-methoxybenzyl)-2-(2-(4-me thoxybenzyl)-2H-tetrazol-5- yl)-6-(trifluoromethyl)benzenesulfonamide (223 mg, 0.286 mmol) was heated in TFA at 60°C for 2 hr. The reaction mixture was concentrated and the residue purified with Gilson (2-45% CH ₃ CN/water with 0.1% TFA) to afford 3-(4-amino-4-(aminomethyl)cyclohexyl)-2-(lH- tetrazol-5-yl)-6-(trifluoromethyl)benzenesulfonamide. LC/MS (M+l) ⁺ = 420.3.

EXAMPLE 498 and 499

3-(cis 4-(2-aminoethyl)cyclohexyl)-2-(lH-tetrazol-5-yl)-6-(trifluor omethyl)benzenesulfonamide and -(trans 4-(2-aminoethyl)cyclohexyl)-2-(lH-tetrazol-5-yl)-6- (trifluoromethyl)benzenesulfonamide

Step A: 3-(4-(Cyanomethylene)cyclohexyl)-N,N-bis(4-methoxybenzyl)-2- (l-(4- methoxybenzyl)- lH-tetrazol-5-yl)-6-(trifluoromethyl)benzenesulfonamide and 3-(4- (cyanomethylene)cyclohexyl)-N,N-bis(4-methoxybenzyl)-2-(2-(4 -methoxybenzyl)-2H-tetrazol- 5-yl)-6-(trifluoromethyl)benzenesulfonamide

To a solution of Potassium Tert-Butoxide (2.8 mL, 2.80 mmol) in THF (0.8 mL) was added Diethyl Cyanomethylphosphonate (500 mg, 2.82 mmol) in THF (0.5 mL). The resulting pale yellow solution was aged for 60 min and a solution of N,N-bis(4-methoxybenzyl)- 2-( 1 -(4-methoxybenzyl)- lH-tetrazol-5 -yl)-3 -(4-oxocyclohexyl)-6-

(trifluoromethyl)benzenesulfonamide and N,N-bis(4-methoxybenzyl)-2-(2-(4-methoxybenzyl)- 2H-tetrazol-5-yl)-3-(4-oxocyclohexyl)-6-(trifluoromethyl)ben zenesulfonamide (300 mg, 0.400 mmol) in THF ( 3 mL) was added while maintaining the temp at 0°C. The reaction turned yellow thick solution during the addition. The reaction was allowed to warm up to rt and stirred overnight. Ether and water were added, and the layers were separated. The product was extracted from water layer twice with ether. The combined organic extracts were dried over a ₂ S04, filtered, and concentrated. The resulting residue was purified by column chromatography (0-50% EtOAc/Hexane) to give the title compounds. LC/MS (M+l) ⁺ = 773.7.

Step B: 3-(4-(2-Aminoethyl)cyclohexyl)-N,N-bis(4-methoxybenzyl)-2-(l -(4- methoxybenzyl)- lH-tetrazol-5-yl)-6-(trifluoromethyl)benzenesulfonamide and 3-(4-(2- aminoethyl)cyclohexyl)-N,N-bis(4-methoxybenzyl)-2-(2-(4-meth oxybenzyl)-2H-tetrazol-5-yl)-6- (trifluoromethyl)benzenesulfonamide

3 -(4-(Cyanomethylene)cyclohexyl)-N,N-bis(4-methoxybenzyl)-2-( 1 -(4- methoxybenzyl)- lH-tetrazol-5-yl)-6-(trifluoromethyl)benzenesulfonamide and 3-(4- (cyanomethylene)cyclohexyl)-N,N-bis(4-methoxybenzyl)-2-(2-(4 -methoxybenzyl)-2H-tetrazol- 5-yl)-6-(trifluoromethyl)benzenesulfonamide (257 mg, 0.333 mmol) was hydrogenated with Pd- C (354 mg, 0.333 mmol) with a ¾ ballon overnight. The reaction mixture was filtered and the filtrates were concentrated to give an crude oil, which was dissolved in 1.5 mL of acetic acid, 1 mL of EtOH, and 2 mL of DCM. Platinum(IV) Oxide (53 mg, 0.233 mmol) was added. The mixture was hydrogenated with a par shaker (40 psi) overnight. LC-MS showed the completion of the reaction. The reaction was filtered and the filtrates were concentrated to give the crude products. LC/MS (M+l) ⁺ = 779.8

Step C: 3-(cis 4-(2-Aminoethyl)cyclohexyl)-2-(lH-tetrazol-5-yl)-6-

(trifluoromethyl)benzenesulfonamide and -(trans 4-(2-aminoethyl)cyclohexyl)-2-(lH-tetrazol- 5-yl)-6-(trifluoromethyl)benzenesulfonamide

3-(4-(2-Aminoethyl)cyclohexyl)-N,N-bis(4-methoxybenzyl)-2-(l -(4- methoxybenzyl)- lH-tetrazol-5-yl)-6-(trifluoromethyl)benzenesulfonamide and 3-(4-(2- aminoethyl)cyclohexyl)-N,N-bis(4-methoxybenzyl)-2-(2-(4-meth oxybenzyl)-2H-tetrazol-5-yl)-6- (trifluoromethyl)benzenesulfonamide (238 mg, 0.306 mmol) was heated in TFA (4 mL) at 60°C for 2 hr. After cooling to room temperature, the reaction mixture was concentrated and the residue was dissolved in DMSO (5 mL, 1 mL per injection) and purified with Gilson (2-52% CH ₃ CN/water with 0.1%TFA, 15 min gradient time). The correct fractions were combined, concentrated and lypholized to give 3-(cis 4-(2-aminoethyl)cyclohexyl)-2-(lH-tetrazol-5-yl)-6- (trifluoromethyl)benzenesulfonamide LC/MS (M+l) ⁺ = 419.5; and -(trans 4-(2- aminoethyl)cyclohexyl)-2-(lH-tetrazol-5-yl)-6-(trifluorometh yl)benzenesulfonamide. LC/MS (M+l) ⁺ = 419.5 EXAMPLES 500 and 501

3-(cis 4-(Aminomethyl)cyclohexyl)-2-(lH-tetrazol-5-yl)-6-(trifluoro methyl)benzenesulfonamide and 3 -(trans 4-(aminomethyl)cyclohexyl)-2-(lH-tetrazol-5-yl)-6- (trifluoromethyl)benzenesulfonamide

Step A: 4'-Cyano-N,N-bis(4-methoxybenzyl)-2-( 1 -(4-methoxybenzyl)- lH-tetrazol-5-yl)-

4-(trifluoromethyl)-2',3',4',5'-tetrahydro-[l, -biphenyl]-3-sulfonamide and 4'-cyano-N,N-bis(4- methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-4-(t rifluoromethyl)-2',3',4',5'- tetrahydro- [1, 1 '-biphenyl] -3 -sulfonamide

3 -Bromo-N,N-bis(4-methoxybenzyl)-2-( 1 -(4-methoxybenzyl)- lH-tetrazol-5-yl)-

6-(trifluoromethyl)benzenesulfonamide and 3-bromo-N,N-bis(4-methoxybenzyl)-2-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)-6-(trifluoromethyl)benzenes ulfonamide (1500 mg, 2.048 mmol), 4-(4,4,5,5-tetramethyl-l,3,2-dioxaborolan-2-yl)cyclohex-3-en ecarbonitrile (716 mg, 3.07 mmol), PdCi ₂ (dppf) (150 mg, 0.205 mmol) and sodium carbonate (434 mg, 4.10 mmol) were placed in a reaction vial. Dioxane (1.54E+04 μΕ) and Water (51 19 μί) were added. The reaction was sealed and degassed and heated at 80°C over a weekend. The reaction mixture was purified by column chromatography (0-60% EtOAc/Hexane) to give the title compounds.

LC/MS (M+l) ⁺ = 759.5

Step B : 3 -(4-(Aminomethyl)cyclohexyl)-N,N-bis(4-methoxybenzyl)-2-( 1 -(4- methoxybenzyl)-lH-tetrazol-5-yl)-6-(trifluoromethyl)benzenes ulfonamide and 3-(4-

(aminomethyl)cyclohexyl)-N,N-bis(4-methoxybenzyl)-2-(2-(4 -methoxybenzyl)-2H-tetrazol-5- yl)-6-(trifluoromethyl)benzenesulfonamide

4'-Cyano-N,N-bis(4-methoxybenzyl)-2-( 1 -(4-methoxybenzyl)- lH-tetrazol-5-yl)- 4-(trifluoromethyl)-2',3',4',5'-tetrahydro-[l, -biphenyl]-3-sulfonamide and 4'-cyano-N,N-bis(4- methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-4-(t rifluoromethyl)-2',3',4',5'- tetrahydro-[l, l'-biphenyl] -3 -sulfonamide (1.2 g, 1.581 mmol) was hydrogenated with Pd(OH) ₂ (1.4 g) as the catalyst at 46 psi for 36 hr. LC-MS showed cyclohexene was reduced, and some of which the CN group was also reduced. The two types of the products were separated with a SCX cartridge to afford 3-(4-cyanocyclohexyl)-N,N-bis(4-methoxybenzyl)-2-(l-(4- methoxybenzyl)- lH-tetrazol-5-yl)-6-(trifluoromethyl)benzenesulfonamide and 3-(4- cyanocyclohexyl)-N,N-bis(4-methoxybenzyl)-2-(2-(4-methoxyben zyl)-2H-tetrazol-5-yl)-6-

(trifluoromethyl)benzenesulfonamide, LC/MS (M+l) ⁺ = 761.7; 3-(4-(aminomethyl)cyclohexyl)-

N,N-bis(4-methoxybenzyl)-2-(l-(4-methoxybenzyl)-lH-tetraz ol-5-yl)-6-

(trifluoromethyl)benzenesulfonamide and 3-(4-(aminomethyl)cyclohexyl)-N,N-bis(4- methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-6-

(trifluoromethyl)benzenesulfonamide. LC/MS (M+l) ⁺ = 765.9

Step C: 3-(c s-4-(Aminomethyl)cyclohexyl)-2-(lH-tetrazol-5-yl)-6-

(trifluoromethyl)benzenesulfonamide and -(trans 4-(aminomethyl)cyclohexyl)-2-(lH-tetrazol-

5-yl)-6-(trifluoromethyl)benzenesulfonamide

3 -(4-(Aminomethyl)cyclohexyl)-N,N-bis(4-methoxybenzyl)-2-( 1 -(4- methoxybenzyl)- lH-tetrazol-5-yl)-6-(trifluoromethyl)benzenesulfonamide and 3-(4- (aminomethyl)cyclohexyl)-N,N-bis(4-methoxybenzyl)-2-(2-(4-me thoxybenzyl)-2H-tetrazol-5- yl)-6-(trifluoromethyl)benzenesulfonamide (310 mg, 0.405 mmol) was heated in TFA (3000 μϊ _^ , 38.9 mmol) at 60°C for 2 hr. After cooling to room temperature, the reaction mixture was concentrated and the residue was purified with Gilson (3-50% CH ₃ CN/water with 0.1% TFA) to afford the title compounds. LC/MS (M+l) ⁺ = 405.4 for both isomers.

EXAMPLES 502 and 503

3-(cis 4-(guanidinomethyl)cyclohexyl)-2-(lH-tetrazol-5-yl)-6- (trifluoromethyl)benzenesulfonamide and -(trans 4-(guanidinomethyl)cyclohexyl)-2-(lH- -5-yl)-6-(trifluoromethyl)benzenesulfonamide

Step A: 3 -(4-(Guanidinomethyl)cyclohexyl)-N,N-bis(4-methoxybenzyl)-2- ( 1 -(4- methoxybenzyl)- lH-tetrazol-5-yl)-6-(trifluoromethyl)benzenesulfonamide and 3-(4- (guanidinomethyl)cyclohexyl)-N,N-bis(4-methoxybenzyl)-2-(2-( 4-methoxybenzyl)-2H-tetrazol- 5-yl)-6-(trifluoromethyl)benzenesulfonamide

3 -(4-(Aminomethyl)cyclohexyl)-N,N-bis(4-methoxybenzyl)-2-( 1 -(4- methoxybenzyl)- lH-tetrazol-5-yl)-6-(trifluoromethyl)benzenesulfonamide and 3-(4- (aminomethyl)cyclohexyl)-N,N-bis(4-methoxybenzyl)-2-(2-(4-me thoxybenzyl)-2H-tetrazol-5- yl)-6-(trifluoromethyl)benzenesulfonamide (135 mg, 0.177 mmol) was dissolved in THF (2 mL), to which, was added lH-Pyrazole-l-Carboxamidine Hydrochloride (150 mg, 1.023 mmol), and DIEA (250 μί, 1.431 mmol). The mixture was stirred at room temperature under ₂ for 48 hr. The reaction mixture was diluted with DCM and washed with a small amount of water. The oragnics were filtered through a pad of a2S0 ₄ . The filtrates were concentrated to give the crude title compounds which were used directly in the next step.

Step B: 3-(cis 4-(guanidinomethyl)cyclohexyl)-2-(lH-tetrazol-5-yl)-6- (trifluoromethyl)benzenesulfonamide and 3 -(trans 4-(guanidinomethyl)cyclohexyl)-2-(lH- tetrazol-5-yl)-6-(trifluoromethyl)benzenesulfonamide

The crude 3-(4-(guanidinomethyl)cyclohexyl)-N,N-bis(4-methoxybenzyl)-2 -(l- (4-methoxybenzyl)-lH-tetrazol-5-yl)-6-(trifluoromethyl)benze nesulfonamide and 3-(4- (guanidinomethyl)cyclohexyl)-N,N-bis(4-methoxybenzyl)-2-(2-( 4-methoxybenzyl)-2H-tetrazol- 5-yl)-6-(trifluoromethyl)benzenesulfonamide was heated in TFA (2 mL) at 60°C for 2 hr. After being cooled to room temperature, the reaction was concentrated to remove TFA and the residue was purified with Gilson (2-52% CH ₃ CN/water with 0.1% TFA). The correct fractions were combined, concentrated and lypholized to afford 3-(cis 4-(guanidinomethyl)cyclohexyl)-2-(lH- tetrazol-5-yl)-6-(trifluoromethyl)benzenesulfonamide and 3-(trans 4- (guanidinomethyl)cyclohexyl)-2-(lH-tetrazol-5-yl)-6-(trifluo romethyl)benzenesulfonamide. LC/MS (M+l) ⁺ = 447.5 for both isomers.

EXAMPLE 504

4-(3-Sulfamoyl-2-(lH-tetrazol-5- -4-(trifluoromethyl)phenyl)cyclohexane-l-carboximidamide

Step A: 4-(3-(N,N-Bis(4-methoxybenzyl)sulfamoyl)-2-(l-(4-methoxybenz yl)-lH-tetrazol- 5-yl)-4-(trifluoromethyl)phenyl)-N-hydroxycyclohexane-l-carb oximidamide and 4-(3-(N,N- bis(4-methoxybenzyl)sulfamoyl)-2-(2-(4-methoxybenzyl)-2H-tet razol-5-yl)-4- (trifluoromethyl)phenyl)-N-hydroxycyclohexane-l-carboximidam ide 4'-Cyano-N,N-bis(4-methoxybenzyl)-2-( 1 -(4-methoxybenzyl)- lH-tetrazol-5-yl)-

4- (trifluoromethyl)-2',3',4',5'-tetrahydro-[l, -biphenyl]-3-sulfonamide and 4'-cyano-N,N-bis(4- methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-4-(t rifluoromethyl)-2',3',4',5'- tetrahydro-[l, l'-biphenyl] -3 -sulfonamide (0.376 g, 0.496 mmol) were placed in a flask and EtOH (5 mL) and then THF (5 mL) were added. Hydroxylamine (0.607 mL, 9.91 mmol) was added. It was observed that some solid precipated out. DMF (2 mL) was then added. The reaction was heated at 80°C with a relux condenser under 2 overnight. The reaction mixture was concentrated and the residue was purified by column chromatography (0-10% MeOH/EtOAc) to give the title compounds. LC/MS (M+l) ⁺ = 792.6

Step B: 4-(3-(N,N-Bis(4-Methoxybenzyl)sulfamoyl)-2-(l -(4-methoxybenzyl)- lH-tetrazol-

5- yl)-4-(trifluoromethyl)phenyl)cyclohexane-l-carboximidamide and 4-(3-(N,N-bis(4- methoxybenzyl)sulfamoyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol- 5-yl)-4- (trifluoromethyl)phenyl)cyclohexane- 1 -carboximidamide

4-(3 -(N,N-Bis(4-methoxybenzyl)sulfamoyl)-2-( 1 -(4-methoxybenzyl)- lH-tetrazol- 5-yl)-4-(trifluoromethyl)phenyl)-N-hydroxycyclohexane-l-carb oximidamide and 4-(3-(N,N- bis(4-methoxybenzyl)sulfamoyl)-2-(2-(4-methoxybenzyl)-2H-tet razol-5-yl)-4- (trifluoromethyl)phenyl)-N-hydroxycyclohexane-l -carboximidamide (183 mg, 0.231 mmol) were dissolved in AcOH (1156 μΚ), to which solution, was added Ammonium Formate (146 mg, 2.31 mmol), and Pd-C (100 mg, 0.094 mmol). The reaction mixture was heated at 120°C for 12 hr. Additional amount of ammonium formate was added and heating was continued at 120°C for 3 hr until LC-MS analysis showed that the starting material was consumed. The reaction mixture was cooled and concentrated. The residue was partitioned between saturated NaHC(¾ aqueous solution and DCM. The organics were separated, washed with brine, dried ( a ₂ S04), filtered and concentrated. The residue was purified by column chromatography (0-10% MeOH/ EtOAc) to give the title compounds. LC/MS (M+l) ⁺ = 777.6

Step C: 4-(3-Sulfamoyl-2-(lH-tetrazol-5-yl)-4-(trifluoromethyl)pheny l)cyclohexane-l- carboximidamide

4-(3 -(N,N-bis(4-methoxybenzyl)sulfamoyl)-2-( 1 -(4-methoxybenzyl)- lH-tetrazol- 5-yl)-4-(trifluoromethyl)phenyl)cyclohexanecarboximidamide and and 4-(3-(N,N-bis(4- methoxybenzyl)sulfamoyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol- 5-yl)-4-

(trifluoromethyl)phenyl)cyclohexane-l -carboximidamide (27 mg, 0.035 mmol) was heated in TFA at 60°C for 2 hr. The reaction mixture was concentrated and the residue was dissolved in DMSO and purified with Gilson (2-80% CH ₃ CN/water with 0.1% TFA). The correct fractions were combined and lyophilized to give 4-(3-Sulfamoyl-2-(lH-tetrazol-5-yl)-4- (trifluoromethyl)phenyl)cyclohexane-l-carboximidamide. LC/MS (M+l) ⁺ = 417.2.

EXAMPLES 505 and 506 cis and trans

3-(cis 4-(4,5-dihydro-lH-imidazol-2-yl)cyclohexyl)-2-(lH-tetrazol-5 -yl)-6- (trifluoromethyl)benzenesulfonamide and -(trans 4-(4,5-dihydro-lH-imidazol-2-yl)cyclohexyl)- 2-(lH-tetrazol-5-yl)-6-(trifluoromethyl)benzenesulfonamide

3 -(4-Cyanocyclohexyl)-N,N-bis(4-methoxybenzyl)-2-( 1 -(4-methoxybenzyl)- 1H- tetrazol-5-yl)-6-(trifluoromethyl)benzenesulfonamide and 3-(4-cyanocyclohexyl)-N,N-bis(4- methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-6-

(trifluoromethyl)benzenesulfonamide (197 mg, 0.259 mmol) was dissolved in MeOH (2589 μΚ) and cooled to 0°C. The reaction mixture was saturated with HC1 gas and then sealed. The mixture was stirred at 0°C and warmed up to room temperature overnight. The mixture was concentrated to give the crude oil. This crude oil (0.205 g, 0.259 mmol) was dissolved in MeOH (2 mL), and treated with tert-butyl (2-aminoethyl)carbamate (0.041 g, 0.259 mmol) and DIEA (0.045 mL, 0.259 mmol). The mixture was stirred at room temperature overnight, and then concentrated to give an oil, which was dissolved in TFA (2 mL) and stirred at room temperature for 2 hr. LC-MS showed the boc group was removed. The reaction mixture was concentrated and stripped with toluene/MeOH several times. TFA (4 mL) and Anisole (0.283 ml, 2.59 mmol) were added to the residue and heated at 60°C for 2 hr. Afetr cooling, the reaction mixture was concentrated to remove TFA. The residue was taken up in DMSO and purified with Gilson(2- 45% CHsCN/water) with 0.1% TFA. The fractions for fast moving isomer and slow moving isomer were combined and concentrated respectively, neutralized with SCX cartridges, then lyophilized. LC/MS (M+l) ⁺ = 444.4 for fast moving isomer; LC/MS (M+l) ⁺ = 444.3 for slow moving isomer. EXAMPLE 507

3-((6-Amino-5-(hydroxymethyl)pyridin-3-yl)ethynyl)-2-(2H-tet razol-5-yl)-6- (trifluoromethyl)benzenesulfonamide

Step A: N,N-Bis(4-methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol- 5-yl)-6-

(trifluoromethyl)-3 -((trimethylsilyl)ethynyl)benzenesulfonamide and N,N-bis(4-methoxybenzyl)-

2-(l-(4-methoxybenzyl)-lH-tetrazol-5-yl)-6-(trifluorometh yl)-3-

((trimethylsilyl)ethynyl)benzenesulfonamide

3-Bromo-N,N-bis(4-methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-t etrazol-5-yl)- 6-(trifluoromethyl)benzenesulfonamide and 3-bromo-N,N-bis(4-methoxybenzyl)-2-(l-(4- methoxybenzyl)-lH-tetrazol-5-yl)-6-(trifluoromethyl)benzenes ulfonamide (1.00 g, 1.37 mmol) was combined with Pd(PPh3) ₄ (0.137 mmol), ethynyltrimethylsilane (4.11 mmol), triethylamine (6.85 mmol) and Cul (0.274 mmol) in dioxane (20 mL) was stirred at 80°C under nitrogen for 16 hr. The reaction was quenched by brine (2 mL) and extracted with ethyl acetate (3 x 6 mL). The combined organic layers were washed with brine (6 mL). The solution was dried over anhydrous Na ₂ S0 ₄ , filtered and concentrated under reduced pressure to give a residue, which was purified by a silica gel column to afford title compounds. LC/MS [M+H] ⁺ : 750.35

Step B: 3-Ethynyl-N,N-bis(4-methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H -tetrazol-5-yl)- 6-(trifluoromethyl)benzenesulfonamide and 3 -ethynyl-N,N-bis(4-methoxybenzyl)-2-( 1 -(4- methoxybenzyl)-lH-tetrazol-5-yl)-6-(trifluoromethyl)benzenes ulfonamide

Sodium carbonate (274 mg, 2.59 mmol) was added to a rapidly stirred solution of N,N-bis(4-methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol- 5-yl)-6-(trifluoromethyl)-3- ((trimethylsilyl)ethynyl)benzenesulfonamide and N,N-bis(4-methoxybenzyl)-2-( 1 -(4- methoxybenzyl)-lH-tetrazol-5-yl)-6-(trifluoromethyl)-3- ((trimethylsilyl)ethynyl)benzenesulfonamide (970 mg, 1.294 mmol) in methanol (15 mL) at room temperature. The mixture and was stirred for 90 min. After this time the reaction was poured into water (10 mL) and extracted with diethyl ether (2 x 30 mL). The organic phase was washed with saturated brine (20 mL), dried (Na ₂ S0 ₄ ), filtered and concentrated in vacuo. The material was used without further purification. LC/MS [M+H] ⁺ : 678.33. Step C: 3-((6-Amino-5-(hydroxymethyl)pyridin-3-yl)ethynyl)-N,N-bis(4 -methoxybenzyl)- 2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-6-(trifluoromethyl) benzenesulfonamide and 3-((6- amino-5-(hydroxymethyl)pyridin-3 -yl)ethynyl)-N,N-bis(4-methoxybenzyl)-2-( 1 -(4- methoxybenzyl)-lH-tetrazol-5-yl)-6-(trifluoromethyl)benzenes ulfonamide

A solution of 3-ethynyl-N,N-bis(4-methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H - tetrazol-5-yl)-6-(trifluoromethyl)benzenesulfonamide and 3-ethynyl-N,N-bis(4-methoxybenzyl)- 2-( 1 -(4-methoxybenzyl)- lH-tetrazol-5-yl)-6-(trifluoromethyl)benzenesulfonamide

(300 mg, 0.443 mmol), (2-amino-5-iodopyridin-3-yl)methanol (133 mg, 0.531 mmol), Pd(PPh ₃ ) ₄ (0.044 mmol), TEA (2.66 mmol), and Cul (0.044 mmol) in THF (5 mL) was stirred for 4 hr at 80°C under a nitrogen atmosphere. The reaction was quenched by brine (15 mL), extracted with ethyl acetate (3 x 30 mL). The combined organic layers were washed with brine (30 mL), dried over anhydrous Na ₂ S0 ₄ , filtered, and concentrated under reduced pressure to give a residue, which was purified by a silica gel column to isolate title compounds. LC/MS [M+H] ⁺ : 800.37. Step D: 3-((6-Amino-5-(hydroxymethyl)pyridin-3-yl)ethynyl)-2-(2H-tet razol-5-yl)-6- (trifluoromethyl)benzenesulfonamide

To a solution of 3-((6-amino-5-(hydroxymethyl)pyridin-3-yl)ethynyl)-N,N-bis(4 - methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-6-

(trifluoromethyl)benzenesulfonamide and 3-((6-amino-5-(hydroxymethyl)pyridin-3-yl)ethynyl)- N,N-bis(4-methoxybenzyl)-2-(l -(4-methoxybenzyl)- lH-tetrazol-5-yl)-6- (trifluoromethyl)benzenesulfonamide (100 mg, 0.125 mmol) in DCM (4 mL) was added TFA (12.5 mmol) and anisole (1.25 mmol). The reaction mixture was heated at 80°C for 1 hr. After removing the volatile the residue was purified by HPLC and then lyophilized to give the title compound. LC/MS [M+H] ⁺ : 440.16.

EXAMPLE 508

3-(2-(6-Amino-5-(hydroxymethyl)pyridin-3-yl)ethyl)-2-(2H-tet razol-5-yl)-6-

(trifluoromethyl)benzenesulfonamide

Step A: 3-(2-(6-Amino-5-(hydroxymethyl)pyridin-3-yl)ethyl)-N,N-bis(4 -methoxybenzyl)- 2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-6-(trifluoromethyl) benzenesulfonamide and 3 -(2-(6- amino-5-(hydroxymethyl)pyridin-3-yl)ethyl)-N,N-bis(4-methoxy benzyl)-2-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)-6-(trifluoromethyl)benzenes ulfonamide

3-((6-Amino-5-(hydroxymethyl)pyridin-3-yl)ethynyl)-N,N-bis(4 -methoxybenzyl)- 2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-6-(trifluoromethyl) benzenesulfonamide and 3-((6- amino-5-(hydroxymethyl)pyridin-3 -yl)ethynyl)-N,N-bis(4-methoxybenzyl)-2-( 1 -(4- methoxybenzyl)-lH-tetrazol-5-yl)-6-(trifluoromethyl)benzenes ulfonamide (1000 mg, 1.250 mmol) and platinum(IV) oxide (142 mg, 0.625 mmol) in AcOH (20 mL) were stirred under a hydrogen atmosphere for 16 hr. The solution was filtered through celite and then concentrated and the title compounds were used without further purification. LC/MS [M+H] ⁺ : 804.48 Step B: 3-(2-(6-Amino-5-(hydroxymethyl)pyridin-3-yl)ethyl)-2-(2H-tet razol-5-yl)-6- (trifluoromethyl)benzenesulfonamide

3-(2-(6-Amino-5-(hydroxymethyl)pyridin-3-yl)ethyl)-N,N-bis(4 -methoxybenzyl)- 2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-6-(trifluoromethyl) benzenesulfonamide and 3-(2-(6- amino-5-(hydroxymethyl)pyridin-3-yl)ethyl)-N,N-bis(4-methoxy benzyl)-2-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)-6-(trifluoromethyl)benzenes ulfonamide were deprotected in the same fashion as in the preceding EXAMPLE with TFA and anisole (1.25 mmol) at 80°C for 1 hr. After removing the volatiles the residue was purified by HPLC and then lyophilized to give the title compound. LC/MS [M+H] ⁺ : 444.20.

EXAMPLE 509

4'-( 1 ,3 -Diaminopropan-2-yl)-2-( lH-tetrazol-5 -yl)-[ 1 , 1 '-biphenyl] -3 -sulfonamide

Step A: diethyl 2-(3 '-(N,N-bis(4-methoxybenzyl)sulfamoyl)-2'-( 1 -(4-methoxybenzyl)- 1H- tetrazol-5-yl)- [1,1 '-biphenyl] -4-yl)malonate and diethyl 2-(3'-(N,N-bis(4- methoxybenzyl)sulfamoyl)-2'-(2-(4-methoxybenzyl)-2H-tetrazol -5-yl)-[l, l'-biphenyl]-4- yl)malonate

3-(5,5-dimethyl-l,3,2-dioxaborinan-2-yl)-N,N-bis(4-methoxybe nzyl)-2-(l-(4- methoxybenzyl)- lH-tetrazol-5-yl)benzenesulfonamide and 3-(5,5-dimethyl-l,3,2-dioxaborinan- 2-yl)-N,N-bis(4-methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tet razol-5-yl)benzenesulfonamide (1000 mg, 1.433 mmol), Xphos precatalyst G2 (169 mg, 0.215 mmol), diethyl 2-(4- bromophenyl)malonate (452 mg, 1.43 mmol), and cesium carbonate (1400 mg, 4.30 mmol) were placed into a microwave vial. Dioxane (1.15E+04 μΚ) and Water (2867 μΚ) were added. The mixture was degassed for 15 min and then heated at 85°C overnight. The reaction mixture was loaded onto a 80 g ESCO column and eluted with 0-50% EtOAc/hexane to give the title compounds. LC/MS (M+l) ⁺ = 820.8

Step B : 4'-( 1 ,3-Dihydroxypropan-2-yl)-N,N-bis(4-methoxybenzyl)-2-( 1 -(4- methoxybenzyl)- lH-tetrazol-5-yl)-[l, l'-biphenyl]-3-sulfonamide and 4'-(l,3-dihydroxypropan-2- yl)-N,N-bis(4-methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetra zol-5-yl)-[l, l'-biphenyl]-3- sulfonamide

Diethyl 2-(3'-(N,N-bis(4-methoxybenzyl)sulfamoyl)-2'-(l-(4-methoxybe nzyl)-lH- tetrazol-5-yl)-[l,l'-biphenyl]-4-yl)malonate and diethyl 2-(3'-(N,N-bis(4- methoxybenzyl)sulfamoyl)-2'-(2-(4-methoxybenzyl)-2H-tetrazol -5-yl)-[l, l'-biphenyl]-4- yl)malonate (1.03 g, 1.26 mmol) was dissolved in THF (10 mL), cooled to -78°C. Under N ₂ , DIBAL-H (6.28 mL, 6.28 mmol) was added dropwise. The reaction mixture was allowed to warm up to room temperature overnight. The reaction was quenched by adding NH ₄ C1 aqueous solution. Celite was added to the reaction mixture and the resulting mixture was stirred at room temperature for 30 min. The mixture was filtered. The filtrates were concentrated and the residue was purified by column chromatography (0-100% EtOAc/hexane) to give the title compounds. LC/MS (M+l) ⁺ = 736.7

Step C: 4'-(l,3-Diazidopropan-2-yl)-N,N-bis(4-methoxybenzyl)-2-(l-(4 -methoxybenzyl)- lH-tetrazol-5-yl)-[l, l'-biphenyl]-3-sulfonamide and 4'-(l,3-diazidopropan-2-yl)-N,N-bis(4- methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-[l, l'-biphenyl]-3-sulfonamide

4'-(l,3-dihydroxypropan-2-yl)-N,N-bis(4-methoxybenzyl)-2-(l- (4- methoxybenzyl)- lH-tetrazol-5-yl)-[ 1, 1 '-biphenyl]-3-sulfonamide and 4'-(l ,3-dihydroxypropan-2- yl)-N,N-bis(4-methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetra zol-5-yl)-[l, l'-biphenyl]-3- sulfonamide (167 mg, 0.227 mmol) was dissolved in DCM (3 mL), at 0°C, DIEA (198 μί, 1.14 mmol) was added followed by methanesulfonyl chloride (53.1 μί, 0.681 mmol) dropwise. The reaction mixture was warmed to room temperature overnight. The reaction mixture was partitioned between DCM and aHC0 ₃ . The organics were washed with brine, dried over a ₂ S04, filtered and concentrated to give a crude product. This crude product (202 mg, 0.227 mmol) was dissolved in DMF (2270 μΐ). Sodium Azide (44.3 mg, 0.681 mmol) was added. The mixture was heated at 70°C overnight. LC-MS showed the reaction was completed. The reaction mixture was diluted with ether and washed with water. The organics were concentrated and purified by column chromatography (0- 50% EtOAc/Hexane) to give the title compounds. LC/MS (M+l) ⁺ = 786.8.

Step D : 4'-( 1 ,3 -Diaminopropan-2-yl)-N,N-bis(4-methoxybenzyl)-2-( 1 -(4-methoxybenzyl)- lH-tetrazol-5-yl)- [1, 1 '-biphenyl] -3 -sulfonamide and 4'-( 1 ,3 -diaminopropan-2-yl)-N,N-bis(4- methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-[l, l'-biphenyl]-3-sulfonamide

4'-(l,3-Diazidopropan-2-yl)-N,N-bis(4-methoxybenzyl)-2-(l-(4 -methoxybenzyl)- lH-tetrazol-5-yl)-[l, l'-biphenyl]-3-sulfonamide and 4'-(l,3-diazidopropan-2-yl)-N,N-bis(4- methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-[l, l'-biphenyl]-3-sulfonamide (130 mg, 0.165 mmol) was dissolved in DCM (1 mL) and MeOH (1 mL). Pd-C (56 mg, 0.526 mmol) was added and the reaction mixture was stirred under an atomosphere of hydrogen for 2 hr. The reaction mixture was filtered and the filtrates were concentrated to give the title compounds, which were used directly in the next step. LC-MS (M+l) ⁺ = 734.9

Step E: 4'-(l,3-Diaminopropan-2-yl)-2-(lH-tetrazol-5-yl)-[l, l'-biphenyl]-3-sulfonamide

4'-(l,3-Diaminopropan-2-yl)-N,N-bis(4-methoxybenzyl)-2-(l-(4 -methoxybenzyl)- lH-tetrazol-5-yl)- [1, 1 '-biphenyl] -3 -sulfonamide and 4'-( 1 ,3 -diaminopropan-2-yl)-N,N-bis(4- methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-[l, l'-biphenyl] -3 -sulfonamide (121 mg, 0.165 mmol) were heated at 60°C for 3 hr. The reaction mixture was cooled and concentrated. The residue was purified with Gilson 3-45% CH ₃ CN/water with 0.1% TFA to give 4'-( 1 ,3 -diaminopropan-2-yl)-2-( lH-tetrazol-5 -yl)- [ 1 , 1 '-biphenyl] -3 -sulfonamide. LC/MS (M+l)+ = 374.4

EXAMPLE 510

4-(3-Sulfamoyl-2-(lH-tetrazol-5-yl)-4-(trifluoromethyl)pheny l)-4,5,6,7- tetrahydrobenzo[i/]thiazole-2-carboxylic acid

Step A: Ethyl 4-oxo-4,5, 6,7-tetrahydrobenzo[i/]thiazole-2-carboxylate

Bromine (2.32 g, 14.5 mmol) was added dropwise to a solution of cycloh

1,2-dione (1.63 g, 14.5 mmol) in diethyl ether (14.5 mL) at 0°C over 10 min. When the addition was complete, the reaction was allowed to come to room temperature and stirred for 15 min. The reaction mixture was concentrated in vacuo. The resulting dark oil was dissolved in DCM and purified by column chromatography (100% DCM) to give a yellow solid, which was triturated in a small amount of ether. Filtration gave an off white solid. The mother liquid was purifed again with column chromatography eluting with 0-30% EtOAc/hexane to give a pale yellow solid. Two batches of solid were combined to give 3 -bromocyclohexane- 1,2-dione. This 3 -bromocyclohexane- 1,2-dione (1399 mg, 7.32 mmol) and ethyl 2-amino-2-thioxoacetate (650 mg, 4.88 mmol) were added to ethanol (1.63E+04 μΕ) and the mixture was heated at 80°C in a sealed tube overnight. LC-MS indicated this reaction was a very clean conversion. After being cooled to room temperature, the reaction mixture was purified with an 80 g ISCO column with solid loading and eluted with 0-5% MeOH/EtOAc. The correct fractions combined and concentrated to give ethyl 4-oxo-4,5,6,7-tetrahydrobenzo[<i]thiazole-2-carboxylate. LC/MS

(M+l) = 226.0

Step B: ((2-(Ethoxycarbonyl)-6,7-dihydrobenzo[i/]thiazol-4-yl)boroni c acid

Ethyl 4-oxo-4,5, 6,7-tetrahydrobenzo[i/]thiazole-2-carboxylate (627 mmol) was dissolved in THF (15 mL), and under N ₂ , NaHMDS (3618 μΐ, 3.62 mmol) was added at -78°C, dropwise. The resulting mixture was kept stirring at this temperature for 1 hr, and N,N-Bis(Trifluoromethylsulfonyl)Aniline (1392 mg, 3.90 mmol) was added. The reaction was stirred at -78°C for 1 hr, and then the reaction mixture was allowed to warm up gradually to room temperature. The reaction mixture was concentrated and purified by column

chromatography (0-40% EtOAc/hexane) to give ethyl 4-(((trifluoromethyl)sulfonyl)oxy)-6,7- dihydrobenzo[d]thiazole-2-carboxylate. In the reaction vessel was placed ethyl 4- (((trifluoromethyl)sulfonyl)oxy)-6,7-dihydrobenzo[(i]thiazol e-2-carboxylate (198 mg, 0.554 mmol), 4,4,4',4',5,5,5',5'-octamethyl-2,2'-bi(l,3,2-dioxaborolane) (422 mg, 1.66 mmol), potassium acetate (163 mg, 1.66 mmol) and PCy3 Pd G2 (33 mg, 0.055 mmol). Then dry dioxane (2.18E+04 μΚ) was added to this flask. This mixture was degassed and then heated at 80°C for 12 hr. LC-MS showed the desired mass. The mixture was cooled, filtered and concentrated. The resulting residue was purified by column chromatography on silica gel (120 g), eluting first with with 0-100% then with 0-30% MeOH/EtOAc to give the desired product (2- (Ethoxycarbonyl)-6,7-dihydrobenzo[i/]thiazol-4-yl)boronic acid. LC/MS (M+l) ⁺ = 254.2 Step C : 4-(3 -(N,N-bis(4-methoxybenzyl)sulfamoyl)-2-( 1 -(4-methoxybenzyl)- lH-tetrazol-

5- yl)-4-(trifluoromethyl)phenyl)-6,7-dihydrobenzo[i/]thiazole- 2-carboxylic acid and 4-(3-(N,N- bis(4-methoxybenzyl)sulfamoyl)-2-(2-(4-methoxybenzyl)-2H-tet razol-5-yl)-4-

(trifluoromethyl)phenyl)-6,7-dihydrobenzo[if|thiazole-2-c arboxylic acid

3- Bromo-N,N-bis(4-methoxybenzyl)-2-(l-(4-methoxybenzyl)-lH-tet razol-5-yl)-

6- (trifluoromethyl)benzenesulfonamide and 3-bromo-N,N-bis(4-methoxybenzyl)-2-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)-6-(trifluoromethyl)benzenes ulfonamide (300 mg, 0.410 mmol), (2-(ethoxycarbonyl)-6,7-dihydrobenzo[i/]thiazol-4-yl)boronic acid (124 mg, 0.491 mmol), PdCl ₂ (dppf) (30.0 mg, 0.041 mmol) and sodium carbonate (87 mg, 0.82 mmol) were placed in a reaction vial. Dioxane (3071 μί) and Water (1024 μΕ) were added. The reaction vessel was sealed and degassed and heated at 80°C overnight. LC-MS showed there were still starting material present. After the reaction mixture cooled to room temperature, more catalyst (16 mg) was added. The reaction was degassed and hetated at 80°C for 20 hr. After the reaction cooled to rt, the mixture was loaded onto the ISCO column and eluted with 0-50%

EtOAc/hexane, then with 0-20% MeOH/EtOAc to give the title compounds. LC/MS (M+l) ⁺ = 833.8.

