TITLE

Substituted Caprolactams and Derivatives Thereof Useful for Treatment of HIV Disease

Cross-reference to Earlier Filed Application

This application is a continuation-in-part of U.S. Patent Application Serial Number 07/965,061, filed October 22, 1992.

FIELD OF THE INVENTION

This invention relates to novel substituted caprolactams, including 4-azacaprolactams, and derivatives thereof which inhibit HIV protease and are useful for treatment of HIV disease. Also included in this invention are pharmaceutical compositions containing such caprolactams, and to methods of using such caprolactams for the treatment of HIV disease.

BACKGROUND OF THE INVENTION

Current treatments for viral diseases usually involve administration of compounds that inhibit viral DNA synthesis. Current treatments for AIDS (Dagani, Chem . Eng . News, November 23, 1987 pp. 41-49) involve administration of agents such as 2 ' , 3 '-dideoxycytidine, trisodium phosphonoformate, ammonium 21-tungsto-9- antimoniate, 1-b-D-ribofuranoxyl-l,2, -triazole-3- carboxamide, 3 '-azido-3 '-deoxythymidine (AZT) , and adriamycin that inhibit viral DNA synthesis; compounds such as AL-721 and polymannoacetate which may prevent

HIV from penetrating the host cell; and compounds which treat the opportunistic infections caused by the immunosupression resulting from HIV infection. None of the current AIDS treatments have proven to be totally effective in treating and/or reversing the disease. In addition, many of the compounds currently used to treat AIDS cause adverse side effects including low platelet count, renal toxicity, and bone marrow cytopenia.

Proteases are enzymes which cleave proteins at specific peptide bonds. Many biological functions are controlled or mediated by proteases and their complementary protease inhibitors. For example, the protease renin cleaves the peptide angiotensinogen to produce the peptide angiotensin I. Angiotensin I is further cleaved by the protease angiotensin converting enzyme (ACE) to form the hypotensive peptide angiotensin II. Inhibitors of renin and ACE are known to reduce high blood pressure in vivo . However, no therapeutically useful renin protease inhibitors have been developed, due to problems of oral availability and in vi vo stability.

The genomes of retroviruses encode a protease that is responsible for the proteolytic processing of one or more polyprotein precursors such as the pol and gag gene products. See ellink, Arch . Virol . ___ϋ 1 (1988) . Retroviral proteases most commonly process the gag precursor into the core proteins, and also process the pol precursor into reverse transcriptase and retroviral protease . The correct processing of the precursor polyproteins by the retroviral protease is necessary for the assembly of the infectious virions . It has been shown that in vi tro mutagenesis that produces protease- defective virus leads to the production of immature core forms which lack infectivity. See Crawford et al., J. Virol . ____i 899 (1985); Katoh et al . , Virology IAS. 280

(1985) . Therefore, retroviral protease inhibition provides an attractive target for antiviral therapy. See Mitsuya, Nature 225. 775 (1987) .

Moore, Bioche . Biophys . Res . Commun . , 159 420 (1989) discloses peptidyl inhibitors of HIV protease. Erickson, European Patent Application No. WO 89/10752 discloses derivatives of peptides which are inhibitors of HIV protease.

U.S. Patent No. 4,652,552 discloses methyl ketone derivatives of tetrapeptides as inhibitors of viral proteases. U.S. Patent No. 4,644,055 discloses halomethyl derivatives of peptides as inhibitors of viral proteases. European Patent Application No. WO 87/07836 discloses L-glutamic acid gamma- monohydroxamate as an antiviral agent.

Japanese Patent Number 02306992 and Kimura, Agric . Biol . Chem . , 5_3_ _. 1811 (1989) describe compounds of the formula:

wherein R is a fatty acid. These compounds were isolated from streptomyces and shown to be useful as peptidoglycan inhibitors. French Patent Number 2396002 describes quaternary amines, of the formula shown below, which are useful as vasodilators :

wherein R~ is hydrogen or ester and R^ is C1-C2 alkyl. The ability to inhibit a viral protease provides a method for blocking viral replication and therefore a treatment for viral diseases, such as AIDS, that may have fewer side effects, be more efficacious, and be less prone to drug resistance when compared to current treatments . The topic of the present invention is substituted caprolactams and derivatives thereof, which compounds are capable of inhibiting HIV protease and are, therefore, useful for combating HIV diseases, such as AIDS. The caprolactams and derivatives thereof of this invention provide significant improvements over protease inhibitors that are known in the art . A large number of compounds have been reported to be inhibitors of proteases, such as renin, but these have suffered from lack of adequate bioavailability and are thus not useful as therapeutic agents, particularly if oral administration is desired. This poor activity has been ascribed to the relatively high molecular weight of most protease inhibitors, to inadequate solubility properties, and to the presence of a number of peptide bonds, which are vulnerable to cleavage by mammalian proteases in vivo and which generally cause the molecules to be extensively bound in human serum. The substituted caprolactams and derivatives thereof of the present invention and described herein have a distinct advantage in this regard, in that they do not contain

-4-

SUBSΠTUTESHEET(RULE26)

peptide bonds, are of low molecular weight, and can be hydrophilic yet still inhibit the viral protease enzyme.

The structures disclosed also have a particular advantage in the presence of a basic amine in the ring; which provides good in vitro potency and aids in formulation, in vivo absorption and CNS penetration of the compound.

The substituted caprolactams of the present invention are particularly useful as inhibitors of HIV protease and similar retroviral proteases.

The compounds of the invention are of low molecular weight and may, therefore, have good oral absorption properties in mammals.

DETAILED DESCRIPTION OF THE INVENTION

[1] There is provided by this invention compound of the formula (I) :

(I)

or a pharmaceutically acceptable salt or prodrug form thereof wherein:

X is S, 0, N-R ⁷ ;

X ¹ is C(R ⁴ ) (R ^4a ) or N-R ⁴ ;

-5-

SUBSΠTUTESHEET(RULE26)

R ⁴ and R ⁷ are independently selected from the following groups:

hydrogen; Ci-Cβ alkyl substituted with 0-3 R ¹¹ ;

C2-C8 alkenyl substituted with 0-3 R ¹¹ ; C2-C8 alkynyl substituted with 0-3 R ¹¹ ; C3-C8 cycloalkyl substituted with 0-3 R ¹¹ ; Cβ-Cio bicycloalkyl substituted with 0-3 R ¹¹ ; aryl substituted with 0-3 R ¹² ; a C6-C14 carbocyclic ring systm substituted with 0-3 R ¹² ;

a 5- to 10-membered heterocyclic ring system containing 1 to 4 heteroatoms independently selected from oxygen, nitrogen or sulfur, said heterocyclic ring system being substituted with 0-3 Rl ;

R ^4a is selected from the following groups :

hydrogen;

C1-C4 alkyl substituted with 1-4 groups selected independently from: halogen or C1-C2 alkoxy; benzyl substituted with 1-4 groups selected independently from: halogen or C1-C2 alkoxy; -OR ² 0; SR °;

R ⁴ and R ^4a can alternatively join to form a 5-7 membered carbocyclic ring substituted with 0-2 R^ ² ;

n is 0, 1, or 2;

R ⁵ is selected from H; halogen; -N(R ²⁰ )2; -SR ²⁰ ; -OR ²⁰ ; or Ci-Cδ alkyl substituted with 0-3 -N(R ²⁰ )2, -SR ²⁰ , or -OR ²⁰ ;

R^ ^a is selected from H, halogen, Cι~C6 alkyl, -N(R ²⁰ )2. -SR ²⁰ , or -OR ²⁰ ;

R5 and R^ ^a can alternatively join to form =0, =S, or a ketal ring;

R ²⁰ and R ²¹ are independently selected from:

hydrogen;

C1-C6 alkyl substituted with 0-3 R ¹¹ ; C3-C6 alkoxyalkyl substituted with 0-3 R ¹¹ ;

C ₁ -C6 alkylcarbonyl substituted with 0-3 R ¹¹ ;

C1-C6 alkoxycarbonyl substituted with 0-3 R~ ~ ; benzoyl substituted with 0-3 R ¹² ; phenoxycarbonyl substituted with 0-3 R ¹² ; phenylaminocarbonyl substituted with 0-3 R^ ² ;

Ci-Cβ alkylsulfenyl substituted with 0-3 R ¹¹ ;

C ₁ -C6 alkylsulfonyl substituted with 0-3 R- ~ ; or any group that, when administered to a mammalian subject, cleaves to form a free hydroxyl, amino or sulfhydryl;

R- - is selected from one or more of the following:

keto, halogen, cyano, -CH2NR ^l3 R ¹⁴ , -NR ¹³ R ¹⁴ , -CO2R ¹³ , -OC(=0)R ¹³ , -OR ¹³ , C2-C6 alkoxyalkyl, -S(0) _m R ¹³ , -NHC(=NH)NHR ¹³ , -C (=NH)NHR ¹³ , -C(=0)NR ¹³ R ¹⁴ , -NR ¹ C(=0)R ¹³ , =NOR ¹⁴ , -NR ¹⁴ C(=0)OR ¹⁴ , -OC(=0)NR ¹³ R ¹⁴ , -NR ¹³ C (=0)NR ¹³ R ¹⁴ , -NR ¹⁴ S02NR ¹³ R ¹⁴ , -NR ¹ S02R ¹³ , -Sθ2NR ¹³ R ¹⁴ , C1-C4 alkyl, C2-C4 alkenyl, C3-C10 cycloalkyl, C3-C6

cycloalkylmethyl, benzyl, phenethyl, phenoxy, benzyloxy, nitro, C7-C10 arylalkyl, hydroxamic acid, hydrazide, boronic acid, sulfonamide, formyl, C3-C6 cycloalkoxy, C ₁ -C ₄ alkyl substituted with -NR ¹³ R ¹⁴ , C1-C4 hydroxyalkyl, methylenedioxy, ethylenedioxy, C3.-C4 haloalkyl, C1-C4 haloalkoxy, C1-C4 alkoxycarbonyl, C1-C4 alkylcarbonyloxy, C1-C4 alkylcarbonyl, C1 _. -C4 alkylcarbonylamino, -OCH2CO2H, 2- (1-morpholino) ethoxy, azido, or -C(R ¹⁴ )=N(OR ¹⁴ ) ;

C1-C4 alkyl substituted with 0-2 R ¹² ,

1-3 amino acids, linked together via amide bonds and linked to R ⁴ or R ⁷ , R ²⁰ , or R ²¹ via the amine or carboxy terminus;

-(C ₁ -C ₃ alkyl) aryl substituted with 0-2 R ¹² ;

a C ₃ -C14 carbocyclic residue substituted with 0-3 R ² ;

aryl substituted with 0-3 R ¹² ; or

a 5- to 10-membered heterocyclic ring system containing 1 to 4 heteroatoms independently selected from oxygen, nitrogen or sulfur, said heterocyclic ring system being substituted with 0-3 Rl ² ;

R ¹² , when a substituent on carbon, is selected from one or more of the following:

phenyl, benzyl, phenethyl, phenoxy, benzyloxy, halogen, hydroxy, nitro, cyano, C1-C alkyl, C3-C6

cycloalkyl, C3-C6 cycloalkylmethyl, C7-C10 arylalkyl, C1-C4 alkoxy, -CO2H, hydroxamic acid, hydrazide, oxime, boronic acid, sulfonamide, formyl, C3-C6 cycloalkoxy, -OR ¹³ , C1-C4 alkyl substituted with -NR ¹³ R ¹⁴ , -NR ¹³ R ¹⁴ , C2-C6 alkoxyalkyl, C1-C4 hydroxyalkyl, methylenedioxy, ethylenedioxy, C1-C4 haloalkyl, C1-C4 haloalkoxy, C1-C4 alkoxycarbonyl, C1-C4 alkylcarbonyloxy, C1-C4 alkylcarbonyl, C1-C4 alkylcarbonylamino, -S(0) _m R ¹³ , -S02NR ¹³ R ¹⁴ , -NHSO2R ¹⁴ , -OCH2C02H, 2- (1-morpholino) ethoxy; or

a 5- or 6-membered heterocyclic ring containing from 1 to 4 heteroatoms independently selected from oxygen, nitrogen or sulfur;

when R ¹² is attached to a saturated carbon atom, it may be carbonyl or thiocarbonyl;

or R ¹² may alternatively be a 3- or 4- carbon chain attached to adjacent carbons on the ring to form a fused 5- or 6-membered ring, said 5- or 6- membered ring being optionally substituted on the aliphatic carbons with halogen, C1-C4 alkyl, C1 _. -C4 alkoxy, hydroxy, or -NR ¹³ R ¹⁴ ;

R ¹² , when a substituent on nitrogen, is selected from one or more of the following:

phenyl, benzyl, phenethyl, hydroxy, C1-C4 hydroxyalkyl, C1-C4 alkoxy, C1-C4 alkyl, C3-C6 cycloalkyl, C3-C6 cycloalkylmethyl, -CH2NR ¹³ R ¹⁴ , -NR ¹³ R ¹⁴ , C2-C6 alkoxyalkyl, C1-C4 haloalkyl, C1-C4 alkoxycarbonyl, -CO2H, C1-C4 alkylcarbonyloxy, C1-C4 alkylcarbonyl, -C (R ¹⁴ )=N (OR ¹⁴ ) ;

.13 is selected from :

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SUBST1TUTE SHEET (RULE 26)

H; phenyl substituted with 0-3 R ^11A ; benzyl substituted with 0-3 R ^11A ; C1-C6 alkyl substituted with 0-3 R ^11A ; C ₂ -C alkenyl substituted with 0-3 R ^11A ;

C1-C6 alkylcarbonyl substituted with 0-3 R ^11A ; C1-C6 alkoxycarbonyl substituted with 0-3 R ^11A ; C1-C6 alkylaminocarbonyl substituted with 0-3 R ^11A ; C3-C6 alkoxyalkyl substituted with 0-3 R ^11A ; an amine protecting group when R ¹³ is bonded to N; a hydroxy protecting group when R ¹³ is bonded to 0;

R ¹⁴ is OH; H; CF ₃ ; C1-C4 alkyl substituted with 0-3 groups selected from OH, C ₁ -C ₄ alkoxy, halogen, NH ₂ ; Ci-Cβ alkoxy; NH ₂ ; C ₂ -C ₆ alkenyl; benzyl; an amine protecting group when R ¹⁴ is bonded to N; a hydroxy protecting group when R ¹⁴ is bonded to 0;

R ¹³ and R ¹⁴ can alternatively join to form -(CH2)4~, ~(CH2)5", -CH2CH2N(R ¹⁵ )CH2CH2-, or -CH2CH2OCH2CH2-;

R ¹⁵ is H or CH3;

m is 0, 1 or 2;

W is selected from:

-N (R ²² )C( = Z)N(R ²³ )-;

-OC(=Z)0-;

-N(R ²² )C( = Z)0-; -C(R ²⁵ ) (R ²⁶ )C( = Z)C(R ²⁷ ) (R ²⁸ )-;

-N(R ²² )C( = Z)C(R ²⁷ ) (R ²⁸ )-;

-C(R ²⁵ ) (R ²⁶ )C(=Z)0-;

-N(R ²² )C(=0)C(=0)N(R ²³ )-;

-N(R ²² )C( = S)C(=S)N(R ²³ )-; -C(R ²⁵ ) (R ²⁶ )C(F2)C(R ²⁷ ) (R ²⁸ )-;

-C(R ²⁵ ) (R ²⁶ )N(CH3) (O)C(R ²⁷ ) (R ²⁸ )-;

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SUBSΠTIJTE SHEET (RULE 26)

-C(R ²⁵ ) (R ²⁶ )N(OR ²⁹ )C(R ²⁷ ) (R ²⁸ )-; -C(R ²⁵ ) (R ²⁶ )C(=Z)S-; -N(R ²² )S(=Z' )N(R ²³ )-; -N(R ²² )S(=Z' )2N(R ²³ )-; -N(R ²² )P(=0) (R ^24a ) (N(R ²³ )-;

-C(R ²⁵ ) -26 )S =Z')C(R ²⁷ ) (R ²⁸ )-; -C(R ²⁵ ) R ²⁶ )S =Z')2C(R ²⁷ ) (R ²⁸ )-; -C(R ²⁵ ) >26 ⁾ P =0) (R ^{2 a} )C(R ²⁷ ) (R ²⁸ )-; -C(R ²⁵ ) R ²⁶ )S =Z')N(R ²³ )-;

-C(R ²⁵ ) R ²⁶ )S =Z')2N(R ²³ )-; -C(R ²⁵ ) (R ²⁶ )S =0)20-; -C(R ²⁵ ) ( RR ^2D 6)P =0) (R ^24a )N(R ²³⁾ -; -C(R ²⁵ ) (R ² ^ )P =0) (R ^24a )0-; -C(R ²⁵ ) (R 26)C F2)C(=0)N(R ²³ )-; -C(R ²⁵ ) (R 26, F2)S(=0)2N(R ²³ )-;

-SC(=Z)-;

-C(R ²⁵ ) (R ²⁶ )C R ³⁴ ) (R ³⁵ )C(R ²⁷ ) (R ²⁸ )-;

-N(R ²² )C(R ³⁴ ) _R 35 _)N(R 23 ₎ _ _;

-N=C(R ³⁶ )N(R ²³ )-;

-N(R ²² )P (R ^24a )N(R ²³ )

-C(=Z)-;

-P(=0) (R ^24a )-;

-S(=Z')-;

-S ⁽ =z' ⁾ 2-;

Z is 0, S, or NR ²⁴ ;

is 0 or NR 24

R ²² is independently selected from the following

hydrogen;

C1-C8 alkyl substituted with 0-3 R ³¹ ; C2-C8 alkenyl substituted with 0-3 R ³¹ ; C2-C8 alkynyl substituted with 0-3 R ³¹ ;

-11-

SUBST1TUTE SHEET (RULE 26)

a C3-C14 carbocyclic ring system substituted with

0-5 R ³¹ or R ³² ; a 5- to 10-membered heterocyclic ring system containing 1 to 4 heteroatoms independently selected from oxygen, nitrogen or sulfur, said heterocyclic ring system being substituted with 0-2 R ³² ;

R ²³ is independently selected from the following:

hydrogen;

C1-C8 alkyl substituted with 0-3 R ³¹ ; C2-C8 alkenyl substituted with 0-3 R ³¹ ; C2-C8 alkynyl substituted with 0-3 R ³¹ ; a C3-C14 carbocyclic ring system substituted with 0-5 R ³¹ or R ³² ;

a 5- to 10-membered heterocyclic ring system containing 1 to 4 heteroatoms independently selected from oxygen, nitrogen or sulfur, said heterocyclic ring system being substituted with 0-2 R ³² ;

R ²⁴ is selected from: hydrogen; hydroxy; amino; C1-C4 alkyl; C1-C4 alkoxy; mono- or di-(Cτ _. -C6 alkyl) amino; cyano; nitro; benzyloxy; -NHSθ2aryl, aryl being optionally substituted with (Cι-C ₆ )alkyl;

R ^24a is selected from: hydroxy; amino; C1-C4 alkyl; C1-C4 alkoxy; mono- or di- (C1 _. -C6 alkyl) amino; cyano; nitro; benzyloxy; or phenoxy;

R ² - ^> is independently selected from the following

hydrogen;

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SUBSΠTIΠΈ SHEET (RULE 26)

Ci-Cβ alkyl substituted with 0-3 R ³¹ ; C2-C8 alkenyl substituted with 0-3 R ³¹ ; C2-C8 alkynyl substituted with 0-3 R ³¹ ; a C3-C14 carbocyclic ring system substituted with 0-3 R ³¹ or R ³² ;

a 5- to 10-membered heterocyclic ring system containing 1 to 4 heteroatoms independently selected from oxygen, nitrogen or sulfur, said heterocyclic ring system being substituted with 0-2 R ³² ;

R ²⁷ is selected from the following:

hydrogen;

C1-C8 alkyl substituted with 0-3 R ³¹ ;

C2-C8 alkenyl substituted with 0-3 R ³¹ ;

C2-C8 alkynyl substituted with 0-3 R ³¹ ;

C3-C8 cycloalkyl substituted with 0-3 R ³¹ ; a C3-C14 carbocyclic ring system substituted with 0-3 R ³¹ or R ³² ;

a 5- to 10-membered heterocyclic ring system containing 1 to 4 heteroatoms independently selected from oxygen, nitrogen or sulfur, said heterocyclic ring system being substituted with 0-2 R ³² ;

R ² ^ is independently selected from:

hydrogen- halogen;

C1-C4 alkyl substituted with 0-3 halogen or C1-C2 alkoxy;

-13-

SUBSCTTUTE SHEET (RULE 26)

benzyl substituted with 0-3 halogen or C1-C2 alkoxy;

_> 28 is independently selected from:

hydrogen; halogen;

C1-C4 alkyl substituted with 0-3 halogen or C1-C2 alkoxy; benzyl substituted with 0-3 halogen or C1-C2 alkoxy;

_29 is selected from:

hydrogen;

C1-C4 alkyl substituted with 0-3 halogen or C1-C2 alkoxy; benzyl substituted with 0-3 halogen or C1-C2 alkoxy;

alternatively, R ²² , R ^, or R ² ^, independently, can join with R ⁴ or R ^4A to form a 5- or 6-membered fused heterocyclic ring or carbocyclic ring substituted with 0-2 R ¹² , said heterocyclic ring containing 1-3 heteroatoms independently selected from N, S, or 0; or

alternatively, R ²³ , R ²⁷ , or R ²⁸ , independently, can join with R ⁷ to form a 5- or 6-membered fused heterocyclic ring or carbocyclic ring substituted with 0-2 R ¹² , said heterocyclic ring containing 1-3 heteroatoms independently selected from N, S, or 0; or

alternatively, R ²² , R ²⁵ , R ²⁶ , R ²³ , R ²⁷ , R ²⁸ , R ³⁴ , or R ³⁵ can join with R^ or R^ to form a 0- to 7-membered bridge to form a carbocyclic or heterocyclic ring, said bridge being substituted with 0-2 R ¹² and said bridge containing 0-3 heteroatoms independently selected from N, S, or 0 (i.e., a 0-π.embered bridge is formed when R ²² , R ²⁵ , R ²⁶ , R ²³ , R ²⁷ , R ²⁸ , R ³⁴ , or R ³ ^ are taken together with R^ or R^ to form a direct bond) ;

R ³¹ is selected from one or more of the following:

keto, halogen, cyano, -CH2NR ¹³ R ¹⁴ , -NR ¹³ R ¹⁴ , -C02R ¹³ , -C(=0)R ¹¹ , -0C(=0)R ¹³ , -OR ¹³ , C2"C6 alkoxyalkyl, -S(0) _m R ¹³ , -NHC (=NH)NHR ¹³ ,

-C.(=NH)NHR ¹³ , -C(=0)NR ¹³ R ¹⁴ , -NR ¹⁴ C (=0) R ¹³ , =NOR ¹⁴ , -NR ¹⁴ C(=0)OR ¹⁴ , -OC(=0)NR ¹³ R ¹⁴ , -NR ¹³ C (=0)NR ¹³ R ¹⁴ , -NR ¹ S02NR ¹³ R ¹⁴ , -NR ¹ S02R ¹³ , -Sθ2NR ^l3 R ¹⁴ , C1-C4 alkyl, C2-C4 alkenyl, C3-C10 cycloalkyl, C3-C6 cycloalkylmethyl, benzyl, phenethyl, phenoxy, benzyloxy, nitro, C7-C10 arylalkyl, hydroxamic acid, hydrazide, oxime, boronic acid, sulfonamide, formyl, C ₃ -C ₆ cycloalkoxy, C ₁ -C ₄ alkyl substituted with -NR ¹³ R ¹⁴ , C1-C4 hydroxyalkyl, methylenedioxy, ethylenedioxy, C1-C4 haloalkyl, C1-C4 haloalkoxy,

C1-C4 alkoxycarbonyl, C1-C4 alkylcarbonyloxy, C1-C4 alkylcarbonyl, C1-C4 alkylcarbonylamino, -OCH2CO2R ¹³ , 2- (1-morpholino) ethoxy, azido, -C(R ¹ )=N(OR ¹⁴ ) ; or

1-3 amino acids, linked together via amide bonds and linked to R ²² , R ²³ , R ²⁵ , R ²⁷ , R ⁴ or R ⁷ via the amine or carboxy terminus;

a C3-C14 carbocyclic residue substituted with 0-5 R ³² ; or

a 5- to 10-membered heterocyclic ring system containing 1 to 4 heteroatoms independently selected from oxygen, nitrogen or sulfur, said heterocyclic ring system being substituted with 0-2 R ³² ;

R ³² , when a substituent on carbon, is selected from one or more of the following:

phenyl, benzyl, phenethyl, phenoxy, benzyloxy, halogen, hydroxy, nitro, cyano, C1-C4 alkyl, C3-C10 cycloalkyl, C3-C6 cycloalkylmethyl, C7-C10 arylalkyl, C1-C4 alkoxy, -CO2H, hydroxamic acid, -CONR ¹³ NR ¹³ R ¹⁴ , hydrazide, oxime, boronic acid, sulfonamide, formyl, C3-C6 cycloalkoxy, -OR ¹³ , C1-C4 alkyl substituted with -NR ¹³ R ¹⁴ , -NR ¹³ R ¹⁴ , C2-C6 alkoxyalkyl, C1-C4 hydroxyalkyl, methylenedioxy, ethylenedioxy, C1-C4 haloalkyl, C1-C4 haloalkoxy, C1-C4 alkoxycarbonyl, C1-C4 alkylcarbonyloxy, C1-C4 alkylcarbonyl, C1-C4 alkylcarbonylamino, -SfOJmR ¹ ^. -S02NR ¹³ R ¹⁴ , -NHS02R ¹⁴ , -OCH2CO2H, 2- (1-morpholino) ethoxy, -C (R ¹⁴ ) =N (OR ¹⁴ ) ; NO ₂ . -OR ¹³ , -NR ⁴⁰ R ⁴¹ , -SO _m R ¹³ , -SO _m NR ¹³ R ¹⁴ , -C (=0)NR ¹³ R ¹⁴ , -OC(=0)NR ¹³ R ¹⁴ , -C (=0) R ^{1 1} , -0C(=0)R ^1] -, -OC02R ¹³ , phenyl, -C(=0)NR ¹³ - (C ₁ -C ₄ alkyl)-NR ¹³ R ¹⁴ , -C(=O)NR ⁴⁰ R ⁴¹ , C ₁ -C ₄ haloalkyl, C ₁ -C haloalkoxy, C ₂ -C ₄ haloalkenyl, C ₁ -C ₄ haloalkynyl, or

-C (=0)NR ¹³ C(R ¹¹ ) ₂ NR ¹³ R ¹⁴ ; -C(=0)NR ¹³ C (R ¹¹ ) ₂ NR ¹³ NR ¹⁴ ; -C (=0)NR ¹³ C(R ^ι:L )2NR ¹³ Cθ2R ¹³ ; -C(=0)NR ¹³ - (C ₁ -C ₄ alkyl) -NR ¹³ C0 ₂ R ¹³ ; or

-C (=0)C (R ^1:L ) ₂ NR ¹³ R ¹⁴ ; -C (=0) C (R ¹¹ ) ₂ NR ¹³ NR ¹⁴ ;

-16-

SUBSΠTIΠΈ SHEET (RULE 26)

-C(=0)C(R ¹¹ ) ₂ NR ¹³ C02R ¹³ ; -C (=0) - (C ₁ -C ₄ alkyl) -NR ¹³ R ¹⁴ ; -C(=0)-(Cι-C ₄ alkyl) -NR ¹³ C0 ₂ R ¹³ ; or

C1-C4 alkoxy substituted with 0-4 groups selected from: R ¹¹ , C3-C6 cycloalkyl, -C0 R ¹³ , -C (=0)NR ¹³ R ¹⁴ , -NR ¹³ R ¹⁴ or OH;

C _3. -C4 alkyl substituted with 0-4 groups selected from: R ¹¹ , =NR ¹⁴ , =NNR ¹³ C(=0)NR ¹³ R ¹⁴ or -NR ¹³ R ¹⁴ ;

C ₂ -C ₄ alkenyl substituted with 0-4 R ¹¹ ;

C ₂ -C ₄ alkynyl substituted with 0-4 R ¹¹ ;

a 5- or 6-membered heterocyclic ring containing from 1 to 4 heteroatoms selected from oxygen, nitrogen or sulfur;

when R ³² is attached to a saturated carbon atom, it may be =0 or =S;

R ³² may alternatively be a 3- or 4- carbon chain attached to adjacent carbons on the ring to form a fused 5- or 6-membered ring, said 5- or 6- membered ring being optionally substituted on the aliphatic carbons with halogen, C1-C4 alkyl, C1-C4 alkoxy, hydroxy, or -NR ¹³ R ¹⁴ ;

R ³² , when a substituent on nitrogen, is selected from one or more of the following:

phenyl, benzyl, phenethyl, hydroxy, C1-C4 hydroxyalkyl, C1-C4 alkoxy, C3 _. -C4 alkyl, C3-C6 cycloalkyl, C3-C6 cycloalkylmethyl, -CH2NR ¹³ R ¹⁴ , -NR ¹³ R ¹⁴ , C2-C6 alkoxyalkyl, C3.-C4 haloalkyl, C1-C4

alkoxycarbonyl, -C02H, C1-C4 alkylcarbonyloxy, C1-C4 alkylcarbonyl, -C (R ¹⁴ ) =N(OR ¹⁴ ) ;

R ³³ is selected from: H;

C1-C3 alkyl substituted at the C2 or C3 carbon with

-N(R ²⁰ )2, -SR ²⁰ , or -OR ²¹ ; or when taken together with R ^{3 a} , form =0, =S, or a ketal group;

R ^33a is selected from: H;

C1-C3 alkyl substituted at the C2 or C3 carbon with -N(R ²⁰ )2, -SR ²⁰ , or -OR ²¹ ; or, when taken together with R ³³ , form =0;

alternatively, R ³³ or R ³³ a can join with R ⁷ to form a fused 5- or 6- membered carbocyclic ring;

R ³⁴ is selected from: hydrogen;

OR ¹³ ;

SR ¹³ ; halogen; N(R ³⁸ ) (R ³⁹ )

C1-C6 alkyl substituted with 0-3 R ¹¹ ;

C1-C6 alkoxy substituted with 0-3 R ¹¹ ;

C1-C6 thioalkyl substituted with 0-3 R ¹¹ ;

R ³ ^ is selected from: hydrogen;

OR ¹³ ;

SR ¹³ ; halogen; N(R ³⁸ ) (R ³⁹ )

C1-C6 alkyl substituted with 0-3 R ¹¹ ;

C1-C6 alkoxy substituted with 0-3 R ¹¹ ; C1-C6 thioalkyl substituted with 0-3 R ¹¹ ;

R ³⁴ and R ³ ^ can be taken together to form a ketal ring, a 3- to 8-membered carbocyclic ring, or a 5- or 6-membered heterocyclic ring containing 1-3 heteroatoms independently selected from the group 0, N, or S, said ring substituted with 0-5 R ¹¹ ;

R ³ 6 is selected from:

C1-C6 alkyl substituted with 0-3 R ¹¹ ;

-COR ³⁷ ;

- _NR 38 _R 39 _;

-CN;

R ³⁷ is selected from: hydrogen;

C1-C6 alkyl substituted with 0-3 R ¹¹ ; hydroxyl; C1-C6 alkoxy substituted with 0-3 R ¹¹ ;

_ _NR 38 _R 39.

R ³⁸ and R ⁹ are independently selected from: hydrogen; Ci-Cβ alkyl substituted with 0-3 R ¹¹ ; or an amine protecting group;

,40 is selected from: H, C ₁ -C ₃ alkyl;

R ⁴¹ is selected from:

-C(=0)NR ¹³ R ¹⁴ ;

-C(=0)NR ¹³ NR ¹⁴ ;

-C (=0)C (R ¹¹ ) ₂ NR ¹³ R ¹⁴ ;

-C (=0) C (R ¹¹ ) ₂ NR ¹³ NR ¹⁴ ; -C (=0) C (R ^{ι :L} ) 2NR ¹³ Cθ2R ¹³ ;

-C(=0)H; -C ( =0) R~ ~ ;

-C(=0) -(C ₁ -C ₄ alkyl) -NR ¹ R ¹⁴ ; -C (=0) - (C ₁ -C ₄ alkyl) -NR ^l3 C0 R ¹³ ; 1-3 amino acids linked together via amide bonds, and linked to the N atom via the carboxy terminus;

provided that :

when R ⁴ and R ^4a are hydrogen and X is N-R ⁷ , at least one of the following is not hydrogen: R ⁷ , R ²² , R ²⁷ or R ²⁸ ;

when R ⁴ and R ^4a are hydrogen and X is S or 0, at least two of the following are not hydrogen: R ²² , R ²⁷ or R ²⁸ .

[2] Preferred compounds of Formula (I) are compounds described above, wherein:

W is selected from:

-N(R ²² )C (=Z)N(R ²³ )-; -0C(=Z)0-;

-N(R ²² )C(=Z)0-;

-C(R ²⁵ ) (R ²⁶ )C(=Z)C(R ²⁷ ) (R ²⁸ )-;

-N(R ²² )C(=Z)C(R ²⁷ ) (R ²⁸ )-;

-C(R ²⁵ ) (R ²⁶ )C(=Z)0-; -N(R ²² )C(=0)C(=0)N(R ²³ )-;

-N(R ²² )C(=S)C(=S)N(R ²³ )-;

-C(R ²⁵ ) (R ²⁶ )C(F2)C(R ²⁷ ) (R ²⁸ )-;

-C(R ²⁵ ) (R ²⁶ )N(CH3) (O)C(R ²⁷ ) (R ²⁸ )-;

-C(R ²⁵ ) (R ²⁶ )N(OR ²⁹ )C(R ²⁷ ) (R ²⁸ )-; -N(R ²² )S(=Z' )N(R ²³ )-;

-N(R ²² )S (=Z' ) 2N(R ²³ )-;

-20-

SUBSTITliTE SHEET (RULE 26)

-N(R ²² P (=0) (R ^24a ) (N(R ²³ )-; -C(R ²⁵ R ²⁶ )S =Z')C(R ²⁷ ) (R ²⁸ )-; -C(R ²⁵ R ²⁶ )S =Z' )2C(R ²⁷ ) (R ²⁸ )-; -C(R ²⁵ R ²⁶ )P =0) (R ^{2 a} )C(R ²⁷ ) (R ²⁸ )-; -C(R ²⁵ R ²⁶ )S =Z' )N(R ²³ )-; -C(R ²⁵ R ²⁶ )S =Z')2N(R ²³ )-; -C(R ²⁵ 26 )S =0)20-; -C(R ²⁵ R ²⁶ )P =0) (R ^24a )N(R ²³ >-; -C(R ²⁵ R ²⁶ )C F2)C(=0)N(R ²³ )-;

-C(R 25 R ²⁶ )C F2)S(=0)2N(R ²³ )-; -C(R 25 R ^2β )C R ³⁴ ) (R ³⁵ )C(R ²⁷ ) (R ²⁸ )-; -N(R ²² C(R 34 R ³⁵ )N(R ²³ )-;

-N(R 22 =C(R 36 N(R ²³ )-;

-N(R ²² P (R 24a N(R ²³ )-;

[3] The present invention includes compounds of Formula (I) described above of the Formula (la) :

(la)

wherein the groups and substituents are as defined above.

[4] The present invention includes compounds of Formula (I) described above of the Formula (la) :

da]

wherein :

X is S, 0 or N-R ⁷ ;

R ⁴ and R ⁷ are independently selected from the following groups :

hydrogen;

C1-C4 alkyl substituted with 0-3 R ¹¹ ; C3-C4 alkenyl substituted with 0-3 R ¹¹ ; C3-C4 alkynyl substituted with 0-3 R ¹¹ ;

R ^4a is hydrogen;

R ⁵ is selected from H; halogen; -N(R ⁰ )2; -SR ²⁰ ; -OR ²⁰ ; or C1-C3 alkyl substituted with 0-3 -N(R ²⁰ )2, -SR ²⁰ , or -OR ²⁰ ;

R^ ^a is selected from hydrogen or fluoro;

R5 and R ^5a can alternatively join to form =0, =S, or a ketal ring;

R ²⁰ and R ²¹ are independently selected from:

hydrogen;

Cι~C _ alkylcarbonyl;

Ci-Cβ alkoxycarbonyl; benzoyl; or any group that, when administered to a mammalian subject, cleaves to form a free hydroxyl, amine or sulfhydryl;

R ¹¹ is selected from one or more of the following:

keto; halogen; cyano; -CH2NR ¹³ R ¹⁴ ; -NR ¹³ R ¹⁴ ; -C02R ¹³ ; -0C(=0)R ¹³ ; -OR ¹³ ; C2~C6 alkoxyalkyl; -S(0) _m R ¹³ ; C2-C4 alkenyl;

C1-C4 alkyl substituted with 0-2 R ¹² ,

a C3-C14 carbocyclic residue substituted with 0-3 R ¹² ;

aryl (C ₁ -C ₃ alkyl) substituted with 0-2 R ¹² ;

aryl substituted with 0-3 R ¹² ; or

a 5- to 10-membered heterocyclic ring system containing 1 to 4 heteroatoms independently selected from oxygen, nitrogen or sulfur, said heterocyclic ring system being substituted with 0-2 R ² ;

R ¹² , when a substituent on carbon, is selected from one or more of the following:

phenyl, benzyl, phenethyl, phenoxy, benzyloxy, halogen, hydroxy, nitro, cyano, C1-C4 alkyl, C3-C6 cycloalkyl, C3-C6 cycloalkylmethyl, C7-C10 arylalkyl, C1-C4 alkoxy, -CO2H, hydroxamic acid, hydrazide, oxime, boronic acid, sulfonamide, formyl, C3-C6 cycloalkoxy, -OR ¹³ , C1-C4 alkyl substituted with

-NR ¹³ R ¹⁴ , -NR ¹³ R ¹⁴ , C2-C6 alkoxyalkyl, C1-C4 hydroxyalkyl, methylenedioxy, ethylenedioxy, C1 _. -C4 haloalkyl, C1-C4 haloalkoxy, C1-C4 alkoxycarbonyl, C1-C4 alkylcarbonyloxy, C1-C4 alkylcarbonyl, C1-C4 alkylcarbonylamino, -S(0) _m R ¹³ , -Sθ2NR ¹³ R ¹⁴ ,

-NHSO2R ¹⁴ , -OCH2CO2H, 2- (1-morpholino)ethoxy; or

a 5- or 6-membered heterocyclic ring containing from 1 to 4 heteroatoms independently selected from oxygen, nitrogen or sulfur;

when R ¹² is attached to a saturated carbon atom, it may be carbonyl or thiocarbonyl;

or R ¹² may alternatively be a 3- or 4- carbon chain attached to adjacent carbons on the ring to form a fused 5- or 6-membered ring, said 5- or 6- membered ring being optionally substituted on the aliphatic carbons with halogen, C1-C4 alkyl, C1-C4 alkoxy, hydroxy, or -NR ¹³ R ¹⁴ ;

R ¹² , when a substituent on nitrogen, is selected from one or more of the following:

phenyl, benzyl, phenethyl, hydroxy, C1-C4 hydroxyalkyl, C1-C4 alkoxy, C1-C4 alkyl, C3-C6 cycloalkyl, C3-C6 cycloalkylmethyl, -CH2NR ¹³ R ¹⁴ , -NR ¹³ R ¹⁴ , C2-C6 alkoxyalkyl, C1-C4 haloalkyl, C1-C4 alkoxycarbonyl, -CO2H, C1-C4 alkylcarbonyloxy, C1-C4 alkylcarbonyl;

R ¹³ is H, C1-C6 alkyl, or C3-C6 alkoxyalkyl; C ₂ -C ₄ alkenyl, phenyl, or benzyl;

R ¹⁴ is OH, H, CF3, C1-C4 alkyl, C ₁ -C ₄ alkoxy, NH ₂ , C ₂ -C ₄ alkenyl, phenyl or benzyl;

R ¹³ and R ¹⁴ can alternatively join to form -(CH2)4~,

-(CH2)5~, -CH2CH2N(R ¹⁵ )CH2CH2-, or -CH2CH2OCH2CH2-;

R ¹⁵ is H or CH3;

m is 0, 1 or 2;

Z is 0, S, N-CN, N-OH, N-OCH3;

R ²² is independently selected from the following:

hydrogen;

C1-C8 alkyl substituted with 0-3 R ³¹ ; C3-C8 alkenyl substituted with 0-3 R ³¹ ; C3-C8 alkynyl substituted with 0-3 R ³¹ ; C3-C6 cycloalkyl substituted with 0-3 R ³¹ ;

R ²⁷ is selected from the following:

hydrogen;

C1-C8 alkyl substituted with 0-3 R ³¹ ; C2-C8 alkenyl substituted with 0-3 R ³¹ ; C3-C8 alkynyl substituted with 0-3 R ³¹ ;

R ²⁸ is hydrogen;

R ³ is selected from one or more of the following:

keto, halogen, cyano, -CH2NR ¹³ R ¹⁴ , -NR ^l3 R ¹⁴ ,

-CO2R ¹³ , -OC(=0)R ¹³ , -OR ¹³ , C2-C6 alkoxyalkyl, -S(0) _m R ¹³ , C1-C4 alkyl, C2-C4 alkenyl, C3-C6 cycloalkyl, C3-C10 cycloalkylmethyl, benzyl, phenethyl, phenoxy, benzyloxy, nitro, C7-C10 arylalkyl, hydroxamic acid, hydrazide, oxime, boronic acid, sulfonamide, formyl, C3-C6

cycloalkoxy, C ₁ -C ₄ alkyl substituted with -NR ¹³ R ¹⁴ , C1-C4 hydroxyalkyl, methylenedioxy, ethylenedioxy,

C1-C4 haloalkyl, C1-C4 haloalkoxy, C1-C4 alkoxycarbonyl, C1-C4 alkylcarbonyloxy, C1-C4 alkylcarbonyl, C1-C4 alkylcarbonylamino,

-OCH2CO2H, 2- (1-morpholino)ethoxy, -C (R ¹⁴ )=N(OR ¹⁴ ) ; or;

a C3-C14 saturated or partially unsaturated carbocyclic residue substituted with 0-5 R ³² ;

aryl substituted with 0-5 R ³² ; or

a 5- to 10-membered heterocyclic ring system containing 1 to 4 heteroatoms independently selected from oxygen, nitrogen or sulfur, said heterocyclic ring system being substituted with 0-2 R ³² ;

R ³² , when a substituent on carbon, is selected from one or more of the following:

phenethyl, phenoxy, C3-C10 cycloalkyl, C3-C6 cycloalkylmethyl, C7-C10 arylalkyl, hydrazide, oxime, boronic acid, C2 ^_ C6 alkoxyalkyl, methylenedioxy, ethylenedioxy, C1-C4 alkylcarbonyloxy, -NHSO2R ¹⁴ , benzyloxy, halogen, 2- (1-morpholino) ethoxy, -CO2R ¹³ , hydroxamic acid, -CONR ¹³ NR ¹³ R ¹⁴ , cyano, boronic acid, sulfonamide, -CHO, C ₃ -C6 cycloalkoxy, -NR ¹³ R ¹⁴ , -C (R ¹⁴ )=N (OR ¹⁴ ) , N0 ₂ , -OR ¹³ , -NR ⁴⁰ R ⁴¹ , -SO _m R ¹³ , -SO _m NR ¹³ R ¹⁴ , -C(=0)NR ^l3 R ¹⁴ , -OC (=0)NR ¹³ R ¹⁴ , -C (=0) R- ~ , -OC(=0)R ⁿ , -OCO2R ¹³ , phenyl, -C(=0)NR ¹³ -(Cι-C ₄ alkyl)-NR ¹³ R ¹⁴ , -C (=0)NR ⁴⁰ R ⁴¹ ,

C1-C ₄ haloalkyl, C ₁ -C ₄ haloalkoxy, C ₂ -C ₄ haloalkenyl, C ₁ -C ₄ haloalkynyl, or

-C (=0)NR ¹³ C (R ¹¹ ) ₂ NR ¹³ R ¹⁴ ; -C (=0)NR ¹³ C (R ¹¹ ) ₂ NR ¹³ NR ¹⁴ ; -C(=0)NR ¹³ C(R ^ι:L )2NR ¹³ Cθ2R ¹³ ;

-C(=0)NR ¹³ -(Cι-C ₄ alkyl)-NR ¹³ C0 R ¹³ ; or

-C (=0) C (R ¹¹ ) NR ¹³ R ¹⁴ ; -C(=0) C (R ¹¹ ) ₂ NR ¹³ NR ¹⁴ ; -C(=0)C(R ^ι:L )2NR ¹³ Cθ2R ¹³ ; -C (=0) - (C1-C4 alkyl) -NR ¹³ R ¹⁴ ; -C(=0)-(Cι-C ₄ alkyl)-NR ¹³ Cθ2R ¹³ ; or

C1-C4 alkoxy substituted with 0-3 groups selected from: R ¹¹ , C3-C6 cycloalkyl, -CO ₂ R ¹³ , -C (=0) NR ¹³ R ¹⁴ , -NR ¹³ R ¹⁴ or OH;

C ₁ -C ₄ alkyl substituted with 0-3 groups selected from: R ¹¹ , =NR ¹⁴ , =NNR ¹³ C (=0)NR ¹³ R ¹⁴ or -NR ¹³ R ¹⁴ ;

C2-C ₄ alkenyl substituted with 0-3 R ¹¹ ;

C2-C ₄ alkynyl substituted with 0-3 R ¹¹ ;

a 5- or 6-membered heterocyclic ring containing from 1 to 4 heteroatoms independently selected from oxygen, nitrogen or sulfur;

when R ³² is attached to a saturated carbon atom, it may be =0 or =S;

R ³² may alternatively be a 3- or 4- carbon chain attached to adjacent carbons on the ring to form a fused 5- or 6-membered ring, said 5- or 6- membered ring being optionally substituted on the aliphatic carbons with halogen, C1-C4 alkyl, C1-C4 alkoxy, hydroxy, or -NR ¹³ R ¹⁴ ;

R ³² , when a substituent on nitrogen, is selected from one or more of the following:

phenyl, benzyl, phenethyl, hydroxy, C1 _. -C4 hydroxyalkyl, C1-C4 alkoxy, C1 _. -C4 alkyl, C3-C6 cycloalkyl, C3-C6 cycloalkylmethyl, -CH2NR ¹³ R ¹⁴ , -NR ¹³ R ¹⁴ , C2-C6 alkoxyalkyl, C1.-C4 haloalkyl, C1-C4 alkoxycarbonyl, -CO2H, C1-C4 alkylcarbonyloxy, C1-C4 alkylcarbonyl, -C (R ¹⁴ ) =N (OR ¹⁴ ) ;

R ³³ is selected from: H;

C1-C3 alkyl substituted at the C2 or C3 carbon with halogen, -N(R ⁰ )2, -SR ²⁰ , or -OR ²¹ ; or, when taken together with R ^{3 a} , form a =0 group;

R-" and the -OR ²¹ group of R ³³ can alternatively join to form: -OS (=0)0-; -0C(=0)0-; -OCH ₂ O-; -OC(=S)0-; -OC(CH ₃ ) ₂ 0-; -OC (OCH ₃ ) (CH ₂ CH ₂ CH ₃ ) 0-; or any group that, when administered to a mammalian subject, cleaves to form a free dihydroxyl;

33a _ _s pj _{or ma} y b _e taken together with R ³³ form =0;

R ⁴⁰ is selected from: H, C ₁ -C ₃ alkyl;

R ⁴¹ is selected from:

-C(=0)NR ¹³ R ¹⁴ ; -C(=0)NR ¹³ NR ¹⁴ ;

-C (=0)C (R ^1:L ) ₂ NR ¹³ R ¹⁴ ;

-C (=0) C (R ¹¹ ) ₂ NR ¹³ NR ¹⁴ ;

-C (=0) C (R ¹¹ ) ₂ NR ¹³ C0 ₂ R ¹³ ;

-C(=0)H; -C(=0)R ¹¹ ;

-C(=0)- (C ₁ -C ₄ alkyl) -NR ¹³ R ¹⁴ ;

-28-

SUBSfTUTESHEET(RULE26)

-C (=0)- (C1-C ₄ alkyl)-NR ¹³ Cθ2R ¹³ ;

1-3 amino acids linked together via amide bonds, and linked to the N atom via the carboxy terminus of the amino acid;

provided that :

when R ⁴ and R ^4a are hydrogen and X is N-R ⁷ , at least one of the following is not hydrogen: R ⁷ , R ²² , R ²⁷ or R ²⁸ ;

when R ⁴ and R ^4a are hydrogen and X is S or 0, at least two of the following are not hydrogen: R ²² , R ²⁷ or R ²⁸ .

