DESCRIPTION

Title of Invention: CYCLOPROPANAMINE COMPOUND AND USE THEREOF

Technical Field

[0001]

The present invention relates to a cyclopropanamine compound having a lysine-specific demethylase-1 (sometimes to be abbreviated as LSDl in the present specification)

inhibitory action, and useful as a medicament such as a prophylactic or therapeutic agent for cancer, schizophrenia, developmental disorders, particularly diseases having

intellectual disability (e.g., autistic spectrum disorders, Rett syndrome, Down's syndrome, Kabuki syndrome, fragile X syndrome, Kleefstra syndrome, neurofibromatosis type 1, Noonan syndrome, tuberous sclerosis), neurodegenerative diseases (e.g., Alzheimer's disease, Parkinson's disease,

spinocerebellar degeneration (e.g., dentatorubural

pallidoluysian atrophy) and Huntington's disease), epilepsy (e.g., Dravet syndrome) or drug dependence, and the like.

[0002]

(Background of the Invention)

LSDl is a demethylation enzyme of histone, catalyzes a demethylation reaction of a monomethylated product and a dimethylated product of the 4th lysine residue of histone H3 (H3K4mel/2), and forms formaldehyde as a by-product. In addition, LSDl forms a complex with, flavin adenine

dinucleotide (FAD) which is a kind of coenzyme, and FAD promotes oxidation of lysine residue by enzymes as a redox mediator .

[0003]

When a compound having a LSDl inhibitory activity is applied to neuronal cells, histone H3 methylation especially H3K4 methylation around GAD1 gene promoter is increased through inhibition of histone demethylation activity of LSDl (Experimental Example 3 to be mentioned later) . There are many publications with analyses of relationship between gene expression level and histone H3K4 methylation status, which conclude that promotion of histone H3K4 methylation at a gene promoter leads to an activated transcription of the gene

(Becker, Nature 2006, 442: 31-32; Ruthenburg et al., Nature Reviews Molecular Cell Biology 2007, 8: 983-994). Therefore, it is assumed that administration of a compound having an LSDl inhibitory activity accumulates histone H3K4 methylation in neurons in the brain, which in turn results in the GAD1 mRNA expression in the brain. It is widely known that the induction of GAD1 mRNA expression in the brain is effective for the treatment of central nervous system diseases. For example, intracerebral injection of a GAD1 gene expression vector to Parkinson' s disease patients is known to induce GADl mRNA expression and improve the symptoms of Parkinson' s disease patients (LeWitt et al. Lancet Neurol. 2011, 10: 309-319;

Carlson, Physiology of Behavior 11 ^th edition 2013) . From the above, it is considered that the administration of an LSDl inhibitor increases the histone H3K4 methylation and results in increase of the GADl expression level in the brain, which may be effective for the treatment of central nervous system diseases.

[0004]

On the other hand, LSDl also catalyzes a demethylation reaction of a methylated product of the 9th lysine residue of histone H3 (H3K9me) . A decrease of the methylation of H3K9 in animal models of some diseases, for example, animal models of cocaine dependence and Kleefstra syndrome has been reported (Science 8 Jan. 2010, 327, 213-216, Genes Dev. Apr. 2005, 19, 815-826) . A decrease of the H3K9 methylation is known to cause abnormally enhanced expression of some genes. Therefore, it is assumed that administration of a compound having an LSDl inhibitory activity accelerates histone H3K9 methylation in neurons in the brain, which in turn decreases the expression of genes abnormally expressed in the brain. From the above, it is considered that LSDl inhibitor is possibly effective for the treatment of some diseases with a decrease of methylated

H3K9.

[0005]

WO 2010/084160 (patent document 1) discloses a compound of the following formula or a pharmaceutically acceptable salt thereof as an LSD1 inhibitor:

0006]

[0007]

wherein R1-R5 are H, halo and the like; R6 is H or alkyl; R7 is H, alkyl or cycloalkyl; R8 is -L-heterocyclyl or -L-aryl wherein ^' L is - (CH ₂ ) _n - (CH ₂ ) n~, - (CH ₂ ) nO (CH ₂ ) _n - or - (CH ₂ ) _n S (CH ₂ ) _n ~, and n is 0,. 1, 2 or 3.

[0008]

WO 2010/043721 (patent document 2) discloses a compound of the following formula or a pharmaceutically acceptable salt thereof as an LSDl inhibitor:

[0009]

[0010]

wherein R1-R5 are H, halo and the like; R6 is H or alkyl; is H, alkyl or cycloalkyl; R8 is -C(=0)NRxRy or -C(=0)Rz wherein Rx and Ry are each independently H, alkyl and the like, and Rz is H, alkoxy and the like.

[0011]

WO 2011/035941 (patent document 3) discloses a compound of the following formula or a pharmaceutically acceptable salt thereof as an LSDl inhibitor:

[0012]

(A')xr(A)-(B)-(Z)-(L)-(D) ^' '

E

[0013]

wherein (A' ) is aryl, arylalkoxy, heterocyclyl and the like; (A) is heteroaryl or aryl; X is 0, 1, 2 or 3; (B) is a

cyclopropyl ring; (Z) is -NH-; (L) is -CH2CH2- and the like;

(D) is -N(-R1)-R2, -0-R3 or -S-R3 wherein Rl _. and R2 are each independently H, alkyl and the like; and R3 is H, alkyl and the like.