Step D: 4-(3-(N,N-Bis(4-methoxybenzyl)sulfamoyl)-2-(l -(4-methoxybenzyl)- lH-tetrazol- 5-yl)-4-(trifluoromethyl)phenyl)-4,5,6,7-tetrahydrobenzo[if| thiazole-2-carboxylic acid and 4-(3- (N,N-bis(4-methoxybenzyl)sulfamoyl)-2-(2-(4-methoxybenzyl)-2 H-tetrazol-5-yl)-4- (trifluoromethyl)phenyl)-4,5,6,7-tetrahydrobenzo[(i]thiazole -2-carboxylic acid

4- (3 -(N,N-bis(4-methoxybenzyl)sulfamoyl)-2-( 1 -(4-methoxybenzyl)- lH-tetrazol- 5-yl)-4-(trifluoromethyl)phenyl)-6,7-dihydrobenzo[i/]thiazol e-2-carboxylic acid and 4-(3-(N,N- bis(4-methoxybenzyl)sulfamoyl)-2-(2-(4-methoxybenzyl)-2H-tet razol-5-yl)-4-

(trifluoromethyl)phenyl)-6,7-dihydrobenzo[if|thiazole-2-c arboxylic (70 mg, 0.084 mmol) was dissolved in MeOH (1 mL) and EtOAc (1 mL). Pd(OH) ₂ (35.4 mg, 0.050 mmol) was added. The mixture was hydrogenated at 50 psi for 22 hr. LC-MS showed about 50% conversion to the desired product. The reaction was filtered and the filtrates were concentrated. The crude product was subjected to hydrogenation again (50 psi) at room temperature for 26 hr in MeOH (1 mL), EtOAc (1 mL) with Pd (OH)2 (41 mg). LC-MS showed the reaction was completed. The reaction was diluted with EtOAc and MeOH, filtered through a Celite pad. The filtrates were concentrated to give the title compounds. LC/MS (M+l) ⁺ = 835.8

Step E: 4-(3-Sulfamoyl-2-(lH-tetrazol-5-yl)-4-(trifluoromethyl)pheny l)-4,5,6,7- tetrahydrobenzo[i/]thiazole-2-carboxylic acid

4-(3 -(N,N-bis(4-methoxybenzyl)sulfamoyl)-2-( 1 -(4-methoxybenzyl)- lH-tetrazol- 5-yl)-4-(trifluoromethyl)phenyl)-4,5,6,7-tetrahydrobenzo[i/] thiazole-2-carboxylic acid and 4-(3- (N,N-bis(4-methoxybenzyl)sulfamoyl)-2-(2-(4-methoxybenzyl)-2 H-tetrazol-5-yl)-4- (trifluoromethyl)phenyl)-4,5,6,7-tetrahydrobenzo[(i]thiazole -2-carboxylic acid (50 mg, 0.060 mmol) was heated in TFA (2 mL) at 60°C for 1.5 hr. The reaction was concentrated and the residue was purified with Gilson (3 - 75% CH ₃ CN/water) with 0.1% TFA. The correct fraction was concentrated and lypholized to give 4-(3-sulfamoyl-2-(lH-tetrazol-5-yl)-4-

(trifluoromethyl)phenyl)-4,5,6,7-tetrahydrobenzo[(i]thiaz ole-2-carboxylic acid. LC/MS (M+l) ⁺ = 475.4.

EXAMPLE 511

4'-(2-Amino-l,4,5,6-tetrahydropyrimidin-5-yl)-2-(lH-tetrazol -5-yl)-[l, r-biphenyl]-3- sulfonamide

4'-( 1 ,3 -diaminopropan-2-yl)-2-( lH-tetrazol-5 -yl)- [1, 1 '-biphenyl] -3 -sulfonamide bis(2,2,2-trifluoroacetate) (42 mg, 0.070 mmol) in MeOH (3491 μΚ) was treated with cyanic bromide (7.4 mg, 0.070 mmol) followed by DIEA (24.39 μί, 0.140 mmol). The mixture was stirred at room temperature overnight. The reaction mixture was concentrated and purified with Gilson (2-65% CHsCN/water with 0.1% TFA). The correct fractions were combined, concentrated and lypholized to give 4'-(2-Amino-l,4,5,6-tetrahydropyrimidin-5-yl)-2-(lH- tetrazol-5-yl)-[l, l'-biphenyl]-3-sulfonamide. LC/MS (M+l) ⁺ = 399.5. EXAMPLES 512-543

Removal of the p-methoxybenzyl protecting groups on REFERENCE EXAMPLES 38-71 immediately above by trifluoroacetic acid.

The previous list of generated PMB protected REFERENCE EXAMPLES 38-71 were dissolved into TFA (100 equivalents) and anisole (10 equivalents). The reaction mixture was heated at 80°C for 1 - 3 hr. After removing the volatiles the crude products were purified by

HPLC and then lyophilized to give the corresponding title compounds in the following Table.

EXAMPLE 544

3-(2-aminobenzo[^]thiazol-4-yl)-6-( iperidin-4-ylmethyl)-2-(2H-tetrazol-5- yl)benzenesulfonamide

Step A: 3-(2-(bis(4-methoxybenzyl)amino)benzo[(ilthiazol-4-yl)-6-bro mo-N.N-bis(4- methoxybenzyl -2-( ^' 2-( ^' 4-methoxybenzyl -2H-tetrazol-5-yl benzenesulfonamide

To a mixture of 3-(2-aminobenzo[d]thiazol-4-yl)-6-bromo-N,N-bis(4- methoxybenzyl)-2-(l-(4-methoxybenzyl)-lH-tetrazol-5-yl)benze nesulfonamide (250 mg, 0.308 mmol), l-(chloromethyl)-4-methoxybenzene (106 mg, 0.677 mmol) in 2-butanone (1.5 mL) at rt l-(chloromethyl)-4-methoxybenzene (106 mg, 0.677 mmol) was added, followed by potassium carbonate (170 mg, 1.23 mmol) and sodium iodide (101 mg, 0.677 mmol). The reaction was stirred under nitrogen overnight at 80°C and monitored by LCMS. More reagents were added until starting material was consumed. The reaction mixture was then filtered, and rinsed by EtOAc. The combined organic layer was evaporated, and the crude product was purified by silica gel column chromatography with EtO Ac/Hex (0-100%) as eluent to give the title compound. LC-MS (IE, m/z): 1054.75 [M+2] ⁺ . Step B: tert-butyl 4-(4-(2-(bis(4-methoxybenzyl)amino)benzo[if|thiazol-4-yl)-2-

(N,N-bis(4-methoxybenzyl)sulfamoyl)-3-(2-(4-methoxybenzyl )-2H-tetrazol-5- yl)benzyl)piperidine- 1 -carboxylate

A microwave vial was charged with tert-butyl 4-(iodomethyl)piperidine- 1 - carboxylate (67.9 mg, 0.209 mmol), Nickel(II) Iodide (9.79 mg, 0.031 mmol), Manganese (17.22 mg, 0.313 mmol), Bathophenanthroline (5.21 mg, 0.016 mmol) and 3-(2-(bis(4- methoxybenzyl)amino)benzo[d]thiazol-4-yl)-6-bromo-N,N-bis(4- methoxybenzyl)-2-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)benzenesulfonamide (110 mg, 0.104 mmol). The vial was sealed, purged with ₂ for 10 min, and filled with DMA (522 μΕ). The resulting mixture was purged with ₂ for another 10 min and heated over the weekend at 80°C. The reaction mixture was filtered over celite to remove the metal. The filtrate was concentrated and purified by silica gel column chromatography (RediSep gold column, 120 g gold column) using 0-100%

EtOAc/hexane as mobile phase (isocratic at 20% and 40% for a while, removed some des-Br product, which came out first) to afford the product. LCMS: (M+H) ⁺ 1 172.46.

Step C: 3-(2-aminobenzo[if|thiazol-4-yl)-6-(piperidin-4-ylmethyl)-2- (2H-tetrazol-5- yl)benzenesulfonamide

To tert-butyl 4-(4-(2-(bis(4-methoxybenzyl)amino)benzo[if|thiazol-4-yl)-2- (N,N- bis(4-methoxybenzyl)sulfamoyl)-3-(2-(4-methoxybenzyl)-2H-tet razol-5-yl)benzyl)piperidine-l- carboxylate (90 mg, 0.077 mmol) was added Anisole (84 μΕ, 0.768 mmol) and TFA (592 μΕ, 7.68 mmol) at rt. The resulting mixture was stirred at rt for 1 hr to remove both Boc and both PMB protection. After removing the volatiles the residue was purified by reverse phase HPLC using DMSO to load sample and 5-55% acetonitrile/water (0.1% TFA as additive) as mobile phase over 10 min to separate desired product from des-Br product. To a solution of the desired mono-PMB intermediate product in DCM (768 μί) was added Anisole (84 μΕ, 0.768 mmol) and TFA (592 μΕ, 7.68 mmol) at rt. The resulting mixture was stirred at 80°C for 1 hr to remove the final PMB protection. After removing the volatiles the residue was purified by reverse phase HPLC using DMSO to load sample and 5-40% acetonitrile/water (0.1% TFA as additive) as mobile phase over 10 min to give the final product. LC-MS (IE, m/z): 471.4 [M+l] ⁺ .

EXAMPLE 545

3-(2-aminobenzo[i/]thiazol-4-yl)-6-(azetidin-3-ylmethyl)-2-( 2H-tetrazol-5- yl)benzenesulfonamide

The title compound was prepared in an analogous fashion to that described for the preparation of 4'-(piperidin-4-yl)-4-(piperidin-4-ylmethyl)-2-(2H-tetrazol- 5-yl)-[l,r-biphenyl]- 3 -sulfonamide (immediately above) using intermediate 3-(2-(bis(4-methoxybenzyl)amino)-lH- benzo[d]imidazol-4-yl)-6-bromo-N,N-bis(4-methoxybenzyl)-2-(2 -(4-methoxybenzyl)-2H- tetrazol-5-yl)benzenesulfonamide and tert-butyl 3-(iodomethyl)azetidine-l-carboxylate. LC-MS (IE, m/z): 443.50 [M+lf.

EXAMPLE 546

6-(azetidin-3-ylmethyl)-3-(imidazo -a]pyridin-3-yl)-2-(2H-tetrazol-5-yl)benzenesulfonamide

The title compound was prepared in an analogous fashion to that described for the preparation of 4'-(piperidin-4-yl)-4-(piperidin-4-ylmethyl)-2-(2H-tetrazol- 5-yl)-[l,r-biphenyl]- 3 -sulfonamide using intermediates 6-bromo-3-iodo-N,N-bis(4-methoxybenzyl)-2-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)benzenesulfonamide, 3-(4,4,5,5-tetramethyl- 1,3,2- dioxaborolan-2-yl)imidazo[l,2-a]pyridine, and tert-butyl 3-(iodomethyl)azetidine-l-carboxylate. LC-MS (IE, m/z): 41 1.58 [M+lf. EXAMPLES 547-562

Synthesis of 4'-substituted 2-(2H-tetrazol-5-yl)-4-(trifluoromethyl)biphenyl-3 -sulfonamides

Step A: Palladium catalyzed C-C coupling of arylherterocyclicbromide and boronic acids or boronic esters (such as pinacol esters).

Into a 50 mL three necked round bottom flask was placed a solution of 3-(N,N- bis(4-methoxybenzyl)sulfamoyl)-2-(2-(4-methoxybenzyl)-2H-tet razol-5-yl)-4- (trifluoromethyl)phenylboronic acid (0.18 g, 0.26 mmol), 2nd generation X-phos precatalyst (30 mg, 0.04 mmol), heterocycle bromide (commercially available, known from the literature, or prepared as described herein) and CS2CO ₃ (0.25 g, 0.77 mmol) in dioxane (1.5 mL) and water (0.4 mL). The resulting mixture was degassed with nitrogen for 3 times and stirred for 16 hr at 80°C. The reaction was quenched with water (8 mL) and extracted with EtOAc (3 x 15 mL). The combined organic layers was washed with water (2 x 20 mL) and brine (2 x 20 mL), dried over anhydrous Na ₂ S0 ₄ and filtered. The filtrate was concentrated under vacuum. The residue was purified by silica gel column chromatography to afford the coupled products.

Step B: Removal of the / methoxybenzyl (PMB) protecting group by TFA.

Into a 50 mL round bottom flask was placed a solution of the coupled products from Step A (0.16 mmol) in DCM (2.0 mL) followed by the additional of TFA (1.0 mL). After the resulting mixture was stirred at ambient temperature for 3 hr, the solvent was removed under vacuum. The residue was dissolved in DCM (0.2 mL), to which was added anisole (1.0 mL, 0.16 mmol) and TFA (2.0 mL, 26.0 mmol). The resulting mixture was stirred at 80°C for 6 hr. After the solvent was removed under vacuum, the residue was purified by Prep-HPLC, typically with the following conditions: Column: X Bridge RP18, 19 x 150 mm, 5 μιη; Mobile Phase A: water (0.05% TFA), Mobile Phase B: ACN; Flow rate: 20 mL/min; Gradient: 10%B to 40%B in 7 min; Detection: UV 254 nm to afford the title compounds in the Table immediately below. Note that when the Aryl group contains a Boc protective group, this group is removed under the conditions of Step B.

Ex. Structure Name Calc'd. LC/MS No. MW m/e

[M+H] ⁺ [M+H] ⁺

547 H 3 - [4- [(35)-3 -aminopyrrolidin- 454.1 454.2

' ^Ν Ν 0 3 -yl]phenyl] -2-(2H-tetrazol-5 - yl)-6-

(trifluoromethyl)benzenesulfon

N amide

H

548 H 3 -[4- [(3 R)-3 -aminopyrrolidin- 454.1 454.2

3 -yl]phenyl] -2-(2H-tetrazol-5 - yl)-6-

(trifluoromethyl)benzenesulfon

N amide

H

549 3 -(2-amino- 1 ,3 -benzothiazol- 442.4 442.2

6-yl)-2-(lH-tetrazol-5-yl)-6- (trifluoromethyl)benzenesulfon

amide

550 3 -(2-amino- 1 ,3 -benzothiazol- 442.4 442.8

5-yl)-2-(lH-tetrazol-5-yl)-6- (trifluoromethyl)benzenesulfon

amide

562 3-(5-aminopyridin-2-yl)-2- 386 386

(lH-tetrazol-5-yl)-6- (trifluoromethyl)benzenesulfon

amide

EXAMPLE 563

N-(azetidin-3-yl)-3'-sulfamoyl-2'-(2H-tetrazol-5-yl)-4'-(tri fluoromethyl)biphi

carboximidamide

Step A: 4'-cyano-N,N-bis(4-methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H- tetrazol-5-yl)-4- (trifluoromethyl)biphenyl-3-sulfonamide

Into a 25-mL round-bottom flask purged and maintained with an inert atmosphere of argon, was placed a solution of 3-bromo-N,N-bis(4-methoxybenzyl)-2-(l-(4-methoxybenzyl)- lH-tetrazol-5-yl)-6-(trifluoromethyl)benzenesulfonamide (0.20 g, 0.27 mmol) in dioxane/water (v : v = 4 : 1, 4 mL). This was followed by the addition of 4-(4,4,5,5-tetramethyl-l,3,2- dioxaborolan-2-yl)benzonitrile (0.13 g, 0.55 mmol), [1, 1'- bis(diphenylphosphino)ferrocene]dichloropalladium(II) (20 mg, 0.03 mmol), a ₂ C0 ₃ (87 mg , 0.82 mmol) at ambient temperature. The reaction mixture was stirred at 80°C for 2 hr under argon atmosphere. The resulting mixture was cooled down to 20°C and the solvent was evaporated under vacuum. The residue was purified by Prep-TLC with EtO Ac/petroleum ether (1/2) to afford the title compound: LCMS (ESI) calc'd for CsgHssFs gOjS [M + H] ⁺ : 755, found 755;

Step B: methyl 2'-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-3'-(N-(4- methoxybenzyl)sulfamoyl)-4'-(trifluoromethyl)biphenyl-4-carb imidate

Into a solution of 4'-cyano-N,N-bis(4-methoxybenzyl)-2-(l-(4-methoxybenzyl)- lH-tetrazol-5-yl)-4-(trifluoromethyl)-[l, r-biphenyl]-3-sulfonamide (100 mg, 0.132 mmol) in dry MeOH (20 mL) was bubbled with dry HC1 (g) at ambient temperature. The saturated HC1 solution was stirred for 5 hr at ambient temperature. The solvent was evaporated under vacuum to afford the crude title compound, which was used directly in the next step without further purification: LCMS (ESI) calc'd for C ₃ 2H ₂₉ F _{3 6} 0 ₅ S [M + H] ⁺ : 667, found 667.

Step C: tert-butyl 3-(2'-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-3'-(N-(4- methoxybenzyl)sulfamoyl)-4'-(trifluoromethyl)biphenyl-4-ylca rboximidamido)azetidine-l- carboxylate

Into a 25-mL round-bottom flask purged and maintained with an inert atmosphere of argon, was placed a solution of methyl 2'-(l-(4-methoxybenzyl)-lH-tetrazol-5-yl)-3'-(N-(4- methoxybenzyl)sulfamoyl)-4'-(trifluoromethyl)-[l, r-biphenyl]-4-carbimidate (0.14 g, 0.13 mmol) in DCM (2 mL). This was followed by the addition of N,N-diisopropylethylamine (65 mg, 0.50 mmol) and tert-butyl 3-aminoazetidine-l-carboxylate (43 mg, 0.25 mmol) at 0°C. The resulting mixture was stirred at 20°C for 24 hr under argon atmosphere. The solvent was evaporated under vacuum and the residue was purified by silica gel column chromatography, eluted with EtOAc/PE (1 : 2) to afford the title compound: LCMS (ESI) calc'd for

C ₃₉ H4iF _{3 8} 0 ₆ S [M + H] ⁺ : 807, found 807;

Step D: N-(azetidin-3-yl)-2'-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)- 3'-(N-(4- methoxybenzyl)sulf amoyl)-4'-(trifluoromethyl)biphenyl-4-carboximidamide

To a solution of tert-butyl 3-(2'-(l-(4-methoxybenzyl)-lH-tetrazol-5-yl)-3'-(N-(4- methoxybenzyl)sulfamoyl)-4'-(trifluoromethyl)-[l, r-biphenyl]-4-ylcarboximidamido)azetidine- 1 -carboxylate (0.12 g, 0.12 mmol) in anisole (1 mL) was added TFA (1 mL) at 0°C. The resulting mixture was stirred at 0°C for 1 hr and then the solvent was evaporated under vacuum. The residue was used directly in the next step without further purification: LCMS (ESI) calc'd for C ₃₄ H ₃₃ F ₃ N ₈ 0 ₄ S [M + H] ⁺ : 707, found 707.

Step E: N-(azetidin-3-yl)-3'-sulfamoyl-2'-(2H-tetrazol-5-yl)-4'-(tri fluoromethyl)biphenyl- 4-carboximidamide

To a solution of N-(azetidin-3-yl)-2'-(l-(4-methoxybenzyl)-lH-tetrazol-5-yl)- 3'-

(N-(4-methoxybenzyl)sulfamoyl)-4'-(trifluoromethyl)-[l, r-biphenyl]-4-carboximidamide (0.10 g, 0.1 1 mmol) in anisole (0.5 mL) was added TFA (3 mL) at ambient temperature. The resulting mixture was stirred at 80°C for 16 hr. The resulting mixture was cooled down to 20°C and the solvent was evaporated under vacuum. The residue was purified by Prep-HPLC with the following conditions: Column: X Bridge C18, 19 x 150 mm, 5 μιη; Mobile Phase A: water (10 mM NH ₄ HCO ₃ ); Mobile Phase B: ACN; Flow rate: 20 mL/min; Gradient: 10-18% B in 8 min; Detection: at 254 nm; Retention time: 6.6 min. The collected fractions were combined and concentrated under reduced pressure to afford the title compound: LCMS (ESI) calc'd for CisHnFs sOzS [M + H] ⁺ : 467, found 467;

EXAMPLE 564

N-(pyrrolidin-3-yl)-3'-sulfamoyl-2'-(2H-tetrazol-5-yl)-4'-(t rifluoromethyl)biphenyl-4- carboximidamide

Step A: tert-butyl 3-(2'-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-3'-(N-(4- methoxybenzyl)sulfamoyl)-4'-(trifluoromethyl)biphenyl-4-ylca rboximidamido)pyrrolidine-l- carboxylate

To a stirred solution of methyl 2'-(l-(4-methoxybenzyl)-lH-tetrazol-5-yl)-3'-(N- (4-methoxybenzyl)sulfamoyl)-4'-(trifluoromethyl)-[l,r-biphen yl]-4-carbimidate (0.35 g, 0.34 mmol) in DCM (3 mL) and MeOH (1 mL) were added DIEA (0.60 ml, 3.41 mmol) and tert- butyl 3-aminopyrrolidine-l-carboxylate (0.32 g, 1.71 mmol) at 0°C under argon atmosphere. The resulting mixture was stirred at ambient temperature for 24 hr under argon atmosphere. The solvent was evaporated under vacuum and the residue was purified by Prep-TLC, eluted with EtOAcA/PE (1 : 2) to afford the title compound: LCMS (ESI) calc'd for C ₄ oH4 ₃ F _{3 8} 0 ₆ S [M + H] ⁺ : 821 , found 821.

Step B: 2'-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-3'-(N-(4-methoxybe nzyl)sulfamoyl)- N-(pyrrolidin-3-yl)-4'-(trifluoromethyl)biphenyl-4-carboximi damide.

A solution of tert-butyl 3-(2'-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-3'-(N-(4- methoxybenzyl)sulfamoyl)-4'-(trifluoromethyl)- [1, 1 '-biphenyl] -4- ylcarboximidamido)pyrrolidine-l-carboxylate (0.26 g, 0.22 mmol) in anisole (1 mL) and TFA (1 mL) was stirred at ambient temperature for 1 hr. The solvent was evaporated under vacuum and the residue was used directly in the next step without further purification: LCMS (ESI) calc'd for CssHssFs sC^S [M + H] ⁺ : 721, found 721 Ste C: N-(pyrrolidin-3-yl)-3'-sulfamoyl-2'-(2H-tetrazol-5-yl)-4'- (trifluoromethyl)biphenyl-4-carboximidamide

A solution of 2'-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-3'-(N-(4- methoxybenzyl)sulfamoyl)-N-(pyrrolidin-3 -yl)-4'-(trifluoromethyl)- [ 1 , 1 '-biphenyl]-4- carboximidamide (0.22 g, 0.18 mmol) in anisole (1 mL) and TFA (3 mL) was stirred at 80°C for 16 hr. The resulting mixture was cooled down to 20°C and the solvent was evaporated under vacuum. The residue was purified by Prep-HPLC with the following conditions: Column: X Bridge C18, 19 x 150 mm, 5 μιη; Mobile Phase A: water (10 mM NH ₄ HCO ₃ ), Mobile Phase B: ACN; Flow rate: 20 mL/min; Gradient: 10-18% B in 8 min; Detection: at 254 nm; Retention time: 6.0 min. The collected fractions were combined and concentrated under reduced pressure to afford the title compound: LCMS (ESI) calc'd for [M + H] ⁺ : 481, found 481.

EXAMPLE 565

N-(3-aminopropyl)-3'-sulfamoyl-2'-(2H-tetrazol-5-yl)-4'-(tri fluoromethyl)biphenyl-4- carboximidamide

Step A: tert-butyl 3-(2'-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-3'-(N-(4- methoxybenzyl)sulfamoyl)-4'-(trifluoromethyl)biphenyl-4-ylca rboximidamido)propylcarbamate

To a solution of methyl 2'-(l-(4-methoxybenzyl)-lH-tetrazol-5-yl)-3'-(N-(4- methoxybenzyl)sulfamoyl)-4'-(trifluoromethyl)-[l,r-biphenyl] -4-carbimidate (0.18 g, 0.21 mmol) in DCM (5 mL) were added DIEA (0.18 mL, 1.05 mmol) and tert-butyl (3- aminopropyl)carbamate (0.15 g, 0.84 mmol) at 0°C under nitrogen. The mixture was stirred at ambient temperature for 36 hr under argon atmosphere. The solvent was evaporated under vacuum and the residue was purified by Prep-TLC, eluted with EtOAc/PE (1 : 2) to afford the crude title compound: LCMS (ESI) calc'd for CsgtL _t sFs sOgS [M + H] ⁺ : 809 , found 809. Step B: N-(3-aminopropyl)-2'-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)- 3'-(N-(4- methoxybenzyl)sulfamoyl)-4'-(trifluoromethyl)biphenyl-4-carb oximidamide A solution of tert-butyl (3-(2'-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-3'-(N-(4- methoxybenzyl)sulfamoyl)-4'-(trifluoromethyl)- [1, 1 '-biphenyl] -4- ylcarboximidamido)propyl)carbamate (0.20 g, 0.20 mmol) in DCM (2 mL) was added TFA (0.5 ml, 6.49 mmol) at 0°C. The resulting mixture was stirred at 0°C for 2 hr. The solvent was evaporated under vacuum and the residue was used directly in the next step without further purification: LCMS (ESI) calc'd for C ₃ 4H ₃ 5F _{3 8} O4S [M + H] ⁺ : 709, found 709.

Step C: N-(3-aminopropyl)-3'-sulfamoyl-2'-(2H-tetrazol-5-yl)-4'- (trifluoromethyl)biphenyl-4-carboximidamide

To a solution of N-(3-aminopropyl)-2'-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)- 3'- (N-(4-methoxybenzyl)sulfamoyl)-4'-(trifluoromethyl)-[l,r-bip henyl]-4-carboximidamide (0.18 g, 0.20 mmol) in anisole (0.5 mL) was added TFA (3 mL, 38.9 mmol) at ambient temperature. The resulting mixture was stirred at 80°C for 3 hr. The reaction mixture was cooled down to 20°C and the solvent was evaporated under vacuum. The residue was purified by Prep-HPLC with the following conditions: Column: X Bridge CI 8, 19 x 150 mm, 5 μιη; Mobile Phase A: water (0.05% TFA), Mobile Phase B: ACN; Flow rate: 20 mL/min; Gradient: 30%B to 70%B in 10 min; Detection: at 254 nm. The collected fractions were combined and concentrated under reduced pressure to afford the title compound: LCMS (ESI) calc'd for C1 ₈ H1 ₉ F _{3 8} O2S [M + H] ⁺ : 469, found 469.

EXAMPLE 566

3-(2-amino-5-fluoro-lH-benzo[d]imidazol-7-yl)-2-(lH-tetrazol -5-yl)-6-

(trifluoromethyl)benzenesulfonamide

Step A: 7-bromo-5-fluoro-lH-benzo[<f]imidazol-2-amine.

To a 25 mL microwave tube was added a solution of 3-bromo-5-fluorobenzene- 1,2-diamine (0.410 g, 2.0 mmol) in 6 mL of methanol, followed by addition of cyanic bromide (0.254 g, 2.40 mmol) and 4 mL of water. The mixture was stirred for 16 hr. TLC showed most SM was converted. The reaction mixture was heated at 80°C for 1 hr and no SM was left. The solvent was removed via rotavapor and the residue was purified via column chromatography (ISCO RediSep gold column, 40g) using 0-10% MeOH/DCM as mobile phase to afford the title compound. LC-MS (M + H) ⁺ : 230.08.

Step B: 3-(2-amino-5-fluoro-lH-benzo[d]imidazol-7-yl)-N,N-bis(4-meth oxybenzyl)-2-(l- (4-methoxybenzyl)-lH-tetrazol-5-yl)-6-(trifluoromethyl)benze nesulfonamide and 3-(2-amino-5- fluoro-lH-benzo[d]imidazol-7-yl)-N,N-bis(4-methoxybenzyl)-2- (2-(4-methoxybenzyl)-2H- tetrazol-5-yl)-6-(trifluoromethyl)benzenesulfonamide

To a 10 mL RBF was added cesium carbonate (63.8 mg, 0.196 mmol), 7-bromo- 5-fluoro-lH-benzo[d]imidazol-2-amine (15.77 mg, 0.069 mmol), 3-(5,5-dimethyl-l,3,2- dioxaborinan-2-yl)-N,N-bis(4-methoxybenzyl)-2-(2-(4-methoxyb enzyl)-2H-tetrazol-5-yl)-6- trifluoromethyl)benzenesulfonamide (50 mg, 0.065 mmol) and Xphos Pd G2 (10.28 mg, 0.013 mmol). The flask was sealed, degassed, and filled with dioxane (0.8ml) and water (0.200 ml). The resulting mixture was heated at 80°C for overnight. The reaction mixture was filtered through a celite pad to removed palladium. The filtrate was diluted with EtOAc and washed with water. The organic layer was dried over anhydrous MgS04, filtered, concentrated and purified by silica gel column chromatography (ISCO RediSep gold column, 40g) using 0-10% MeOH/DCM as mobile phase and the title compound was isolated. LC/MS (M+H) ⁺ : 799.7. Step C: 3-(2-amino-5-fluoro-lH-benzo[d]imidazol-7-yl)-2-(lH-tetrazol -5-yl)-6- (trifluoromethyl)benzenesulfonamide

To a solution of 3-(2-amino-5-fluoro-lH-benzo[d]imidazol-7-yl)-N,N-bis(4- methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-6-

(trifluoromethyl)benzenesulfonamide (15 mg, 0.019 mmol) in DCM (200 μΐ) was added anisole (20 μΐ, 0.187 mmol) and TFA (144 μΐ, 1.868 mmol) at 0°C. The reaction mixture was stirred at 80°C for 1 hr. After removing the volatile, the residue was dissolved in 1 mL of DMSO and purified by Gilson using 3 to 60% water (0.05% TFA) in acetonitrile (0.05% TFA) to afford the title compound. LC/MS (M+H) ⁺ : 443.34.

EXAMPLE 567

3-(2-amino-5-(trifluoromethyl)-lH-benzo[d]imidazol-7-yl)-N,N -bis(4-methoxybenzyl)-2-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)-6-(trifluoromethyl) benzenesulfonamide

Step A: 7-bromo-5-(trifluoromethyl)-lH-benzo[(i]imidazol-2-amine.

To a 25 mL microwave tube was added a solution of 3-bromo-5- (trifluoromethyl)benzene-l,2-diamine (0.510 g, 2.0 mmol) in 6 mL of methanol, followed by addition of cyanic bromide (0.254 g, 2.40 mmol) and 4 mL of water. The mixture was stirred for 16 hr. TLC showed most SM was converted. The reaction mixture was heated at 80°C for 1 hr and no SM was left. The solvent was removed via rotavapor and the residue was purified via column chromatography (ISCO RediSep gold column, 40g) using 0-10% MeOH/DCM as mobile phase to afford the title compound. LC-MS (M + H) ⁺ : 280.10.

Step B: 3-(2-amino-5-(trifluoromethyl)-lH-benzo[d]imidazol-7-yl)-N,N -bis(4- methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-6-

(trifluoromethyl)benzenesulfonamide and 3-(2-amino-5-(trifluoromethyl)- lH-benzo[d]imidazol-

7-yl)-N,N-bis(4-methoxybenzyl)-2-(l-(4-methoxybenzyl)-lH- tetrazol-5-yl)-6-

(trifluoromethyl)benzenesulfonamide

To a 10 mL RBF was added cesium carbonate (63.8 mg, 0.196 mmol), 7-bromo-

5- (trifluoromethyl)-lH-benzo[d]imidazol-2-amine (19.20 mg, 0.069 mmol), 3-(5,5-dimethyl- l,3,2-dioxaborinan-2-yl)-N,N-bis(4-methoxybenzyl)-2-(2-(4-me thoxybenzyl)-2H-tetrazol-5-yl)-

6- trifluoromethyl)benzenesulfonamide (50 mg, 0.065 mmol) and Xphos Pd G2 (10.28 mg, 0.013 mmol). The flask was sealed, degassed, and filled with dioxane (0.8 ml) and water (0.2 ml). The resulting mixture was heated at 80°C for overnight. The reaction mixture was filtered through a celite pad to removed palladium. The filtrate was diluted with EtOAc and washed with water. The organic layer was dried over anhydrous MgS04, filtered, concentrated and purified by silica gel column chromatography (ISCO RediSep gold column, 40g) using 0-10% MeOH/DCM as mobile phase and the title compound was isolated. LC/MS (M+H) ⁺ : 853.84.

Step C: 3-(2-amino-5-(trifluoromethyl)-lH-benzo[d]imidazol-7-yl)-N,N -bis(4- methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-6-(t rifluoromethyl)

benzenesulfonamide To a solution of 3-(2-amino-5-trifluoromethyl-lH-benzo[d]imidazol-7-yl)-N,N- bis(4-methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl )-6-(trifluoromethyl)benzene- sulfonamide (20 mg, 0.023 mmol) in DCM (0.2 ml) was added anisole (26 μΐ, 0.24 mmol) and TFA (181 μΐ, 2.35 mmol) at 0°C. The reaction mixture was stirred at 80°C for 1 hr. After removing the volatile, the residue was dissolved in 1 mL of DMSO and purified by Gilson using 3 to 60% water (0.05% TFA) in acetonitrile (0.05% TFA) to afford the title compound. LC/MS (M+H) ⁺ : 493.36.

EXAMPLE 568

3-(2-amino-4-methyl-lH-benzo[d]imidazol-7-yl)-2-(lH-tetrazol -5-yl)-6- (trifluoromethyl)benzenesulfonamide

Step A: 7-bromo-4-methyl-lH-benzo[i/]imidazol-2-amine.

To a 25 mL microwave tube was added a solution of 3-bromo-4-methylbenzene- 1,2-diamine (201 mg, 1.0 mmol) in 6 mL of methanol, followed by addition of cyanic bromide (127 mg, 1.20 mmol) and 4 mL of water. The mixture was stirred for 16 hr. TLC showed most SM was converted. The reaction mixture was heated at 80°C for 1 hr and no SM was left. The solvent was removed via rotavapor and the residue was purified via column chromatography (ISCO RediSep gold column, 40g) using 0-10% MeOH/DCM as mobile phase to afford the title compound. LC-MS (M + H) ⁺ : 228.10.

Step B: 3-(2-amino-4-methyl-lH-benzo[d]imidazol-7-yl)-N,N-bis(4-meth oxybenzyl)-2- (2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-6-(trifluoromethyl)be nzenesulfonamide and 3-(2-amino- 4-methyl- lH-benzo[d]imidazol-7-yl)-N,N-bis(4-methoxybenzyl)-2-(l -(4-methoxybenzyl)- 1H- tetrazol-5-yl)-6-(trifluoromethyl)benzenesulfonamide

To a 10 mL RBF was added cesium carbonate (63.8 mg, 0.196 mmol), 7-bromo- 4-methyl-lH-benzo[d]imidazol-2-amine (15.5 mg, 0.069 mmol), 3-(5,5-dimethyl-l,3,2- dioxaborinan-2-yl)-N,N-bis(4-methoxybenzyl)-2-(2-(4-methoxyb enzyl)-2H-tetrazol-5-yl)-6- (trifluoromethyl)benzenesulfonamide (and its tetrazole PMB isomer) (50 mg, 0.065 mmol) and Xphos Pd G2 (10.28 mg, 0.013 mmol). The RBF was sealed, degassed, and filled with dioxane (0.8 ml) and water (0.2 ml). The resulting mixture was heated at 80°C for overnight, then was cooled and filtered through a celite pad to removed palladium. The filtrate was diluted with EtOAc, then was washed with water. The organic layer was dried over anhydrous MgS04, filtered, concentrated and purified by silica gel column chromatography (ISCO RediSep gold column, 40g) using 0-10% MeOH/DCM as mobile phase to afford the title compounds. LC/MS (M+H) ⁺ : 799.9.

Step C: 3-(2-amino-4-methyl-lH-benzo[d]imidazol-7-yl)-2-(lH-tetrazol -5-yl)-6- (trifluoromethyl)benzenesulfonamide

To a solution of 3-(2-amino-4-methyl-lH-benzo[d]imidazol-7-yl)-N,N-bis(4- methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-6-

(trifluoromethyl)benzenesulfonamide (20mg, 0.025 mmol) in DCM (200 μΐ) was added anisole (27.2 μΐ, 0.250 mmol) and TFA (193 μΐ, 2.504 mmol) at 0°C. The reaction mixture was stirred at 80°C for 1 hr. After removing the volatile, the residue was dissolved in 1 mL of DMSO and purified by Gilson using 3 to 60% water (0.05% TFA) in acetonitrile (0.05% TFA). LC/MS (M+H) ⁺ : 439.33.

EXAMPLE 569

3-(2-amino-5-cyano-lH-benzo[d]imidazol-7-yl)-2-(lH-tetrazol- 5-yl)-6- (trifluoromethyl)benzenesulfonamide

Step A: 2-amino-7-bromo-lH-benzo[i/]imidazole-5-carbonitrile.

To a 25 mL microwave tube was added a solution of 3,4-diamino-5- bromobenzonitrile (212 mg, 1.0 mmol) in 6 mL of methanol, followed by addition of cyanic bromide (127 mg, 1.20 mmol) and 4 mL of water. The mixture was stirred for 16 hr. TLC showed most SM was converted. The reaction mixture was heated at 80°C for 1 hr and no SM was left. The solvent was removed via rotavapor and the residue was purified via column chromatography (ISCO RediSep gold column, 40g) using 0-10% MeOH/DCM as mobile phase to afford the title compound. LC-MS (M + H) ⁺ : 238.89.

Step B: 3-(2-amino-5-cyano-lH-benzo[d]imidazol-7-yl)-N,N-bis(4-metho xybenzyl)-2-(l- (4-methoxybenzyl)-lH-tetrazol-5-yl)-6-(trifluoromethyl)benze nesulfonamide and 3-(2-amino-5- cyano-lH-benzo[d]imidazol-7-yl)-N,N-bis(4-methoxybenzyl)-2-( 2-(4-methoxybenzyl)-2H- tetrazol-5-yl)-6-(trifluoromethyl)benzenesulfonamide

To a 10 mL RBF was added cesium carbonate (63.8 mg, 0.196 mmol), 2- amino-7-bromo-lH-benzo[d]imidazole-5-carbonitrile (16.26 mg, 0.069 mmol), 3-(5,5-dimethyl- l,3,2-dioxaborinan-2-yl)-N,N-bis(4-methoxybenzyl)-2-(2-(4-me thoxybenzyl)-2H-tetrazol-5-yl)- 6-(trifluoromethyl)benzenesulfonamide (50 mg, 0.065 mmol) and Xphos Pd G2 (10.28 mg,

0.013 mmol). The vial was sealed, degassed, and filled with Dioxane (0.8ml) and Water (0.200 ml). The resulting mixture was heated at 80°C ovenight. The reaction mixture was filtered through a celite pad to remove palladium. The filtrate was diluted with EtOAc and washed with water. The organic layer was dried over anhydrous MgS04, filtered, concentrated and purified by silica gel column chromatography (ISCO RediSep gold column, 40g) using 0-20%

MeOH/DCM as mobile phase to afford the title compound. LC/MS (M+H) ⁺ : 810.8.