[5] Preferred compounds of Formula (la) described above, wherein:

R ⁴ and R ⁷ are independently selected from the following groups :

hydrogen; C1-C4 alkyl substituted with 0-3 R ¹¹ ;

C3-C4 alkenyl substituted with 0-3 R ¹¹ ;

R ⁵ is -OR ²⁰ ;

R ^5a is H;

R ²⁰ is H or any group that, when administered to a mammalian subject, cleaves to form a free hydroxyl;

R is selected from one or more of the following:

keto; halogen; -CH2NR ¹³ R ¹⁴ ; -NR ¹³ R ¹⁴ ; -OR ¹³ ; C2-C alkoxyalkyl; C2-C4 alkenyl;

^c 3~ ^c 10 cycloalkyl substituted with 0-2 R ¹² ; C1-C4 alkyl substituted with 0-2 R ¹² ,

aryl (C _3. -C ₃ alkyl) substituted with 0-2 R ¹² ; aryl substituted with 0-3 R ¹² ; or

a 5- to 10-membered heterocyclic ring system containing 1 to 4 heteroatoms independently selected from oxygen, nitrogen or sulfur, said heterocyclic ring system being substituted with 0-2 R ¹² ;

R ¹² , when a substituent on carbon, is selected from one or more of the following:

phenyl, benzyl, phenethyl, phenoxy, benzyloxy, halogen, C1 _. -C4 alkyl, C7-C10 arylalkyl, C1-C4 alkoxy, -CO2H, hydroxamic acid, hydrazide, oxime, boronic acid, sulfonamide, formyl, C3-C6 cycloalkoxy, -OR ¹³ , C1-C4 alkyl substituted with -NR ¹³ R ¹⁴ , -NR ¹³ R ¹⁴ , methylenedioxy, C1-C4 haloalkyl, C1 _. -C4 alkylcarbonyl, C1-C4 alkylcarbonylamino, -OH, hydroxymethyl; or

a 5- or 6-membered heterocyclic ring containing from 1 to 4 heteroatoms selected from oxygen, nitrogen or sulfur;

R ² , when a substituent on nitrogen, is benzyl or methyl;

R ¹³ is H, C1-C4 alkyl, or C3-C6 alkoxyalkyl, C ₂ -C alkenyl, or benzyl;

R ¹⁴ is OH, H, CF ₃ , C1-C4 alkyl, C^C alkoxy, NH ₂ , C ₂ -C ₄ alkenyl, or benzyl;

R ¹³ and R ¹⁴ can alternatively join to form -(CH2)4~,

-(CH2)5~, -CH2CH2N(R ¹⁵ )CH2CH2~, or -CH2CH2OCH2CH2-;

Z is 0, S, or N-CN;

R ²² is independently selected from the following:

hydrogen;

C3 _. -C8 alkyl substituted with 0-3 R ³¹ ; C2-C6 alkenyl substituted with 0-3 R ³¹ ; C2-C alkynyl substituted with 0-3 R ³¹ ;

R ²⁷ is selected from the following:

hydrogen; C1-C4 alkyl substituted with 0-3 R ³¹ ;

C2-C4 alkenyl substituted with 0-3 R ³¹ ;

R ³ is selected from one or more of the following:

keto, halogen, -CH2NR ¹³ R ¹⁴ , -NR ¹³ R ¹⁴ , -OR ¹³ , C2-C4 alkoxyalkyl, C1-C4 alkyl, C2-C alkenyl, C3-C10 cycloalkyl, -C (R ¹⁴ )=N (OR ¹⁴ ) , -C0 ₂ R ¹³ , -S(0) _m R ¹³ ;

aryl substituted with 0-5 R ³² ; or

a 5- to 10-membered heterocyclic ring system containing 1 to 4 heteroatoms independently selected from oxygen, nitrogen or sulfur, said heterocyclic ring system being substituted with 0-2 R ³² ;

R ^, when a substituent on carbon, is selected from one or more of the following:

phenethyl, phenoxy, C3-C10 cycloalkyl, C3-C6 cycloalkylmethyl, C7-C10 arylalkyl, hydrazide, oxime, boronic acid, C2-C6 alkoxyalkyl, methylenedioxy, ethylenedioxy, C1-C4 alkylcarbonyloxy, -NHSO2R ¹⁴ , benzyloxy, halogen, 2- (1-morpholino) ethoxy, -CO2R ¹³ , hydroxamic acid, -CONR ¹³ NR ¹³ R ¹⁴ , cyano, boronic acid, sulfonamide, -CHO, C3-C ₆ cycloalkoxy, -NR ¹³ R ¹⁴ ,

-C(R ¹ )=N(OR ¹⁴ ) , NO ₂ , -OR ¹³ , -NR ⁴⁰ R ⁴¹ , -SO _m R ¹³ ,

-SO _m NR ¹³ R ¹⁴ , -C (=0)NR ¹³ R ¹⁴ , -OC (=0)NR ¹³ R ¹⁴ ,

-C(=0)R ^1:L , -OC(=0)R , -OCO2R ¹³ , phenyl, -C(=0)NR ¹³ -(Cι-C ₄ alkyl) -NR ¹³ R ¹⁴ , -C (=0)NR ⁴⁰ R ⁴¹ ,

C1-C4 haloalkyl, C ₁ -C ₄ haloalkoxy, C ₂ -C ₄ haloalkenyl,

C ₁ -C4 haloalkynyl, or

C1-C4 alkoxy substituted with 0-3 groups selected from: R ¹¹ , C ₃ -C ₆ cycloalkyl, -C0 ₂ R ¹³ , -C (=0)NR ¹³ R ¹⁴ , -NR ¹³ R ¹⁴ or OH;

C1-C ₄ alkyl substituted with 0-3 groups selected from: R ¹¹ , =NR ¹⁴ , =NNR ¹³ C (=0) NR ¹³ R ¹⁴ or -NR ¹³ R ¹⁴ ;

C ₂ -C ₄ alkenyl substituted with 0-3 R ¹¹ ;

C ₂ -C ₄ alkynyl substituted with 0-3 R ¹¹ ;

a 5- or 6-membered heterocyclic ring containing from 1 to 4 heteroatoms independently selected from oxygen, nitrogen or sulfur;

R ³² , when a substituent on nitrogen, is benzyl or methyl;

-32-

SUBST1TUTE SHEET (RULE 26)

R ³³ is hydrogen or, when taken together with R ³³ , form a =0 group;

provided that :

when R ⁴ is hydrogen and X is N-R ⁷ , at least one of the following is not hydrogen: R ⁷ , R ²² , or R ²⁷ ;

when R ⁴ is hydrogen and X is S or 0, at least two of the following are not hydrogen: R ²² or R ²⁷ .

[6] More preferred are compounds of Formula (la) described above, wherein:

R ⁴ and R ⁷ are independently selected from the following groups :

hydrogen;

C1-C3 alkyl substituted with 0-3 R ¹¹ ;

R ¹¹ is selected from one or more of the following:

halogen, -OR ¹³ ;

C3-C10 cycloalkyl substituted with 0-2 R ¹² ; C1-C4 alkyl substituted with 0-2 R ¹² , aryl (C ₁ -C3 alkyl) substituted with 0-2 R ¹² ; aryl substituted with 0-2 R ¹² ; or a heterocyclic ring system selected from pyridyl, pyrimidinyl, triazinyl, furanyl, thienyl, pyrrolyl, pyrazolyl, imidazolyl, tetrazolyl, benzofuranyl, indolyl, quinolinyl, isoquinolinyl, oxazolidinyl, said heterocyclic ring system being substituted with 0-2 R ¹² ;;

R ¹² , when a substituent on carbon, is selected from one or more of the following:

benzyloxy, halogen, methyl, C1-C4 alkoxy, CF3, 2- (1-morpolino)ethoxy, -CO2H, hydroxamic acid, hydrazide, oxime, cyano, boronic acid, sulfonamide, formyl, C3-C6 cycloalkoxy, C1-C4 alkyl substituted with -NR ¹³ R ¹⁴ , -NR ¹³ R ¹⁴ , -OH, hydroxymethyl; or

R ¹² , when a substituent on nitrogen, is methyl;

R ¹³ is H, C ₁ -C ₄ alkyl, C ₂ -C ₄ alkenyl, or benzyl;

Z is 0 or N-CN;

R ²⁷ is selected from the following:

hydrogen;

C1-C4 alkyl substituted with 0-3 R ³¹ ; C3-C4 alkenyl substituted with 0-3 R ³¹ ;

R ³¹ is selected from one or more of the following:

halogen, -OR ¹³ , C1-C4 alkyl, C3-C10 cycloalkyl, -C(R ¹⁴ )=N(OR ¹⁴ ) , -C0 ₂ R ¹³ , -S(0) _m R ¹³ ;

aryl substituted with 0-5 R ³² ; or

a heterocyclic ring system selected from pyridyl, pyrimidinyl, triazinyl, furanyl, thienyl, pyrrolyl, pyrazolyl, imidazolyl, tetrazolyl, benzofuranyl, indolyl, quinolinyl, isoquinolinyl, oxazolidinyl, said heterocyclic ring being substituted with 0-2

R ³² ;

R ³² , when a substituent on carbon, is selected from one or more of the following:

benzyloxy, halogen, 2- (1-morpholino)ethoxy, -C02R ¹³ , hydroxamic acid, -CONR ¹³ NR ¹³ R ¹⁴ , cyano, boronic acid, sulfonamide, formyl, C3-C ₁ 0 cycloalkoxy, -NR ¹³ R ¹⁴ , -C(R ¹⁴ )=N (OR ¹⁴ ) , NO2, -OR ¹³ , NR ⁴⁰ R ⁴¹ , -SOmR ¹³ , -SO _m NR ¹³ R ¹⁴ , -C (=0)NR ¹³ R ¹⁴ , -OC(=0)NR ¹³ R ¹⁴ , -C(=0)R ^1:L , -OC(=0)R ⁿ , -OCO2R ¹³ , phenyl, -C (=0)NR ¹³ - (C1-C ₄ alkyl) -NR ¹³ R ¹⁴ ,

-C(=O)NR ⁴⁰ R ⁴¹ , C ₁ -C ₄ haloalkyl, C ₁ -C ₄ haloalkoxy, C ₂ -C ₄ haloalkenyl, C ₁ -C ₄ haloalkynyl, -C (=0) NR ¹³ R ¹⁴ ; -C (=0) C (R ¹¹ ) ₂ NR ¹³ R ¹⁴ ; -C (=0) C (R ¹¹ ) ₂ NR ¹³ NR ¹⁴ ; -C(=0)C(R ^1:L ) ₂ NR ¹³ C0 ₂ R ¹³ ; -C(=0)- (C ₁ -C4 alkyl) -NR ¹³ R ¹⁴ ; -C(=0)-(Cι-C ₄ alkyl) -NR ¹³ C0 R ¹³ ; or

C1-C4 alkoxy substituted with 0-3 groups selected from: R ¹¹ , C ₃ -C ₆ cycloalkyl, -C (=0) NR ¹³ R ¹⁴ , -NR ¹³ R ¹⁴ or OH;

C ₁ -C ₄ alkyl substituted with 0-3 groups selected from: R ¹¹ , =NR ¹⁴ , =NNR ¹³ C (=0)NR ¹³ R ¹⁴ or -NR ¹³ R ¹⁴ ;

C ₂ -C ₄ alkenyl substituted with 0-3 R ¹¹ ;

C ₂ -C ₄ alkynyl substituted with 0-3 R ¹¹ ;

a 5- or 6-membered heterocyclic ring containing from 1 to 4 heteroatoms independently selected from oxygen, nitrogen or sulfur;

R ³² , when a substituent on nitrogen, is methyl.

[7] Further preferred compounds of the present invention are compounds of Formula (la) described above, wherein :

R ⁴ and R ⁷ are selected from benzyl, fluorobenzyl, pyrrolylmethyl, methoxybenzyl, isobutyl, nitrobenzyl or aminobenzyl;

R ^b is -OH;

R ¹³ is H, C ₁ -C ₄ alkyl, C ₂ -C alkenyl, or benzyl;

R ¹⁴ is OH, H, CF ₃ , C ₁ -C ₄ alkyl, C ₁ -C ₄ alkoxy, NH ₂ , C ₂ -C ₄ alkenyl, or benzyl;

R ¹³ and R ¹⁴ can alternatively join to form -(CH2)4~,

-(CH2)5~, -CH2CH2N(R ¹⁵ )CH2CH2", or -CH2CH2OCH2CH2-;

R ²² is independently selected from the following:

hydrogen;

C1-C8 alkyl substituted with 0-2 R ³¹ ; C2-C6 alkenyl substituted with 0-2 R ³¹ ; C2-C alkynyl substituted with 0-2 R ³¹ ;

R ²⁷ is H or C1-C4 alkyl substituted with 0-3 R ³¹ ;

R ³² , when a substituent on carbon, is selected from one or more of the following:

-CONH ₂ , -C0 ₂ H, -CHO, -CH ₂ NH0H, -CH ₂ NR ¹³ R ¹⁴ , -NR ¹³ R ¹⁴ , hydroxy, hydroxymethyl, -C (R ¹⁴ )=N (OR ¹⁴ ) , halogen, methoxy, methyl, nitro, cyano, allyloxy, -CO2CH3, -NHCHO, -NHCOCH3, -OCO2CH3, -CH=NCH2CH2θH,

-OCONHCH2C6H5, -OCONHCH3, oxazolidinyl, -C=C-CH2θH,

-COCH3, hydroxyethyl, C ₁ -C ₃ alkyl (said alkyl substituted with 0-4 halogen, or OH), tetrazolyl, -OCH2CONH2, -CONHNH2, -CH=NNHCONH2, -CONHOCH3, -CH2CH (OH)CH2θH, adamantamido, hydroxyethoxy, dihydroxyethyl, -C(NH2)=NH, -CONHCH3, -B(OH)2, benzyloxy, -CONHCH2CH3, -CON (CH2CH3) 2, methylthio, -SO2CH3- -NHCONH2, -NHCONHCH3, -NHCOCH2N(CH3)2, -NHCOCH2NHCH3, -NHCOCH2NHCO2CH2C6H5, -NHCOCH2NH2, -NHCOCH(CH3)NHCO2CH2C6H5, -NHCOCH (CH2C6H5)NHC02CH2C6H5, -NHCOCH (CH3)NH2,

-NHCOCH (CH2C6H5)NH2, -CO2CH2CH3, -CONHCH2CH2CH3, -CONHCH(CH3)2, -CH2"imidazole, -COC(CH3)3, -CH(OH)CF3, -CO-imidazole, -COCF3, -COCH2CH3, -COCH2CH2CH3, pyrazolyl, -SO2NH2, -C (CH2CH3) =N (OH) or -C (CF3) =N (OH) , phenyl, acetoxy, hydroxyamino,

-N(CH ₃ ) (CHO) , cyclopropylmethoxy, -CONR ¹³ R ¹⁴ , -CONHOH, (diethylaminoethyl) aminocarbonyl, (N-ethyl,N-methylaminoethyl) aminocarbonyl, (4-methylpiperazinylethyl)aminocarbonyl, pyrrolidinylethyl) aminocarbonyl,

(piperidinylethyl) aminocarbonyl, -NHCOCH ₂ NHCH3, N- (2- (4-morpholino) ethyl) aminocarbonyl, N- (2- (N, N- dimethylamino) ethyl) aminocarbonyl .

[8] More further preferred compounds of Formula (la) described above, wherein:

X is N-R ⁷ ;

R ⁴ and R ⁷ are benzyl;

R ^4a is hydrogen;

R ⁵ is -OH;

Z is 0 or N-CN;

R ²⁸ is hydrogen;

R ²² and R ²⁷ are independently selected from the group consisting of:

hydrogen, allyl, methyl, ethyl, propyl, cyclopropylmethyl, n-butyl, i-butyl, CH2CH=C (CH3) 2, pyridinylmethyl, methallyl, n-pentyl, i-pentyl, hexyl, benzyl, isoprenyl, propargyl, picolinyl, methoxyethyl, cyclohexylmethyl, dimethyl-butyl, ethoxyethyl, met yl-oxazolinylmethyl, naphthylmethyl, methyloxazolinylmethyl, vinyloxyethyl, pentafluorobenzyl, quinolinylmethyl, carboxybenzyl, chloro-thienyl, benzyloxybenzyl, phenylbenzyl, adamantylethyl, cyclopropylmethoxybenzyl, methoxybenzyl, methylbenzyl, ethoxybenzyl, hydroxybenzyl, hydroxymethylbenzyl, aminobenzyl, formylbenzyl, cyanobenzyl, cinnamyl, allyloxybenzyl, fluorobenzyl, difluorobenzyl, chlorobenzyl, chloromethylbenzyl, fluoromethylbenzyl, iodobenzyl, bromobenzyl, cyclobutylmethyl, formaldoximebenzyl, cyclopentylmethyl, nitrobenzyl, (H ₂ NC (=0) ) -benzyl, carbomethoxybenzyl, carboethoxybenzyl, tetrazolylbenzyl, and dimethylallyl, aminomethylbenzyl, (O-benzyl-formaldoxime)benzyl, (O-methyl-formaldoxime)benzyl, (CH3O2CO) -benzyl,

(HOCH2CH2N=CH) -benzyl, N-benzylaminocarbonylbenzyl, N-methylaminobenzyl, N-ethylaminobenzyl, N-ethylaminomethylbenzyl, acetylbenzyl, acetoxybenzyl, N-hydroxylaminobenzyl, phenylmethyl- boronic acid, N-hydroxylaminomethylbenzyl, (hydroxyl) ethylbenzyl, (CH3C (=N0H) ) -benzyl,

(H2NNHC(=0) ) -benzyl, (H2NC (=0)NHN=CH)-benzyl, (CH3ONHC (=0) )-benzyl, (HONHC (=0) ) -benzyl, (CH3NHC (=0) ) -benzyl,

N,N-dimethylaminocarbonylbenzyl, (HOCH2CH (OH) CH2O) - benzyl, hydroxyethoxybenzyl (oxazolidinyl) -benzyl, (hydroxyl) hexyl, hexenyl, (hydroxy) octyl, (hydroxyl)pentyl, (carboxy)pentyl, (carbomethoxy)pentyl, (methylthio)benzyl, (methylsulfonyl)benzyl, N,N-dimethylaminomethylbenzyl,

N-methylaminomethylbenzyl, glycylaminobenzyl, N,N-dimethylglycylaminobenzyl, alanylaminobenzyl, (N-phenylmethoxycarbonyl) alanylaminobenzyl, phenylalanylaminobenzyl, (N-phenylmethoxycarbonyl) phenylalanylaminobenzyl, (CH3CH2NHC (=0) ) -benzyl, N,N-diethylaminocarbonylbenzyl, N-ethylaminocarbonylbenzyl, N-propylaminocarbonylbenzyl, N,N-diisopropylaminocarbonylbenzyl, N, N-di-n- propylaminocarbonylbenzyl, (hydroxypropynyl)benzyl, (imidazolyl-C (=0) ) -benzyl, trifluoroacetylbenzyl, (pyrazolyl) enzyl, (H2NSO2) -benzyl, dihydroxyethylbenzyl, (MeHNC (=0)NH) -benzyl, (H2NC (=0)NH) -benzyl, (HC (=0)NH)-benzyl, methanesulfonylpentyl, methoxypentyl, N-formyl-N- methylaminobenzyl, acetylaminobenzyl, propionylbenzyl, butyrylbenzyl, (CH3CH2C (=N0H) ) - benzyl, (trifluorohydroxyethy1)benzyl, (CF3C (=NOH) ) -benzyl, (N-methylglycyl) aminobenzyl, ( (4-morpholino)ethyl)aminocarbonylbenzyl,

(N,N-dimethylaminoethyl)aminocarbonylbenzyl, (N,N-diethylaminoethyl) aminocarbonylbenzyl, (4-methylpiperazin-l-ylethyl) aminocarbonylbenzyl, (benzyl-NHC (=0) 0)benzyl, (CH3NHC (=0) 0)benzyl, (NH ₂ C(=0)CH ₂ 0)benzyl, (NH ₂ C (=NH) )benzyl,

( (N-phenylmethoxycarbonyl) glycylamino) enzyl,

(imidazolylmethyl)benzyl, ( (CH ₃ ) ₃ C-C (=0) )benzyl, (N-methyl-N-ethylaminoethyl) aminocarbonylbenzyl, (pyrrolidinylethyl)aminocarbonylbenzyl, (piperidinylethyl) aminocarbonylbenzyl .

[9] Preferred compounds of the invention of Formula (la) are compounds of Formula (lb) :

or a pharmaceutically acceptable salt or prodrug form thereof wherein:

X is S, O or N-R ⁷ ;

R ⁴ and R ⁷ are independently selected from the following groups :

hydrogen;

C1-C4 alkyl substituted with 0-3 R ¹¹ ;

C3-C4 alkenyl substituted with 0-3 R ¹¹ ;

R ¹ is selected from one or more of the following:

keto; halogen; cyano; -CH2NR ¹³ R ¹⁴ ; -NR ^l3 R ¹⁴ ; -CO2R ¹³ ; -OC (=0)R ¹³ ; -OR ¹³ ; C2-C6 alkoxyalkyl; -S(0) _m R ¹³ ; C2-C4 alkenyl;

a C5-C14 carbocyclic residue substituted with 0-3 R ¹² ;

aryl (C ₁ -C ₃ alkyl) substituted with 0-2 R ¹² ;

aryl substituted with 0-3 R ¹² ; or

a 5- to 10-membered heterocyclic ring system containing 1 to 4 heteroatoms independently selected from oxygen, nitrogen or sulfur, said heterocyclic ring system being substituted with 0-2 R ¹² ;

R ¹² , when a substituent on carbon, is selected from one or more of the following:

phenyl, benzyl, phenethyl, phenoxy, benzyloxy, halogen, C1-C4 alkyl, C7-C10 arylalkyl, C1 _. -C4 alkoxy, -CO2H, hydroxamic acid, hydrazide, oxime, boronic acid, sulfonamide, formyl, C3-C6 cycloalkoxy, -OR ¹³ , C1-C4 alkyl substituted with -NR ¹³ R ¹⁴ , -NR ¹³ R ¹⁴ , methylenedioxy, C1-C4 haloalkyl, C1-C4 alkylcarbonyl, C1-C4 alkylcarbonylamino, -OH, hydroxymethyl; or

a 5- or 6-membered heterocyclic ring containing from 1 to 4 heteroatoms selected from oxygen, nitrogen or sulfur;

R ² , when a substituent on nitrogen, is benzyl or methyl;

R ¹³ is H, C1-C4 alkyl, or C3-C6 alkoxyalkyl, C ₂ -C ₄ alkenyl, or benzyl;

R ¹⁴ is OH, H, CF ₃ , or C1-C4 alkyl, C ₁ -C ₄ alkoxy, NH ₂ , C ₂ -C alkenyl, or benzyl;

R ¹³ and R ¹⁴ can alternatively join to form -(CH2)4~,

-(CH2)5-, -CH2CH2N(R ¹⁵ )CH2CH2-, or -CH2CH2OCH2CH2-;

R ¹⁵ is H or CH3;

R ²² is independently selected from the following:

hydrogen;

C1-C8 alkyl substituted with 0-3 R ³¹ ; C2-C6 alkenyl substituted with 0-3 R ³¹ ; C2-C4 alkynyl substituted with 0-1 R ³¹ ;

R ²⁷ is selected from the following:

hydrogen;

C1-C4 alkyl substituted with 0-3 R ³¹ ; C2-C4 alkenyl substituted with 0-3 R ³¹ ;

R ³¹ is selected from one or more of the following:

keto, halogen, -CH2NR ¹³ R ¹⁴ , -NR ¹³ R ¹⁴ , -OR ¹³ , C2-C alkoxyalkyl, C1-C4 alkyl, C2-C4 alkenyl, C3-C10 cycloalkyl, -C (R ¹⁴ ) = (OR ¹⁴ ) , -CO ₂ R ¹³ , -S(0) _m R ¹³ ;;

aryl substituted with 0-5 R ³² ; or

a 5- to 10-membered heterocyclic ring system containing 1 to 4 heteroatoms independently selected from oxygen, nitrogen or sulfur, said heterocyclic ring system being substituted with 0-2 R ³² ;

R ³² , when a substituent on carbon, is selected from one or more of the following:

phenethyl, phenoxy, C3-C6 cycloalkyl, C3-C6 cycloalkylmethyl, C7-C10 arylalkyl, hydrazide, oxime, boronic acid, C2-C6 alkoxyalkyl, methylenedioxy, ethylenedioxy, C1-C4 alkylcarbonyloxy, -NHSO2R ¹⁴ , benzyloxy, halogen, 2- (1-morpholino) ethoxy, -CO2R ¹³ , hydroxamic acid, -CONR ¹³ NR ¹ R ¹⁴ , cyano, boronic acid, sulfonamide, -CHO, C3-C6 cycloalkoxy, -NR ¹³ R ¹⁴ , -C(R ¹⁴ )=N(OR ¹⁴ ) , N0 ₂ , -OR ¹³ , -NR ⁰ R ⁴¹ , -SO _m R ¹³ , -SOmNR ¹³ R ¹⁴ , -C (=0)NR ¹³ R ¹ , -OC (=0)NR ¹³ R ¹⁴ , -C (=0) R ^{1 1} , -OC(=0)R ^1:1 , -OCO2R ¹³ , phenyl, -C (=0)NR ¹³ - (C ₁ -C ₄ alkyl)-NR ¹³ R ¹⁴ , -C (=0)NR ⁴⁰ R ⁴¹ , C ₁ -C ₄ haloalkyl, C ₁ -C ₄ haloalkoxy, C ₂ -C ₄ haloalkenyl, C ₁ -C ₄ haloalkynyl, or

C1-C4 alkoxy substituted with 0-3 groups selected from: R ¹¹ , C ₃ -C ₆ cycloalkyl, -C0 ₂ R ¹³ , -C (=0)NR ¹³ R ¹⁴ , -NR ¹³ R ¹⁴ or OH;

C ₁ -C ₄ alkyl substituted with 0-3 groups selected from: R ¹¹ , =NR ¹⁴ , =NNR ¹³ C (=0) NR ¹³ R ¹⁴ or -NR ¹³ R ¹⁴ ;

C ₂ -C ₄ alkenyl substituted with 0-3 R ¹¹ ;

C ₂ -C ₄ alkynyl substituted with 0-3 R ¹¹ ;

a 5- or 6-membered heterocyclic ring containing from 1 to 4 heteroatoms independently selected from oxygen, nitrogen or sulfur;

R ³² , when a substituent on nitrogen, is benzyl or methyl;

m is 0, 1, or 2;

R ³³ is hydrogen or, when taken together with R ³³ , form a =0 group;

R ⁴⁰ is selected from: H, C ₁ -C3 alkyl;

R ⁴¹ is selected from: -C(=0)NR ¹³ R ¹⁴ ; -C(=0)NR ¹³ NR ¹⁴ ; -C (=0)C (R ¹¹ ) NR ¹³ R ¹⁴ ; -C(=0)C(R ¹¹ ) ₂ NR ¹³ NR ¹⁴ ;

-C (=0) C (R ¹¹ ) ₂ NR ¹³ Cθ2R ¹³ ; -C(=0)H; -C(=0)R ^1:L ;

-C(=0)-(Cι-C ₄ alkyl) -NR ¹³ R ¹⁴ ; -C(=0)-(Cι-C4 alkyl)-NR ¹³ C0 R ¹³ ;

1-3 amino acids linked together via amide bonds, and linked to the N atom via the carboxy terminus;

provided that :

when R ⁴ is hydrogen and X is N-R ⁷ , at least one of the following is not hydrogen: R ⁷ , R ²² , or R ²⁷ ;

when R ⁴ is hydrogen and X is S or 0, at least two of the following are not hydrogen: R ²² or R ²⁷ .

[10] Preferred compounds of the invention of Formula (lb) are compounds of Formula (Ic) :

(Ic) wherein:

R ⁴ and R ⁷ are independently selected from the following groups :

hydrogen;

C1-C4 alkyl substituted with 0-3 R ¹¹ ;

C3-C4 alkenyl substituted with 0-3 R ¹¹ ;

R ¹ is selected from one or more of the following:

keto, halogen, -CH2NR ¹³ R ¹⁴ , -NR ¹³ R ¹⁴ , -OR ¹³ , C2-C4 alkoxyalkyl, C1 _. -C4 alkyl, C2-C4 alkenyl, C3-C6 cycloalkyl;

aryl (C ₁ -C ₃ alkyl) substituted with 0-2 R ¹² ;

aryl substituted with 0-3 R ¹² ; or

a 5- to 10-membered heterocyclic ring system containing 1 to 4 heteroatoms independently selected from oxygen, nitrogen or sulfur, said heterocyclic ring system being substituted with 0-2 R ¹² ;

R ¹² , when a substituent on carbon, is selected from one or more of the following:

phenyl, benzyl, phenethyl, phenoxy, benzyloxy, halogen, C1-C4 alkyl, C7-C10 arylalkyl, C1-C4 alkoxy, -CO2H, hydroxamic acid, hydrazide, oxime, boronic acid, sulfonamide, formyl, C3-C6 cycloalkoxy, -OR ¹³ , C1 _. -C4 alkyl substituted with

-NR ¹³ R ¹⁴ , -NR ¹³ R ¹⁴ , methylenedioxy, C2.-C4 haloalkyl, C1-C4 alkylcarbonyl, C1-C4 alkylcarbonylamino, -OH, hydroxymethyl; or

a 5- or 6-membered heterocyclic ring containing from 1 to 4 heteroatoms selected from oxygen, nitrogen or sulfur;

R ¹² , when a substituent on nitrogen, is benzyl or methyl;

R ¹³ is H, C3 _. -C4 alkyl, or C3-C6 alkoxyalkyl, C ₂ -C ₄ alkenyl, or benzyl;

R ¹⁴ is OH, H, CF ₃ , or C1-C4 alkyl, C ₁ -C ₄ alkoxy, NH ₂ , C ₂ - C ₄ alkenyl, or benzyl;

R ¹³ and R ¹⁴ can alternatively join to form -(CH2) ₄ ~,

-(CH2)5 ^~ , -CH2CH2N(R ¹ 5)CH2CH2", or -CH2CH2OCH2CH2-;

R ¹⁵ is H or CH3;

R ²² is independently selected from the following:

hydrogen;

C1-C8 alkyl substituted with 0-3 R ³¹ ; ^C 2 ^-C 6 alkenyl substituted with 0-3 R ³¹ ; C2-C4 alkynyl substituted with 0-1 R ³¹ ;

R ²⁷ is selected from the following:

hydrogen;

C1-C4 alkyl substituted with 0-3 R ³¹ ;

C2-C4 alkenyl substituted with 0-3 R ³¹ ;

R »3- ⁵ 1 ¹ is selected from one or more of the following:

keto, halogen, -CH2NR ¹³ R ¹⁴ , -NR ¹³ R ¹⁴ , -OR ¹³ , C2-C4 alkoxyalkyl, C1 _. -C4 alkyl, C2-C4 alkenyl, C3-C10 cycloalkyl, -C(R ¹⁴ )=N(OR ¹⁴ ) , -C0 ₂ R ¹³ , -S(0) _m R ¹³ ;

aryl substituted with 0-5 R ³² ; or

a 5- to 10-membered heterocyclic ring system containing 1 to 4 heteroatoms independently selected from oxygen, nitrogen or sulfur, said heterocyclic ring system being substituted with 0-2 R ³² ;

R ³² , when a substituent on carbon, is selected from one or more of the following:

phenethyl, phenoxy, C3-C6 cycloalkyl, C3-C6 cycloalkylmethyl, C7-C10 arylalkyl, hydrazide, oxime, boronic acid, C2-Cβ alkoxyalkyl, methylenedioxy, ethylenedioxy, C1-C4 alkylcarbonyloxy, -NHSO2R ¹⁴ , benzyloxy, halogen, 2- (1-morpholino) ethoxy, -CO2R ¹³ , hydroxamic acid, -CONR ¹³ NR ¹ R ¹⁴ , cyano, boronic acid, sulfonamide, -CHO, C3-C ₆ cycloalkoxy, -NR ¹³ R ¹⁴ , -C (R ¹⁴ )=N(OR ¹⁴ ) , N0 ₂ , -OR ¹³ , -NR ⁴⁰ R ⁴¹ , -SO _m R ¹³ , -SOmNR ¹³ R ¹⁴ , -C(=0)NR ¹³ R ¹⁴ , -OC (=0)NR ¹³ R ¹⁴ , -C(=0)R ⁿ , -0C(=0)R ^1:L , -OCO2R ¹³ , phenyl, -C(=0)NR ¹³ -(Cι-C alkyl)-NR ¹³ R ¹⁴ , -C (=0)NR ⁴⁰ R ⁴ - , C ₁ -C ₄ haloalkyl, C ₁ -C ₄ haloalkoxy, C ₂ -C ₄ haloalkenyl, C ₁ -C ₄ haloalkynyl; or

C1-C4 alkoxy substituted with 0-3 groups selected from: R ¹¹ , C3-C6 cycloalkyl, -CO ₂ R ¹³ , -C (=0) NR ¹³ R ¹⁴ , -NR ¹³ R ¹⁴ or OH;

C1-C ₄ alkyl substituted with 0-3 groups selected from: R ¹¹ , =NR ¹⁴ , =NNR ¹³ C (=0)NR ¹³ R ¹⁴ or -NR ¹³ R ¹⁴ ;

C ₂ -C ₄ alkenyl substituted with 0-3 R ¹¹ ;

C ₂ -C ₄ alkynyl substituted with 0-3 R ¹¹ ;

a 5- or 6-membered heterocyclic ring containing from 1 to 4 heteroatoms independently selected from oxygen, nitrogen or sulfur;

R ³² , when a substituent on nitrogen, is benzyl or methyl;

m is 0, 1, or 2;

R ³³ is hydrogen or, when taken together with R ³³ , form a =0 group;

R ⁴⁰ is selected from: H, C ₁ -C ₃ alkyl;

R ⁴¹ is selected from:

-C(=0)NR ¹³ R ¹⁴ ;

-C(=0)NR ¹³ NR ¹⁴ ;

-C(=0)C(R ^ι:ι ) ₂ NR ¹³ R ¹⁴ ; -C(=0)C(R ^1;L ) ₂ NR ¹³ NR ¹⁴ ;

-C (=0) C (R ¹¹ ) ₂ NR ¹³ C0 ₂ R ¹³ ;

-C(=0)H;

-C(=0)R ¹¹ /

-C(=0)-(Cι-C ₄ alkyl)-NR ¹³ R ¹⁴ ; -C(=0)- (C ₁ -C ₄ alkyl) -NR ¹³ C0 ₂ R ¹³ ;

1-3 amino acids linked together via amide bonds, and linked to the N atom via the carboxy terminus;

provided that :

when R ⁴ is hydrogen at least one of the following is not hydrogen: R ⁷ , R ²² , or R ²⁷ .

[11] More preferred compounds of Formula (Ic) are described above, wherein:

R ⁴ and R ⁷ are selected from benzyl, fluorobenzyl, pyrrolylmethyl, methoxybenzyl, isobutyl, nitrobenzyl or aminobenzyl;

R ¹³ is H, C ₁ -C ₄ alkyl, C ₂ -C ₄ alkenyl, or benzyl;

R ¹⁴ is OH, H, CF ₃ , C ₁ -C ₄ alkyl, C ₁ -C alkoxy, NH ₂ , C2-C ₄ alkenyl, or benzyl;

R ³ and R ⁴ can alternatively join to form -(CH2)4~,

-(CH2)5~, -CH2CH2N(R ¹⁵ )CH2CH2~, or -CH2CH2OCH2CH2-;

R ²² and R ²⁷ are independently selected from the following:

hydrogen;

C1-C8 alkyl substituted with 0-2 R ³¹ ; C2-C6 alkenyl substituted with 0-2 R ³¹ ; C2-C4 alkynyl substituted with 0-2 R ³¹ ;

R ³¹ is selected from one or more of the following:

halogen, -OR ¹³ , C1 _. -C4 alkyl, C3-C10 cycloalkyl, -C(R ¹⁴ )=N(OR ¹⁴ ) , -C0 ₂ R ¹³ , -S(0) _m R ¹³ ;

aryl substituted with 0-5 R ³² ; or

a heterocyclic ring system chosen from pyridyl, pyrimidinyl, triazinyl, furanyl, thienyl, pyrrolyl, pyrazolyl, imidazolyl, tetrazolyl, benzofuranyl, indolyl, quinolinyl, isoqu'inolinyl, oxazolidinyl, said heterocyclic ring being substituted with 0-2 R ³² ;

R ³² , when a substituent on carbon, is selected from one or more of the following:

-CONH ₂ , -C0 H, -CHO, -CH ₂ NHOH, -CH ₂ NR ¹³ R ¹⁴ , -NR ¹³ R ¹⁴ , hydroxy, hydroxymethyl, -C (R ¹⁴ ) =N (OR ¹⁴ ) , halogen, methoxy, methyl, nitro, cyano, allyloxy, -CO2CH3, -NHCHO, -NHCOCH3, -OCO2CH3, -CH=NCH2CH2θH, -OCONHCH2C6H5, -OCONHCH3, oxazolidinyl, -C=C-CH2θH, -COCH3, hydroxyethyl, C ₁ -C3 alkyl (said alkyl substituted with 0-4 halogen, or OH), tetrazolyl, -OCH2CONH2, -CONHNH2, -CH=NNHCONH2, -CONHOCH3, -CH2CH (OH) CH2OH, adamantamido, hydroxyethoxy, dihydroxyethyl, -C(NH2)=NH, -CONHCH3, -B(OH)2, benzyloxy, -CONHCH2CH3, -CON (CH2CH3) 2, methylthio, -SO2CH3, -NHCONH2, -NHCONHCH3, -NHCOCH2N(CH3) 2,

-NHCOCH2NHCH3, -NHCOCH2NHCO2CH2C6H5, -NHCOCH2NH2, -NHCOCH (CH3)NHCO2CH2C6H5,

-NHCOCH (CH2C6H5)NHC02CH2C6H5, -NHCOCH (CH3)NH2, -NHCOCH (CH2C6H5)NH2, -CO2CH2CH3, -CONHCH2CH2CH3, -CONHCH(CH3)2, -CH2-imidazole, -COC(CH3)3,

-CH(OH)CF3, -CO-imidazole, -COCF3, -COCH2CH3, -COCH2CH2CH3, pyrazolyl, -SO2NH2, -C (CH2CH3) =N (OH) or -C (CF3) =N (OH) , phenyl, acetoxy, hydroxyamino, -N (CH ₃ ) (CHO) , cyclopropylmethoxy, -CONR ¹³ R ¹⁴ , -CONHOH, (diethylaminoethyl) aminocarbonyl,

(N-ethyl,N-methylaminoethyl) aminocarbonyl,

(4-methylpiperazinylethyl)aminocarbonyl, pyrrolidinylethyl) aminocarbonyl,

(piperidinylethyl) aminocarbonyl, -NHCOCH ₂ NHCH3, N- (2- (4-morpholino) ethyl)aminocarbonyl, N- (2- (N, N- dimethylamino) ethyl) aminocarbonyl;

R ³² , when a substituent on nitrogen, is methyl.

[12] Specifically preferred compounds of Formula (Ic) are described above, wherein:

R ⁴ and R ⁷ are selected from benzyl, fluorobenzyl, pyrrolylmethyl, methoxybenzyl, isobutyl, nitrobenzyl or aminobenzyl;

R ²² and R ²⁷ are independently selected from the group consisting of:

hydrogen, allyl, methyl, ethyl, propyl, cyclopropylmethyl, n-butyl, i-butyl, CH2CH=C (CH3) 2, pyridinylmethyl, ethallyl, n-pentyl, i-pentyl, hexyl, benzyl, isoprenyl, propargyl, picolinyl, methoxyethyl, cyclohexylmethyl, dimethyl-butyl, ethoxyethyl, methyl-oxazolinylmethyl, naphthylmethyl, methyloxazolinylmethyl, vinyloxyethyl, pentafluorobenzyl, quinolmylmethyl, carboxybenzyl, chloro-thienyl, benzyloxybenzyl, phenylbenzyl, adamantylethyl, cyclopropylmethoxybenzyl, methoxybenzyl, methylbenzyl, ethoxybenzyl, hydroxybenzyl, hydroxymethylbenzyl, aminobenzyl, formylbenzyl, cyanobenzyl, cinnamyl, allyloxybenzyl, fluorobenzyl, difluorobenzyl, chlorobenzyl, chloromethylbenzyl, fluoromethylbenzyl, iodobenzyl,

bromobenzyl, cyclobutylmethyl, formaldoximebenzyl, cyclopentylmethyl, nitrobenzyl, (H ₂ NC (=0) ) -benzyl, carbomethoxybenzyl, carboethoxybenzyl, tetrazolylbenzyl, and dimethylallyl, aminomethylbenzyl, (O-benzyl-formaldoxime)benzyl, (O-methyl-formaldoxime) enzyl, (CH3O2CO) -benzyl, (HOCH2CH2N=CH) -benzyl, N-benzylaminocarbonylbenzyl, N-methylaminobenzyl, N-ethylaminobenzyl, N-ethylaminomethylbenzyl, acetylbenzyl, acetoxybenzyl, N-hydroxylaminobenzyl, phenylmethyl- boronic acid, N-hydroxylaminomethylbenzyl, (hydroxyl) ethylbenzyl, (CH3C (=N0H) ) -benzyl, (H2NNHC(=0) ) -benzyl, (H2NC (=0)NHN=CH) -benzyl, (CH3ONHC (=0) ) -benzyl, (HONHC (=0) ) -benzyl, (CH3NHC(=0) ) -benzyl,

N,N-dimethylaminocarbonylbenzyl, (HOCH2CH (OH) CH2O) - benzyl, hydroxyethoxybenzyl (oxazolidinyl) -benzyl, (hydroxyl) exyl, hexenyl, (hydroxy) octyl, (hydroxyl) pentyl, (carboxy) pentyl, (carbo ethoxy)pentyl, (methylthio)benzyl, (methylsulfonyl) benzyl, N,N-dimethylaminomethylbenzyl,

N-methylaminomethylbenzyl, glycylaminobenzyl, N,N-dimethylglycylaminobenzyl, alanylaminobenzyl, (N-phenylmethoxycarbonyl) alanylaminobenzyl, phenylalanylaminobenzyl, (N-phenylmethoxycarbonyl) phenylalanylaminobenzyl, (CH3CH2NHC (=0) ) -benzyl, N,N-diethylaminocarbonylbenzyl, N-ethylaminocarbonylbenzyl, N-propylaminocarbonylbenzyl,

N,N-diisopropylaminocarbonylbenzyl, N, N-di-n- propylaminocarbonylbenzyl, (hydroxypropynyl)benzyl, (imidazolyl-C (=0) )-benzyl, trifluoroacetylbenzyl, (pyrazolyl)benzyl, (H2NSO2)-benzyl, dihydroxyethylbenzyl, (MeHNC (=0)NH) -benzyl, (H2NC (=0)NH) -benzyl, (HC (=0)NH) -benzyl,

-52-

SUBSnTUTE SHEET (RULE 26)

methanesulfonylpentyl, methoxypentyl, N-formyl-N- methylaminobenzyl, acetylaminobenzyl, propionylbenzyl, butyrylbenzyl, (CH3CH2C (=N0H) ) - benzyl, (trifluorohydroxyethyl)benzyl, (CF3C (=N0H) ) -benzyl, (N-methylglycyl) aminobenzyl, ( (4-morpholino) ethyl)aminocarbonylbenzyl, (N,N-dimethylaminoethyl)aminocarbonylbenzyl, (N,N-diethylaminoethyl) aminocarbonylbenzyl, (4-methylpiperazin-l-ylethyl)aminocarbonylbenzyl, (benzyl-NHC (=0)0)benzyl, (CH3NHC (=0)O)benzyl, (NH ₂ C (=0) CH ₂ 0)benzyl, (NH ₂ C (=NH) )benzyl,

( (N-phenylmethoxycarbonyl)glycylamino)benzyl, (imidazolylmethyl)benzyl, ( (CH3) ₃ C-C (=0) ) benzyl,

(N-methyl-N-ethylaminoethyl) aminocarbonylbenzyl, (pyrrolidinylethyl)aminocarbonylbenzyl, (piperidinylethyl) aminocarbonylbenzyl .

[13] Still more specifically preferred compounds of Formula (Ic) are described above, wherein:

R ⁴ and R ⁷ are benzyl;

R ²² and R ²⁷ are imdependently selected from the group consisting of:

hydrogen, allyl, methyl, ethyl, propyl, cyclopropylmethyl, n-butyl, i-butyl, CH2CH=C (CH3) 2, pyridinylmethyl, methallyl, n-pentyl, i-pentyl, hexyl, benzyl, isoprenyl, propargyl, picolinyl, methoxyethyl, cyclohexylmethyl, dimethyl-butyl, ethoxyethyl, methyl-oxazolinylmethyl, naphthylmethyl, methyloxazolinylmethyl, vinyloxyethyl, pentafluorobenzyl, quinolmylmethyl, carboxybenzyl, chloro-thienyl, benzyloxybenzyl, phenylbenzyl, adamantylethyl, cyclopropylmethoxybenzyl, methoxybenzyl,

-53-

SUBSJTTUTE SHEET (RULE 26)

methylbenzyl, ethoxybenzyl, hydroxybenzyl, hydroxymethylbenzyl, aminobenzyl, formylbenzyl, cyanobenzyl, cinna yl, allyloxybenzyl, fluorobenzyl, difluorobenzyl, chlorobenzyl, chloromethylbenzyl, fluoromethylbenzyl, iodobenzyl, bromobenzyl, cyclobutylmethyl, formaldoximebenzyl, cyclopentylmethyl, nitrobenzyl, (H ₂ NC (=0) )-benzyl, carbomethoxybenzyl, carboethoxybenzyl, tetrazolylbenzyl, and di ethylallyl, aminomethylbenzyl, (O-benzyl-formaldoxime)benzyl, (O-methyl-formaldoxime)benzyl, (CH3O2CO)-benzyl, (HOCH2CH2N=CH) -benzyl, N-benzylaminocarbonylbenzyl, N-methylaminobenzyl, N-ethylaminobenzyl, N-ethylaminomethylbenzyl, acetylbenzyl, acetoxybenzyl, N-hydroxylaminobenzyl, phenylmethyl- boronic acid, N-hydroxylaminomethylbenzyl, (hydroxyl) ethylbenzyl, (CH3C (=N0H) ) -benzyl, (H2NNHC (=0) ) -benzyl, (H2NC (=0)NHN=CH) -benzyl, (CH3ONHC (=0) )-benzyl, (HONHC (=0) ) -benzyl, (CH3NHC(=0) ) -benzyl,

N, N-dimethylaminocarbonylbenzyl, (HOCH2CH (OH) CH2O) - benzyl, hydroxyethoxybenzyl (oxazolidinyl) -benzyl, (hydroxyl) hexyl, hexenyl, (hydroxy) octyl, (hydroxyl)pentyl, (carboxy)pentyl, (carbomethoxy)pentyl, (methylthio)benzyl, (methylsulfonyl) benzyl, N,N-dimethylaminomethylbenzyl,

N-methylaminomethylbenzyl, glycylaminobenzyl, N,N-dimethylglycylaminobenzyl, alanylaminobenzyl, (N-phenylmethoxycarbonyl) alanylaminobenzyl, phenylalanylaminobenzyl, (N-phenylmethoxycarbonyl) phenylalanylaminobenzyl, (CH3CH2NHC (=0) ) -benzyl, N,N-diethylaminocarbonylbenzyl, N-ethylaminocarbonylbenzyl, N-propylaminocarbonylbenzyl,

N,N-diisopropylaminocarbonylbenzyl, N, N-di-n-

-54-

SUBSCTTUTE SHEET (RULE 26)

propylaminocarbonylbenzyl, (hydroxypropynyl)benzyl, (imidazolyl-C(=0) )-benzyl, trifluoroacetylbenzyl, (pyrazolyl)benzyl, (H2NSO2)-benzyl, dihydroxyethylbenzyl, (MeHNC(=0)NH) -benzyl, (H2NC(=0)NH)-benzyl, (HC (=0)NH)-benzyl, methanesulfonylpentyl, methoxypentyl, N-formyl-N- methylaminobenzyl, acetylaminobenzyl, propionylbenzyl, butyrylbenzyl, (CH3CH2C(=N0H) )- benzyl, (trifluorohydroxyethyl)benzyl, (CF3C (=NOH) )-benzyl, (N-methylglycyl) aminobenzyl, ( (4-morpholino) ethyl)aminocarbonylbenzyl, (N,N-dimethylaminoethyl) aminocarbonylbenzyl, (N,N-diethylaminoethyl) aminocarbonylbenzyl, (4-methylpiperazin-l-ylethyl) aminocarbonylbenzyl, (benzyl-NHC(=0)0)benzyl, (CH3NHC (=0) 0)benzyl, (NH ₂ C(=0)CH ₂ 0)benzyl, (NH ₂ C(=NH) )benzyl, ( (N-phenylmethoxycarbonyl) glycylamino)benzyl, (imidazolylmethyl)benzyl, ( (CH3) C-C(=0) )benzyl,

(N-methyl-N-ethylaminoethyl)aminocarbonylbenzyl, (pyrrolidinylethyl) aminocarbonylbenzyl, (piperidinylethyl)aminocarbonylbenzyl.

[14] Most specifically preferred compounds of Formula (Ic) are compounds of Formula (Id) :

(Id)

selected from the group consisting of

the compound of the Formula (Id) wherein R ²² is hydrogen and R ⁷ is hydrogen;

the compound of the Formula (Id) wherein R ²² is hydrogen and R ⁷ is benzyl;

the compound of the Formula (Id) wherein R ²² is cyclopropylmethyl and R ⁷ is hydrogen;

[11] Another embodiment of the present invention are compounds of Formula (I) of the Formula (Ila) :

(Ila) or a pharmaceutically acceptable salt or prodrug form thereof, wherein:

X is S, O, N-R ⁷ ;

R ⁴ and R ⁷ are independently selected from the following groups :

hydrogen;

Cι-C8 alkyl substituted with 0-3 R ¹¹ ;

C2-C8 alkenyl substituted with 0-3 R ¹¹ ;

C2-C8 alkynyl substituted with 0-3 R ¹¹ ;

C3-C8 cycloalkyl substituted with 0-3 R ¹¹ ; C6-C10 bicycloalkyl substituted with 0-3 R ¹¹ ; aryl substituted with 0-3 R ¹² ;

a C6-C1 carbocyclic residue substituted with 0-3 R ¹² ; a heterocyclic ring system substituted with 0-2 R ¹² , composed of 5 to 10 atoms including at least one, preferably 1-4, nitrogen, oxygen or sulfur atom;

R ^4a is selected from the following groups :

hydrogen;

C1-C4 alkyl substituted with halogen or Cχ-C2 alkoxy; benzyl substituted with halogen or C1-C2 alkoxy;

-OR ²⁰ ; or SR ²⁰ ;

R ⁴ and R ^4a can alternatively join to form a 5-7 membered carbocyclic ring substituted with 0-2 R ¹² ;

R5 is selected from =0; H; halogen; Ci-Cβ alkyl substituted with 0-3 -OH; -N(R ²⁰ )2; -SR ²⁰ ; or -OR ⁰ ;

R^ ^a is selected from hydrogen, halogen, C1-C6 alkyl, -N(R ²⁰ )2, -SR ²⁰ , or -OR ²⁰ ;

R5 and R^ ^a can alternatively join to form =0, =S, or a ketal ring;

.20 and R ²¹ are independently selected from:

hydrogen;

C1-C6 alkyl substituted with 0-3 R ¹¹ ; C3-C6 alkoxyalkyl substituted with 0-3 R ¹¹ ; Ci-Cβ alkylcarbonyl substituted with 0-3 R- ~ ; C1-C6 alkoxycarbonyl substituted with 0-3 R ¹¹ ; benzoyl substituted with 0-3 R ¹² ;

phenoxycarbonyl substituted with 0-3 R ¹² ; phenylaminocarbonyl substituted with 0-3 R ¹² ; Ci-C _δ alkylsulfenyl substituted with 0-3 R ¹¹ ; Ci-Cβ alkylsulfonyl substituted with 0-3 R ; or any group that, when administered to a mammalian subject, cleaves to form a free hydroxyl, amino or sulfhydryl;

s selected from one or more of the following:

keto, halogen, cyano, -CH2NR ¹³ R ¹⁴ , -NR ¹³ R ¹⁴ , -CO2R ¹³ , -0C(=0)R ¹³ , -OR ¹³ , C2-C6 alkoxyalkyl, -S(0) _m R ¹³ , -NHC(=NH)NHR ¹³ , -C (=NH) NHR ¹³ , -C(=0)NR ¹³ R ¹⁴ , -NR ¹⁴ C(=0)R ¹³ , =NOR ¹⁴ , -NR ¹ C(=0)OR ¹⁴ , -OC(=0)NR ¹³ R ¹⁴ , -NR ¹³ C (=0) NR ¹³ R ¹⁴ , -NR ¹ S02NR ¹³ R ¹⁴ , -NR ¹⁴ Sθ2R ¹³ , -Sθ2NR ¹³ R ¹⁴ , C1-C4 alkyl, C2-C alkenyl, C3-C10 cycloalkyl, C3-C6 cycloalkylmethyl, benzyl, phenethyl, phenoxy, benzyloxy, nitro, C7-C10 arylalkyl, hydroxamic acid, hydrazide, boronic acid, sulfonamide, formyl, C3-C6 cycloalkoxy, C ₁ -C ₄ alkyl substituted with -NR ¹³ R ¹⁴ , C1-C4 hydroxyalkyl, methylenedioxy, ethylenedioxy, C1-C4 haloalkyl, C1-C4 haloalkoxy, C1-C4 alkoxycarbonyl, C1-C4 alkylcarbonyloxy, C1-C4 alkylcarbonyl, C1-C4 alkylcarbonylamino,

-OCH2CO2H, 2- (1-morpholino) ethoxy, azido, or -C(R ¹⁴ )=N(OR ¹⁴ ) ;

1-3 amino acids, linked together via amide bonds and linked to R ⁴ or R ⁷ , R ²⁰ , or R ²¹ via the amine or carboxy terminus;

-(C ₁ -C3 alkyl) aryl substituted with 0-2 R ¹² ;

-58-

SUBSCTTUTE SHEET (RULE 26)

a C5-C14 carbocyclic residue substituted with 0-3 R ¹² ;

aryl substituted with 0-3 R ¹² ; or

a 5- to 10-membered heterocyclic ring system containing 1 to 4 heteroatoms independently selected from oxygen, nitrogen or sulfur, said heterocyclic ring system being substituted with 0-3 R ¹² ;

R ¹² , when a substituent on carbon, is selected from one or more of the following:

phenyl, benzyl, phenethyl, phenoxy, benzyloxy, halogen, hydroxy, nitro, cyano, C1-C4 alkyl, C3-C6 cycloalkyl, C3-C6 cycloalkylmethyl, C7-C10 arylalkyl, C1-C4 alkoxy, -CO2H, hydroxamic acid, hydrazide, oxime, boronic acid, sulfonamide, formyl, C3-C6 cycloalkoxy, -OR ¹³ , C1 _. -C4 alkyl substituted with -NR ¹³ R ¹⁴ , -NR ¹³ R ¹⁴ , C2-C6 alkoxyalkyl, C1-C4 hydroxyalkyl, methylenedioxy, ethylenedioxy, C1-C4 haloalkyl, C1-C4 haloalkoxy, C1-C4 alkoxycarbonyl, C1-C4 alkylcarbonyloxy, C1-C4 alkylcarbonyl, C1-C4 alkylcarbonylamino, -S(0) _m R ¹³ , -S02NR ¹³ R ¹⁴ ,

-NHSO2R ¹⁴ , -OCH2CO2H, 2- (1-morpholino) ethoxy; or

a 5- or 6-membered heterocyclic ring containing from 1 to 4 heteroatoms independently selected from oxygen, nitrogen or sulfur;

when R ² is attached to a saturated carbon atom, it may be carbonyl or thiocarbonyl;

or R ¹² may alternatively be a 3- or 4- carbon chain attached to adjacent carbons on the ring to form a

fused 5- or 6-membered ring, said 5- or 6- membered ring being optionally substituted on the aliphatic carbons with halogen, C1-C4 alkyl, C1-C4 alkoxy, hydroxy, or -NR ¹ R ¹⁴ ;

R ¹² , when a substituent on nitrogen, is selected from one or more of the following:

phenyl, benzyl, phenethyl, hydroxy, C1-C4 hydroxyalkyl, C1-C4 alkoxy, C1-C4 alkyl, C3-C6 cycloalkyl, C3-C6 cycloalkylmethyl, -CH2NR ¹³ R ¹⁴ ,

-NR ¹³ R ¹⁴ , C2-C6 alkoxyalkyl, C1-C4 haloalkyl, C1-C4 alkoxycarbonyl, -CO2H, C1-C4 alkylcarbonyloxy,

C1-C4 alkylcarbonyl, -C (R ¹⁴ )=N (OR ¹⁴ ) ;

R ¹³ is selected from:

H; phenyl substituted with 0-3 R ^11A ; benzyl substituted with 0-3 R ^11A ; C1-C6 alkyl substituted with 0-3 R ^11A ;

C ₂ -C ₄ alkenyl substituted with 0-3 R ^11A ;

C1-C6 alkylcarbonyl substituted with 0-3 R ^11A ;

Ci-Cβ alkoxycarbonyl substituted with 0-3 R ^11A ;

Ci-Cς alkylaminocarbonyl substituted with 0-3 R ^11A ; C3-C6 alkoxyalkyl substituted with 0-3 R ^11A ; an amine protecting group when R ¹³ is bonded to N; a hydroxy protecting group when R ¹³ is bonded to 0;

R ¹⁴ is OH, H, CF3; C1-C4 alkyl substituted with 0-3 groups selected from OH, C ₁ -C ₄ alkoxy, halogen,

NH ₂ ; Ci-Cβ alkoxy; NH ₂ ; C ₂ -C ₆ alkenyl; or benzyl; an amine protecting group when R ¹⁴ is bonded to N; a hydroxy protecting group when R ¹⁴ is bonded to 0;

R ¹³ and R ¹⁴ can alternatively join to form -(CH2)4~,

-(CH2)5-, -CH2CH2N(R ¹⁵ )CH2CH2~, or -CH2CH2OCH2CH2-;

_15 is H or CH3;

m is 0, 1 or 2;

Z is 0, S, or NR ²⁴ ;

R ²² is independently selected from the following:

hydrogen;

C1-C8 alkyl substituted with 0-3 R ³¹ ; C2-C8 alkenyl substituted with 0-3 R ³¹ ; C2-C8 alkynyl substituted with 0-3 R ³¹ ; a C3-C14 carbocyclic ring system substituted with

0-5 R ³¹ or R ³² ; a 5- to 10-membered heterocyclic ring system containing 1 to 4 heteroatoms independently selected from oxygen, nitrogen or sulfur, said heterocyclic ring system being substituted with 0-2 R ³² ;

R ²³ is independently selected from the following:

hydrogen;

C1-C8 alkyl substituted with 0-3 R ³¹ ; C2-C8 alkenyl substituted with 0-3 R ³¹ ; C2-C8 alkynyl substituted with 0-3 R ³¹ ; a C3-C14 carbocyclic ring system substituted with 0-5 R ³¹ or R ³² ;

a 5- to 10-membered heterocyclic ring system containing 1 to 4 heteroatoms independently selected from oxygen, nitrogen or sulfur, said

heterocyclic ring system being substituted with 0-2 R ³² ;

R ²⁴ is selected from: hydrogen; hydroxy; amino; C1-C4 alkyl; C1-C4 alkoxy; mono- or di-(Cι-Cς alkyl)amino; cyano; nitro; benzyloxy; -NHSθ2aryl, aryl being optionally substituted with (Cι-C ₆ )alkyl;

alternatively, R ²² , R ² ^, or R ^, independently, can join with R ⁴ or R ^4A to form a 5- or 6-membered fused heterocyclic ring or carbocyclic ring substituted with 0-2 R ¹² , said heterocyclic ring containing 1-3 heteroatoms independently selected from N, S, or 0; or

alternatively, R ²³ , R ²⁷ , or R ²⁸ , independently, can join with R ⁷ to form a 5- or 6-membered fused heterocyclic ring or carbocyclic ring substituted with 0-2 R ¹² , said heterocyclic ring containing 1-3 heteroatoms independently selected from N, S, or 0; or

alternatively, R ²² , R ²³ , R ²⁷ or R ²⁸ can join with R^ or R ³³ to form a 0- to 7-membered bridge to form a carbocyclic or heterocyclic ring, said bridge being substituted with 0-2 R ¹² and said bridge containing 0-3 heteroatoms independently selected from N, S, or 0 (i.e., a 0-membered bridge is formed when R ²² , R ²⁷ , R ²⁸ , or R ²³ are taken together with R ⁵ or R ³³ to form a direct bond) ;

R ³¹ is selected from one or more of the following:

keto, halogen, cyano, -CH2NR ¹³ R ¹⁴ , -NR ¹³ R ¹⁴ , -CO2R ¹³ , -C(=0)R ¹¹ , -0C(=0)R ¹³ , -OR ¹³ , C2-C6

-62-

SUBST1TUTE SHEET (RULE 26)

alkoxyalkyl, -S(0) _m R ¹³ , -NHC (=NH)NHR ¹³ , -C(=NH)NHR ¹³ , -C(=0)NR ¹³ R ¹⁴ , -NR ¹⁴ C (=0)R ¹³ , =NOR ¹⁴ , -NR ¹ C(=0)OR ¹⁴ , -OC(=0)NR ¹³ R ¹⁴ , -NR ¹³ C (=0)NR ¹³ R ¹⁴ , -NR ¹⁴ S02NR ¹³ R ¹⁴ , -NR ¹ S02R ¹³ , -Sθ2NR ¹³ R ¹⁴ , C1-C4 alkyl, C2-C4 alkenyl, C3-C10 cycloalkyl, C3-C6 cycloalkylmethyl, benzyl, phenethyl, phenoxy, benzyloxy, nitro, C7-C10 arylalkyl, hydroxamic acid, hydrazide, oxime, boronic acid, sulfonamide, formyl, C3-C6 cycloalkoxy, C ₁ -C ₄ alkyl substituted with -NR ¹³ R ¹⁴ , C1-C4 hydroxyalkyl, methylenedioxy, ethylenedioxy, C1-C4 haloalkyl, C1-C4 haloalkoxy, C1-C4 alkoxycarbonyl, C1-C4 alkylcarbonyloxy, C1-C4 alkylcarbonyl, C1-C4 alkylcarbonylamino, -OCH2CO2R ¹³ , 2- (1-morpholino) ethoxy, azido, -C(R ¹ )=N(OR ¹⁴ ) ; or

1-3 amino acids, linked together via amide bonds and linked to R ²² , R ²³ , R ²⁵ , R ²⁷ , R ⁴ or R ⁷ via the amine or carboxy terminus;

a C5-C14 carbocyclic residue substituted with 0-3 R ³² ;

a C5-C14 carbocyclic residue substituted with 0-5 R ³² ; or

a 5- to 10-membered heterocyclic ring system containing 1 to 4 heteroatoms independently selected from oxygen, nitrogen or sulfur, said heterocyclic ring system being substituted with 0-2 R ³² ;

R ³² , when a substituent on carbon, is selected from one or more of the following:

phenyl, benzyl, phenethyl, phenoxy, benzyloxy, halogen, hydroxy, nitro, cyano, C1-C4 alkyl, C3-C10 cycloalkyl, C3-C6 cycloalkylmethyl, C7-C10 arylalkyl, C1 _. -C4 alkoxy, -CO2H, hydroxamic acid, -CONR ¹³ NR ¹ R ¹⁴ , hydrazide, oxime, boronic acid, sulfonamide, formyl, C3-C6 cycloalkoxy, -OR ¹³ , C1 _. -C4 alkyl substituted with -NR ¹³ R ¹⁴ , -NR ¹³ R ¹⁴ , C2-C6 alkoxyalkyl, C1-C4 hydroxyalkyl, methylenedioxy, ethylenedioxy, C1-C4 haloalkyl, C1-C4 haloalkoxy, C3 _. -C4 alkoxycarbonyl, C1-C4 alkylcarbonyloxy, C1-C4 alkylcarbonyl, C1-C4 alkylcarbonylamino, -S(0)π _. R ¹³ , -Sθ2NR ¹³ R ¹⁴ , -NHS02R ¹⁴ , -OCH2CO2H,

2- (1-morpholino)ethoxy, -C (R ¹⁴ ) =N (OR ¹⁴ ) ; N0 , -OR ¹³ , -NR ⁴⁰ R ⁴¹ , -SO _m R ¹³ , -SO _m NR ¹³ R ¹⁴ , -C (=0)NR ¹³ R ¹⁴ , -OC(=0)NR ¹³ R ¹⁴ , -C(=0)R , -0C (=0) R ^{1 1} , -OCO2R ¹³ , phenyl, -C (=0)NR ¹³ - (C ₁ -C ₄ alkyl) -NR ¹³ R ¹⁴ , -C(=O)NR ⁴⁰ R ⁴¹ , C _! -C ₄ haloalkyl, C ₁ -C ₄ haloalkoxy, C ₂ -C ₄ haloalkenyl, C ₁ -C haloalkynyl, or

-C(=0)NR ¹ C(R ¹¹ ) ₂ NR ¹³ R ¹ 4; -C(=0)NR ¹ C (R ¹¹ ) ₂ NR ¹³ NR ¹⁴ ; -C (=0) NR ¹³ C (R ¹¹ ) ₂ NR ¹³ C0 ₂ R ¹³ ; -C (=0)NR ¹³ - (C ₁ -C ₄ alkyl) -NR ¹³ C0 R ¹³ ; or

-C (=0) C (R ¹¹ ) ₂ NR ¹³ R ¹⁴ ; -C (=0) C (R ¹¹ ) ₂ NR ¹³ NR ¹⁴ ; -C (=0)C(R ¹¹ ) ₂ NR ¹³ C0 ₂ R ¹³ ; -C (=0)- (C ₁ -C ₄ alkyl) -NR ¹³ R ¹⁴ ; -C (=0)- (C ₁ -C ₄ alkyl) -NR ¹³ C0 ₂ R ¹³ ; or

C3.-C4 alkoxy substituted with 0-4 groups selected from: R ¹¹ , C ₃ -C ₆ cycloalkyl, -C0 ₂ R ¹³ , -C (=0)NR ¹³ R ¹⁴ , _ _NR 13 _R 14 _{or 0H;}

C ₁ -C ₄ alkyl substituted with 0-4 groups selected from: R ¹¹ , =NR ¹⁴ , =NNR ¹³ C (=0)NR ¹³ R ¹⁴ or -NR ¹³ R ¹⁴ ;

C ₂ -C ₄ alkenyl substituted with 0-4 R ¹¹ ;

C ₂ -C ₄ alkynyl substituted with 0-4 R ¹¹ ;

a 5- or 6-membered heterocyclic ring containing from 1 to 4 heteroatoms selected from oxygen, nitrogen or sulfur;

when R ³² is attached to a saturated carbon atom, it may be =0 or =S;

R ³² may alternatively be a 3- or 4- carbon chain attached to adjacent carbons on the ring to form a fused 5- or 6-membered ring, said 5- or 6- membered ring being optionally substituted on the aliphatic carbons with halogen, C1-C4 alkyl, C1-C4 alkoxy, hydroxy, or -NR ¹³ R ¹⁴ ;

R ³² , when a substituent on nitrogen, is selected from one or more of the following:

phenyl, benzyl, phenethyl, hydroxy, C1-C4 hydroxyalkyl, C1-C4 alkoxy, C1-C4 alkyl, C3-C6 cycloalkyl, C3-C6 cycloalkylmethyl, -CH2NR ¹³ R ¹⁴ , -NR ¹³ R ¹⁴ , C2-C6 alkoxyalkyl, C1-C4 haloalkyl, C1-C4 alkoxycarbonyl, -CO2H, C1-C4 alkylcarbonyloxy, C1-C4 alkylcarbonyl, -C (R ¹⁴ ) =N (OR ¹⁴ ) ;

R ³³ is selected from: H;

C1-C3 alkyl substituted at the C2 or C3 carbon with -N(R ²⁰ )2. -SR ²⁰ , or -OR ²¹ ; or when taken together with R ^33a , form =0, =S, or a ketal group;

_R 33a j _^s selected from: H;

C1-C3 alkyl substituted at the C2 or C3 carbon with

-N(R ²⁰ )2, -SR ²⁰ , or -OR ²¹ ; or, when taken together with R ³³ , form =0;

alternatively, R ³³ or R ^33a can join with R ⁷ to form a fused 5- or 6- membered carbocyclic ring;

R ⁴⁰ is selected from: H, C ₁ -C3 alkyl;

R ⁴¹ is selected from:

-C(=0)NR ¹³ R ¹⁴ ;

-C(=0)NR ¹³ NR ¹⁴ ;

-C(=0)C(R ^ι:L ) ₂ NR ^l3 R ¹⁴ ;

-C (=0) C (R ¹¹ ) ₂ NR ¹³ NR ¹⁴ ; -C(=O)C(R ¹¹ )2NR ¹³ C02R ¹³ ;

-C(=0)H;

-C(=0)R ^ι:L ;

-C(=0)-(Cι-C ₄ alkyl)-NR ¹³ R ¹⁴ ;

-C(=0)- (C1-C4 alkyl)-NR ¹³ Cθ2R ¹³ ; 1-3 amino acids linked together via amide bonds, and linked to the N atom via the carboxy terminus;

provided that :

when R ⁴ and R ^4a are hydrogen and X is N-R ⁷ , at least one of the following is not hydrogen: R ⁷ , R ²² , R ²⁷ or R ²⁸ ;

when R ⁴ and R ^a are hydrogen and X is S or 0, at least two of the following are not hydrogen: R ²² , R ²⁷ or R ²⁸ .

[16] Preferred compounds of Formula (Ila) described above are those compounds of Formula (lib) :

(Ub)

wherein:

R ⁴ and R ⁷ are independently selected from the following groups :

hydrogen;

C1-C4 alkyl substituted with 0-3 R ¹¹ ;

C3-C4 alkenyl substituted with 0-3 R ¹¹ ;

R ¹¹ is selected from one or more of the following:

keto, halogen, -CH2NR ¹³ R ¹⁴ , -NR ¹³ R ¹⁴ , -OR ¹³ , C2-C4 alkoxyalkyl, C1-C4 alkyl, C2-C alkenyl, C3-C6 cycloalkyl;

aryl(Cι-C ₃ alkyl) substituted with 0-2 R ¹² ;

aryl substituted with 0-3 R ¹² ; or

a 5- to 10-membered heterocyclic ring system containing 1 to 4 heteroatoms independently selected from oxygen, nitrogen or sulfur, said heterocyclic ring system being substituted with 0-2 R ¹² ;

-67-

SUBST1TUTESHEET(RULE26)

R ² , when a substituent on carbon, is selected from one or more of the following:

phenyl, benzyl, phenethyl, phenoxy, benzyloxy, halogen, C1-C4 alkyl, C7-C10 arylalkyl, C1-C4 alkoxy, -CO2H, hydroxamic acid, hydrazide, oxime, boronic acid, sulfonamide, formyl, C3-C6 cycloalkoxy, -OR ¹³ , C1-C4 alkyl substituted with -NR ¹³ R ¹⁴ , -NR ¹³ R ¹⁴ , methylenedioxy, C1-C4 haloalkyl, C1-C4 alkylcarbonyl, C1-C4 alkylcarbonylamino, -OH, hydroxymethyl; or

a 5- or 6-membered heterocyclic ring containing from 1 to 4 heteroatoms selected from oxygen, nitrogen or sulfur;

R ¹² , when a substituent on nitrogen, is benzyl or methyl;

R ¹³ is H, C3 _. -C4 alkyl, or C3-C6 alkoxyalkyl, C ₂ -C ₄ alkenyl, or benzyl;

R ¹⁴ is OH, H, CF3, or C1-C4 alkyl, C ₁ -C ₄ alkoxy, NH ₂ , C ₂ -C ₄ alkenyl, or benzyl;

R ¹³ and R ¹⁴ can alternatively join to form -(CH2)4~, -(CH2)5~, -CH2CH2N(R ¹⁵ )CH2CH2 ^~ , or -CH2CH2OCH2CH2-;

R ²² and R ²³ are independently selected from the following:

hydrogen;

C1-C8 alkyl substituted with 0-3 R ³¹ ; C2-C6 alkenyl substituted with 0-3 R ³¹ ; C2-C4 alkynyl substituted with 0-1 R ³¹ ;

-68-

SUBSriTUTESHEET(RULE26)

R ³ is selected from one or more of the following:

keto, halogen, -CH2NR ¹³ R ¹⁴ , -NR ¹³ R ¹⁴ , -OR ¹³ , C2-C4 alkoxyalkyl, C1-C4 alkyl, C2-C alkenyl, C3-C10 cycloalkyl, -C (R ¹⁴ )=N(OR ¹⁴ ) , -C0 ₂ R ¹³ , -S(0) _m R ¹³ ;;

aryl substituted with 0-3 R ³² ; or

a 5- to 10-membered heterocyclic ring system containing 1 to 4 heteroatoms independently selected from oxygen, nitrogen or sulfur, said heterocyclic ring system being substituted with 0-2 R ³² ;

R ³² , when a substituent on carbon, is selected from one or more of the following:

phenethyl, phenoxy, C3-C6 cycloalkyl, C3-C6 cycloalkylmethyl, C7-C10 arylalkyl, hydrazide, oxime, boronic acid, C2-C6 alkoxyalkyl, methylenedioxy, ethylenedioxy, C1-C4 alkylcarbonyloxy, -NHSO2R ¹⁴ , benzyloxy, halogen, 2- (1-morpholino) ethoxy, -CO2R ¹³ , hydroxamic acid, -CONR ^l3 NR ¹³ R ¹⁴ , cyano, boronic acid, sulfonamide, -CHO, C ₃ -C6 cycloalkoxy, -NR ¹³ R ¹⁴ , -C(R ¹⁴ )=N(OR ¹⁴ ) , N0 ₂ , -OR ¹³ , -NR ⁴⁰ R ⁴¹ , -SO _m R ¹³ , -SO _m NR ¹³ R ¹⁴ , -C(=0)NR ¹³ R ¹⁴ , -OC (=0)NR ¹³ R ¹⁴ , -C(=0)R ¹¹ , -OC (=0) R- - _f -OCO2R ¹³ , phenyl, -C(=0)NR ¹³ -(Cι-C ₄ alkyl)-NR ¹³ R ¹⁴ , -C (=0)NR ⁴⁰ R ⁴¹ ,

C ₁ -C ₄ haloalkyl, C ₁ -C haloalkoxy, C ₂ -C ₄ haloalkenyl, C ₁ -C ₄ haloalkynyl, or

C1-C4 alkoxy substituted with 0-3 groups selected from: R ¹¹ , C ₃ -C ₆ cycloalkyl, -C0 ₂ R ¹³ , -C (=0)NR ^l3 R ¹⁴ , -NR ¹³ R ¹⁴ or OH;

C ₁ -C alkyl substituted with 0-3 groups selected from: R ¹¹ , =NR ¹⁴ , =NNR ¹³ C(=0)NR ¹³ R ¹⁴ or -NR ¹³ R ¹⁴ ;

C2-C ₄ alkenyl substituted with 0-3 R ¹¹ ;

C ₂ -C ₄ alkynyl substituted with 0-3 R ¹¹ ;

a 5- or 6-membered heterocyclic ring containing from 1 to 4 heteroatoms independently selected from oxygen, nitrogen or sulfur;

R ³² , when a substituent on nitrogen, is benzyl or methyl;

R ³³ is hydrogen or, when taken together with R ³³ , form a =0 group;

provided that :

when R ⁴ is hydrogen at least one of the following is not hydrogen: R ⁷ , R ²² , or R ²⁷ .

[17] Another preferred embodiment of Formula (I) are compounds of Formula (Ilia)

(Ilia)

-70-

SUBSCTTUTE SHEET (RULE 26)

or a pharmaceutically acceptable salt or prodrug form thereof, wherein:

R ⁴ and R ⁷ are independently selected from the following groups :

hydrogen;

Ci-Cβ alkyl substituted with 0-3 R ¹¹ ;

C2-C8 alkenyl substituted with 0-3 R ¹¹ ; C2-C8 alkynyl substituted with 0-3 R ¹¹ ;

C3-C8 cycloalkyl substituted with 0-3 R ¹¹ ;

C6-C10 bicycloalkyl substituted with 0-3 R ¹¹ ; aryl substituted with 0-3 R ¹² ; a Cg-Ci carbocyclic residue substituted with 0-3 R ¹² ; a heterocyclic ring system substituted with 0-2

R ¹² , composed of 5 to 10 atoms including at least one, preferably 1-4, nitrogen, oxygen or sulfur atom;

n is 0, 1, or 2;

R ¹¹ is selected from one or more of the following:

keto, halogen, cyano, -CH2NR ¹³ R ¹⁴ , -NR ^l3 R ¹⁴ ,

-CO2R ¹³ , -OC(=0)R ¹³ , -OR ¹³ , C2-C6 alkoxyalkyl, -S(0) _m R ¹³ , -NHC(=NH)NHR ¹³ , -C(=NH)NHR ¹³ , -C(=0)NR ¹³ R ¹⁴ , -NR ¹ C(=0)R ¹³ , =NOR ¹⁴ , -NR ¹⁴ C(=0)OR ¹⁴ , -OC(=0)NR ¹³ R ¹⁴ , -NR ¹³ C (=0)NR ¹³ R ¹ , -NR ¹ S02NR ¹³ R ¹⁴ , -NR ¹⁴ S02R ¹³ , -Sθ2NR ¹³ R ¹ , C1-C alkyl, C2-C4 alkenyl, C3-C10 cycloalkyl, C3-C6 cycloalkylmethyl, benzyl, phenethyl, phenoxy, benzyloxy, nitro, C7-C10 arylalkyl, hydroxamic acid, hydrazide, boronic acid, sulfonamide, formyl, C ₃ -C ₆ cycloalkoxy, C ₁ -C alkyl substituted with -NR ¹³ R ¹⁴ , C1-C4 hydroxyalkyl, methylenedioxy,

-71-

SUBSCTTUTE SHEET (RULE 26)

ethylenedioxy, C1-C4 haloalkyl, C1-C4 haloalkoxy, C1-C4 alkoxycarbonyl, C1-C4 alkylcarbonyloxy, C1-C4 alkylcarbonyl, C1-C4 alkylcarbonylamino, -OCH2CO2H, 2- (1-morpholino) ethoxy, azido, or -C(R ¹⁴ )=N(OR ¹⁴ ) ;

1-3 amino acids, linked together via amide bonds and linked to R ⁴ or R ⁷ , R ²⁰ , or R ²¹ via the amine or carboxy terminus;

-(C ₁ -C3 alkyDaryl substituted with 0-2 R ¹² ,

a C5-C14 carbocyclic residue substituted with 0-3 R ¹² ;

iryl substituted with 0-3 R ¹² ; or

a 5- to 10-membered heterocyclic ring system containing 1 to 4 heteroatoms independently selected from oxygen, nitrogen or sulfur, said heterocyclic ring system being substituted with 0-3 R ² ;

R ¹² , when a substituent on carbon, is selected from one or more of the following:

phenyl, benzyl, phenethyl, phenoxy, benzyloxy, halogen, hydroxy, nitro, cyano, C1-C4 alkyl, C3-C6 cycloalkyl, C3-C6 cycloalkylmethyl, C7-C10 arylalkyl, C1-C4 alkoxy, -CO2H, hydroxamic acid, hydrazide, oxime, boronic acid, sulfonamide, formyl, C3-C6 cycloalkoxy, -OR ¹³ , C1-C4 alkyl substituted with -NR ¹³ R ¹⁴ , -NR ¹³ R ¹⁴ , C2-C6 alkoxyalkyl, C1-C4 hydroxyalkyl, methylenedioxy, ethylenedioxy, C1-C4 haloalkyl, C1-C4 haloalkoxy, C1-C4 alkoxycarbonyl,

C1-C4 alkylcarbonyloxy, C1-C4 alkylcarbonyl, C1-C4 alkylcarbonylamino, -S(0) _m R ¹³ , -Sθ2NR ¹³ R ¹⁴ , -NHSO2R ¹⁴ , -OCH2CO2H, 2- (1-morpholino) ethoxy; or

a 5- or 6-membered heterocyclic ring containing from 1 to 4 heteroatoms independently selected from oxygen, nitrogen or sulfur;

when R ¹² is attached to a saturated carbon atom, it may be carbonyl or thiocarbonyl;

or R ¹² may alternatively be a 3- or 4- carbon chain attached to adjacent carbons on the ring to form a fused 5- or 6-membered ring, said 5- or 6- membered ring being optionally substituted on the aliphatic carbons with halogen, C1-C4 alkyl, C3 _. -C4 alkoxy, hydroxy, or -NR ¹³ R ¹⁴ ;

R ² , when a substituent on nitrogen, is selected from one or more of the following:

phenyl, benzyl, phenethyl, hydroxy, C1 _. -C4 hydroxyalkyl, C1-C4 alkoxy, C1-C4 alkyl, C3-C6 cycloalkyl, C3-C6 cycloalkylmethyl, -CH2NR ¹³ R ¹⁴ , -NR ¹³ R ¹⁴ , C2-C6 alkoxyalkyl, C1-C4 haloalkyl, C1-C4 alkoxycarbonyl, -CO2H, C1-C4 alkylcarbonyloxy, C1-C4 alkylcarbonyl, -C (R ¹⁴ ) =N (OR ¹⁴ ) ;

R ³ is selected from: H; phenyl substituted with 0-3 R ^11A ; benzyl substituted with 0-3 R ^11A ;

C1-C6 alkyl substituted with 0-3 R ^11A ;

C ₂ -C ₄ alkenyl substituted with 0-3 R ^11A ; C1-C6 alkylcarbonyl substituted with 0-3 R ^11A ;

C1-C6 alkoxycarbonyl substituted with 0-3 R ^11A ;

C1-C6 alkylaminocarbonyl substituted with 0-3 R ^11A ; C3-C6 alkoxyalkyl substituted with 0-3 R ^11A ; an amine protecting group when R ¹³ is bonded to N; a hydroxy protecting group when R ¹³ is bonded to 0;

R ¹⁴ is OH, H, CF3; C1-C4 alkyl substituted with 0-3 groups selected from OH, C ₁ -C ₄ alkoxy, halogen, NH ₂ ; C ₁ -C ₆ alkoxy; NH ₂ ; C ₂ -C ₆ alkenyl; or benzyl; an amine protecting group when R ¹⁴ is bonded to N; a hydroxy protecting group when R ¹⁴ is bonded to 0;

R ¹³ and R ¹⁴ can alternatively join to form -(CH2)4~,

-(CH2)5 ^~ , -CH2CH2N(R ¹⁵ )CH2CH2~, or -CH2CH2OCH2CH2-;

R ¹⁵ is H or CH3;

m is 0, 1 or 2;

R ²² is independently selected from the following:

hydrogen;

C1-C8 alkyl substituted with 0-3 R ³¹ ;

C2-C8 alkenyl substituted with 0-3 R ³¹ ;

C2-C8 alkynyl substituted with 0-3 R ³¹ ; a C3-C14 carbocyclic ring system substituted with 0-5 R ³¹ or R ³² ; a 5- to 10-membered heterocyclic ring system containing 1 to 4 heteroatoms independently selected from oxygen, nitrogen or sulfur, said heterocyclic ring system being substituted with 0-2

R ³² ;

R ²³ is independently selected from the following:

hydrogen;

C1-C8 alkyl substituted with 0-3 R ³¹ ; C2-C8 alkenyl substituted with 0-3 R ³¹ ; C2-C8 alkynyl substituted with 0-3 R ³¹ ; a C3-C14 carbocyclic ring system substituted with 0-5 R ³¹ or R ³² ;

a 5- to 10-membered heterocyclic ring system containing 1 to 4 heteroatoms independently selected from oxygen, nitrogen or sulfur, said heterocyclic ring system being substituted with 0-2 R ³² ;

alternatively, R ²² can join with R ⁴ to form a 5- or 6- membered fused heterocyclic ring or carbocyclic ring substituted with 0-2 R ¹² , said heterocyclic ring containing 1-3 heteroatoms independently selected from N, S, or 0; or

alternatively, R ²³ can join with R ⁷ to form a 5- or 6- membered fused heterocyclic ring or carbocyclic ring substituted with 0-2 R ¹² , said heterocyclic ring containing 1-3 heteroatoms independently selected from N, S, or 0; or

alternatively, R ²² , R ²⁷ or R ²⁸ can join with R^ or R ³³ to form a 0- to 7-membered bridge to form a carbocyclic or heterocyclic ring, said bridge being substituted with 0-2 R ² and said bridge containing 0-3 heteroatoms independently selected from N, S, or 0 (i.e., a 0-membered bridge is formed when R ²² , R ²⁷ , or R ²⁸ are taken together with R^ or R ³³ to form a direct bond) ;

R ³¹ is selected from one or more of the following:

keto, halogen, cyano, -CH2NR ¹³ R ¹⁴ , -NR ¹³ R ¹⁴ , -CO2R ¹³ , -C(=0)R ¹¹ , -OC(=0)R ¹³ , -OR ¹³ , C2-C6 alkoxyalkyl, -S(0) _m R ¹³ , -NHC (=NH)NHR ¹³ , -C(=NH)NHR ¹³ , -C(=0)NR ¹³ R ¹⁴ , -NR ¹ C (=0) R ¹³ , =N0R ¹⁴ , -NR ¹ C(=0)0R ¹⁴ , -OC(=0)NR ¹³ R ¹⁴ , -NR ¹³ C (=0)NR ¹³ R ¹⁴ , -NR ¹⁴ S02NR ¹³ R ¹⁴ , -NR ¹⁴ Sθ2R ¹³ , -Sθ2NR ¹³ R ¹⁴ , C1-C4 alkyl, C2-C4 alkenyl, C3-C10 cycloalkyl, C3-C6 cycloalkylmethyl, benzyl, phenethyl, phenoxy, benzyloxy, nitro, C7-C10 arylalkyl, hydroxamic acid, hydrazide, oxime, boronic acid, sulfonamide, formyl, C ₃ -C ₆ cycloalkoxy, C ₁ -C alkyl substituted with -NR ¹³ R ¹⁴ , C1-C4 hydroxyalkyl, methylenedioxy, ethylenedioxy, C1-C4 haloalkyl, C1-C4 haloalkoxy, C1-C4 alkoxycarbonyl, C1-C4 alkylcarbonyloxy, C1-C4 alkylcarbonyl, C1-C4 alkylcarbonylamino, -OCH2CO2R ¹³ , 2- (1-morpholino) ethoxy, azido, -C(R ¹⁴ )=N(OR ¹⁴ ) ; or

1-3 amino acids, linked together via amide bonds and linked to R ²² , R ²³ , R ²⁵ , R ²⁷ , R ⁴ or R ⁷ via the amine or carboxy terminus;

a C5-C14 carbocyclic residue substituted with 0-3 R ³² ;

a C5-C14 carbocyclic residue substituted with 0-5 R ³² ; or

a 5- to 10-membered heterocyclic ring system containing 1 to 4 heteroatoms independently selected from oxygen, nitrogen or sulfur, said heterocyclic ring system being substituted with 0-2 R ³² ;

R ³² , when a substituent on carbon, is selected from one or more of the following:

phenyl, benzyl, phenethyl, phenoxy, benzyloxy, halogen, hydroxy, nitro, cyano, C1-C4 alkyl, C3-C10 cycloalkyl, C3-C6 cycloalkylmethyl, C7-C10 arylalkyl, C1-C4 alkoxy, -CO2H, hydroxamic acid, -CONR ¹³ NR ¹ R ¹⁴ , hydrazide, oxime, boronic acid, sulfonamide, formyl, C3-C6 cycloalkoxy, -OR ¹³ , C1-C4 alkyl substituted with -NR ¹³ R ¹⁴ , -NR ¹³ R ¹⁴ , C2-C6 alkoxyalkyl, C1-C4 hydroxyalkyl, methylenedioxy, ethylenedioxy, C1-C4 haloalkyl, C1-C4 haloalkoxy, C1-C4 alkoxycarbonyl, C1-C4 alkylcarbonyloxy, C1-C4 alkylcarbonyl, C1-C4 alkylcarbonylamino, -S(0) _m R ¹³ , -Sθ2NR ¹³ R ¹⁴ , -NHSO2R ¹⁴ , -OCH2CO2H,

2- (1-morpholino) ethoxy, -C (R ¹⁴ ) =N (OR ¹⁴ ) ; N0 , -OR ¹³ , -NR ⁴⁰ R ⁴¹ , -SO _m R ¹³ , -SO _m NR ¹³ R ¹⁴ , -C (=0)NR ¹³ R ¹⁴ , -OC(=0)NR ¹³ R ¹⁴ , -C(=0)R ^1;L , -0C(=0)R ¹¹ , -OCO2R ¹³ , phenyl, -C (=0)NR ¹³ - (C ₁ -C ₄ alkyl) -NR ¹³ R ¹⁴ , -C(=O)NR ⁴⁰ R ⁴¹ , C ₁ -C ₄ haloalkyl, C ₁ -C ₄ haloalkoxy, C ₂ -C ₄ haloalkenyl, C ₁ -C ₄ haloalkynyl, or

-C (=0) NR ¹³ C (R ¹¹ ) ₂ NR ¹³ R ¹⁴ ; -C (=0)NR ¹³ C (R ¹¹ ) NR ¹³ NR ¹⁴ ; -C (=0) NR ¹³ C (R ¹¹ ) ₂ NR ¹³ C02R ¹³ ; -C(=0)NR ¹³ -(Cι-C ₄ alkyl)-NR ¹³ C0 ₂ R ¹³ ; or

-C (=0) C (R ¹¹ ) NR ¹³ R ¹⁴ ; -C (=0) C (R ¹¹ ) ₂ NR ¹³ NR ¹⁴ ; -C(=0)C(R ¹¹ )2NR ¹³ C0 ₂ R ¹³ ; -C (=0) - (C ₁ -C4 alkyl) -NR ¹³ R ¹⁴ ; -C (=0)- (C ₁ -C4 alkyl) -NR ¹³ Cθ ₂ R ¹³ ; or

C1-C4 alkoxy substituted with 0-4 groups selected from: R ¹¹ , C3-C ₆ cycloalkyl, -CO ₂ R ¹³ , -C (=0) NR ¹³ R ¹⁴ , -NR ¹³ R ¹⁴ or OH;

C ₁ -C ₄ alkyl substituted with 0-4 groups selected from: R ¹¹ , =NR ¹⁴ , =NNR ¹³ C (=0)NR ¹³ R ¹⁴ or -NR ¹³ R ¹⁴ ;

C2-C ₄ alkenyl substituted with 0-4 R ¹¹ ;

C ₂ -C ₄ alkynyl substituted with 0-4 R ¹¹ ;

a 5- or 6-membered heterocyclic ring containing from 1 to 4 heteroatoms selected from oxygen, nitrogen or sulfur;

when R ³² is attached to a saturated carbon atom, it may be =0 or =S;

R ³² may alternatively be a 3- or 4- carbon chain attached to adjacent carbons on the ring to form a fused 5- or 6-membered ring, said 5- or 6- membered ring being optionally substituted on the aliphatic carbons with halogen, C1-C4 alkyl, C1-C4 alkoxy, hydroxy, or -NR ¹³ R ¹⁴ ;

R ³² , when a substituent on nitrogen, is selected from one or more of the following:

phenyl, benzyl, phenethyl, hydroxy, C1-C4 hydroxyalkyl, C1-C4 alkoxy, C1-C4 alkyl, C3-C6 cycloalkyl, C3-C6 cycloalkylmethyl, -CH2NR ¹³ R ¹⁴ , -NR ¹³ R ¹⁴ , C2-C6 alkoxyalkyl, C1-C4 haloalkyl, C1-C4 alkoxycarbonyl, -CO2H, C1-C4 alkylcarbonyloxy, C1-C ₄ alkylcarbonyl, -C (R ¹⁴ ) =N (OR ¹⁴ ) ;

R ⁴⁰ is selected from: H, C ₁ -C3 alkyl;

R ⁴¹ is selected from: -C(=0)NR ¹³ R ¹⁴ ; -C (=0)NR ¹³ NR ¹⁴ ;

-78-

SUBST1TUTESHEET(RULE26)

-C (=0) C (R ¹¹ ) NR ¹³ R ¹⁴ ; -C (=0) C (R ¹¹ ) ₂ NR ¹³ NR ¹⁴ ; -C (=0) C (R ¹¹ ) ₂ NR ¹³ C0 ₂ R ¹³ ; -C(=0)H; -C(=0)R ^1:ι ;

-C(=0)-(Cι-C ₄ alkyl) -NR ¹³ R ¹⁴ ; -C (=0) - (C ₁ -C ₄ alkyl)-NR ¹³ Cθ2R ¹³ ;

1-3 amino acids linked together via amide bonds, and linked to the N atom via the carboxy terminus;

provided that :

when R ⁴ is hydrogen, at least two of the following is not hydrogen: R ⁷ , R ²² or R ²³ ;

[18] Preferred compounds of formula (Ilia) are compounds described above, wherein:

R ⁴ and R ⁷ are selected from benzyl, fluorobenzyl, pyrrolylmethyl, methoxybenzyl, isobutyl, nitrobenzyl or aminobenzyl;

R ²² and R ²³ are independently selected from the group consisting of:

hydrogen, allyl, methyl, ethyl, propyl, cyclopropylmethyl, n-butyl, i-butyl, CH2CH=C (CH3) 2, pyridinylmethyl, methallyl, n-pentyl, i-pentyl, hexyl, benzyl, isoprenyl, propargyl, picolinyl, methoxyethyl, cyclohexylmethyl, dimethyl-butyl, ethoxyethyl, methyl-oxazolinylmethyl, naphthylmethyl, methyloxazolinylmethyl, vinyloxyethyl, pentafluorobenzyl, quinolinylmethyl,

carboxybenzyl, chloro-thienyl, benzyloxybenzyl, phenylbenzyl, adamantylethyl, cyclopropylmethoxybenzyl, methoxybenzyl, methylbenzyl, ethoxybenzyl, hydroxybenzyl, hydroxymethylbenzyl, aminobenzyl, formylbenzyl, cyanobenzyl, cinnamyl, allyloxybenzyl, fluorobenzyl, difluorobenzyl, chlorobenzyl, chloromethylbenzyl, fluoromethylbenzyl, iodobenzyl, bromobenzyl, cyclobutylmethyl, formaldoximebenzyl, cyclopentylmethyl, nitrobenzyl, (H ₂ NC (=0) )-benzyl, carbomethoxybenzyl, carboethoxybenzyl, tetrazolylbenzyl, and dimethylallyl, aminomethylbenzyl, (O-benzyl-formaldoxime)benzyl, (O-methyl-formaldoxime)benzyl, (CH3O2CO) -benzyl, (HOCH2CH2N=CH) -benzyl, N-benzylaminocarbonylbenzyl, N-methylaminobenzyl, N-ethylaminobenzyl, N-ethylaminomethylbenzyl, acetylbenzyl, acetoxybenzyl, N-hydroxylaminobenzyl, phenylmethyl- boronic acid, N-hydroxylaminomethylbenzyl, (hydroxyl) ethylbenzyl, (CH3C (=N0H) )-benzyl,

(H2NNHC(=0) )-benzyl, (H2NC (=0)NHN=CH)-benzyl, (CH3ONHC (=0) )-benzyl, (HONHC (=0) ) -benzyl, (CH3NHC (=0) ) -benzyl,

N, N-dimethylaminocarbonylbenzyl, (HOCH2CH (OH) CH2O) - benzyl, hydroxyethoxybenzyl (oxazolidinyl) -benzyl, (hydroxyl) hexyl, hexenyl, (hydroxy) octyl, (hydroxyl)pentyl, (carboxy)pentyl, (carbomethoxy)pentyl, (methylthio)benzyl, (methylsulfonyl)benzyl, N,N-dimethylaminomethylbenzyl,

N-methylaminomethylbenzyl, glycylaminobenzyl,

N, -dimethylglycylaminobenzyl, alanylaminobenzyl, (N-phenylmethoxycarbonyl) alanylaminobenzyl, phenylalanylaminobenzyl, (N-phenylmethoxycarbonyl) phenylalanylaminobenzyl, (CH3CH2NHC (=0) ) -benzyl,

N,N-diethylaminocarbonylbenzyl,

-80-

SUBST1TUTESHEET(RULE26)

N-ethylaminocarbonylbenzyl, N-propylaminocarbonylbenzyl,

N,N-diisopropylaminocarbonylbenzyl, N, N-di-n- propylaminocarbonylbenzyl, (hydroxypropynyl)benzyl, (imidazolyl-C(=0) )-benzyl, trifluoroacetylbenzyl, (pyrazolyl)benzyl, (H2 SO2)-benzyl, dihydroxyethylbenzyl, (MeHNC(=0)NH)-benzyl, (H2NC (=0)NH) -benzyl, (HC(=0)NH) -benzyl, methanesulfonylpentyl, methoxypentyl, N-formyl-N- methylaminobenzyl, acetylaminobenzyl, propionylbenzyl, butyrylbenzyl, (CH3CH2C (=N0H) )- benzyl, (trifluorohydroxyethyl)benzyl, (CF3C (=N0H) ) -benzyl, (N-methylglycyl) aminobenzyl, ( (4-morpholino)ethyl) aminocarbonylbenzyl, (N,N-dimethylaminoethyl) aminocarbonylbenzyl, (N,N-diethylaminoethyl) aminocarbonylbenzyl, (4-methylpiperazin-l-ylethyl) aminocarbonylbenzyl, (benzyl-NHC (=0)0)benzyl, (CH ₃ NHC (=0)0)benzyl, (NH ₂ C (=0) CH ₂ 0)benzyl, (NH ₂ C (=NH) )benzyl, ( (N-phenylmethoxycarbonyl)glycylamino)benzyl,

(imidazolylmethyl)benzyl, ( (CH ₃ ) 3C-C (=0) )benzyl, (N-methyl-N-ethylaminoethyl) aminocarbonylbenzyl, (pyrrolidinylethyl)aminocarbonylbenzyl, (piperidinylethyl)aminocarbonylbenzyl .