Step C : 3 -(2-amino-5-cyano- 1 H-benzo [d] imidazol-7-yl)-2-( 1 H-tetrazol-5 -yl)-6-

(trifluoromethyl)benzenesulfonamide

To a solution of 3-(2-amino-5-cyano-lH-benzo[d]imidazol-7-yl)-N,N-bis(4- methoxybenzyl)-2-(l -(4-methoxybenzyl)- 1 H-tetrazol-5 -yl)-6-

(trifluoromethyl)benzenesulfonamide and 3-(2-amino-5-cyano- lH-benzo[d]imidazol-7-yl)-N,N- bis(4-methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl )-6-

(trifluoromethyl)benzenesulfonamide (20 mg, 0.025 mmol) in DCM (200 μΐ) was added anisole (26.8 μΐ, 0.247 mmol) and TFA (190 μΐ, 2.470 mmol) at 0°C. The reaction mixture was stirred at 80°C for 1 hr. After removing the volatile, the residue was dissolved in 1 mL of DMSO and purified by Gilson using 3 to 60% water (0.05% TFA) in acetonitrile (0.05% TFA). LC/MS (M+H) ⁺ : 450.37.

EXAMPLE 570

3-(2-amino-lH-imidazo[4,5-b]pyridin-7-yl)-2-(lH-tetrazol-5-y l)-6- (trifluoromethy l)benzenesulfonamide

Step A: 3-(2,3-diaminopyridin-4-yl)-N,N-bis(4-methoxybenzyl)-2-(l-(4 -methoxybenzyl)- lH-tetrazol-5-yl)-6-(trifluoromethyl)benzenesulfonamide and 3-(2,3-diaminopyridin-4-yl)-N,N- bis(4-methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl )-6- (trifluoromethyl)benzenesulfonamide

To a 10 niL RBF was added cesium carbonate (280 mg, 0.860 mmol), 2- bromopyridine-3,4-diamine (53.9 mg, 0.287 mmol), (3-(N,N-bis(4-methoxybenzyl)sulfamoyl)-2- (2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-4-(trifluoromethyl)ph enyl)boronic acid (200 mg, 0.287 mmol) and Xphos Pd G2 (22.56 mg, 0.029 mmol). The vial was sealed, degassed, and filled with dioxane (2.4 ml) and water (0.6 ml). The resulting mixture was heated at 80°C for 2 hr. The reaction mixture was filtered through a celite pad. The filtrate was diluted with EtOAc and washed with water. The organic layer was dried over anhydrous MgS04, filtered, concentrated and purified by silica gel column chromatography (ISCO RediSep gold column, 24 g) using 0- 10% MeOH/DCM as mobile phase (3% and 6% isostatic) to afford the title compound. LC/MS (M+H) ⁺ : 761.37.

Step B: 3-(2-amino-lH-imidazo[4,5-b]pyridin-7-yl)-N,N-bis(4-methoxyb enzyl)-2-(l-(4- methoxybenzyl)-lH-tetrazol-5-yl)-6-(trifluoromethyl)benzenes ulfonamide and 3-(2-amino-lH- imidazo[4,5-b]pyridin-7-yl)-N,N-bis(4-methoxybenzyl)-2-(2-(4 -methoxybenzyl)-2H-tetrazol-5- yl)-6-(trifluoromethyl)benzenesulfonamide

To a 10 mL microwave tube was added a solution of 3-(2,3-diaminopyridin-4-yl)-

N,N-bis(4-methoxybenzyl)-2-( 1 -(4-methoxybenzyl)- 1 H-tetrazol-5-yl)-6- (trifluoromethyl)benzenesulfonamide and 3-(2,3-diaminopyridin-4-yl)-N,N-bis(4- methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-6- (trifluoromethyl)benzenesulfonamide (82 mg, 0.108 mmol) and di(lH-imidazol-l- yl)methanimine (17.37 mg, 0.108 mmol) in 2 mL of DMF. The mixture was refluxed at 120°C for overnight. LC-MS showed formation of the desired product. DMF was removed under vacuum and the residual was chromatographed by silica gel column chromatography (ISCO RediSep gold column 24 g) using 0-20% methanol/DCM as mobile phase to afford the title compound. LC/MS (M+H) ⁺ : 786.78.

Step C: 3-(2-amino-lH-imidazo[4,5-b]pyridin-7-yl)-2-(lH-tetrazol-5-y l)-6- (trifluoromethyl)benzenesulfonamide

To a solution of 3-(2-amino-lH-imidazo[4,5-b]pyridin-7-yl)-N,N-bis(4- methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-6-

(trifluoromethyl)benzenesulfonamide (17 mg, 0.022 mmol) in DCM (0.2 mL) was added anisole (23.51 μϊ _^ , 0.216 mmol) and TFA (167 μϊ _^ , 2.163 mmol) at 0°C. The reaction mixture was stirred at 80°C for 1 hr. After removing the volatile, the residue was dissolved in 1 mL of DMSO and purified by Gilson using 3 to 60% water (0.05% TFA) in acetonitrile (0.05% TFA) to afford the title compound. LC/MS (M+H) ⁺ : 426.38.

EXAMPLE 571

3-(2-amino-lH-imidazo[4,5-c]pyridin-7-yl)-2-(lH-tetrazol-5-y l)-6-

(trifluoromethyl)benzenesulfonamide

Step A: 3-(4,5-diaminopyridin-3-yl)-N,N-bis(4-methoxybenzyl)-2-(l-(4 -methoxybenzyl)- 1 H-tetrazol-5-yl)-6-(trifluoromethyl)benzenesulfonamide and 3 -(4,5-diaminopyridin-3 -yl)-N,N- bis(4-methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl )-6- (trifluoromethyl)benzenesulfonamide

To a 10 ml RBF was added cesium carbonate (140 mg, 0.430 mmol), 5- bromopyridine-3,4-diamine (27.0 mg, 0.143 mmol), (3-(N,N-bis(4-methoxybenzyl)sulfamoyl)-2- (2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-4-(trifluoromethyl)ph enyl)boronic acid (100 mg, 0.143 mmol) and Xphos Pd G2 (11.28 mg, 0.014 mmol). The RBF was sealed, degassed, and filled with dioxane (1.2 ml) and water (0.3 ml). The resulting mixture was heated at 80°C for 2 hr. The reaction mixture was filtered through a celite pad. The filtrate was diluted with EtOAc and washed with water. The organic layer was dried over anhydrous MgSO_i, filtered, concentrated and purified by silica gel column chromatography ( ISCO RediSep gold column, 24 g) using 0- 10% MeOH/DCM as mobile phase (3% and 6% isostatic) to afford the title compounds. LC/MS (M+H) ⁺ : 761.71.

Step B : 3 -(2-amino- 1 H-imidazo [4,5-c]pyridin-7-yl)-N,N-bis(4-methoxybenzyl)-2-( 1 -(4- methoxybenzyl)-lH-tetrazol-5-yl)-6-(trifluoromethyl)benzenes ulfonamide and 3-(2-amino-lH- imidazo[4,5-c]pyridin-7-yl)-N,N-bis(4-methoxybenzyl)-2-(2-(4 -methoxybenzyl)-2H-tetrazol-5- yl)-6-(trifluoromethyl)benzenesulfonamide

To a 10 mL sealed tube was added a solution of 3-(4,5-diaminopyridin-3-yl)-N,N- bis(4-methoxybenzyl)-2-( 1 -(4-methoxybenzyl)- 1 H-tetrazol-5-yl)-6- (trifluoromethyl)benzenesulfonamide and 3-(4,5-diaminopyridin-3-yl)-N,N-bis(4- methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-6-

(trifluoromethyl)benzenesulfonamide (42 mg, 0.055 mmol) and di(lH-imidazol-l- yl)methanimine (8.90 mg, 0.055 mmol) in DMF (3 mL). The mixture was stirred for overnight at 120°C. The solvent was removed in vacuum and the residue was purified by column chromatography (ISCO RediSep Gold column 24g) using 0-20% methanol/DCM as mobile phase to afford the title compounds. LC/MS (M+H) ⁺ : 786.68.

Step C : 3 -(2-amino- 1 H-imidazo [4,5-c]pyridin-7-yl)-2-( 1 H-tetrazol-5 -yl)-6-

(trifluoromethyl)benzenesulfonamide

To a solution of 3-(2-amino-lH-imidazo[4,5-c]pyridin-7-yl)-N,N-bis(4- methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-6- (trifluoromethyl)benzenesulfonamide (17 mg, 0.022 mmol) in DCM (0.2 ml) was added anisole (23.51 μΐ, 0.216 mmol) and TFA (167 μΐ, 2.163 mmol) at 0°C. The reaction mixture was stirred at 80°C for 1 hr. After removing the volatile, the residue was dissolved in 1 mL of DMSO and purified by Gilson using 3 to 60% water (0.05% TFA) in acetonitrile (0.05% TFA). LC/MS (M+H) ⁺ : 426.48.

EXAMPLE 572

3-((6-amino-2-methylpyridin-3-yl)methyl)-2-(2H-tetrazol-5-yl )benzenesulfonamide

Step A: N,N-bis(4-methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol- 5-yl)-3- vinylbenzenesulfonamide

Into a 100 mL three necked round bottom flask was placed a solution of 3-bromo- N,N-bis(4-methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol- 5-yl)benzenesulfonamide (1.00 g, 1.51 mmol), potassium vinyltrifluoroborate (0.40 g, 3.01 mmol), PdC dppf) (0.11 g, 0.15 mmol) and a ₂ C0 ₃ (0.48 g, 4.51 mmol) in dioxane (12 mL) and water (2.5 mL). The resulting mixture was degassed with nitrogen for 3 times and stirred for overnight at 90°C. The solvent was removed under reduced pressure. The residue was diluted with EtOAc (100 mL), washed with water (2 x 30 mL) and brine (30 mL), dried over anhydrous Na ₂ S0 ₄ and filtered. The filtrate was concentrated under reduced and the residue was purified by silica gel column chromatography, eluted with EtOAc/PE (1 : 2) to give the title compound: LCMS (ESI) calc'd for C ₃₃ H ₃₃ N5O5S [M + H] ⁺ : 612, found 612;

Step B: 3-formyl-N,N-bis(4-methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H- tetrazol-5- yl)benzenesulfonamide

Into a 100 mL round bottom flask was placed a solution of N,N-bis(4- methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-3-vi nylbenzenesulfonamide (0.65 g, 1.06 mmol) and 4-methylmorpholine N-oxide (0.16 g, 1.38 mmol) in ACN (9 mL) and water (1.8 mL) followed by the additional of a solution of Os0 ₄ (30 mg) in water (0.5 mL) with stirring at ambient temperature. After the resulting mixture was stirred at ambient temperature for 1 hr, NaI0 ₄ (0.68 g, 3.19 mmol) was added and the resulting mixture was stirred at ambient temperature for 1 hr. The reaction mixture with heavy precipitate was filtered through celite, washed with EtOAc (20 mL). The combined organic layers were concentrated under vacuum to give the title compound: LCMS (ESI) calc'd for C ₃ 2H ₃ i ₅ 0 ₆ S [M + H] ⁺ : 614, found 614;

Step C: 3-(hydroxymethyl)-N,N-bis(4-methoxybenzyl)-2-(2-(4-methoxybe nzyl)-2H- tetrazol-5-yl)benzenesulfonamide Into a 100 niL round bottom flask was placed a solution of 3-formyl-N,N-bis(4- methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)benze nesulfonamide (0.63 g, 1.03 mmol) in MeOH (10 mL), NaBH ₄ (78 mg, 2.06 mmol) was added in portions at 0°C. The reaction mixture was stirred at ambient temperature for 1 hr and then quenched with ice water (5 mL), diluted with water (10 mL) and extracted with ethyl acetate (3 x 20 mL). The combined organic layers were washed with water (30 mL) and brine (30 mL), dried over anhydrous Na ₂ S0 ₄ and filtered. The filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography, eluting with EtOAc/PE (2 : 1) to give the title compound: LCMS (ESI) calc'd for C ₃ 2H _{33 5} 0 ₆ S [M + H] ⁺ : 616, found 616;

Step D: 3-(bromomethyl)-N,N-bis(4-methoxybenzyl)-2-(2-(4-methoxybenz yl)-2H- tetrazol-5-yl)benzenesulfonamide

Into a 100 mL round bottom flask was placed a solution of 3-(hydroxymethyl)- N,N-bis(4-methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol- 5-yl)benzenesulfonamide (0.43 g, 0.70 mmol) in DCM (10 mL). To this solution was added PBr ₃ (0.20 mL, 2.01 mmol) with stirring at 0°C. The resulting mixture was stirred at ambient temperature for 30 min. and then quenched with water (5 mL), diluted with water (10 mL) and extracted with EtOAc (3 x 20 mL). The combined organic layers were washed with water (20 mL), brine (20 mL), dried over anhydrous Na ₂ S0 ₄ and filtered. The filtrate was concentrated under reduced pressure and the residue was purified by silica gel column chromatography, eluted with EtOAc/PE(l : 3) to give the title compound: LCMS (ESI) calc'd for C ₃ 2H ₃₂ Br ₅ 0 ₅ S [M + H] ⁺ : 678, 680 (1 : 1), found 678, 680 (1 : 1);

Step E: 3 -((6-amino-2-methylpyridin-3 -yl)methyl)-N,N-bis(4-methoxybenzyl)-2-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)benzenesulfonamide

Into a 50 mL three necked round bottom flask were placed 3-(bromomethyl)-N,N- bis(4-methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl )benzenesulfonamide (0.27 g, 0.40 mmol), 6-methyl-5-(4,4,5,5-tetramethyl-l,3,2-dioxaborolan-2-yl)pyri din-2-amine (0.14 g, 0.60 mmol), PdCl ₂ (dppf) (29 mg, 0.04 mmol) and a ₂ C0 ₃ (0.13 g, 1.20 mmol) in Dioxane (5 mL) and water (1.0 mL). The reaction mixture was degassed with nitrogen for 3 times and stirred for 4 hr at 80°C. The resulting mixture was poured into water (5 mL), extracted with EtOAc (3 x 15 mL). The combined organic layers were washed with water (15 mL), brine (15 mL), dried over anhydrous Na ₂ S0 ₄ and filtered. The filtrate was concentrated under reduced pressure and the residue was purified by silica gel column chromatography, eluted with

EtOAc/PE (1 : 1) to give the title compound: LCMS (ESI) calc'd for C ₃₈ H ₃₉ 7O5S [M + H] ⁺ : 706, found 706;

Step F : 3-((6-amino-2-methylpyridin-3-yl)methyl)-2-(2H-tetrazol-5- yl)benzenesulfonamide

Into a 50 mL round bottom flask was placed a solution of 3-((6-amino-2- methylpyridin-3-yl)methyl)-N,N-bis(4-methoxybenzyl)-2-(2-(4- methoxybenzyl)-2H-tetrazol-5- yl)benzenesulfonamide (0.20 g, 0.28 mmol) in DCM (2.0 mL), anisole (2.0 mL) and TFA (4.0 mL). The resulting mixture was stirred at 85°C for 16 hr. The solvent was removed under reduced and the residue was purified by Prep-HPLC with the following conditions: Column: T 3, 19 x 150 mm, 5 μιη; Mobile Phase A: water (0.05% TFA), Mobile Phase B: ACN; Flow rate: 20 mL/min; Gradient: 5%B to 30% B in 8 min; Detection: UV 254 nm. The collected fractions were combined and concentrated under reduced pressure to give the title compound: LCMS (ESI) calc'd for d^NvC^S [M + H] ⁺ : 346, found 346;

EXAMPLE 573

3-((6-amino-4-methylpyridin-3-yl)methyl)-2-(2H-tetrazol-5-yl )benzenesulfonamide

Step A: 3-((6-amino-4-methylpyridin-3-yl)methyl)-N,N-bis(4-methoxybe nzyl)-2-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)benzenesulfonamide

To a stirred solution of 3-(bromomethyl)-N,N-bis(4-methoxybenzyl)-2-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl) benzene sulfonamide (0.20 g, 0.30 mmol) in dioxane/water (4/1) (5 ml) were added l, l '-bis(diphenyl phosphino)ferrocene]dichcloropalladium (22 mg, 0.03 mmol), 4-methyl-5-(4,4,5,5-tetramethyl-l,3,2-dioxaborolan-2-yl) pyridin-2 -amine (0.10 g, 0.44 mmol), a ₂ C0 ₃ (94 mg, 0.88 mmol) at ambient temperature. After the resulting mixture was degassed with nitrogen for 3 times and stirred at 80°C for 2 hr under nitrogen, it was cooled down to room temperature and the solids were filtered out. The filtrate was concentrated and the residue was purified by silica gel column chromatography, eluteding with EtOAc/PE (10/1) to give the title compound: LCMS (ESI) calc'd for C ₃₈ H ₃₉ 7O5S [M + H] ⁺ : 706, found 706.

Step B: 3-((6-amino-4-methylpyridin-3-yl)methyl)-2-(2H-tetrazol-5- yl)benzenesulfonamide

To a stirred solution of 3-((6-amino-4-methylpyridin-3-yl)methyl)-N, N-bis(4- methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl) benzenesulfonamide (0.16 g, 0.18 mmol) in DCM (2 ml) and anisole (2 ml) was added TFA (0.10 g, 0.89 mmol) at ambient temperature. The resulting mixture was stirred at 80°C for 16 hr and then concentrated under reduced pressure. The residue was purified by Prep-HPLC with the following conditions:

Column, Xbridge CI 8, 19 x 150 mm; mobile phase: water (0.05% TFA) and acetonitrile (hold 34% acetonitrile for 8 min, hold 100% for 2 min, down to 34% in 2 min); Detector, UV 220 and 254 nm; retention time: 6.18 min. The collected fractions were combined and concentrated under reduced pressure to afford 30 mg (37%) of 3-((6-amino-4-methylpyridin-3-yl)methyl)-2- (2H-tetrazol-5-yl)benzenesulfonamide 2,2,2-trifluoroacetate as a colorless solid: LCMS (ESI) calc'd for C14H15N7O2S [M + H] ⁺ : 346, found 346.

EXAMPLE 574

6-(((ls,4s)-4-aminocyclohexyl)methyl)-3-(6-aminopyridin-3-yl )-2-(2H-tetrazol-5- yl)benzenesulfonamide

H ₂

Step A: 3-(6-aminopyridin-3-yl)-6-bromo-N,N-bis(4-methoxybenzyl)-2-( 2-(4- methoxybenzyl)-2H-tetrazol-5-yl)benzenesulfonamide

Into a 100-mL round bottom flask was placed a solution of 6-bromo-3-iodo-N,N- bis(4-methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl )benzenesulfonamide (2.00 g, 2.53 mmol), 5-(4,4,5,5-tetramethyl-l,3,2-dioxaborolan-2-yl)pyridin-2-ami ne (0.89 g, 4.05 mmol) and Pd(PPh ₃ ) ₄ (0.29 g, 0.25 mmol) and Na ₂ C03 (0.81 g, 7.59 mmol) in dioxane (40 mL) and water (8 mL) at ambient temperature. The resulting mixture was degassed with nitrogen and stirred at 80°C for 16 hr under nitrogen and then quenched with water (200 rnL) and extracted with EtOAC (3 x 200 rnL). The combined organics were washed with brine (500 mL), dried over anhydrous Na ₂ S0 ₄ and filtered. The filtrate was evaporated under reduced pressure and the residue was purified by a silica gel column chromatography, eluted with EtOAc/petroleum ether (4/1) to afford the title compound: LCMS (ESI) calc'd for [M + H] ⁺ : 756, 758 (1 : 1), found 756, 758 (1 : 1).

Step B : 3 -(6-(bis(4-methoxybenzyl)amino)pyridin-3 -yl)-6-bromo-N,N-bis(4- methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)benze nesulfonamide

To a stirred solution of 3-(6-aminopyridin-3-yl)-6-bromo-N,N-bis(4- methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)benze nesulfonamide (2.00 g, 2.64 mmol) in DMF (30 mL) was added NaH (0.19 g, 7.93 mmol) at 0°C. The resulting mixture was stirred for 30 min at ambient temperature, and then 4-methoxybenzyl bromide (1.59 g, 7.93 mmol) was added dropwise at 0°C. After the resulting mixture was stirred for 3 hours at ambient temperature, the reaction was quenched with water (20 mL) and extracted with EtOAc (3 x 20 mL). The combined organic layers were washed with brine (2 x 20 mL), dried over anhydrous Na ₂ S0 ₄ and filtered. The filtrate was concentrated under reduced pressure and the residue was purified by silica gel chromatography, eluted with EtOAc/PE (1/3) to give the title compound: LCMS (ESI) calc'd for C ₅₂ H ₅ oBr ₇ 0 ₇ S [M + H] ⁺ : 996, 998 (1 : 1), found 996, 998 (1 : 1).

Step C: tert-butyl (ls,4s)-4-(4-(6-(bis(4-methoxybenzyl)amino)pyridin-3-yl)-2-( N,N- bis(4-methoxybenzyl)sulfamoyl)-3-(2-(4-methoxybenzyl)-2H-tet razol-5- yl)benzyl)cyclohexylcarbamate

Into a 50 mL round bottom flask was placed a solution of 3-(6-(bis(4- methoxybenzyl)amino)pyridin-3-yl)-6-bromo-N,N-bis(4-methoxyb enzyl)-2-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)benzenesulfonamide (0.20 g, 0.20 mmol), tert-butyl ((15,45)- 4-(iodomethyl)cyclohexyl)carbamate (0.14 g, 0.40 mmol), Mn (22 mg, 0.40 mmol), L (12 mg, 0.04 mmol), bathophenanthroline (10 mg, 0.03 mmol) and benzonitrile (4 mg, 0.04 mmol) in DMA (1.2 mL). The resulting mixture was degassed with nitrogen for 3 times, then TMSC1 (5 μί, 0.04 mmol) was added at 0°C and stirred for 2 hr at 60°C. The reaction mixture was quenched with water (10 mL) and extracted with EtOAc (3 x 5 mL). The combined organic layers were washed with water (25mL), brine (25mL), dried over anhydrous Na ₂ S0 ₄ and filtered. The filtrate was concentrated under vacuum and the residue was purified by Prep-HPLC with the following conditions: Column: X Bridge RP18, 19 x 150 mm, 5 μιη; Mobile Phase A: water (0.05% TFA), Mobile Phase B: ACN; Flow rate: 20 mL/min; Gradient: 52% B to 90% B in 10 min; Detection: UV 254 nm. The collected fractions were concentrated under vacuum to afford the title compound: LCMS (ESI) calc'd for [M + H] ⁺ : 1 129, found 1129.

Step D: 6-(((ls,4s)-4-aminocyclohexyl)methyl)-3-(6-aminopyridin-3-yl )-2-(2H-tetrazol-5- yl)benzenesulfonamide

Into a 10 mL round bottom flask was placed a solution of tert-butyl ((ls,4s)-4-(4- (6-(bis(4-methoxybenzyl)amino)pyridin-3-yl)-2-(N,N-bis(4-met hoxybenzyl)sulfamoyl)-3-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)benzyl)cyclohexyl)carbamate (0.15 g, 0.13 mmol) in DCM (2 mL), TFA (1 mL, 26.00 mmol) was added. After the resulting mixture was stirred at ambient temperature for 2 hr, the solvent was removed under vacuum. The residue was dissolved in DCM (0.5 mL), and then anisole (1 mL) and trifluoroacetic acid (2 mL, 26.0 mmol) was added sequentially. The resulting mixture was stirred at 80°C for 16 hr. The solvent was removed under reduced pressure and the residue was purified by Prep-HPLC with the following conditions: Column: X Bridge RP18, 19 x 150 mm, 5 μιη; Mobile Phase A: water (0.05%

NH ₄ HCO ₃ ), Mobile Phase B: ACN; Flow rate: 20 mL/min; Gradient: 5% B to 16% B in 7 min; Detection: UV 254 nm. The collected fractions were concentrated under reduced pressure to afford the title compound: LCMS (ESI) calc'd for [M + H] ⁺ : 429, found 429.

EXAMPLES 575-581

In the similar way to 6-(((ls,4s)-4-aminocyclohexyl)methyl)-3-(6-aminopyridin-

3-yl)-2-(2H-tetrazol-5-yl)benzenesulfonamide, the following compounds were synthesized starting from 3-(6-(bis(4-methoxybenzyl)amino)pyridin-3-yl)-6-bromo-N,N-bi s(4- methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)benze nesulfonamide and using alkyl halides prepared as described above.

Ex. Structure Name Calc'd. LC/MS

No. MW m/e

[M+H] ⁺ [M+H] ⁺ 581 3 -(6-aminopyridin-3 -yl)-6-(2- 429 429

(piperidin-4-yl)ethyl)-2-( 1H- tetrazol-5-yl)benzenesulfonamide

EXAMPLE 582

4-(((lr,4r)-4-aminocyclohexyl)methyl)-4'-(pyrrolidin-3-yl)-2 -(2H-tetrazol-5-yl)-[ 1 , 1 '-biphenyl]- -sulfonamide

Step A : tert-butyl 3-(3'-(N,N-bis(4-methoxybenzyl)sulfamoyl)-4'-bromo-2'-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)biphenyl-4-yl)pyrrolidine-l- carboxylate

Into a 50-mL round bottom flask was added a solution of sodium carbonate (0.40 g, 3.79 mmol) in dioxane (10 mL)/water (2.5 mL) (v/v 4: 1) at ambient temperature. Then tetrakis(triphenylphosphine)palladium(0) (0.15 g, 0.13 mmol), tert-butyl 3-(4-(4,4,5,5- tetramethyl-l,3,2-dioxaborolan-2-yl)phenyl)pyrrolidine-l-car boxylate (0.76 g, 2.02 mmol) and 6-bromo-3-iodo-N,N-bis(4-methoxybenzyl)-2-(2-(4-methoxybenzy l)-2H-tetrazol-5- yl)benzenesulfonamide (1.00 g, 1.26 mmol) were added sequentially. The resulting mixture was degassed with nitrogen for 3 times and then stirred for 4 hr at 100°C under nitrogen. The resulting mixture was quenched and extracted by EtOAc (3 x 20 mL). The organic layers were combined and concentrated under reduced pressure. The residue was purified by a silica gel column chromatography, edluted with EtOAc/DCM/petroleum ether (1/1/5) to afford the title compound: LCMS (ESI) calc'd for C ₄₆ H4 ₉ Br ₆ 0 ₇ S [M + H] ⁺ : 909, 911 (1 : 1), found 909, 911 (1 : 1).

Step B : tert-butyl 3-(3'-(N,N-bis(4-methoxybenzyl)sulfamoyl)-4'-(((lr,4r)-4-(te rt- butoxycarbonylamino)cyclohexyl)methyl)-2'-(2-(4-methoxybenzy l)-2H-tetrazol-5-yl)biphenyl-4- yl)pyrrolidine- 1 -carboxylate Into a 50 mL round bottom flask were placed tert-butyl 3-(3'-(N,N-bis(4- methoxybenzyl)sulfamoyl)-4'-bromo-2'-(2-(4-methoxybenzyl)-2H -tetrazol-5-yl)-[l, r-biphenyl]- 4-yl)pyrrolidine-l-carboxylate (0.30 g, 0.33 mmol), tert-butyl ((lR,4R)-4- (iodomethyl)cyclohexyl)carbamate (0.45 g, 1.32 mmol), bathophenanthroline (16 mg, 0.049 mmol), manganese (36 mg, 0.659 mmol), nickel (II) iodide (21 mg, 0.07 mmol), and dry pyridine (5 μί, 0.07 mmol) in DMA (2 mL). The resulting mixture was degassed with nitrogen for 3 times and stirred for 18 hr at 80°C. The reaction mixture was quenched with water (5 mL) and extracted with EtOAc (3 x 15 mL). The combined organic layers were washed with water (15 mL) and brine (15 mL), dried over anhydrous sodium sulfate and filtered. The filtrate was concentrated under vacuum. The residue was purified by Prep-TLC with

EtOAc/DCM/petroleum ether (l/l/2)to give the title compound: LCMS (ESI) calc'd for C5 ₈ H71 7O ₉ S [M + H] ⁺ : 1042, found 1042.

Step C: 4-(((lr,4r)-4-aminocyclohexyl)methyl)-4'-(pyrrolidin-3-yl)-2 -(2H-tetrazol-5-yl)- [1, 1 '-biphenyl] -3 -sulfonamide

Into a 50 mL three necked round bottom flask were placed a solution of tert-butyl

3-(3'-(N,N-bis(4-methoxybenzyl)sulfamoyl)-4'-(((lR,4R)-4- ((tert- butoxycarbonyl)amino)cyclohexyl)methyl)-2'-(2-(4-methoxybenz yl)-2H-tetrazol-5-yl)-[l,l'- biphenyl]-4-yl)pyrrolidine-l-carboxylate (0.11 g, 0.11 mmol) in DCM (2 mL), trifluoroacetic acid (2 mL, 26.00 mmol). The resulting mixture was stirred at ambient temperature for 2 hr and then the solvent was removed under reduced pressure. The residue was dissolved in DCM (1 mL), and then Anisole (1 mL, 0.1 1 mmol), trifluoroacetic acid (2 mL, 26.0 mmol) was added sequentially. After the reaction mixture was stirred at 80°C for 16 hr, the solvent was removed under reduced pressure. The residue was purified by Prep-HPLC with the following conditions: Column: X Bridge CI 8, 19 x 150 mm, 5 μιη; Mobile Phase A: water (0.05% TFA), Mobile Phase B: ACN; Flow rate: 20 mL/min; Gradient: 30% B to 70%B in 10 min; Detection: UV 254 nm. The collected fractions were combined and concentrated under reduced pressure to afford the title compound: LCMS (ESI) calc'd for C ₂ 4H ₃ i ₇ 02S [M + H] ⁺ : 482, found 482.

EXAMPLES 583-588

In the similar way to 4-(((lr,4r)-4-aminocyclohexyl)methyl)-4'-(pyrrolidin-3-yl)- 2-(2H-tetrazol-5-yl)-[l, l'-biphenyl] -3 -sulfonamide, the following compounds were synthesized starting from tert-butyl 3-(3'-(N,N-bis(4-methoxybenzyl)sulfamoyl)-4'-bromo-2'-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)biphenyl-4-yl)pyrrolidine-l- carboxylate.

Ex. Structure Name Calc'd. LC/MS No. MW m/e

[M+H] ⁺ [M+H] ⁺

583 4-(((ls,4s)-4- 482.23 482.2 aminocyclohexyl)methyl)-4'- (pyrrolidin-3 -yl)-2-( 1 H- tetrazol-5-yl)-[l, l'- biphenyl] -3 -sulfonamide

584 4-(2-((lr,4s)-4- 496.24 496.3 aminocyclohexyl)ethyl)-4'- (pyrrolidin-3 -yl)-2-( 1 H- tetrazol-5-yl)-[l, l'- biphenyl] -3 -sulfonamide

585 4-(2-((ls,4r)-4- 496.24 496.3 aminocyclohexyl)ethyl)-4'- (pyrrolidin-3 -yl)-2-( 1 H- tetrazol-5-yl)-[l, l'- biphenyl] -3 -sulfonamide

586 4-(((lr,4r)-4- 496.24 496.4

(aminomethyl)cyclohexyl)m

ethyl)-4'-(pyrrolidin-3-yl)-2- (lH-tetrazol-5-yl)-[l, l'- biphenyl] -3 -sulfonamide 587 4-(((ls,4s)-4- 496.24 496.2

(aminomethyl)cyclohexyl)m

ethyl)-4'-(pyrrolidin-3-yl)-2- (lH-tetrazol-5-yl)-[l, l'- biphenyl] -3 -sulfonamide

588 4-(piperidin-4-ylmethyl)-4'- 468.21 468.3

(pyrrolidin-3 -yl)-2-(2H- tetrazol-5-yl)-[l, l'- biphenyl] -3 -sulfonamide

EXAMPLES 589 and 590

3-((lr,4r)-4-(aminomethyl)cyclohexyl)-6-(piperidin-4-ylmethy l)-2-(2H-tetrazol-5- yl)benzenesulfonamide and 3-((lr,4r)-4-(aminomethyl)cyclohexyl)-6-(piperidin-4-ylmethy l)-2- (2H-tetraz -5 -yl)benzenesulfonamide

Step A: 6-bromo-3-(4-cyanocyclohex-l-enyl)-N,N-bis(4-methoxybenzyl)- 2-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)benzenesulfonamide

A degassed solution of tetrakis(triphenylphosphine) palladium (0) (14.62 mg, 0.013 mmol), sodium carbonate (40 mg, 0.38 mmol), 4-(4,4,5,5-tetramethyl-l,3,2-dioxaborolan- 2-yl)cyclohex-3-enecarbonitrile (35 mg, 0.15 mmol), 6-bromo-3-iodo-N,N-bis(4- methoxybenzyl)-2-(l-(4-methoxybenzyl)-lH-tetrazol-5-yl)benze nesulfonamide (0.10 g, 0.127 mmol) in dioxane/water (4/1) (4 mL) was stirred at 80°C for 2 hr under nitrogen. The mixture was concentrated under vacuum and the residue was purified by Prep-TLC with EtOAc/PE (1/2) to afford the title compound: LCMS (ESI) calc'd for CssHsvBr eOjS [M + H] ⁺ : 769, 771 (1 : 1), found: 769, 771 (1 : 1). Step B: tert-butyl 4-(2-(N,N-bis(4-methoxybenzyl)sulfamoyl)-4-(4-cyanocyclohex- l- enyl)-3-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)benzyl)piperid ine-l-carboxylate

In the 10 niL sealed tube, tert-butyl 4-(iodomethyl)piperidine-l-carboxylate (1.01 g, 3.12 mmol), 4,7-diphenyl-l, 10-phenanthroline (0.08 g, 0.23 mmol), nickel(II) iodide (0.15 g, 0.47 mmol), manganese (0.26 g, 4.68 mmol) was added to a stirred mixture of 4-bromo-4'- cyano-N,N-bis(4-methoxybenzyl)-2-(l-(4-methoxybenzyl)-lH-tet razol-5-yl)-2',3',4',5'- tetrahydro-[l, l'-biphenyl] -3 -sulfonamide (1.20 g, 1.56 mmol) in DMAc (3 mL) at ambient temperature. The resulting mixture was bubbled with argon for 10 min and then stirred for 16 hr at 80 °C under argon and then quenched with water (10 mL). The resulting mixture was extracted with EtOAc (3 x 50 mL), dried over anhydrous Na ₂ S0 ₄ and concentrated under reduced pressure. The residue was purified by silica gel column chromatography, eluted with EtOAc/PE (1/2) to afford the residue which was purified by Prep-HPLC with the following conditions: Column: X bridge CI 8, 19 x 150 mm, 5 μιη; Mobile phase A: water (10 mM

NH ₄ HC0 ₃ ) and Mobile phase B: ACN; Flow rate: 20 mL/min; Gradient: 75-85% B in 8min; Detection: UV 220 and 254 nm. The collected fractions were combined and concentrated under reduced pressure to afford the title compound: LCMS (ESI) calc'd for ₉ H ₅₇ N ₇ O ₇ S [M + H] ⁺ : 888, found: 888.

Step C: tert-butyl 4-(2-(N,N-bis(4-methoxybenzyl)sulfamoyl)-4-(4-((teri- butoxycarbonylamino)methyl)cyclohex-l-enyl)-3-(2-(4-methoxyb enzyl)-2H-tetrazol-5- yl)benzyl)piperidine- 1 -carboxylate

In the 25 mL round bottom flask, di-tert-butyl dicarbonate (74 mg, 0.34 mmol) was added to a stirred mixture of tert-butyl 4-((3-(N,N-bis(4-methoxybenzyl)sulfamoyl)- 4'-cyano-2-(l-(4-methoxybenzyl)-lH-tetrazol-5-yl)-2',3',4',5 '-tetrahydro-[l,l'-biphenyl]-4- yl)methyl)piperidine- 1 -carboxylate (0.15 g, 0.17 mmol) in MeOH (3 mL) at ambient temperature under hydrogen (2 atm). The resulting mixture was stirred for 2 hr at ambient temperature under hydrogen and then the solids were filtered out. The filtrate was concentrated and the residue was purified by Prep-TLC with EtOAC/PE (1/2) to afford the title compound: LCMS (ESI) calc'd for C5 ₄ H ₆₉ 70 ₉ S [M + H] ⁺ : 992, found: 992.

Step D: tert-butyl 4-(2-(N,N-bis(4-methoxybenzyl)sulfamoyl)-4-(4-((tert- butoxycarbonylamino)methyl)cyclohexyl)-3-(2-(4-methoxybenzyl )-2H-tetrazol-5- yl)benzyl)piperidine- 1 -carboxylate In the 20 sealed tube, dihydroxypalladium (0.16 g, 0.23 mmol) was added to a stirred mixture of tert-butyl 4-((3-(N,N-bis(4-methoxybenzyl)sulfamoyl)-4'-(((tert- butoxycarbonyl)amino)methyl)-2-(2-(4-methoxybenzyl)-2H-tetra zol-5-yl)-2',3',4',5'-tetrahydro- [l, l'-biphenyl]-4-yl)methyl)piperidine-l-carboxylate (0.15 g, 0.15 mmol) in MeOH (3 mL) at ambient temperature. After the resulting mixture was stirred at ambient temperature for 16 hr under hydrogen at 15 atm, the solids were filtered out and the filtrate was concentrated under vacuum to afford the title compound: LCMS (ESI) calc'd for C54H71N7O ₉ S [M + H] ⁺ : 994, found: 994.

Step E: 3 -(4-(aminomethyl)cyclohexyl)-N,N-bis(4-methoxybenzyl)-2-(2-( 4- methoxybenzyl)-2H-tetrazol-5-yl)-6-(piperidin-4-ylmethyl)ben zenesulfonamide

In the 25 round bottom flask, 2,2,2-trifluoroacetic acid (14.91 mg, 0.13 mmol) was added dropwise to a stirred mixture of tert-butyl 4-(2-(N,N-bis(4- methoxybenzyl)sulfamoyl)-4-(4-(((tert-butoxycarbonyl)amino)m ethyl)cyclohexyl)-3-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)benzyl)piperidine-l-carboxyl ate (0.13 g, 0.13 mmol) in anisole (1 mL) at ambient temperature. The resulting mixture was stirred at ambient temperature for 1 hr and then concentrated under vacuum. The residue was used in the next step directly without further purification: LCMS (ESI) calc'd for C44H55N7O5S [M + H] ⁺ : 794, found: 794.

Step F: 3-((lr,4r)-4-(aminomethyl)cyclohexyl)-6-(piperidin-4-ylmethy l)-2-(2H-tetrazol-5- yl)benzenesulfonamide and 3-((lr,4r)-4-(aminomethyl)cyclohexyl)-6-(piperidin-4-ylmethy l)-2- (2H-tetrazol-5 -yl)benzenesulfonamide

In the 100 mL round bottom flask, 2,2,2-trifluoroacetic acid (0.14 g, 1.26 mmol) was added dropwise to a stirred mixture of 3-(2-aminoquinolin-8-yl)-N,N-bis(4-methoxybenzyl)- 2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-6-(trifluoromethyl) benzenesulfonamide (0.10 g, 0.13 mmol) in anisole and DCM (1/1) (2 mL) at ambient temperature. The resulting mixture was stirred for 16 hr at 80°C and then concentrated under vacuum. The residue was purified by Prep- HPLC with the following conditions: Column: X Bridge CI 8, 19 x 150 mm, 5 μιη; Mobile Phase A: water (10 mM NH4HCO ₃ ), Mobile Phase B: ACN; Flow rate: 20 mL/min; Gradient: 10-36% B in 8 min; Detection: UV 254 nm. The collected fractions were combined and concentrated under reduced pressure to afford the faster eluting isomer: LCMS (ESI) calc'd for C2 ₀ H ₃ 1 7O2S [M + H] ⁺ : 434, found: 434; ¾ NMR (300 MHz, CD ₃ OD): 7.58 (d, J= 5.4 Hz, 1H), 7.39 (d, J= 6.3 Hz, 1H), 3.33-3.31 (m, 2H), 3.15-3.12 (m, 2H), 2.97 (d, J= 5.7 Hz, 1H), 2.87-2.76 (m, 2H), 1.99-1.96 (m, 2H), 1.88-1.71 (m, 3H), 1.71-1.61 (m, 2H) 1.53-1.35 (m, 9H) and the slower eluting isomer: LCMS (ESI) calc'd for C2 ₀ H ₃ 1 7O2S [M + H] ⁺ : 434, found: 434; ¾ NMR (300 MHz, CD3OD): 7.58 (d, J= 3.9 Hz, 1H), 7.39 (d, J= 9.0 Hz, 1H), 3.31-3.11 (m, 3H), 2.90-2.79 (m, 2H), 2.66 (d, J= 5.1 Hz, 1H), 1.95-1.77 (m, 8H), 1.68-1.41 (m, 7H), 0.88-0.72 (m, 2H).