[19] Another embodiment of Formula (I) are compounds of Formula (IVa) or (IVb) :

(IVa;

(ivb)

or a pharmaceutically acceptable salt or prodrug form thereof, wherein:

R ⁴ and R ⁷ are independently selected from the following groups :

hydrogen;

Ci-Cβ alkyl substituted with 0-3 R ¹¹ ;

C2-C8 alkenyl substituted with 0-3 R ¹¹ ;

C2-C8 alkynyl substituted with 0-3 R ¹¹ ;

C3-C8 cycloalkyl substituted with 0-3 R ¹¹ ; Cβ-Cio bicycloalkyl substituted with 0-3 R ¹¹ ; aryl substituted with 0-3 R ¹² ; a C6-C14 carbocyclic residue substituted with 0-3

R ¹² ; a heterocyclic ring system substituted with 0-2 R ¹² , composed of 5 to 10 atoms including at least one, preferably 1-4, nitrogen, oxygen or sulfur atom;

R5 is selected from =0; H; halogen; Cχ-C6 alkyl substituted with 0-3 -OH; -N(R ⁰ )2 -SR ²⁰ ; or -OR ²⁰ ;

R ²⁰ is selected from:

hydrogen;

C1-C6 alkyl substituted with 0-3 R ¹¹ ;

-82-

SUBSTΓTUTE SHEET (RULE 26)

C3-C6 alkoxyalkyl substituted with 0-3 R ¹¹ ; C1-C6 alkylcarbonyl substituted with 0-3 R- - ; C1-C6 alkoxycarbonyl substituted with 0-3 R ¹¹ ; benzoyl substituted with 0-3 R ¹² ; phenoxycarbonyl substituted with 0-3 R ¹² ; phenylaminocarbonyl substituted with 0-3 R ² ; C ₁ -C6 alkylsulfenyl substituted with 0-3 R ¹¹ ; Ci-Cβ alkylsulfonyl substituted with 0-3 R- ~ ; or any group that, when administered to a mammalian subject, cleaves to form a free hydroxyl, amino or sulfhydryl;

s selected from one or more of the following:

keto, halogen, cyano, -CH2NR ¹³ R ¹⁴ , -NR ¹³ R ¹⁴ ,

-CO2R ¹³ , -OC(=0)R ¹³ , -OR ¹³ , C2-C6 alkoxyalkyl, -S(0)mR ¹³ , -NHC(=NH)NHR ¹³ , -C (=NH)NHR ¹³ , -C(=0)NR ¹³ R ¹⁴ , -NR ¹⁴ C(=0)R ¹³ , =NOR ¹⁴ , -NR ¹⁴ C(=0)OR ¹⁴ , -OC(=0)NR ¹³ R ¹⁴ , -NR ¹³ C (=0)NR ¹³ R ¹⁴ , -NR ¹ S02NR ¹³ R ¹⁴ , -NR ¹⁴ S02R ¹³ , -Sθ2NR ¹³ R ¹⁴ , C1-C4 alkyl, C2-C4 alkenyl, C3-C10 cycloalkyl, C3-C6 cycloalkylmethyl, benzyl, phenethyl, phenoxy, benzyloxy, nitro, C7-C10 arylalkyl, hydroxamic acid, hydrazide, boronic acid, sulfonamide, formyl, C ₃ -C ₆ cycloalkoxy, C ₁ -C ₄ alkyl substituted with -NR ¹³ R ¹⁴ , C1-C4 hydroxyalkyl, methylenedioxy, ethylenedioxy, C1-C4 haloalkyl, C1-C4 haloalkoxy, C1-C4 alkoxycarbonyl, C1 _. -C4 alkylcarbonyloxy, C1-C4 alkylcarbonyl, C1-C4 alkylcarbonylamino, -OCH2CO2H, 2- (1-morpholino)ethoxy, azido, or -C(R ¹⁴ )=N(OR ¹⁴ ) ;

1-3 amino acids, linked together via amide bonds and linked to R ⁴ or R ⁷ , R ²⁰ , or R ²¹ via the amine or carboxy terminus;

-83-

SUBSCTTUTE SHEET (RULE 26)

-(C ₁ -C3 alkyl) aryl substituted with 0-2 R ¹² ;

a C5-C14 carbocyclic residue substituted with 0-3 R ² ;

aryl substituted with 0-3 R ¹² ; or

a 5- to 10-membered heterocyclic ring system containing 1 to 4 heteroatoms independently selected from oxygen, nitrogen or sulfur, said heterocyclic ring system being substituted with 0-3 R ¹² ;

R ¹² , when a substituent on carbon, is selected from one or more of the following:

phenyl, benzyl, phenethyl, phenoxy, benzyloxy, halogen, hydroxy, nitro, cyano, C1-C4 alkyl, C3-C6 cycloalkyl, C3-C6 cycloalkylmethyl, C7-C10 arylalkyl, C1-C4 alkoxy, -CO2H, hydroxamic acid, hydrazide, oxime, boronic acid, sulfonamide, formyl, C3-C6 cycloalkoxy, -OR ¹³ , C1-C4 alkyl substituted with -NR ¹³ R ¹⁴ , -NR ¹³ R ¹⁴ , C2-C6 alkoxyalkyl, C1-C4 hydroxyalkyl, methylenedioxy, ethylenedioxy, C1-C4 haloalkyl, C1-C4 haloalkoxy, C1-C4 alkoxycarbonyl, C1-C4 alkylcarbonyloxy, C1-C4 alkylcarbonyl, C1-C4 alkylcarbonylamino, -S(0) _m R ¹³ , -Sθ2NR ¹³ R ¹⁴ , -NHSO2R ¹⁴ , -OCH2CO2H, 2- (1-morpholino)ethoxy; or

a 5- or 6-membered heterocyclic ring containing from 1 to 4 heteroatoms independently selected from oxygen, nitrogen or sulfur;

when R ¹² is attached to a saturated carbon atom, it may be carbonyl or thiocarbonyl;

or R ¹² may alternatively be a 3- or 4- carbon chain attached to adjacent carbons on the ring to form a fused 5- or 6-membered ring, said 5- or 6- membered ring being optionally substituted on the aliphatic carbons with halogen, C1-C alkyl, C1-C4 alkoxy, hydroxy, or -NR ¹³ R ¹⁴ ;

R ² , when a substituent on nitrogen, is selected from one or more of the following:

phenyl, benzyl, phenethyl, hydroxy, C1-C4 hydroxyalkyl, C1 _. -C4 alkoxy, C1 _. -C4 alkyl, C3-C6 cycloalkyl, C3-C6 cycloalkylmethyl, -CH2NR ¹³ R ¹⁴ , -NR ¹³ R ¹⁴ , C2-C6 alkoxyalkyl, C3 _. -C4 haloalkyl, C1-C4 alkoxycarbonyl, -CO2H, C1-C4 alkylcarbonyloxy, C1-C4 alkylcarbonyl, -C (R ¹⁴ )=N (OR ¹⁴ ) ;

R ¹³ is selected from: H; phenyl substituted with 0-3 R ^11A ; benzyl substituted with 0-3 R ^11A ;

C1-C6 alkyl substituted with 0-3 R ^11A ;

C ₂ -C ₄ alkenyl substituted with 0-3 R ^11A ; i-Cβ alkylcarbonyl substituted with 0-3 R ^11A ;

Ci-Cβ alkoxycarbonyl substituted with 0-3 R ^11A ;

Cχ-C6 alkylaminocarbonyl substituted with 0-3 R ^11A ;

C3-C6 alkoxyalkyl substituted with 0-3 R ^11A ; an amine protecting group when R ¹³ is bonded to N; a hydroxy protecting group when R ¹³ is bonded to 0;

R ¹⁴ is OH, H, CF3; C1-C4 alkyl substituted with 0-3 groups selected from OH, C ₁ -C ₄ alkoxy, halogen, NH ₂ ; Ci-Cβ alkoxy; NH2; C ₂ -C ₆ alkenyl; or benzyl; an amine protecting group when R ¹⁴ is bonded to N; a hydroxy protecting group when R ¹⁴ is bonded to 0;

-85-

SUBSCTTUTE SHEET (RULE 26)

R ¹³ and R ¹⁴ can alternatively join to form -(CH2)4~, -(CH2)5-/ -CH2CH2N(R ¹⁵ )CH2CH2~, or -CH2CH2OCH2CH2-;

R ¹⁵ is H or CH3;

m is 0, 1 or 2;

R ²² is independently selected from the following:

hydrogen;

C1-C8 alkyl substituted with 0-3 R ³¹ ;

C2-C8 alkenyl substituted with 0-3 R ³¹ ;

C2-C8 alkynyl substituted with 0-3 R ³¹ ; a C3-C14 carbocyclic ring system substituted with 0-5 R ³¹ or R ³² ; a 5- to 10-membered heterocyclic ring system containing 1 to 4 heteroatoms independently selected from oxygen, nitrogen or sulfur, said heterocyclic ring system being substituted with 0-2

R ³² ;

R ²³ is independently selected from the following:

hydrogen;

C1-C8 alkyl substituted with 0-3 R ³¹ ; C2-C8 alkenyl substituted with 0-3 R ³¹ ; C2-C8 alkynyl substituted with 0-3 R ³¹ ;

a C3-C14 carbocyclic ring system substituted with 0-5 R ³¹ or R ³² ;

a 5- to 10-membered heterocyclic ring system containing 1 to 4 heteroatoms independently selected from oxygen, nitrogen or sulfur, said

-86-

SUBSCTTUTE SHEET (RULE 26)

heterocyclic ring system being substituted with 0- 2 R ³² ;

alternatively, R ²² can join with R ⁴ to form a 5- or 6- membered fused heterocyclic ring or carbocyclic ring substituted with 0-2 R ¹² , said heterocyclic ring containing 1-3 heteroatoms independently selected from N, S, or 0; or

alternatively, R ²³ can join with R ⁷ to form a 5- or 6- membered fused heterocyclic ring or carbocyclic ring substituted with 0-2 R ¹² , said heterocyclic ring containing 1-3 heteroatoms independently selected from N, S, or 0; or

alternatively, R ²² or R ²³ can join with R^ to form a 0- to 7-membered bridge to form a carbocyclic or heterocyclic ring, said bridge being substituted with 0-2 R ¹² and said bridge containing 0-3 heteroatoms independently selected from N, S, or 0 (i.e., a 0-membered bridge is formed when R ²² or R ²³ are taken together with R^ to form a direct bond) ;

R ³¹ is selected from one or more of the following:

keto, halogen, cyano, -CH2NR ¹³ R ¹⁴ , -NR ¹³ R ¹⁴ , -Cθ2R ¹³ , -C(=0)R ⁿ , -OC(=0)R ¹³ , -OR ¹³ , C2-C6 alkoxyalkyl, -S(0) _m R ¹³ , -NHC (=NH)NHR ¹³ , -C(=NH)NHR ¹³ , -C (=0)NR ¹³ R ¹ , -NR ¹⁴ C (=0)R ¹³ , =NOR ¹⁴ , -NR ¹ C(=0)OR ¹⁴ , -OC (=0)NR ¹³ R ¹⁴ , -NR ¹³ C (=0)NR ¹³ R ¹⁴ , -NR ¹⁴ S02NR ¹³ R ¹⁴ , -NR ¹⁴ S02R ¹³ , -Sθ2NR ¹³ R ¹⁴ , C1-C4 alkyl, C2-C4 alkenyl, C3-C10 cycloalkyl, C3-C6 cycloalkylmethyl, benzyl, phenethyl, phenoxy, benzyloxy, nitro, C7-C10 arylalkyl, hydroxamic acid, hydrazide, oxime, boronic acid, sulfonamide,

formyl, C ₃ -C ₆ cycloalkoxy, C ₁ -C ₄ alkyl substituted with -NR ¹³ R ¹⁴ , C1-C4 hydroxyalkyl, methylenedioxy, ethylenedioxy, C1-C4 haloalkyl, C1-C4 haloalkoxy, C1-C4 alkoxycarbonyl, C1-C4 alkylcarbonyloxy, C1-C4 alkylcarbonyl, C1-C4 alkylcarbonylamino,

-OCH2CO2R ¹³ , 2- (1-morpholino)ethoxy, azido, -C(R ¹ )=N(OR ¹⁴ ) ; or

1-3 amino acids, linked together via amide bonds and linked to R ²² , R ²³ , R ⁴ or R ⁷ via the amine or carboxy terminus;

a C5-C14 carbocyclic residue substituted with 0-3

>32.

a C5-C14 carbocyclic residue substituted with 0-5 R ³² ; or

a 5- to 10-membered heterocyclic ring system containing 1 to 4 heteroatoms independently selected from oxygen, nitrogen or sulfur, said heterocyclic ring system being substituted with 0-2 R ³² ;

R ³² , when a substituent on carbon, is selected from one or more of the following:

phenyl, benzyl, phenethyl, phenoxy, benzyloxy, halogen, hydroxy, nitro, cyano, C1-C4 alkyl, C3-C10 cycloalkyl, C3-C6 cycloalkylmethyl, C7-C10 arylalkyl, C1-C4 alkoxy, -CO2H, hydroxamic acid, -CONR ¹³ NR ¹³ R ¹⁴ , hydrazide, oxime, boronic acid, sulfonamide, formyl, C3-C6 cycloalkoxy, -OR ¹³ , C1-C4 alkyl substituted with -NR ¹³ R ¹⁴ , -NR ^l3 R ¹⁴ , C2-C6 alkoxyalkyl, C1-C4 hydroxyalkyl, methylenedioxy,

ethylenedioxy, C3.-C4 haloalkyl, C1-C4 haloalkoxy, C1-C4 alkoxycarbonyl, C1-C4 alkylcarbonyloxy, C1-C4 alkylcarbonyl, C1-C4 alkylcarbonylamino, -S(0) _m R ¹³ , -S02NR ¹³ R ¹⁴ , -NHS02R ¹⁴ , -OCH2CO2H, 2- (1-morpholino) ethoxy, -C (R ¹ ) =N (OR ¹⁴ ) ; N0 ₂ , -OR ¹³ , -NR ⁰ R ⁴¹ , -SO _m R ¹³ , -SO _m NR ¹³ R ¹⁴ , -C (=0)NR ¹³ R ¹⁴ , -OC(=0)NR ¹³ R ¹⁴ , -C(=0)R , -OC(=0)R , -OCO2R ¹³ , phenyl, -C (=0)NR ¹³ - (C ₁ -C ₄ alkyl)-NR ¹³ R ¹⁴ , -C(=O)NR ⁴⁰ R ⁴¹ , C ₁ -C ₄ haloalkyl, C ₁ -C ₄ haloalkoxy, C ₂ -C ₄ haloalkenyl, C ₁ -C ₄ haloalkynyl, or

-C (=0) NR ¹³ C (R ¹¹ ) 2NR ¹³ R ¹⁴ ; -C (=0)NR ¹³ C (R ¹¹ ) ₂ NR ¹³ NR ¹⁴ ; -C (=0)NR ¹³ C(R ¹¹ )2NR ¹³ C02R ¹³ ; -C(=0)NR ¹³ -(Cι-C4 alkyl) -NR ¹³ C0 ₂ R ¹³ ; or

-C (=0) C (R ¹¹ ) NR ¹³ R ¹⁴ ; -C (=0) C (R ¹¹ ) ₂ NR ¹³ NR ¹⁴ ; -C(=0)C(R ^ι:L )2NR ¹³ Cθ ₂ R ¹³ ; -C(=0)- (C ₁ -C ₄ alkyl) -NR ¹³ R ¹⁴ ; -C (=0)- (C1-C4 alkyl)-NR ¹³ Cθ ₂ R ¹³ ; or

C1-C4 alkoxy substituted with 0-4 groups selected from: R ¹¹ , C ₃ -C ₆ cycloalkyl, -CO ₂ R ¹³ , -C (=0) NR ¹³ R ¹⁴ , -NR ¹³ R ¹⁴ or OH;

C ₁ -C ₄ alkyl substituted with 0-4 groups selected from: R ¹¹ , =NR ¹⁴ , =NNR ¹³ C (=0) NR ¹³ R ¹⁴ or -NR ¹³ R ¹⁴ ;

C ₂ -C ₄ alkenyl substituted with 0-4 R ¹¹ ;

C ₂ -C ₄ alkynyl substituted with 0-4 R ¹¹ ;

a 5- or 6-membered heterocyclic ring containing from 1 to 4 heteroatoms selected from oxygen, nitrogen or sulfur;

when R ³² is attached to a saturated carbon atom, it may be =0 or =S;

-89-

SUBSCTTUTE SHEET (RULE 26)

R ³² may alternatively be a 3- or 4- carbon chain attached to adjacent carbons on the ring to form a fused 5- or 6-membered ring, said 5- or 6- membered ring being optionally substituted on the aliphatic carbons with halogen, C1-C4 alkyl, C1-C4 alkoxy, hydroxy, or -NR ¹³ R ¹⁴ ;

R ³² , when a substituent on nitrogen, is selected from one or more of the following:

phenyl, benzyl, phenethyl, hydroxy, C1-C4 hydroxyalkyl, C1-C4 alkoxy, C1-C4 alkyl, C3-C6 cycloalkyl, C3-C6 cycloalkylmethyl, -CH2NR ¹³ R ¹⁴ , -NR ¹³ R ¹⁴ , C2-C6 alkoxyalkyl, C1-C4 haloalkyl, C1-C4 alkoxycarbonyl, -CO2H, C1 _. -C4 alkylcarbonyloxy, C1-C4 alkylcarbonyl, -C (R ¹⁴ ) =N (OR ¹⁴ ) ;

R 40 is selected from: H, C ₁ -C ₃ alkyl;

R ⁴¹ is selected from: -C(=0)NR ¹³ R ¹⁴ ; -C(=0)NR ¹³ NR ¹⁴ ; -C(=0)C(R ^1:L ) ₂ NR ¹³ R ¹⁴ ; -C(=0)C(R ^ι;L ) ₂ NR ¹³ NR ¹⁴ ;

-C (=0) C (R ¹¹ ) ₂ NR ¹³ C0 ₂ R ¹³ ; -C(=0)H; -C(=0)R ^ι:ι ;

-C(=0)-(Cι-C alkyl)-NR ¹³ R ¹⁴ ; -C(=0)-(Ci-C ₄ alkyl)-NR ¹³ C0 ₂ R ¹³ ;

1-3 amino acids linked together via amide bonds, and linked to the N atom via the carboxy terminus;

provided that :

when R ⁴ is hydrogen, at least one of the following is not hydrogen: R ⁷ , R ²² or R ²³ ;

when R ⁴ and R ⁷ are hydrogen, at least two of the following are not hydrogen: R ²² or R ²³ .

[20] Preferred compounds of the Formula (IVa) and Formula (IVb) as described above are those compounds wherein:

R ⁴ and R ⁷ are selected from benzyl, fluorobenzyl, pyrrolylmethyl, methoxybenzyl, isobutyl, nitrobenzyl or aminobenzyl;

R ⁵ is -OH;

R ²² and R ²³ are independently selected from the group consisting of:

hydrogen, allyl, methyl, ethyl, propyl, cyclopropylmethyl, n-butyl, i-butyl, CH2CH=C (CH3) 2, pyridinylmethyl, methallyl, n-pentyl, i-pentyl, hexyl, benzyl, isoprenyl, propargyl, picolinyl, methoxyethyl, cyclohexylmethyl, dimethyl-butyl, ethoxyethyl, methyl-oxazolinylmethyl, naphthylmethyl, methyloxazolinylmethyl, vinyloxyethyl, pentafluorobenzyl, quinolinylmethyl, carboxybenzyl, chloro-thienyl, benzyloxybenzyl, phenylbenzyl, adamantylethyl, cyclopropylmethoxybenzyl, methoxybenzyl, ethylbenzyl, ethoxybenzyl, hydroxybenzyl, hydroxymethylbenzyl, aminobenzyl, formylbenzyl, cyanobenzyl, cinnamyl, allyloxybenzyl, fluorobenzyl, difluorobenzyl, chlorobenzyl,

chloromethylbenzyl, fluoromethylbenzyl, iodobenzyl, bromobenzyl, cyclobutylmethyl, formaldoximebenzyl, cyclopentylmethyl, nitrobenzyl, (H ₂ NC (=0) ) -benzyl, carbomethoxybenzy1, carboethoxybenzyl, tetrazolylbenzyl, and dimethylallyl, aminomethylbenzyl, (O-benzyl-formaldoxime)benzyl,

(O-methyl-formaldoxime)benzyl, (CH3O2CO) -benzyl,

(HOCH2CH2N=CH) -benzyl, N-benzylaminocarbonylbenzyl, N-methylaminobenzyl, N-ethylaminobenzyl, N-ethylaminomethylbenzyl, acetylbenzyl, acetoxybenzyl, N-hydroxylaminobenzyl, phenylmethyl- boronic acid, N-hydroxylaminomethylbenzyl,

(hydroxyl) ethylbenzyl, (CH3C (=NOH) ) -benzyl,

(H2NNHC (=0) ) -benzyl, (H2NC (=0) NHN=CH) -benzyl, (CH3ONHC (=0) ) -benzyl, (H0NHC (=0) ) -benzyl,

(CH3NHC (=0) )-benzyl,

N,N-dimethylaminocarbonylbenzyl, (HOCH2CH (OH) CH2O)- benzyl, hydroxyethoxybenzyl (oxazolidinyl) -benzyl,

(hydroxyl) hexyl, hexenyl, (hydroxy) octyl, (hydroxyl)pentyl, (carboxy)pentyl,

(carbomethoxy)pentyl, (methyIthio)benzyl,

(methylsulfonyl)benzyl, N,N-dimethylarninomethylbenzyl,

N-methylaminomethylbenzyl, glycylaminobenzyl, N,N-dimethylglycylaminobenzyl, alanylaminobenzyl,

(N-phenylmethoxycarbonyl) alanylaminobenzyl, phenylalanylaminobenzyl, (N-phenylmethoxycarbonyl) phenylalanylaminobenzyl, (CH3CH2NHC (=0) ) -benzyl,

N,N-diethylaminocarbonylbenzyl, N-ethylaminocarbonylbenzyl, N-propylaminocarbonylbenzyl,

N, N-diisopropylaminocarbonylbenzyl, N, N-di-n- propylaminocarbonylbenzyl, (hydroxypropynyl)benzyl, (imidazolyl-C (=0) ) -benzyl, trifluoroacetylbenzyl, (pyrazolyl)benzyl, (H2NSO2) -benzyl, dihydroxyethylbenzyl, (MeHNC (=0)NH) -benzyl,

(H2NC (=0)NH) -benzyl, (HC (=0)NH) -benzyl, methanesulfonylpentyl, methoxypentyl, N-formyl-N- methylaminobenzyl, acetylaminobenzyl, propionylbenzyl, butyrylbenzyl, (CH3CH2C(=N0H) )- benzyl, (trifluorohydroxyethyl)benzyl,

(CF3C (=N0H) ) -benzyl, (N-methylglycyl) aminobenzyl, ( (4-morpholino) ethyl)aminocarbonylbenzyl, (N,N-dimethylaminoethyl)aminocarbonylbenzyl, (N,N-diethylaminoethyl)aminocarbonylbenzyl, (4-methylpiperazin-l-ylethyl)aminocarbonylbenzyl, (benzyl-NHC (=0)0)benzyl, (CH3NHC(=0)0)benzyl, (NH ₂ C(=0)CH 0) enzyl, (NH ₂ C(=NH) ) enzyl, ( (N-phenylmethoxycarbonyl) glycylamino)benzyl, (imidazolylmethyl)benzyl, ( (CH ₃ ) ₃ C-C (=0) )benzyl, (N-methyl-N-ethylaminoethyl)aminocarbonylbenzyl, (pyrrolidinylethyl)aminocarbonylbenzyl, (piperidinylethyl)aminocarbonylbenzyl .

[21] Another embodiment of the present invention are compounds of Formula (I) having the Formula (Va) :

(Va) or a pharmaceutically acceptable salt or prodrug form thereof, wherein:

R ⁴ and R ⁷ are independently selected from the following groups :

hydrogen;

C1-C8 alkyl substituted with 0-3 R ¹¹ ;

C2-C8 alkenyl substituted with 0-3 R ¹¹ ; C2-C8 alkynyl substituted with 0-3 R ¹¹ ; C3-C8 cycloalkyl substituted with 0-3 R ¹¹ ; 6~Ci0 bicycloalkyl substituted with 0-3 R ¹¹ ; aryl substituted with 0-3 R ¹² ; a C6-C14 carbocyclic residue substituted with 0-3 R ¹² ; a heterocyclic ring system substituted with 0-2 R ¹² , composed of 5 to 10 atoms including at least one, preferably 1-4, nitrogen, oxygen or sulfur atom;

R5 is selected from =0; H; halogen; Cχ-C6 alkyl substituted with 0-3 -OH; -N(R ²⁰ )2; -SR ²⁰ ; or -OR ²⁰ ;

R ²⁰ is selected from:

hydrogen;

C1-C6 alkyl substituted with 0-3 R ¹¹ ; C3-C6 alkoxyalkyl substituted with 0-3 R ¹¹ ;

C -C _ alkylcarbonyl substituted with 0-3 R ¹¹ ;

Ci-Cδ alkoxycarbonyl substituted with 0-3 R ¹¹ ; benzoyl substituted with 0-3 R ¹² ; phenoxycarbonyl substituted with 0-3 R ¹² ; phenylaminocarbonyl substituted with 0-3 R ¹² ;

C ₁ -C ₆ alkylsulfenyl substituted with 0-3 R ¹ ;

C ₁ -C ₆ alkylsulfonyl substituted with 0-3 R ¹¹ ; or any group that, when administered to a mammalian subject, cleaves to form a free hydroxyl, amino or sulfhydryl;

R ¹¹ is selected from one or more of the following:

keto, halogen, cyano, -CH2NR ¹³ R ¹⁴ , -NR ¹³ R ¹⁴ , -CO2R ¹³ , -OC(=0)R ¹³ , -OR ¹³ , C2-C6 alkoxyalkyl,

-S(0) _m R ¹³ , -NHC(=NH)NHR ¹³ , -C (=NH) NHR ¹³ , -C(=0)NR ¹³ R ¹⁴ , -NR ¹⁴ C(=0)R ¹³ , =NOR ¹⁴ ,

-NR ¹⁴ C(=0)OR ¹⁴ , -OC(=0)NR ¹³ R ¹⁴ , -NR ¹³ C (=0)NR ¹ R ¹⁴ , -NR ¹ S02NR ¹³ R ¹⁴ , -NR ¹⁴ Sθ2R ¹³ , -Sθ2NR ¹³ R ¹⁴ , C1-C4 alkyl, C2-C4 alkenyl, C3-C10 cycloalkyl, C3-C6 cycloalkylmethyl, benzyl, phenethyl, phenoxy, benzyloxy, nitro, C7-C10 arylalkyl, hydroxamic acid, hydrazide, boronic acid, sulfonamide, formyl, C3-C6 cycloalkoxy, C ₁ -C ₄ alkyl substituted with -NR ¹³ R ¹⁴ , C1-C4 hydroxyalkyl, methylenedioxy, ethylenedioxy, C1-C4 haloalkyl, C1-C4 haloalkoxy, C1-C4 alkoxycarbonyl, C1-C4 alkylcarbonyloxy, C1 _. -C4 alkylcarbonyl, C1-C4 alkylcarbonylamino, -OCH2CO2H, 2- (1-morpholino) ethoxy, azido, or -C(R ¹⁴ )=N(OR ¹⁴ ) ;

1-3 amino acids, linked together via amide bonds and linked to R ⁴ or R ⁷ , R ²⁰ , or R ²¹ via the amine or carboxy terminus;

-(C ₁ -C ₃ alkyl) aryl substituted with 0-2 R ¹² ;

a C5-C14 carbocyclic residue substituted with 0-3 R ¹² ;

aryl substituted with 0-3 R ² ; or

a 5- to 10-membered heterocyclic ring system containing 1 to 4 heteroatoms independently selected from oxygen, nitrogen or sulfur, said heterocyclic ring system being substituted with 0-3 R ² ;

R ¹² , when a substituent on carbon, is selected from one or more of the following:

-95-

SUBSCTTUTE SHEET (RULE 26)

phenyl, benzyl, phenethyl, phenoxy, benzyloxy, halogen, hydroxy, nitro, cyano, C1-C4 alkyl, C3-C6 cycloalkyl, C3-C6 cycloalkylmethyl, C7-C10 arylalkyl, C1-C alkoxy, -CO2H, hydroxamic acid, hydrazide, oxime, boronic acid, sulfonamide, formyl, C3-C6 cycloalkoxy, -OR ¹³ , C1 _. -C4 alkyl substituted with -NR ¹³ R ¹⁴ , -NR ¹³ R ¹⁴ , C2-C6 alkoxyalkyl, C1-C4 hydroxyalkyl, methylenedioxy, ethylenedioxy, C3 _. -C4 haloalkyl, C1-C4 haloalkoxy, C1-C4 alkoxycarbonyl, C1-C4 alkylcarbonyloxy, C1-C4 alkylcarbonyl, C1-C4 alkylcarbonylamino, -S(0) _m R ¹³ , -Sθ2NR ¹³ R ¹⁴ , -NHSO2R ¹⁴ , -OCH2CO2H, 2- (1-morpholino) ethoxy; or

a 5- or 6-membered heterocyclic ring containing from 1 to 4 heteroatoms independently selected from oxygen, nitrogen or sulfur;

when R ¹² is attached to a saturated carbon atom, it may be carbonyl or thiocarbonyl;

or R ¹² may alternatively be a 3- or 4- carbon chain attached to adjacent carbons on the ring to form a fused 5- or 6-membered ring, said 5- or 6- membered ring being optionally substituted on the aliphatic carbons with halogen, C1-C4 alkyl, C1-C4 alkoxy, hydroxy, or -NR ¹ R ¹⁴ ;

R ² , when a substituent on nitrogen, is selected from one or more of the following:

phenyl, benzyl, phenethyl, hydroxy, C1-C4 hydroxyalkyl, C1-C4 alkoxy, C1-C4 alkyl, C3-C6 cycloalkyl, C3-C6 cycloalkylmethyl, -CH2NR ¹³ R ¹⁴ , -NR ¹³ R ¹⁴ , C2-C6 alkoxyalkyl, C1-C4 haloalkyl, C1-C4

-96-

SUBSΠTLΠΈ SHEET (RULE 26)

alkoxycarbonyl, -CO2H, C1-C4 alkylcarbonyloxy, C1-C4 alkylcarbonyl, -C(R ¹⁴ )=N(OR ¹⁴ ) ;

R ¹³ is selected from: H; phenyl substituted with 0-3 R ^11A ; benzyl substituted with 0-3 R ^11A ;

C1-C6 alkyl substituted with 0-3 R ^11A ;

C ₂ -C ₄ alkenyl substituted with 0-3 R ^11A ; C1-C6 alkylcarbonyl substituted with 0-3 R ^11A ;

C1-C6 alkoxycarbonyl substituted with 0-3 R ^11A ;

C1-C6 alkylaminocarbonyl substituted with 0-3 R ^11A ;

C3-C6 alkoxyalkyl substituted with 0-3 R ^11A ; an amine protecting group when R ¹³ is bonded to N; a hydroxy protecting group when R ¹³ is bonded to 0;

R ¹⁴ is OH, H, CF3; C1-C4 alkyl substituted with 0-3 groups selected from OH, C ₁ -C ₄ alkoxy, halogen, H2; C1-C ₆ alkoxy; NH2; C2-C ₆ alkenyl; or benzyl; an amine protecting group when R ¹⁴ is bonded to N; a hydroxy protecting group when R ¹⁴ is bonded to 0;

R ¹³ and R ¹⁴ can alternatively join to form -(CH2)4~,

-(CH2)5~, -CH2CH2N(R ¹⁵ )CH2CH2", or -CH2CH2OCH2CH2-;

R ¹⁵ is H or CH3;

is 0, 1 or 2;

R ²² is independently selected from the following:

hydrogen;

C1-C8 alkyl substituted with 0-3 R ³¹ ; C2-C8 alkenyl substituted with 0-3 R ³¹ ; C2-C8 alkynyl substituted with 0-3 R ³¹ ;

a C3-C14 carbocyclic ring system substituted with

0-5 R ³¹ or R ³² ; a 5- to 10-membered heterocyclic ring system containing 1 to 4 heteroatoms independently selected from oxygen, nitrogen or sulfur, said heterocyclic ring system being substituted with 0-2 R ³² ;

R ²³ is independently selected from the following:

hydrogen;

C1-C8 alkyl substituted with 0-3 R ³¹ ; C2-C8 alkenyl substituted with 0-3 R ³¹ ; C2-C8 alkynyl substituted with 0-3 R ³¹ ;

a C3-C14 carbocyclic ring system substituted with 0-5 R ³¹ or R ³² ;

a 5- to 10-membered heterocyclic ring system containing 1 to 4 heteroatoms independently selected from oxygen, nitrogen or sulfur, said heterocyclic ring system being substituted with 0-2 _R 32.

alternatively, R ²² can join with R ⁴ to form a 5- or 6- membered fused heterocyclic ring or carbocyclic ring substituted with 0-2 R ¹² , said heterocyclic ring containing 1-3 heteroatoms independently selected from N, S, or 0; or

alternatively, R ²³ can join with R ⁷ to form a 5- or 6- membered fused heterocyclic ring or carbocyclic ring substituted with 0-2 R ¹² , said heterocyclic ring containing 1-3 heteroatoms independently selected from N, S, or 0; or

alternatively, R ²² ' R ²⁷ or R ²⁸ can join with R ⁵ to form a 0- to 7-membered bridge to form a carbocyclic or heterocyclic ring, said bridge being substituted with 0-2 R ¹² and said bridge containing 0-3 heteroatoms independently selected from N, S, or 0 (i.e., a 0-membered bridge is formed when R ²² , R ²⁷ , or R ²⁸ are taken together with R^ to form a direct bond) ;

R ³¹ is selected from one or more of the following:

keto, halogen, cyano, -CH2NR ¹³ R ¹⁴ , -NR ^l3 R ¹⁴ , -C02R ¹³ , -C(=0)R ⁿ , -OC(=0)R ¹³ , -OR ¹³ , C2~C6 alkoxyalkyl, -S(0) _m R ¹³ , -NHC (=NH)NHR ¹³ , -C(=NH)NHR ¹³ , -C (=0)NR ¹³ R ¹⁴ , -NR ¹⁴ C (=0) R ¹³ , =NOR ¹⁴ , -NR ¹⁴ C(=0)OR ¹⁴ , -OC(=0)NR ¹³ R ¹⁴ , -NR ¹³ C (=0)NR ¹³ R ¹ , -NR ¹ S02NR ¹³ R ¹⁴ , -NR ¹⁴ S02R ¹³ , -Sθ2NR ¹³ R ¹⁴ , C1-C4 alkyl, C2-C4 alkenyl, C3-C10 cycloalkyl, C3-C6 cycloalkylmethyl, benzyl, phenethyl, phenoxy, benzyloxy, nitro, C7-C10 arylalkyl, hydroxamic acid, hydrazide, oxime, boronic acid, sulfonamide, formyl, C ₃ -C ₆ cycloalkoxy, C ₁ -C ₄ alkyl substituted with -NR ¹³ R ¹⁴ , C1-C4 hydroxyalkyl, methylenedioxy, ethylenedioxy, C1-C4 haloalkyl, C1-C4 haloalkoxy, C1-C4 alkoxycarbonyl, C1-C4 alkylcarbonyloxy, C1-C4 alkylcarbonyl, C1 _. -C4 alkylcarbonylamino, -OCH2CO2R ¹³ , 2- (1-morpholino) ethoxy, azido, -C(R ¹⁴ )=N(OR ¹⁴ ) ; or

1-3 amino acids, linked together via amide bonds and linked to R ²² , R ²³ , R ²⁵ , R ²⁷ , R ⁴ or R ⁷ via the amine or carboxy terminus;

a C5-C14 carbocyclic residue substituted with 0-3 R ³² ;

a C5-C14 carbocyclic residue substituted with 0-5 R ³² ; or

a 5- to 10-membered heterocyclic ring system containing 1 to 4 heteroatoms independently selected from oxygen, nitrogen or sulfur, said heterocyclic ring system being substituted with 0-2 R ³² ;

R ³² , when a substituent on carbon, is selected from one or more of the following:

phenyl, benzyl, phenethyl, phenoxy, benzyloxy, halogen, hydroxy, nitro, cyano, C1-C4 alkyl, C3-C10 cycloalkyl, C3-C6 cycloalkylmethyl, C7-C10 arylalkyl, C1-C4 alkoxy, -CO2H, hydroxamic acid, -CONR ¹³ NR ¹³ R ¹⁴ , hydrazide, oxime, boronic acid, sulfonamide, formyl, C3-C6 cycloalkoxy, -OR ¹³ , C1-C4 alkyl substituted with -NR ¹³ R ¹⁴ , -NR ¹³ R ¹⁴ , C2-C6 alkoxyalkyl, C1-C4 hydroxyalkyl, methylenedioxy, ethylenedioxy, C1-C4 haloalkyl, C1-C4 haloalkoxy, C1-C4 alkoxycarbonyl, C1-C4 alkylcarbonyloxy, C1-C4 alkylcarbonyl, C1-C4 alkylcarbonylamino, -S(0) _m R ¹³ , -S02NR ¹³ R ¹⁴ , -NHSO2R ¹⁴ , -OCH2CO2H,

2- (1-morpholino) ethoxy, -C (R ¹⁴ ) =N (OR ¹⁴ ) ; NO ₂ , -OR ¹³ , -NR ⁴⁰ R ⁴¹ , -SO _m R ¹³ , -SO _m NR ¹³ R ¹⁴ , -C (=0)NR ¹³ R ¹⁴ , -OC(=0)NR ¹³ R ¹⁴ , -C (=Q) R ¹ - , -OC (=0)R ¹¹ , -OCO2R ¹³ , phenyl, -C (=0)NR ¹³ - (C ₁ -C ₄ alkyl) -NR ¹ R ¹⁴ , -C(=O)NR ⁴⁰ R ⁴¹ , C ₁ -C ₄ haloalkyl, C ₁ -C ₄ haloalkoxy, C ₂ -C ₄ haloalkenyl, C ₁ -C haloalkynyl, or

-C(=0)NR ¹³ C(R ¹¹ ) ₂ NR ¹³ R ¹⁴ ; -C(=0)NR ¹³ C (R ¹¹ ) ₂ NR ¹³ NR ¹⁴ ; -C (=0)NR ¹³ C (R ¹¹ ) ₂ NR ¹³ C0 ₂ R ¹³ ; alkyl) -NR ¹³ C0 R ¹³ ; or

-100-

SUBSΠTUTESHEET(RULE26)

-C (=0) C (R ¹¹ ) ₂ NR ¹ R ¹⁴ ; -C (=0) C (R ¹¹ ) ₂ NR ¹³ NR ¹⁴ ; -C(=0)C(R ^1:L )2NR ¹³ C0 ₂ R ¹³ ; -C (=0) - (C ₁ -C4 alkyl)-NR ¹³ R ¹⁴ ; -C(=0)- (C1-C4 alkyl)-NR ¹³ C0 ₂ R ¹³ ; or

C1-C4 alkoxy substituted with 0-4 groups selected from: R ¹¹ , C ₃ -C6 cycloalkyl, -C0 ₂ R ¹³ , -C (=0)NR ¹³ R ¹⁴ , -NR ¹³ R ¹⁴ or OH;

C ₁ -C ₄ alkyl substituted with 0-4 groups selected from: R ¹¹ , =NR ¹⁴ , =NNR ¹³ C (=0)NR ¹³ R ¹⁴ or -NR ¹³ R ¹⁴ ;

C ₂ -C ₄ alkenyl substituted with 0-4 R ¹¹ ;

C ₂ -C ₄ alkynyl substituted with 0-4 R ¹¹ ;

a 5- or 6-membered heterocyclic ring containing from 1 to 4 heteroatoms selected from oxygen, nitrogen or sulfur;

when R ³² is attached to a saturated carbon atom, it may be =0 or =S;

R ³² may alternatively be a 3- or 4- carbon chain attached to adjacent carbons on the ring to form a fused 5- or 6-membered ring, said 5- or 6- membered ring being optionally substituted on the aliphatic carbons with halogen, C1-C4 alkyl, C1-C4 alkoxy, hydroxy, or -NR ¹³ R ¹⁴ ;

R ³² , when a substituent on nitrogen, is selected from one or more of the following:

phenyl, benzyl, phenethyl, hydroxy, C1-C4 hydroxyalkyl, C1-C4 alkoxy, C1-C4 alkyl, C3-C6 cycloalkyl, C3-C6 cycloalkylmethyl, -CH2NR ¹³ R ¹⁴ ,

-101-

SUBSCTTUTE SHEET (RULE 26)

-NR ³ R ¹⁴ , C2-C6 alkoxyalkyl, C1-C4 haloalkyl, C1-C4 alkoxycarbonyl, -CO2H, C1-C4 alkylcarbonyloxy, C1-C4 alkylcarbonyl, -C (R ¹⁴ ) =N (OR ¹⁴ ) ;

,40 is selected from: H, C ₁ -C3 alkyl;

R ⁴¹ is selected from: -C(=0)NR ¹ R ¹⁴ ; -C(=0)NR ¹³ NR ¹⁴ ; -C(=0)C(R ¹¹ ) ₂ NR ¹³ R ¹⁴ ; -C(=0) C (R ¹¹ ) ₂ NR ¹³ NR ¹⁴ ; -C (=0) C (R ¹¹ ) ₂ NR ¹³ Cθ2R ¹³ ; -C(=0)H; -C(=0)R ^1:1 ; -C(=0)-(Cι-C ₄ alkyl) -NR ¹³ R ¹⁴ ;

-C (=0) - (C ₁ -C ₄ alkyl) -NR ¹³ C0 ₂ R ¹³ ;

1-3 amino acids linked together via amide bonds, and linked to the N atom via the carboxy terminus;

provided that : when R ⁴ is hydrogen, at least one of the following is not hydrogen: R ⁷ , R ²² or R ²³ ; when R ⁴ and R ⁷ are hydrogen, at least two of the following are not hydrogen: R ²² or R ²³ .

[22] Preferred compounds of Formula (Va) as described above are those compounds wherein :

R ⁴ and R ⁷ are selected from benzyl, fluorobenzyl, pyrrolylmethyl, methoxybenzyl, isobutyl, nitrobenzyl or aminobenzyl;

R ⁵ is OH or =0;

R ²² and R ²³ are independently selected from the group consisting of:

hydrogen, allyl, methyl, ethyl, propyl, cyclopropylmethyl, n-butyl, i-butyl, CH2CH=C (CH3) 2. pyridinylmethyl, methallyl, n-pentyl, i-pentyl, hexyl, benzyl, isoprenyl, propargyl, picolinyl, methoxyethyl, cyclohexylmethyl, dimethyl-butyl, ethoxyethyl, methyl-oxazolinylmethyl, naphthylmethyl, methyloxazolinylmethyl, vinyloxyethyl, pentafluorobenzyl, quinolinylmethyl, carboxybenzyl, chloro-thienyl, benzyloxybenzyl, phenylbenzyl, adamantylethyl, cyclopropylmethoxybenzyl, methoxybenzyl, methylbenzyl, ethoxybenzyl, hydroxybenzyl, hydroxymethylbenzyl, aminobenzyl, formylbenzyl, cyanobenzyl, cinnamyl, allyloxybenzyl, fluorobenzyl, difluorobenzyl, chlorobenzyl, chloromethylbenzyl, fluoromethylbenzyl, iodobenzyl, bromobenzyl, cyclobutylmethyl, formaldoximebenzyl, cyclopentylmethyl, nitrobenzyl, (H ₂ NC (=0) ) -benzyl, carbomethoxybenzyl, carboethoxybenzyl, tetrazolylbenzyl, and dimethylallyl, aminomethylbenzyl, (0-benzyl-formaldoxime)benzyl, (0-methyl-formaldoxime) benzyl, (CH3O2CO) -benzyl,

(HOCH2CH2N=CH)-benzyl, N-benzylaminocarbonylbenzyl, N-methylaminobenzyl, N-ethylaminobenzyl, N-ethylaminomethylbenzyl, acetylbenzyl, acetoxybenzyl, N-hydroxylaminobenzyl, phenylmethyl- boronic acid, N-hydroxylaminomethylbenzyl, (hydroxyl) ethylbenzyl, (CH3C (=NOH) ) -benzyl, (H2NNHC(=0) ) -benzyl, (H2NC (=0)NHN=CH) -benzyl, (CH3θNHC(=0) ) -benzyl, (HONHC (=0) ) -benzyl,

(CH3NHC (=0) )-benzyl, N,N-dimethylaminocarbonylbenzyl, (HOCH2CH (OH) CH2O)- benzyl, hydroxyethoxybenzyl (oxazolidinyl) -benzyl,

(hydroxyl) hexyl, hexenyl, (hydroxy) octyl,

(hydroxyl)pentyl, (carboxy) pentyl,

(carbomethoxy)pentyl, (methylthio)benzyl,

(methylsulfonyl)benzyl, N,N-dimethylaminomethylbenzyl,

N-methylaminomethylbenzyl, glycylaminobenzyl,

N,N-dimethylglycylaminobenzyl, - alanylaminobenzyl,

(N-phenylmethoxycarbonyl)alanylaminobenzyl, phenylalanylaminobenzyl, (N-phenylmethoxycarbonyl) phenylalanylaminobenzyl, (CH3CH2NHC (=0) ) -benzyl, N,N-diethylaminocarbonylbenzyl, N-ethylaminocarbonylbenzyl, N-propylaminocarbonylbenzyl,

N,N-diisopropylaminocarbonylbenzyl, N, N-di-n- propylaminocarbonylbenzyl, (hydroxypropynyl)benzyl,

(imidazolyl-C (=0) ) -benzyl, trifluoroacetylbenzyl,

(pyrazolyl)benzyl, (H2NSO2)-benzyl, dihydroxyethylbenzyl, (MeHNC (=0) NH) -benzyl,

(H2NC (=0)NH) -benzyl, (HC (=0)NH) -benzyl, methanesulfonylpentyl, methoxypentyl, N-formyl-N- methylaminobenzyl, acetylaminobenzyl, propionylbenzyl, butyrylbenzyl, (CH3CH2C (=N0H) ) - benzyl, (trifluorohydroxyethyl)benzyl, (CF3C (=N0H) ) -benzyl, (N-methylglycyl) aminobenzyl, ( (4-morpholino) ethyl) aminocarbonylbenzyl,

(N,N-dimethylaminoethyl) aminocarbonylbenzyl, (N,N-diethylaminoethyl) aminocarbonylbenzyl, (4-methylpiperazin-l-ylethyl)aminocarbonylbenzyl, (benzyl-NHC (=0)0)benzyl, (CH3NHC (=0) 0)benzyl, (NH ₂ C (=0)CH ₂ 0)benzyl, (NH ₂ C (=NH) )benzyl,

( (N-phenylmethoxycarbonyl) glycylamino)benzyl, (imidazolylmethyl)benzyl, ( (CH3) ₃ C-C (=0) )benzyl,

(N-methyl-N-ethylaminoethyl)aminocarbonylbenzyl, (pyrrolidinylethyl)aminocarbonylbenzyl, (piperidinylethyl) aminocarbonylbenzyl .

[23] Another preferred embodiment of the present invention are those compounds of Formula (I) of the Formulae (Ie) or (If) or (Ig) :

(Ie)

(if)

or a pharmaceutically acceptable salt or prodrug form thereof, wherein:

R ⁴ and R ⁷ are independently selected from the following groups :

hydrogen;

Cl-Cδ alkyl substituted with 0-3 R ¹¹ ;

-105-

SUBSCTTUTE SHEET (RULE 26)

C2-C8 alkenyl substituted with 0-3 R ¹¹ ; C2-C8 alkynyl substituted with 0-3 R ¹¹ ; C3-C8 cycloalkyl substituted with 0-3 R ¹¹ ; C6- i0 bicycloalkyl substituted with 0-3 R-- ; aryl substituted with 0-3 R ¹² ; a C6~Ci4 carbocyclic residue substituted with 0-3 R ¹² ; a heterocyclic ring system substituted with 0-2 R ¹² , composed of 5 to 10 atoms including at least one, preferably 1-4, nitrogen, oxygen or sulfur atom;

R ⁵ is -OR ²⁰ ;

R ²⁰ is H or any group that, when administered to a mammalian subject, cleaves to form a free hydroxyl;

R ¹¹ is selected from one or more of the following:

keto, halogen, cyano, -CH2NR ¹³ R ¹⁴ , -NR ¹³ R ¹⁴ ,

-CO2R ¹³ , -OC(=0)R ¹³ , -OR ¹³ , C2-C6 alkoxyalkyl, -S(0) _m R ¹³ , -NHC(=NH)NHR ¹³ , -C (=NH)NHR ¹³ , -C(=0)NR ¹³ R ¹⁴ , -NR ¹⁴ C(=0)R ¹³ , =NOR ¹⁴ , -NR ¹⁴ C(=0)OR ¹⁴ , -OC(=0)NR ¹³ R ¹⁴ , -NR ¹ C (=0)NR ¹³ R ¹⁴ , -NR ¹⁴ S02NR ¹³ R ¹⁴ , -NR ¹⁴ S02R ¹³ , -Sθ2NR ¹³ R ¹⁴ , C1-C4 alkyl, C2-C alkenyl, .C3-C10 cycloalkyl, C3-C6 cycloalkylmethyl, benzyl, phenethyl, phenoxy, benzyloxy, nitro, C7-C10 arylalkyl, hydroxamic acid, hydrazide, boronic acid, sulfonamide, formyl, C ₃ -C6 cycloalkoxy, C ₁ -C ₄ alkyl substituted with -NR ¹³ R ¹⁴ , C1-C4 hydroxyalkyl, methylenedioxy, ethylenedioxy, C1-C4 haloalkyl, C1-C4 haloalkoxy, C1-C4 alkoxycarbonyl, C1-C4 alkylcarbonyloxy, C3 _. -C4 alkylcarbonyl, C1-C4 alkylcarbonylamino,

-OCH2CO2H, 2- (1-morpholino) ethoxy, azido, or -C(R ¹⁴ )=N(OR ¹⁴ ) ;

1-3 amino acids, linked together via amide bonds 5. and linked to R ⁴ or R ⁷ , R ²⁰ , or R ²¹ via the amine or carboxy terminus;

-(C ₁ -C3 alkyl)aryl substituted with 0-2 R ¹² ;

0 a C5-C14 carbocyclic residue substituted with 0-3 R ¹² ;

aryl substituted with 0-3 R ¹² ; or

5 a 5- to 10-membered heterocyclic ring system containing 1 to 4 heteroatoms independently selected from oxygen, nitrogen or sulfur, said heterocyclic ring system being substituted with 0-3 R ² ;

R ¹² , when a substituent on carbon, is selected from one or more of the following:

phenyl, benzyl, phenethyl, phenoxy, benzyloxy, halogen, hydroxy, nitro, cyano, C1-C4 alkyl, C3-C6 cycloalkyl, C3-C6 cycloalkylmethyl, C7-C10 arylalkyl, C1-C4 alkoxy, -CO2H, hydroxamic acid, hydrazide, oxime, boronic acid, sulfonamide, formyl, C3-C6 cycloalkoxy, -OR ¹³ , C1-C4 alkyl substituted with -NR ¹³ R ¹⁴ , -NR ¹³ R ¹⁴ , C2"C6 alkoxyalkyl, C1-C4 hydroxyalkyl, methylenedioxy, ethylenedioxy, C1-C4 haloalkyl, C1-C4 haloalkoxy, C1-C4 alkoxycarbonyl, C1-C4 alkylcarbonyloxy, C1-C4 alkylcarbonyl, C1-C4 alkylcarbonylamino, -S(0) _m R ¹³ , -Sθ2NR ^l3 R ¹⁴ , -NHS02R ¹⁴ , -OCH2CO2H, 2- (1-morpholino) ethoxy; or

-107-

SUBST1TUTE SHEET (RULE 26)

a 5- or 6-membered heterocyclic ring containing from 1 to 4 heteroatoms independently selected from oxygen, nitrogen or sulfur;

when R ¹² is attached to a saturated carbon atom, it may be carbonyl or thiocarbonyl;

or R ¹² may alternatively be a 3- or 4- carbon chain attached to adjacent carbons on the ring to form a fused 5- or 6-membered ring, said 5- or 6- membered ring being optionally substituted on the aliphatic carbons with halogen, C1 _. -C4 alkyl, C1 _. -C4 alkoxy, hydroxy, or -NR ¹³ R ¹⁴ ;

R ¹² , when a substituent on nitrogen, is selected from one or more of the following:

phenyl, benzyl, phenethyl, hydroxy, C1-C4 hydroxyalkyl, C1-C4 alkoxy, C1-C4 alkyl, C3-C6 cycloalkyl, C3-C6 cycloalkylmethyl, -CH2NR ¹³ R ¹⁴ ,

-NR ¹ R ¹⁴ , C2-C6 alkoxyalkyl, C1-C4 haloalkyl, C1-C4 alkoxycarbonyl, -CO2H, C1-C4 alkylcarbonyloxy,

C1-C4 alkylcarbonyl, -C (R ¹⁴ )=N (OR ¹⁴ ) ;

R ¹³ is selected from:

H; phenyl substituted with 0-3 R ^11A ; benzyl substituted with 0-3 R ^11A ; C1-C6 alkyl substituted with 0-3 R ^11A ;

C ₂ -C ₄ alkenyl substituted with 0-3 R ^11A ;

C1-C6 alkylcarbonyl substituted with 0-3 R ^11A ;

C1-C6 alkoxycarbonyl substituted with 0-3 R ^11A ;

Ci-Cβ alkylaminocarbonyl substituted with 0-3 R ^11A ; C3-C6 alkoxyalkyl substituted with 0-3 R ^11A ; an amine protecting group when R ¹³ is bonded to N;

a hydroxy protecting group when R ¹³ is bonded to 0;

R ¹⁴ is OH, H, CF3; C1-C4 alkyl substituted with 0-3 groups selected from OH, C ₁ -C ₄ alkoxy, halogen, NH2; Ci-Cg alkoxy; NH2; C ₂ -C6 alkenyl; or benzyl; an amine protecting group when R ¹⁴ is bonded to N; a hydroxy protecting group'when R ¹⁴ is bonded to 0;

R ¹³ and R ¹⁴ can alternatively join to form -(CH2)4~, -(CH2)5~, -CH2CH2N(R ¹⁵ )CH2CH2", or -CH2CH2OCH2CH2-;

R ¹⁵ is H or CH3;

m is 0, 1 or 2;

.22 is independently selected from the following:

hydrogen;

C1-C8 alkyl substituted with 0-3 R ³¹ ; C2-C8 alkenyl substituted with 0-3 R ³¹ ;

C2-C8 alkynyl substituted with 0-3 R ³¹ ; a C3-C14 carbocyclic ring system substituted with 0-5 R ³¹ or R ³² ; a 5- to 10-membered heterocyclic ring system containing 1 to 4 heteroatoms independently selected from oxygen, • nitrogen or sulfur, said heterocyclic ring system being substituted with 0-2 _R 32.

R ²⁷ is independently selected from the following:

hydrogen;

C1-C8 alkyl substituted with 0-3 R ³¹ ; C2-C8 alkenyl substituted with 0-3 R ³¹ ; C2-C8 alkynyl substituted with 0-3 R ³¹ ;

-109-

SUBSCTTUTE SHEET (RULE 26)

a C3-C14 carbocyclic ring system substituted with 0-5 R ³¹ or R ³² ;

a 5- to 10-membered heterocyclic ring system containing 1 to 4 heteroatoms independently selected from oxygen, nitrogen or sulfur, said heterocyclic ring system being substituted with 0-2 R ³² ;

alternatively, R ²² can join with R ⁴ to form a 5- or 6- membered fused heterocyclic ring or carbocyclic ring substituted with 0-2 R ¹² , said heterocyclic ring containing 1-3 heteroatoms independently selected from N, S, or 0; or

alternatively, R ²⁷ can join with R ⁷ to form a 5- or 6- membered fused heterocyclic ring or carbocyclic ring substituted with 0-2 R ¹² , said heterocyclic ring containing 1-3 heteroatoms independently selected from N, S, or 0; or

alternatively, R ²² or R ²⁷ can join with R^ to form a 0- to 7-membered bridge to form a carbocyclic or heterocyclic ring, said bridge being substituted with 0-2 R ¹² and said bridge containing 0-3 heteroatoms independently selected from N, S, or 0 (i.e., a 0-membered bridge is formed when R ²² or R ²⁷ are taken together with R^ to form a direct bond) ;

R ³¹ is selected from one or more of the following:

keto, halogen, cyano, -CH2NR ¹³ R ¹⁴ , -NR ¹ R ¹⁴ , -C02R ¹³ , -C(=0)R ⁿ , -OC(=0)R ¹³ , -OR ¹³ , C2-C6 alkoxyalkyl, -S(0) _m R ¹³ , -NHC (=NH)NHR ¹³ ,

-C(=NH)NHR ¹³ , -C(=0)NR ¹³ R ¹⁴ , -NR ¹⁴ C (=0) R ¹³ , =NOR ¹⁴ ,

-110-

SUBST1TUTE SHEET (RULE 26)

-NR ¹⁴ C(=0)OR ¹⁴ , -OC(=0)NR ¹³ R ¹⁴ , -NR ¹³ C(=0)NR ¹³ R ¹⁴ , -NR ¹⁴ S02NR ¹³ R ¹⁴ , -NR ¹⁴ S02R ¹³ , -Sθ2NR ¹³ R ¹⁴ , C1-C4 alkyl, C2-C4 alkenyl, C3-C10 cycloalkyl, C3-C6 cycloalkylmethyl, benzyl, phenethyl, phenoxy, benzyloxy, nitro, C7-C10 arylalkyl, hydroxamic acid, hydrazide, oxime, boronic acid, sulfonamide, formyl, C3-C6 cycloalkoxy, C ₁ -C ₄ alkyl substituted with -NR R ¹⁴ , C1-C4 hydroxyalkyl, methylenedioxy, ethylenedioxy, C1-C4 haloalkyl, C1-C4 haloalkoxy, C1-C4 alkoxycarbonyl, C1-C4 alkylcarbonyloxy, C1-C4 alkylcarbonyl, C1-C4 alkylcarbonylamino, -OCH2CO2R ¹³ , 2- (1-morpholino) ethoxy, azido, -C(R ¹⁴ )=N(OR ¹⁴ ) ; or

1-3 amino acids, linked together via amide bonds and linked to R ²² , R ²³ , R ²⁵ , R ²⁷ , R ⁴ or R ⁷ via the amine or carboxy terminus;

a C5-C14 carbocyclic residue substituted with 0-3 R ³² ;

a C5-C14 carbocyclic residue substituted with 0-5 R ³² ; or

a 5- to 10-membered heterocyclic ring system containing 1 to 4 heteroatoms independently selected from oxygen, nitrogen or sulfur, said heterocyclic ring system being substituted with 0-2 R ³² ;

R ³² , when a substituent on carbon, is selected from one or more of the following:

phenyl, benzyl, phenethyl, phenoxy, benzyloxy, halogen, hydroxy, nitro, cyano, C1-C4 alkyl, C3-C10

cycloalkyl, C3-C6 cycloalkylmethyl, C7-C10 arylalkyl, C1-C4 alkoxy, -CO2H, hydroxamic acid, -CONR ¹³ NR ¹ R ¹⁴ , hydrazide, oxime, boronic acid, sulfonamide, formyl, C3-C6 cycloalkoxy, -OR ¹³ , C1-C4 alkyl substituted with -NR ¹³ R ¹⁴ , -NR ¹³ R ¹⁴ , C2-C6 alkoxyalkyl, C1-C4 hydroxyalkyl, methylenedioxy, ethylenedioxy, C1-C4 haloalkyl, C1-C4 haloalkoxy, C1-C4 alkoxycarbonyl, C1-C4 alkylcarbonyloxy, C1-C4 alkylcarbonyl, C1-C4 alkylcarbonylamino, -S(0) _m R ¹³ , -S02NR ¹³ R ¹⁴ , -NHS02R ¹⁴ , -OCH2C02H,

2- (1-morpholino)ethoxy, -C(R ¹⁴ )=N(OR ¹⁴ ) ; NO ₂ , -OR ¹³ , -NR ⁴⁰ R ⁴¹ , -SO _m R ¹³ , -SO _m NR ¹³ R ¹⁴ , -C (=0)NR ¹³ R ¹⁴ , -OC(=0)NR ¹³ R ¹⁴ , -C(=0)R ¹¹ -OC (=0) R ^{1 1} , -OCO2R ¹³ , phenyl, -C (=0) NR ¹³ - (C ₁ -C ₄ alkyl) -NR ¹³ R ¹⁴ , -C (=O)NR ⁴⁰ R ⁴¹ , C ₁ -C ₄ haloalkyl, C ₁ -C ₄ haloalkoxy, C ₂ -C ₄ haloalkenyl, C ₁ -C ₄ haloalkynyl, or

-C (=0) NR ¹³ C (R ¹¹ ) ₂ NR ¹³ R ¹⁴ ; -C (=0)NR ¹³ C (R ¹¹ ) NR ¹³ NR ¹⁴ ; -C (=0)NR ¹³ C (R ¹¹ ) 2NR ¹³ Cθ2R ¹³ ; -C(=0)NR ¹³ -(Cι-C ₄ alkyl) -NR ¹³ C0 ₂ R ¹³ ; or

-C (=0)C (R ¹¹ ) ₂ NR ¹³ R ¹⁴ ; -C (=0)C(R ¹¹ ) ₂ NR ¹³ NR ¹⁴ ; -C (=0)C (R ¹¹ ) NR ¹³ C0 ₂ R ¹³ ; -C(=0)- (C ₁ -C ₄ alkyl)-NR ¹³ R ¹⁴ ; -C (=0)- (C1-C4 alkyl) -NR ¹³ C0 ₂ R ¹³ ; or

C1-C4 alkoxy substituted with 0-4 groups selected from: R ¹¹ , C ₃ -C ₆ cycloalkyl, -C0 ₂ R ¹³ , -C (=0) NR ¹³ R ¹⁴ , -NR ¹³ R ¹⁴ or OH;

C ₁ -C ₄ alkyl substituted with 0-4 groups selected from: R ¹¹ , =NR ¹⁴ , =NNR ¹³ C (=0)NR ¹³ R ¹⁴ or -NR ¹³ R ¹⁴ ;

C ₂ -C ₄ alkenyl substituted with 0-4 R ¹¹ ;

C ₂ -C ₄ alkynyl substituted with 0-4 R ¹¹ ;

a 5- or 6-membered heterocyclic ring containing from 1 to 4 heteroatoms selected from oxygen, nitrogen or sulfur;

or R ³² may be a 3- or 4- carbon chain attached to adjacent carbons on the ring to form a fused 5- or 6-membered ring, said 5- or 6- membered ring being optionally substituted on the aliphatic carbons with halogen, C1-C4 alkyl, C1-C4 alkoxy, hydroxy, or -NR ¹³ R ¹⁴ ; or, when R ³² is attached to a saturated carbon atom, it may be =0 or =S;

R ³² , when a substituent on nitrogen, is selected from one or more of the following:

phenyl, benzyl, phenethyl, hydroxy, C1-C4 hydroxyalkyl, C1-C4 alkoxy, C1-C4 alkyl, C3-C6 cycloalkyl, C3-C6 cycloalkylmethyl, -CH2NR ¹³ R ¹⁴ , -NR ¹³ R ¹⁴ , C2-C6 alkoxyalkyl, C1-C4 haloalkyl, C1.-C4 alkoxycarbonyl, -CO2H, C1-C4 alkylcarbonyloxy, C1-C4 alkylcarbonyl, -C(R ¹⁴ ) =N(OR ¹⁴ ) ;

>40 is selected from: H, C ₁ -C3 alkyl;

R ⁴¹ is selected from:

-C(=0)NR ¹³ R ¹⁴ ;

-C(=0)NR ¹³ NR ¹⁴ ;

-C (=0) C (R ¹¹ ) ₂ NR ¹³ R ¹⁴ ; -C(=0)C(R ¹¹ ) ₂ NR ¹³ NR ¹⁴ ;

-C (=0) C (R ¹¹ ) ₂ NR ¹³ C0 R ¹³ ;

-C(=0)H;

-C(=0)R ¹¹ ;

-C(=0)-(Cι-C ₄ alkyl) -NR ¹³ R ¹⁴ ; -C(=0)-(Cι-C ₄ alkyl) -NR ¹³ C0 ₂ R ¹³ ;

1-3 amino acids linked together via amide bonds, and linked to the N atom via the carboxy terminus;

provided that :

when R ⁴ is hydrogen, at least two of the following is not hydrogen: R ⁷ , R ²² or R ²⁷ .

[24] Preferred compounds of formulae (Ie) or (If) or (Ig) are compounds described above, wherein:

R ⁵ is -OR ²⁰ ;

R ²⁰ is H or any group that, when administered to a mammalian subject, cleaves to form a free hydroxyl;

R ⁴ and R ²⁷ are selected from benzyl, fluorobenzyl, pyrrolylmethyl, methoxybenzyl, isobutyl, nitrobenzyl or aminobenzyl;

R ²² and R ⁷ are independently selected from the group consisting of:

hydrogen, allyl, methyl, ethyl, propyl, cyclopropylmethyl, n-butyl, i-butyl, CH2CH=C (CH3) 2 _. pyridinylmethyl, methallyl, n-pentyl, i-pentyl, hexyl, benzyl, isoprenyl, propargyl, picolinyl, methoxyethyl, cyclohexylmethyl, dimethyl-butyl, ethoxyethyl, methyl-oxazolinylmethyl, naphthylmethyl, methyloxazolinylmethyl, vinyloxyethyl, pentafluorobenzyl, quinolinylmethyl, carboxybenzyl, chloro-thienyl, benzyloxybenzyl, phenylbenzyl, adamantylethyl,

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SUBSπTUTESHEET(RULE26)

cyclopropylmethoxybenzyl, methoxybenzyl, methylbenzyl, ethoxybenzyl, hydroxybenzyl, hydroxymethylbenzyl, aminobenzyl, formylbenzyl, cyanobenzyl, cinnamyl, allyloxybenzyl, fluorobenzyl, difluorobenzyl, chlorobenzyl, chloromethylbenzyl, fluoromethylbenzyl, iodobenzyl, bromobenzyl, cyclobutylmethyl, formaldoximebenzyl, cyclopentylmethyl, nitrobenzyl, (H ₂ NC (=0) ) -benzyl, carbomethoxybenzyl, carboethoxybenzyl, tetrazolylbenzyl, and dimethylallyl, aminomethylbenzyl, (O-benzyl-formaldoxime)benzyl, (O-methyl-formaldoxime)benzyl, (CH3O2CO)-benzyl, (HOCH2CH2N=CH) -benzyl, N-benzylaminocarbonylbenzyl, N-methylaminobenzyl, N-ethylaminobenzyl, N-ethylaminomethylbenzyl, acetylbenzyl, acetoxybenzyl, N-hydroxylaminobenzyl, phenylmethyl- boronic acid, N-hydroxylaminomethylbenzyl, (hydroxyl) ethylbenzyl, (CH3C (=N0H) ) -benzyl, (H2NNHC (=0) ) -benzyl, (H2NC (=0)NHN=CH) -benzyl, (CH3θNHC(=0) ) -benzyl, (HONHC (=0) ) -benzyl, (CH3NHC (=0) ) -benzyl,

N,N-dimethylaminocarbonylbenzyl, (HOCH2CH (OH) CH2O) - benzyl, hydroxyethoxybenzyl (oxazolidinyl) -benzyl, (hydroxyl) hexyl, hexenyl, (hydroxy) octyl, (hydroxyl) pentyl, (carboxy) pentyl,

(carbomethoxy)pentyl, (methylthio)benzyl, (methylsulfonyl)benzyl, N,N-dimethylaminomethylbenzyl, N-methylaminomethylbenzyl, glycylaminobenzyl, N,N-dimethylglycylaminobenzyl, alanylaminobenzyl, (N-phenylmethoxycarbonyl)alanylaminobenzyl, phenylalanylaminobenzyl, (N-phenylmethoxycarbonyl) phenylalanylaminobenzyl, (CH3CH2NHC (=0) ) -benzyl,

N,N-diethylaminocarbonylbenzyl, N-ethylaminocarbonylbenzyl, N-propylaminocarbonylbenzyl,

N,N-diisopropylaminocarbonylbenzyl, N, N-di-n- propylaminocarbonylbenzyl, (hydroxypropynyl)benzyl, (imidazolyl-C (=0) ) -benzyl, trifluoroacetylbenzyl, (pyrazolyl)benzyl, (H2NSO2) -benzyl, dihydroxyethylbenzyl, (MeHNC (=0)NH) -benzyl, (H2NC (=0)NH)-benzyl, (HC (=0)NH)-benzyl, methanesulfonylpentyl, methoxypentyl, N-formyl-N- ethylaminobenzyl, acetylaminobenzyl, propionylbenzyl, butyrylbenzyl, (CH3CH2C (=N0H) ) - benzyl, (trifluorohydroxyethyl)benzyl,

(CF3C (=N0H) ) -benzyl, (N-methylglycyl) aminobenzyl, ( (4-morpholino) ethyl) aminocarbonylbenzyl, (N,N-dimethylaminoethyl) aminocarbonylbenzyl, (N,N-diethylaminoethyl) aminocarbonylbenzyl, (4-methylpiperazin-l-ylethyl) aminocarbonylbenzyl, (benzyl-NHC (=0)0)benzyl, (CH3NHC (=0)0)benzyl, (NH ₂ C (=0) CH 0)benzyl, (NH ₂ C (=NH) )benzyl, ( (N-phenylmethoxycarbonyl) glycylamino)benzyl, (imidazolylmethyl)benzyl, ( (CH3) 3C-C (=0) )benzyl, (N-methyl-N-ethylaminoethyl) aminocarbonylbenzyl, (pyrrolidinylethyl) aminocarbonylbenzyl, (piperidinylethyl) aminocarbonylbenzyl .

In the present invention it has been discovered that the compounds above are useful as inhibitors of HIV protease and similar retroviral proteases, and for the treatment of HIV infection and associated diseases, and similar retrovirus infections. The present invention also provides methods for the treatment of HIV infection and associated diseases by administering to a host infected with HIV a therapeutically effective antiviral amount of a compound of formula (I) as described above. By therapeutically effective amount, it is meant an amount of a compound of

the present invention effective to inhibit HIV infection or treat the symptoms of HIV infection in a host.

Also provided by this invention are pharmaceutical compositions containing a pharmaceutically acceptable carrier and a therapeutically effective compound of formula (I) described above.

The compounds herein described may have asymmetric centers. All chiral, diastereomeric, and racemic forms are included in the present invention. Many geometric isomers of olefins, C=N double bonds, and the like can also be present in the compounds described herein, and all such stable isomers are contemplated in the present invention. It will be appreciated that certain compounds of the present invention contain an asymmetrically substituted carbon atom, and may be isolated in optically active or racemic forms. It is well known in the art how to prepare optically active forms, such as by resolution of racemic forms or by synthesis, from optically active starting materials. Also, it is realized that cis and trans geometric isomers of the compounds of the present invention are described and may be isolated as a mixture of isomers or as separated isomeric forms. All chiral, diastereomeric, racemic forms and all geometric isomeric forms of a structure are intended, unless the specific stereochemistry or isomer form is specifically indicated. When any variable (for example, R ¹¹ , R ¹² , R ¹³ , R ¹⁴ , R ³¹ , R ³² , and m) occurs more than one time in any constituent or in formula (I) or (II), or any other formula herein, its definition on each occurrence is independent of its definition at every other occurrence. Thus, for example, if a group is shown to be substituted with 0-3 R ¹¹ , then said group may optionally be

substituted with up to three R ¹¹ and R ¹¹ at each occurrence is selected independently from the defined list of possible R ¹¹ . Also, for example, in -N(R ²⁰ )2, each of the R ²⁰ substituents may be independently selected from the list of possible R ²⁰ groups defined. Also, combinations of substituents and/or variables are permissible only if such combinations result in stable compounds .

As used herein, "alkyl" is intended to include both branched and straight-chain saturated aliphatic hydrocarbon groups having the specified number of carbon atoms; "haloalkyl" is intended to include both branched and straight-chain saturated aliphatic hydrocarbon groups having the specified number of carbon atoms, substituted with 1 or more halogen; "alkoxy" represents an alkyl group of indicated number of carbon atoms attached through an oxygen bridge; "cycloalkyl" is intended to include saturated ring groups, including mono-,bi- or poly-cyclic ring systems, such as cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl and cyclooctyl; and "biycloalkyl" is intended to include saturated bicyclic ring groups such as [3.3.0]bicyclooctane, [4.3.0]bicyclononane, [4.4.O]bicyclodecane (decalin) , [2.2.2]bicyclooctane, and so forth. "Alkenyl" is intended to include hydrocarbon chains of either a straight or branched configuration and one or more unsaturated carbon-carbon bonds which may occur in any stable point along the chain, such as ethenyl, propenyl, and the like; and "alkynyl" is intended to include hydrocarbon chains of either a straight or branched configuration and one or more triple carbon-carbon bonds which may occur in any stable point along the chain, such as ethynyl, propynyl and the like. "Halo" or "halogen" as used herein refers to fluoro, chloro, bromo, and iodo; and "counterion" is

used to represent a small, negatively charged species such as chloride, bromide, hydroxide, acetate, sulfate, and the like.

As used herein, "aryl" is intended to mean phenyl or naphthyl. As used herein, "carbocycle" or

"carbocyclic residue" or "carbocyclic ring system" is intended to mean any stable 3*- to 7- membered monocyclic or bicyclic or 7- to 14-membered bicyclic or tricyclic or an up to 26-membered polycyclic carbon ring, any of which may be saturated, partially unsaturated, or aromatic. Examples of such carbocyles include, but are not limited to, cyclopropyl, cyclopentyl, cyclohexyl, phenyl, biphenyl, naphthyl, indanyl, adamantyl, or tetrahydronaphthyl (tetralin) . As used herein, the term "heterocycle" or

"heterocyclic ring system" is intended to mean a stable 5- to 7- membered monocyclic or bicyclic or 7- to 10- membered bicyclic heterocyclic ring which is either saturated or unsaturated, and which consists of carbon atoms and from 1 to 4 heteroatoms independently selected from the group consisting of N, 0 and S and wherein the nitrogen and sulfur heteroatoms may optionally be oxidized, and the nitrogen may optionally be quaternized, and including any bicyclic group in which any of the above-defined heterocyclic rings is fused to a benzene ring. The heterocyclic ring may be attached to its pendant group at any heteroatom or carbon atom which results in a stable structure. The heterocyclic rings described herein may be substituted on carbon or on a nitrogen atom if the resulting compound is stable. Examples of such heterocycles include, but are not limited to, pyridyl, pyrimidinyl, furanyl, thienyl, pyrrolyl, pyrazolyl, imidazolyl, tetrazolyl, benzofuranyl, benzothiophenyl, indolyl, indolenyl, quinolinyl, isoquinolinyl or benzimidazolyl, piperidinyl, 4-piperidonyl, pyrrolidinyl, 2-

pyrrolidonyl, pyrrolinyl, tetrahydrofuranyl, tetrahydroquinolinyl, tetrahydroisoquinolinyl, decahydroquinolinyl or octahydroisoquinolinyl, azocinyl, triazinyl, 6H-1 , 2, 5-thiadiazinyl, 2H, 6H- 1 , 5, 2- dithiazinyl, thiophenyl, thianthrenyl, furanyl, pyranyl, isobenzofuranyl, chromenyl, xanthenyl, phenoxathiinyl, 2-ϊ-pyrrolyl, pyrrole, imidazolyl, pyrazolyl, isothiazolyl, isoxazole, pyridinyl, pyrazinyl, pyrimidinyl, pyridazinyl, indolizinyl, isoindole, 3H- indole, indole, liϊ-indazole, purinyl, 4#-quinolizinyl, isoquinolinyl, quinolinyl, phthalazinyl, naphthyridinyl, quinoxalinyl, quinazolinyl, cinnolinyl, pteridinyl, 4a#-carbazole, carbazole, β-carbolinyl, phenanthridinyl, acridinyl, perimidinyl, phenanthrolinyl, phenazinyl, phenarsazinyl, phenothiazinyl, furazanyl, phenoxazinyl, isochromanyl, chromanyl, pyrrolidinyl, pyrrolinyl, imidazolidinyl, imidazolinyl, pyrazolidinyl, pyrazolinyl, piperidinyl, piperazinyl, indolinyl, isoindolinyl, quinuclidinyl, morpholinyl or oxazolidinyl. Also included are fused ring and spiro compounds containing, for example, the above heterocycles .

The term "boronic acid" as used herein means a group of the formula -B(R ³⁴ ) (R ³⁵ ) , wherein R ³⁴ and R ³⁵ are independently selected from: -OH; -F; -NR ^l R ¹⁴ ; or Cι-C8~alkoxy; or R ³⁴ and R ³ ^ can alternatively be taken together to form: a cyclic boron ester where said chain or ring contains from 2 to 20 carbon atoms and, optionally, 1-4 heteroatoms independently selected from N, S, or O; a divalent cyclic boron amide where said chain or ring contains from 2 to 20 carbon atoms and, optionally, 1-4 heteroatoms independently selected from N, S, or 0; a cyclic boron amide-ester where said chain or ring contains from 2 to 20 carbon atoms and, optionally, 1-4 heteroatoms independently selected from

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SUBSHTUTE SHEET (RULE 26)

N, S, or O. Such cyclic boron esters, boron amides, or boron amide-esters may also be optionally substituted with 1-5 groups independently selected from R ¹¹ .

Boron esters include boronic acid protecting groups, including moieties derived from diols, for example pinanediol and pinacol to form pinanediol boronic acid ester and the pinacol boronic acid, respectively. Other illustrations of diols useful for deriving boronic acid esters are perfluoropinacol, ethylene glycol, diethylene glycol, 1, 2-ethanediol, 1, 3-propanediol, 1, 2-propanediol, 1, 2-butanediol, 1, -butanediol, 2, 3-butanediol, 2, 3-hexanediol, 1,2-hexanediol, catechol, 1,2-diisopropylethanediol, 5, 6-decanediol, 1, 2-dicyclohexylethanediol .

The term "substituted", as used herein, means that an one or more hydrogen on the designated atom is replaced with a selection from the indicated group, provided that the designated atom's normal valency is not exceeded, and that the substitution results in a stable compound. When a substitent is keto (i.e., =0), then 2 hydrogens on the atom are replaced.

By "stable compound" or "stable structure" is meant herein a compound that is sufficiently robust to survive isolation to a useful degree of purity from a reaction mixture, and formulation into an efficacious therapeutic agent .

As used herein, the term "any group that, when administered to a mammalian subject, cleaves to form a free hydroxyl, amino or sulfhydryl" means any group bonded to an 0, N, or S atom, respectively, which is cleaved from the 0, N, or S atom when the compound is administered to a mammalian subject to provide a compound having a remaining free hydroxyl, amino, or

-121-

SUBSXITUTE SHEET (RULE 26)

sulfhydryl group, respectively. Examples of groups that, when administered to a mammalian subject, are cleaved to form a free hydroxyl, amino or sulfhydryl, include but are not limited to, Ci-Cδ alkyl substituted with 0-3 R ¹¹ , C3-C6 alkoxyalkyl substituted with 0-3

R ¹¹ , C ₁ -C6 alkylcarbonyl substituted with 0-3 R ¹¹ , Cτ _. -C6 alkoxycarbonyl substituted with 0-3 R ¹¹ , Ci-Cδ alkylaminocarbonyl substituted with 0-3 R ¹¹ , benzoyl substituted with 0-3 R ² , phenoxycarbonyl substituted with 0-3 R ² , phenylaminocarbonyl substituted with 0-3 R ¹² . Examples of group that, when administered to a mammalian subject, are cleaved to form a free hydroxyl, amino or sulfhydryl, include hydroxy, amine or sulfhydryl protecting groups, respectively. As used herein, the term "amine protecting group" means any group known in the art of organic synthesis for the protection of amine groups. Such amine protecting groups include those listed in Greene and Wuts, "Protective Groups in Organic Synthesis" John Wiley & Sons, New York (1991) and "The Peptides:

Analysis, Synthesis, Biology, Vol. 3, Academic Press, New York (1981), the disclosure of which is hereby incorporated by reference. Any amine protecting group known in the art can be used. Examples of amine protecting groups include, but are not limited to, the following: 1) acyl types such as formyl, trifluoroacetyl, phthalyl, and p-toluenesulfonyl; 2) aromatic carbamate types such as benzyloxycarbonyl (Cbz) and substituted benzyloxycarbonyls, 1- (p-biphenyl) -1- methylethoxycarbonyl, and 9-fluorenylmethyloxycarbonyl (Fmoc) ; 3) aliphatic carbamate types such as tert- butyloxycarbonyl (Boc) , ethoxycarbonyl, diisopropylmethoxycarbonyl, and allyloxycarbonyl; 4) cyclic alkyl carbamate types such as cyclopentyloxycarbonyl and adamantyloxycarbonyl; 5) alkyl types such as triphenylmethyl and benzyl; 6)

trialkylsilane such as trimethylsilane; and 7) thiol containing types such as phenylthiocarbonyl and dithiasuccinoyl.

By a "ketal ring" or "ketal" group is meant any ketal protecting group which can be hydroyzed to form a carbonyl . Such ketal rings or ketal protecting groups are well known in the art of organic synthesis and typically include, for example, substituted or unsubstituted carbocyclic diethers, dithioethers, or mixed ethers. Such ketal protecting groups include those listed in Greene and Wuts, "Protective Groups in Organic Synthesis" John Wiley & Sons, New York (1991)

The term "amino acid" as used herein means an organic compound containing both a basic amino group and an acidic carboxyl group. Included within this term are natural amino acids, modified and unusual amino acids, as well as amino acids which are known to occur biologically in free or combined form but usually do not occur in proteins. Included within this term are modified and unusual amino acids, such as those disclosed in, for example, Roberts and Vellaccio (1983) The Peptides, 5: 342-429, the teaching of which is hereby incorporated by reference. Modified or unusual amino acids which can be used to practice the invention include, but are not limited to, D-amino acids, hydroxylysine, 4-hydroxyproline, an N-Cbz-protected amino acid, ornithine, 2, -diaminobutyric acid, homoarginine, norleucine, N-methylaminobutyric acid, naphthylalanine, phenylglycine, β-phenylproline, tert-leucine, 4-aminocyclohexylalanine, N-methyl- norleucine, 3, 4-dehydroproline, N,N- dimethylaminoglycine, N-methylaminoglycine, 4-aminopiρeridine-4-carboxylic acid, 6-aminocaproic acid, trans-4- (aminomethyl) -cyclohexanecarboxylic acid, 2-, 3-, and 4- (aminomethyl) -benzoic acid, 1-aminocyclopentanecarboxylic acid,

1-aminocyclopropanecarboxylic acid, and 2-benzyl-5- aminopentanoic acid.

The term "amino acid residue" as used herein means that portion of an amino acid (as defined herein) that is present in a peptide.

The term "peptide" as used herein means a compound that consists of two or more amino acids (as defined herein) that are linked by means of a peptide bond. The term "peptide" also includes compounds containing both peptide and non-peptide components, such as pseudopeptide or peptide mimetic residues or other non-amino acid components. Such a compound containing both peptide and non-peptide components may also be referred to as a "peptide analog". The term "peptide bond" means a covalent amide linkage formed by loss of a molecule of water between the carboxyl group of one amino acid and the amino group of a second amino acid.

As used herein, "pharmaceutically acceptable salts and prodrugs" refer to derivatives of the disclosed compounds that are modified by making acid or base salts, or by modifying functional groups present in the compounds in such a way that the modifications are cleaved, either in routine manipulation or in vi vo, to the parent compounds. Examples include, but are not limited to, mineral or organic acid salts of basic residues such as amines; alkali or organic salts of acidic residues such as carboxylic acids; acetate, formate and benzoate derivatives of alcohols and amines; and the like.

"Prodrugs" are considered to be any covalently bonded carriers which release the active parent drug according to formula (I) in vi vo when such prodrug is administered to a mammalian su ject. Prodrugs of the compounds of formula (I) are prepared by modifying

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SUBSXITUTESHEET(RULE26)

functional groups present in the compounds in such a way that the modifications are cleaved, either in routine manipulation or in vivo, to the parent compounds. Prodrugs include compounds of formula (I) wherein hydroxy, amine, or sulfhydryl groups are bonded to any group that, when administered to a mammalian subject, cleaves to form a free hydroxyl, amino, or sulfhydryl group, respectively. Examples of prodrugs include, but are not limited to, acetate, formate and benzoate derivatives of alcohol and amine functional groups in the compounds of formula (I); and the like.

Pharmaceutically acceptable salts of the compounds of the invention can be prepared by reacting the free acid or base forms of these compounds with a stoichiometric amount of the appropriate base or acid in water or in an organic solvent, or in a mixture of the two; generally, nonaqueous media like ether, ethyl acetate, ethanol, isopropanol, or acetonitrile are preferred. Lists of suitable salts are found in Remington's Pharmaceutical Sciences. 17th ed., Mack

Publishing Company, Easton, PA, 1985, p. 1418, the disclosure of which is hereby incorporated by reference.

Synthesis

Compounds of the invention can be prepared by methods described herein, or variations thereon as appreciated by those skilled in the art . Preferred methods include, but are not limited to, those described below.

Any of the compounds can be derived from the joining of two amino acids derivatives, followed by elaboration of substituents as necessary. Natural amino acids are available in abundance, and a great array of unnatural amino acids have been prepared by techniques

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SUBSΠTUTESHEET(RULE26)

well known to those skilled in the art of organic synthesis. D.C. Roberts and F. Vellaccio provide a comprehensive listing of unnatural amino acids, and techniques for the synthesis of many variations thereof .The Peptides, Vol. 5: Analysis. Synthesis. Bioloσv.

Academic Press, NY, 1983] . A more recent description of additional routes to chirally pure unnatural amino acids is found in Cintas, P. Tetrahedron, 47(32), 6079-111, 1991. Thus, one skilled in the art can synthesize the amino acid precursors used in the preparation of the compounds of the invention by a judicious selection of one or more of the methods outlined above. Each of the references cited herein are hereby incorporated by reference.

The substituent R ⁴ is chosen first, and the corresponding amino acid III with the desired stereochemistry is synthesized or purchased as necessary:

III

wherein R ⁴ has the meaning designated above. If substituents on R ⁴ are deemed to be sensitive to the reaction conditions employed in the following steps, then appropriate protecting groups are used, and the desired substituents are freed from protection at the end of the sequence. Extensive descriptions of the correct choice of protecting groups for various reaction conditions, and the correct method of removal, are

described in T.W. Greene and P.G.M. Wuts, Protec ive Groups in Organic Synthesis. 2nd Edition, Wiley, New York, 1991.

A protecting group is also chosen for the amine terminal of amino acid III. For example, the above reference can be used to assist the choice of protecting group, or M. Bodanzky and A. Bodanzky in The Practice of Peptide Synthesis. Springer-Verlag, Berlin, 1984 can be consulted. A preferred amine protecting group is the N- carbobenzyloxy (CBZ) group. In the following structures, a protecting group is designated PG.

IV

The protected amino acid is then converted to the protected amino epoxide by known techniques, such as the Wittig or Petersen olefination of a protected amino aldehyde followed by epoxidation of the olefin; or by addition of a methylene sulfur ylide to an amino aldehyde or by the following, preferred method: treatment of the protected amino acid with diazomethane to generate the diazoketone, followed by treatment with aqueous hydrochloric acid to generate the chloroketone, followed by reduction with a hydride reducing agent, preferably a metal borohydride to form the chloroalcohol. Stereochemistry of the hydroxyl group can be controlled by the choice of reducing agent; preferably a mixture can be obtained which can optionally be separated by chromatography and each

-127-

SUBST1TUTESHEET(RULE26)

diastereomer can be evaluated independently. This step is followed by base-catalyzed elimination of hydrogen chloride in an aprotic solvent, preferably potassium tert-butoxide in tetrahydrofuran, to form the protected amino epoxide V.

HCl, H ₂ 0

I KO ^l Bu

Next the desired R ²⁷ substituent is chosen, with the desired stereochemistry, and the appropriate acid is synthesized or purchased. Protecting groups are added as necessary to the functionality on R ²⁷ . The acid terminus is protected, preferably with the t-butyl ester, to form compound VI:

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SUBSCTTUTE SHEET (RULE 26)

V I

V and VI are coupled in the presence of a solvent, preferably methanol, at a temperature between 0 and 100°C, to form the amino alcohol VII:

VII

The hydroxyl group of VII is protected, preferably with a silyl protecting group such as t-butyldimethylsilyl (TBDMS) chloride. The selected protective group must withstand the conditions used to remove the nitrogen and carboxy protecting groups. The wide variety of protecting groups described in the references above make the selection of the proper combination of groups straightforward to one skilled in the art .

The amine and acid protecting groups are removed to form amino acid VIII :

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SUBSCTTUTE SHEET (RULE 26)

which depending on cleavage conditions used may be isolated as a salt of the amines. VIII is cyclized to the lactam IX: any number of standard conditions can be used to form lactams, although the preferred procedure involves activating the carboxylate with a group such as dicylohexylcarbodiimide under conditions dilute enough to favor intramolecular condensation.

IX

Intermediate IX can be deprotected to form hydroxy lactam X. In instances where the protecting group is TBDMS, the preferred cleavage conditions are tetra-n- butylammonium fluoride in tetrahydrofuran.

When R ⁴ and R ²⁷ are benzyl, X is Example 1. Other representative compounds of the invention are listed in Table 1.

Alternatively, IX can be further modified to add substituents R ⁷ and R ²² . Beginning with the protected alcohol, using methods known to one skilled in the art one may alkylate either the amide nitrogen or the basic nitrogen with a group R ²² -LG or R ⁷ -LG, respectively, where LG is a leaving group. If alkylation of the basic nitrogen is desired while keeping the amide nitrogen unsubstituted, it is advantageous to protect the amide nitrogen using one of the many protective groups discussed in the above references . A preferred protecting group is benzyl, which can be selectively removed from the basic nitrogen by hydrogenolysis.

For obtaining compounds with R ⁷ ≠ hydrogen and R ²² = hydrogen, the preferred method is to treat IX with a base, such as potassium carbonate, in a polar aprotic solvent, such as dimethylformamide, and add to the mixture between 0 and 100°C an alkylating agent R ⁷ -LG, preferably an alkyl chloride, bromide iodide, or tosylate. Preferred alkylating agents are substituted benzyl chlorides, substituted Cι-C ^~ alkyl bromides, (heterocyclic)methyl chlorides and substituted (alicyclic)methyl bromides and tosylates.

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SUBST1TUTE SHEET (RULE 26)

I X X I

If compounds wherein R ²² = R ⁷ ≠ hydrogen are desired, the preferred method is that described in the preceding paragraph, but substituting a stronger base, preferably sodium hydride, for potassium carbonate and employing 2 equivalents alkylating agent. If R ⁷ ≠ R ²² , the product XI can be further alkylated in the same fashion to give XII, by substituting a stronger base, preferably sodium hydride, for potassium carbonate and employing 1 equivalent alkylating agent R ²² -LG. Preferred alkylating agents are as described above.

X I XI I

For the case in which R ²² ≠ H and R ⁷ = H, as exemplified in XIII, a preferred method is one in which the above procedures are followed, such that IX is first alkylated with benzyl bromide in dimethylformamide (DMF)

in the presence of postassium carbonate; the material is purified and subjected to R ²² -LG in the presence of sodium hydride in DMF to give Xlla; after which the N- benzyl is removed by catalytic hydrogenation or preferably by transfer hydrogenation, e.g. formic acid and palladium on carbon in methanol.

Xlla XIII

(R ⁷ = CH2Ph)

The protecting group on XI-XIII is removed to give removed structure XIV, where Z = 0 as described above. The representative compounds of the invention listed in Table 1 can be prepared by these methods.

XIV

By the proper manipulation and choice of protecting groups by one skilled in the art, compounds of the formula II, wherein X is S or 0, can be obtained by substitution of a suitably protected form of acid Via in the above described sequences. Further modification of these compounds are detailed above.

Via

The preferred compounds are those in which Z = 0; however, standard techniques can be employed to convert the carbonyl oxygen to sulfur or an amidine or substituted amidine. These techniques are described in detail in copending application U.S. Patent Application 07/883,944, filed May 15, 1992, which is incorporated by reference .