EXAMPLES 591-592

In the similar way to 3-((lr,4r)-4-(aminomethyl)cyclohexyl)-6-(piperidin-4- ylmethyl)-2-(2H-tetrazol-5-yl)benzenesulfonamide and 3-((lr,4r)-4-(aminomethyl)cyclohexyl)- 6-(piperidin-4-ylmethyl)-2-(2H-tetrazol-5-yl)benzenesulfonam ide, the following compounds were s nthesized.

EXAMPLE 593

4'-(aminomethyl)-4-(piperidin-4-ylmethyl)-2-(2H-tetrazol-5-y l)biphenyl-3-sulfonamide

Η

N— S0 ₂ NH ₂ Step A: benzyl 4-((3-(N,N-bis(4-methoxybenzyl)sulfamoyl)-4'-cyano-2-(2-(4- methoxybenzyl)-2H-tetrazol-5 -yl)biphenyl-4-yl)methyl)piperidine- 1 -carboxylate

To a stirred mixture of 4-bromo-4'-cyano-N,N-bis(4-methoxybenzyl)-2-(l-(4- methoxybenzyl)-lH-tetrazol-5-yl)-[l,l'-biphenyl]-3-sulfonami de (0.20 g, 0.26 mmol) in DMA (2.6 mL) was added benzyl 4-(iodomethyl)piperidine- 1 -carboxylate (0.38 mg, 1.05 mmol) at ambient temperature under Ar. To the reaction mixture were added 4,7-diphenyl-l, 10- phenanthroline (17 mg, 0.05 mmol), nickel (II) iodide (16 mg, 0.05 mmol), manganese (29 mg, 0.52 mmol), benzonitrile (5 mg, 0.05 mmol) and chlorotrimethylsilane (6 mg, 0.05 mmol) sequentially. After the resulting mixture was heated for 2 hr at 40°C under Ar, it was quenched with water (5 mL) and extracted with EtOAc (3 x 10 mL). The combined organic layers were washed with brine (2 x 10 mL), dried over anhydrous Na ₂ S0 ₄ , concentrated under reduced pressure. The residue was purified by Prep-TLC with EtOAc/PE (1/1) to afford the title compound, which was used in the next reaction directly. LCMS (ESI) calc'd for C52H51 7O7S [M + If: 918, found 918.

Step B: 4'-(aminomethyl)-N,N-bis(4-methoxybenzyl)-2-(2-(4-methoxyben zyl)-2H- tetrazol-5-yl)-4-(piperidin-4-ylmethyl)biphenyl-3-sulfonamid e

To a stirred solution of benzyl 4-((3-(N,N-bis(4-methoxybenzyl)sulfamoyl)-4'- cyano-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-[l, l'-biphenyl]-4-yl)methyl)piperidine-l- carboxylate (0.1 1 g, 0.12 mmol) in EtOAc (3 mL) was added dihydroxypalladium (8 mg, 0.012 mmol) and five drops of HCl (1 Ν, aq.) at ambient temperature. The reaction mixture was stirred under hydrogen (1.5 atm) for 48 hr at ambient temperature, and then filtered through celite. The filtrate was concentrated under reduced pressure to afford the title compound, which was used in the next step directly without further purification. LCMS (ESI) calc'd for C ₃ 6H ₄ i ₇ 0 ₄ S [M + If : 668, found 668.

Step C: 4'-(aminomethyl)-4-(piperidin-4-ylmethyl)-2-(2H-tetrazol-5-y l)biphenyl-3-sulfonamide

To a stirred solution of 4'-(aminomethyl)-N,N-bis(4-methoxybenzyl)-2-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)-4-(piperidin-4-ylmethyl)-[ 1 , 1 '-biphenyl]-3 -sulfonamide (60 mg, 0.08 mmol) (crude) in anisole (2 mL, 0.08 mmol) was added TFA (4 mL, 0.08 mmol) at 0°C. The reaction mixture was heated for 16 hr at 80°C and then concentrated under reduced pressure. The residue was purified by Prep-HPLC with the following conditions: Column, X bridge CI 8 , 19 x 150 mm; Mobile phase: water (0.05% NH ₄ HCO ₃ ) and acetonitrile; Gradient: hold 34% acetonitrile for 8 min, hold 100% for 2 min, down to 34% in 2 min; Detector: UV 220 and 254 nm. The collected fractions was concentrated under reduced pressure to afford the title compound: LCMS (ESI) calc'd for [M + 1] ⁺ : 428, found 428.

EXAMPLE 594

4'-(guanidinomethyl)-4-(piperidin-4-ylmethyl)-2-(2H-tetrazol -5-yl)biphenyl-3-sulfonamide

Step A: tert-butyl 4-((4'-(aminomethyl)-3-(N,N-bis(4-methoxybenzyl)sulfamoyl)-2 -(2-(4- methoxybenzyl)-2H-tetrazol-5 -yl)biphenyl-4-yl)methyl)piperidine- 1 -carboxylate

To a stirred solution of tert-butyl 4-((3-(N,N-bis(4-methoxybenzyl)sulfamoyl)-4'- cyano-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-[l, l'-biphenyl]-4-yl)methyl)piperidine-l- carboxylate (0.1 1 g, 0.12 mmol) in EtOAc (3 mL), dihydroxypalladium (8 mg, 0.01 mmol) and five drops of HQ (1 Ν, aq.) were added at ambient temperature. The reaction mixture was stirred under hydrogen (15 atm) for 48 hr at ambient temperature, and then filtered and concentrated to afford the title compound, which was used in the next reaction directly without further purification. LCMS (ESI) calc'd for C49H57N7O7S [M + i : 888, found 888.

Step B: tert-butyl 4-((3-(N,N-bis(4-methoxybenzyl)sulfamoyl)-4'-(guanidinomethy l)-2-(2-

(4-methoxybenzyl)-2H-tetrazol-5-yl)biphenyl-4-yl)methyl)p iperidine-l -carboxylate

To a stirred mixture of tert-butyl 4-((4'-(aminomethyl)-3-(N,N-bis(4- methoxybenzyl)sulfamoyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol- 5-yl)-[l,l'-biphenyl]-4- yl)methyl)piperidine- 1 -carboxylate (60 mg, 0.07 mmol) and lH-pyrazole- 1 -carboximidamide (22 mg, 0.20 mmol) in DMF (1 mL), DIEA (26 mg, 0.20 mmol) was added dropwise at 0°C. The resulting mixture was stirred for 4 h at ambient temperature and then quenched with water (5 mL), extracted with EtOAc (2 x 10 mL). The combined organic layers were washed with brine (2 x 10 mL), dried over anhydrous Na ₂ S0 ₄ and concentrated under reduced pressure. The residue was purified Prep-TLC, eluted with DCM/MeOH (5/1) to afford the title compound, which was used in the next step directly. LCMS (ESI) calc'd for C5 ₀ H5 ₉ N ₉ O7S [M + 1] : 930, found 930.

Step C: 4'-(guanidinomethyl)-4-(piperidin-4-ylmethyl)-2-(2H-tetrazol -5-yl)biphenyl-3- sulfonamide

To a stirred solution of tert-butyl 4-((3-(N,N-bis(4-methoxybenzyl)sulfamoyl)-4'-

(guanidinomethyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl )-[l, -biphenyl]-4- yl)methyl)piperidine-l-carboxylate (40 mg, 0.04 mmol) in anisole (1 mL, 0.04 mmol), TFA (1 mL, 0.04 mmol) was added dropwise at 0°C. After the reaction mixture was stirred for 2 hr at ambient temperature, it was concentrated to afford 60 mg crude of 4'-(guanidinomethyl)-N-(4- methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-4-(p iperidin-4-ylmethyl)-[l, l'- biphenyl]-3 -sulfonamide which was used directly in the next step without further purification. LCMS (ESI) calc'd for C ₃ 7H4 ₃ N ₉ O4S [M + 1] ⁺ : 710, found 710.

To a stirred solution of 4'-(guanidinomethyl)-N-(4-methoxybenzyl)-2-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)-4-(piperidin-4-ylmethyl)-[l ,r-biphenyl]-3-sulfonamide (60 mg, 0.09 mmol) (crude) in anisole (5 mL) was added TFA (10 mL, 0.09 mmol) at 0°C. The resulting mixture was heated for 16 hr at 80°C and then concentrated under reduced pressure. The residue was purified by Prep-HPLC with the following conditions: Column, X bridge CI 8 , 19 x 150 mm; mobile phase: water (0.05% NH ₄ HCO ₃ ) and acetonitrile; Gradient: hold 34% acetonitrile for 8 min, hold 100% for 2 min, down to 34% in 2 min; Detector: UV 220 and 254 nm. The collected fractions were concentrated under reduced pressure to afford the title compound: LCMS (ESI) calc'd for C21H27N9O2S [M + if: 470, found 470.

EXAMPLE 595

4-((( 1 r,4r)-4-aminocyclohexyl)methyl)-4'-(azetidin-3 -yl)-2-(2H-tetrazol-5 -yl)- [ 1 , 1 '-biphenyl]-3 - sulfonamide

Step A: tert-butyl (lr,4r)-4-(hydroxymethyl)cyclohexylcarbamate

To a stirred solution of (lR,4R)-4-((tert- butoxycarbonyl)amino)cyclohexanecarboxylic acid (2.00 g, 8.22 mmol) in THF (20 mL), borane (8.22 mL, 16.44 mmol) was added dropwise at 0°C. After the resulting mixture was stirred for 6 hr at ambient temperature, it was quenched with water (20 mL) and extracted with EtOAc (2 x 40 mL). The combined organic layers were washed brine (2 x 30 mL), dried over anhydrous Na ₂ S0 ₄ and concentrated under reduced pressure to afford the title compound: ^X H NMR (400 MHz, CDC1 ₃ ): δ 4.62 (s, 1H), 3.48 (d, J= 6.4 Hz, 2H), 3.01-2.98 (m, 2H), 1.89-1.71 (m, 4H), 1.70-1.61 (m, 1H), 1.49 (s, 9H), 1.05-0.90 (m, 4H).

Step B: tert-butyl (lr,4r)-4-(iodomethyl)cyclohexylcarbamate

To a stirred mixture of tert-butyl ((lR,4R)-4- (hydroxymethyl)cyclohexyl)carbamate (1.70 g, 7.41 mmol), triphenylphosphine (2.33 g, 8.90 mmol) and lH-imidazole (0.60 g, 8.90 mmol) in THF (30 mL), I ₂ (2.26 g, 8.90 mmol) in 10 mL of THF was added dropwise at 0°C. After the resulting mixture was stirred 12 hr at ambient temperature, it was quenched with water (50 mL) and extracted with EtOAc (3 x 50 mL). The combined organic layers were washed with aqueous a ₂ S0 ₃ (aq.) (2 x 50 mL), dried over anhydrous Na ₂ S0 ₄ and concentrated under redcued pressure. The residue was purified by silica gel column chromatography, eluting with EtOAc/PE (1/5) to afford the title compound: ^X H NMR (400 MHz, CDCI ₃ ): δ 4.46 (s, 1H), 3.45 (s, 1H), 3.11 (d, J = 8.4 Hz, 2H), 2.12-1.89 (m, 4H), 1.45 (s, 9H), 1.18- 1.01 (m, 4H).

Step C: tert-butyl 3-(3'-(N,N-bis(4-methoxybenzyl)sulfamoyl)-4'-(((lr,4r)-4-(te rt- butoxycarbonylamino)cyclohexyl)methyl)-2'-(2-(4-methoxybenzy l)-2H-tetrazol-5-yl)biphenyl-4- yl)azetidine- 1 -carboxylate

To a stirred mixture of tert-butyl 3-(3'-(N,N-bis(4-methoxybenzyl)sulfamoyl)-4'- bromo-2'-( 1 -(4-methoxybenzyl)- lH-tetrazol-5-yl)-[ 1 , 1 '-biphenyl]-4-yl)azetidine- 1 -carboxylate (0.30 g, 0.34 mmol) and tert-butyl ((lR,4R)-4-(iodomethyl)cyclohexyl)carbamate (0.23 g, 0.67 mmol) in DMA (3.9 mL), 4,7-diphenyl-l, 10-phenanthroline (17 mg, 0.05 mmol), nickel (II) iodide (21 mg, 0.07 mmol), manganese (37 mg, 0.67 mmol) and pyridine (5 μί, 0.07 mmol) was added at ambient temperature under Ar sequentially. The resulting mixture was heated for 24 hr at 80°C under Ar and then quenched with water (5 mL) and extracted with EtOAc (3 x 10 mL). The combined organic layers were washed with brine (2 x 10 mL), dried over anhydrous Na ₂ S0 ₄ and concentrated under reduced pressure. The residue was purified by Prep-TLC and the combined organic fractions were concentrated under reduced pressure to afford the title compound, which was used in the next step directly. LCMS (ESI) calc'd for C57H ₆₉ 7O ₉ S [M + H] ⁺ : 1028, found: 1028.

Step D: tert-butyl 3-(3'-(N,N-bis(4-methoxybenzyl)sulfamoyl)-4'-(((lr,4r)-4-(te rt- butoxycarbonylamino)cyclohexyl)methyl)-2'-(2-(4-methoxybenzy l)-2H-tetrazol-5-yl)biphenyl-4- yl)azetidine- 1 -carboxylate

To a stirred solution of tert-butyl 3-(3'-(N,N-bis(4-methoxybenzyl)sulfamoyl)-4'- (((lR,4R)-4-((tert-butoxycarbonyl)amino)cyclohexyl)methyl)-2 '-(2-(4-methoxybenzyl)-2H- tetrazol-5-yl)-[l, l'-biphenyl]-4-yl)azetidine-l-carboxylate (90 mg, 0.09 mmol) in anisole (1 mL), TFA (1.4 mL, 17.51 mmol) was added dropwise at 0°C. After the resulting solution was stirred at 0°C for 2 hr, it was concentrated under reduced pressure. The residue was evaporated with anisole (10 mL) for 3 times under reduced pressure and used in the next step directly.

Step E: 6-[(4-aminocyclohexyl)methyl]-3-[4-(azetidin-3-yl)phenyl]-2- (lH-tetrazol-5- yl)benzenesulfonamide

To a stirred solution of 4-(((lR,4R)-4-aminocyclohexyl)methyl)-4'-(azetidin-3- yl)-N-(4-methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5 -yl)-[l, l'-biphenyl]-3- sulfonamide (0.10 g, 0.14 mmol, crude) in anisole (0.2 mL) TFA (2 mL, 28.30 mmol) was added at ambient temperature. After the resulting mixture was heated at 80°C for 16 hr, it was concentrated under reduced pressure. The residue was purified by Prep-HP LC with following condition: Column: X Bridge CI 8, 19 x 150 mm, 5 μιη; Mobile Phase A: water (0.05% TFA), Mobile Phase B: ACN; Flow rate: 20 mL/min; Gradient: 5-15% B in 8 min; Detected: at UV 254 nm and 220 nm. The collected fractions were concentrated under reduced pressure to afford the title compound: LCMS (ESI) calc'd for [M + H] ⁺ : 468, found: 468.

EXAMPLES 596-602

In the similar way to 4-(((lr,4r)-4-aminocyclohexyl)methyl)-4'-(azetidin-3-yl)-2- (2H-tetrazol-5-yl)-[l, l'-biphenyl]-3-sulfonamide, the following compounds were synthesized starting from tert-butyl 3-(3'-(N,N-bis(4-methoxybenzyl)sulfamoyl)-4'-bromo-2'-(l-(4- methoxybenzyl)-lH-tetrazol-5-yl)-[l,l'-biphenyl]-4-yl)azetid ine-l-carboxylate and alkyl halides repared as described herein.

EXAMPLE 603

3-[4-[4-(4-piperidylmethyl)-3-sulfamoyl-2-(2H-tetrazol-5-yl) phenyl]phenyl]azetidine-l- carboxamidine

Step A : benzyl 4-(iodomethyl)piperidine- 1 -carboxylate

A solution of I ₂ (9.77 g, 38.50 mmol) in THF (5 mL) was added in dropwise to a stirred solution of benzyl 4-(hydroxymethyl)piperidine- 1 -carboxylate (8.00 g, 32.10 mmol), 1H- imidazole (2.62 g, 38.50 mmol) and triphenylphosphine (10.10 g, 38.50 mmol) in THF (15 mL) at ambient temperature in a period of 4 hr. The reaction mixture was then quenched with water (30 mL), diluted with water (40 mL) and extracted with EtOAc (3 x 40 mL). The combined organic layers were washed with water (20 mL) and brine (20 mL), dried over anhydrous Na ₂ S0 ₄ and concentrated under reduced pressure. The residue was purified by silica gel, eluted with EtOAc/PE (1/10) to afford the title compound: LCMS (ESI) calc'd for Οι ₄ Η ₁₈ ΓΝ0 ₂ [M + H] ⁺ : 360, found 360.

Step B : benzyl 4-((3-(N,N-bis(4-methoxybenzyl)sulfamoyl)-4'-(l-(tert- butoxycarbonyl)azetidin-3-yl)-2-(2-(4-methoxybenzyl)-2H-tetr azol-5-yl)biphenyl-4- yl)methyl)piperidine- 1 -carboxylate

To the solution mixture of tert-butyl 3-(3'-(N,N-bis(4-methoxybenzyl)sulfamoyl)-

4'-bromo-2'-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-[l,r-b iphenyl]-4-yl)azetidine-l-carboxylate (0.50 g, 0.56 mmol), benzyl 4-(iodomethyl)piperidine- 1 -carboxylate (0.40 g, 1.12 mmol), nickel iodide (35 mg, 0.11 mmol), 4,7-diphenyl-l,10-phenanthroline (28 mg, 0.08 mmol) and manganese (61 mg, 1.12 mmol) in DMA (5 mL) were added benzonitrile (12 mg, 0.112 mmol) (one drop) and chlorotrimethylsilane (12 mg, 0.112 mmol) (one drop) at ambient temperature under Argon sequencely. The resulting mixture was stirred at 40°C for 2 hr under Argon and then filtered. The filtrate was concentrated under reduced pressure and the residue was purified by silica gel, eluted with EtOAc/PE (40/60) to afford the title compound: LCMS (ESI) calc'd for CsgHes vOgS [M + H] ⁺ : 1048, found 1048.

Step C : benzyl 4-((4'-(azetidin-3-yl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5- yl)-3-(N-(4- methoxybenzyl)sulfamoyl)biphenyl-4-yl)methyl)piperidine-l-ca rboxylate

To the solution of benzyl 4-((3-(N,N-bis(4-methoxybenzyl)sulfamoyl)-4'-(l-(tert- butoxycarbonyl)azetidin-3 -yl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-[ 1 , 1 '-biphenyl]-4- yl)methyl)piperidine- 1 -carboxylate (0.16 g, 0.15 mmol) in DCM (16 mL) was added TFA (1.6 mL, 20.77 mmol) at 0°C and stirred at 0°C for 2 hr. The reaction was quenched with water (5 mL) and adjusted to pH 10 with aHC0 ₃ , extracted with DCM (3 x 20 mL). The combined organic layers were washed with water (20 mL) and brine (20 mL), dried over anhydrous Na ₂ S0 ₄ and concentrated under vacuum to afford the title compound. LCMS (ESI) calc'd for C ₄₆ H ₄₉ N ₇ 0 ₆ S [M + H] ⁺ : 828, found 828. Step D : benzyl 4-((4'-(l-carbamimidoylazetidin-3-yl)-2-(2-(4-methoxybenzyl) -2H- tetrazol-5-yl)-3-(N-(4-methoxybenzyl)sulfamoyl)biphenyl-4-yl )methyl)piperidine-l-carboxylate

The solution of benzyl 4-((4'-(azetidin-3-yl)-2-(2-(4-methoxybenzyl)-2H-tetrazol- 5-yl)-3 -(N-(4-methoxybenzyl)sulfamoyl)-[ 1 , 1 '-biphenyl]-4-yl)methyl)piperidine- 1 -carboxylate (0.13 g, 0.15 mmol), DIEA (0.11 mL, 0.60 mmol) and 7H-pyrazole-l-carboxamidine hydrochloride (89 mg, 0.60 mmol) in DMF (3 mL) was stirred at ambient temperature for 3 hr under nitrogen and then quenched with water (30 mL), diluted with water (30 mL) and extracted with EtOAc (3 x 20 mL). The combined organic layers were washed with water (20 mL) and brine (20 mL), dried over anhydrous Na ₂ S0 ₄ and concentrated under reduced presure. The residue was purified by silica gel, eluted with MeOH/DCM (10/90) to afford the title compound: LCMS (ESI) calc'd for C ₄₇ H5i ₉ 0 ₆ S [M + H] ⁺ : 870, found 870.

Step E : 3-(2'-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-3'-(N-(4-methox ybenzyl)sulfamoyl) -4'-(piperidin-4-ylmethyl)biphenyl-4-yl)azetidine-l-carboxim idamide

To a stirred solution of benzyl 4-((4'-(l-carbamimidoylazetidin-3-yl)-2-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)-3-(N-(4-methoxybenzyl)sulfa moyl)-[l,l'-biphenyl]-4- yl)methyl)piperidine-l -carboxylate (50 mg, 0.06 mmol) in MeOH (5 mL) was added Pd(OH) ₂ (40 mg, 0.06 mmol) at ambient temperature. After the reaction mixture was degassed with hydrogen for 3 times and stirred under hydrogen for 1 hr at ambient temperature, the resulting mixture was filtered and the filter cake was washed with DCM (3 x 10 mL). The combined organic layers were concentrated under reduced pressure to afford the title compound: LCMS (ESI) calc'd for C ₃₉ H _{45 9} 0 ₄ S [M + H] ⁺ : 736, found 736.

Step F: 3-[4-[4-(4-piperidylmethyl)-3-sulfamoyl-2-(2H-tetrazol-5-yl) phenyl]phenyl]azeti dine- 1 -carboxamidine

A mixture solution of 3-(2'-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-3'-(N-(4- methoxybenzyl)sulfamoyl)-4'-(piperidin-4-ylmethyl)-[l,r-biph enyl]-4-yl)azetidine-l- carboximidamide (45 mg, 0.06 mmol) and TFA (5 mL) in DCM (1 mL) was stirred at 80°C for 16 hr. The resulting solution was concentrated under reduced pressure and the residue was dissolved with water (50 mL), extracted with EtOAc (3 x 20 mL) and concentrated to afford the crude product. The crude product was purified by Prep-HPLC with the following conditions: Column, Sunfire C 18, 19 x 150 mm; Mobile phase: water (0.05% NH ₄ HC0 ₃ ) and acetonitrile; Gradient time: 7 min. B%: 40%-80%; Detector; UV 220 and 254 nm. The collected fractions were combined and concentrated under reduced pressure to afford the title compound. LCMS (ESI) calc'd for [M + H] ⁺ : 496, found 496; ¾ NMR (400 MHz, DMSO-i¾): δ 7.83 (s, 2H), 7.40 (d, J= 8.0 Hz, 1H), 7.32 (d, J= 8.0 Hz, 1H), 7.27 (s, 2H), 7.11 (d, J= 8.4 Hz, 2H), 6.85 (d, J= 8.4 Hz, 2H), 4.41-4.37 (m, 2H), 3.97-3.94 (m, 2H), 3.88-3.81 (m, 1H), 3.04-3.00 (m, 2H), 2.91-2.88 (m, 2H), 2.42-2.37 (m, 2H), 1.74-1.70 (m, 1H), 1.57-1.54 (m, 2H), 1.14-1.09 (m, 2H).

EXAMPLE 604

4-[[4-[4-(azetidin-3-yl)phenyl]-2-sulfamoyl-3-(2H-tetrazol-5 -yl)phenyl]methyl]piperidine-l- carboxamidine

Step A: tert-butyl 3-(3'-(N,N-bis(4-methoxybenzyl)sulfamoyl)-2'-(2-(4-methoxybe nzyl)-

2H-tetrazol-5-yl)-4'-(piperidin-4-ylmethyl)biphenyl-4-yl) azetidine-l-carboxylate

The solution of benzyl 4-((3-(N,N-bis(4-methoxybenzyl)sulfamoyl)-4'-(l-(tert- butoxycarbonyl)azetidin-3-yl)-2-(2-(4-methoxybenzyl)-2H-tetr azol-5-yl)-[l , 1 '-biphenyl]-4- yl)methyl)piperidine-l-carboxylate (1.10 g, 1.05 mmol), Pd(OH) ₂ (0.74 g, 1.05 mmol) and HCl (two drops, 1 Ν) in MeOH (4 mL) and DCM (5 mL) was degassed with H ₂ for 3 times and stirred under ¾ atmosphere for 1 hr at ambient temperature. The resulting mixture was filtered and the filtrate was concentrated under vacuum to afford the title compound: LCMS (ESI) calc'd for C51H5 ₉ N7O7S [M+l : 914, found 914.

Step B : tert-butyl 3-(3'-(N,N-bis(4-methoxybenzyl)sulfamoyl)-4'-((l- carbamimidoylpiperidin-4-yl)methyl)-2'-(2-(4-methoxybenzyl)- 2H-tetrazol-5-yl)biphenyl-4- yl)azetidine- 1 -carboxylate

A mixture solution of tert-butyl 3-(3'-(N,N-bis(4-methoxybenzyl)sulfamoyl)-2'- (2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-4'-(piperidin-4-ylmet hyl)-[l,r-biphenyl]-4-yl)azetidine- 1 -carboxylate (0.21 g, 0.23 mmol), DIEA (0.24 niL, 1.38 mmol) and lH-pyrazole-1- carboxamidine hydrochloride (0.15 g, 1.03 mmol) in DMF (5 mL) was stirred at ambient temperature for 16 hr. The resulting mixture was quenched with water (20 mL), diluted with water (20 mL) and extracted with EtOAc (3 x 30 mL). The combined organic layers were washed with water (20 mL) and brine (20 mL), dried over anhydrous sodium sulfate and concentrated under reduced pressure to afford the title compound: LCMS (ESI) calc'd for C ₅ 2H ₆ i 90 ₇ S [M+lf: 956, found 956.

Step C : 4-((4'-(azetidin-3-yl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5- yl)-3-(N-(4- methoxybenzyl)sulfamoyl)biphenyl-4-yl)methyl)piperidine-l-ca rboximidamide

A mixture solution of tert-butyl-3-(3'-(N,N-bis(4-methoxybenzyl)sulfamoyl)-4'-

((l-carbamimidoylpiperidin-4-yl)methyl)-2'-(2-(4-methoxyb enzyl)-2H-tetrazol-5-yl)-[l,r- biphenyl]-4-yl)azetidine-l -carboxylate (0.10 g, 0.1 1 mmol) and TFA (2 mL, 26.00 mmol) in DCM (3 mL) was stirred at ambient temperature for 1 hr. The resulting mixture was concentrated under reduced pressure to afford the crude title compound: LCMS (ESI) calc'd for C39H45N9O4S [M+lf: 736, found 736.

Step D : 4-[[4-[4-(azetidin-3-yl)phenyl]-2-sulfamoyl-3-(2H-tetrazol-5 - yl)phenyl]methyl]piperidine- 1 -carboxamidine

A solution of 4-((4'-(azetidin-3-yl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5- yl)-3- (N-(4-methoxybenzyl)sulfamoyl)-[l,r-biphenyl]-4-yl)methyl)pi peridine-l-carboximidamide (0.10 g, 0.14 mmol), TFA (5 mL, 64.90 mmol) and anisole (0.5 mL, 4.58 mmol) in DCM (0.5 mL) was stirred at 80°C for 16 hr. The resulting mixture was concentrated under reduced pressure and the residue was purified by Prep-HPLC with the following conditions: Column: X Bridge RP18, 19 x 150 mm, 5 μιη; Mobile Phase A: water (0.05% NH4HCO ₃ ); Mobile Phase B: ACN; Flow rate: 20 mL/min; Gradient: 5% B to 35% B in 7 min; Detection: UV 254 nm. The collected fractions were combined and concentrated under vacuum to afford the title compound: LCMS (ESI) calc'd for [M+l] ⁺ : 496, found 496.

EXAMPLE 605

3 -[4-(azetidin-3 -yl)phenyl] -6-[( 1 , 1 -dimethylpiperidin- 1 -ium-4-yl)methyl] -2-(2H-tetrazol-5 - yl)benzenesulfonamide

Step A : 4-((3-(N,N-bis(4-methoxybenzyl)sulfamoyl)-4'-(l-(ter?-butoxy carbonyl)azetidin- 3-yl)-2-(2-(4-methoxybenzyl)-2H etrazol-5-yl)bi

A mixture solution of tert-butyl 3-(3'-(N,N-bis(4-methoxybenzyl)sulfamoyl)-2'- (2-(4-methoxybenzyl)-2H4etrazol-5-yl)-4'-(piperidin-4-ylmeth yl)-[l, r-biphenyl]-4-yl)azetidine- 1-carboxylate (0.20 g, 0.22 mmol), K ₂ C0 ₃ (0.18 g, 1.31 mmol) and Mel (0.08 mL, 1.31 mmol) in acetone (4 mL) was stirred at ambient temperature for 1 hr. The resulting mixture was filtered and the filtrate was concentrated under reduced pressure to afford the title compound: LCMS (ESI) calc'd for C ₅ 3H _{64 7} 0 ₇ S ⁺ [M] ⁺ : 942, found 942.

Step B : 4-((4'-(azetidin-3-yl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5- yl)-3-(N-(4- methoxybenzyl)sulfamoyl)biphenyl-4-yl)methyl)- 1 , 1 -dimethylpiperidinium

A mixture solution of 4-((3-(N,N-bis(4-methoxybenzyl)sulfamoyl)-4'-(l-(tert- butoxycarbonyl)azetidin-3-yl)-2-(2-(4-methoxybenzyl)-2H-tetr azol-5-yl)-[l,l'-biphenyl]-4- yl)methyl)-l,l-dimethylpiperidin-l-ium (0.20 g, 0.21 mmol) and TFA (3 mL, 38.90 mmol) in DCM (2 mL) was stirred at ambient temperature for 1 hr. The resulting mixture was concentrated under reduced pressure to afford the title compound, which was used in the next step directly: LCMS (ESI) calc'd for C ₄ oH4 _{8 7} 0 ₄ S ⁺ [M] ⁺ : 722, found 722.

Step C : 3-[4-(azetidin-3-yl)phenyl]-6-[(l, l-dimethylpiperidin-l-ium-4-yl)methyl]-2-(2H-t etrazol-5 -yl)benzenesulfonamide

A mixture solution of 4-((4'-(azetidin-3-yl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-

5-yl)-3 -(N-(4-methoxybenzyl)sulfamoyl)-[ 1 , 1 '-biphenyl]-4-yl)methyl)- 1 , 1 -dimethylpiperidin- 1 - ium (0.20 g, 0.28 mmol), TFA (10 mL, 130 mmol) and anisole (0.5 mL, 4.58 mmol) in DCM (1 mL) was stirred at 80°C for 16 hr. The resulting mixture was concentrated under reduced pressure and the residue was purified by Prep-HPLC with the following conditions: Column: X Bridge C18, 19 x 250 mm, 5 μιη; Mobile Phase A: water (0.05% NH ₄ HC0 ₃ ), Mobile Phase B: ACN; Flow rate: 20 mL/min; Gradient: 28% B to 85% B in 8min; Detection: UV 254 nm. The collected fractions were combined and concentrated under reduced pressure to afford the title compound. LCMS (ESI) calc'd for C ₂₄ H _{32 7} 0 ₂ S ⁺ [M + H] ⁺ : 482, found 482; ^X H NMR (400 MHz, DMSO-i/ ₆ ): δ 7.85 (brs, 2H), 7.46 (d, J= 8.0 Hz, 1H), 7.36 (d, J= 8.0 Hz, 1H), 7.06 (d, J = 8.0 Hz, 2H), 6.79 (d, J= 8.0 Hz, 2H), 3.73-3.68 (m, 3H), 3.57-3.51 (m, 2H), 3.41-3.35 (m, 4H), 3.15-3.06 (m, 8H), 1.97-1.95 (m, 1H), 1.79-1.69 (m, 4H).

EXAMPLE 606

6-[[l-(2-aminoethyl)-4-piperidyl]methyl]-3-[4-(azetidin-3-yl )phenyl]-2-(2H-tetrazol-5- yl)benzenesulfonamide

Step A : tert-butyl 3-(3'-(N,N-bis(4-methoxybenzyl)sulfamoyl)-4'-((l-(2-(tert-bu toxycarbo nylamino)ethyl)piperidin-4-yl)methyl)-2'-(2-(4-methoxybenzyl )-2H-tetrazol-5-yl)biphenyl-4-yl) azetidine- 1 -carboxylate

A mixture solution of tert-butyl 3-(3'-(N,N-bis(4-methoxybenzyl)sulfamoyl)-2'- (2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-4'-(piperidin-4-ylmet hyl)-[l,r-biphenyl]-4-yl)azetidine- 1-carboxylate (0.15 g, 0.16 mmol), Mg ₂ S0 ₄ (0.19 g, 1.64 mmol), acetic acid (10 mg, 0.16 mmol), tert-butyl-2-oxoethylcarbamate (0.13 g, 0.82 mmol) and sodium triacetoxyborohydride (70 mg, 0.33 mmol) in MeOH (0.5 mL) was stirred at ambient temperature for 16 hr. The reaction mixture was quenched with water (20 mL), diluted with water (20 mL) and extracted with EtOAc (3 x 20 mL). The combined organic layers were washed with water (20 mL) and brine (20 mL), dried over anhydrous Na ₂ S0 ₄ and concentrated under reduced pressure to afford the title compound: LCMS (ESI) calc'd for [M + H] ⁺ : 1057, found 1057.

Step B : 4-((l-(2-aminoethyl)piperidin-4-yl)methyl)-4'-(azetidin-3-yl )-N-(4- methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)biphe nyl-3-sulfonamide

To a stirred solution of tert-butyl 3-(3'-(N,N-bis(4-methoxybenzyl)sulfamoyl)-4'- ((l-(2-((tert-butoxycarbonyl)amino)ethyl)piperidin-4-yl)meth yl)-2'-(2-(4-methoxybenzyl)-2H- tetrazol-5-yl)-[l, l'-biphenyl]-4-yl)azetidine-l-carboxylate (0.17 g, 0.16 mmol) in DCM (10 mL) was added dropwise TFA (1 niL, 12.98 mmol) at 0°C and stirred at 0°C for 2 hr. The resulting mixture was concentrated under reduced pressure to afford the title compound, which was used in the next step directly: LCMS (ESI) calc'd for C4 ₀ H4 _{8 8} O4S [M + H] ⁺ : 737, found 737.

Step C : 6- [ [ 1 -(2-aminoethyl)-4-piperidyl]methyl] -3 - [4-(azetidin-3 -yl)phenyl]-2-(2H- tetrazol-5-yl)benzenesulfonamide

A solution of 4-(( 1 -(2-aminoethyl)piperidin-4-yl)methyl)-4'-(azetidin-3 -yl)-N-(4- methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-[l, l'-biphenyl]-3-sulfonamide (0.10 g, 0.14 mmol), TFA (10 mL, 130 mmol) and anisole (0.015 mL, 0.136 mmol) in DCM (1 mL) was stirred at 80°C for 3 hr. The reaction mixture was concentrated under reduced pressure and the residue was purified by Prep-HPLC with the following conditions: Column: X Bridge RP18, 19 x 150 mm, 5 μιη; Mobile Phase A: water (0.05% NH ₄ HCO ₃ ), Mobile Phase B: ACN; Flow rate: 20 mL/min; Gradient: 5% B to 15% B in 10 min; Detection: UV 254 nm. The collected fractions were combined and concentrated under reduced pressure to afford the title compound: LCMS (ESI) calc'd for C ₂₄ H _{32 8} O ₂ S [M + H] ⁺ : 497, found 497.

EXAMPLE 607

3-[4-(azetidin-3-yl)phenyl]-6-[[l-(2-hydroxyethyl)-4-piperid yl]methyl]-2-(2H-tetrazol-5- yl)benzenesulfonamide

Η

Step A : tert-butyl 3-(4'-((l-(2-(benzyloxy)ethyl)piperidin-4-yl)methyl)-3'-(N,N -bis(4- methoxybenzyl)sulfamoyl)-2'-(2-(4-methoxybenzyl)-2H-tetrazol -5-yl)biphenyl-4-yl)azetidine-l- carboxylate

A mixture solution of tert-butyl 3-(3'-(N,N-bis(4-methoxybenzyl)sulfamoyl)-2'- (2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-4'-(piperidin-4-ylmet hyl)-[l,r-biphenyl]-4-yl)azetidine- 1-carboxylate (0.10 g, 0.1 1 mmol), Mg ₂ S0 ₄ (0.13 g, 1.09 mmol), acetic acid (7 mg, 0.12 mmol), benzyloxyacetaldehyde (82 mg, 0.55 mmol) and sodium triacetoxyborohydride (46 mg, 0.22 mmol) in MeOH (0.5 mL) was stirred at ambient temperature for 16 hr, and then the resulting mixture was quenched with water (20 mL), diluted with water (20 mL) and extracted with EtOAc (3 x 20 mL). The combined organic layers were washed with water (20 mL) and brine (20 mL), dried over anhydrous Na ₂ S0 ₄ and concentrated under reduced pressure to afford the tittle compound, which was used in the next reaction directly: LCMS (ESI) calc'd for

CSOHO TOSS [M + H] ⁺ : 1048, found 1048.

Step B : tert-butyl 3-(3'-(N,N-bis(4-methoxybenzyl)sulfamoyl)-4'-((l-(2- hydroxyethyl)piperidin-4-yl)methyl)-2'-(2-(4-methoxybenzyl)- 2H-tetrazol-5-yl)biphenyl-4- yl)azetidine- 1 -carboxylate

A mixture solution of tert-butyl 3-(4'-((l-(2-(benzyloxy)ethyl)piperidin-4- yl)methyl)-3'-(N,N-bis(4-methoxybenzyl)sulfamoyl)-2'-(2-(4-m ethoxybenzyl)-2H-tetrazol-5-yl)- [l, l'-biphenyl]-4-yl)azetidine-l -carboxylate (70 mg, 0.07 mmol), Pd(OH) ₂ (47 mg, 0.07 mmol) and AcOH (4 μΐ, 0.07 mmol) in MeOH (4 mL) was stirred at ambient temperature for 16 hr under hydrogen at 1.5 atm. The resulting mixture was filtered and the filtrate was concentrated to afford the title compound, which was used in the next reaction directly: LCMS (ESI) calc'd for CJSHSS TOSS [M + H] ⁺ : 958, found 958.

Step C : 4'-(azetidin-3-yl)-4-((l -(2 -hydroxy ethyl)piperidin-4-yl)methyl)-N-(4- methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)biphe nyl-3-sulfonamide

A mixture solution of tert-butyl-3-(3'-(N,N-bis(4-methoxybenzyl)sulfamoyl)-4'- ((l-(2-hydroxyethyl)piperidin-4-yl)methyl)-2'-(2-(4-methoxyb enzyl)-2H-tetrazol-5-yl)-[l,r- biphenyl]-4-yl)azetidine-l -carboxylate (60 mg, 0.06 mmol) and TFA (1 mL, 12.98 mmol) in DCM (10 mL) was stirred at ambient temperature for 1 hr. The reaction mixture was concentrated under reduced pressure to afford the title compound, which was used in the next step directly. LCMS (ESI) calc'd for G1 ₀ H47N7O5S [M + H] ⁺ : 738, found 738.