The preferred compounds are those in which R ^4a and R ² ^ are hydrogen. However, compounds in which R ^a and R ² ^ are substituted benzyl or substituted lower alkyl can be prepared by choosing alpha, alpha '-substituted amino acids as starting materials. For example, if, in structure III, the alpha hydrogen is replaced by substituted benzyl or substituted lower alkyl, then the product derived from the synthesis described herein is XV:

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SUBSCTTUTE SHEET (RULE 26)

XV

and if in structure VI the alpha hydrogen is replaced by substituted benzyl or substituted lower alkyl then the product of the above-described sequence is XVI. These alpha, alpha' substituted amino acids can be prepared by the means described in the references above, and by other means well known to skilled in the art of organic synthesis .

XVI

Compounds in which the side chains on the same side of the seven-membered ring are joined to form a fused ring are contemplated as part of this invention.

Specifically, compound XVII can be formed by choosing amino acid VI such that R ²⁷ is protected 4-hydroxybutyl (n=2) or protected 3-hydroxypropyl . Release of the hydroxy group, conversion to the tosylate or mesylate in

dilute solution in a polar aprotic solvent at 0-100°C in the presence of a weak base will result in the fused ring system.

XVII

If a similar procedure is employed with R ⁴ , and the resulting tosylate or mesylate is heated in dilute solution with a stronger base such as sodium hydride in a polar aprotic solvent, the fused ring system XVIII can be obtained.

XVIII

The absolute and relative stereochemistry of the ring substituents are important for the degree of binding of these compounds to the HIV protease active site. Although a preferred diastereo er is shown in

-136-

SUBSCTTUTE SHEET (RULE 26)

structure XIX, other diastereomers are also active and are contemplated as part of this invention. Control over stereochemistry is obtained by choice of starting materials III and VI, and by choice of reducing agent to form chloroalcohol as described above.

XIX

Other compounds of this invention can be prepared as outlined by the schemes below, using the methods and procedures described herein, or additionally, the methods and procedures described in US Patent Application No.USSN 08/023,439, filed 2/26/93.

The compounds of the general formula XX can be prepared as shown in Scheme 1. The compound of the general formula XXa and XXc can be prepared according to the method described by A. S. Dutt and J. S. Morley (J. Chem. Soc. Perkin I. 1712, (1975)) . Treatment of

XXa with 1 equivalent of ethylene oxide would provide intermediate XX (where R = H) which can be activated to XXb (where R = mesylate or tosylate) by methods well known to the skilled in the art. The resulting intermediate then heated in solvents such as methanol, ethanol, etc. in the presence of XXc to provide XXd. The compound XXe could be obtained by treatment of XXd with acids such as trifluoroacetic acid or hydrochloric acid in a suitable solvent. The intermediate XXe can be

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SUBST1TUTE SHEET (RULE 26)

cyclized to XXf by treatment with carbonyldiimidazole (CDI) and then alkylated with sodium hydride to give the desired XXg (where R ²² = R ² ^) .

The compounds of general formula XXI can be prepared as detailed in Scheme 2. Hydrazine XXIa (EP 521827 A) is treated with triethylsilyl chloride according to the method of Corey et al. (J. Am. Chem. Soc. , 1971, 93, 7319), followed by aqueous hydrolysis, to give XXIb. Carbonyl diimidazole cyclization followed by alkylation under the standard procedure gives XXId. Deprotection by HCl/MeOH yields XXIe.

As further detailed in Scheme 2 continued, XXIf is treated with KCN followed by protection, Dibal-H reduction to give XXIg, and further reaction with hydrazine to provide XXIi. XXIi could be reacted with C1C(=0)C1 (phosgene), followed by treatment with triethylamine to give XXIk which can be cyclized to XXII by heating in toluene. Following the same alkylation & deprotection procedures as described previously, the desired XXIe can be obtained.

The compounds of general formula XXIII are shown in Scheme 4. Compound XXIIIa (T. Minoto, et al . EP 0490667A2; Y. Yabe, et al . EP 0498680A; R. Herranz, et al. J. Org. Chem., 1990, 55, 2232) was protected as the THP ether and the methyl ester hydrolyzed to give XXIIIb, which was coupled with O-benzyl phenylalanine using 1, 3-dicyclohexylcarbodiimide (DCC) . Hydrogenolysis of the O-benzyl group and phenylmethoxycarbonyl (CBZ) protecting groups would give XXIIId, which was then cyclized with DCC to give XXIIIe. Standard alkylation was performed to give XXIIIf, which was then hydrolyzed in acidic medium to give the desired XXIIIg.

XXIV

Any of the compounds of formula XXIV described in Scheme 5 can be derived from the joining of an amino acid derivative and a hydroxy-protected statine derivative, followed by elaboration of substituents as necessary. Natural amino acids are available in abundance, and a great array of unnatural amino acids have been prepared by techniques well known to those skilled in the art of organic synthesis. D.C. Roberts and F. Vellaccio provide a comprehensive listing of unnatural amino acids, and techniques for the synthesis of many variations thereof. .The Peptides. Vol. 5: Analysis. Synthesis, Biology; Academic Press, NY 1983. A more recent description of additional routes to chirally pure unnatural amino acids is in: Asymmetric synthesis of .alpha.-amino acids from carbohydrates as chiral templates; Cintas, P. Tetrahedron. 1991, 47(32), 6079- 111. Thus one skilled in the art can synthesize the amino acid precursors used in the preparation of the compounds of the invention by a judicious selection of one or more of the methods outlined above, which articles are hereby incorporated by reference. Statine derivatives are also well known in the literature and can be prepared by methods disclosed in EP 0 401 675 Al . Other methods are described in the series cited above (The Peptides. Vol. 5: Analysis. Synthesis. Biology;

-139-

SUBST1TUTE SHEET (RULE 26)

Academic Press, NY 1983] and by Bringmann et al. in Synlett (5), 253-255 (1990); by Kessler and Schudok in Synthesis (6) 457-8 (1990); and by Nishi and Morisawa in Heterocycles 29(9), 1835-42 (1989) . The statine hydroxyl is protected if necessary; the preferred protecting group is tert-butyldimethylsilyl . The amino acid is protected at the carboxyl group, the statine derivative is protected at the amino group, and the amide bond is formed using techniques described in the references. The preferred N-protecting group is phenylmethoxycarbonyl (CBZ) , the preferred carboxylic acid protecting group is tert-butyl ester, and the preferred coupling reagent is 1,3- dicyclohexylcarbodiimide . The product XXIVc is isolated and purified if necessary, and protecting groups are removed by standard methods; if the preferred groups are employed, the CBZ protecting group is removed by treatment with 10% palladium on carbon in the presence of ethanol, tetrahydrofuran and hydrogen gas, or by the action of palladium oxide in ethanol/water in the presence of cyclohexene. The preferred t-butyl ester is removed with 25% triflouracetic acid in dichloromethane . These steps yield XXIVd. Compound XXIVd is cyclized using standard techniques to XXIVe. Dicyclohexylcarbodiimide is the preferred cyclization reagent. The amide nitrogens are alkylated if desired; the preferred alkylating agents are benzylic or allylic bromides, or alkyl iodides or tosylates, in the presence of sodium hydride in an aprotic solvent . One or two alkyl groups can be provided depending on the stoichiometry of the alkylating agent and base .

Removal of the hydroxyl protecting group using standard conditions, preferably tetra-n-butyl ammonium flouride, yields the desired product XXIV.

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SUBSΠTUTESHEET(RULE26)

Compounds of the general formula XXVI can be synthesized using Scheme 7. Norstatin, XXVIa can be hydrogenated to remove CBZ protecting group and the resulting amine can be reprotected using t- butoxycarbonyl (BOC) . p-Methoxyphenylmethyl protecting groups are alkylated on both the alcohol and acid; afterwhich basic hydrolysis yields XXVIb. Condensation with t-butyl 2-benzylcarbazate (A.S. Dutta and J.S. Morley, J. Chem. Soc. Perkin I, 1975, 1712) was facilitated using DCC. The BOC group can be removed using acid conditons and the resulting diamine cyclized with carbonyldiimidazole to give XXVId. Alkylation as previously described, deprotection using dichlorodicyanobenzoquinone (DDQ) followed by HCl/MeOH will yield XXVIf. Sequential alkylation with different alkylating agents can also be performed.

The compounds of the present invention may be prepared using methods known in the art of organic synthesis. The compounds may be synthesized, for example, in accordance with the synthetic schemes set forth below.

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SUBSCTTUTE SHEET (RULE 26)

Scheme 1

NHBoc I XXc

BocNH V ocHN HN.

BocHN

O7 B NHBoc I I R' / \ ,NH ,N

,-y R ^* OR R" ^f R

XXa XXb XXd

R ²² = R ²³ XXf XXe

XXg

Scheme 2

XXIa XXIb

- 143-

SUBST1TUTE SHEET (RULE 26)

Scheme 2 (continued)

Dibal-H

Toluene

XXIi

(l) RCl/NaH

ClCOCl (2) BnCI

(3) HCl Dioxane

XXIe

XXIm

HCl/Dioxane

Scheme 3

XXIId

NHBoc I H N XXc

^_ —

XXIIf XXIIe

XXIIj XXIIi

Scheme 4

Dicyclohexyl- carbodiimide XXIDc

H _2> 5% PdC

R^R ²² - ^ R ⁷ = R ² = /"Q^

OTHP OH

Scheme 5

XXIVa

Statine derivative; XXIVb

P, P, P" = protecting group Natural or unnatural amino acid

XXIVc

XXIVd XX IVe

XXIV XXIVf

Scheme 7

MPM = Melhoxyphenylmeihyl

Dicyclohexyl NH ₂ I carbodiimide

BOC ' ^N ^Ph

XXVIc XXVId

NaH, DMF

THPO

H

The synthesis of representative compounds of the present invention is described in further detail below .

1 . Preparation of N-Carbobenzyloxy-D- Phenylalanine chloromethylketone

One equivalent [EQ] (15g)of CBZ-D-phenylalanine was dissolved in tetrahydrofuran [THF, 33ml] (1.5M) The solution was cooled to -20°C (internal) using a dry ice/CCl4 bath and 4-methylmorpholine (5.5ml, 1 EQ) was added dropwise, maintaining a temperature below -15°C, followed by isobutylchloroformate (6.5ml, 1 EQ) maintaining a temperature below -15°C. After stirring for 15 min at -15°C the precipitate was filtered and washed with 50ml cold THF. The combined THF solution was contained in a 1L Erlenmeyer cooled in an ice bath and added to this an excess of diazomethane in ether (see prep below) . After stirring for 25min, the bath was removed and stirred until reaction temperature reached ~18°C. The reaction was recooled in ice bath and ~40ml 4M HCl in dioxane was added, until bubbling ceased and solution became nearly colorless. The pH was checked to confirm acidity and concentrated invacuo. Further evaporation was carried out in high vacuum overnight to afford 18.65g of the desired product, M.P. 88°C. NMR (CDCI3) : consistent with assigned structure.

2. Preparation of Diazomethane

A commercially available diazomethane distillation kit was charged with 2- (2-ethoxyethoxy) ethanol (84ml), anhydrous ether (84ml) and a solution of potassium hydroxide (15g) in distilled water (24ml) . Upon heating to 60°C, a solution of N-methyl-N-nitroso-p- toluenesulfonamide (30g, Diazald®) in anhydrous ether (270ml) was added at the rate of product distillation. Once the 270ml of expected diazomethane in ether was recovered, an additional amount of ether (100ml) was added to the reaction vessel and 50ml of. distillate was collected. The diazomethane in ether was stored cold until ready for use.

CBZ-D-Phenyalanine Chloromethyl Alcohol

Zinc chloride in ether (1.0M, 136ml) was added dropwise to a mechanically stirred flask containing a solution of sodium borohydride (10.30g, 1.25 EQ) in ether (552ml) . A solution of Z-D-phenylalanine chloroketone (36g) (from step 1 above) in tetrahydrofuran (0.27M) was added dropwise and allowed to stir at room temperature overnight. The reaction was quenched by dropwise addition of water (400ml), followed by hydrochloric acid (IN, 200ml) and ethyl acetate (250ml) . Upon separation of the layers, the organic layer was washed with water, saturated sodium bicarbonate and brine. Following drying over magnesium sulfate, the volatiles were removed in vacuo to recover 30.42g of crude product. Recrystallization using ethyl acetate (100ml) afforded 9.73g of two isomers. These

were carried through as a mixture. NMR (CDCI3) : consistent with assigned structure. Mass Spec. 334.21 (M+H) .

4. CBZ-D-Phenylalanine Epoxide

CBZ-D-phenylalanine chloroalcohol (9.73g) from step 3 was dissolved in tetrahydrofuran (0.16M) and cooled in an ice bath. Potassium tert-butoxide (1.0M in THF, 32ml, 1.1 EQ) was added dropwise with stirring under nitrogen. Thin Layer Chromatography (Tic) after 30 min in 6:2:2 toluene: ethyl acetate: hexanes indicated reaction is complete. The reaction mixture was concentrated in vacuo and partitioned between ethyl acetate and water. The organic layer was washed with brine and dried over sodium sulfate. Filtration and concentration in vacuo afforded 7.98g of the desired product. NMR (CDCI3) : consistent with assigned structure. Mass Spec. 298 (M+H); 315.17 (M+NH ₄ ) .

5. Epoxide Condensation with L-phenylalanine tert-Butylester

The commercially available amine (as the HCl salt) was converted to the free base by dissolution in saturated sodium bicarbonate and extraction with ethyl acetate. After drying and removal of the volatiles, free

amine (2.11g, 1 EQ) was added to a solution of above described epoxide (from step 4) (2.84g) in methanol (0.2M) and heated until judged complete. Concentration in vacuo gave 4.95g of the desired product. NMR (CDCI3) consistent with assigned structure. Mass Spec. 519.29 (M+H) .

6. tert-Butyldimethylsilyl Protection on Hydroxyl Group

The previously described product (4.95g) (from step 5) dissolved in anhydrous dimethylformamide (1.2M), was reacted with t-butyldimethylsilyl chloride (2.83g, 2.2 EQ) and imidazole (1.75g, 3 EQ) at room temperature overnight. Tic (2% methanol in chloroform) indicated reaction was complete. The reaction was worked up by adding saturated sodium bicarbonate (100ml) and stirring for 10 minutes. Methylene chloride was added, the organic layer was separated, washed with brine and dried over sodium sulfate. Concentration in vacuo and purification on silica gel using 6:1:3 toluene: ethyl acetate: hexanes afforded 3.24g of the product. NMR (CDCI3) : consistent with assigned structure. Mass Spec 633.37 (M+H) .

7. Removal of the CBZ Protecting Group

The CBZ-protected amino acid (from step 6) (3.24g) was dissolved in tetrahydrofuran (66ml) and glacial acetic acid (6ml) . Following a evacuation and purge sequence with nitrogen, palladium on carbon (10%, 200mg) was added. After an evacuation and purge sequence using hydrogen, the reaction was allowed to stir until judged complete by Tic. The catalyst was filtered off and washed with THF/HOAc .Upon concentration in vacuo and further drying on high vacuum, the recovered acetate salt was used directly in the next step. NMR (CDCI3) : consistent with assigned structure. Mass Spec 499.34 (M+H) .

8. Acid Catalyzed Hydrolysis of the t-Butyl Ester

The t-butyl ester (from step 7) (lOOmg) was dissolved in methylene chloride (8ml) and trifluoroacetic acid (2.6ml) at a concentration of

0.02M. Upon stirring under nitrogen, the reaction was

judged complete by Tic. Concentrated in vacuo while keeping cold, followed by further drying on high vacuum overnight afforded a product which was used directly in the next reaction. NMR (CDCI3) : consistent with assigned structure. Mass Spec. 443.27 (M+H) .

9. General Procedure for Cyclization (Lactam Formation)

To a solution of the previously described product (from step 8) (3.08g) in tetrahydrofuran (140ml, 0.05M) was added 4-methylmorpholine (2.68 ml, 3.5 EQ) , 1- hydroxybenzotriazole hydrate (0.942g, 1 EQ) and 1,3- dicyclohexylcarbodiimide (1.45g, 1 EQ) . After stirring at room temperature under nitrogen for 3 days, the precipitated dicyclohexylurea was filtered away and the filtrate was partitioned between methylene chloride and water. The organics were washed with saturated sodium bicarbonate and brine, dried over sodium sulfate and concentrated in vacuo. The crude material was purified by preparative thin layer chromatography (2mm thickness silica gel plate) using toluene: ethyl acetate: methanol. NMR (CDCI3) : consistent with assigned structure. Mass Spec. 425.26 (M+H) .

Example 1

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SUBSTΓΓUTE SHEET (RULE 26)

10. Fluoride-induced Deprotection of the t-Butyldimethylsilyl Ether

A solution of silyl ether (from step 9 above) (38mg) dissolved in tetrabutylammonium fluoride (IM solution in tetrahydrofuran, 1.5ml) was allowed to stir under nitrogen until judged complete by Tic. The reaction was quenched by addition of saturated sodium bicarbonate and stirred for 10 minutes. After diluting with methylene chloride, the layers were separated and the organics were dried over sodium sulfate. Following concentration in vacuo and purification by preparative Tic using Toluene: Ethyl Acetate: Methanol, 18mg of the desired product was isolated. NMR (CDCI3) : consistent with assigned structure. Mass Spec. 311.18 (M+H) .

11. Benzylation of Basic Amine

A solution of the starting lactam (from step 9) (62.5 mg) was dissolved in anhydrous N,N- dimethylformamide (0.15ml, IM) and allowed to stir with

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SUBSΠTUTE SHEET (RULE 26)

potassium carbonate (30.5mg, 1.5 EQ) at room temperature under nitrogen for 10 minutes. Benzyl bromide (0.026ml, 1.5 EQ) was added and the reaction was stirred until judged complete by Tic. After partitioning between methylene chloride and water, the organic phase was washed with saturated sodium bicarbonate, brine and dried over sodium sulfate. Concentration in vacuo affored 50mg of the desired product. NMR (CDCI3) : consistent with assigned structure. Mass Spec. M+H 515.31

Example 2

12 . Deprotection of Benzylated Compound

Material f rom step 11 (above ) was treated as described above for step 10 . NMR (CDCI3 ) : consistent with assigned st ructure . Mass Spec . 401 (M+H) .

13 . Selective Debenzylation of Cyclized

N-benzylamine (Formic Acid Procedure)

A general procedure based on that described in J. Org. Chem, 1979, _______ 3442 was used. The starting

N-benzyl amine (from step 11) (30mg) was dissolved in MeOH (0.02M) with formic acid (-5%, 3ml) . Following the addition of palladium on Carbon (10%, 30mg) , the reaction was stirred under nitrogen until judged complete by Tic. The catalyst was removed and the filtrate was concentrated in vacuo before the silyl ether cleavage. NMR (CDCI3) : consistent with assigned structure. Mass Spec. 425.26 (M+H) .

Using the above-described techniques or variations thereof appreciated by those of skill in the art of chemical synthesis, the compounds of Tables shown below can also be prepared.

Table 1

XIV

R ' E 22 R 27

H H H H H H H H H H

benzyl H

7 benzyl H H 8 benzyl H H 9 benzyl H H

0 benzyl H H

1 benzyl H H

2 benzyl H H

3 benzyl

Example R4 R7 R22 R2

14 benzyl H H

15 H 16 H 17 H

18 H

19 H

20 H benzyl 0

1 H benzyl

2 benzyl 0

3 H cyclopropyl 0 methyl 4 benzyl benzyl benzyl 0 5 benzyl benzyl cyclopropyl benzyl O methyl 6 benzyl H benzyl isobutyl 0 7 H benzyl (m-HO- ethyl 0 C6H )CH ₂ 8 benzyl benzyl (1T.-HOCH2- (1T.-HOCH2-

C6H ₄ )CH ₂ C6H ₄ )CH2 9 benzyl benzyl naphthyl naphthyl 0 0 benzyl benzyl cyclopropyl methyl O methyl 1 benzyl benzyl benzyl methyl 0 2 benzyl H benzyl CH2-CONH2 0 3 benzyl benzyl cyclopropyl cyclopropyl 0 methyl methyl

Example E - & ' .22 R27

34 benzyl H benzyl (3,4-di-F- 0 C6H ₄ )CH2 35 benzyl H benzyl cyclopropyl 0 methyl 36 benzyl H (m-HO- cyclopropyl O C6H ₄ )CH2 methyl

37 benzyl H (m-HOCH2- (m-HOCH2~ 0 C6H4)CH ₂ C6H ₄ )CH2

Utility

The compounds of formula (I) possess retroviral protease inhibitory activity and are therefore useful as antiviral agents for the treatment of viral diseases. More particularly, the compounds of formula (I) possess HIV protease inhibitory activity and are effective as inhibitors of HIV growth. The protease inhibitory activity of the compounds of the present invention is demonstrated using standard assays of protease activity, for example, using the assay described below for assaying inhibitors of HIV protease activity. The ability of the compounds of the present invention to inhibit viral growth or infectivity is demonstrated in standard assay of viral growth or infectivity, for example, using the assays described below.

A compound is considered to be active if it has an IC50 or Ki value of less than about 1 mM for the inhibition of HIV protease or HIV viral growth or infectivity.

HIV Protease Inhibition Assay- Spectroscopic Method

-160-

SUBSΠTUTE SHEET (RULE 26)

Material,. :

Protease: Inclusion bodies of E. coli harboring plasmid containing HIV protease under the control of an inducible T7 promoter were prepared according to Cheng et . al (1990) Gene 87: 243. Inclusion bodies were solubilized in 8 M urea, 50 mM tris pH 8.0. Protease activity was recovered by dilution 20-fold into buffer containing 50 mM sodium acetate pH 5.5, 1 mM EDTA, 10% glycerol and 5% ethylene glycol. Enzyme was used at a final concentration of 1.0-10 ug/ml (ug = microgram) .

Substrate: Peptide of sequence: Ala-Thr-His-Gln- Val-Tyr-Phe (N02) -Val-Arg-Lys-Ala, containing para-nitrophenylalanine (Phe(Nθ2)), was prepared by solid phase peptide synthesis as previously described by Cheng et al. (1990) Proc. Natl. Acad. Sci. USA 87: 9660. Stock solutions of 10 m were prepared in DMSO.

Inhibitory compounds were dissolved in sufficient DMSO to make 2.5 or 25 mM stock solutions. All further dilutions were done in DMSO.

Reaction :

Compound (1-5 uL) (uL or ul = microliter) and HIV protease were mixed in buffer containing 50 mM MES, pH 6.5, 1 M NaCl, 1 mM EDTA, 1 mM dithiothreitol, 10% glycerol. Reactions were initiated by the addition of peptide substrate to a final concentration of 240 uM (uM = micromolar) , and absorbance at 300 nM monitored for 10 min. Values of Ki for inhibitor binding were determined from percent activity measurements in the presence and absence of known concentration of inhibitor, using a value of 0.07 mM for the Km of the substrate (Cheng et al . (1990) Proc. Natl. Acad. Sci. USA 87: 9660) .

The HIV-1 protease inhibitory activity of representative compounds of the invention is shown in Table 2 (below) .

HIV Protease Inhibition Assay- HPLC Method

Materials:

Protease: Inclusion bodies of E. coli harboring plasmid containing plasmid T1718R with a synthetic gene coding for a single-chain tethered dimer of HIV protease were prepared as described in Cheng et al. (Proc. Natl. Acad. Sci. USA, 87, 9660-9664, 1990) . Active protease was prepared as described therein by extraction with 67% acetic acid, dilution 33-fold with water, dialysis against water and then against a "refolding buffer" consisting of 20 mM MES, 1 mM dithiothreitol and 10% glycerol. Protease was stored as a stock preparation at 10 uM in refolding buffer.

Substrate: Peptide of sequence: aminobenzoyl-Ala- Thr-His-Gln-Val-Tyr-Phe (NO ₂ ) -Val-Arg-Lys-Ala containing p-nitrophenylalanine, was prepared by solid phase synthesis as previously described Cheng et al . , op.cit .

Stock solutions of 2 mM substrate were prepared in DMSO. Inhibitory compounds were dissolved in sufficient

DMSO to make 3 mM stock solutions. All further dilutions were prepared in "assay buffer": 1 M NaCl, 50 mM MES, pH 5.5, 1 mM EDTA, ImM DTT, 20% glycerol.

Reactions :

Enzyme reaction: In a 2 ml screw-cap centrifuge tube were added 50 ul protease (final concentration 0.25 nM) and 100 ul inhibitory compound (final concentration 0.1-12,500) . After 15 min preincubation at room temperature, the reaction was started with the addition of 50 ul substrate (final concentration 5 uM) . Incubation was carried out at 30 C. for 1 hr . The reaction was stopped with 1 ml 0.1 M ammonium hydroxide.

HPLC measurement of product formation: The product (aminobenzoyl-Ala-Thr-His-Gln-Val-Tyr) was separated from substrate on a Pharmacia MonoQ anion exchange column. The injection volume was 200 ul . The mobile phases were: A (20 mM trisHCl, pH 9.0, 0.02% sodium azide, 10% acetonitrile) , B (20 mM tris HCl, pH 9.0, •0.02% sodium azide, 0.5 M ammonium formate, 10% acetonitrile) . The mobile phases were pumped at 1 ml/min, with a gradient from 0 to 30% B in 5 min, 100 % B for 4 min to wash the column, and a re-equilibration for 4 min. The retention time of the product was 3.6 min. Detection with a Shimadzu model RF535 fluorescence monitor was at 330 nm (excitation) and 430 (emission) . The Ki was calculated from the formula Ki = 1/ ( ( (Km+S- FA*S) / (FA*Km) )-l) where I = inhibitory concentration, S = substrate concentration, FA = fractional activity = cm peak height with inhibitor/cm peak height without inhibitor, and Km = Michaelis constant = 20 uM.

HIV Yield Reduction Cell Assay

Materials: MT-2, a human T-cell line, was cultured in RPMI medium supplemented with 5% (v/v) heat inactivated fetal calf serum (FCS) , L-glutamine and gentamycin. Human immunodeficiency virus strains, HIV (3B) and HIV(RF) were propagated in H-9 cells in RPMI with 5% FCS. Poly-L-lysine (Sigma) coated cell culture plates were prepared according to the method of Harada et al. (1985) Science 229: 563-566. MTT, 3-(4,5- dimethyl-thiazol-2yl) -2, 5-diphenyltetrazolium bromide, was obtained from Sigma.

Method: Test compounds were dissolved in dimethylsulfoxide to 5 mg/mL and serially diluted into RPMI medium to ten times the desired final concentration. MT-2 cells (5 x 10^/mL) in 2.3 mL were mixed with 0.3 ml of the appropriate test compound

solution and allowed to sit for 30 minutes at room temperature. HIV (3B) or HIV (RF) (~5 x 10 ⁵ plaque forming units/mL) in 0.375 ml was added to the cell and compound mixtures and incubated for one hour at 36°C. The mixtures were centrifuged at 1000 rpm for 10 minutes and the supernatants containing unattached virus were discarded. The cell pellets were suspended in fresh RPMI containing the appropriate concentrations of test compound and placed in a 36°C, 4% Cθ2 incubator. Virus was allowed to replicate for 3 days. Cultures were centrifuged for 10 minutes at 1000 rpm and the supernatants containing cell free progeny virus were removed for plaque assay.

The virus titers of the progeny virus produced in the presence or absence of test compounds were determined by plaque assay. Progeny virus suspensions were serially diluted in RPMI and 1.0 mL of each dilution was added to 9 ml of MT-2 cells in RPMI. Cells and virus were incubated for 3 hours at 36°C to allow for efficient attachment of the virus to cells.

Aliquots of each virus and cell mixture were added equally to two wells of a six well poly-L-lysine coated culture plate and incubated overnight at 36°C, 4% CO2. Liquid and unattached cells were removed prior to the addition of 1.5 mL of RPMI with 0.75% (w/v) Seaplaque agarose (FMC Corp.) and 5% FCS. Plates were incubated for 3 days and a second RPMI/agarose overlay was added. After an additional 3 days at 36°C, 4% CO2, a final overlay of phosphate-buffered saline with 0.75% Seaplaque agarose and 1 mg MTT/mL was added. The plates were incubated overnight at 36°C. Clear plaques on a purple background were counted and the number of plaque forming units of virus was calculated for each sample. The antiviral activity of test compounds was determined by the percent reduction in the virus titer with respect to virus grown in the absence of any inhibitors.

-164-

SUBSTJTUTESHEET(RULE26)

HIV Low Multiplicity Assay

Materials: MT-2, a human T-cell line, was cultured in RPMI medium supplemented with 5% (v/v) heat inactivated fetal calf serum (FCS) , L-glutamine and gentamycin (GIBCO) . Human immunodeficiency virus strains HIV (3B) and HIV (RF) were propagated in H-9 cells in RPMI with 5% FCS. XTT, benzene-sulfonic acid, 3, 3 '- [1- [ (phenyl-amino)carbonyl]-3, 4-tetrazolium]bis (4- methoxy-6-nitro) -, sodium salt, was obtained from Starks Associates, Inc.

Method: Test compounds were dissolved in dimethyl- sulfoxide to 5 mg/ml and serially diluted into RPMI medium to ten times the desired final concentration.

MT-2 cells (5 x lθVθ.1 mL) were added to each well of a 96 well culture plate and 0.02 mL of the appropriate test compound solution was added to the cells such that each compound concentration was present in two wells. The cells and compounds were allowed to sit for 30 minutes at room temperature. HIV(3B) or HIV(RF) (-5 x 10- ^> plaque forming units/mL) was diluted in medium and added to the cell and compound mixtures to give a multiplicity of infection of 0.01 plaque forming unit/cell. The mixtures were incubated for 7 days at

36°C, during which time the virus replicated and caused the death of unprotected cells. The percentage of cells protected from virus induced cell death was determined by the degree of metabolism of the tetrazolium dye, XTT. In living cells, XTT was metabolized to a colored formazan product which was quantitated spectrophotometrically at 450 nm. The amount of colored formazan was proportional to the number of cells protected from virus by the test compound. The concentration of compound protecting either 50% (IC ₅₀ )

or 90% (IC _9Q ) with respect to an uninfected cell culture was determined.

The HIV inhibitory activity of representative compounds of the present invention in the whole cell infectivity assay described above is shown in Table 2.

Table 2

Example Number Ki XQ90 l +++ +++

24 ++ +++

The IC ₉ Q values in Table 2 are indicated as: +++ = <10 ug/mL.

In the Tables herein the Ki values were determined using the assay conditions described above under HIV Protease Inhibition Assay-HPLC Method. The Ki values are indicated as follows: +++ = <10 nM; ++ = 10 nM to 1 uM; + = >1 uM.

In the Tables herein the IC ₉ o values were determined using the assay conditions described above under HIV Low Multiplicity Assay. The IC ₉ o values are indicated as follows: +++ = <10 ug/mL; ++ = 10 to 100 ug/mL; + = >100 ug/mL.

Dosage and Formulation

The antiviral compounds of this invention can be administered as treatment for viral infections by any

means that produces contact of the active agent with the agent's site of action, the viral protease, in the body of a mammal. They can be administered by any conventional means available for use in conjunction with pharmaceuticals, either as individual therapeutic agents or in a combination of therapeutic agents. They can be administered alone, but generally administered with a pharmaceutical carrier selected on the basis of the chosen route of administration and standard pharmaceutical practice.

The dosage administered will, of course, vary depending upon known factors, such as the pharmacodynamic characteristics of the particular agent and its mode and route of administration; the age, health and weight of the recipient; the nature and extent of the symptoms; the kind of concurrent treatment; the frequency of treatment; and the effect desired. A daily dosage of active ingredient can be expected to be about 0.001 to 1000 milligrams per kilogram of body weight, with the preferred dose being 0.1 to about 30 mg/kg.

Dosage forms (compositions suitable for administration contain from about 1 milligram to about 100 milligrams of active ingredient per unit. In these pharmaceutical compositions the active ingredient will ordinarily be present in an amount of about 0.5-95% by weight based on the total weight of the composition.

The active ingredient can be administered orally in solid dosage forms, such as capsules, tablets, and powders, or in liquid dosage forms, such as elixirs, syrups, and suspensions. It can also be administered parenterally, in sterile liquid dosage forms.

Gelatin capsules contain the active ingredient and powdered carriers, such as lactose, starch, cellulose derivatives, magnesium stearate, stearic acid, and the like. Similar diluents can be used to make compressed

tablets. Both tablets and capsules can be manufactured as sustained release products to provide for continuous release of medication over a period of hours. Compressed tablets can be sugar coated or film coated to mask any unpleasant taste and protect the tablet from the atmosphere, or enteric coated for selective disintegration in the gastrointestinal tract.

Liquid dosage forms for oral administration can contain coloring and flavoring to increase patient acceptance.

In general, water, a suitable oil, saline, aqueous dextrose (glucose) , and related sugar solutions and glycols such as propylene glycol or polyethylene glycols are suitable carriers for parenteral solutions. Solutions for parenteral administration preferably contain a water soluble salt of the active ingredient, suitable stabilizing agents, and if necessary, buffer substances. Antioxidizing agents such as sodium bisulfite, sodium sulfite, or ascorbic acid, either alone or combined, are suitable stabilizing agents.

Also used are citric acid and its salts and sodium EDTA. In addition, parenteral solutions can contain preservatives, such as benzalkonium chloride, methyl- or propyl-paraben, and chlorobutanol . Suitable pharmaceutical carriers are described in Remington's Pharmaceutical Sciences. Mack Publishing Company, a standard reference text in this field.

Useful pharmaceutical dosage-forms for administration of the compounds of this invention can be illustrated as follows :

Capsule?

A large number of unit capsules are prepared by filling standard two-piece hard gelatin capsules each with 100 milligrams of powdered active ingredient, 150

milligrams of lactose, 50 milligrams of cellulose, and 6 milligrams magnesium stearate .

Soft Gelatin Capsules A mixture of active ingredient in a digestable oil such as soybean oil, cottonseed oil or olive oil is prepared and injected by means of a positive displacement pump into gelatin to form soft gelatin capsules containing 100 milligrams of the active ingredient. The capsules are washed and dried.

Tablets

A large number of tablets are prepared by conventional procedures so that the dosage unit was 100 milligrams of active ingredient, 0.2 milligrams of colloidal silicon dioxide, 5 milligrams of magnesium stearate, 275 milligrams of microcrystalline cellulose, 11 milligrams of starch and 98.8 milligrams of lactose. Appropriate coatings may be applied to increase palatability or delay absorption.

Formula (Ic)

Formula (Ilia) Formula (IVa) Formula (IVb)

Formula (Va)

Table 3 [a]

Formula (Ic), R ⁴ =R ²⁷ =benzyl, R ²² =R ⁷ =Table Ex. No .0 .1 .2 l[a] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 2 [a] - (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

3 [a] m-(N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

4 [a] -trifluorocarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

5 [a] i-i-formaldoximebenzyl m-acetoximebenzyl benzyl

6 [a] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

7 [a] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

8 [a] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 4 [a]

Formula (Ic) , R ⁴ =R ²⁷ =fluorobenzyl, R ²² =R ⁷ =Table

Ex. o .0 .1 .2

9 [a] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

10 [a] m-(N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

11 [a] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 12 [a] m-trifluorocarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

13[a] m-formaldoximebenzyl m-acetoximebenzyl benzyl

14 [a] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

15 [a] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

16 [a] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 5 [a]

Formula (Ic) , R =R ²⁷ =pyrrolylmethyl , R ² =R ⁷ =Table

Ex . No . 0 . 1 .2

17 [a] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

18 [a] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl ) aminobenzyl

19 [a] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

20 [a] m-trifluorocarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

21 [a] m-formaldoximebenzyl m-acetoximebenzyl benzyl

22 [a] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

23 [a] m-imidazolylbenzyl p-f luorobenzyl pyridinylmethyl

24 [a] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 6 [a]

Formula (Ic), R ⁴ =R ²⁷ =methoxybenzyl, R ²² =R ⁷ =Table

Ex . No . 0 .1 .2

25 [a] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

26 [a] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl)aminobenzyl

27 [a] m-(N-methylamino) m-(N-methylamino) m-formylbenzyl carbonylbenzyl benzyl .

28 [a] m-trifluorocarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

29[a] m-formaldoximebenzyl m-acetoximebenzyl benzyl

30 [a] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

31 [a] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

32 [a] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 7 [a ]

Formula ( Ic) , R ⁴ =R ^{2 7} =isobutyl , R ² =R ⁷ =Table

Ex . No . 0 . 1

33 [a] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

34 [a] m-(N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

35 [a] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

36 [a] m-trifluorocarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

37 [a] m-formaldoximebenzyl m-acetoximebenzyl benzyl

38 [a] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

39 [a] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

40 [a] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 8 [a]

Formula (Ic), R ⁴ =R ²⁷ =p-nitrobenzyl, R ²² =R ⁷ =Table

Ex. o .0 .1 .2

41 [a] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

42 [a] m-(N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

43 [a] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

44 [a] m-trifluorocarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

45 [a] m-formaldoximebenzyl m-acetoximebenzyl benzyl

46[a] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

47 [a] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

48 [a] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 9 [a]

Formula ( Ic) , R ⁴ =R ²⁷ =m-aminobenzyl , R ²² =R ⁷ =Table

.0 .1 .2

49 [a] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

50 [a] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

51 [a] m-(N-methylamino) m-(N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

52 [a] m-trifluorocarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

53 [a] m-formaldoximebenzyl m-acetoximebenzyl benzyl

54 [a] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

55 [a] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

56 [a] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 10[a]

Formula (Ic), R ⁴ =R ⁷ =pyridinylmethyl, R ²² =R ⁷ =Table

Ex.No .0 .1 .2

57 [a] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

58 [a] m- (N, -dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl)aminobenzyl

59 [a] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

60 [a] m-trifluorocarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

61 [a] m-formaldoximebenzyl m-acetoximebenzyl benzyl

62 [a] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

63 [a] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

64 [a] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 11 [a]

Formula ( Ic) , R ⁴ =R ²⁷ =m-hydroxybenzyl, R ² =R ⁷ =Table

Ex . No .0 .1 .2

65[a] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

66 [a] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl)aminobenzyl

67 [a] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 68 [a] m-trifluorocarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

69 [a] m-formaldoximebenzyl m-acetoximebenzyl benzyl

70 [a] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

71 [a] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

72 [a] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 12 [a]

Formula (Ic) , R ⁴ =R ²⁷ =p-hydroxybenzyl, R ²² =R ⁷ =Table

Ex.No .0 .1 .2

73 [a] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

74 [a] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

75 [a] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

76 [a] m-trifluorocarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

77 [a] m-formaldoximebenzyl m-acetoximebenzyl benzyl

78 [a] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

79[a] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

80 [a] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 13 [a]

Formula (Ic) , R ⁴ =R ⁷ =m-aminocarbonybenzyl, R ² =R ⁷ =Table Ex.No .0 .1 .2

81 [a] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

82 [a] m-(N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl)aminobenzyl

83[a] m-(N-methylamino) m-(N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

84 [a] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

85[a] m-formaldoximebenzyl m-acetoximebenzyl benzyl

86[a] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

87 [a] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

88 fa] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 14 [a]

Formula ( I c) , R ⁴ =R ^{2 7} =p-hydroxymethylbenzyl , R _. ^z 22= ₌ R _R 7'=-Table

Ex . o . 0 . 1

89[a] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

90 [a] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl)aminobenzyl

91 [a] m- (N-methylamino) m-(N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

92 [a] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

93[a] m-formaldoximebenzyl m-acetoximebenzyl benzyl

94 [a] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

95 [a] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

96[a] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 15 [a]

Formula (Ic) , R ⁴ =R ²⁷ =m-hydroxycarbonylbenzyl, R ²² =R ⁷ =Table

Ex.No .0 .1 .2

97 [a] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

98 [a] m-(N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

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SUBST1TUTESHEET(RULE26)

99 [a] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

100 [a] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

101 [a] m-formaldoximebenzyl m-acetoximebenzyl benzyl

102 [a] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

103 [a] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

10 [a] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 16 [a]

Formula ( Ic) , R ⁴ =R ⁷ =benzyl , R ² =m-hydroxymethylbenzyl ,

R ⁷ =Table Ex . No . 0 . 1 .2

105 [a ] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 106 [a] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

107 [a] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

108 [a] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

109 [a] m-formaldoximebenzyl m-acetoximebenzyl benzyl

110 [a] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 111 [a] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

112 [a] m-acetylbenzyl -aminosulfonylbenzyl m-methoxybenzyl

Table 17 [a ]

Formula ( Ic ) , R ⁴ =R ⁷ =benzyl , R ² =p-hydroxymethylbenzyl ,

R ⁷ =Table Ex . No . 0 . 1 .2

113 [a] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 11 [ a ] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl ) aminobenzyl 115 [a ] m- (N-methylamino) m- (N-methylamino) m-f ormylbenzyl carbonylbenzyl benzyl

- 176-

SUBSTJTUTE SHEET (RULE 26)

116 [a] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

117 [a] m-formaldoximebenzyl m-acetoximebenzyl benzyl

118 [a] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

119 [a] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

120 [a] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 18 [a]

Formula (Ic) , R ⁴ =R =benzyl, R ²² =m-hydroxybenzyl,

R ⁷ =Table Ex.No .0 .1 .2

121 [a] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

122 [a] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

123 [a] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 12 [a] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

125 [a] m-formaldoximebenzyl m-acetoximebenzyl benzyl 126 [a] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 127 [a] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

128 [a] m-acetylbenzyl -aminosulfonylbenzyl m-methoxybenzyl

Table 19[a]

Formula (Ic) , R ⁴ =R ²⁷ =benzyl, R ²² =m- (N,N-dimethylamino glycyl) aminobenzyl, R ⁷ =Table

Ex.No .0 .1 .2

129 [a] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

130 [a] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

131 [a] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

132 [a] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

133 [a] m-formaldoximebenzyl m-acetoximebenzyl benzyl

-177-

SUBSCTTUTE SHEET (RULE 26)

13 [a] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 135 [a] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl 136 [a] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 20 [a]

Formula ( Ic) , R ⁴ =R ²⁷ =benzyl , R ²² =m-aminocarbonylbenzyl,

R ⁷ =Table Ex . o . 0 . 1 .2

137 [a] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

138 [a] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

139 [a _. m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

140 [a] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

141 [a] m-formaldoximebenzyl m-acetoximebenzyl benzyl

142 [a] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 143[a] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

144 [a] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 21 [a ]

Formula ( Ic) , R ⁴ =R ⁷ =benzyl , R ² =p-hydroxybenzyl ,

R ⁷ =Table Ex . No . 0 . 1 .2

145 [a] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 146 [a] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

147 [a] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

148 [a] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

149 [a] m-formaldoximebenzyl m-acetoximebenzyl benzyl

150 [a] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 151 [a] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

152 [a. m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

-178-

SUBSTΠTJTE SHEET (RULE 26)

Table 22 [ a ]

Formula ( I c ) , R ⁴ =R ^{2 7} =benzyl , R ²² =m- (N-methylaminocarbonyl benzyl , R ⁷ =Table Ex . No . 0 . 1 .2

153 [a ] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 15 [a] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

155 [a] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 156 [a ] m-trif luorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

157 [a] m-formaldoximebenzyl m-acetoximebenzyl benzyl

158 [a] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

159 [a] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

160 [a] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 23 [a]

Formula (Ic), R ⁴ =R ⁷ =benzyl, R ²² =m- (N-methylamino) enzyl,

R ⁷ =Table Ex.No .0 .1 .2

161 [a] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

162 [a] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

163 [a] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 16 [a] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

165 [a] m-formaldoximebenzyl m-acetoximebenzyl benzyl 166 [a] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 167 [a] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

168 [a] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 24 [a]

Formula (Ic), R ⁴ =R ⁷ =benzyl, R ² =m-formyllbenzyl, R ⁷ =Table

Ex.No .0 .1 .2

169 [a] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

170 [a] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl)aminobenzyl

171 [a] m- (N-methylamino) m-(N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 172 [a] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl 173[a] m-formaldoximebenzyl m-acetoximebenzyl benzyl 17 [a] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

175 [a] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

176 [a] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 25 [ a]

Formula ( Ic) , R ⁴ =R ⁷ =benzyl , R ² =m-trif luorocarbonylbenzyl ,

R ⁷ =Table Ex . No .0 . 1 .2

177 [a ] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 178 [a] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

179 [a] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

180 [a] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

181 [a] m-formaldoximebenzyl m-acetoximebenzyl benzyl

182 [a] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

183 [a] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

184 [a] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 26 [a .