Step D : 3-[4-(azetidin-3-yl)phenyl]-6-[[l-(2-hydroxyethyl)-4-piperid yl]methyl]-2-(2H- tetrazol-5-yl)benzenesulfonamide

A mixture solution of 4'-(azetidin-3-yl)-4-((l-(2-hydroxyethyl)piperidin-4- yl)methyl)-N-(4-methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tet razol-5-yl)-[ 1 , 1 '-biphenyl]-3- sulfonamide (50 mg, 0.07 mmol) in anisole (0.5 mL), TFA (10 mL) and DCM (0.5 mL) was stirred at 80°C for 4 hr. The reaction mixture was concentrated under vacuum and the residue was purified by Prep-HPLC with the following conditions: Column: X Bridge CI 8, 19 x 250 mm, 5 μιη; Mobile Phase A: water (0.05% NH4HCO ₃ ), Mobile Phase B: ACN; Flow rate: 20 mL/min; Gradient: 5% B to 20% B in 8 min; Detection: UV 254 nm. The collected fractions were combined and concentrated under vacuum to afford the title compound: LCMS (ESI) calc'd for C24H ₃ 1N7O ₃ S [M + H] ⁺ : 498, found 498; ^X H NMR (400 MHz, DMSO-i¾): 7.82 (brs, 2H), 7.41 (d, J= 8.0 Hz, 1H), 7.34 (d, J= 8.0 Hz, 1H), 7.13 (d, J= 8.1 Hz, 2H), 6.87 (d, J= 8.1 Hz, 2H), 4.42 (brs, 1H), 4.15-4.1 1 (m, 2H), 3.97-3.92 (m, 3H), 3.51-3.49 (m, 2H), 3.05 (d, J= 6.4 Hz, 2H), 2.90-2.83 (m, 2H), 2.49-2.42 (m, 2H), 2.03-1.95 (m, 2H), 1.71-1.58 (m, 3H), 1.32-1.25 (m, 2H).

EXAMPLE 608

3-[4-[l-(2-hydroxyethyl)azetidin-3-yl]phenyl]-6-(4-piperidyl methyl)-2-(2H-tetrazol-5- yl)benzenesulfonamide

Step A : 4'-(l -(2 -hydroxy ethy l)azetidin-3-y l)-4-(piperidin-4-y lmethy l)-2-(2H-tetrazol-5 - yl)biphenyl-3 -sulfonamide

A mixture solution of benzyl 4-((4'-(azetidin-3-yl)-2-(2-(4-methoxybenzyl)-2H- tetrazol-5-yl)-3-(N-(4-methoxybenzyl)sulfamoyl)biphenyl-4-yl )methyl)piperidine-l-carboxylate (0.15 mg, 0.18 mmol), Mg ₂ S0 ₄ (0.13 g, 1.09 mmol), acetic acid (7 mg, 0.1 1 mmol), 2-(tert- butyldimethylsilyloxy)acetaldehyde (0.32 mg, 1.81 mmol) and sodium triacetoxyborohydride (46 mg, 0.22 mmol) in MeOH (0.5 mL) was stirred at ambient temperature for 16 hr. The reaction mixture was quenched with water (20 mL), diluted with water (20 mL) and extracted with EtOAc (3 x 20 mL). The combined organic layers were washed with water (20 mL) and then brine (20 mL), dried over anhydrous Na ₂ S0 ₄ and concentrated under reduced pressure to afford the title compound, which was used in next step directly : LCMS (ESI) calc'd for C ₅ 4H ₆ 7 70 ₇ SSi [M + H] ⁺ : 986, found 986.

Step B : 4'-(l-(2-(tert-butyldimethylsilyloxy)ethyl)azetidin-3-yl)-N- (4-methoxybenzyl)-2- (2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-4-(piperidin-4-ylmeth yl)biphenyl-3-sulfonamide A mixture solution of benzyl-4-((4'-(l-(2-(tert- butyldimethylsilyloxy)ethyl)azetidin-3-yl)-2-(2-(4-methoxybe nzyl)-2H-tetrazol-5-yl)-3-(N-(4- methoxybenzyl)sulfamoyl)biphenyl-4-yl)methyl)piperidine-l-ca rboxylate (67 mg, 0.07 mmol), Pd(OH) ₂ (47 mg, 0.07 mmol) and AcOH (4 μί, 0.07 mmol) in MeOH (4 mL) was stirred at ambient temperature for 16 hr. The resulting mixture was filtered and the filtrate was concentrated under reduced pressure to afford the title compound, which was used in the next step directly: LCMS (ESI) calc'd for C ₄₆ H ₆₁ N ₇ O ₅ SS1 [M + H] ⁺ : 852, found 852.

Step C: 4'-(l-(2-hydroxyethyl)azetidin-3-yl)-N-(4-methoxybenzyl)-2-( 2-(4- methoxybenzyl)-2H-tetrazol-5-yl)-4-(piperidin-4-ylmethyl)bip henyl-3-sulfonamide

A mixture solution of 4'-(l-(2-(tert-butyldimethylsilyloxy)ethyl)azetidin-3-yl)-N-

(4-methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl )-4-(piperidin-4-ylmethyl)biphenyl- 3-sulfonamide (50 mg, 0.06 mmol) and TBAF (0.15 g, 0.58 mmol) in THF (10 mL) was stirred at ambient temperature for 1 hr and then the resulting mixture was concentrated under reduced pressure and the residue was purified by Prep-HPLC with the following conditions: Column: X Bridge C 18, 19 x 250 mm, 5 μιη; Mobile Phase A: water (0.05% TFA), Mobile Phase B: ACN; Flow rate: 20 mL/min; Gradient: 30%B to 70%B in 10 min; Detection: UV 254 nm; Retention time: 5.8 min. The collected fractions were combined and concentrated to afford the title compound, which was used in next step directly: LCMS (ESI) calc'd for C ₄₀ H ₄₇ N ₇ O ₅ S [M + H] ⁺ : 738, found 738.

Step D: 3-[4-[l-(2-hydroxyethyl)azetidin-3-yl]phenyl]-6-(4-piperidyl methyl)-2-(2H- tetrazol-5-yl)benzenesulfonamide

A mixture solution of 4'-(l -(2 -hydroxy ethyl)azetidin-3-yl)-N-(4-methoxybenzyl)- 2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-4-(piperidin-4-ylme thyl)biphenyl-3-sulfonamide (30 mg, 0.04 mmol), anisole (0.5 mL, 4.58 mmol) and TFA (10 mL, 0.13 mmol) in DCM (0.5 mL) was stirred at ambient temperature for 4 hr. The resulting mixture was concentrated under vacuum and the residue was purified by Prep-HPLC with the following conditions: Column: X Bridge C18, 19 x 250 mm, 5 μιη; Mobile Phase A: water (0.05% NH ₄ HCO ₃ ), Mobile Phase B: ACN; Flow rate: 20 mL/min; Gradient: 5% B to 20% B in 8 min; Detection: UV 254 nm. The collected fractions were combined and concentrated under reduced pressure to afford the title compound: LCMS (ESI) calc'd for C ₂₄ H ₃₁ N7O ₃ S [M + H] ⁺ : 498, found 498; ^X H NMR (400 MHz, DMSO-i/ ₆ ): 7.53-7.47 (m, 2H), 7.10 (d, J= 8.0 Hz, 2H), 6.97 (d, J= 8.4 Hz, 2H), 3.93- 3.85 (m, 2H), 3.79-3.71 (m, 1H), 3.62-3.59 (m, 2H), 3.37-3.32 (m, 2H), 3.23-3.16 (m, 2H), 2.94- 2.88 (m, 2H), 2.76-2.72 (m, 2H), 2.12-2.03 (m, 1H), 1.96-1.90 (m, 2H), 1.59-1.30 (m, 4H).

EXAMPLE 609

2-[4-[[4-[4-(azetidin-3-yl)phenyl]-2-sulfamoyl-3-(2H-tetrazo l-5-yl)phenyl]methyl]-l- piperidyl]acetamide

Step A : tert-butyl 3-(4'-((l-(2-amino-2-oxoethyl)piperidin-4-yl)methyl)-3'-(N,N -bis(4-met hoxybenzyl)sulfamoyl)-2'-(2-(4-methoxybenzyl)-2H-tetrazol-5- yl)biphenyl-4-yl)azetidine-l-carb oxylate

A solution mixture of tert-butyl 3-(3'-(N,N-bis(4-methoxybenzyl)sulfamoyl)-2'- (2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-4'-(piperidin-4-ylmet hyl)-[l,r-biphenyl]-4-yl)azetidine- 1-carboxylate (0.15 g, 0.16 mmol), K ₂ CO ₃ (0.1 1 mg, 0.82 mmol) and 2-chloroacetamide (77 mg, 0.82 mmol) in DMF (10 mL) was stirred at 60°C for 3 hr. The resulting mixture was quenched with water (20 mL), diluted with water (60 mL) and extracted with EtOAc (3 x 40 mL). The combined organic layers were washed with water (20 mL) and brine (20 mL), dried over anhydrous Na ₂ S0 ₄ and concentrated under vacuum to afford the title compound, which was used in next step directly.: LCMS (ESI) calc'd for Csstfe sOgS [M + H] ⁺ : 971, found 971.

Step B: 2-(4-((4'-(azetidin-3-yl)-3-(N,N-bis(4-methoxybenzyl)sulfamo yl)-2-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)biphenyl-4-yl)methyl)piperid in-l-yl)acetamide

A solution of tert-butyl-3-(4'-((l-(2-amino-2-oxoethyl)piperidin-4-yl)meth yl)-3'- (N,N-bis(4-methoxybenzyl)sulfamoyl)-2'-(2-(4-methoxybenzyl)- 2H-tetrazol-5-yl)-[l,l'- biphenyl]-4-yl)azetidine- 1-carboxylate (0.15 g, 0.15 mmol) and TFA (2.5 mL, 32.40 mmol) in DCM (20 mL) was stirred at ambient temperature for 30 min and then it was concentrated under reduced pressure to afford the title compound, which was used in next step directly: LCMS (ESI) calc'd for [M + H] ⁺ : 871, found 871. Step C : 2-[4-[[4-[4-(azetidin-3-yl)phenyl]-2-sulfamoyl-3-(2H-tetrazo l-5- yl)phenyl] methyl]- 1 -piperidyl]acetamide

A solution of 2-(4-((4'-(azetidin-3-yl)-3-(N,N-bis(4-methoxybenzyl)sulfamo yl)-2- (2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-[l,r-biphenyl]-4-yl)m ethyl)piperidin-l-yl)acetamide (0.13 g, 0.15 mmol) in TFA (10 mL, 130 mmol) was stirred at 80°C for 2 hr and then the resulting mixture was concentrated under vacuum and the residue was purified by Prep-HPLC with the following conditions: Column: X Bridge RP18, 19 x 150 mm, 5 μιη; Mobile Phase A: water (0.05% NH ₄ HCO ₃ ), Mobile Phase B: ACN; Flow rate: 20 mL/min; Gradient: 5% B to 25% B in 7 min; Detection: UV 254 nm. The collected fractions were combined and concentrated under vacuum to afford the title compound: LCMS (ESI) calc'd for C24H30 8O3S [M + H] ⁺ : 51 1, found 511 ; 'H NMR (300 MHz, DMSO-i¾): δ 8.51 (brs, 1H), 7.82 (s, 2H), 7.43-7.32 (m, 2H), 7.14-7.1 1 (m, 4H), 6.87 (d, J= 10.8 Hz, 2H), 4.17 (s, 2H), 3.97-3.96 (m, 3H), 3.06 (d, J= 8.0 Hz, 2H), 2.81-2.71 (m, 4H), 2.01-1.93 (m, 2H), 1.65-1.57 (m, 3H), 1.38-1.34 (m, 2H).

EXAMPLE 610

3-(2-amino-3H-benzo[d]imidazol-5-yl)-6-(piperidin-4-ylmethyl )-2-(2H-tetrazol-5- yl)benzenesulfonamide

Step A : 2-nitro-4-(4,4,5,5-tetramethyl-l,3,2-dioxaborolan-2-yl)benze namine

Into a 500-mL round-bottom flask purged and maintained with an inert atmosphere of argon, was placed a solution of 4,4,4',4',5,5,5',5'-octamethyl-2,2'-bi(l,3,2- dioxaborolane) (25.70 g, 101.00 mmol) , 4-bromo-2-nitroaniline (20.00 g, 92.00 mmol) and potassium acetate (27.10 g, 276.00 mmol) in DMF (250 mL). This was followed by the addition of PdOAc ₂ (0.62 g, 2.76 mmol) at ambient temperature. The resulting mixture was stirred at 85°C for 20 hr under argon and then it was cool down to 20°C, quenched with water (200 mL) and filtered. The filtrate was concentrated under reduced pressure and the residue was purified by silica gel column chromatography, eluted with EA in PE (50%) to afford the crude product. The crude was recrystallized from PE/EtOAc (200 mL/10 mL) and dried over in vacuum to afford the title compound: LCMS (ESI) calc'd for C ₁₂ H ₁₇ BN ₂ 04 [M + H] ⁺ : 265, found 265; ^X H NMR (400 MHz, DMSO-i/ ₆ ): δ 8.26 (s, 1H), 7.70 (s, 2H), 7.55 (d, J= 8.4 Hz, 1H) , 6.97 (d, J = 8.4 Hz, 1H), 1.27 (s, 12H).

Step B : 4-(4,4,5,5-tetramethyl-l,3,2-dioxaborolan-2-yl)benzene-l,2-d iamine

Into a 250-mL round-bottom flask, was placed a solution of 2-nitro-4-(4,4,5,5- tetramethyl-l,3,2-dioxaborolan-2-yl)aniline (7.40 g, 25.20 mmol) in MeOH (50 mL) and DCM (50 mL). This was followed by the additional of Pd/C (134 g, 126 mmol, wet 10%) at ambient temperature. The reaction mixture was degassed with nitrogen for 3 times and stirred under hydrogen for 16 hr at ambient temperature. The resulting mixture was filtered and the filter cake was washed with DCM (3 x 10 mL). The combined organic layers were concentrated in vacuo and purified by silica gel column chromatography, eluted with EA in PE (30%) to afford the title compound: LCMS (ESI) calc'd for Ci ₂ H ₁₉ B ₂ 0 ₂ [M + H] ⁺ : 235, found 235; ^X H NMR (400 MHz, CD ₃ C1): δ 7.23 (d, J= 7.6 Hz, 1H), 7.17 (s, 1H), 6.70 (d, J= 8.0 Hz, 1H) , 3.19 (br, 4H), 1.32 (s, 12H) .

Step C : 6-(4,4,5,5-tetramethyl-l,3,2-dioxaborolan-2-yl)-lH-benzo[d]i midazol-2-amine

Into a 50-mL round-bottom flask purged and maintained with an inert atmosphere of argon, was placed a solution of 4-(4,4,5,5-tetramethyl-l,3,2-dioxaborolan-2-yl)benzene-l,2- diamine (2.00 g, 7.69 mmol) in MeOH (10 mL). This was followed by the additional of cyanogen bromide (0.83 g, 7.69 mmol) at 0°C. The resulting mixture was stirred at 0°C for 2 hr under argon and then it was quenched with aqueous saturated a ₂ C0 ₃ (30 mL) and extracted with EtOAc (3 x 30 mL). The combined organic layers were washed with brine (70 mL), dried over anhydrous a ₂ S0 ₄ and concentrated in vacuo. The residue was recrystallized from DCM (100 mL) to afford the title compound: LCMS (ESI) calc'd for Ci ₃ H ₁₈ B ₃ 0 ₂ [M + H] ⁺ : 260, found 260; 'H NMR (400 MHz, DMSO-i¾): δ 10.70 (br, 1H), 7.40 (s, 1H), 7.23 (d, J= 8.0 Hz, 1H), 7.06 (d, J= 7.6 Hz, 1H), 6.24 (s, 2H), 1.23 (s, 12H) .

Step D : 3-(2-amino-3H-benzo[d]imidazol-5-yl)-6-bromo-N,N-bis(4-metho xybenzyl)-2-(2- (4-methoxybenzyl)-2H-tetrazol-5-yl)benzenesulfonamide

Into a 25-mL round-bottom flask purged and maintained with an inert atmosphere of argon, was placed a solution of 6-bromo-3-iodo-N,N-bis(4-methoxybenzyl)-2-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)benzenesulfonamide (0.63 g, 0.80 mmol), 6-(4,4,5,5- tetramethyl-l,3,2-dioxaborolan-2-yl)-lH-benzo[i/]imidazol-2- amine (0.25 g, 0.96 mmol) and Pd(PPh ₃ ) ₄ (0.14 g, 0.12 mmol) in dioxane (7 mL). This was followed by the addition of a ₂ C03 (0.26 g, 2.41 mmol) in water (1.5 mL) at ambient temperature. After the resulting mixture was stirred at 80°C for 18 hr under argon, it was cooled down to 20°C, quenched with water (50 mL) and extracted with EtOAc (3 x 50 mL). The combined organics were washed with brine (2 x 50 mL), dried over anhydrous Na ₂ S0 ₄ and concentrated in vacuo. The residue was purified by silica gel column chromatography, eluted with EtOAc/PE (100/1) to afford the title compound: LCMS (ESI) calc'd for CssHsjBr sOjS [M + H] ⁺ : 795, 797 (1 : 1), found 795, 797 (1 : 1).

Step E: tert-butyl 4-(4-(2-amino-3H-benzo[d]imidazol-5-yl)-2-(N,N-bis(4- methoxybenzyl)sulfamoyl)-3-(2-(4-methoxybenzyl)-2H-tetrazol- 5-yl)benzyl)piperidine-l- carboxylate

Into a 10-mL round-bottom flask purged and maintained with an inert atmosphere of argon, was placed a solution of 3-(2-amino-lH-benzo[i/]imidazol-6-yl)-6-bromo-N,N-bis(4- methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)benze nesulfonamide (0.10 g, 0.13 mmol), tert-butyl 4-(iodomethyl)piperidine-l-carboxylate (82 mg, 0.25 mmol), 4,7-diphenyl-

1,10-phenanthroline (8.35 mg, 0.025 mmol), nickel iodine (7.85 mg, 0.03 mmol) and manganese (14 mg, 0.25 mmol) in DMA (1 mL). This was followed by the addition of benzonitrile (1.30 mg, 0.013 mmol) at ambient temperature and chlorotrimethylsilane (0.14 mg, 1.26 μιηοΐ) at 0°C. The resulting mixture was stirred at 40°C for 2 hr under argon and then cooled down to 20°C, quenched with water (10 mL) and extracted with EtOAc (3 x 10 mL). The combined organic phases were washed with brine (2 x 20 mL), dried over anhydrous Na ₂ S0 ₄ and concentrated in vacuo. The residue was purified by Prep-HPLC: Column: X Bridge C18, 19 x 150 mm, 5 μιη; Mobile Phase A: water (0.05% TFA), Mobile Phase B: ACN; Flow rate: 20 mL/min; Gradient: 30% B to 70% B in 10 min; Detection: UV 254 nm. to afford the title compound: LCMS (ESI) calc'd for [M + H] ⁺ : 914, found 914.

Step F : 3-(2-amino-3H-benzo[d]imidazol-5-yl)-N,N-bis(4-methoxybenzyl )-2-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)-6-(piperidin-4-ylmethyl)ben zenesulfonamide

Into a 25-mL round-bottom flask , was placed a solution of /er/-butyl 4-(4-(2- amino-lH-benzo[i/]imidazol-6-yl)-2-(N,N-bis(4-methoxybenzyl) sulfamoyl)-3-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)benzyl)piperidine-l-carboxyl ate (25 mg, 0.03 mmol) in DCM (2 mL). This was followed by the addition of TFA (0.5 mL, 6.49 mmol) dropwise with stirring at 0°C. The resulting mixture was stirred at 0°C for 1 hr and then the solvent was evaporated in vacuo to afford the title compound. The crude product was used directly in the next step without further purification: LCMS (ESI) calc'd for C44H47N ₉ O5S [M + H] ⁺ : 814, found 814.

Step G : 3-(2-amino-3H-benzo[d]imidazol-5-yl)-6-(piperidin-4-ylmethyl )-2-(2H-tetrazol- 5-yl)benzenesulfonamide

To a stirred solution of 3-(2-amino-lH-benzo[i/]imidazol-6-yl)-N,N-bis(4- methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-6-(p iperidin-4- ylmethyl)benzenesulfonamide (20 mg, 0.02 mmol) in anisole (1 mL) was added TFA (3 mL, 38.9 mmol) at ambient temperature. The resulting mixture was stirred at 80°C for 3 hr and then cool down to 20°C. The solvent was evaporated and the residue was purified by Prep-HPLC with the following conditions: Column: X Bridge RP18, 19 x 150 mm, 5 μιη; Mobile Phase A: water (0.05% NH4HCO ₃ ), Mobile Phase B: ACN; Flow rate: 20 mL/min; Gradient: 3%B to 18%B in 7 min; Detection: UV 254 nm. The collected fractions were combined and

concentrated in vacuo to give the title compound: LCMS (ESI) calc'd for C2 ₀ H2 _{3 9} O2S [M - H] ^~ : 452, found 452; ^X H NMR (400 MHz, DMSO-i/ ₆ ): δ 7.83 (s, 2H), 7.44 (d, J= 8.0 Hz, 1H), 7.32 (d, J= 8.0 Hz, 1H), 6.78 (d, J= 8.0 Hz, 1H), 6.64 (s, 1H), 6.42 (s, 1H), 6.01 (s, 2H), 3.20-3.10 (s, 2H), 3.07 (d, J= 6.4 Hz, 2H), 2.76-2.73 (m, 2H), 1.98-1.82 (m, 1H), 1.75-1.71 (m, 2H), 1.40- 1.37 (m, 2H) .

EXAMPLE 61 1

3-(2-amino-3H-benzo[i/]imidazol-5-yl)-6-(azetidin-3-ylmethyl )-2-(2H-tetrazol-5- yl)benzenesulfonamide

Step A : tert-butyl 3-(4-(2-amino-3H-benzo[d]imidazol-5-yl)-2-(N,N-bis(4- methoxybenzyl)sulfamoyl)-3-(2-(4-methoxybenzyl)-2H-tetrazol- 5-yl)benzyl)azetidine-l- carboxylate

To a stirred mixture of 3-(2-amino-3a,7a-dihydro-lH-benzo[i/]imidazol-6-yl)-6- bromo-N,N-bis(4-methoxybenzyl)-2-(l-(4-methoxybenzyl)-lH-tet razol-5- yl)benzenesulfonamide (0.10 g, 0.13 mmol) in DMA (1.3 mL) was added tert-butyl 3- (iodomethyl)azetidine-l-carboxylate (0.15 g, 0.50 mmol) at ambient temperature under Ar. To the resulting mixture was added 4,7-diphenyl-l,10-phenanthroline (17 mg, 0.05 mmol), nickel (II) iodide (16 mg, 0.05 mmol), manganese (28 mg, 0.50 mmol), benzonitrile (5 mg, 0.05 mmol) and chlorotrimethylsilane (6 mg, 0.05 mmol) at ambient temperature. After the resulting mixture was heated for 2 hr at 60°C under Ar, the reaction was quenched with water (5 mL) and extracted with EtOAc (3 x 10 mL). The combined organic layers were washed with brine (2 x 10 mL), dried over anhydrous Na ₂ S0 ₄ and concentrated in vacuo. The residue was purified by Prep-TLC with DCM/MeOH (15/1) to afford the title compound, which was used in the next reaction directly. LCMS (ESI) calc'd for [M + if: 886, found 886.

Step B : 3-(2-amino-3H-benzo[d]imidazol-5-yl)-6-(azetidin-3-ylmethyl) -N-(4- methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)benze nesulfonamide

To a stirred solution of /er/-butyl 3-(4-(2-amino-lH-benzo[i/]imidazol-6-yl)-2- (N,N-bis(4-methoxybenzyl)sulfamoyl)-3-(2-(4-methoxybenzyl)-2 H-tetrazol-5- yl)benzyl)azetidine-l-carboxylate (60 mg, 0.07 mmol) in anisole (1 mL, 0.07 mmol) was dropwise added TFA (1 mL, 0.07 mmol) at 0°C. The reaction mixture was stirred for 2 hr at ambient temperature and concentrated in vacuo to afford the title compound, which was used directly: LCMS (ESI) calc'd for C ₃₉ H ₃ 5N ₉ O4S [M + i : 666, found 666.

Step C : 3-(2-amino-3H-benzo[d]imidazol-5-yl)-6-(azetidin-3-ylmethyl) -2-(2H-tetrazol-5- yl)benzenesulfonamide

To a stirred mixture of 3-(2-amino-lH-benzo[i/]imidazol-6-yl)-6-(azetidin-3- ylmethyl)-N,N-bis(4-methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H -tetrazol-5- yl)benzenesulfonamide (70 mg, 0.00 mmol) (crude) in anisole (1 mL) was added TFA (2 mL) at ambient temperature. The resulting solution was stirred for 3 hr at 80°C and then concentrated in vacuo. The residue was purified by Prep-HPLC with the following conditions: Column, X bridge CI 8 , 19 x 150 mm; Mobile phase A: water (0.05% NH ₄ HC0 ₃ ), Mobile phase A:

acetonitrile; Gradient: (hold 34% acetonitrile for 8 min, hold 100% for 2 min, down to 34% in 2 min; Detector: UV 220 and 254 nm. The collected fractions were concentrated in vacuo to afford the title compound: LCMS (ESI) calc'd for C ₁₈ H _{19 9} 0 ₂ S [M + if: 426, found 426; ¾ NMR (400 MHz, CD ₃ OD): δ 7.59 (d, J= 8.0 Hz, 1H), 7.54-7.51 (m, 1H), 6.99 (d, J= 8.4 Hz, 1H), 6.84 (d, J= 8.8 Hz, 1H), 6.76 (d, J= 6.4 Hz, 1H),4.10-3.99 (m, 3H), 3.66-3.48 (m, 4H). EXAMPLE 612

3-(2-amino-3H-benzo[d]imidazol-4-yl)-6-(piperidin-4-ylmethyl )-2-(2H-tetrazol-5- yl)benzenesulfonamide

Step A : 2-nitro-3-(4,4,5,5-tetramethyl-l,3,2-dioxaborolan-2-yl)benze namine

Into a 50-mL round-bottom flask purged and maintained with an inert atmosphere of argon, was placed a solution of 3-bromo-2-nitroaniline (20.00 g, 92 mmol) in 1,4-dioxane (300 mL). This was followed by the addition of [ 1, 1'- bis(diphenylphosphino)ferrocene]dichloropalladium(II) (3.37 g, 4.61 mmol), potassium acetate (27.10 g, 276 mmol) and 4,4,4',4',5,5,5',5'-octamethyl-2,2'-bi(l,3,2-dioxaborolane) (35.10 g, 138 mmol) at ambient temperature. After the resulting mixture was stirred at 85°C for 16 hr under argon, it was filtered out and the filtrate was concentrated in vacuo. The residue was purified by silica gel column chromatography, eluted with EtOAc/PE (1/1) to afford the title compound: LCMS (ESI) calc'd for Ci ₂ H ₁₇ B ₂ 04 [M + H] ⁺ : 265, found 265.

Step B : 3-(4,4,5,5-tetramethyl-l,3,2-dioxaborolan-2-yl)benzene-l,2-d iamine

Into a 250-mL round-bottom flask, was placed a solution of 2-nitro-3 -(4,4,5,5- tetramethyl-l,3,2-dioxaborolan-2-yl)aniline (5.00 g, 18.93 mmol) in DCM (20 mL) and MeOH (20 mL). This was followed by the additional of Pd/C (20.15 g, 18.93 mmol) at ambient temperature. The resulting mixture was degassed with nitrogen for 3 times, and then bubbled with hydrogen for 3 times. After the resulting mixture was stirred under hydrogen for 16 hr at ambient temperature at 1.5 atm, it was filtered and the filter cake was washed with DCM (3 x 10 mL). The combined organic layers were concentrated in vacuo and purified by silica gel column chromatography, eluted with EtOAc/PE (2/3) to afford the title compound: LCMS (ESI) calc'd for Ci ₂ H ₁₉ B ₂ 0 ₂ [M + H] ⁺ : 235, found 235. Step C : 5',6'-diamino-4-bromo-N,N-bis(4-methoxybenzyl)-2-(2-(4-metho xybenzyl)-2H- tetrazol-5 -yl)biphenyl-3 -sulfonamide

Into a 50-mL round-bottom flask purged and maintained with an inert atmosphere of argon, was placed a solution of 6-bromo-3-iodo-N,N-bis(4-methoxybenzyl)-2-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)benzenesulfonamide (0.77 g, 0.97 mmol), 3-(4,4,5,5- tetramethyl-l,3,2-dioxaborolan-2-yl)benzene-l,2-diamine (0.50 g, 2.13 mmol) and Pd(Ph ₃ P) ₄ (0.11 g, 0.10 mmol) in dioxane (10 mL). This was followed by the addition of a ₂ C0 ₃ (0.31 g, 2.90 mmol) in water (1 mL) at ambient temperature. The resulting mixture was stirred at 80°C for 18 hr under argon and then was cooled down to 20°C, quenched with water (50 mL) and extracted with EtOAc (3 x 50 mL). The combined organic phase was washed with brine (3 x 50 mL), dried over anhydrous Na ₂ S0 ₄ and concnetrated under reduced pressure. The residue was purified by silica gel column chromatography, eluted with EA/PE (3/2) to afford the title compound, which was used in the next step directly. LCMS (ESI) calc'd for C ₃ 7H ₃₆ Br 705S [M + H] ⁺ : 770, 772 (1 : 1), found 770, 772 (1 : 1).

Step D : 3-(2-amino-3H-benzo[d]imidazol-4-yl)-6-bromo-N,N-bis(4-metho xybenzyl)-2-(2- (4-methoxybenzyl)-2H-tetrazol-5-yl)benzenesulfonamide

Into a 25-mL round-bottom flask purged and maintained with an inert atmosphere of argon, was placed a solution of 2',3'-diamino-4-bromo-N,N-bis(4-methoxybenzyl)-2-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)-[l,l'-biphenyl]-3-sulfonami de (1.4 g, 1.82 mmol) in MeOH (5 mL) and DCM (5 mL). This was followed by the addition of cyanogen bromide (0.19 g, 1.82 mmol) at 0°C. The resulting mixture was stirred at 25°C for 16 hr under a atmosphere of argon. The reaction was quenched with aqueous saturated sodium bicarbonate (50 mL) and extracted with EtOAc (3 x 50 mL). The combined organic layers were washed with brine (2 x 50 mL), dried over anhydrous Na ₂ S0 ₄ and concentrated under reduced pressure. The residue was recrystallized from DCM/EA/PE (10 mL/10 mL/50 mL). The solid was collected by filtration and dried in vacuo and then was purified by silica gel column chromatography, eluted with EtOAc in Petroleum ether (80%) to afford the title compound: LCMS (ESI) calc'd for

CssHssBr sOjS [M + H] ⁺ : 795, 797 (1 : 1), found 795, 797 (1 : 1).

Step E : tert-butyl 4-(4-(2-amino-3H-benzo[d]imidazol-4-yl)-2-(N,N-bis(4- methoxybenzyl)sulfamoyl)-3-(2-(4-methoxybenzyl)-2H-tetrazol- 5-yl)benzyl)piperidine-l- carboxylate Into a 10-mL round-bottom flask purged and maintained with an inert atmosphere of argon, was placed a solution of 3-(2-amino-lH-benzo[( Jimidazol-7-yl)-6-bromo-N,N-bis(4- methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)benze nesulfonamide (0.20 g, 0.25 mmol), tert-butyl 4-(iodomethyl)piperidine-l-carboxylate (0.33 g, 1.01 mmol), 4,7-diphenyl- 1,10-phenanthroline (33 mg, 0.10 mmol), nickel iodide (17 mg, 0.05 mmol) and manganese (55 mg, 1.01 mmol) in DMA (3 mL). This was followed by the addition of benzonitrile (26 mg, 0.25 mmol) at ambient temperature and chlorotrimethylsilane (27.3 mg, 0.251 mmol) at 0°C. The resulting mixture was stirred at 60°C for 2 hr under a atmosphere of argon. The reaction mixture was allowed to cool to 20°C, quenched with water (10 mL) and extracted with EtOAc (3 x 10 mL), the combined organic layers were washed with brine (2 x 20 mL), dried over anhydrous Na ₂ S0 ₄ and filtered. The filtrate was evaporated under reduced pressure and the residue was purified by Prep-HPLC with the following conditions: Column: X Bridge RP CI 8, 19 x 150 mm, 5 μιη; Mobile Phase A: water (10 mM NH ₄ HC0 ₃ ), Mobile Phase B: ACN; Flow rate: 20 mL/min; Gradient: 65-65%B in 12 min; Detection: at 254 nm. The collected fractions were combined and concentrated in vacuo to afford the title compound: LCMS (ESI) calc'd for C4 ₉ H55N ₉ O7S [M + H] ⁺ : 914, found 914.

Step F : 3-(2-amino-3H-benzo[d]imidazol-4-yl)-N,N-bis(4-methoxybenzyl )-2-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)-6-(piperidin-4-ylmethyl)ben zenesulfonamide

Into a 25-mL round-bottom flask, was placed a solution of tert-butyl 4-(4-(2- amino- lH-benzo[i/]imidazol-7-yl)-2-(N,N-bis(4-methoxybenzyl)sulfam oyl)-3-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)benzyl)piperidine-l-carboxyl ate (0.10 g, 0.11 mmol) in DCM (2 mL). This was followed by the addition of TFA (0.5 mL, 6.49 mmol) dropwise with stirring at 0°C. The resulting mixture was stirred at 0°C for 1 hr and then evaporated under reducing pressure to afford the title compound, which was used directly in the next step without further purification: LCMS (ESI) calc'd for C ₄₄ H ₄₇ N ₉ 0 ₅ S [M + H] ⁺ : 814, found 814.

Step G : 3-(2-amino-3H-benzo[d]imidazol-4-yl)-6-(piperidin-4-ylmethyl )-2-(2H-tetrazol- 5 -yl)benzenesulfonamide

To a solution of 3-(2-amino-lH-benzo[i/]imidazol-7-yl)-N,N-bis(4- methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-6-(p iperidin-4- ylmethyl)benzenesulfonamide (90 mg, 0.09 mmol) in anisole (0.5 mL) was added TFA (3 mL, 38.9 mmol) at ambient temperature. After the resulting mixture was stirred at 80°C for 2 hr, it was cooled down to 20°C and the solvent was evaporated. The residue was purified by Prep- HPLC with the following conditions: Column: X Bridge RP CI 8, 19 x 150 mm, 5 μιη; Mobile Phase A: water (10 mM NH ₄ HCO ₃ ), Mobile Phase B: ACN; Flow rate: 20 mL/min; Gradient: 5- 25%B in 8 min; Detection: at 254 nm. The collected fractions were combined and concentrated under reducing pressure to afford the title compound: LCMS (ESI) calc'd for C2 ₀ H2 _{3 9} O2S [M - FfJ ^" : 452, found 452; 'H NMR (400 MHz, DMSO-i¾): δ 7.86 (s, 2H), 7.63 (s, 1H), 7.35 (d, J= 8.4 Hz, 1H), 6.85 (d, J= 8.4 Hz, 1H) , 6.44 (s, 1H), 6.08 (s, 1H), 6.04 (d, J= 8.0 Hz, 2H), 3.17- 3.08 (m, 4H), 2.51-2.49 (m, 2H), 1.80 (s, 1H), 1.67-1.51 (m, 2H), 1.42-1.33 (m, 2H).

EXAMPLES 613-621

Parallel synthesis of N-substituted 4'-(piperidin-4-yl)-2-(lH-tetrazol-5-yl)-[l,l'-biphenyl]-3- sulfonamides

A) polystyrene bound sodium cyanoborohydride

Step A: 2-(l-(4-methoxybenzyl)-lH-tetrazol-5-yl)-4'-(piperidin-4-yl) -[l,r-biphenyl]-3- sulfonamide 2,2,2-trifluoroacetate and 2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-4'-(piperidin-4- yl)-[l,l'-biphenyl]-3-sulfonamide 2,2,2-trifluoroacetate (47 mg, 0.076 mmol) in MeOH (0.500 mL) and Tetrahydrofuran (0.5 mL) were treated with an excess of polystyrene bound sodium cyanoborohydride. Then commercially available or known tert-butoxycarbonyl protected aminoaldehydes (2 equivalents, 0.152 mmol) were added in separate vials prepared as described and each of these mixtures was stirred for 3 hours. The organics were removed via pipette to leave behind the resin. The solvents were removed in the genevac under reduced pressure.

Step B: To firstly remove the boc-protecting group, ANISOLE (0.100 mL, 0.912 mmol), CH ₂ C1 ₂ (0.7 mL) and TFA (0.3 mL) were added and the mixtures were stirred at room temperature for 2 hours. Then TFA (1 mL) was added and the mixtures were stirred at 65°C for 2.5 hours. The mixtures were allowed to cool, and the volatile organics were removed in the genenvac. 1 mL of DMSO was added to each vial and the mixtures were purified using mass directed reverse phase HPLC to afford the examples in the table below.

Ex. Structure Name Calc'd LC/MS

No. MW m/e

yl)benzenesulfonamide

EXAMPLES 622-638

Parallel synthesis of 3-(6-aminopyridin-3-yl)-2-(2H-tetrazol-5-yl)benzenesulfonami des

Step A

Step A: Copper catalyzed C-N coupling of pyridyl bromide with primary and secondary amines.

3-(6-bromopyridin-3-yl)-N,N-bis(4-methoxybenzyl)-2-(l-(4-met hoxybenzyl)-lH- tetrazol-5-yl)benzenesulfonamide (40 mg, 0.054 mmol), Bis(2- isobutyrylcyclohexanone)copper(II) (commercially available from Aldrich; 9.23 mg, 0.022 mmol) and commercially available or known primary and secondary amines (0.054 mmol) were stirred at 100°C for 18 hours. The mixtures were allowed to cool. Then 1 mL DCM and 1 mL water were added. The organics were separated and concentrated in vacuo.

Step B : Removal of the ara-methoxybenzyl protective groups.

The residue from Step A was dissolved in TFA (1 mL) and treated with anisole (0.029 mL, 0.270 mmol). The mixture was stirred at 65°C for 2 hr. The mixtures were allowed to cool. The volatile organics were removed under reduced pressure in the genevac. Then 1 ml DMSO was added and the crude materials and others made in the same way were purified by mass directed reverse hase HPLC to afford Examples 622-638.

EXAMPLES 639-646

Parallel synthesis of 3-(2-aminobenzo[d]thiazol-4-yl)-2-(lH-tetrazol-5-yl)benzenes ulfonamides

Step A: Coupling of primary and secondary amines to 3-(2-bromobenzo[d]thiazol-4-yl)- N,N-bis(4-methoxybenzyl)-2-( 1 -(4-methoxybenzyl)- lH-tetrazol-5-yl)benzenesulfonamide and 3-(2-bromobenzo[d]thiazol-4-yl)-N,N-bis(4-methoxybenzyl)-2-( 2-(4-methoxybenzyl)-2H- tetrazol-5-yl)benzenesulfonamide.

A mixture of 3-(2-bromobenzo[d]thiazol-4-yl)-N,N-bis(4-methoxybenzyl)-2-( l- (4-methoxybenzyl)-lH-tetrazol-5-yl)benzenesulfonamide and 3-(2-bromobenzo[d]thiazol-4-yl)- N,N-bis(4-methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol- 5-yl)benzenesulfonamide (40 mg, 0.050 mmol), DBU (0.030 mL, 0.201 mmol) and commercially available primary or secondary amines (0.100 mmol) in Dioxane (1 mL) were added to a microwave vial, and heated at 150°C for 15 mintues. The crude reaction mixture was concentrated in the genevac under reduced pressure.

Step B : Removal of the ara-methoxybenzyl protective groups.

The residues from Step A were treated with TFA (1.0 mL) and stirred at 65°C for 4 hours. The mixtures were allowed to cool and the volatile organics removed in the genevac under reduced pressure. Then 1 ml DMSO was added and the crude materials and others made in the same way were purified by mass directed reverse phase HPLC to afford Examples 639- 646. Note that in some cases the amines used contained a tert-butoxycarbonyl protected amino group. In those cases when the amines used contained a second amino group protected with a tert-butoxycarbonyl protective group, this group was also removed under the para- methoxybenzyl protective group removal conditions.