Formula ( Ic) , R ⁴ =R ²⁷ =benzyl , R ²² =m-hydroxyamidinobenzyl ,

R ⁷ =Table Ex . No . 0 . 1 .2

185 [a] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

-180-

SUBSCTTUTE SHEET (RULE 26)

186 [a] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl ) aminobenzyl

187 [a] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

188 [a] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

189[a] m-formaldoximebenzyl m-acetoximebenzyl benzyl

190 [a] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

191 [a] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

192[a] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 27 [a]

Formula ( Ic) , R ⁴ =R ²⁷ =benzyl, R ²² =m-triazolylbenzyl ,

R ⁷ =Table Ex . No . 0 . 1 .2

193 [a] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 194 [ a ] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

195 [a] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 196fa] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl 197 [a] m-formaldoximebenzyl m-acetoximebenzyl benzyl

198 [a] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

199 [a] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

200 [a] m-acetylbenzyl -aminosulfonylbenzyl m-methoxybenzyl

Table 28 [a]

Formula (Ic), R ⁴ =R ⁷ =benzyl, R ²² =m-formaldoximebenzyl,

R ⁷ =Table Ex.No .0 .1 .2

201 [a] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

202 [a] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl)aminobenzyl

203 [a] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

204 [a] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

205 [a] m-formaldoximebenzyl m-acetoximebenzyl benzyl 206 [a] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 207 [a] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

208 [a] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 29 [a]

Formula ( I c ) , R ⁴ =R ^{2 7} =benzyl , R ²² =m-acetoximebenzyl ,

R ⁷ =Table Ex . No . 0 . 1 .2

209 [a] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

210 [a] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

211 [a] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 212 [a] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

213 [a] m-formaldoximebenzyl m-acetoximebenzyl benzyl 21 [a] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 215 fa] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

216 [a] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 30 [a ]

Formula ( I c ) , R ⁴ =R ^{2 7} =benzyl , R ²² =benzyl , R ⁷ =Table

Ex . No . 0 . 1 .2

217 [a] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

218 [a] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

219 [a] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

220 [a] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

221 [a] m-formaldoximebenzyl m-acetoximebenzyl benzyl

222 [a] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 223 [a] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl 224 [a] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 31 [a]

Formula ( Ic) , R ⁴ =R =benzyl, R ² =m-hydroxycarbonylbenzyl ,

R ⁷ =Table Ex . No . 0 . 1 .2

225 [a] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 226 [a] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

227 [ a ] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

228 [a] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

229 fa] m-formaldoximebenzyl m-acetoximebenzyl benzyl

230 [a] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

231 [a] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

232 [a] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 32 [a]

Formula (Ic) , R ⁴ =R ⁷ =benzyl, R ²² =m-tetrazolylbenzyl, R ⁷ =Table

Ex.No .0 .1 .2

233 [a] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

234 [a] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

235 [a] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

236fa] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

237 fa] m-formaldoximebenzyl m-acetoximebenzyl benzyl 238 [a] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 239 [a] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

240 [a] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 33 [a]

Formula (Ic) , R ⁴ =R ⁷ =benzyl, R ² =m-pyrazolylbenzyl,

R ⁷ =Table Ex.No .0 .1 .2

241 [a] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

242 [a] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl)aminobenzyl

243 fa] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

24 [a] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

245 fa] m-formaldoximebenzyl m-acetoximebenzyl benzyl 246 [a] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 247 [a] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

248 [a] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 34 [a]

Formula (Ic) , R ⁴ =R ²⁷ =benzyl, R ² =m-imidazolylbenzyl,

R ⁷ =Table Ex.No .0 .1 .2

249 [a] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

250 fa] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

251 [a] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 252 [a] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

253 [a] m-formaldoximebenzyl m-acetoximebenzyl benzyl

254 [a] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

255 [a] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

256 [a] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 35[a]

-184-

SUBSTJTUTE SHEET (RULE 26)

Formula (Ic) , R ⁴ =R ²⁷ =benzyl, R ²² =p-fluorobenzyl,

R ⁷ =Table Ex. o .0 .1 .2

257 [a] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

258 [a] m- (N, -dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

259 [a] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 260 [a] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

261 [a] m-formaldoximebenzyl m-acetoximebenzyl benzyl

262 [a] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

263[a] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

26 [a] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 36 [a ]

Formula ( Ic) , R ⁴ =R ²⁷ =benzyl , R ² =pyridinylmethyl , R ⁷ =Table

Ex . No . 0 . 1 .2

265 [a] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

266 [a] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

267 [a] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 268 [a] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl 269 [a] m-formaldoximebenzyl m-acetoximebenzyl benzyl

270 [a] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

271 [a] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

272 [a] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 37 [a ]

Formula ( I c ) , R ⁴ =R ^{2 7} =benzyl , R ² =m-acetylbenzyl ,

R ⁷ =Table

Ex . No

273 [a] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

274 fa] m- (N, -dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl)aminobenzyl

275[a] m-(N-methylamino) m-(N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

276 [a] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

277[a] m-formaldoximebenzyl m-acetoximebenzyl benzyl

278 [a] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

279 [a] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

280 [a] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 38 fa]

Formula (Ic) , R ⁴ =R ² =benzyl, R ² =m-aminosulf onylbenzyl,

R ⁷ =Table Ex. No .0 .1 .2

281 [a] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 282 [a] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

283 [a] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

284 [a] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

285 [a] m-formaldoximebenzyl m-acetoximebenzyl benzyl 286[a] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 287 [a] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

288 [a] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 39[a]

Formula (Ic) , R ⁴ =R ²⁷ =benzyl, R ²² =m-methoxybenzyl,

R ⁷ =Table Ex. No .0 .1 .2

289 [a] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 290 fa] - (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

291 [a] - (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

292 [a] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

293[a] m-formaldoximebenzyl m-acetoximebenzyl benzyl 294 fa] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 295 [a] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

296 [a] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 3 [b]

Formula (Ie), R =R ²⁷ =benzyl, R ²² =R ⁷ =Table

Ex.No .0 .1 lib] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 2[b] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

3[b] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

4[b] m-trifluorocarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

5[b] m-formaldoximebenzyl m-acetoximebenzyl benzyl 6[b] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 7[b] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl 8[b] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table [b]

Formula (Ie) , R ⁴ =R ²⁷ =fluorobenzyl, R ²² =R ⁷ =Table

Ex.No .0 .1 .2

9 [b] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

10 [b] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

11 [b] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

12 [b] m-trifluorocarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

13 [b] m-formaldoximebenzyl m-acetoximebenzyl benzyl

14 [b] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

15fb] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

16 [b] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 5[b]

Formula (Ie), R ⁴ =R ²⁷ =pyrrolylmethyl, R ² =R ⁷ =Table

Ex.No .0 .1 .2

17 [b] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

18 [b] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl)aminobenzyl

19 [b] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

20 [b] m-trifluorocarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

21 [b] m-formaldoximebenzyl m-acetoximebenzyl benzyl

22 [b] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

23 [b] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

24 fb] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 6[b]

Formula (Ie) , R ⁴ =R ²⁷ =rnethoxybenzyl, R =R ⁷ =Table

Ex.No .0 .1 .2

25 fb] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

26 fb] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

27 [b] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

28 [b] m-trifluorocarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

29 [b] m-formaldoximebenzyl m-acetoximebenzyl benzyl

30 [b] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

31 [b] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

32 [b] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 7 [b]

-li

Formula (Ie) , R =R ²⁷ =isobutyl, R ²² =R ⁷ =Table Ex.No .0 .1 .2

33 [b] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

34 [b] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

35 [b] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

36 [b] m-trifluorocarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

37 [b] m-formaldoximebenzyl m-acetoximebenzyl benzyl

38 [b] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 39 fb] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

40 [b] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 8 [b]

Formula ( I e ) , R ⁴ =R ^{2 7} =p-nit robenzyl , R ²² =R ⁷ =Table

Ex . No . 0 . 1 .2

41 [b] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

42 [b] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

43 [b] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 4 fb] m-trifluorocarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

45 [b] m-formaldoximebenzyl m-acetoximebenzyl benzyl

46 fb] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

47 [b] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

48 [b] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 9 [b]

Formula ( Ie ) , R ⁴ =R ²⁷ =m-aminobenzyl , R ²² =R ⁷ =Table

Ex . No . 0 . 1 .2

49 [b] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

50 [b] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

51 [b] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

52 [b] m-trifluorocarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

53[b] m-formaldoximebenzyl m-acetoximebenzyl benzyl

54 [b] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

55[b] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

56 [b] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 10 [b]

Formula ( Ie ) , R ⁴ =R ⁷ =pyridinylmethyl , R ² =R ⁷ =Table

Ex . No . 0 . 1 . 2

57 [b] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

58 [b] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl)aminobenzyl

59 fb] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

60 [b] m-trifluorocarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

61 [b] m-formaldoximebenzyl m-acetoximebenzyl benzyl

62 [b] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

63 [b] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

64 [b] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 11 [b]

Formula (Ie), R ⁴ =R ²⁷ =m-hydroxybenzyl, R ²² =R ⁷ =Table

Ex.No .0 .1 .2

65fb] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

66 [b] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

67 fb] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

68 [b] m-trifluorocarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

69 fb] m- ormaldoximebenzyl m-acetoximebenzyl benzyl

70 fb] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

71 [b] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

72 [b] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 12 [b]

Formula ( Ie ) , R ⁴ =R ^{2 7} =p-hydroxybenzyl , R ² =R ⁷ =Table

Ex . No . 0 .1 .2

73 [b] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

74 [b] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

75 [b] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

76 [b] m-trifluorocarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

77 [b] m-formaldoximebenzyl m-acetoximebenzyl benzyl

78 [b] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

79 [b] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

80 [b] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 13 [b]

Formula (Ie) , R =R ²⁷ =m-aminocarbonybenzyl, R ²² =R ⁷ =Table

Ex.No .0 .1 .2

81 [b] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

82 fb] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

83 [b] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

84 fb] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

85 [b] m-formaldoximebenzyl m-acetoximebenzyl benzyl

86 [b] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 87 fb] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

88 [b] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 14 [b]

-191-

SUBSTΪTUTESHEET(RULE26)

Formula (Ie) , R ⁴ =R ²⁷ =p-hydroxymethylbenzyl, R ² =R ⁷ =Table Ex. o .0 .1 .2

89 [b] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

90[b] m-(N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl)aminobenzyl

91 [b] m-(N-methylamino) m-(N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

92 [b] m-trifluorcarbonyl ^* m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

93 [b] m-formaldoximebenzyl m-acetoximebenzyl benzyl

94 [b] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

95 [b] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl 96fb] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 15 [b]

Formula (Ie), R ⁴ =R ²⁷ =m-hydroxycarbonylbenzyl, R ² =R =Table

Ex.No .0 .1 .2

97 fb] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

98 fb] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl)aminobenzyl

99[b] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

100 [b] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

101 [b] m-formaldoximebenzyl m-acetoximebenzyl benzyl

102 [b] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

103 [b] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

104 [b] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 16fb]

Formula ( Ie) , R ⁴ =R ²⁷ =benzyl , R ²² =m-hydroxymethylbenzyl ,

R ⁷ =Table Ex . No . 0 . 1 .2

105 [b] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

106 [b] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

107 [b] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

108 [b] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl,

109[b] m-formaldoximebenzyl m-acetoximebenzyl benzyl 110 [b] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl lllfb] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl 112 [b] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 17 [b]

Formula ( Ie) , R ⁴ =R ²⁷ =benzyl , R ²² =p-hydroxymethylbenzyl ,

R ⁷ =Table Ex . No .0 . 1 .2

113 [b] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

11 [b] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

115 [b] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 116 [b] m-trif luorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

117 fb] m-formaldoximebenzyl m-acetoximebenzyl benzyl 118 [b] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 11 [b] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

120 [b] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 18 [b]

Formula ( Ie ) , R ⁴ =R ^{2 7} =benzyl , R ² =m-hydroxybenzyl ,

R ⁷ =Table Ex . No . 0 . 1 .2

121 fb] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 122 fb] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl ) aminobenzyl

-193-

SUBSTJTUTE SHEET (RULE 26)

123 fb] m-(N-methylamino) m-(N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 124 [b] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

125[b] m-formaldoximebenzyl m-acetoximebenzyl benzyl 126[b] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 127 fb] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl 128 [b] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 19 [b]

Formula ( Ie ) , R ⁴ =R ⁷ =benzyl , R =m- (N, N-dimethylamino glycyl ) aminobenzyl , R ⁷ =Table Ex . No . 0 . 1 .2

129 [b] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 130 [b] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

131 [b] m-(N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

132 fb] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

133[b] m-formaldoximebenzyl m-acetoximebenzyl benzyl 13 [b] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 135 [b] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

136[b] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 20 [b]

Formula ( Ie ) , R ⁴ =R ⁷ =benzyl , R =m-aminocarbonylbenzyl ,

R ⁷ =Table Ex . No . 0 . 1 .2

137 [b] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 138 [b] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl 139 fb] m- (N-methylamino) m- (N-methylamino) m-f ormylbenzyl carbonylbenzyl benzyl

- 1 94-

SUBSTΪTUTE SHEET (RULE 26)

140 [b] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

141 fb] m-formaldoximebenzyl m-acetoximebenzyl benzyl

142 [b] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

143[b] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

144fb] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 21 [b]

Formula ( Ie ) , R ⁴ =R ²⁷ =benzyl, R ² =p-hydroxybenzyl ,

R ⁷ =Table Ex . No . 0 . 1 .2

145 [b] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 146 [b] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

147 [b] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 148 [b] m-trif luorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

149 [b] m-formaldoximebenzyl m-acetoximebenzyl benzyl 150 [b] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 151 [b] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

152 [b] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 22 [b]

Formula ( Ie ) , R ⁴ =R ²⁷ =benzyl , R ²² =m- (N-methylaminocarbonyl benzyl , R ⁷ =Table Ex . No . 0 . 1 .2

153 [b] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

154 [b] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

155 [b] m- (N-methylamino) m- (N-methylamino) m-f ormylbenzyl carbonylbenzyl benzyl

156 [b] m-trif luorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

157 fb] m-formaldoximebenzyl m-acetoximebenzyl benzyl

158 [b] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 159 fb] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl 160 [b] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 23 [b]

Formula ( Ie) , R ⁴ =R ²⁷ =benzyl, R =m- (N-methylamino) benzyl ,

R ⁷ =Table Ex . o .0 . 1 .2

161 fb] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 162 [b] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

163 [b] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 16 [b] m-trif luorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

165fb] m-formaldoximebenzyl m-acetoximebenzyl benzyl 166[b] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 167 [b] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

168 [b] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 2 [b]

Formula (Ie), R =R ⁷ =benzyl, R ²² =m-formyllbenzyl, R ⁷ =Table

Ex.No .0 .1 .2

169[b] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

170 [b] m-(N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

171 [b] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 172[b] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

173fb] m-formaldoximebenzyl m-acetoximebenzyl benzyl 17 [b] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 175[b] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

176[b] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 25 [b]

Formula (Ie) , R ⁴ =R ²⁷ =benzyl, R ²² =m-trifluorocarbonylbenzyl, R ⁷ =Table

Ex.No .0 .1 .2

177 [b] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

178 [b] m- (N, -dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

179 [b] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 180 fb] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

181 [b] m-formaldoximebenzyl m-acetoximebenzyl benzyl 182 [b] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 183 [b] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

18 [b] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 26[b]

Formula (Ie), R =R ²⁷ =benzyl, R ² =m-hydroxyamidinobenzyl, R =Table

Ex.No .0 .1 .2

185 fb] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

186 fb] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

187 fb] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 188 [b] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

189 [b] m-formaldoximebenzyl m-acetoximebenzyl benzyl 190 [b] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 191 [b] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

192 [b] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 27 [b]

Formula (Ie), R ⁴ =R ²⁷ =benzyl, R ²² =m-triazolylbenzyl, R ⁷ =Table

Ex.No .0 .1 .2

193[b] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

194 [b] m- (N, -dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl 195fb] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 196fb] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl 197 [b] m-formaldoximebenzyl m-acetoximebenzyl benzyl 198 [b] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 199 [b] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl 200 [b] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 28 [b]

Formula ( Ie) , R ⁴ =R ^{2 7} =benzyl, R ² =m-formaldoximebenzyl,

R ⁷ =Table Ex. No .0 .1 .2

201 [b] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 202 [b] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl ) aminobenzyl

203 fb] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 20 [b] m-trif luorcarbonyl m-hydroxyamidinc m-triazolylbenzyl benzyl benzyl

205 [b] m-formaldoximebenzyl m-acetoximebenzyl benzyl 206 [b] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 207 [b] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

208 [b] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 29 [b]

Formula ( Ie) , R ⁴ =R ^{2 7} =benzyl , R ² =m-acetoximebenzyl ,

R ⁷ =Table Ex . No . 0 . 1 .2

209 fb] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

210 [b] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl 211 [b] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 212 [b] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

213 [b] m-formaldoximebenzyl m-acetoximebenzyl benzyl 214 [b] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 215 [b] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl 216 [b] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 30fb]

Formula (Ie) , R ⁴ =R ²⁷ =benzyl, R ²² =benzyl, R ⁷ =Table Ex.No .0 .1

217 [b] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 218 [b] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

219 fb] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 220 fb] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

221 [b] m-formaldoximebenzyl m-acetoximebenzyl benzyl 222 [b] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 223 [b] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl 22 [b] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 31 [b]

Formula ( Ie ) , R ⁴ =R ⁷ =benzyl , R ²² =m-hydroxycarbonylbenzyl ,

R ⁷ =Table Ex . No . 0 . 1 .2

225 [b] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 226 [b] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl ) aminobenzyl 227 [b] m- (N-methylamino) m- (N-methylamino) m-f ormylbenzyl carbonylbenzyl benzyl

228 fb] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

229fb] m-formaldoximebenzyl m-acetoximebenzyl benzyl

230 fb] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

231 [b] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

232 fb] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 32 fb]

Formula ( Ie) , R ⁴ =R ²⁷ =benzyl, R ²² =m-tetrazolylbenzyl,

R ⁷ =Table Ex . o . 0 . 1 .2

233 fb] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 23 [b] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

235 [b] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 236 [b] m-trif luorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

237 fb] m-formaldoximebenzyl m-acetoximebenzyl benzyl 238fb] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 239fb] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

240 [b] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 33 [b]

Formula (Ie), R ⁴ =R ²⁷ =benzyl, R ²² =rn-pyrazolylbenzyl,

R ⁷ =Table Ex.No .0 .1 .2

241 [b] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 242 fb] m-(N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

243fb] m-(N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

244 [b] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

245[b] m-formaldoximebenzyl m-acetoximebenzyl benzyl

246 [b] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

247 [b] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

248 [b] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 34 [b]

Formula ( Ie ) , R ⁴ =R ²⁷ =benzyl, R ² =m-imidazolylbenzyl, R =Table

Ex . No . 0 . 1 .2

249 [b] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

250 [b] m-(N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

251 fb] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 252 [b] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

253 [b] m-formaldoximebenzyl m-acetoximebenzyl benzyl 25 [b] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 255 [b] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

256 [b] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 35 [b]

Formula ( Ie ) , R =R ² =benzyl , R ²² =p-f luorobenzyl ,

R ⁷ =Table Ex . No .0 .1 .2

257 [b] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 258 [b] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

259 [b] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 260 [b] m-trif luorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

261 [b] m-formaldoximebenzyl m-acetoximebenzyl benzyl 262 [b] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 263 [b] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

26 [b] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 36 fb]

Formula ( Ie ) , R ⁴ =R ^{2 7} =benzyl , R =pyridinylmethyl ,

R ⁷ =Table Ex . o .0 . 1 .2

265 fb] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 266 [b] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

267 [b] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 268 [b] m-trif luorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

269 fb] m-formaldoximebenzyl m-acetoximebenzyl benzyl 270 [b] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 271 fb] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

272 [b] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 37 [b]

Formula ( Ie ) , R ⁴ =R ² =benzyl , R ²² =m-acetylbenzyl ,

R ⁷ =Table Ex . No . 0 . 1 .2

273 [b] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 274 [b] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl ) aminobenzyl

275 [b] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 276 [b] m-trif luorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

277 [b] m-formaldoximebenzyl m-acetoximebenzyl benzyl 278 [b] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 279[b] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

280 [b] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 38 [b]

Formula (Ie), R ⁴ =R ²⁷ =benzyl, R ² =m-aminosulfonylbenzyl, R ⁷ =Table

Ex.No .0 .1 .2

281 [b] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

282 [b] m-(N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl 283 [b] m- (N-methylamino) m-(N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 284 [b] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl 285 [b] m-formaldoximebenzyl m-acetoximebenzyl benzyl 286[b] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 287 [b] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl 288 [b] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 39 [b]

Formula ( Ie ) , R ⁴ =R ²⁷ =benzyl , R ²² =m-methoxybenzyl ,

R ⁷ =Table Ex . No . 0 . 1 .2

289 [b] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 290 [b] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

291 [b] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 292 [b] m-trif luorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

293 [b] m-formaldoximebenzyl m-acetoximebenzyl benzyl 29 [b] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 295 [b] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

296 fb] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 3 [ c]

Formula ( I f ) , R ⁴ =R ²⁷ =benzyl , R ² =R ⁷ =Table Ex . No . 0 . 1 .2

1 [ c] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 2 [c] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl ) aminobenzyl

3 [ c ] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

4 [ c ] m-trifluorocarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

5[c] m-formaldoximebenzyl m-acetoximebenzyl benzyl 6[c] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl tc] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl 8[c] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table [c]

Formula ( If ) , R ⁴ =R ²⁷ =f luorobenzyl , R ²² =R ⁷ =Table Ex . No .0 .1 .2

9 f c ] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 10 [ c] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl ) aminobenzyl life] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 12 fc] m-trifluorocarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

13 [c] m-formaldoximebenzyl m-acetoximebenzyl benzyl

14 [c] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

15 [c] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

16 [c] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 5 [c ]

Formula ( I f ) , R ⁴ =R ⁷ =pyrrolylmethyl , R ²² =R ⁷ =Table

Ex . No .0 .1 .2

17 [c] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

18 fc] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl)aminobenzyl

19 [c] -(N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

20 [c] m-trifluorocarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

21 [c] m-formaldoximebenzyl m-acetoximebenzyl benzyl

-204-

SUBSTJTUTESHEET(RULE26)

22 [c] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

23 [c] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

24 [c] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 6[c]

Formula (If), R ⁴ =R ²⁷ =methoxybenzyl, R ² =R ⁷ =Table

Ex.No .0 .1 .2

25 [c] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

26 [c] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl)aminobenzyl

27 [c] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 28 [c] m-trifluorocarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

29 [c] m-formaldoximebenzyl m-acetoximebenzyl benzyl

30 [c] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

31 [c] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

32 [c] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 7 [c]

Formula ( I f ) , R ⁴ =R ²⁷ =isobutyl , R ²² =R ⁷ =Table

Ex.No .0 .1

33 [c] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

34 [c] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

35 [c] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

36 [c] m-trifluorocarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

37 [c] m-formaldoximebenzyl m-acetoximebenzyl benzyl

38 [c] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

39 fc] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

40 fc] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 8[c]

Formula (If), R ⁴ =R ⁷ =p-nitrobenzyl, R ²² =R ⁷ =Table

Ex.No .0 .1 .2

41 fc] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

42 [c] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl)aminobenzyl

43[c] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

44 [c] m-trifluorocarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

45fc] m-formaldoximebenzyl m-acetoximebenzyl benzyl

46 fc] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

47 [c] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

48 [c] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 9[c]

Formula (If), R ⁴ =R ²⁷ =m-aminobenzyl, R ²² =R ⁷ =Table

Ex.No .0 .1 .2

49 [c] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

50 [c] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl)aminobenzyl

51 [c] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

52 [c] m-trifluorocarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

53 fc] m-formaldoximebenzyl m-acetoximebenzyl benzyl

54 [c] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

55 [c] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

56 [c] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 10[c]

Formula (If), R ⁴ =R ⁷ =pyridinylmethyl, R ²² =R ⁷ =Table

Ex.No .0 .1 .2

57 [c] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

58 [c] m- (N, -dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

59 [c] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

60 [c] m-trif luorocarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

61 [c] m-formaldoximebenzyl m-acetoximebenzyl benzyl

62 [c] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

63 [c] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

64 [c] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table life]

Formula (If) , R ⁴ =R ²⁷ =m-hydroxybenzyl, R ²² =R ⁷ =Table

Ex.No .0 .1 .2

65 [c] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

66 fc] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

67 [c] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 68 [c] m-trifluorocarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

69 [c] m-formaldoximebenzyl m-acetoximebenzyl benzyl

70 [c] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

71 [c] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

72 [c] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 12 [c]

Formula (If) , R ⁴ =R ²⁷ =p-hydroxybenzyl, R ² =R ⁷ =Table

Ex.No .0 .1 .2

73 fc] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

74 [c] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

75 [c] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

76 [c] m-trifluorocarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

77 [c] m-formaldoximebenzyl m-acetoximebenzyl benzyl

78 [c] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

79 [c] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

80 fc] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 13fc]

Formula (If), R ⁴ =R ²⁷ =m-aminocarbonybenzyl, R ²² =R ⁷ =Table

Ex.No .0 .1 .2

81 [c] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

82 [c] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

83 [c] - (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

84 fc] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

85[c] m-formaldoximebenzyl m-acetoximebenzyl benzyl

86[c] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

87 [c] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

88 [c] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 1 [c]

Formula (If), R =R ²⁷ =p-hydroxymethylbenzyl, R ²² =R ⁷ =Table

Ex.No .0 .1 .2

89 [c] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

90 [c] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl)aminobenzyl

91 [c] m- (N-methylamino) m- (N-methylamino) m-f ormylbenzyl carbonylbenzyl benzyl

92 [c] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

93 [c] m-formaldoximebenzyl m-acetoximebenzyl benzyl

94 [c] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

95 [c] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

96 fc] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 15 [c]

-208-

SUBSOTTUTE SHEET (RULE 26)

Formula (If), R ⁴ =R ²⁷ =m-hydroxycarbonylbenzyl, R ²² =R ⁷ =Table Ex.No .0 .1 .2

97 fc] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

98 [c] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl)aminobenzyl

99[c] m-(N-methylamino) m-(N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 100[c] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

101 [c] m-formaldoximebenzyl m-acetoximebenzyl benzyl 102[c] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 103 [c] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

104 [c] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 16 [c]

Formula ( I f ) , R =R ²⁷ =benzyl , R ²² =m-hydroxymethylbenzyl ,

R ⁷ =Table Ex . No . 0 . 1 .2

105 [c] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 106 f c] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

107 [c] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 108 [c] m-trif luorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

109fc] m-formaldoximebenzyl m-racetoximebenzyl benzyl 110 [c] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl lllfc] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

112 [c] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 17 [c]

Formula ( I f ) , R ⁴ =R ^{2 7} =benzyl , R ²² =p-hydroxymethylbenzyl ,

R ⁷ =Table Ex . No . 0 . 1 .2

113 [c] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

-209-

SUBSCTTUTE SHEET (RULE 26)

11 fc] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

115 [c] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 116 [c] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

117 [c] m-formaldoximebenzyl m-acetoximebenzyl benzyl

118 [c] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 119 [c] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

120 [c] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 18 [c]

Formula ( I f ) , R =R ^{2 7} =benzyl , R ² =m-hydroxybenzyl ,

R ⁷ =Table Ex . No . 0 . 1 .2

121 [c ] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 122 [c] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl ) aminobenzyl

123 fc] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

124 [c] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

125 [c] m-formaldoximebenzyl m-acetoximebenzyl benzyl

126 [c] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

127 [c] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

128 [c] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 1 9 [ c]

Formula ( I f ) , R ⁴ =R ^{2 7} =benzyl , R ²² =m- (N, N-dimethylamino glycyl ) aminobenzyl , R ⁷ =Table Ex . No . 0 . 1 .2

129 [c] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 130 [c] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl ) aminobenzyl

-210-

SUBSTJTUTE SHEET (RULE 26)

131 fc] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

132 [c] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

133 [c] m-formaldoximebenzyl m-acetoximebenzyl benzyl 134 fc] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 135 [c] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

136fc] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 20[c]

Formula (If) , R =R ²⁷ =benzyl, R ²² =m-aminocarbonylbenzyl,

R ⁷ =Table Ex.No .0 .1 .2

137 [c] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

138 [c] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

139 [c] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 140 [c] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

141 [c] m-formaldoximebenzyl m-acetoximebenzyl benzyl 14 [c] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 143 [c] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

144 [c] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 21 [c]

Formula ( I f ) , R ⁴ =R ²⁷ =benzyl , R ²² =p-hydroxybenzyl ,

R ⁷ =Table Ex . No . 0 . 1 .2

145 [c] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 146 [c] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl ) aminobenzyl 147 [c] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

148 [c] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

149 [c] m-formaldoximebenzyl m-acetoximebenzyl benzyl

150 [c] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

151 [c] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl 152 fc] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 22 fc]

Formula ( If ) , R ⁴ =R ^{2 7} =benzyl , R ²² =m- (N-methylaminocarbonyl benzyl , R ⁷ =Table Ex . NO . 0 . 1 .2

153 [ c ] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 154 [c] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

155 [c] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 156 [ c] m-trif luorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

157 [c] m-formaldoximebenzyl m-acetoximebenzyl benzyl 158 [c] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 159 [c] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

160 [c] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 23[c]

Formula (If), R ⁴ =R ²⁷ =benzyl, R ² =m- (N-methylamino)benzyl, R ⁷ =Table

Ex.No .0 .1 .2

161 [c] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

162 [c] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

163 [c] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

164 [c] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

165 [c] m-formaldoximebenzyl m-acetoximebenzyl benzyl

166 [c] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

167 [c] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

168 [c] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 2 [c]

Formula (If), R ⁴ =R ²⁷ =benzyl, R ²² =m-formyllbenzyl,

R ⁷ =Table Ex.No .0 .1 .2

169 [c] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

170 [c] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

171 [c] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

172 [c] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

173 [c] m-formaldoximebenzyl m-acetoximebenzyl benzyl

174 [c] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 175 [c] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

176 [c] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 25 [c]

Formula (If), R ⁴ =R ²⁷ =benzyl, R ² =m-trifluorocarbonylbenzyl,

R ⁷ =Table Ex.No .0 .1 .2

177 [c] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

178 [c] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl)aminobenzyl

179 [c] m-(N-methylamino) m-(N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 180 [c] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

181 fc] m-formaldoximebenzyl m-acetoximebenzyl benzyl 182 [c] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 183 [c] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

184 [c] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 26 [c]

Formula (If) , R ⁴ =R ²⁷ =benzyl, R ²² =m-hydroxyamidinobenzyl, R ⁷ =Table

Ex.No .0 .1 .2

185 [c] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

186[c] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl)aminobenzyl

187 [c] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 188 fc] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

189 [c] m-formaldoximebenzyl m-acetoximebenzyl benzyl 190 [c] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 191 [c] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

192 fc] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 27 [c]

Formula ( If ) , R ⁴ =R ²⁷ =benzyl , R ²² =m-triazolylbenzyl ,

R ⁷ =Table Ex . No . 0 . 1 .2

193 [c] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 19 [c] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl ) aminobenzyl

195 [ c] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 196 [c] m-trif luorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

197 [c] m-formaldoximebenzyl m-acetoximebenzyl benzyl 198 [c] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 199[c] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

200 [c] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 28[c]

Formula (If), R ⁴ =R ²⁷ =benzyl, R ²² =m-formaldoximebenzyl, R ⁷ =Table

-214-

SUBSCTTUTE SHEET (RULE 26)

Ex . o . 0 .1 .2

201 fc] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

202 [c] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl)aminobenzyl 203[c] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 204 [c] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

205 [c] m-formaldoximebenzyl m-acetoximebenzyl benzyl

206 [c hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

207 [c] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl 208 [c] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 29 [c]

Formula (If), R ⁴ =R ⁷ =benzyl, R ²² =m-acetoximebenzyl,

R ⁷ =Table Ex.No .0 .1 .2

209 [c] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

210 [c] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

211 [c] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 212 [c] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

213 [c] m-formaldoximebenzyl m-acetoximebenzyl benzyl 214 [c] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 215 [c] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

216 [c] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 30 [c]

Formula ( If ) , R ⁴ =R ²⁷ =benzyl , R ²² =benzyl , R ⁷ =Table Ex . No . 0 . 1 .2

217 [c] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 218 [c] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

219fc] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

220 [c] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

221 [c] m-formaldoximebenzyl m-acetoximebenzyl benzyl 222[c] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazclylbenzyl ■223[c] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

224fc] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 31 [c]

Formula ( I f ) , R ⁴ =R ²⁷ =benzyl , R ²² =m-hydroxycarbonylbenzyl ,

R ⁷ =Table Ex . No . 0 . 1 .2

225 [ c] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 226 f c] - (N, -dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

227 [c] m-(N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

228 [c] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

229 [c] m-formaldoximebenzyl m-acetoximebenzyl benzyl 230 [c] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 231 fc] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

232 [c] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 32 fc]

Formula (If) , R ⁴ =R ⁷ =benzyl, R ²² =m-tetrazolylbenzyl,

R ⁷ =Table Ex.No .0 .1 .2

233 [c] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

234 [c] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl)aminobenzyl 235 [c] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

236 [c] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

237 [c] m-formaldoximebenzyl m-acetoximebenzyl benzyl

238 [c] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

239 [c] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

240 [c] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 33 fc]

Formula ( I f ) , R =R ² =benzyl , R ²² =m-pyrazolylbenzyl , R ⁷ =Table

Ex . No . 0 . 1 .2

241 [c] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

242 [c] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

243 [c] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 244 [c] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

245 [c] m-formaldoximebenzyl m-acetoximebenzyl benzyl 246 [c] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 247 [c] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

248 [c] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 34 [c]

Formula (If), R ⁴ =R ²⁷ =benzyl, R ² =m-imidazolylbenzyl,

R ⁷ =Table Ex.No .0 .1 .2

249 fc] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

250 [c] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl)aminobenzyl

251 [c] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

252 [c] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

253 [c] m-formaldoximebenzyl m-acetoximebenzyl benzyl

254 [c] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 255[c] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl 256[c] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 35 fc]

Formula ( I f ) , R ⁴ =R ²⁷ =benzyl , R ²² =p-f luorobenzyl ,

R ⁷ =Table Ex . No .0 . 1 .2

257 f c] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 258 [c] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

259 [c] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 260 [c] m-t rifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

261[c] m-formaldoximebenzyl m-acetoximebenzyl benzyl 262 fc] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 263[c] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

264 [c] m-acetylbenzyl -aminosulfonylbenzyl m-methoxybenzyl

Table 36 [c]

Formula ( I f ) , R =R ^{2 7} =benzyl , R ²² =pyridinylmethyl ,

R ⁷ =Table Ex . No . 0 . 1 .2

265 f c] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 266 f c] - (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl ) aminobenzyl

267 f c] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 268 [c] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

269 [c] m-formaldoximebenzyl m-acetoximebenzyl benzyl 270[c] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 271 fc] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

272 [c] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 37 f c]

Formula ( I f ) , R ⁴ =R ²⁷ =benzyl , R ² =m-acetylbenzyl ,

R ⁷ =Table Ex . No .0 . 1 .2

273 [c] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 274 [c] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

275 [c] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 276 [c] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

277 [c] m-formaldoximebenzyl m-acetoximebenzyl benzyl 278[c] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 279fc] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

280 [c] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 38 [c]

Formula ( If) , R ⁴ =R ⁷ =benzyl, R ² =m-aminosulfonylbenzyl,

R ⁷ =Table Ex . No . 0 . 1 .2

281 [c] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 282 f c ] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

283 [c] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 284 [ c] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

285[c] m-formaldoximebenzyl m-acetoximebenzyl benzyl 286[c] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 287 [c] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

288 [c] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 39 [c]

Formula (If), R ⁴ =R ² =benzyl, R ² =m-methoxybenzyl, R ⁷ =Table

Ex . No . 0 .1 .2

289 [c] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 290 [c] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl ) aminobenzyl

291[c] m-(N-methylamino) m-(N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

292 [c] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl 293 fc] m-formaldoximebenzyl m-acetoximebenzyl benzyl 294[c] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 295fc] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl 296 [c] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 3 [d]

Formula ( I l ia ) , R ⁴ =R ²³ =benzyl , R ²² =R ⁷ =Table

Ex . No . 0 . 1 l f d] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

2 [d] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

3 [d] m- (N-methylamino) m- (N-methylamino) m-f ormylbenzyl carbonylbenzyl benzyl

4 [d] m-trifluorocarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

5 (d] m-formaldoximebenzyl m-acetoximebenzyl benzyl 6 [d] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 7 [d] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl 8 [d] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 4 [d]

Formula (Ilia), R ⁴ =R ²³ =fluorobenzyl, R ²² =R ⁷ =Table

Ex. o .0 .1 .2

9 [d] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

10fd] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl)aminobenzyl

11 [d] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

12 fd] m-trifluorocarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

13 [d] m-formaldoximebenzyl m-acetoximebenzyl benzyl 14 fd] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 15 [d] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

16 [d] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 5[d]

Formula (Ilia), R ⁴ =R ²³ =pyrrolylmethyl, R ²² =R ⁷ =Table

Ex.No .0 .1 .2

17 [d] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

18 [d] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

19 [d] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

20 [d] m-trifluorocarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

21 [d] m-formaldoximebenzyl m-acetoximebenzyl benzyl

22 [d] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

23 [d] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

24 [d] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 6 [ d ]

Formula ( I l ia ) , R ⁴ =R ³ =methoxybenzyl , R =R ⁷ =Table Ex . No . 0 . 1 .2

25 [d] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 26 [d] m- (N, -dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

27 [d] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

28 [d] m-trifluorocarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

29 [d] m-formaldoximebenzyl m-acetoximebenzyl benzyl

-221-

SUBSCTTUTE SHEET (RULE 26)

30 [d] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

31 [d] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

32 [d] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 7 fd]

Formula ( I l ia ) , R ⁴ =R ²³ =isobutyl , R ²² =R ⁷ =Table

Ex . No . 0 . 1 .2

33fd] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

34 [d] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

35[d] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 36 fd] m-trifluorocarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

37 [d] m-formaldoximebenzyl m-acetoximebenzyl benzyl

38 [d] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

39 [d] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

40 [d] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 8 [d]

Formula ( I l ia ) , R ⁴ =R ²³ =p- ^■ nit robenzyl , R ² =R ⁷ =Table

Ex . No . 0 . 1 .2

41 [d] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

42 [d] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl 43 fd] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 44 fd] m-trifluorocarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

45 [d] m-formaldoximebenzyl m-acetoximebenzyl benzyl

46 [d] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

47 [d] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

48 [d] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 9[d]

-222-

SUBSCTTUTE SHEET (RULE 26)

Formula ( I l ia ) , R ⁴ =R ^{2 3} =m -aminobenzyl , R ²² =R ⁷ =Table Ex . No . 0 . 1 . 2

49 [d] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 50 fd] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl ) aminobenzyl

51 [d] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

52 [d] m-trifluorocarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

53 [d] m-formaldoximebenzyl m-acetoximebenzyl benzyl

54 [d] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

55 [d] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl 56 [d] m-acetylbenzyl -aminosulfonylbenzyl m-methoxybenzyl

Table 10 [ d]

Formula ( I l i a ) , R ⁴ =R ^{2 3} =pyridinylmethyl , R ^{2 2} =R ⁷ =Table

Ex . No . 0 . 1 .2

57 [d] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

58 [d] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

59 [d] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

60 [d] m-trifluorocarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

61 [d] m-formaldoximebenzyl m-acetoximebenzyl benzyl

62 [d] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

63 [d] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

64 [d] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 11 fd]

Formula (Ilia), R ⁴ =R ²³ =m-hydroxybenzyl, R ²² =R ⁷ =Table

Ex.No .0 .1 .2

65 [d] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

66 [d] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

67 [d] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

68 fd] m-trifluorocarbonyl m-hydroxyamidino m-triazolylbenzy benzyl benzyl

69 fd] m-formaldoximebenzyl m-acetoximebenzyl benzyl

70 [d] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzy

71 [d] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

72 [d] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 12 [d]

Formula ( I l ia ) , R ⁴ =R ²³ =p- ^• hydroxybenzyl , R ²² =R ⁷ =Table

Ex . No . 0 .1

73 [d] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

74 [d] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl 75 fd] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 76 fd] m-trifluorocarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

77 [d] m-formaldoximebenzyl m-acetoximebenzyl benzyl

78 [d] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

79 [d] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl 80 [d] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 13 [d]

Formula (Ilia) , R ⁴ =R ²³ =m-aminocarbonybenzyl, R ²² =R ⁷ =Table

Ex.No .0 .1 .2

81 [d] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

82 [d] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

83 [d] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

84 [d] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

85 [d] m-formaldoximebenzyl m-acetoximebenzyl benzyl

86 [d] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

87 fd] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

88 [d] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 14 f d]

Formula ( I lia) , R =R ²³ =p- •hydroxymethylbenzyl , R ² =R =Table

Ex. No .0 .1 .2

89 fd] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

90 [d] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

91 [d] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

92 [d] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

93 fd] m-formaldoximebenzyl m-acetoximebenzyl benzyl

94 fd] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

95 [d] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

96 [d] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 15 [d]

Formula (Ilia), R ⁴ =R ²³ =m-hydroxycarbonylbenzyl,

R ²² =R ⁷ =Table

Ex.No .1 .2 97[d] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 98 [d] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl 99 [d] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 100 [d] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl 101 [d] m-formaldoximebenzyl m-acetoximebenzyl benzyl 102 [d] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 103 fd] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl 104 [d] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 16[d]

Formula (Ilia), R ⁴ =R ²³ =benzyl, R ²² =m-hydroxymethylbenzyl,

R ⁷ =Table Ex. o .0 .1 .2

105 [d] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 106 fd] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

107 [d] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 108 [d] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

109 fd] m-formaldoximebenzyl m-acetoximebenzyl benzyl 110 [d] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 111 fd] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

112 [d] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 17 [d]

Formula (Ilia), R ⁴ =R ²³ =benzyl, R ² =p-hydroxymethylbenzyl, R ⁷ =Table

Ex. No .0 .1 .2

113 [d] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 11 [d] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

115 [d] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 116 [d] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

117 [d] m-formaldoximebenzyl m-acetoximebenzyl benzyl 118 [d] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 119 fd] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

120 [d] m-acetylbenzyl m-aminosul onylbenzyl m-methoxybenzyl

Table 18 [d] Formula (Ilia), R ⁴ =R ²³ =benzyl, R ²² =m-hydroxybenzyl, R ⁷ =Table Ex. No .0 .1 .2

121 [d] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 122 [d] m-(N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl 123 [d] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 124 [d] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl 125 fd] m-formaldoximebenzyl m-acetoximebenzyl benzyl 126 [d] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 127 [d] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl 128 [d] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 1 9 [d]

Formula ( I l ia ) , R ⁴ =R ²³ =benzyl , R ^{2 2} =m- (N, N-dimethylamino glycyl ) aminobenzyl , R ⁷ =Table Ex . No . 0 . 1 .2

129 fd] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 130 [d] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

131 [d] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 132 [d] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

133 [d] m-formaldoximebenzyl m-acetoximebenzyl benzyl 134 [d] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 135 [d] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

136 [d] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 20 [d]

Formula ( I l ia ) , R ⁴ =R ² =benzyl , R ²² =m-aminocarbonylbenzyl ,

R ⁷ =Table Ex . No . 0 . 1 .2

137 [d] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 138 [d] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl ) aminobenzyl

139fd] m-(N-methylamino) m-(N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

140fd] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

141 fd] m-formaldoximebenzyl m-acetoximebenzyl benzyl 142 [d] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 143 [d] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

144 [d] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 21 fd]

Formula ( I l ia ) , R ⁴ =R ^{2 3} =benzyl , R ²² =ρ-hydroxybenzyl ,

R ⁷ =Table Ex . No . 0 . 1 .2

145 [d] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 146 [d] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl ) aminobenzyl

147 [d] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 148 [d] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

149 [d] m-formaldoximebenzyl m-acetoximebenzyl benzyl 150[d] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 151 [d] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

152 [d] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 22 [d]

Formula ( I l ia ) , R ⁴ =R ²³ =benzyl , R ²² =m- (N-methylaminocarbonyl benzyl , R ⁷ =Table Ex . No . 0 . 1 .2

153 [d] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 154 f d] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl ) aminobenzyl 155 [d] m- (N-methylamino) m- (N-methylamino) m-f ormylbenzyl carbonylbenzyl benzyl

156 [d] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

157 [d] m-formaldoximebenzyl m-acetoximebenzyl benzyl

158 [d] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

159 fd] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

160 fd] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 23 [d]

Formula ( I lia) , R ⁴ =R =benzyl, R ²² =m- (N-methylamino) benzyl ,

R ⁷ =Table Ex . No .0 .1 .2

161 [d] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 162 [d] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

163 [d] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 16 [d] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

165 fd] m-formaldoximebenzyl m-acetoximebenzyl benzyl 166 [d] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 167 [d] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

168 [d] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 24 [d]

Formula (Ilia), R ⁴ =R ²³ =benzyl, R ² =m-formyllbenzyl,

R ⁷ =Table Ex.No .0 .1 .2

169 [d] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

170 [d] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl)aminobenzyl

171 [d] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

172 [d] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

173 [d] m-formaldoximebenzyl m-acetoximebenzyl benzyl

174 [d] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

175 [d] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

176 [d] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 25 [d]

Formula ( I l ia ) , R ⁴ =R ²³ =benzyl , R ²² =m- trif luorocarbonylbenzyl , R ⁷ =Table

Ex . o . 0 . 1 .2

177 [d] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

178 [d] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl)aminobenzyl

179 [d] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 180 [d] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

181 [d] m-formaldoximebenzyl m-acetoximebenzyl benzyl 182 [d] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 183 [d] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

184 fd] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 2 6 [d]

Formula ( I l ia ) , R =R ^{2 3} =benzyl , R ² =m-hydroxyamidinobenzyl ,

R ⁷ =Table Ex . No . 0 . 1 .2

185 [d] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 186 [d] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

187 [d] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 188 [d] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

189 [d] m-formaldoximebenzyl m-acetoximebenzyl benzyl 190 [d] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 191 [d] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

192 [d] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

-230-

SUBSTJTUTESHEET(RULE26)

Table 27 [d]

Formula ( I lia) , R ⁴ =R ²³ =benzyl , R ²² =m-triazolylbenzyl ,

R ⁷ =Table Ex. o .0 .1 .2

193 fd] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 194 [d] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl ) aminobenzyl

195 [d] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 196 [d] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

197 fd] m-formaldoximebenzyl m-acetoximebenzyl benzyl 198 [d] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 199 [d] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

200 [d] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 28 [d]

Formula ( Ilia) , R ⁴ =R ²³ =benzyl, R ² =m-formaldoximebenzyl,

R ⁷ =Table Ex . o . 0 . 1 .2

201 [d] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 202 [d] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

203 [d] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 204 [d] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

205 [d] m-formaldoximebenzyl m-acetoximebenzyl benzyl 206 [d] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 207 fd] m-imidazolylbenzyJ p-fluorobenzyl pyridinylmethyl

208 [d] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 29 [d]

Formula ( I l ia ) , R ⁴ =R ² =benzyl , R ²² =m-acetoximebenzyl , R ⁷ =Table

Ex . No . 0 .1 .2

209 [d] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

210 fd] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl)aminobenzyl 211 [d] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 212 [d] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl 213[d] m-formaldoximebenzyl m-acetoximebenzyl benzyl 214 [d] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 215[d] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl 216[d] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 30 [d]

Formula ( I l ia ) , R ⁴ =R ²³ =benzyl , R ² =benzyl , R ⁷ =Table

Ex . No . 0 . 1 .2

217 [d] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

218 [d] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

219 [d] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 220 [d] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

221 fd] m-formaldoximebenzyl m-acetoximebenzyl benzyl 222 [d] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 223 [d] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

224 [d] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 31 [d]

Formula ( I l ia ) , R ⁴ =R ³ =benzyl , R ²² =m-hydroxycarbonylbenzyl ,

R ⁷ =Table Ex . No . 0 . 1 .2

225 [d] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 226 [d] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

227[d] m- (N-methylamino) m-(N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

228 [d] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

229fd] m-formaldoximebenzyl m-acetoximebenzyl benzyl 230[d] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 231 [d] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

232fd] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 32 fd]

Formula ( I lia) , R ⁴ =R ²³ =benzyl , R ² =m-tetrazolylbenzyl,

R ⁷ =Table Ex . No . 0 . 1 .2

233 [d] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 23 [d] m- (N, -dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

235 [d] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 236 [d] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

237 [d] m-formaldoximebenzyl m-acetoximebenzyl benzyl 238 fd] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 239 [d] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

240 [d] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 33 [d]

Formula ( I lia ) , R ⁴ =R =benzyl , R ²² =m-pyrazolylbenzyl ,

R ⁷ =Table Ex . No .0 .1 .2

241 fd] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 242 [d] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl ) aminobenzyl 243 [d] m- (N-methylamino) m- (N-methylamino) m-f ormylbenzyl carbonylbenzyl benzyl

24 [d] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

245[d] m-formaldoximebenzyl m-acetoximebenzyl benzyl

246 [d] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

24 [d] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

248 fd] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 34 [d]

Formula ( I lia) , R =R ² =benzyl, R ²² =m-imidazolylbenzyl ,

R ⁷ =Table Ex . No .0 . 1 .2

249 [d] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 250 [d] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

251 [d] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 252 [d] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

253 fd] m-formaldoximebenzyl m-acetoximebenzyl benzyl 25 [d] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 255 [d] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

256 [d] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 35 fd]

Formula (Ilia), R ⁴ =R ² =benzyl, R ² =p-fluorobenzyl,

R ⁷ =Table Ex.No .0 .1 .2

257 fd] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

258 [d] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

259 [d] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

260 [d] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

261 [d] m-formaldoximebenzyl m-acetoximebenzyl benzyl

262 [d] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 263 [d] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl 264 [d] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 36 [d]

Formula ( Ilia) , R ⁴ =R ³ =benzyl, R ²² =pyridinylmethyl, R ⁷ =Table

Ex . No . 0 . 1 .2

265 [d] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

266 [d] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

267 [d] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 268 [d] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

269 [d] m-formaldoximebenzyl m-acetoximebenzyl benzyl 270 [d] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 271 [d] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

272 [d] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 37 [d]

Formula ( I l ia ) , R ⁴ =R ²³ =benzyl , R ²² =m-acetylbenzyl ,

R ⁷ =Table Ex . o . 0 . 1 .2

273 [d] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 274 [d] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl ) aminobenzyl

275 [d] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 276 [d] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

277 fd] m-formaldoximebenzyl m-acetoximebenzyl benzyl 278 [d] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 279 [d] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

280 [d] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

-235-

SUBSCTTUTE SHEET (RULE 26)

Table 38[d]

Formula (Ilia) , R ⁴ =R =benzyl, R ² =m-aminosulfonylbenzyl, R ⁷ =Table

Ex.No .0 .1 .2

281 fd] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

282 [d] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl)aminobenzyl

283 fd] m- (N-methylamino) m-(N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 284 [d] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

285 [d] m-formaldoximebenzyl m-acetoximebenzyl benzyl 286 [d] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 287 [d] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

288 [d] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 39 [d]

Formula ( I l ia ) , R ⁴ =R ²³ =benzyl , R ² =m-methoxybenzyl , R ⁷ =Table

Ex . No . 0 . 1 .2

289 [d] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 290 [d] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl ) aminobenzyl

291 [d] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 292 fd] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

293 [d] m-formaldoximebenzyl m-acetoximebenzyl benzyl 29 fd] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 295 fd] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