Ex. Structure Name Calc'd LC/MS

No. Mass m/e

EXAMPLES 647-652

Parallel synthesis of 3 -substituted 2-(lH-tetrazol-5-yl)benzenesulfonamides

Step A

Step A: Palladium catalyzed C-C coupling of arylboronic ester and arylbromides. In a glove box under a dry nitrogen atomosphere, arylbromides (0.3 mmol) (commercially available, known from the literature) and Ad2nBuP Biphenyl Pre-Catalyst (6.71 mg, 10.0 μιηοΐ) and 200 μΐ, of 1.5 N degassed aq. CS2CO ₃ solution were added into 2 drum vials. 1.0 mL of a solution of the mixture of 3-(5,5-dimethyl-l,3,2-dioxaborinan-2-yl)-N,N- bis(4-methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl )benzenesulfonamide and 3-(5,5- dimethyl-l,3,2-dioxaborinan-2-yl)-N,N-bis(4-methoxybenzyl)-2 -(l-(4-methoxybenzyl)-lH- tetrazol-5-yl)benzenesulfonamide from Reference Example 9 (70 mg, 0.1 mmol) in Toluene were added into each vial. The vials were capped and heated at 1 10°C with stirring for 20 hr. After the vials were cooled to room temperature, the solvent was removed in a GeneVac. Into each residue was added 600 of H ₂ 0 and 2 mL of EtOAc. The organic layers were transferred into 2 dram vials. The organic solvent was removed in GeneVac to afford the crude

intermediates which were deprotected without further purification in the subsequent step.

Step B: Removal of the p-methoxybenzyl (PMB) protecting group by TFA treatment

The residues from Step A were each added TFA 0.7 mL alone with anilsole (0.3 mL). The vials were sealed and heated at 55°C under stirring. The pressure was released periodically by unscrewing the cap. After 5 hr, the reactions were monitored by UPLC. The mixtures were cooled to room temperature and filtered through filters. The filtrates were concentrated in a GeneVac. The residues were dissolved in DMSO. Each crude mixture was filtered into a 96-well tray and purified with HPLC. The crude products were purified by mass triggered reverse phase HPLC using the following conditions: [column: Waters XBridge CI 8, or Waters Sunfire C18, 5μιη , 19x100 mm; solvent: gradient range 3 -28% initial to 60-95% final MeCN (0.1% TFA) in water (0.1% TFA) 50 or 70 mL/min; 8 min run time] to afford

EXAMPLES 647 to 652.

EXAMPLES 653-667

Parallel synthesis of 3-N-substituted-2-(lH-tetrazol-5-yl)-6-(trifluromethyl)benze nesulfonamides

C-N displacement of secondary amines on arylbromide.

To 5-mL microwave vials, secondary amines (0.164 mmol) (commercially available, known from the literature) and K2CO ₃ solid (37.7 mg, 0.273 mmol) were added followed by addition of 1 mL DMF solution of the mixture of 3-bromo-N,N-bis(4- methoxybenzyl)-2-(l -(4-methoxybenzyl)- lH-tetrazol-5-yl)-6-

(trifluoromethyl)benzenesulfonamide and 3-bromo-N,N-bis(4-methoxybenzyl)-2-(2-(4- methoxybenzyl)-2H-tetrazol-5-yl)-6-(trifluoromethyl)benzenes ulfonamide from Reference Example 24 (40 mg, 0.055mmol). The vials were capped and heated at 140°C with stirring for 2 hr. After the vials were cooled to room temperature, the solvent was removed in a GeneVac. Into each residue was added 500 of 3 N HC1 and 2 mL of EtOAc. The organic layers were transferred into 2 dram vials. The organic solvent was removed in GeneVac to afford the crude intermediates which were deprotected without further purification in the subsequent step.

Step B: Removal of the p-methoxybenzyl (PMB) protecting group by TFA treatment

The residues from Step A were each added TFA 0.7 mL alone with anilsole (0.3 mL). The vials were sealed and heated at 55°C under stirring. The pressure was released periodically by unscrewing the cap. After 5 hr, the reactions were monitored by UPLC. The mixtures were cooled to room temperature and filtered through filters. The filtrates were concentrated in a GeneVac. The residues were dissolved in DMSO. Each crude mixture was filtered into a 96-well tray and purified with HPLC. The crude products were purified by mass triggered reverse phase HPLC using the following conditions: [column: Waters XBridge CI 8, or Waters Sunfire C18, 5μιη , 19x100 mm; solvent: gradient range 10 -35% initial to 45-95% final MeCN (0.1% TFA) in water (0.1% TFA) 50 or 70 mL/min; 8 min run time] to afford Examples 653-667.

EXAMPLES 668-678

Parallel synthesis of 4'-[N-substituted piperidin-4-yl]-2-(lH-tetrazol-5-yl)-4- (trifluoromethyl)biphenyl-3-sulfonamides

Step A: Reductive amination of aldehydes on piperidin.

To 2 dram vials, aldehydes (0.13 mmol) (commercially available, known from the literature) was added into 1 mL MeOH solution of the mixture of N,N-bis(4-methoxybenzyl)- 2-( 1 -(4-methoxybenzyl)- 1 H-tetrazol-5-yl)-4'-(piperidin-4-yl)-4-(trifluoromethyl)- [ 1 , 1 '-biphenyl] - 3 -sulfonamide and N,N-bis(4-methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol- 5-yl)-4'- (piperidin-4-yl)-4-(trifluoromethyl)-[l,r-biphenyl] -3 -sulfonamide from Example 269, prior to TFA removal of the ara-methoxybenzyl protective groups, (30 mg, 0.043 mmol) followed by addition of 2 drops of acetic acid. The vials were capped and stirring at room temerature for 20 min. MP-CNBH3 (90 mg, 2.4 mmol/g) was then added to each vial. The vials were capped and stirring at room temperature for 20 hr. The crude reactions were monitored by UPLC. Once the reaction was finished, the mixture were filtered and the solvent were removed in a GeneVac to afford the crude intermediates which were deprotected without further purification in the subsequent step.

Step B: Removal of the boc and p-methoxybenzyl (PMB) protecting group by TFA treatment

The residues from Step A were each added TFA 0.7 mL alone with thioanilsole (0.3 mL). The vials were sealed and stirred at room temperature. After 5 hr, the reactions were monitored by UPLC. The mixtures were concentrated in a GeneVac. The residues were dissolved in DMSO. Each crude mixture was filtered into a 96-well tray and purified with HPLC. The crude products were purified by mass triggered reverse phase HPLC to afford corresponding intermediates.

Step C: Removal of the p-methoxybenzyl (PMB) protecting group by TFA treatment

To the intermediates from Step B, was added TFA 0.7 mL. The vials were sealed and heated at 55°C under stirring. The pressure was released periodically by unscrewing the cap. After 5 hr, the reactions were monitored by UPLC. The mixtures were cooled to room temperature and filtered through filters. The filtrates were concentrated in a GeneVac. The residues were dissolved in DMSO. Each crude mixture was filtered into a 96-well tray and purified with HPLC. The crude products were purified by mass triggered reverse phase HPLC using the following conditions: [column: Waters XBridge C18, or Waters Sunfire C18, 5μιη,

19x100 mm; solvent: gradient range 3-28% initial to 45-100% final MeCN (0.1% TFA) in water (0.1% TFA) 50 or 70 mL/min; 8 min run time] to afford Examples 668-678.

Ex. Structure Name Calc'd. LC/MS

No. MW m/e

[M+H] ⁺ [M+H] ⁺

EXAMPLES 679-705

Parallel synthesis of ?ra«s-4'-N-substituted cyclohexyl-2-(lH-tetrazol-5-yl)-6- (trifluoromethyl)benzensulfonamides

Step A: Reductive amination of ketones on cyclohexylamine.

To 2 dram vials, ketones (0.12 mmol) (commercially available, known from the literature) was added into 1 mL MeOH solution of the mixture (S)-3-((lr,4S)-4- aminocyclohexyl)-N,N-bis(4-methoxybenzyl)-2-(l-(4-methoxyben zyl)-lH-tetrazol-5-yl)-6- (trifluoromethyl)benzenesulfonamide and 3-((lr,4r)-4-aminocyclohexyl)-N,N-bis(4- methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-6-

(trifluoromethyl)benzenesulfonamide from Example 820, prior to removal of the para- methoxybenzyl protective groups, (30 mg, 0.04 mmol) followed by addition of 2 drops of acetic acid. The vials were capped and stirring at room temperature for 20 min. MP-CNBH ₃ (90 mg, 2.4 mmol/g) was then added to each vial. The vials were capped and stirring at room temperature for 20 hr. The crude reactions were monitored by UPLC. Once reactions were finished, the mixture were filtered and the solvent were removed in a GeneVac to afford the crude intermediates which were deprotected without further purification in the subsequent step.

Step B: Removal of the boc and p-methoxybenzyl (PMB) protecting group by TFA treatment To the residues from Step A, were each added TFA 0.7 mL and thioanilsole (0.3 mL). The vials were sealed and stirred at room temperature. After 5 hr, the reactions were monitored by UPLC. The mixtures were concentrated in a GeneVac. The residues were dissolved in DMSO. Each crude mixture was filtered into a 96-well tray and purified with HPLC. The crude products were purified by mass triggered reverse phase HPLC to afford corresponding intermediates.

Step C: Removal of the p-methoxybenzyl (PMB) protecting group by TFA treatment

To the intermediates from Step B were added TFA 0.7 mL. The vials were sealed and heated at 55°C under stirring. The pressure was released periodically by unscrewing the cap. After 5 hr, the reactions were monitored by UPLC. The mixtures were cooled to room temperature and filtered through filters. The filtrates were concentrated in a GeneVac. The residues were dissolved in DMSO. Each crude mixture was filtered into a 96-well tray and purified with HPLC. The crude products were purified by mass triggered reverse phase HPLC using the following conditions: [column: Waters XBridge C I 8, or Waters Sunfire C I 8, 5μιη , 19x100 mm; solvent: gradient range 3-45% initial to 45- 100% final MeCN (0.1% TFA) in water (0.1% TFA) 50 or 70 mL/min; 8 min run time] to afford Examples 679-705.

Ex. Structure Name Calc'd. LC/MS No. MW m/e

[M+H] ⁺ [M+H] ⁺

679 3-{4-[(3aS,6S,7aS)- 514.22 514.21 octahydro-lH-indol-6- ylamino]cyclohexyl}-2- (lH-tetrazol-5-yl)-6- (trifluoromethyl)benzene

sulfonamide

EXAMPLES 706-753

Parallel synthesis of 3 -substituted 2-(lH-tetrazol-5-yl)-6-(trifluromethyl)benzenesulfonamides

Step A

Step A: Palladium catalyzed C-C coupling of arylboronic ester and arylbromides. In a glove box under a dry nitrogen atomosphere, arylbromides (0.133 mmol) (commercially available, known from the literature) and 2 ^nd Generation Xphos Pre-Catalyst (5.23 mg, 6.65 μιηοΐ) and 266 μΐ, of IN degassed aq. CS2CO3 solution were added into 2 dram vials. 1.0 mL of a solution of the mixture of 3-(5,5-dimethyl-l,3,2-dioxaborinan-2-yl)-N,N- bis(4-methoxybenzyl)-2-( 1 -(4-methoxybenzyl)- 1 H-tetrazol-5-yl)-6-

(trifluoromethyl)benzenesulfonamide and 3-(5,5-dimethyl-l,3,2-dioxaborinan-2-yl)-N,N-bis(4- methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-6-

(trifluoromethyl)benzenesulfonamide (50 mg, 0.067 mmol) in 1,4-Dioxane were added into each vial. The vials were capped and heated at 85°C with stirring for 20 hr. After the vials were cooled to room temperature, the solvent was removed in a GeneVac. Into each residue was added 600 μϊ _^ of H ₂ 0 and 2 mL of EtOAc. The organic layers were transferred into 2 dram vials. The organic solvent was removed in GeneVac to afford the crude intermediates which were deprotected without further purification in the subsequent step.

Step B: Removal of the p-methoxybenzyl (PMB) protecting group by TFA treatment

To the residues from Step A were each added TFA 0.7 mL and anisole (0.3 mL).

The vials were sealed and heated at 55°C under stirring. The pressure was released periodically by unscrewing the cap. After 5 hr, the reactions were monitored by UPLC. The mixtures were cooled to room temperature and filtered through filters. The filtrates were concentrated in a GeneVac. The residues were dissolved in DMSO. Each crude mixture was filtered into a 96- well tray and purified with HPLC. The crude products were purified by mass triggered reverse phase HPLC using the following conditions: [column: Waters XBridge CI 8, or Waters Sunfire C18, 5μιη , 19x100 mm; solvent: gradient range 3 -28% initial to 45-95% final MeCN (0.1% TFA) in water (0.1% TFA) 50 or 70 mL/min; 8 min run time] to afford EXAMPLES 706-753. Note that some aryl halides included tert-butoxycarbonyl protected amino groups; in these instances TFA treatment also led to removal of the tert-butoxycarbonyl protective group.

Ex. Structure Name Calc'd. LC/MS

No. MW m/e

[M+H] ⁺ [M+H] ⁺

sulfonamide 463.09 463.08

EXAMPLES 754-784

Parallel synthesis of 3-N-substituted-2-(lH-tetrazol-5-yl)-6-(trifluromethyl)benze nesulfonamides

C-N displacement of secondary amines on arylbromide.

To 5-mL microwave vials, secondary amines (0.164 mmol) (commercially available, known from the literature) and K2CO ₃ solid (37.7 mg, 0.273 mmol) were added followed by addition of 1 mL DMF solution of the mixture of 3-bromo-N,N-bis(4- methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-6-

(trifluoromethyl)benzenesulfonamide and 3 -bromo-N,N-bis(4-methoxybenzyl)-2-( 1 -(4- methoxybenzyl)- lH-tetrazol-5-yl)-6-(trifluoromethyl)benzenesulfonamide from Reference Example 24 (40 mg, 0.055mmol). The vials were capped and heated at 140°C with stirring for 2 hr. After the vials were cooled to room temperature, the solvent was removed in a GeneVac. Into each residue was added 500 of 3 N HCl and 2 mL of EtOAc. The organic layers were transferred into 2 dram vials. The organic solvent was removed in GeneVac to afford the crude intermediates which were deprotected without further purification in the subsequent step.

Step B: Removal of the boc and p-methoxybenzyl (PMB) protecting group by TFA treatment

To the residues from Step A were each added TFA 0.7 mL and thioanisole (0.3 mL). The vials were sealed and stirred at room temperature. After 5 hr, the reactions were monitored by UPLC. The mixtures were concentrated in a GeneVac. The residues were dissolved in DMSO. Each crude mixture was filtered into a 96-well tray and purified with HPLC. The crude products were purified by mass triggered reverse phase HPLC to afford corresponding intermediates.

Step C: Removal of the p-methoxybenzyl (PMB) protecting group by TFA treatment To the intermediates from Step B were added TFA 0.7 mL. The vials were sealed and heated at 55°C under stirring. The pressure was released periodically by unscrewing the cap. After 5 hr, the reactions were monitored by UPLC. The mixtures were cooled to room temperature and filtered through filters. The filtrates were concentrated in a GeneVac. The residues were dissolved in DMSO. Each crude mixture was filtered into a 96-well tray and purified with HPLC. The crude products were purified by mass triggered reverse phase HPLC using the following conditions: [column: Waters XBridge C18, or Waters Sunfire C 18, 5μιη , 19x100 mm; solvent: gradient range 3-45% initial to 45- 100% final MeCN (0.1% TFA) in water 0.1% TFA) 50 or 70 mL/min; 8 min run time] to afford EXAMPLES 754-784.

1 amide

EXAMPLES 785-799

Parallel synthesis of N-substituted 4'-piperidin-2-(lH-tetrazol-5-yl)-[l,l'-biphenyl]-4- (trifluromethyl)-3 -sulfonamides

Reductive amination of ketones on piperidine.

To 2 dram vials, ketones (0.246 mmol) (commercially available, known from the literature) was added into 1 mL MeOH solution of the mixture of N,N-bis(4-methoxybenzyl)-2- (l-(4-methoxybenzyl)-lH etrazol-5-yl)-4'-(piperidin-4-yl)-4-(trifluoromethyl)-[l,r-b iphenyl]-3- sulfonamideand 3-((trans-4-aminocyclohexyl)-N,N-bis(4-methoxybenzyl)-2-(l-( 4- methoxyhenzyl)-lH-tetrazol-5-yl)-4-(trifluromethyl)-[l,l '-biphenyl]-3 -sulfonamide and N,N- bis(4-methoxybenzyl)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl )-4'-(piperidin-4-yl)-4- (trifluoromethyl)-[l,r-biphenyl]-3 -sulfonamide from Reference Example (50 mg, 0.062 mmol) followed by addition of 2 drops of acetic acid. The vials were capped and stirring at room temerature for 20 min. MP-CNBH ₃ (120 mg, 2.4 mmol/g) was then added to each vial. The vials were capped and stirring at room temerature for 20 hr. The crude reactions were monitored by UPLC. Once reactions were finished, the mixtures were filtered and the solvent were removed in a GeneVac to afford the crude intermediates which were deprotected without further purification in the subsequent step.

Step B: Removal of the boc and p-methoxybenzyl (PMB) protecting group by TFA treatment

To the residues from Step A were each added TFA 0.7 mL and thioanisole (0.3 mL). The vials were sealed and stirred at room temperature. After 5 hr, the reactions were monitored by UPLC. The mixtures were concentrated in a GeneVac. The residues were dissolved in DMSO. Each crude mixture was filtered into a 96-well tray and purified with HPLC. The crude products were purified by mass triggered reverse phase HPLC to afford corresponding intermediates. Step C: Removal of the p-methoxybenzyl (PMB) protecting group by TFA treatment

To the intermediates from Step B were added TFA 0.7 mL. The vials were sealed and heated at 55°C under stirring. The pressure was released periodically by unscrewing the cap. After 5 hr, the reactions were monitored by UPLC. The mixtures were cooled to room temperature and filtered through filters. The filtrates were concentrated in a GeneVac. The residues were dissolved in DMSO. Each crude mixture was filtered into a 96-well tray and purified with HPLC. The crude products were purified by mass triggered reverse phase HPLC using the following conditions: [column: Waters XBridge C18, or Waters Sunfire C18, 5 μιη, 19x100 mm; solvent: gradient range 3-45% initial to 45-100% final MeCN (0.1% TFA) in water (0.1% TFA) 50 or 70 mL/min; 8 min run time] to afford EXAMPLES 785-799.

EXAMPLES 800-818

Parallel synthesis of 4'-(l-substituted-azetidin-3-yl)-2-(lH-tetrazol-5-yl)-4- (trifluoromethyl)biphenyl-3-sulfonamides.

Step A: Reductive amination of ketones on azetidine.

To 2 dram vials, ketones (0.255 mmol) (commercially available, known from the literature) was added into 1 mL MeOH solution of the mixture of 4'-(azetidin-3-yl)-N,N-bis(4- methoxybenzyl)-2-(l -(4-methoxybenzyl)- lH-tetrazol-5-yl)-4-(trifluoromethyl)-[ 1, 1 '-biphenyl] - 3 -sulfonamide and 4'-(azetidin-3-yl)-N,N-bis(4-methoxybenzyl)-2-(2-(4-methoxyb enzyl)-2H- tetrazol-5-yl)-4-(trifluoromethyl)-[l,r-biphenyl]-3-sulfonam ide from Example 433, prior to removal of the ara-methoxybenzyl protective groups (50 mg, 0.064 mmol) followed by addition of 2 drops of acetic acid. The vials were capped and stirring at room temerature for 20 min. MP-CNBH ₃ (120 mg, 2.4 mmol/g) was then added to each vial. The vials were capped and stirring at room temerature for 20 hr. The crude reactions were monitored by UPLC. Once the reaction was finished, the mixtures were filtered and the solvent were removed in a GeneVac to afford the crude intermediates which were deprotected without further purification in the subsequent step.

Step B: Removal of the Boc and p-methoxybenzyl (PMB) protecting group by TFA treatment

The residues from Step A were each added TFA 0.7 mL alone with thioanilsole (0.3 mL). The vials were sealed and stirred at roo temperature. After 5 hr, the reactions were monitored by UPLC. The mixtures were concentrated in a GeneVac. The residues were dissolved in DMSO. Each crude mixture was filtered into a 96-well tray and purified with HPLC. The crude products were purified by mass triggered reverse phase HPLC to afford corresponding intermediates.

Step C: Removal of the p-methoxybenzyl (PMB) protecting group by TFA treatment

To the intermediates from Step B was added TFA 0.7 mL. The vials were sealed and heated at 55°C under stirring. The pressure was released periodically by unscrewing the cap. After 5 hr, the reactions were monitored by UPLC. The mixtures were cooled to room temperature and filtered through filters. The filtrates were concentrated in a GeneVac. The residues were dissolved in DMSO. Each crude mixture was filtered into a 96-well tray and purified with HPLC. The crude products were purified by mass triggered reverse phase HPLC using the following conditions: [column: Waters XBridge C18, or Waters Sunfire C18, 5μιη , 19x100 mm; solvent: gradient range 3-45% initial to 45-100% final MeCN (0.1% TFA) in water (0.1% TFA) 50 or 70 mL/min; 8 min run time] to afford EXAMPLES 800-818.

Ex. Structure Name Calc'd. LC/MS

No. MW m/e

[M+H] ⁺ [M+H] ⁺

118

4'-[l-(pyrrolidin-3- ylmethyl)azetidin-3 -yl]-2-

(lH-tetrazol-5-yl)-4- (trifluoromethyl)biphenyl- 3 -sulfonamide 508.17 508.17

The following General Methods were used in making EXAMPLES 819-840

Method 1 : General coupling procedure between an aryl halide core substrate and boronic ester or acid

The aryl halide core substrate (1.0 mmol), an aryl boronic ester or acid (1.2 mmol), sodium carbonate (2.5 mmol) and Pd(dppf)Ci2 ( 0.1 mmol) were placed in a reaction vessel. To the reaction vessel was added 1,4-Dioxane (6 ml) and Water (1.5 ml). 2 was bubbled through for 10 min. Then the reaction was heated at 80°C overnight. The reaction mixture was diluted with water (60 ml) and extracted with EtOAc (2 X 50 ml). The organic phase was concentrated by reduced pressure. The residue was purified by column

chromatography to give the product.

Method 2: General coupling procedure between an aryl boronic ester or acid core substrate and an aryl halide

To a reaction flask was added an aryl boronic ester (0.3 mmol) core substrate, an aryl halide compound (0.6 mmol), CS2CO ₃ (0.9 mmol) and second generation xphos precatalyst (0.06 mmol). Dioxane (2 ml) and water (0.5 ml) were added to this flask. 2 was bubbled through for 10 min. This mixture was then heated at 75°C overnight. The mixture was cooled, saturated aHC03 was addded to the reaction mixture which was then extracted with EtOAc (2X60 ml). The combined organic phase was concentrated under reduced pressure. The residue was purified by column chromatography on silica gel to give the product.

Method 3: General procedure for remove Boc protecting group on nitrogen

This method is used when in addition to PMB protection on tetrazole and sulfonamide there is also Boc protection on an amino group present in the intermediate.

The N-Boc protected starting material ( 0.7 mmol) was dissolved in DCM (4 ml). TFA (8 ml) was added at room temperature and the mixture was stirred at room temperature for 2 hr. The reaction mixture was concentrated to afford the crude Boc fall off product. The crude material was placed on the vacuum for 3 hours and used as is.

Method 4: General procedure for remove N-PMB protecting group on nitrogen

The N-PMB protected starting material (0.16 mmol) was dissolved in 3 ml of TFA, heated to 80°C for 2 hr. The reaction mixture was concentrated. The residue was purified by Gilson reverse phase HPLC to give the pure product.

Method 5: General reaction procedure between an aryl halide core substrate and an amine

To an aryl halide core (210 mg, 0.287 mmol) in DMF (3 ml), were added potassium carbonate (238 mg, 1.720 mmol) and an amine (115 mg, 0.573 mmol) in a microwave vial. The mixture was stirred in a microwave reactor at 130°C for 1 hour. The mixtures were diluted with water (25 ml), extracted with EtOAc (2X25 ml). The combined organic phase was dried (MgSC^), concentrated under reduced pressure. The residue was purified by column chromatography on silica gel, eluting with EtOAc/isohexane to give the product.

EXAMPLE 819 and 820

3-((ls,4s)-4-aminocyclohexyl)-2-(lH-tetrazol-5-yl)-6-(triflu oromethyl)benzenesulfonamide and 3-((lr,4r)-4-aminocyclohexyl)-2-(lH-tetrazol-5-yl)-6-(triflu oromethyl)benzenesulfonamide

Step A: tert-butyl (3 '-(N,N-bis(4-methoxybenzyl)sulfamoyl)-2'-( 1 -(4-methoxybenzyl)- 1H- tetrazol-5-yl)-4'-(trifluoromethyl)-2,3,4,5-tetrahydro-[l,r- biphenyl]-4-yl)carbamate

Starting from 3-bromo-N,N-bis(4-methoxybenzyl)-2-( 1 -(4-methoxybenzyl)- 1H- tetrazol-5-yl)-6-(trifluoromethyl)benzenesulfonamide and tert-butyl (4-(4,4,5,5-tetramethyl- l,3,2-dioxaborolan-2-yl)cyclohex-3-en-l-yl)carbamates, Method 1 was used to provide the title compound.

Step B: tert-butyl (4-(3-(N,N-bis(4-methoxybenzyl)sulfamoyl)-2-(l-(4-methoxyben zyl)- lH-tetrazol-5-yl)-4-(trifluoromethyl)phenyl)cyclohexyl)carba mate

Palladium hydroxide (176 mg, 0.251 mmol) was added to a stirred solution of tert-butyl (3 '-(N,N-bis(4-methoxybenzyl)sulfamoyl)-2'-(l -(4-methoxybenzyl)- lH-tetrazol-5-yl)- 4'-(trifluoromethyl)-2,3,4,5-tetrahydro-[l, -biphenyl]-4-yl)carbamate (710 mg, 0.836 mmol) in methanol(10 ml) and DCM (6 ml) at RT. The mixture solution was degased by reduced pressure and refilled with 2 and vacuum applied again. Then the reaction mixture was hydrogenated (balloon or 45 PSI) at room temperature overnight. The reaction mixture was filtered through a celite pad and washed with EtOAc. The filtrate was concentrated and the residue was purified by column chromatography on silica gel, eluting with EtOAc/isohexane to give the title compound.

Step C: 3-((ls,4s)-4-aminocyclohexyl)-2-(lH-tetrazol-5-yl)-6- (trifluoromethyl)benzenesulfonamide and 3-((lr,4r)-4-aminocyclohexyl)-2-(lH-tetrazol-5-yl)-6- (trifluoromethyl)benzenesulfonamide

Starting from tert-butyl (4-(3-(N,N-bis(4-methoxybenzyl)sulfamoyl)-2-(l-(4- methoxybenzyl)- lH-tetrazol-5-yl)-4-(trifluoromethyl)phenyl)cyclohexyl)carba mates, Methods 3 and 4 were applied to give, after HPLC separation, the separated cis and trans title compounds.

EXAMPLE 821

3 -[4-(aminomethyl)- 1 -piperidyl]-2-( lH-tetrazol-5-yl)-6-(trifluoromethyl)benzenesulfonamide

Step A: 3 -(4-cyanopiperidin- 1 -yl)-N,N-bis(4-methoxybenzyl)-2-( 1 -(4-methoxybenzyl)- lH-tetrazol-5-yl)-6-(trifluoromethyl)benzenesulfonamide

Starting from 3-bromo-N,N-bis(4-methoxybenzyl)-2-(l -(4-methoxybenzyl)- 1Η- tetrazol-5-yl)-6-(trifluoromethyl)benzenesulfonamide and piperidine-4-carbonitrile, the title compound was obtained by using Method 5.

Step B : 3 -(4-(aminomethyl)piperidin- 1 -yl)-N,N-bis(4-methoxybenzyl)-2-(l -(4- methoxybenzyl)-lH-tetrazol-5-yl)-6-(trifluoromethyl)benzenes ulfonamide

Platinum(rV) oxide (22 mg, 0.098 mmol) was added to a stirred solution of 3-(4- cyanopiperidin-l-yl)-N,N-bis(4-methoxybenzyl)-2-(l -(4-methoxybenzyl)- lH-tetrazol-5-yl)-6- (trifluoromethyl)benzenesulfonamide (150 mg, 0.197 mmol) in HOAc (1 mL), methanol(l mL) and DCM (1 ml) at rt. The mixture solution was degased by reduced pressure and then hydrogenated (using small balloon) at room temperature overnight. The reaction mixture was filtered through celite and washed with DCM and MeOH. The filtrate was concentrated to afford the title compound.

Step C: 3-[4-(aminomethyl)-l-piperidyl]-2-(lH-tetrazol-5-yl)-6- (trifluoromethyl)benzenesulfonamide

Starting from 3-(4-(aminomethyl)piperidin-l-yl)-N,N-bis(4-methoxybenzyl)-2 -(l- (4-methoxybenzyl)-lH-tetrazol-5-yl)-6-(trifluoromethyl)benze nesulfonamide, method 4 was applied to afford the title compound. LC/MS: Cal'd mass: 405.12; Observed mass 406.52 (M+H) ⁺ .

General procedure for the synthesis of guanidine containing analogs from the corresponding amines:

To a corresponding core substrate containing an amine (0.2 mmol) in THF (2.0 mL) was added IH-pyrazole-l-carboxamidine hydrochloride ( 0.45 mmol) and Hunig's base (1.0 mmol). The reaction mixture was stirred at rt under nitrogen overnight. The mixture was diluted with ethyl acetate (2 X 25 mL), washed with brine (25 mL), dried (MgS0 ₄ ), filtered and the solvent was evaporated under reduced pressure. The residue was deprotected by using Method 4 to ive the crude product which was purified by Gilson HPLC to give the pure product.

EXAMPLE 827

3-[4-(?ra«s-2-aminoethylamino)cyclohexyl]-2-(lH-tetrazol -5-yl)-6- (trifluoromethyl)benzenesulfonamide

tert-Butyl (2-oxoethyl)carbamate (98 mg, 0.615 mmol) and sodium cyanoborohydride (38.6 mg, 0.615 mmol) were added to a stirred solution of starting material 3- ((lr,4r)-4-aminocyclohexyl)-2-(lH-tetrazol-5-yl)-6-(trifluor omethyl)benzenesulfonamide (80 mg, 0.205 mmol) in methanol at room temperature. The resulting mixture was stirred at room temperature overnight. The reaction mixture was diluted with water (3 mL) and the mixture was stirred for 30 min, filtered through a celite pad. The filtrate was concentrated to afford the crude product. Then followed by using deprtection Method 3 to afford the title product. LC/MS: Cal'd mass 433.15; Observed 434.37 [M+l] ⁺ .

EXAMPLE 828

3-((ls,4s)-4-((2-aminoethyl)amino)cyclohexyl)-2-(lH-tetrazol -5-yl)-6- (trifluoromethyl)benzenesulfonamide

Step A: tert-butyl (2-(((ls,4s)-4-(3-sulfamoyl-2-(lH-tetrazol-5-yl)-4-

(trifluoromethyl)phenyl)cyclohexyl)amino)ethyl)carbamate

tert-butyl (2-oxoethyl)carbamate (53.8 mg, 0.338 mmol) was added to a stirred solution of starting material 3-((ls,4s)-4-aminocyclohexyl)-2-(lH-tetrazol-5-yl)-6- (trifluoromethyl)benzenesulfonamide (44 mg, 0.113 mmol) in methanol(2 ml) at room temperature and the mixture was stirred at room temperature overnight. The mixture was diluted with water (3 ml) and the mixture was stirred for 30 min and filtered through a celite pad. The filtrate was concentrated to afford the crude product, tert-butyl (2-(((ls,4s)-4-(3-sulfamoyl-2- (lH-tetrazol-5-yl)-4-(trifluoromethyl)phenyl)cyclohexyl)amin o)ethyl)carbamate.

Step B : 3 -(( 1 s,4s)-4-((2-aminoethyl)amino)cyclohexyl)-2-( 1 H-tetrazol-5-yl)-6- (trifluoromethyl)benzenesulfonamide Using deprotection Method 3 tert-butyl (2-(((ls,4s)-4-(3-sulfamoyl-2-(lH- tetrazol-5-yl)-4-(trifluoromethyl)phenyl)cyclohexyl)amino)et hyl)carbamate was converted to the title product. LC/MS: Calc'd mass 433.15; Observed 434.30 [M+lf.

EXAMPLE 829

3-[4-(2-aminoethylamino)-l-piperidyl]-2-(lH-tetrazol-5-yl)-6 -

(trifluoromethyl)benzenesulfonamide

Sodium acetate (26.0 mg, 0.317 mmol) was added to 3-(4-aminopiperidin-l-yl)- N-(4-methoxybenzyl)-2-(l-(4-methoxybenzyl)-lH-tetrazol-5-yl) -6- (trifluoromethyl)benzenesulfonamide (100 mg, 0.158 mmol) in THF (2 ml) and MeOH (2 ml). Followed by adding tert-butyl (2-oxoethyl)carbamate (50.4 mg, 0.317 mmol), sodium cyanotrihydroborate (49.7 mg, 0.792 mmol) and acetic acid (9.06 μΐ, 0.158 mmol). The mixture was stirred at rt under nitrogen overnight. To the reaction flask was added another 2 equvalent of sodium cyanotrihydroborate (49.7 mg, 0.792 mmol) and stirred for 5 hr. The mixture was diluted with ethyl acacate (30 ml), washed with brine ( 25 mL), the organic phase was dried (MgS0 ₄ ), filtered and the solvent was evaporated under reduced pressure. The residue was purified by column chromatography on silica gel 12 g, eluting with EtOAc/isohexane to give as the intermediate tert-butyl (2-((l-(2-(l-(4-methoxybenzyl)-lH-tetrazol-5-yl)-3-(N-(4- methoxybenzyl)sulfamoyl)-4-(trifluoromethyl)phenyl)piperidin -4-yl)amino)ethyl)carbamate. This intemediate product was treated with Method 3 and 4 to afford the titled compound.

LC/MS: Calc'd mass 434.14; Observed 435.36 [M+lf.

EXAMPLE 830

3-[4-[(l-aminocyclopropyl)methylamino]cyclohexyl]-2-(lH-tetr azol-5-yl)-6- (trifluoromethyl)benzenesulfonamide

tert-Butyl (l-formylcyclopropyl)carbamate (47.0 mg, 0.254 mmol) was added to 3-((lr,4r)-4-aminocyclohexyl)-N-(4-methoxybenzyl)-2-(l-(4-me thoxybenzyl)-lH-tetrazol-5-yl)- 6-(trifluoromethyl)benzenesulfonamide (80 mg, 0.127 mmol)in DCE. Followed by adding sodium triacetoxyborohydride (67.2 mg, 0.317 mmol) and acetic acid (10.89 μΐ, 0.190 mmol). The reaction mixture was stirred at 45 °C under 2 for 5 hr. The mixture was diluted with water and extracted with EtOAc twice (2X30 ml). The combined organic phase was washed with saturated aHC03, brine (30 mL), dried (MgS0 ₄ ), filtered and the solvent was evaporated under reduced pressure. The residue was purified by column chromatography on silica gel eluting with EtO Ac/is ohexane to give the intermediate tert-butyl (l-((((lr,4r)-4-(2-(l-(4-methoxybenzyl)- lH-tetrazol-5-yl)-3-(N-(4-methoxybenzyl)sulfamoyl)-4-

(trifluoromethyl)phenyl)cyclohexyl)amino)methyl)cycloprop yl)carbamate. This intermediate product was treated with Method 3 and 4 to afford the title product. LC/MS: Calc'd mass 459.17; Observed mass 460.45 [M+l .

EXAMPLES 831 and 832

3 -(( 1 s,4s)-4-(piperidin-4-yl)cyclohexyl)-2-( 1 H-tetrazol-5 -yl)-6- (trifluoromethyl)benzenesulfonamide and 3-((lr,4r)-4-(piperidin-4-yl)cyclohexyl)-2-(lH- tetrazol-5-yl)-6-(trifluoromethyl)benzenesulfonamide

Step A: 2'-(l-(4-methoxybenzyl)-lH-tetrazol-5-yl)-3'-( -(4-methoxybenzyl)sulfamoyl)- 4'-(trifluoromethyl)- 1,2,3, 6-tetrahydro-[l,l'-biphenyl]-4-yl trifluoromethanesulfonate

To a solution of N-(4-methoxybenzyl)-2-(l-(4-methoxybenzyl)-lH-tetrazol-5-yl) - 3-(4-oxocyclohexyl)-6-(trifluoromethyl)benzenesulfonamide (190 mg, 0.302 mmol) and 1,1,1- trifluoro-N-phenyl-N-((trifluoromethyl)sulfonyl)methanesulfo namide (108 mg, 0.302 mmol) in THF (4.0 niL) was added sodium bis(trimethylsilyl)amide (0.392 ml, 0.392 mmol) at -78°C. After stirring at -78°C for 30 min, saturated aHC03 (50 ml) was added and the mixture was extracted with EtOAc (2X50 ml). The combined organic layer was washed with brine, dried over MgS0 ₄ and concentrated. The residue was purified by column chromatography on silica gel, eluting with EtOAc/hexane to give the title compound.

Step B: tert-butyl 4-(2'-(l-(4-methoxybenzyl)-lH-tetrazol-5-yl)-3'-(N-(4- methoxybenzyl)sulfamoyl)-4'-(trifluoromethyl)- 1 ,2,3,6-tetrahydro-[ 1 , 1 '-biphenyl]-4-yl)-3 ,6- dihydropyridine- 1 (2H)-carboxylate

2'-(l-(4-methoxybenzyl)-lH-tetrazol-5-yl)-3'-(N-(4-methoxybe nzyl)sulfamoyl)- 4'-(trifluoromethyl)-l,2,3,6-tetrahydro-[l, -biphenyl]-4-yl trifluoromethanesulfonate (71 mg, 0.093 mmol), tert-butyl 4-(4,4,5,5-tetramethyl-l,3,2-dioxaborolan-2-yl)-5,6-dihydrop yridine- l(2H)-carboxylate (72.1 mg, 0.233 mmol), Pd(dppf)Ci ₂ (17.05 mg, 0.023 mmol) and sodium carbonate (19.8 mg, 0.186 mmol) were placed in a reaction vessel. Dioxane (1.5 mL) and Water (0.5 mL) was added. The mixture was sealed and degassed and heated at 95°C, and stirred overnight. The reaction mixture was cooled to room temperature, filterted through a celite pad. The filtrated was concentrated and the residue was loaded onto silica gel column and eluted with EtOAc/hexane to give the title compound.

Step C: tert-butyl 4-(4-(2-(l-(4-methoxybenzyl)-lH-tetrazol-5-yl)-3-(N-(4- methoxybenzyl)sulfamoyl)-4-(trifluoromethyl)phenyl)cyclohexy l)piperidine-l-carboxylate

Dihydroxypalladium (27.0 mg, 0.038 mmol) was added to a stirred solution of starting material tert-butyl 4-(2'-(l-(4-methoxybenzyl)-lH-tetrazol-5-yl)-3'-(N-(4- methoxybenzyl)sulfamoyl)-4'-(trifluoromethyl)- 1 ,2,3,6-tetrahydro-[ 1, 1 '-biphenyl]-4-yl)-5,6- dihydropyridine-l(2H)-carboxylate (102 mg, 0.128 mmol) in methanol(2 ml) and DCM (2 ml) at RT. The mixture solution was degased by reduced pressure and then hydrogenated (using small balloon) at room temperature for overnight. The reaction mixture was filtered through a celite pad and washed with EtOAc. The filtrate was concentrated and the residue was purified by column chromatography on silica gel, eluting with EtOAc/isohexane to give the title compound.

Step 4: 3 -(( 1 s,4s)-4-(piperidin-4-yl)cyclohexyl)-2-( lH-tetrazol-5-yl)-6-

(trifluoromethyl)benzenesulfonamide and 3 -(( 1 r,4r)-4-(piperidin-4-yl)cyclohexyl)-2-( 1 H- tetrazol-5-yl)-6-(trifluoromethyl)benzenesulfonamide Used deprotection Method 3 and 4 to afford the titled compounds after HPLC separation of the isomers. LC/MS: Calc'd mass 458.17; Observed Cis 459.35 [M+1] and Trans 459.36 [M+l .

EXAMPLE 833

3-(3-azaspiro[5.5]undecan-9-yl)-2-(lH-tetrazol-5-yl)-6-(trif luoromethyl)benzenesulfonamide

Step A: tert-butyl 9-(((trifluoromethyl)sulfonyl)oxy)-3-azaspiro[5.5]undec-8-en e-3- carboxylate

To a solution of tert-butyl 9-oxo-3-azaspiro[5.5]undecane-3-carboxylate (1.0 g, 3.74 mmol) and in THF (20 mL) was added sodium bis(trimethylsilyl)amide (4.86 ml, 4.86 mmol) at -78°C. After stirring at -78°C for 30 min, 1 , 1 , 1-trifluoro-N-phenyl-N- ((trifluoromethyl)sulfonyl)methanesulfonamide (1.60 g, 4.49 mmol) was added as solid and stirred for 50 minutes. To the reaction was added saturated aHC0 ₃ (100 mL) and the mixture was extracted with EtOAc (2X100 mL). The organic layer was washed with brine, dried over MgS0 ₄ , filtered and concentrated. The residue was purified by column chromatography on silica gel, eluting with EtOAc/hexane to give the title compound.

Step B: tert-butyl 9-(4,4,5,5-tetramethyl- l,3,2-dioxaborolan-2-yl)-3-azaspiro[5.5]undec-

8-ene-3-carboxylate

4,4,4',4',5,5,5',5'-Octamethyl-2,2'-bi(l ,3,2-dioxaborolane) (0.763 g, 3.00 mmol), tert-butyl 9-(((trifluoromethyl)sulfonyl)oxy)-3-azaspiro[5.5]undec-8-en e-3-carboxylate (1.0g, 2.504 mmol), Pd(dppf)Cl ₂ (0.183 g, 0.250 mmol) and potassium acetate (0.737 g, 7.51 mmol) were placed in a reaction vessel. Dioxane (15 mL) was added. The mixture was sealed and degassed. The reaction was stirred at 80°C overnight. The reaction mixture was cooled to rt and filtered through a celite pad. The filtrate was concentrated and the residue was purified by silica gel column chromatgraph and eluted with EtOAc/hexane to give the title compound.

Step C: tert-butyl 9-(3-(N,N-bis(4-methoxybenzyl)sulfamoyl)-2-(l -(4-methoxybenzyl)- lH-tetrazol-5-yl)-4-(trifluoromethyl)phenyl)-3-azaspiro[5.5] undec-8-ene-3-carboxylate Coupling Method 1 was applied tert-butyl 9-(4,4,5,5-tetramethyl-l,3,2- dioxaborolan-2-yl)-3-azaspiro[5.5]undec-8-ene-3-carboxylate and 3-bromo-N,N-bis(4- methoxybenzyl)-2-( 1 -(4-methoxybenzyl)- lH-tetrazol-5-yl)-6- (trifluoromethyl)benzenesulfonamide to afford the title compound.

Step D: tert-butyl 9-(3-(N,N-bis(4-methoxybenzyl)sulfamoyl)-2-(l-(4-methoxybenz yl)- lH-tetrazol-5-yl)-4-(trifluoromethyl)phenyl)-3-azaspiro[5.5] undecane-3-carboxylate

Dihydroxypalladium (182 mg, 0.259 mmol) was added to a stirred solution of starting material tert-butyl 9-(3-( ,N-bis(4-methoxybenzyl)sulfamoyl)-2-(l-(4-methoxybenzyl)- lH-tetrazol-5-yl)-4-(trifluoromethyl)phenyl)-3-azaspiro[5.5] undec-8-ene-3-carboxylate (780 mg, 0.864 mmol) in methanol (6 ml) and DCM (6 mL) at RT. The mixture solution was degased by reduced pressure and then hydrogenated (using small balloon) at room temperature for overnight. The reaction mixture was filtered through celite. The filtrate was concentrated and the residue was purified by column chromatography on silica gel, eluting with EtOAc/isohexane to give the title compound.

Step E: 3-(3-azaspiro[5.5]undecan-9-yl)-2-(lH-tetrazol-5-yl)-6- (trifluoromethyl)benzenesulfonamide

Used deprotection Method 3 and 4 to afford the title compound. LC/MS: Calc'd mass 444.16; Observed 445.41 [M+l .

EXAMPLE 834

3-[3-[(l-aminocyclopropyl)methyl]-3-azaspiro[5.5]undecan-9-y l]-2-(lH-tetrazol-5-yl)-6-

(trifluoromethyl)benzenesulfonamide

tert-Butyl (l-formylcyclopropyl)carbamate (108 mg, 0.584 mmol) was added to N-(4-methoxybenzyl)-2-( 1 -(4-methoxybenzyl)- 1 H-tetrazol-5-yl)-3 -(3 -azaspiro [5.5 ]undecan-9- yl)-6-(trifluoromethyl)benzenesulfonamide (200 mg, 0.292 mmol) in DCE (2.5 mL). Sodium triacetoxyborohydride (155 mg, 0.730 mmol) and acetic acid (0.025 ml, 0.438 mmol) were added. The mixture was stirred at RT under nitrogen for 4 hr. Then mixture was diluted with water and extracted with EtOAc twice (50mL). The combined organic phase was washed with saturated NaHC03, brine ( 2 x 30 ml), dried (MgS0 ₄ ), filtered through a celite pad and the solvent was evaporated under reduced pressure. The residue was purified by column

chromatography on silica gel, eluting with EtOAc/isohexane to give tert-butyl (l-((9-(2-(l-(4- methoxybenzyl)-lH-tetrazol-5-yl)-3-(N-(4-methoxybenzyl)sulfa moyl)-4- (trifluoromethyl)phenyl)-3-azaspiro[5.5]undecan-3-yl)methyl) cyclopropyl)carbamate. Followed by using deprotection Method 3 and 4 to afford the title product. LC/MS: Calc'd mass 513.21 ; Observed mass 514.50 [M+l .

EXAMPLE 835

3-[l-(4-piperidyl)-4-piperidyl -2-(lH-tetrazol-5-yl)-6-(trifluoromethyl)benzenesulfonamide

Step A: tert-butyl 4-(3-(N,N-bis(4-methoxybenzyl)sulfamoyl)-2-(l-(4-methoxybenz yl)- lH-tetrazol-5-yl)-4-(trifluoromethyl)phenyl)-3 ,6-dihydropyridine- 1 (2H)-carboxylate

Coupling Method 1 was applied to 3-bromo-N,N-bis(4-methoxybenzyl)-2-(l-(4- methoxybenzyl)-lH-tetrazol-5-yl)-6-(trifluoromethyl)benzenes ulfonamide and tert-butyl 4- (4,4,5, 5-tetramethyl-l,3,2-dioxaborolan-2-yl)-3,6-dihydropyridine-l (2H)-carboxylate to afford the title compound.

Step B: tert-butyl 4-(3-(N,N-bis(4-methoxybenzyl)sulfamoyl)-2-(l-(4-methoxybenz yl)- lH-tetrazol-5-yl)-4-(trifluoromethyl)phenyl)piperidine-l-car boxylate

Dihydroxypalladium (0.303 g, 0.431 mmol) was added to a stirred solution of starting material tert-butyl 4-(3-(N,N-bis(4-methoxybenzyl)sulfamoyl)-2-(l-(4-methoxybenz yl)- lH-tetrazol-5-yl)-4-(trifluoromethyl)phenyl)-5,6-dihydropyri dine-l(2H)-carboxylate (1.2 g, 1.437 mmol) in methanol (6 mL) and DCM (6 mL) at RT. The mixture solution was degased by reduced pressure. The reaction mixture was then hydrogenated (using small balloon) at room temperature overnight. The reaction mixture was filtered through celite and washed with EtOAc. The filtrate was concentrated and the residue was purified by column chromatography on silica gel, eluting with EtOAc/isohexane to give the title compound.

Step C: N-(4-methoxybenzyl)-2-(l-(4-methoxybenzyl)lH-tetrazol-5-yl)- 3-(piperidin-4- yl)-6-(trifluoromethyl)benzenesulfonamide

Depropection Method 3 was applied to tert-butyl 4-(3-(N,N-bis(4- methoxybenzyl)sulfamoyl)-2-(l-(4-methoxybenzyl)-lH-tetrazol- 5-yl)-4- (trifluoromethyl)phenyl)piperidine-l-carboxylate to afford the title compound.

Step D: tert-butyl 4-(2-(l-(4-methoxybenzyl)-lH-tetrazol-5-yl)-3-(N-(4- methoxybenzyl)sulfamoyl)-4-(trifluoromethyl)phenyl)-[l,4'-bi piperidine]-r-carboxylate

tert-Butyl 4-oxopiperidine-l-carboxylate (145 mg, 0.730 mmol) and titanium(iv) isopropoxide (0.288 mL, 0.973 mmol) were added to N-(4-methoxybenzyl)-2-(l-(4- methoxybenzyl)-lH-tetrazol-5-yl)-3-( iperidin-4-yl)-6-(trifluoromethyl)benzenesulfonamide (150 mg, 0.243 mmol) in EtOH (2 mL). The reaction was heated to 70°C for overnight. The reaction was cooled to RT, and sodium cyanotrihydroborate (61.1 mg, 0.973 mmol) was added. The reaction mixture was stirred at rt under nitrogen for 1 hr. The mixture was diluted with water and extracted with EtOAc (2X30 mL). The combined organic phase was washed with saturated aHC03, brine (2 x 30mL), dried (MgS0 ₄ ), filtered and the solvent was evaporated under reduced pressure. The residue was purified by column chromatography on silica gel, eluting with EtOAc/isohexane to give the title compound.

Step E: 3-[l-(4-piperidyl)-4-piperidyl]-2-(lH-tetrazol-5-yl)-6- (trifluoromethyl)benzenesulfonamide

Using deprotection procedure 3 and 4 was applied to tert-butyl 4-(2-(l-(4- methoxybenzyl)-lH-tetrazol-5-yl)-3-(N-(4-methoxybenzyl)sulfa moyl)-4-

(trifluoromethyl)phenyl)-[l,4'-bipiperidine]-r-carboxylat e to afford the titled product. LC/MS: Calc'd mass 459.17 Observed mass 460.43 [M+l .

EXAMPLE 836

3-(2-aminoindan-4-yl)-2-(lH-tetrazol-5-yl)-6-(trifluoromethy l)benzenesulfonamide

Step A: 3-(2-hydroxy-2,3-dihydro-lH-inden-4-yl)-N,N-bis(4-methoxyben zyl)-2-(l-(4- methoxybenzyl)-lH-tetrazol-5-yl)-6-(trifluoromethyl)benzenes ulfonamide

To a reaction vessel, was added (3-(N,N-bis(4-methoxybenzyl)sulfamoyl)-2-(l- (4-methoxybenzyl)-lH-tetrazol-5-yl)-4-(trifluoromethyl)pheny l) boronic acid(200 mg, 0.287 mmol), 4-bromo-2,3-dihydro-lH-inden-2-ol (122 mg, 0.573 mmol), cesium carbonate (280 mg, 0.860 mmol) and 2nd generation xphos precatalyst (45.1 mg, 0.057 mmol). Dioxane (1.5 ml) and water (0.5 ml) were added to this flask. The reaction mixture was degased with bubbled under 2 for 10 min. This mixture was then heated at 66°C for overnight. The mixture was cooled, diluted with satured NaHC03, and extracted with EtOAc. The organic phase was concentrated under reduced pressure. The residue was purified by column chromatography on silica gel, eluting with hexane/EtOAc to give the title compound.

Step B : 4-(3 -(N,N-bis(4-methoxybenzyl)sulfamoyl)-2-( 1 -(4-methoxybenzyl)- lH-tetrazol-

5-yl)-4-(trifluoromethyl)phenyl)-2,3-dihydro-lH-inden-2-y l methanesulfonate

Triethylamine (0.043 mL, 0.305 mmol) and methanesulfonyl chloride (0.012 mL, 0.153 mmol) was added to a stirred solution of starting material 3-(2-hydroxy-2,3-dihydro-lH- inden-4-yl)-N,N-bis(4-methoxybenzyl)-2-( 1 -(4-methoxybenzyl)- lH-tetrazol-5-yl)-6- (trifluoromethyl)benzenesulfonamide (80 mg, 0.102 mmol) in dichloromethane (2 mL) at 0°C and the mixture was stirred at 0°C for 5 hr. The mixture was diluted with aqueous sodium hydrogen carbonate (20 mL) and the mixture was extracted with dichloromethane (2x 30 mL). The organic phase was washed with HQ (0.5M, 20 mL), dried (MgSC^) and concentrated to give crude title compound, which was taken as is for next step.

Step C: 3-(2-azido-2,3-dihydro-lH-inden-4-yl)-N,N-bis(4-methoxybenzy l)-2-(l-(4- methoxybenzyl)-lH-tetrazol-5-yl)-6-(trifluoromethyl)benzenes ulfonamide

Sodium azide (33.1 mg, 0.509 mmol) was added to a stirred solution of starting material 4-(3-( ,N-bis(4-methoxybenzyl)sulfamoyl)-2-(l -(4-methoxybenzyl)- lH-tetrazol-5-yl)- 4-(trifluoromethyl)phenyl)-2,3-dihydro-lH-inden-2-yl methanesulfonate (88 mg, 0.102 mmol) in dimethylsulfoxide (2 mL) at room temperature and the mixture was stirred at room temperature for overnight. The mixture was diluted with water (30 ml) and the mixture was extracted with diethyl ether (2x 30 mL). The organic phase was washed with brine, dried (MgSC^) and concentrated. The residue was purified by column chromatography on silica gel, eluting with EtOAc/isohexane to give the title compound.

Step D : 3 -(2-amino-2,3 -dihydro- lH-inden-4-yl)-N,N-bis(4methoxybenzyl)-2-( 1 -(4- methoxybenzyl)-lH-tetrazol-5-yl)-6-(trifluoromethyl)benzenes ulfonamide

Pd-C (27.6 mg, 0.026 mmol) was added to a stirred solution of starting material 3-

(2-azido-2,3-dihydro-lH-inden-4-yl)-N,N-bis(4-methoxybenz yl)-2-(l-(4-methoxybenzyl)-lH- tetrazol-5-yl)-6-(trifluoromethyl)benzenesulfonamide (70 mg, 0.086 mmol) in DCM (1 ml) at RT and the mixture solution was degased by reduced pressure. Then the reaction mixture was hydrogenated (using small balloon) at room temperature for 2 hours. The reaction mixture was filtered through celite and washed with MeOH. The filtrate was concentrated and the residue was purified by column chromatography on silica gel, eluting with EtOAc/isohexane to give the title compound.

Step E: 3-(2-aminoindan-4-yl)-2-(lH-tetrazol-5-yl)-6- (trifluoromethyl)benzenesulfonamide

3-(2-Amino-2,3-dihydro- lH-inden-4-yl)-N,N-bis(4methoxybenzyl)-2-(l -(4- methoxybenzyl)-lH-tetrazol-5-yl)-6-(trifluoromethyl)benzenes ulfonamide was subjected to deprotection Method 4 to afford the title product. LC/MS: Calc'd mass 424.09; Observed 425.18

EXAMPLE 837

(5)-2,3-diamino-N-((lr,45)-4-(3-sulfamoyl-2-(lH-tetrazol-5-y l)-4-

(trifluoromethyl)phenyl)cyclohexyl)propanamide

Step A: (5)-2,5-dioxopyrrolidin-l-yl 2,3-bis((tert-butoxycarbonyl)amino)propanoate

N,N,N',N-Tetramethyl-0-(N-succinimidyl)uronium tetrafluoroborate (193 mg, 0.641 mmol) was added to a stirred mixture of starting material(S)-2,3-bis((tert- butoxycarbonyl)amino)propanoic acid (150 mg, 0.493 mmol) in dichloromethane (2 mL) at 0°C and the mixture was stirred at room temperature for 2 hr to give the title compound which was used as is for next step.

Step B: di-tert-butyl ((S)-3-oxo-3-(((lr,4S)-4-(3-sulfamoyl-2-(lH-tetrazol-5-yl)^-

(trifluoromethyl)phenyl)cyclohexyl)amino)propane-l,2-diyl )dicarbamate

(5)-2,5-Dioxopyrrolidin-l-yl 2,3-bis((tert-butoxycarbonyl)amino)propanoate (80 mg, 0.200 mmol) was added to a stirred solution of starting material 3-((lr,4r)-4- aminocyclohexyl)-2-(lH-tetrazol-5-yl)-6-(trifluoromethyl)ben zenesulfonamide (60 mg, 0.154 mmol) in dimethylformamide (2 ml) at 0°C and the mixture was stirred at 0°C for 2 hr. The mixture was diluted with water (30 mL), and extracted with dichloromethane ( 2x 30 mL). The combined organic phase was dried (MgSC^) and concentrated. The residue was used as is.

Step C: (5)-2,3-diamino-N-((lr,45)-4-(3-sulfamoyl-2-(lH-tetrazol-5-y l)-4- (trifluoromethyl)phenyl)cyclohexyl)propanamide

TFA (1.0 mL, 13 mmol) was added to a stirred solution of starting material di- tert-butyl ((S)-3 -oxo-3 -((( 1 r,4S)-4-(3 -sulfamoyl-2-( 1 H-tetrazol-5 -yl)-4-

(trifluoromethyl)phenyl)cyclohexyl)amino)propane-l,2-diyl )dicarbamate (30 mg, 0.044 mmol) in dichloromethane (1 ml) at room temperature and the mixture was stirred at room temperature for 2 hr. The mixture was concentrated. The residue was purified by Gilson HPLC reverse phase (C-18), eluting with acetonitrile/water to give the title compound after lyophilization. LC/MS: Calc'd mass 476.16; Observed 477.47 [M+l] ⁺ .

EXAMPLE 838

3-(4 -aminocyclohexyl)-6- -(4-piperidyl)ethyl]-2-(2H-tetrazol-5-yl)benzenesulfonamide

Step A: tert-butyl 4-(2-(3-(N,N-bis(4methoxybenzyl)sulfamoyl)-4'-((teri- butoxycarbonyl)amino)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-y l)-2',3',4',5'-tetrahydro-[l,r- biphenyl]-4-yl)ethyl)piperidine- 1 -carboxylate

A microwave vial was charged with 4,7-diphenyl-l, 10-phenanthroline (21.86 mg, 0.066 mmol), tert-butyl 4-(2-iodoethyl)piperidine- 1 -carboxylate (297 mg, 0.877 mmol), nickel(II) iodide (41.1 mg, 0.132 mmol), tert-butyl (3'-(N,N-bis(4-methoxybenzyl)sulfamoyl)-4'- bromo-2'-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-2,3,4,5-tetr ahydro-[l,r-biphenyl]-4- yl)carbamate (377 mg, 0.438 mmol) and manganese (48.2 mg, 0.877 mmol). The vial was sealed, purged with N ₂ for 10 min, and filled with DMA (2 ml), benzonitrile (9.04 μΐ, 0.088 mmol) and chlorotrimethylsilane (0.011 ml, 0.088 mmol). The resulting mixture was purged with 2 for another 5 min, and heated for 3 hr at 60°C. The reaction mixture was filtered over celite to remove metal. The filtrate was concentrated and purified by silica gel column chromatography to afford the title compound.

Step B: tert-butyl 4-(2-(N,N-bis(4-methoxybenzyl)sulfamoyl)-4-(4-((/ert- butoxycarbonyl)amino)cyclohexyl)-3-(2-(4-methoxybenzyl)-2H-t etrazol-5- yl)phenethyl)Piperidine- 1 -carboxylate

Dihydroxypalladium (164 mg, 0.234 mmol) was added to a stirred solution of starting material tert-butyl 4-(2-(3-(N,N-bis(4-methoxybenzyl)sulfamoyl)-4'-((tert- butoxycarbonyl)amino)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-y l)-2',3',4',5'-tetrahydro-[l,r- biphenyl]-4-yl)ethyl)piperidine-l -carboxylate (387 mg, 0.390 mmol) in methanol (3 ml) and EtOAc (2 ml) at RT. The mixture solution was degased. And then hydrogenated (Parr shaker, 45 PSI) at room temperature overnight. The reaction mixture was filtered through celite and washed with EtOAc. The filtrate was concentrated and the residue was purified by column chromatography on silica gel, eluting with EtOAc/isohexane to give the title compound.

Step C: 3-(4-aminocyclohexyl)-N,N-bis(4-methoxybenzyl-2-(2-(4-methox ybenzyl)-2H- tetrazol-5-yl)-6-(2-(piperidin-4-yl)ethyl)benzenesulfonamide

tert-Butyl 4-(2-(N,N-bis(4-methoxybenzyl)sulfamoyl)-4-(4-((tert- butoxycarbonyl)amino)cyclohexyl)-3-(2-(4-methoxybenzyl)-2H-t etrazol-5- yl)phenethyl)Piperidine- 1 -carboxylate was subjected to deprotection Method 3 to afford the title compound.

Step D: 3-(4 -aminocyclohexyl)-6-[2-(4-piperidyl)ethyl]-2-(2H-tetrazol-5- yl)benzenesulfonamide

3-(4-Aminocyclohexyl)-N,N-bis(4-methoxybenzyl-2-(2-(4-methox ybenzyl)-2H- tetrazol-5-yl)-6-(2-(piperidin-4-yl)ethyl)benzenesulfonamide was subjected to deprotection Method 4 to afford the title compound. LC/MS: Calc'd mass 433.22; Observed 217.77 [M+2]/2. EXAMPLE 839

3-(4-aminocyclohexyl)-6-(piperidin-4-ylmethyl)-2-(2H-tetrazo l-5-yl)benzenesulfonamide

Step A: tert-butyl 4-((3 -(N,N-bis(4-methoxybenzyl)sulfamoyl)-4'-((tert- butoxycarbonyl)amino)-2-(2-(4-methoxybenzyl)-2H-tetrazol-5-y l)-2',3',4',5'-tetrahydro-[l,r- biphenyl]-4-yl)methyl)piperidine-l-carboxylate

A microwave vial was charged with 4,7-diphenyl-l, 10-phenanthroline (22.91 mg, 0.069 mmol), tert-butyl 4-(iodomethyl)piperidine-l-carboxylate (448 mg, 1.378 mmol), nickel(II) iodide (43.1 mg, 0.138 mmol), tert-butyl (3'-(N,N-bis(4-methoxybenzyl)sulfamoyl)-4'- bromo-2'-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-2,3,4,5-tetr ahydro-[l,r-biphenyl]-4- yl)carbamate (395 mg, 0.459 mmol) and manganese (50.5 mg, 0.919 mmol). The vial was sealed, purged with 2 for 10 min, and filled with DMA (2 ml), benzonitrile (9.47 μΐ, 0.092 mmol) and chlorotrimethylsilane (0.012 ml, 0.092 mmol). The resulting mixture was purged with 2 for another 5 min, and heated for 3 hr at 45°C. The reaction mixture was filtered over celite to remove metal. The filtrate was concentrated and purified by silica gel column chromatography using EtOAc/hexane as mobile phase to afford the title compound.

Step B: tert-butyl 4-(2-(N,N-bis(4-methoxybenzyl)sulfamoyl)-4-(4-((teri- butoxycarbonyl)amino)cyclohexyl)-3-(2-(4-methoxybenzyl)-2H-t etrazol-5-yl)benzyl)piperidine- 1 -carboxylate

Dihydroxypalladium (129 mg, 0.184 mmol) was added to a solution of starting material tert-butyl 4-((3-(N,N-bis(4-methoxybenzyl)sulfamoyl)-4'-((tert-butoxyca rbonyl)amino)- 2-(2-(4-methoxybenzyl)-2H-tetrazol-5-yl)-2',3',4',5'-tetrahy dro-[l, l'-biphenyl]-4- yl)methyl)piperidine- 1 -carboxylate (300 mg, 0.307 mmol) in methanol (3 ml) and EtOAc (3 ml) at RT. This was followed by adding acetic acid (0.5 ml). The mixture solution was degased, and then hydrogenated (45 PSI) at room temperature for overnight. The reaction mixture was filtered through celite and washed with MeOH. The filtrate was concentrated and the residue was purified by column chromatography on silica gel, eluting with EtOAc/isohexane to give the title compound.

Step C: 3-(4-aminocyclohexyl)-N-(4-methoxybenzyl)-2-(2-(4-methoxyben zyl)-2H- tetrazol-5-yl)-6-(piperidin-4-ylmethyl)benzenesulfonamide

tert-Butyl 4-(2-(N,N-bis(4-methoxybenzyl)sulfamoyl)-4-(4-((tert- butoxycarbonyl)amino)cyclohexyl)-3-(2-(4-methoxybenzyl)-2H-t etrazol-5-yl)benzyl)piperidine- 1-carboxylate was subjected to deprotection Method 3 to afford the title compound.

Step D: 3-(4-aminocyclohexyl)-6-(piperidin-4-ylmethyl)-2-(2H-tetrazo l-5- yl)benzenesulfonamide

3-(4-Aminocyclohexyl)-N-(4-methoxybenzyl)-2-(2-(4-methoxyben zyl)-2H- tetrazol-5-yl)-6-(piperidin-4-ylmethyl)benzenesulfonamide was subjected to deprotection Method 4 to afford the title compound. LC/MS: Calc'd mass 419.21; Observed 210.92 [M+2]/2.

EXAMPLE 840

3-([l,2,4]triazolo[l,5-a]pyridin-8-yl)-2-(lH-tetrazol-5-yl)- 6- (trifluoromethyl)benzenesulfonamide

Step A: 3-([l,2,4]triazolo[l,5-a]pyridin-8-yl)-N,N-bis(4-methoxybenz yl)-2-(l-(4- methoxybenzyl)-lH-tetrazol-5-yl)-6-(trifluoromethyl)benzenes ulfonamide

8-(Tributylstannyl)-[l,2,4]triazolo[l,5-a]pyridine (1.014 g, 2.484 mmol) and Pd(Pli ₃ P)4 (0.221 g, 0.191 mmol) were added to a stirred solution of starting material 3-bromo- N,N-bis(4-methoxybenzyl)-2-( 1 -(4-methoxybenzyl)- 1 H-tetrazol-5-yl)-6- (trifluoromethyl)benzenesulfonamide (1.4 g, 1.9 mmol) in toluene (50 mL) at room temperature and the mixture was stirred at 70°C for overnight. The mixture was concentrated, dissolved in EtOAc 30 ml, diluted with brine (30 mL) and the mixture was extracted with ethyl acacate (2 x 50 mL). The residue was purified by column chromatography on silica gel, eluting with EtOAc/isohexane to give the title compound. Ste B: 3-([l,2,4]triazolo[l,5-a]pyridin-8-yl)-2-(lH-tetrazol-5-yl)- 6- (trifluoromethyl)benzenesulfonamide

3 -([ 1 ,2,4]Triazolo [ 1 ,5 -a]pyridin-8-yl)-N,N-bis(4-methoxybenzyl)-2-( 1 -(4- methoxybenzyl)-lH-tetrazol-5-yl)-6-(trifluoromethyl)benzenes ulfonamide was subjected to Method 4 to afford the title compound. LC/MS: Calc'd mass 410.05; observed mass 411.30

BIOLOGICAL ASSAYS

Enzyme Activity: Determination of IC5 ₀

The Class B enzyme activities were measured in the presence of the test inhibitor in a fluorescence assay against a commercially available substrate consisting of a cephalosporin core linking 7-hydroxycoumarin to fluorescein (CCF2-FA). The enzyme (NDM-1, IMP-1 or VIM-1) and the substrate were diluted in 100 mM ΚΗ ₂ Ρ0 ₄ buffer (pH 7) containing 0.005% Tween-20 and 10 μΜ ZnS0 ₄ . In the assay, the final concentration of enzyme was 1 pM, 2 pM and 30 pM for NDM-1, IMP-1 and VIM-1, respectively, and the final concentration of CCF2-FA was 1.25 μΜ. The test inhibitor was dissolved in dimethylsulfoxide and diluted 1 :50 in the assay, resulting in a final concentration range of 20 uM to 0.00063 uM. In a 384-well microplate, the test inhibitor was incubated with the metallo-p-lactamase enzyme and the substrate for 2 hours at 25°C. Fluorescence at 460 nm following excitation at 405 nm was measured. The IC5 ₀ value was determined from semi-logarithmic plots of enzyme inhibition versus inhibitor concentration, with a curve generated using a 4-parameter fit.

Representative compounds of the present invention exhibit inhibition of Class B β-lactamases in this assay. For example, the compounds of Examples 1-840 were tested in this assay and were found to have the IC5 ₀ values shown in Table 1. Antibiotic Potentiation Activity: Determination of Synergistic Concentration

The concentrations of metallo- -lactamase inhibitors required to restore the susceptibility of various strains of bacteria to inactive concentrations of antibiotics were determined in an assay that assessed bacterial growth by measuring the optical density at 600 nm (OD ₆ oo). The bacterial strains tested included the clinical strains Escherichia coli expressing NDM-1 (CLB30005, CLB30016), Serratia marcescens expressing IMP-1 (CL5741), and

Klebsiella pneumoniae expressing VIM-1 (IHMA599644). Inhibitor activity was measured in the presence and absence of imipenem in a 384-well microplate.

The clinical strains CLB30016, CL5741 and IHMA599644 were grown on trypticase soy agar containing 5% sheep's blood. The clinical strain CLB30005 was grown on Mueller Hinton broth agar containing 8 ug/ml imipenem. The bacteria on agar plates were incubated at 35°C with humidity overnight. The following day, individual colonies from each clinical strain were picked and resuspended in 5 ml saline to attain an OD ₆ oo of 0.14, 0.11, 0.15 and 0.13, for CLB30005, CLB30016, CL5741 and IHMA599644, respectively. These were further diluted 1 : 100 into 1.1X CAMHB and used to inoculate the test wells as described below.

Imipenem in 10 mM 3-(N-morpholino)propanesulfonic acid (MOPS, pH 7) was stored in single use aliquots at -80°C. Test inhibitors were dissolved in dimethylsulfoxide and diluted 1 :50 in the assay, resulting in a final concentration range of 200 uM to 0.195 μΜ. On the day of the assay, 4 μΐ of antibiotic was added to 45 ul of bacteria followed by 1 μΐ of test compound and mixed by pipetting and with an orbital shaker. The concentration of antibiotic used in the assay was 4 μg/ml, or optionally 1 μg/ml. Microplates were covered and incubated at 35°C for 22 hours to 24 hours. At the end of the incubation, absorbance was determined using a spectrophotometer. The synergistic concentration of MBLI was determined by identifying the lowest concentration of test compound in the presence of a given concentration of antibiotic that was required to inhibit 95% of the growth of the bacteria. The results for Examples 1-840 are reported in Table 1, expressed as the concentration of compound that potentiated the action of antibiotic (imipenem) affecting 95% inhibition of bacterial growth (MITC95).

Representative compounds of the present invention do not have any or have minimal intrinsic antibacterial activity but display a synergistic effect when used in combination with a beta-lactam antibiotic. For example, in general, the compounds of Examples 1-840 were determined to restore susceptibility to imipenem for one or more of the test organisms at concentrations of 100 μΜ or less.

Table 1. Inhibition of metallo-P-lactamases (IMP-1, NDM-1, VIM-1) and antibiotic potentiation vs. MBL-expressing bacteria by Examples 1-840. 3.74 0.972 26.7 12.5 12.5 >200

12.12 1.494 52.8 6.25 3.125 200

1668 132.1 874.7 50 3.125 1.563 200

34.39 4.96 18.83 1.56 0.781 6.25

18.05 3.458 77.8 0.7813 0.5859 25

70.59 16.62 832 1.172 1.172 100

3094 150.9 1438 150 3.125 >200

2683 137.9 1011 50 1.953 100

789.7 38.74 218.7 50 1.953 75

1211 26.43 205.9 50 2.344 200

2392 280.8 5537 25 0.7813 200

2574 345.6 8139 50 1.563 >200

3048 42.2 560.1 200 3.125 200

246.8 30.43 1151 9.375 0.3906 200

10520 542.7 9964 200 1.563 0.7813 >200

2094 309.9 2462 75 1.172 >200

293.4 34.59 293.8 12.5 0.3906 37.5

1206 85.04 496.2 25 0.7813 50

302 14.54 99.07 25 0.5859 28.13

4156 344.7 5359 50 0.7813 >200

644.4 19.14 181.8 33.33 0.3906 66.67

4047 21.58 61.68 150 0.5859 12.5

37.87 2.709 89.13 12.5 2.344 200

27.44 2.74 4193 31.25 9.375 >200

17.91 1.705 96.61 6.25 1.563 100

73.27 4.411 37.05 6.25 0.5859 37.5

204.6 42.28 937.4 18.75 2.344 >200

52.7 3.48 144.2 12.5 1.953 200

13.23 1.826 43.98 14.06 2.344 200

28.85 4.194 29.67 4.688 1.563 25

227.2 14.54 189.6 12.5 0.5859 100

36.12 4.379 94.95 6.25 2.344 200 16.49 3.175 27.78 4.688 3.906 75

58 6.336 62.03 6.25 0.5859 25

211.2 8.475 186.1 100 1.563 100

1557 48.91 1322 50 0.7813 100

247.7 13.43 587.6 50 1.953 200

20000 904.6 4994 >200 4.688 >200

140.1 1.103 29.07 18.75 0.7813 75

910.7 2.158 56.97 75 2.344 62.5

81.86 1.99 33.66 12.5 2.344 75

236.7 5.055 26.4 18.75 0.7813 25

105.1 1.995 28.9 18.75 1.563 150

78.58 1.22 14.48 18.75 0.7813 75

48.66 0.6366 22.16 12.5 2.344 25

156.4 6.489 66.65 18.75 1.563 100

1610 26.44 474.8 18.75 0.9766 50

9.964 4.569 98.08 3.906 6.25 >200

42.7 17.07 243.7 6.25 6.25 >200

53.84 12.04 2905 28.13 9.375 >200

202.5 19.32 147 18.75 0.7813 100

3967 48.65 60.23 150 1.563 25

2384 81.82 541.8 50 0.3906 25

571.2 34.65 255.4 37.5 0.9766 37.5

22.18 1.429 7.793 3.125 1.953 0.5859 12.5

520.3 5.974 43.59 50 0.3906 25

707.7 3.079 23.16 50 0.7813 6.25

94.61 1.812 28.02 37.5 2.344 150

67.44 11.03 1073 3.125 0.7813 200

907.6 95.45 2086 18.75 3.906 200

87.3 2.983 243.3 12.5 1.953 100

318.6 54.67 1023 12.5 4.688 >200

197 2.241 15.49 25 0.5859 12.5

830.2 27.53 180 50 0.7813 75 92 2530 41.05 208.5 50 0.3906 37.5

93 330.9 3.166 89.85 18.75 0.7813 25

94 164.1 6.317 234.4 12.5 2.344 100

95 534 1.515 374.7 106.3 3.906 >200

96 109 1.306 3.551 15.63 1.758 25

97 1572 71.14 1615 18.75 0.5859 200

98 319.9 2.7 29.38 7.813 0.9766 0.7813 18.75

99 208 6.984 104 28.13 9.375 >200

100 145.9 29.57 940.1 14.06 7.031 >200

101 517 40.91 111.5 14.06 3.906 125

102 173.6 128.1 524.3 53.13 9.375 >200

103 310.6 49.44 2641 15.63 9.375 >200

104 286.7 16.78 107.1 15.63 0.9766 25

105 374.2 14.35 70.36 31.25 0.9766 18.75

106 1799 9.626 961.8 62.5 3.906 200

107 365.2 10.01 194 15.63 3.906 200

108 255.1 5.802 45.02 18.75 1.172 37.5

109 38.94 2.21 0.6366 12.89 12.5 18.75

110 445.2 51.89 1364 28.13 9.375 >200

111 9.375 1.172 18.75

113 14830 15.44 313 200 3.125 50

115 543.5 7.811 54.43 18.75 0.25 37.5

116 225.7 5.428 1238 9.375 1.563 200

117 133.7 5.179 134.8 6.25 1.172 100

118 1330 44.2 491.7 18.75 0.7813 50

119 548.4 16.21 261.4 18.75 1.563 50

120 777 1.415 4.994 18.75 0.7813 4.688

121 372.8 7.371 187.1 25 3.125 >200

122 63.09 3.08 248.6 4.688 4.688 >200

123 414.6 8.303 309.2 18.75 1.563 >200

124 68.93 4.341 258.6 6.25 2.344 >200

125 326 6.55 172.1 9.375 1.953 25 126 864.2 166.3 14390 25 6.25 >200

127 157.3 1.112 84.22 4.688 1.172 37.5

128 452.7 7.953 1140 9.375 1.563 >200

129 176 3.707 37.88 9.375 0.7813 12.5

130 267.2 10.6 41.8 9.375 1.172 37.5

131 187.4 0.7001 16.94 3.125 0.7813 3.125

132 755.1 2.727 26.7 12.5 1.172 6.25

133 4922 21.55 107.8 37.5 0.3906 6.25

134 22.62 0.2802 11.08 0.7813 0.5859 3.125

135 62.61 4.471 61.85 1.172 1.172 18.75

136 1692 24.79 150.1 25 1.563 37.5

137 2534 30.71 560.8 25 1.172 25

138 354.3 6.78 166.3 37.5 1.563 >200

139 98.37 0.6366 5.781 6.25 0.1953 12.5

140 160.4 7.677 388.2 6.25 0.5859 50

141 2335 61.54 2582 37.5 0.7813 200

142 80.95 8.197 418.8 6.25 1.563 >200

143 98.46 20.74 380 4.688 0.7813 200

144 4500 121.1 1540 200 3.125 >200

145 2410 190.6 6409 75 0.7813 >200

146 766.4 65.53 2796 50 1.172 >200

147 103.2 16.43 1097 18.75 3.125 >200

148 550.4 131 3076 50 6.25 >200

149 492.9 23.67 861.4 6.25 1.563 150

150 1940 147.6 5650 6.25 0.7813 200

151 31.8 1.25 31.46 1.563 1.172 37.5

152 252.4 14.22 91.39 12.5 4.688 200

153 71.28 8.253 251.7 2.344 4.688 >200

154 10.76 3.28 80.79 0.3906 2.344 100

155 92.66 2.999 16.17 2.344 3.125 75

156 507.9 13.07 390.8 9.375 0.5859 50

157 560.8 28.66 1048 6.25 0.3906 50 158 387.1 15.96 351.9 12.5 3.125 200

159 525.9 33.99 3390 18.75 3.125 >200

160 251 8.999 279.6 9.375 0.7813 75

161 306.4 20.1 874.3 6.25 1.563 150

162 571.3 18.93 690.5 12.5 1.563 200

163 326.7 17.7 437.4 12.5 3.125 >200

164 5.498 2.934 50.63 0.3906 1.563 200

165 213.6 1.243 11.59 9.375 0.5859 37.5

166 74.5 6.892 18.82 3.906 2.344 100

167 260.4 12.36 1030 9.375 1.563 200

168 864.9 39.38 50.27 6.25 0.25 2.172

169 111 3.74 57.59 3.125 2.344 50

170 576.7 21.92 3470 9.375 1.563 200

171 118.6 8.564 128.1 6.25 2.344 25

172 720.3 16.52 420.7 18.75 4.688 100

173 148.9 4.392 85.64 6.25 4.688 >200

174 402.8 4.543 262.4 12.5 2.344 100

175 12370 552.4 3087 37.5 0.7813 75

176 72.78 6.432 148.3

177 667.7 12.83 733 37.5 6.25 >200

178 1023 28.43 65.53 12.5 0.25 9.375

179 405.9 10.82 1439 37.5 3.125 >200

180 112.6 9.911 22.43 3.125 0.3906 0.5 4.688

181 374.8 27.87 184 12.5 1.953 0.6727 18.75

182 348.1 32.41 91.42 100 4.688 200

183 339.3 11.51 172.7 50 4.688 75

184 601.5 66.91 163.7 37.5 0.5859 25

185 1478 135 2021 75 2.344 >200

186 563.7 97.14 1859 100 18.75 >200

187 28.93 2.809 149.6 25 15.63 >200

188 767.7 36.5 4127 37.5 2.344 >200

189 704.4 23.25 685.2 37.5 1.563 100 190 3150 231.8 1300 100 10.42 >200

191 75.98 7.747 45.87 15.63 9.375 75

192 439.1 36.44 98.14 50 1.953 50

193 2655 373.7 813 150 0.7813 37.5

194 2272 248.1 906.8 75 0.7813 62.5

195 2629 78.54 290.8 50 0.3906 12.5

196 1590 45.61 50.31 125 1.953 25

197 581.7 130.1 70.21 1.563 0.3906 1.563

198 1166 68.38 101.1 3.125 0.3906 2.344

199 324.9 12.96 24.79 6.25 0.3906 3.125

200 962.9 30.23 35.64 75 2.083 50

201 1447 66.21 67.11 50 0.7813 18.75

202 23.8 11.51 118.2 2.344 0.3906 25

203 1426 18.62 43.57 50 0.3906 9.375

204 2855 59.05 237.8 37.5 0.3906 12.5

205 112.9 14.3 24.13 6.25 0.3906 9.375

206 91.45 11.42 14.18 4.125 0.1953 0.375 3.125

207 373.3 35.11 200.9 12.5 0.1953 0.5 18.75

208 588.9 94.73 568.5 37.5 3.646 >200

209 516.4 26.33 5.454 75 2.604 37.5

210 420.9 11.76 25.48 25 0.5208 15.63

211 537.1 45.57 242 31.25 0.3906 200

212 414.6 7.909 13.08 18.75 0.3906 3.125

213 564.3 50.98 62.38 37.5 1.042 100

214 98.4 13.21 128.7 3.344 0.1953 0.375 37.5

215 1856 90.92 493.9 18.75 0.1953 0.25 12.5

216 456.3 40.35 96.66 12.5 1.172 18.75

217 480.6 43.03 49.29 12.5 4.688 150

218 484.1 101.9 105.8 25 12.5 100

219 10410 1061 457.6 37.5 4.688 12.5

220 2387 22.79 233.7 75 12.5 >200

221 6169 251.1 6175 100 4.688 200 222 20000 5150 793.8 75 12.5 12.5

223 1305 157.3 583.4 25 4.688 200

224 1093 246.7 1181 18.75 4.688 200

225 76.16 142.4 225.8 2.344 9.375 50

226 3869 481.4 709.7 50 6.25 12.5

227 7070 888.4 260.5 75 3.125 6.25

228 3207 371.9 342.7 37.5 1.563 37.5

229 466.3 204.4 2.221 50 12.5 6.25

230 796.7 206.1 163.6 18.75 1.563 37.5

231 422.7 10.79 325.7 18.75 4.688 >200

232 7638 892.3 166.2 >200 50 150

233 195.2 60.92 97.6 6.25 0.7813 37.5

234 1448 24.46 1171 100 4.688 >200

235 3435 141.8 1728 200 12.5 >200

236 222.9 38.59 187.6 25 18.75 >200

237 580.8 101.6 239.1 125 18.75 >200

238 188.5 30.77 96.89 9.375 3.125 125

239 3711 382.9 945.1 50 1.563 50

240 3406 418.4 937.8 37.5 1.172 25

241 335.1 67.66 774.2 12.5 1.563 >200

242 1115 102.7 270.2 25 0.3906 6.25

243 1509 67.13 204.2 100 18.75 >200

244 681.9 51.19 125.4 18.75 1.563 37.5

245 9779 266 460.1 50 0.3906 12.5

246 2805 30.22 78.28 150 0.5859 12.5

247 479.3 14.62 115.7 25 0.3906 37.5

248 134 4.491 132 4.688 0.1875 12.5

249 104.4 7.548 86.98 3.125 0.7813 50

250 109.1 18.02 194.7 4.688 0.7813 100

251 42.51 5.852 71.64 6.25 0.7813 200

252 111500 591.1 156100

253 46290 440.1 170000 >200 3.125 >200 254 20000 1052 20000 >200 3.125 >200

255 20000 699 20000 >200 25 >200

256 6260 229.7 8441 100 0.7813 >200

257 8277 546.6 9229 150 1.563 >200

258 887.6 12.87 147.1 37.5 1.302 15.63

259 10.07 10.96 3.1 1 1.584 3.125

260 6.723 11.17 0.7966 1.563 6.25 6.25

261 1.717 6.586 10.21 1.563 6.25 100

262 72.42 31.46 28.15 6.25 3.125 25

263 21.02 3.275 11.46 0.7813 0.7813 18.75

264 16.95 4.607 4.397 0.3828 0.04688 1.781

265 6.932 2.653 1.263 0.4271 0.125 4.775

266 12.56 2.082 0.6886 0.7813 3.125 9.375

267 2.005 1.815 2.955 0.2552 0.7383 6.25

268 1.639 2.012 0.898 0.25 2.229 9.375

269 1.429 1.213 0.317 0.3125 0.7383 1.969

270 4.864 2.559 1.684 0.3906 1.563 6.25

271 23.44 11.38 11.7 0.5859 0.3906 2.344

272 49.04 7.168 5.544 1.563 0.7813 0.7813

273 3.213 0.5809 0.1648 0.3906 4.688 6.25

274 0.6366 0.6366 0.6366 0.1953 0.7813 4.688

275 6.702 3.679 0.6366 0.7813 3.125 9.375

276 8.749 5.507 3.385 0.3906 0.7813 1.563

277 5270 295.9 1226 125 12.5 >200

278 535.8 8.497 79.1 37.5 3.125 100

279 2166 32.34 183.5 25 0.5859 75

280 15.83 1.44 20.41 6.25 0.5859 3.125

281 42.86 0.3417 12.16 3.125 0.7813 12.5

282 265.9 21.52 182.9 1.563 0.7813 12.5

283 500.1 32.99 307.8 2.344 0.5859 12.5

284 102.2 12.66 55.52 1.563 0.7813 4.688

285 25.08 2.825 18.02 0.7813 0.3906 3.125 286 204.5 6.145 12.73 3.125 0.7813 3.125