296 [d] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 3[e]

Formula (IVa) , R =R ²³ =benzyl, R ² =R ⁷ =Table Ex.No .0 .1

1 [e] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 2[e] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl)aminobenzyl 3[e] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 4[e] m-trifluorocarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl 5 [e] m-formaldoximebenzyl m-acetoximebenzyl benzyl 6[e] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

7 [e] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

8 [e] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table [e]

Formula (IVa), R ⁴ =R ²³ =fluorobenzyl, R ²² =R ⁷ =Table

Ex.No .0 .1 .2

9 [e] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

10 [e] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl)aminobenzyl life] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 12 [e] m-trifluorocarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

13 [e] m-formaldoximebenzyl m-acetoximebenzyl benzyl

14 [e] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

15 [e] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

16 [e] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 5[e]

Formula (IVa), R ⁴ =R ²³ =pyrrolylmethyl, R ²² =R ⁷ =Table

Ex.No .0 .1 .2

17 [e] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

18 [e] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl)aminobenzyl

19 [e] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

20 [e] m-trifluorocarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

21 [e] m-formaldoximebenzyl m-acetoximebenzyl benzyl

22 [e] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

23 [e] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

24 [e] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 6[e]

Formula (IVa), R ⁴ =R ²³ =methoxybenzyl, R ² =R ⁷ =Table

Ex.No .0 .1 .2

25[e] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

26 [e] m-(N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl 2 [e] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 28 [e] m-trifluorocarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

29 [e] m-formaldoximebenzyl m-acetoximebenzyl benzyl

30 [e] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

31 [e] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

32 [e ] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 7 [e]

Formula ( IVa ) , R ⁴ =R ²³ =isobutyl , R ²² =R ⁷ =Table

Ex . No . 0 . 1 .2

33 [e] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

34 [e] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

35 [e] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

36 [e] m-trifluorocarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

37 [e] m-formaldoximebenzyl m-acetoximebenzyl benzyl

38 [e] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

39 [e] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

40 [e] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 8 [e]

Formula ( IVa ) , R ⁴ =R ²³ =p-nitrobenzyl , R =R ⁷ =Table

Ex . No . 0 .1 .2

41 [e] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

42 [e] m- (N, -dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl)aminobenzyl

43 [e] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

44 [e] m-trifluorocarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

45 [e] m-formaldoximebenzyl m-acetoximebenzyl benzyl

46 [e] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

47 [e] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

48 [e] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 9[e]

Formula (IVa), R ⁴ =R ²³ =m-aminobenzyl, R ²² =R ⁷ =Table

Ex.No .0 .1 .2

49 [e] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

50 [e] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

51 [e] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

52 [e] m-trifluorocarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

53 [e] m-formaldoximebenzyl m-acetoximebenzyl benzyl

54 [e] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

55 [e] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

56 [e] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 10 [e]

Formula (IVa), R ⁴ =R ²³ =pyridinylmethyl, R ²² =R ⁷ =Table

Ex.No .0 .1 .2

57 [e] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 58 [e] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

59 [e] m- (N-methylamino) m-(N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

60 [e] m-trifluorocarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl 61 fe] m-formaldoximebenzyl m-acetoximebenzyl benzyl 62 [e] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 63 [e] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl 64 [e] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table life]

Formula (IVa), R ⁴ =R ²³ =m-hydroxybenzyl, R ²² =R ⁷ =Table

Ex.No .0 .1 .2

65 [e] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

66 [e] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl)aminobenzyl 67 [e] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 68 [e] m-trifluorocarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl 69 [e] m-formaldoximebenzyl m-acetoximebenzyl benzyl 70 fe] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 71 [e] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl 72 fe] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 12 fe]

Formula (IVa), R ⁴ =R ²³ =p-hydroxybenzyl, R ²² =R ⁷ =Table

Ex.No .0 .1 .2

73 [e] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

74 fe] m-(N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl)aminobenzyl 75 [e] m-(N-methylamino) m-(N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

76 [e] m-trifluorocarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

77 [e] m-formaldoximebenzyl m-acetoximebenzyl benzyl

78 [e] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

79 fe] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

80 [e] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 13 [e]

Formula (IVa) , R =R ²³ =m- aminocarbonybenzyl , R ²² =R ⁷ =Table

Ex.No .0 . 1 .2

81 [e] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

82 [e] m-(N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl)aminobenzyl

83 [e] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

84 [e] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

85 [e] m-formaldoximebenzyl m-acetoximebenzyl benzyl

86 [e] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 87 [e] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl 88 [e] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 14 [e ]

Formula ( IVa ) , R ⁴ =R ² =p-hydroxymethylbenzyl, R ²² =R ⁷ =Table

Ex .No . 0 .1 .2

89 [e] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

90 [e] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl 91 [e] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 92 [e] m-trif luorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

93 [e] m-formaldoximebenzyl m-acetoximebenzyl benzyl

94 [e] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

95 [e] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

96 [e] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 15 fe]

Formula (IVa), R ⁴ =R ² =m-hydroxycarbonylbenzyl, R ²² =R ⁷ =Table

Ex.No .0 .1 .2 97[e] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 98 fe] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl)aminobenzyl

99[e] mm-- ((NN--mmeetthhyyllaammiinnoo)) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

100 [e] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

101 [e] m-formaldoximebenzyl m-acetoximebenzyl benzyl

102 [e] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

103 [e] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

10 [e] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 1 6 [e]

Formula ( IVa ) , R ⁴ =R ³ =benzyl , R ² =m-hydroxymethylbenzyl ,

R ⁷ =Table Ex . No . 0 . 1 .2

105 [e] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 106 [e] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl ) aminobenzyl

107 [e] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 108 [e] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl 109 [e] m-formaldoximebenzyl m-acetoximebenzyl benzyl

110 [e] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

111 [e] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

112 [e] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 17 fe]

Formula ( IVa) , R ⁴ =R ²³ =benzyl , R ²² =p-hydroxymethylbenzyl ,

R ⁷ =Table Ex . No .0 .1 .2

113 fe] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 114 [e] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

115 [e] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 116 fe] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

117 [e] m-formaldoximebenzyl m-acetoximebenzyl benzyl 118 [e] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 119 [e] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

120 [e] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 18 [e]

Formula ( IVa ) , R ⁴ =R ² =benzyl , R ²² =m-hydroxybenzyl ,

R ⁷ =Table Ex . No . 0 .1 .2

121 [e] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 122 [e] m- (N, -dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl ) aminobenzyl

123 [e] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 124 [e] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

125 [e] m-formaldoximebenzyl m-acetoximebenzyl benzyl 126 [e] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 127 [e] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

128 [e] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 19 fe]

Formula (IVa), R ⁴ =R ²³ =benzyl, R ²² =m- (N,N-dimethylamino glycyl)aminobenzyl, R ⁷ =Table Ex.No .0 .1 .2

-243-

SUBSCTTUTE SHEET (RULE 26)

129 [e] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

130 [e] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl ) aminobenzyl

131 [e] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 132 [e] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl 133 [e] m-formaldoximebenzyl m-acetoximebenzyl benzyl 134 [e] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 135 [e] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl 136 fe] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 20 [e ]

Formula ( IVa ) , R ⁴ =R ² =benzyl , R ² =m-aminocarbonylben zyl ,

R ⁷ =Table Ex . No . 0 . 1 .2

137 [e ] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 138 [e] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

139 [e] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

140 [e] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

141 [e] m-formaldoximebenzyl m-acetoximebenzyl benzyl

142 [e] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 143 [e] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

144 [e] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 21 [e]

Formula ( IVa ) , R ⁴ =R ^{2 3} =benzyl , R ²² =p-hydroxybenzyl ,

R =Table Ex . No . 0 . 1 .2

145 [e] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 146 [e] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

-244 -

SUBSCTTUTE SHEET (RULE 26)

147 [e] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

148 [e] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

149 [e] m-formaldoximebenzyl m-acetoximebenzyl benzyl

150 [e] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

151 [e] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

152 [e] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 22 [e]

Formula ( IVa ) , R ⁴ =R ² =benzyl , R ²² =m- (N-methylaminocarbonyl benzyl , R ⁷ =Table Ex . No . 0 . 1 .2

153 [e] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 15 [e] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

155 [e] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 156 [e] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

157 [e] m-formaldoximebenzyl m-acetoximebenzyl benzyl 158 [e] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 159 [e] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

160 [e] m-acetylbenzyl -aminosulfonylbenzyl m-methoxybenzyl

Table 23 [e]

Formula ( IVa) , R ⁴ =R ² =benzyl , R =m- (N-methylamino) benzyl ,

R ⁷ =Table Ex . No . 0 . 1 .2

161 [e] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 162 [e] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl ) aminobenzyl 163 [e] m- (N-methylamino) m- (N-methylamino) m-f ormylbenzyl carbonylbenzyl benzyl

164 [e] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

165 fe] m-formaldoximebenzyl m-acetoximebenzyl benzyl

166 [e] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

167 [e] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

168 [e] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 2 [e]

Formula (IVa), R ⁴ =R ² =benzyl, R ²² =m-formyllbenzyl, R =Table

Ex.No .0 .1 .2

169 [e] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

170 [e] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

171 fe] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

172 [e] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

173 [e] m-formaldoximebenzyl m-acetoximebenzyl benzyl

174 [e] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 175 [e] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

176 [e] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 25 [ e ]

Formula ( IVa ) , R ⁴ =R ²³ =benzyl , R ²² =m-t ri f luorocarbonyl benzyl , R =Table Ex . No . 0 . 1 .2

177 [e] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 178 [e] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl ) aminobenzyl

179 f e] m- (N-methylamino) m- (N-methylamino) m- formylbenzyl carbonylbenzyl benzyl

180 f e] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

181 [e] m-formaldoximebenzyl m-acetoximebenzyl benzyl

182 [e] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

183 fe] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

184 [e] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 26 fe]

Formula ( IVa) , R ⁴ =R ² =benzyl, R ² =m-hydroxyamidinobenzyl,

R ⁷ =Table Ex. o .0 .1 .2

185 [e] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 186 fe] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl ) aminobenzyl

187 [e] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 188 [e] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

189 [e] m-formaldoximebenzyl m-acetoximebenzyl benzyl 190 [e] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 191 fe] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

192 [e] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 27 [e ]

Formula ( IVa ) , R =R ²³ =benzyl , R ² =m-triazolylbenzyl ,

R ⁷ =Table Ex . No . 0 . 1 .2

193 fe] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 194 [e] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl ) aminobenzyl

195 [e] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 196 [e] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

197 [e] m-formaldoximebenzyl m-acetoximebenzyl benzyl

198 [e] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 199fe] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

200 [e] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 28 fe]

Formula (IVa) , R ⁴ =R ²³ =benzyl, R =m-formaldoximebenzyl,

R ⁷ =Table Ex. o .0 .1 .2

201 [e] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 202 [e] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

203 fe] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 20 fe] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

205 [e] m-formaldoximebenzyl m-acetoximebenzyl benzyl 206 [e] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 207 [e] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

208 [e] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 29[e]

Formula (IVa), R ⁴ =R ³ =benzyl, R ²² =m-acetoximebenzyl,

R ⁷ =Table Ex. No .0 .1 .2

209 [e] m-hydroxymethylbenzyl p-nydroxymethylbenzyl m-hydroxybenzyl 210 fe] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

211 [e] m-(N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 212 fe] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl 213 [e] m-formaldoximebenzyl m-acetoximebenzyl benzyl

214 [e] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

215[e] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

216 [e] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 30[e]

Formula (IVa), R ⁴ =R ²³ =benzyl, R ² =benzyl, R ⁷ =Table Ex. No .0 .1 .2

217[e] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

218 [e] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl)aminobenzyl

219[e] m-(N-methylamino) m-(N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 220[e] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl 221 [e] m-formaldoximebenzyl m-acetoximebenzyl benzyl

222 [e] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

223[e] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

224 [e] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 31 [e]

Formula ( IVa ) , R ⁴ =R ²³ =benzyl , R ²² =m-hydroxycarbonylbenzyl ,

R ⁷ =Table Ex . No . 0 .1 .2

225 [e] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 226 [e] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

227 [e] m-(N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 228 [e] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl 229 [e] m-formaldoximebenzyl m-acetoximebenzyl benzyl

230 [e] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

231 [e] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

232 [e] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 32 fe]

Formula ( IVa ) , R ⁴ =R ³ =benzyl , R ² =m-tet razolylbenzyl ,

R ⁷ =Table Ex . No . 0 . 1 .2

233 [e] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 234 f e] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl ) aminobenzyl

235fe] m-(N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

236 [e] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

237 [e] m-formaldoximebenzyl m-acetoximebenzyl benzyl 238 fe] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 239fe] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

240[e] m-acetylbenzyl -aminosulfonylbenzyl m-methoxybenzyl

Table 33 [e]

Formula ( IVa ) , R =R ² =benzyl , R ²² =m-pyrazolylbenzyl ,

R ⁷ =Table Ex . No . 0 . 1 .2

241 [e] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 242 [e] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

243 [e] - (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 244 [e] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

245 [e] m-formaldoximebenzyl m-acetoximebenzyl benzyl 246 [e] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 247fe] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

248 [e] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 34 [e]

Formula (IVa), R ⁴ =R ²³ =benzyl, R ²² =m-imidazolylbenzyl, R ⁷ =Table

Ex.No .0 .1 .2

249 [e] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

250 [e] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl)aminobenzyl

251 [e] m- (N-methylamino) m-(N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

-250-

SUBS ΓΓUTE SHEET (RULE 26)

252[e] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

253[e] m-formaldoximebenzyl m-acetoximebenzyl benzyl

25 [e] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

255[e] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

256fe] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 35 [e]

Formula ( IVa) , R ⁴ =R ² =benzyl , R ²² =p-fluorobenzyl,

R ⁷ =Table Ex . No . 0 .1 .2

257 f e] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 258 [e] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

259 [e] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 260 [e] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

261 [e] m-formaldoximebenzyl m-acetoximebenzyl benzyl 262 [e] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 263 [e] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

26 [e] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 36 [e]

Formula ( IVa ) , R ⁴ =R ^{2 3} =benzyl , R ²² =pyridinylmethyl ,

R ⁷ =Table Ex . No .0 .1 .2

265 [e] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

266 [e] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

267 [e] m- (N-methylamino) m~ (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

268 [e] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

269 [e] m-formaldoximebenzyl m-acetoximebenzyl benzyl

270 [e] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 271 [e] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl 272 [e] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 37 [e]

Formula ( IVa) , R ⁴ =R ²³ =benzyl, R ² =m-acetylbenzyl, R ⁷ =Table

Ex.No .0 .1 .2

273[e] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

27 [e] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl)aminobenzyl

275[e] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 276 [e] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

277 [e] m-formaldoximebenzyl m-acetoximebenzyl benzyl 278 [e] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 279 fe] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

280 [e] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 38 [e]

Formula ( IVa ) , R ⁴ =R ²³ =benzyl , R ²² =m-aminosul f onylbenzyl ,

R ⁷ =Table Ex . o . 0 . 1 .2

281 [e] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 282 [e] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

283[e] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

284 [e] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

285 [e] m-formaldoximebenzyl m-acetoximebenzyl benzyl

286 [e] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 287 [e] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

288 [e] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 39 [e]

Formula ( IVa ) , R ⁴ =R ²³ =benzyl , R ²² =m-methoxybenzyl ,

R ⁷ =Table Ex . No . 0 . 1 .2

289 [e] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 290 [e] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) minobenzyl

291 [e] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

292 [e] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

293 [e] m-formaldoximebenzyl m-acetoximebenzyl benzyl 294 [e] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 295 fe] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

296 fe] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 3 [ f ]

Formula ( IVb ) , R ⁴ =R ²³ =benzyl , R ²² =R ⁷ =Table

Ex . No .0 .1 .2 i f f ] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

2[f] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl 3[f] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 4[f] m-trifluorocarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

5[f] m-formaldoximebenzyl m-acetoximebenzyl benzyl 6[f] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 7[f] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl 8[f] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 4 [ f ] Formula ( IVb) , R =R ^{2 3} =f luorobenzyl , R ²² =R =Table

Ex . No . 0 . 1 .2

9[f] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

10 [ f ] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

11 [f] - (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

12 [f] m-trifluorocarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

13 [f] m-formaldoximebenzyl m-acetoximebenzyl benzyl

14 [f] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

15 [f] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

16[f] m-acetylbenzyl -aminosulfonylbenzyl m-methoxybenzyl

Table 5[f]

Formula (IVb), R ⁴ =R ²³ =pyrrolylmethyl, R ²² =R ⁷ =Table

Ex.No .0 .1 .2

17 [f] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

18 [f] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

19 [f] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 20 [f] m-trifluorocarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

21 [f] m-formaldoximebenzyl m-acetoximebenzyl benzyl

22 [f] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

23 ff] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

24 [f] m-acetylbenzyl -aminosulfonylbenzyl m-methoxybenzyl

Table 6[f]

Formula (IVb), R ⁴ =R ³ =methoxybenzyl, R ²² =R ⁷ =Table

Ex.No .0 .1 .2

25 [f] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

26 [f] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

27 [f] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

40

28 [f] m-trifluorocarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

29[f] m-formaldoximebenzyl m-acetoximebenzyl benzyl

30[f] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

31[f] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

32[f] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 7(f]

Formula (IVb), R =R ²³ =isobutyl, R ² =R ⁷ =Table

Ex.No .0 .1 .2

33ff] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

34[f] m-(N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl)aminobenzyl

35[f] m- (N-methylamino) m-(N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 36[f] m-trifluorocarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

37[f] m-formaldoximebenzyl m-acetoximebenzyl benzyl

38 [f] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

39[f] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

40 ff] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 8 [ f ]

Formula ( IVb) , R ⁴ =R ²³ =p- nitrobenzyl , R ²² =R ⁷ =Table

Ex .No . 0 . 1 .2

41 [f] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

42[f] m-(N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl)aminobenzyl

43ff] m-(N-methylamino) m-(N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

44 [f] m-trifluorocarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl 45 f f ] m-formaldoximebenzyl m-acetoximebenzyl benzyl 46 [f] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 47 f f ] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

-255-

SUBSCTTUTE SHEET (RULE 26)

48 f f ] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 9 [ f ]

Formula ( IVb) , R ⁴ =R ²³ =m- aminobenzyl , R ² =R ⁷ =Table

Ex.No .0 .1

49 f f] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

50 f f ] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl 51 [ f ] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 52 [ f ] m-trif luorocarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl 53 [f ] m-formaldoximebenzyl m-acetoximebenzyl benzyl 5 [f ] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 55 f f ] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl 56 f f ] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 10[f]

Formula (IVb), R ⁴ =R ³ =pyridinylmethyl, R ²² =R ⁷ =Table

Ex. o .0 .1 .2

57 [f] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

58 [f] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

59 [f] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 60 [f] m-trifluorocarbonyl m-hydroxyamidino m- riazolylbenzyl benzyl benzyl

61 [f] m-formaldoximebenzyl m-acetoximebenzyl benzyl

62 [f] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

63 [f] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

64 [f] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 11 [f]

Formula (IVb) , R ⁴ =R ²³ =m-hydroxybenzyl, R ² =R ⁷ =Table

Ex.No .0 .1 .2

65 [f] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

66 [f] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl)aminobenzyl

67 [f] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

68 [f] m-trifluorocarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

69 [f] m-formaldoximebenzyl m-acetoximebenzyl benzyl 70 ff] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 71 [f] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

72 [f] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 12 [ f ]

Formula ( IVb) , R ⁴ =R ²³ =p- hydroxybenzyl , R ²² =R ⁷ =Table

Ex .No . 0 . 1 .2

73 [f] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

74 [f] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl 75 [f] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

76 [f] m-trifluorocarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

77 [f] m-formaldoximebenzyl m-acetoximebenzyl benzyl

78 [f] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

79 [f] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

80 [f] m-acetylbenzyl -aminosulfonylbenzyl m-methoxybenzyl

Table 13 ff]

Formula (IVb) , R ⁴ =R ²³ =m-aminocarbonybenzyl, R ²² =R ⁷ =Table

Ex.No .0 .1 .2

81 [f] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

82 [f] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

83 [f] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl ' benzyl

-257-

SUBSCTTUTE SHEET (RULE 26)

84 [f] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

85 ff] m-formaldoximebenzyl m-acetoximebenzyl benzyl

86 [f] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

87 [f] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

88 [f] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 14 [f]

Formula (IVb), R ⁴ =R ²³ =p- hydroxymethylbenzyl , R ²² =R ⁷ =Table

Ex.No .0 .1 .2

89 ff] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

90 [f] m-(N, -dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

91 [f] m- (N-methylamino) m- (N-methylamino) m-f ormylbenzyl carbonylbenzyl benzyl 92 ff] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

93 [f] m-formaldoximebenzyl m-acetoximebenzyl benzyl

94 ff] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

95 [f] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

96 [f] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 15[f]

Formula (IVb), R ⁴ =R ² =m-hydroxycarbonylbenzyl, R ²² =R ⁷ =Table

Ex. No .0 .1 .2

97[f] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 98[f] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

99[f] mm-- ((NN--mmeetthhyyllaammiinnoo)) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 100 [f] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

101 [f] m-formaldoximebenzyl m-acetoximebenzyl benzyl 102 [f] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 103 [f] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

-258-

SUBSΠTUTE SHEET (RULE 26)

104 [ f ] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 16 [f]

Formula (IVb), R ⁴ =R =benzyl, R ²² =m-hydroxymethylbenzyl, R ⁷ =Table

Ex.No .0 .1 .2

105[f] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

106[f] m-(N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl)aminobenzyl

107ff] m-(N-methylamino) -(N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 108 ff] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

109 [f] m-formaldoximebenzyl m-acetoximebenzyl benzyl 110ff] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl lllff] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

112[f] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 17 [f]

Formula (IVb), R ⁴ =R ²³ =benzyl, R ²² =p-hydroxymethylbenzyl, R ⁷ =Table

Ex.No .0 .1 .2

113 [f] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

114 [f] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl)aminobenzyl

115 [f] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 116ff] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl 117 ff] m-formaldoximebenzyl m-acetoximebenzyl benzyl

118 [f] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

119[f] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

120 [f] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 18ff]

Formula (IVb) , R ⁴ =R ² =benzyl, R =m-hydroxybenzyl,

R ⁷ =Table Ex. o .0 .1 .2

121 ff] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 122 [f] m- (N, -dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

123 [f] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

124 [f] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

125 [f] m-formaldoximebenzyl m-acetoximebenzyl benzyl 126 [f] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 127 [f] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

128 [f] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 19[f]

Formula (IVb) , R ⁴ =R ²³ =benzyl, R ²² =m- (N, N-dimethylamino glycyl) aminobenzyl, R ⁷ =Table Ex. o .0 .1 .2

129 ff] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 130 [f] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

131 [f] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 132 [f] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

133 [f] m-formaldoximebenzyl m-acetoximebenzyl benzyl 134 [f] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 135 [f] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

136 [f] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 20[f]

Formula (IVb), R ⁴ =R ²³ =benzyl, R ² =m-aminocarbonylbenzyl, R ⁷ =Table

Ex. No .1

-260-

SUBSTΓΓUTE SHEET (RULE 26)

40

137[f] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 138[f] m-(N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl)aminobenzyl 139 [f] m-(N-methylamino) m-(N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 140[f] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl 141[f] m-formaldoximebenzyl m-acetoximebenzyl benzyl 142[f] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzy1 143[f] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl 144 ff] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 21 [f]

Formula ( IVb) , R ⁴ =R ²³ =benzyl , R ² =p-hydroxyben zyl ,

R ⁷ =Table Ex . No . 0 . 1 .2

145 f f] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 146 f f ] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

147 [f] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 148 [f ] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

149[f] m-formaldoximebenzyl m-acetoximebenzyl benzyl 150 [f] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 151 [f] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

152[f] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 22 [f]

Formula (IVb), R ⁴ =R ² =benzyl, R ²² =m- (N-methylaminocarbonyl benzyl, R ⁷ =Table Ex.No .0 .1 .2

153[f] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

154 [f] m-(N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl)aminobenzyl

0

155[f] m-(N-methylamino) m-(N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

156[f] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzy benzyl benzyl

157[f] m-formaldoximebenzyl m-acetoximebenzyl benzyl 158 ff] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzy 159[f] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

160[f] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 23 [f]

Formula ( IVb) , R ⁴ =R ²³ =benzyl , R ²² =m- (N-methylamino) benzyl ,

R ⁷ =Table Ex . No . 0 . 1 .2

161 [f] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 162 [f] m- (N, -dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

163 [f] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 164 f f] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzy benzyl benzyl

165ff] m-formaldoximebenzyl m-acetoximebenzyl benzyl 166[f] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzy 167[f] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

168 [f] m-acetylbenzyl -aminosulfonylbenzyl m-methoxybenzyl

Table 2 [ f ]

Formula ( IVb) , R ⁴ =R ² =benzyl , R ²² =m-formyllbenzyl ,

R ⁷ =Table Ex . No . 0 . 1 .2

169 [f] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 170 [f ] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl 171 f f] m- (N-methylamino) m- (N-methylamino) m-f ormylbenzyl carbonylbenzyl benzyl

172 ff] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

173ff] m-formaldoximebenzyl m-acetoximebenzyl benzyl

174 [f] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

175[f] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

176 f f] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 25 [ f ]

Formula ( IVb) , R =R ²³ =benzyl , R ²² =m- trif luorocarbonylbenzyl , R ⁷ =Table

Ex . No .0 . 1 .2

177ff] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

178 [f] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl 179[f] m-(N-methylamino) m-(N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 180 [f] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

181 [f] m-formaldoximebenzyl m-acetoximebenzyl benzyl 182[f] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 183 ff) m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl 184 [f] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 26[f]

Formula (IVb), R ⁴ =R ²³ =benzyl, R ²² =m-hydroxyamidinobenzyl, R ⁷ =Table

Ex.No .0 .1 .2

185 [f] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

186[f] m-(N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl)aminobenzyl

18 [f] m- (N-methylamino) m-(N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

188 [f] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

189 [f] m-formaldoximebenzyl m-acetoximebenzyl benzyl

190 [f] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 191 [f] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl 192 [f] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 27 [f]

Formula (IVb), R ⁴ =R ²³ =benzyl, R ²² =m-triazolylbenzyl, R ⁷ =Table

Ex.No .0 .1 .2

193 [f] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

194 [f] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl)aminobenzyl

195 [f] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 196 [f] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

197 [f] m-formaldoximebenzyl m-acetoximebenzyl benzyl 198 ff] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 199 [f] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

200 [f] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 28[f]

Formula (IVb) , R ⁴ =R ² =benzyl, R ²² =m-formaldoximebenzyl,

R ⁷ =Table E .No .0 .1 .2

201 [f] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

202 [f] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

203 [f] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 204 [f] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

205 [f] m-formaldoximebenzyl m-acetoximebenzyl benzyl 206 ff] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 207 [f] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

208 [f] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 29[f]

Formula (IVb) , R ⁴ =R ² =benzyl, R ²² =m-acetoximebenzyl,

R ⁷ =Table Ex. No .0 .1 .2

209 [f] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

210 ff] m-(N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

211 ff] m- (N-methylamino) m- (N-methylamino) m-formylbenzy1 carbonylbenzyl benzyl 212 ff] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

213 [f] m-formaldoximebenzyl m-acetoximebenzyl benzyl 214 [f] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 215 [f] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

216 [f] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 30 [f]

Formula (IVb), R =R ²³ =benzyl, R ²² =benzyl, R ⁷ =Table Ex. No .0 .1 .2

217 [f ] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 218 [f] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

219 [f] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 220 [f] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

221 ff] m-formaldoximebenzyl m-acetoximebenzyl benzyl 222 [f] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 223 [f] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl 224 [f] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 31 [f] Formula (IVb), R ⁴ =R ²³ =benzyl, R ²² =m-hydroxycarbonylbenzyl, R ⁷ =Table Ex. No .0 .1 .2

225[f] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 226ff] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl 227 ff] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 228 [f] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl 229 [f] m-formaldoximebenzyl m-acetoximebenzyl benzyl 230 [f] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 231 [f] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl 232 [f] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 32 [f ]

Formula ( IVb) , R ⁴ =R ³ =benzyl , R ²² =m-tet razolylbenzyl ,

R ⁷ =Table Ex . No . 0 . 1 .2

233 [ f ] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 234 [f ] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

235 [f] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 236 [ f ] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

237 [f] m-formaldoximebenzyl m-acetoximebenzyl benzyl 238 ff] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 239 [f] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

240 [f] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 33 [ f ]

Formula ( IVb) , R ⁴ =R ^{2 3} =benzyl , R ²² =m-pyra zolylbenzyl ,

R ⁷ =Table Ex . No . 0 . 1 .2

241 [ f ] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 242 [ f ] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl ) aminobenzyl

243 ff] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

244 [f] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

245 [f] m-formaldoximebenzyl m-acetoximebenzyl benzyl 246 [f] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 247 ff] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

248 [f] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 34 [f]

Formula (IVb), R ⁴ =R ²³ =benzyl, R ² =m-imidazolylbenzyl, R ⁷ =Table

Ex.No .0 .1 .2

249 [f] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

250 ff] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl)aminobenzyl

251 [f] m- (N-methylamino) m-(N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 252 [f] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

253 [f] m-formaldoximebenzyl m-acetoximebenzyl benzyl 254 [f] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 255 [f] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

256 [f] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 35 [ f ]

Formula ( IVb) , R =R ²³ =benzyl , R ² =p- f luorobenzyl ,

R ⁷ =Table Ex . No . 0 . 1 .2

257 [f ] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 258 [ f ] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl ) aminobenzyl 259 [f ] m- (N-methylamino) m- (N-methylamino ) m-formylbenzyl carbonylbenzyl benzyl

260[f] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

261 [f] m-formaldoximebenzyl m-acetoximebenzyl benzyl

262 [f] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

263ff] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

264 ff] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 36[f]

Formula (IVb), R ⁴ =R ²³ =benzyl, R ²² =pyridinylmethyl,

R ⁷ =Table Ex. No .0 .1 .2

265 ff] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 266 [f] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

267 [f] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 268 [f] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

269ff] m-formaldoximebenzyl m-acetoximebenzyl benzyl 270 ff] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 271 [f] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

272[f] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 37 [f]

Formula (IVb), R ⁴ =R ²³ =benzyl , R ² =m-acetylbenzyl,

R ⁷ =Table Ex. No .0 .1 .2

273 ff] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

274 [f] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

275 [f] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

276 ff] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

277 [f] m-formaldoximebenzyl m-acetoximebenzyl benzyl

278 [f] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 279ff] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl 280[f] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 38 f f]

Formula ( IVb) , R =R ² =benzyl , R ²² =m-aminosulfonylbenzyl ,

R ⁷ =Table Ex . No .0 .1 .2

281 ff] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 282 f f ] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

283 f f ] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 284 f f ] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

285 ff] m-formaldoximebenzyl m-acetoximebenzyl benzyl 286[f] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 287[f] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

288 [f] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 39 [ f ]

Formula ( IVb) , R ⁴ =R ²³ =benzyl , R ² =m-methoxybenzyl ,

R ⁷ =Table Ex . No .0 . 1 .2

289 [ f ] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 290 [f ] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl ) aminobenzyl

291 [f] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 292[f] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl 293[f] m-formaldoximebenzyl m-acetoximebenzyl benzyl

294 [f] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

295 [f] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

296[f] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 3[g]

Formula (Va) , R =R ²³ =benzyl, R ²² =R ⁷ =Table

Ex.No .0 .1 i[g] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 2[g] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

3fg] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl fg] m-trifluorocarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

5[g] m-formaldoximebenzyl m-acetoximebenzyl benzyl 6[g] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 7[g) m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl 8[g] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table [g]

Formula (Va) , R ⁴ =R ³ =fluorobenzyl, R ² =R ⁷ =Table

Ex.No .0 .1 .2

9fg] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

10 [g] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl)aminobenzyl

11 [g] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 12 [g] m-trifluorocarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

13 [g] m-formaldoximebenzyl m-acetoximebenzyl benzyl

14 [g] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

15 [g] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

16 [g] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 5[g]

Formula (Va) , R ⁴ =R ²³ =pyrrolylmethyl, R ²² =R ⁷ =Table

Ex.No .0 .1 .2

17 [g] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

-270-

SUBS ΓΠJTE SHEET (RULE 26)

18 [g] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

19[g] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

20 [g] m-trifluorocarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

21 [g] m-formaldoximebenzyl m-acetoximebenzyl benzyl

22 fg] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

23 [g] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

24 [g] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 6[g]

Formula (Va) , R ⁴ =R ²³ =methoxybenzyl, R ²² =R ⁷ =Table

Ex.No .0 .1 .2

25 [g] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

26 [g] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl)aminobenzyl

27 [g] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

28 [g] m-trifluorocarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

29 [g] m-formaldoximebenzyl m-acetoximebenzyl benzyl

30 [g] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

31 [g] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

32 [g] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 7 [g]

Formula (Va ) , R ⁴ =R ²³ =isobutyl , R ²² =R ⁷ =Table

Ex . No . 0 . 1 . 2

33 fg] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

34 [g] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

35 [g] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

36 [g] m-trifluorocarbonyl m-hydroxyamidxno m-triazolylbenzyl benzyl benzyl

37 [g] m-formaldoximebenzyl m-acetoximebenzyl benzyl

38 [g] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

39 [g] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

40 [g] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 8 [g]

Formula (Va ) , R ⁴ =R ³ =p-nitrobenzyl , R ² =R ⁷ =Table

Ex . No . 0 . 1 .2

41 [g] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

42 [g] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) amxnobenzyl

43 [g] m- (N-methylamxno) m- (N-methylamxno) m-formylbenzyl carbonylbenzyl benzyl

44 [g] m-trxfluorocarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

45 [g] m-formaldoximebenzyl m-acetoximebenzyl benzyl

46 [g] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

47 [g] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

48 [g] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 9[g]

Formula (Va) , R ⁴ =R ²³ =m-aminobenzyl, R ² =R =Table

Ex.No .0 .1 .2

49 [g] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

50 [g] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

51 [g] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

52 [g] m-trifluorocarbonyl m-hydroxyamidxno m-triazolylbenzyl benzyl benzyl

53 [g] m-formaldoximebenzyl m-acetoximebenzyl benzyl

54 [g] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

55 [g] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

56 fg] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 10 [g]

Formula (Va) , R ⁴ =R ²³ =pyridinylmethyl, R ²² =R ⁷ =Table

Ex.No .0 .1 .2

57 [g] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

58 fg] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl)aminobenzyl

59 [g] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

60 [g] m-trifluorocarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

61 [g] m-formaldoximebenzyl m-acetoximebenzyl benzyl

62 [g] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

63 [g] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

6 [g] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 11 [g]

Formula (Va) , R ⁴ =R ²³ =m-hydroxybenzyl, R ²² =R ⁷ =Table

Ex.No .0 .1 .2

65 [g] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

66 [g] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

67 [g] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

68 fg] m-trifluorocarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

69 [g] m-formaldoximebenzyl m-acetoximebenzyl benzyl

70 [g] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

71 [g] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

72 [g] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 12 [g]

Formula (Va) , R ⁴ =R ²³ =p-hydroxybenzyl, R ²² =R ⁷ =Table

Ex.No .0 .1 .2

73 [g] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

74 [g] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

75 [g] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

76 [g] m-trifluorocarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

77 [g] m-formaldoximebenzyl m-acetoximebenzyl benzyl

78 [g] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 79 [g] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

80 fg] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 13 [g]

Formula (Va) , R =R ²³ =m-aminocarbonybenzyl, R ² =R ⁷ =Table

Ex.No .0 .1 .2

81 [g] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

82 [g] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

83 [g] m- (N-methylamino) m-(N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

84 [g] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

85 [g] m-formaldoximebenzyl m-acetoxxmebenzyl benzyl

86 [g] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

87 [g] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

88 [g] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 14 [g]

Formula (Va) , R ⁴ =R ²³ =p-hydroxymethylbenzyl, R ²² =R ⁷ =Table

Ex.No .0 .1 .2

89 [g] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

90 fg] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl)aminobenzyl 91 [g] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

92 [g] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

93fg] m-formaldoximebenzyl m-acetoximebenzyl benzyl

94[g] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

95fg] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl 96fg] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 15 [g]

Formula (Va) , R ⁴ =R ² =m-hydroxycarbonylbenzyl, R ²² =R ⁷ =Table

Ex.No .0 .1 .2

97 [g] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

98 fg] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

99 [g] m- (N-methylamino) m-(N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 100 fg] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

101 fg] m-formaldoximebenzyl m-acetoximebenzyl benzyl 102 [g] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 103[g] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

104 [g] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 16 [g]

Formula (Va ) , R ⁴ =R ²³ =benzyl , R ² =m-hydroxymethylbenzyl ,

R ⁷ =Table Ex . No . 0 .1 .2

105 [g] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 106 [g] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

107 [g] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 108 [g] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

109 [g] m-formaldoximebenzyl m-acetoximebenzyl benzyl 110 [g] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

lll f g] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl 112 [g] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 17 [g]

Formula (Va) , R =R ² =benzyl, R ² =p-hydroxymethylbenzyl,

R ⁷ =Table Ex . No . 0 . 1 .2

113 [g] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 114 [g] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

115 f g] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 116 [g] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

117 [g] m-formaldoximebenzyl m-acetoximebenzyl benzyl 118 fg] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 119 [g] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

120 [g] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 18 [g]

Formula (Va ) , R ⁴ =R ²³ =benzyl , R ² =m-hydroxybenzyl ,

R ⁷ =Table Ex . No . 0 . 1 .2

121 [g] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 122 [g] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

123 [g] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 124 [g] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

125 fg] m-formaldoximebenzyl m-acetoximebenzyl benzyl 126 [g] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 127 [g] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

128 [g] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 19 [g]

Formula (Va ) , R ⁴ =R ³ =benzyl , R ^{2 2} =m- (N, N-dimethylamino glycyl ) aminobenzyl , R ⁷ =Table Ex . No . 0 . 1 .2

129 fg] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 130 [g] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

131 [g] m- (N-methylamino) m-(N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 132 [g] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

133 [g] m-formaldoximebenzyl m-acetoximebenzyl benzyl 134 [g] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 135 [g] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

136 [g] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 20 fg]

Formula (Va ) , R =R ³ =benzyl , R ² =m-aminocarbonylbenzyl ,

R ⁷ =Table Ex . No . 0 . 1 .2

137 [g] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 138 [g] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

139 [g] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 140 [g] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

141 [g] m-formaldoximebenzyl m-acetoximebenzyl benzyl 142 [g] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 143 [g] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

144 [g] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 21 [g] Formula (Va ) , R ⁴ =R ²³ =benzyl , R ²² =p-hydroxybenzyl , R ⁷ =Table

Ex . No . 1

145[g] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 146[g] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl)aminobenzyl 147 [g] -(N-methylamino) m-(N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 148 [g] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl 149fg] m-formaldoximebenzyl m-acetoximebenzyl benzyl 150 [g] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 151 [g] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl 152 [g] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 22 [g]

Formula (Va ) , R ⁴ =R ² =benzyl , R ² =m- (N-methylaminocarbonyl benzyl , R ⁷ =Table Ex . No . 0 . 1 .2

153 [g] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 154 [g] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

155 [g] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 156 [g] m-trif luorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

157 [g] m-formaldoximebenzyl m-acetoximebenzyl benzyl 158 [g] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 159 [g] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

160 [g] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 23 [g]

Formula (Va ) , R ⁴ =R ²³ =benzyl , R ²² =m- (N-methylamino) benzyl , R ⁷ =Table

Ex . No . 0 . 1 .2

161 f g] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

162 [g] m- (N, -dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

163 [g] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

16 [g] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzy benzyl benzyl

165 [g] m-formaldoximebenzyl m-acetoximebenzyl benzyl 166 [g] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzy 167 [g] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

168 [g] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 24 [ g ]

Formula (Va ) , R ⁴ =R ²³ =benzyl , R ² =m-f ormyllbenzyl ,

R ⁷ =Table Ex . No . 0 . 1 .2

169 [g] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 170 fg] , m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

171 [g] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 172 [g] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzy benzyl benzyl

173 fg] m-formaldoximebenzyl m-acetoximebenzyl benzyl 174 [g] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzy 175 [g] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

176 [g] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 25 [g]

Formula (Va) , R ⁴ =R ² =benzyl, R ² =m-trifluorocarbonylbenzyl, R ⁷ =Table

Ex.No .0 .1 .2

177 [g] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

178 fg] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

179 [g] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

180 [g] m-trxfluorcarbonyl m-hydroxyamidxno m-trxazolylbenzyl benzyl benzyl

181 [g] m-formaldoximebenzyl m-acetoximebenzyl benzyl

182 [g] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

183 [g] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

184 [g] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 26[g]

Formula (Va) , R ⁴ =R ²³ =benzyl, R ²² =m-hydroxyamidinobenzyl, R ⁷ =Table

Ex.No .0 .1 .2

185 [g] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

186 [g] m- (N, N-dxmethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

187 [g] m- (N-methylamino) m- (N-methylamxno) m-formylbenzyl carbonylbenzyl benzyl 188 [g] m-trxfluorcarbonyl m-hydroxyamidxno m-trxazolylbenzyl benzyl benzyl

189 [g] m-formaldoxxmebenzyl m-acetoximebenzyl benzyl 190 [g] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 191 [g] m-imidazolylbenzyl p-fluorobenzyl pyrxdinylmethyl

192 [g] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 27 [g]

Formula (Va) , R ⁴ =R ² =benzyl, R ² =m-triazolylbenzyl,

R ⁷ =Table Ex.No .0 .1 .2

193 [g] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

194 [g] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

195 [g] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

196 [g] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

19 [g] m-formaldoxxmebenzyl m-acetoximebenzyl benzyl

198 [g] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzy

199 [g] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

200 [g] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 28 [g]

Formula (Va) , R ⁴ =R ²³ =benzyl, R ²² =m-formaldoximebenzyl,

R ⁷ =Table Ex.No .0 .1 .2

201 [g] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 202 [g] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

203 [g] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

204 [g] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

205 [g] m-formaldoximebenzyl m-acetoximebenzyl benzyl

206 [g] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

207 [g] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

208 [g] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 29[g]

Formula (Va) , R ⁴ =R =benzyl, R ² =m-acetoximebenzyl,

R ⁷ =Table E .No .0 .1 .2

209 [g] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

210 [g] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

211 [g] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

212 [g] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

213 [g] m-formaldoximebenzyl m-acetoximebenzyl benzyl

214 [g] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

215 [g] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

216 [g] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 30 [g]

Formula (Va) , R ⁴ =R ³ =benzyl, R ² =benzyl, R ⁷ =Table

Ex. No .0 .1 .2

217 [g] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

218 [g] m- (N, -dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl)aminobenzyl

219 fg] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

220 [g] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

221 fg] m-formaldoximebenzyl m-acetoximebenzyl benzyl

222 [g] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

223 [g] m-xmidazolylbenzyl p-fluorobenzyl pyridinylmethyl

22 [g] m-acetylbenzyl m-amxnosulfonylbenzyl m-methoxyoenzyl

Table 31 [g]

Formula (Va) , R ⁴ =R =benzyl, R ² =m-hydroxycarbonylbenzyl,

R ⁷ =Table Ex. No .0 .1 .2

225 [g] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

226 [g] m- (N, N-dxmethylamxno m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

227 [g] m- (N-methylamxno) m- (N-methylamxno) m-f ormylDenzyl carbonylbenzyl benzyl

228 [g] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

229 [g] m-formaldoximebenzyl m-acetoximebenzyl benzyl

230 [g] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

231 [g] m-xmidazolylbenzyl p-fluorobenzyl pyridinylmethyl

232 [g] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 32 [g] Formula (Va) , R ⁴ =R ²³ =benzyl, R ² =m-tetrazolylbenzyl, R ⁷ =Table Ex. No .0 .1 .2

233 [g] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

234 [g] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl)aminobenzyl

235 [g] m- (N-methylamino) m-(N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

236 [g] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

237 [g] m-formaldoximebenzyl m-acetoximebenzyl benzyl

238 [g] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

239 [g] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

240 [g] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 33 [g]

Formula (Va) , R ⁴ =R ³ =benzyl, R ² =m-pyrazolylbenzyl,

R ⁷ =Table Ex.No .0 .1 .2

241 fg] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

242 [g] m- (N,N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl)aminobenzyl

243 fg] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

24 [g] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

245 [g] m-formaldoximebenzyl m-acetoximebenzyl benzyl

246 [g] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

247 fg] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

248 [g] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 34 [g]

Formula (Va) , R ⁴ =R =benzyl , R ² =m-imidazolylbenzyl ,

R ⁷ =Table Ex . No . 0 . 1 .2

249 [g] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

250 [g] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

251 [g] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl

252 [g] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

253 [g] m-formaldoximebenzyl m-acetoximebenzyl benzyl 25 [g] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 255 [g] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

256 [g] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 35 f g]

Formula (Va ) , R ⁴ =R ³ =benzyl , R ² =p- f luorobenzyl ,

R ⁷ =Table Ex . o . 0 . 1 .2

257 [g] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 258 [g] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

259 [g] m- (N-methylamino) m- (N-methylamino) m-formylbenzyl carbonylbenzyl benzyl 260 [g] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

261 [g] m-formaldoximebenzyl m-acetoximebenzyl benzyl 262 [g] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 263 [g] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

264 [g] m-acetyibenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 36 [g]

Formula (Va ) , R ⁴ =R ²³ =benzyl , R ² =pyridinylmethyl ,

R ⁷ =Table Ex . No . 0 . 1 .2

265 [g] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 266 [g] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl ) aminobenzyl 267 [g] m- (N-methylamino) m- (N-methylamino) m-f ormylbenzyl carbonylbenzyl benzyl

268 [g] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

269 fg] m-formaldoximebenzyl m-acetoximebenzyl benzyl

270 [g] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

271 [g] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

272 [g] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 37 [g]

Formula (Va ) , R ⁴ =R ²³ =benzyl, R ²² =m-acetylbenzyl ,

R ⁷ =Table Ex . No . 0 . 1 .2

273 [g] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl 27 [g] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

275 [g] m- (N-methylamino) m- (N-methylaminc) m-formylbenzyl carbonylbenzyl benzyl 276 [g] m-trifluorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

277 [g] m-formaldoximebenzyl m-acetoximebenzyl benzyl 278 [g] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl 279 [g] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

280 [g] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 38 [g]

Formula (Va ) , R =R ² =benzyl , R ² =m-aminosulfonylbenzyl ,

R ⁷ =Table Ex . No . 0 .1 .2

281 [g] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

282 [g] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl ) aminobenzyl

283 [g] - (N-methylamino) m- (N-methylamino) m-f ormylbenzyl carbonylbenzyl benzyl

284 [g] m-trif luorcarbonyl m-hydroxyamidino m-triazolylbenzyl benzyl benzyl

285 [g] m-formaldoximebenzyl m-acetoximebenzyl benzyl

286 [g] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

287 [g] m-imidazolylbenzyl p-fluorobenzyl pyridinylmethyl

288 [g] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl

Table 39 [g]

Formula (Va ) , R =R ³ =benzyl , R ²² =m-methoxybenzyl ,

R ⁷ =Table Ex . No . 0 . 1 .2

28 fg] m-hydroxymethylbenzyl p-hydroxymethylbenzyl m-hydroxybenzyl

290 [g] m- (N, N-dimethylamino m-aminocarbonylbenzyl p-hydroxybenzyl glycyl) aminobenzyl

291 [g] m- (N-methylamino) m- (N-methylamino) m-f ormylbenzyl carbonylbenzyl benzyl

292 [g] m-trxfluorcarbonyl m-hydroxyamxdino m-trxazolylbenzyl benzyl benzyl

293 [g] m-formaldoximebenzyl -acetoxxmebenzyl benzyl

29 [g] hydroxycarbonylbenzyl m-tetrazolylbenzyl m-pyrazolylbenzyl

295 [g] m-xmidazolylbenzyl p-fluorobenzyl pyridinylmethyl

296 [g] m-acetylbenzyl m-aminosulfonylbenzyl m-methoxybenzyl