287 159 0.7338 33.98 18.75 9.375 37.5

288 88.86 1.307 9.778 9.375 1.563 75

289 120.6 13.54 452.1 31.25 3.125 >200

290 19.71 0.6366 34.29 19.53 3.516 >200

291 98.64 1.472 221.7 4.688 3.906 >200

292 416 3.651 192.6 18.75 3.516 >200

293 86.54 1.023 232.4 9.375 1.953 >200

294 29.36 0.6366 192.7 0.6406 0.3802 37.5

295 16.06 0.6366 126.4 1.563 1.953 >200

296 54.84 0.6366 127.4 3.125 1.953 >200

297 20000 2479 20000 >200 12.5 >200

298 776 71.66 250.6 8.333 0.1953 0.04688 12.5

299 443.9 11.76 110.4 18.75 0.1953 37.5

300 372.7 37.21 31.55 12.5 1.172 9.375

301 1383 8.195 281.9 37.5 0.7813 25

302 110.5 5.851 38.47 3.906 0.3906 150

303 58.98 5.063 44.57 2.344 0.9766 18.75

304 50.27 29.19 102.7 7.031 6.25 >200

305 332.6 50.22 102.6 4.688 1.953 18.75

306 3737 104.4 299.9 50 1.172 25

307 4887 173.9 96.18 50 1.172 12.5

308 192.1 11.33 164.2 9.375 2.344 75

309 326.4 1.347 31.5 8.333 0.3906 0.7813 5.729

310 419.8 0.9943 45.98 9.375 0.1953 0.02344 4.167

311 128.9 1.108 8.162 3.906 0.1953 0.7813 4.688

312 107.4 0.9498 6.495 5.469 0.3906 0.5859 3.125

313 66.94 0.7696 13.44 3.906 0.4635 0.5859 7.031

314 291.7 3.652 26.9 5.469 0.1953 0.3906 3.906

315 510.1 11.6 33.39 4.688 0.3906 3.125

316 69.27 5.109 67.73 2.344 0.9766 12.5

317 359.9 5.384 46.03 9.375 0.125 0.1875 18.75 318 295.4 2.134 24.6 6.25 0.1953 0.0625 4.688

319 62.16 0.5506 0.8864 3.906 0.3906 3.906 3.906

320 294.3 14.41 35.92 9.375 0.6836 6.25

321 93.53 19.25 199.3 6.25 1.563 50

322 321.3 36.48 3649 25 7.813 200

323 70.58 7.692 150.7 12.5 2.344 200

324 1022 104.8 404.3 32.81 13.28 37.5

325 228.3 1.298 13.12 25 3.125 37.5

326 370 3.648 135.5 18.75 3.32 37.5

327 534.1 37.73 215.8 12.5 0.7813 100

328 324.9 20.44 473.4 6.25 1.563 125

329 87.07 8.257 682.7 1.563 0.7813 200

330 118 12.49 401.3 4.688 1.563 50

331 392 30.62 1185 6.25 1.172 150

332 192.5 11.49 554 3.125 0.5859 100

333 185.7 10.65 335.1 4.688 0.7813 50

334 385 10.59 129 3.125 0.3906 9.375

335 228.2 14.99 226.7 3.125 0.3906 25

336 379.3 34.04 634 4.688 0.7813 100

337 69.83 4.379 321.1 2.344 0.3906 75

338 75.43 4.526 151.5 3.125 0.5859 25

339 42.33 4.537 610.7 1.563 0.5859 >200

340 90.24 5.137 158.4 1.563 0.3906 25

341 22.13 2.938 786.3 1.172 0.7813 >200

342 46.04 4.643 80.44 0.7813 3.125 25

343 372.9 24.73 1179 9.375 1.563 100

344 241.6 32.78 585.2 4.688 2.344 100

345 213.4 18.49 269.1 4.688 1.563 50

346 232.1 11.74 407.6 2.344 1.563 150

347 184.6 12.2 844.4 3.125 2.344 200

348 1330 25.41 850.8 9.375 1.172 75

349 61.08 4.32 636.6 2.344 6.25 >200 350 39.69 5.799 246.2 1.563 1.172 >200

351 331.8 18.1 414 3.125 1.563 150

352 547.4 38.02 916.3 6.25 1.563 >200

353 28.02 4.098 689.2 1.172 2.344 100

354 16.35 7.325 324.7 2.344 2.344 200

355 466.7 14 868.7 4.688 1.563 150

356 1536 24.14 646 12.5 1.563 75

357 181.6 12.54 286.9 4.688 3.125 25

358 287.8 32.83 386.8 4.688 3.125 75

359 103.9 13.01 1865 3.125 4.688 >200

360 37.59 1.518 231.7 2.344 2.344 >200

361 138.9 12.94 271.4 3.125 2.344 25

362 115.8 11.3 493.8 3.125 0.7813 75

363 233 21.45 494.8 6.25 3.125 100

364 100.1 9.17 211.7 3.125 1.563 25

365 52.1 5.367 390.4 2.344 1.563 75

366 257.1 18.23 1543 3.125 1.172 150

367 60.28 7.525 1003 3.125 3.125 200

368 417 23.38 1676 9.375 1.563 >200

369 727.6 25.2 667.4 12.5 3.125 200

370 45.83 7.346 624.2 1.563 1.563 200

371 78.29 8.504 370.1 2.344 0.7813 100

372 15.7 4.914 469.8 1.563 7.813 >200

373 246.8 11.26 241 3.125 1.563 50

374 263.5 16.03 277.2 3.125 0.7813 37.5

375 97.6 6.127 533.3 3.125 1.563 >200

376 96.62 14.45 50.39 4.688 2.344 15.63

377 73.73 5.269 256.4 3.125 1.563 200

378 261.9 24.58 406.8 6.25 3.125 50

379 318.3 27.28 639 4.688 1.563 200

380 335.2 22.19 263.1 4.688 1.563 62.5

381 25.42 2.246 356.8 0.7813 1.563 50 382 212.3 12.77 220.4 3.125 1.563 50

383 51.62 4.664 269.2 1.563 1.563 200

384 292.7 13.63 224.9 4.688 1.953 50

385 498.6 12.52 356.6 6.25 1.563 50

386 32.05 3.228 120 1.563 6.25 >200

387 144.9 10.61 444.6 3.125 2.344 100

388 48.57 4.275 272.5 1.563 1.563 200

389 63.96 3.333 146 2.344 1.563 75

390 482.8 12.16 221.7 6.25 0.7813 62.5

391 348.1 18.85 400.6 2.344 1.172 50

392 393.7 7.877 454.9 3.125 2.344 75

393 337.7 10.82 508.6 4.688 1.563 200

394 195.4 11.3 657.9 3.125 2.344 >200

395 225.7 14.43 343 3.125 1.563 100

396 22.39 3.206 180.9 1.172 1.172 100

397 37.26 3.926 246.1 9.375 3.906 >200

398 1214 42.99 312 50 1.563 100

399 15100 117.3 12420 >200 3.906 >200

400 166.1 1.639 18.45 12.5 0.25 6.25

401 645.8 7.314 7.569 6.25 0.09375 0.8906

402 389.4 8.087 348.8 6.25 0.3906 25

403 184 2.338 15.45 4.688 0.125 6.25

404 71.38 0.8173 5.411 1.708 0.0625 2.563

405 67.64 4.231 16.87 1.563 1.563 62.5

406 250.4 1.652 1.736 6.25 1.172 3.125

407 114.7 25.75 133 3.125 3.125 >200

408 84.28 1.376 14.91 4.688 0.3906 75

409 445.3 26.91 236.9 12.5 1.563 >200

410 107.3 4.108 19.24 3.125 0.5859 18.75

411 102.3 4.836 27.76 3.125 0.7813 25

412 1389 25.9 25.79 25 0.3906 3.125

413 340.4 2.125 2.085 9.375 0.5859 4.688 414 176.9 6.014 19.86 4.688 2.344 18.75

415 32.3 0.5796 1.099 1.172 0.5859 3.125

416 56.47 2.416 13.72 6.25 2.344 25

417 49.78 0.7597 8.533 2.344 1.953 9.375

418 118.2 1.184 12.96 6.25 0.3906 6.25

419 1037 51.9 468.6 25 0.25 25

420 217.2 4.742 30.71 9.375 1.563 18.75

421 18.84 0.291 2.298 25 3.125 >200

422 55.95 1.305 22.59 25 3.125 100

423 1.288 0.3783 0.7105 0.125 1.086 3.125

424 80.77 18.89 32.7 1.563 0.7813 15.63

425 15.95 13.52 4.067 0.5859 0.3906 1.563

426 353.2 9.281 259.9 9.375 0.4063 25

427 108.9 29.79 450.1 4.688 0.25 75

428 345.2 0.6829 17.26 6.25 0.0625 1.531

429 498.8 2.585 30.03 6.25 0.0625 2.344

430 6.377 52.29 50.83 0.3906 1.563 3.125

431 3.745 17.94 0.4318 0.125 2.563 1.531

432 11.67 47.86 4.721 0.3906 6.25 18.75

433 0.5632 0.8747 0.9836 0.1875 0.6406 0.7656

434 1.853 1.783 0.1754 0.09375 0.543 0.7656

435 11.07 12.04 2.374 0.25 1.281 3.125

436 12.85 9.318 3.043 0.2552 0.375 0.8542

437 7.823 7.947 8.002 0.3906 0.3906 3.125

438 4.05 3.674 10.75 0.25 0.125 2.563

439 20.58 11.88 4.05 0.5859 0.7813 1.563

440 3.371 3.912 0.3572 0.0625 0.25 0.7656

441 22.05 11.3 0.8382 1.563 1.172 0.7813

442 16.54 11.78 0.2676 0.5859 1.172 0.7813

443 1.341 0.9092 0.4972 0.09375 0.7734 0.8906

444 3.275 2.495 1.349 0.3906 2.344 4.688

445 1.169 1.276 1.339 0.125 1.547 4.688 446 19.35 15.39 0.252 0.3906 1.563 1.563

447 4.263 7.129 0.1712 0.125 1.086 0.8906

448 2.165 2.095 0.9617 0.1953 3.125 6.25

449 0.5371 0.6534 0.8151 0.1953 0.7813 6.25

450 1.284 1.623 1.8 0.03125 18.75 75

451 47.08 0.9766 0.4764 3.125 1.563 3.125

452 124.8 1.221 1.984 9.375 1.563 4.688

453 110.7 6.885 0.6651 12.5 4.688 6.25

454 67.01 111.1 19.63 12.5 100 200

454 1.925 2.019 1.892 0.0625 0.7656 6.25

455 6.295 3.374 2.835 0.3906 0.5859 1.563

456 9.795 4.583 3.441 0.5859 0.5859 1.172

457 3.047 1.102 0.8031 0.1953 0.3906 1.172

458 2.386 22.14 2.125 0.125 3.125 3.125

459 86.63 1116 112.2 1.172 6.25 3.125

460 16.58 3.973 10.38 0.3906 0.5859 1.563

461 4.068 1.918 1.667 1.563 1.563 4.688

462 11.52 3.803 8.131 1.563 0.7813 18.75

463 6.579 4.415 4.419 0.1953 0.7813 0.7813

464 18.74 3.821 1.949 1.563 0.7813 1.563

465 3.305 2.703 1.635 3.125 3.125 12.5

466 54.63 10.54 3.723 1.563 0.7813 1.563

467 34.78 10.19 4.751 1.563 0.7813 1.563

468 13.49 9.948 3.813 1.563 0.7813 1.563

469 29.72 10.65 7.655 1.563 0.7813 1.563

470 3.233 27.02 101.1 1.563 0.7813 12.5

471 8.684 2.722 2.048 1.563 0.7813 1.563

472 0.661 0.5053 13.42 0.7813 1.172 75

473 7.296 4.47 1.416 0.5859 4.688 4.688

474 3.913 0.5226 0.5489 0.4453 0.09375 1.531

475 13.67 5.126 1.919 0.7813 0.7813 3.125

476 3.982 1.791 0.2627 0.5859 1.563 1.563 477 6.378 1.009 0.722 0.5859 0.7813 6.25

478 88.07 24.6 0.6388 2.344 0.7813 0.7813

479 30.32 6.658 0.373 1.563 0.3906 0.7813

480 9.143 0.8705 0.2643 0.7813 0.7813 2.344

481 7.106 1.462 0.4205 0.543 0.125 1.922

482 7.239 0.8886 0.1941 3.125 1.563 3.125

483 2.122 0.7548 0.2163 25 6.25 12.5

484 6.585 1.22 0.322 0.3828 0.25 1.708

485 4.977 1.568 0.1965 12.5 3.125 6.25

486 1.191 0.1918 0.1341 0.1367 1.208 4.531

487 56.37 102.5 70.38 1.563 1.563 25

488 18.79 7.896 3.445 0.7813 1.563 4.688

489 20.7 19.63 9.83 0.7813 1.563 9.375

490 5.607 2.569 2.351 0.375 1.281 9.375

491 1.107 0.4347 0.5047 0.0625 0.6406 3.792

492 15.99 17.27 12.3 0.3906 3.125 12.5

493 4.499 1.694 0.1333 0.3906 1.563 3.125

494 12.97 4.429 0.4271 1.172 0.3906 1.563

495 4.26 1.866 22.09 0.5859 2.344 25

496 1.091 0.5061 0.3968 0.3906 1.172 3.125

497 25.8 3.064 59.45 0.3906 0.5859 6.25

498 5.502 2.148 6.366 0.1953 0.3906 4.688

499 7.043 1.933 0.3277 0.1953 0.7813 1.172

500 9.861 3.519 12.2 1.563 2.344 31.25

501 5.388 1.521 0.5163 1.563 1.172 1.563

502 1.188 0.5204 1.444 1.563 1.563 9.375

503 4.202 1.141 0.1833 0.1953 0.1953 0.7813

505 22.21 9.543 0.9368 6.25 6.25 12.5

506 35.71 2.217 41.42 6.25 4.688 100

507 4.313 11.53 3.272 0.5859 4.688 25

508 2.366 4.554 1.662 0.0625 0.8359 3.125

509 928.7 57.36 395.8 12.5 1.563 50 510 47.35 3.422 12.81 200 50 >200

511 14.29 4.803 41.62 3.125 3.125 100

512 46.05 161.7 3.903 0.9766 9.375 2.344

513 3.612 9.349 1.176 9.375 12.5 9.375

514 6.076 1.148 0.1377 1.172 3.125 9.375

515 3.676 0.6027 0.3086 0.3906 4.688 6.25

516 12.63 2.404 0.2769 0.7813 6.25 6.25

517 37.21 5.884 0.937 3.125 3.125 1.563

518 1.624 0.7754 0.3422 0.3906 1.563 6.25

519 766.1 3.784 24.55 100 1.563 37.5

520 52.63 24.82 1.956 3.125 3.125 3.125

521 559.3 3.439 19.68 12.5 1.563 12.5

522 263.3 3.403 52.89 18.75 2.344 50

523 1210 20.17 226.3 9.375 0.125 4.125

524 5.132 24.75 1.048 6.25 12.5 12.5

0.0896

525 6.853 0.5412 8 12.5 3.125 4.688

526 4.575 1.848 1.586 100 25 50

527 10.64 7.025 2.894 12.5 6.25 12.5

528 0.4248 0.02476 0.1456 3.125 1.563 12.5

529 6.299 2.201 0.991 0.7813 3.906 9.375

530 25.91 1.149 0.2999 0.5859 3.125 4.688

531 32.14 2.069 8.362 12.5 6.25 12.5

532 6.415 0.5975 3.962 12.5 12.5 12.5

533 16.62 0.8776 2.875 12.5 3.125 12.5

534 9.529 0.4442 0.8425 25 6.25 12.5

535 6.855 0.8443 2.709 25 6.25 50

536 39.36 2.71 4.121 50 6.25 25

537 19.24 14.34 66.73 50 50 >200

538 53.75 1.402 40.3 50 6.25 100

539 7.618 0.192 1.854 12.5 3.125 25

540 20.82 0.1993 6.702 6.25 1.563 12.5

541 7.207 0.1326 5.106 6.25 3.125 25 542 7.898 11.49 6.434 6.25 25 100

543 1.161 2.62 3.21 12.5 50 >200

544 19.21 0.7275 2.235 3.125 0.7813 1.563

545 21.8 2.724 7.686 3.125 0.7813 3.125

546 177.8 33.76 38.65 12.5 1.563 12.5

547 9.136 9.316 1.175 3.125 6.25 6.25

548 10.48 7.537 0.5188 3.125 3.125 1.563

549 0.4723 0.2556 0.0629 3.125 1.563 6.25

550 2.521 0.7533 0.3153 3.125 3.125 12.5

551 3.803 0.1419 0.2602 0.7813 0.3906 1.563

552 7.198 1.325 0.2618 1.563 0.3906 1.563

553 0.9585 0.0499 0.0624 3.125 3.125 3.125

554 0.8178 0.1151 0.3631 1.563 3.125 3.125

555 8.916 1.962 0.1768 6.25 0.5859 3.125

556 2.973 0.1251 0.1218 12.5 25 12.5

557 8.084 3.052 0.6556 6.25 0.3906 6.25

558 1.957 0.1447 0.1777 6.25 6.25 6.25

559 0.5342 0.439 0.2124 6.25 12.5 12.5

560 0.8979 0.7272 0.2118 3.125 6.25 6.25

561 0.9929 0.1534 0.4339 0.09375 0.668 2.563

562 7.55 5.003 2.35 0.3906 0.5859 3.125

563 45.94 53.8 5.024 6.25 3.125 3.125

564 301 261.8 36.33 25 25 50

565 199.9 186.7 11.3 25 12.5 12.5

566 2.676 0.2332 0.5079 3.125 0.7813 3.125

567 3.771 0.2992 0.2251 6.25 3.125 6.25

568 1.169 0.0983 0.1611 1.563 0.3906 1.563

569 1.617 0.215 0.3094 3.125 6.25 6.25

570 4.06 0.33 0.49 6.25 3.125 6.25

571 14.85 1.71 5.06 3.125 0.7813 6.25

572 701.4 14.65 8.979 25 0.5859 6.25

573 668.2 38.65 41.38 12.5 0.7813 12.5 574 35.88 1.495 7.943 3.125 0.3906 3.125

575 59.45 3.149 6.977 3.125 0.3906 6.25

576 164.4 12.32 24.81 6.323 0.5969 4.24

577 29.62 2.47 10.38 3.125 0.7813 12.5

578 47.08 1.852 11.13 12.5 3.125 50

579 17.79 1.636 3.121 3.125 0.7813 12.5

580 22.67 0.869 13.41 6.25 1.563 12.5

581 267.8 8.228 36.83 6.25 0.3906 12.5

582 17.36 3.986 1.567 1.563 0.7813 1.563

583 12.01 6.527 23.6 6.25 3.125 6.25

584 10.23 2.048 1.606 1.563 1.563 6.25

585 16.99 2.202 4.583 3.125 0.7813 6.25

586 7.143 2.342 1.164 1.563 0.7813 1.563

587 2.829 0.7982 11.53 1.563 0.7813 6.25

588 28.76 6.27 2.61 3.125 1.563 1.563

589 146.4 8.746 93.88 4.688 1.172 9.375

590 24.51 8.273 8.349 2.344 1.172 2.344

591 320.1 16 574.4 6.25 1.563 25

592 84.09 8.598 34.82 3.125 1.563 12.5

593 272.7 38.18 31.56 6.25 1.563 3.125

594 51.69 13.38 5.406 1.563 0.7813 1.563

595 42.56 4.342 1.297 3.125 0.7813 1.563

596 10.59 4.385 7.464 1.563 0.7813 1.563

597 45.98 8.861 1.239 3.125 1.563 1.563

598 135.2 15.25 4.409 3.125 1.563 1.563

599 6.434 2.117 5.332 3.125 1.563 3.125

600 43.77 2.557 0.8611 6.25 1.563 3.125

601 13.06 1.656 0.5866 3.125 1.563 1.563

602 21.02 3.954 2.472 3.125 1.563 1.563

603 31.94 21.55 4.73 1.563 3.125 1.563

604 41.66 3.315 0.8991 6.25 1.563 1.563

605 159.9 11.7 3.886 6.25 6.25 3.125 606 51.42 17.69 1.124 3.125 0.7813 1.563

607 42.18 11.34 2.068 3.125 1.563 1.563

608 127.1 30.42 45.01 6.25 6.25 6.25

609 83.93 21.27 1.636 12.5 6.25 3.125

610 114.4 2.918 6.392 3.125 0.3906 1.563

611 343.8 17.69 20.11 12.5 0.3906 1.563

612 65.47 1.63 7.23 2.563 0.5 1.281

613 36.3 14.1 252.9 0.543 0.25 18.75

614 11.6 5.891 505 1.563 1.172 >200

615 16.71 9.836 620.7 1.172 0.7813 >200

616 14.43 4.365 276 0.5859 0.3906 75

617 9.665 10.02 334.1 0.2969 0.25 37.5

618 16.1 11.67 345.1 0.3906 0.3906 75

619 10.77 8.235 388.3 0.9766 0.7813 150

620 8.364 10.67 1034 2.344 7.813 >200

621 6.018 2.569 508.4 1.563 3.906 >200

622 85.57 4.395 142.4 6.25 0.9766 >200

623 79.49 7.937 206.9 6.25 1.953 150

624 86.23 10.17 559 12.5 7.813 >200

625 203.1 36.95 1348 12.5 2.344 >200

626 68.52 9.128 355.9 12.5 4.688 >200

627 415.2 32.89 830.2 12.5 1.172 100

628 649.7 44.97 164 12.5 0.9766 12.5

629 798.8 43.6 668.4 25 4.688 100

630 388.3 32.33 634.9 12.5 1.172 50

631 39.91 8.253 110 6.25 1.953 25

632 254.3 26.78 482.2 6.25 1.172 100

633 66.39 4.885 119.9 4.833 0.125 37.5

634 1283 14.1 163 18.75 0.5859 6.25

635 91.49 4.924 258.1 7.813 2.148 112.5

636 37.25 1.536 88.91 4.688 0.3906 >200

637 924.6 52.02 452.9 25 2.344 50 638 595.5 55.04 181.2 12.5 0.7813 12.5

639 187 1.975 10.52 25 1.563 6.25

640 193.7 0.8547 9.842 100 1.563 100

641 26.5 1.016 4.462 25 6.25 25

642 51.9 1.015 8.997 25 1.563 50

643 101.1 2.338 12.28 25 1.563 25

644 32.44 1.339 13.84 37.5 4.688 75

645 88.79 1.157 5.292 100 1.563 50

646 31.84 0.851 5.098 50 3.125 100

647 617.6 14.08 83.94 18.75 0.25 6.25

648 95.67 5.11 15.27 6.25 1.563 12.5

649 48.38 2.868 12.83 3.125 2.344 12.5

650 1262 22.06 46.84 100 1.563 50

651 899.7 9.85 40.66 37.5 1.172 6.25

652 167.3 5.372 27.35 12.5 1.563 25

653 4.821 2.818 4.501 0.3906 1.563 6.25

654 19.65 6.853 1.226 1.172 4.688 9.375

655 7.799 0.9846 0.2252 0.5859 2.344 9.375

656 2.838 1.978 0.8004 0.125 0.5781 3.125

657 10.16 9.664 2.091 0.7813 2.344 4.688

658 6.997 5.12 5.264 0.7813 2.344 12.5

659 36.29 18.77 6.402 2.344 15.63 25

660 10.43 4.699 1.31 0.3906 2.344 6.25

661 0.9648 1.007 0.2195 0.0625 2.703 2.75

662 37.11 11.62 4.585 1.953 6.25 12.5

663 2.944 2.459 0.7899 0.125 0.8906 3.125

664 38.5 18.06 51.96 0.418 0.25 6.25

665 29.84 7.48 0.9985 1.172 1.563 4.688

666 150.5 57.02 14.72 4.688 2.344 12.5

667 75.02 19.68 1.48 2.344 3.125 9.375

668 2.796 9.316 7.04 3.125 1.563 50

669 0.6879 3.922 8.993 2.344 2.344 >200 670 1.076 4.109 3.529 3.125 1.563 25

671 2.004 4.133 5.647 1.563 1.172 37.5

672 2.513 3.659 3.381 4.688 6.25 75

673 1.354 10.06 9.066 3.125 3.125 62.5

674 2.469 6.629 17.39 6.25 3.125 75

675 1.942 4.525 14.68 6.25 4.688 150

676 1.258 5.589 9.104 6.25 12.5 >200

677 0.5406 4.165 19.37 12.5 12.5 >200

678 5.005 15.3 20.75 6.25 9.375 150

679 75.31 19.79 21.23 3.125 1.563 50

680 86.6 41.38 5.159 3.125 1.563 6.25

681 16.1 8.72 7.104 3.125 1.563 6.25

682 27.37 4.125 0.6843 6.25 6.25 12.5

683 153.7 31.49 28.07 12.5 3.125 50

684 75.73 38.65 10.76 6.25 3.125 12.5

685 75.79 29.98 4.88 6.25 1.563 25

686 31.71 9.53 15.65 6.25 1.563 12.5

687 94.32 25.22 27.81 6.25 3.125 25

688 158.1 44.06 13.43 6.25 1.563 12.5

689 52.07 26.83 6.43 6.25 6.25 12.5

690 75.86 12.6 5.259 3.125 1.563 25

691 51.82 10.59 6.132 3.125 0.7813 3.125

692 19.81 6.359 12.7 3.125 1.563 6.25

693 97.84 36.86 11.6 6.25 3.125 12.5

694 18.65 4.842 2.458 1.563 0.3906 1.563

695 42.26 13.57 13.18 3.125 0.7813 6.25

696 5.26 1.094 2.381 1.563 0.3906 3.125

697 6.421 1.611 6.327 3.125 0.7813 6.25

698 29.57 10.01 6.518 3.125 0.7813 3.125

699 58.83 18 4.722 6.25 3.125 6.25

700 16.69 3.944 0.9583 3.125 0.3906 1.563

701 62.89 15.44 12.68 3.125 0.7813 6.25 702 25.19 4.016 2.248 3.125 0.7813 1.563

703 38.04 6.143 8.379 3.125 0.3906 12.5

704 51.63 14.84 7.175 6.25 1.563 6.25

705 61.14 18.23 5.7 4.688 2.344 12.5

706 12.38 4.52 0.6321 6.25 3.125 1.563

707 6.674 5.592 0.2492 6.25 3.125 1.563

708 1.599 0.3796 0.1443 6.25 1.563 6.25

709 16.4 6.578 0.2892 25 6.25 6.25

710 2.085 0.8901 0.1679 6.25 6.25 12.5

711 3.541 1.012 0.2237 12.5 6.25 6.25

712 126.3 58.73 13.56 100 25 50

713 3.535 3.272 0.8193 6.25 3.125 3.125

714 31.73 5.046 0.7991 12.5 1.563 3.125

715 27.37 25.31 0.7292 12.5 6.25 3.125

716 5.435 8.075 2.792 3.125 6.25 25

717 2.625 1.637 0.598 3.125 1.563 3.125

718 2.396 1.506 1.732 6.25 12.5 25

719 3.68 3.04 0.5528 3.125 3.125 3.125

720 16.12 3.035 1.04 12.5 6.25 3.125

721 9.18 3.025 0.8072 6.25 6.25 1.563

722 21.66 20.76 1.457 25 12.5 6.25

723 17.18 7.781 1.265 25 6.25 12.5

724 2.445 1.152 0.8617 6.25 6.25 12.5

725 0.9197 0.7671 1.271 6.25 12.5 25

726 58.85 26.75 1.212 25 12.5 3.125

727 1.968 2.131 0.9145 3.125 3.125 25

728 4.156 2.585 3.996 6.25 3.125 25

729 6.972 4.847 7.369 6.25 6.25 25

730 3.574 2.797 5.997 3.125 3.125 50

731 117.4 61.26 22.09 50 25 50

732 0.3839 0.5336 0.6898 3.125 0.7813 25

733 34.29 33.46 1.466 25 12.5 6.25 734 34.39 31.35 3.269 25 12.5 12.5

735 1.698 3.03 0.3883 3.125 3.125 6.25

736 3.229 3.232 1.595 6.25 6.25 6.25

737 3.023 4.951 4.286 3.125 6.25 25

738 2.28 1.276 3.412 6.25 3.125 50

739 6.822 3.837 2.767 25 25 >200

740 0.4555 0.2292 1.15 6.25 6.25 50

741 6.115 4.653 2.739 25 25 >200

742 1.836 2.009 0.6571 12.5 12.5 25

743 0.9012 0.4093 0.1466 6.25 3.125 6.25

744 18.13 16.29 0.9071 12.5 6.25 12.5

745 1.501 1.055 0.1748 3.125 0.7813 3.125

746 2.593 2.269 0.234 6.25 6.25 6.25

747 11.17 5.716 0.8655 25 6.25 12.5

748 1.248 0.8331 0.2477 6.25 0.7813 6.25

749 4.123 2.347 0.2622 12.5 3.125 6.25

750 21.46 4.747 0.4323 6.25 1.563 3.125

751 5.631 0.9619 0.108 3.125 0.7813 3.125

752 6.247 2.327 0.6772 12.5 1.563 25

753 2.022 1.006 0.7536 12.5 12.5 100

754 868.9 596.1 7.675 50 25 12.5

755 22.14 13.93 0.1909 6.25 6.25 3.125

756 89.14 78.09 339.4 12.5 12.5 >200

757 110.6 82.79 352.7 25 12.5 >200

758 45.76 29.64 2.444 6.25 6.25 6.25

759 40.9 22.51 45.64 3.125 3.125 12.5

760 2.08 5.645 1.515 25 100 100

761 103.7 46.03 48.31 100 100 >200

762 123.4 73.22 14.22 6.25 3.125 6.25

763 46.4 37.67 73.58 3.125 1.563 50

764 68.66 272.7 27.68 50 100 >200

765 131 93.29 124.7 3.125 6.25 25 766 120.4 133.9 8.519 25 25 12.5

767 222.6 208.2 4.579 50 200 12.5

768 36.66 24.63 0.906 6.25 12.5 3.125

769 11.41 7.478 0.9983 25 100 50

770 251.4 366.4 7.51 50 50 3.125

771 227.3 30.7 22.93 50 25 50

772 113.6 33.89 13.89 50 12.5 50

773 17.16 31.82 1.112 6.25 6.25 3.125

774 29.08 62.59 1.351 25 25 6.25

775 35.8 9.043 5.193 6.25 3.125 12.5

776 55.86 15.22 15.92 50 25 25

777 51.32 23.31 6.733 12.5 12.5 6.25

778 159.9 146.6 0.6876 1.563 3.125 1.172

779 6.701 6.425 0.1095 0.3906 1.172 2.344

780 31.67 17.7 0.2737 1.563 1.563 2.344

781 53.72 12.01 2.694 1.563 0.7813 3.125

782 397.2 182.1 9.504 4.688 6.25 3.125

783 13.4 4.914 1.927 0.5859 1.172 2.344

784 48.28 41.72 15.54 3.125 3.125 31.25

785 1.093 4.212 12.19 3.125 1.563 25

786 2.084 6.196 12.03 3.125 1.563 50

787 1.711 7.094 8.101 3.125 1.563 25

788 0.4378 2.828 35.65 6.25 6.25 >200

789 0.4725 2.396 16.5 3.125 3.125 100

790 0.8705 3.573 7.258 3.125 0.7813 12.5

791 1.197 6.26 11.1 1.563 0.7813 50

792 1.549 7.313 4.379 3.125 3.125 25

793 1.023 7.004 4.659 3.125 1.563 25

794 1.764 6.442 10.99 3.125 1.563 50

795 1.098 5.226 6.57 3.125 1.563 25

796 0.3449 2.062 17.97 6.25 6.25 >200

797 1.508 5.569 9.919 3.125 3.125 25 798 2.351 6.051 13.3 3.125 1.563 25

799 1.051 3.889 15.01 3.125 3.125 >200

800 5.139 2.683 14.32 6.25 0.7813 12.5

801 2.798 2.217 9.446 6.25 3.125 100

802 4.266 3.246 17.19 6.25 6.25 100

803 13.03 4.866 13.22 6.25 6.25 100

804 5.781 3.854 8.72 6.25 3.125 50

805 7.581 3.769 19.65 6.25 3.125 50

806 7.672 4.679 5.016 6.25 6.25 12.5

807 5.158 3.974 19.92 6.25 1.563 25

808 8.442 3.573 25.3 3.125 1.563 25

809 11.35 4.022 27.9 6.25 3.125 50

810 8.919 7.063 26.78 6.25 3.125 100

811 9.419 4.775 27.89 6.25 1.563 100

812 5.766 2.699 3.885 6.25 1.563 12.5

813 9.862 6.273 20.58 6.25 6.25 100

814 12.46 8.077 22.5 6.25 6.25 100

815 6.014 4.843 18.01 3.125 1.563 100

816 16.27 6.615 13.46 6.25 1.563 12.5

817 14.99 4.457 9.501 6.25 1.563 12.5

818 8.6 4.384 17.24 3.125 1.563 12.5

819 97.09 14.29 27.41 1.823 0.8464 3.385

820 39.42 13.52 0.6593 0.7813 0.3906 0.7813

821 55.15 18.05 0.4959 6.25 12.5 12.5

822 2.246 1.442 0.1955 0.0938 0.6406 1.086

823 25.45 17.48 0.666 0.3906 1.172 1.172

824 59.19 53.13 0.7024 0.7813 1.563 0.7813

825 0.4988 0.1567 0.0805 1.563 0.7813 3.125

826 1.453 0.4908 1.359 3.125 1.563 25

827 22.55 5.718 2.588 0.3906 0.3906 1.172

828 72.88 8.291 73.33 1.563 0.7813 6.25

829 93.3 59.75 1.077 0.9766 0.7813 0.7813 830 3.821 1.934 0.2471 0.724 0.25 0.8542

831 0.8916 0.8174 2.837 3.125 2.344 50

832 1.456 0.5015 0.2118 3.125 1.563 4.688

833 4.307 0.7403 3.335 3.125 1.563 12.5

834 5.449 1.486 13.31 6.25 6.25 50

835 232 95.98 190.4 6.25 3.125 100

836 133.7 54.93 2.386 4.688 2.344 1.563

837 21.17 8.677 2.902 0.5859 1.563 6.25

838 1679 68.26 61.16 12.5 3.125 6.25

839 359.2 56.88 19.33 6.25 3.125 6.25

840 14.1 2.492 0.4603 12.5 3.125 6.25