[0014]

WO 2011/042217 (patent document 4) discloses a compound of the following formula or a pharmaceutically acceptable salt thereof as an LSDl inhibitor:

[0015]

( A ' )x-(A)-(B)-(Z)-(L)-C(=0)NH ₂

(I)

[0016]

wherein (A' ) is aryl, arylalkoxy, arylalkyl, heterocyclyl and the like; (A) is heteroaryl or aryl; X is 0, 1, 2 or 3; (B) is a cyclopropyl ring; (Z) is -NH-; (L) is - (C¾) _m CRlR2- wherein m is 0, 1, 2, 3, 4, 5 or 6; and Rl and R2 are each independently H or Cl-6 alkyl.

[0017]

US 2010/0324147 (patent document 5) discloses a compound of the following formula or a salt thereof as an LSDl inhibitor:

[0018]

[0019]

wherein X is a bond, 0, S or NH; and RA, RB, RC, RD and RE are each independently H, Cl-7 alkyl and the like.

[0020]

WO 2010/143582 (patent document 6) discloses a compound of the following formula or a pharmaceutically acceptable salt thereof as an LSD1 inhibitor:

[0021]

C I )

[0022]

wherein R ¹ is H, an alkyl group optionally having a substituent attached thereto and the like; R ² is an alkylene group optionally having a substituent attached thereto; R ³ is an alkyl group optionally having a substituent attached thereto, a phenyl group optionally having a substituent attached thereto and the like; R ⁴ is an alkyl group optionally having a substituent attached thereto, a phenyl group optionally having a substituent attached thereto and the like; and X is 0, NH ₂ , NHCO, CONH, S or CH ₂ .

[0023]

J. Am. Chem. Soc. 2010, 132, 6827-6833 (non-patent document 1) discloses compounds of the following formu an LSD 1/2 inhibitor:

[0024]

@ HC1

(13b)

©HC1

(14e)

[0025] WO 2012/156531 (patent document 7) discloses use of an LSDl inhibitor for the prophylaxis or treatment of

inflammatory diseases.

[0026]

WO 2012/156537 (patent document 8) discloses use of an

LSDl inhibitor for the prophylaxis or treatment of thrombosis, thrombus formation or circulatory diseases.

[0027]

WO 2012/135113 (patent document 9) discloses, as an LSDl inhibitor, a compound of the following formula or a

pharmaceutically acceptable salt thereof:

[0028]

[0029]

wherein

Ri is selected from the group consisting of Ci-6 alkyl, - S02Me, -NS0 ₂ Ph, arylalkoxy, C3-7 cycloalkyl, -NC(0)Ra, 1-methyl-lH- pyrazol-4-yl, hydroxy, C1-4 alkoxy, halogen, amide, amino, substituted amino and -C(0)0Ra;

R2 is H or COOH;

each R3 is independently selected from the group consisting of aryl, heteroaryl, H, Ci-e alkyl, -S0 ₂ Ra, -NC(0)Ra, -CH ₂ C(0)ORa, -C(0)ORa, -C(0)Ra, -C (0) RaRb, substituted amino, amino, urea, amide, sulfonamide, arylalkyl and heteroarylalkyl;

each Ra is independently H, phenyl, phenylmethyl, 3,5- dimethylisoxazol-4-yl, 1, 2-dimethyl-lH-imidazol-4-yl, C3-7 cycloalkyl, Ci-6 alkyl, C1-4 alkoxy, C1-3 alkylamino or -NHPh; Rb is H or C1-3 alkyl, or when attached to the same atom, Ra and Rb together form a 5- or 6-membered heterocycloalkyl ring;

R ₄ is Ci-4 alkyl, acyl, -C(0)CF ₃ or H;

W is -(CH2)i-4 or -CH(Rc) (CH2)o-3 wherein Rc is CN or C1-4 alkyl; Y is N or C;

X is N or C;

Z is 0 or (CH2) _q wherein q is 0-2, and when q is 0, Z is a bond;

m is 0-3, n is 0-3;

provided that when Z is O, Y is N and X is C;

also provided that when X is C, at least one of the R3 groups attached to X is not H.

[0030]

WO 2013/022047 (patent document 10) discloses, as an LSD1 inhibitor, the compound of the following formula or a salt thereof.

[0031]

[0032]

wherein

A is a hydrocarbon group optionally having substituent ( s ) , or a heterocyclic group optionally having substituent (s) ;

R is a hydrogen atom, a hydrocarbon group optionally having substituent (s) , or a heterocyclic group optionally having substituent (s) ; or

A and R are optionally bonded to each other to form a ring optionally having substituent (s) ;

Q ¹ , Q ² , Q ³ and Q ⁴ are each independently a hydrogen atom or a substituent; Q ¹ and Q ² , and Q ³ and Q ⁴ , are each optionally bonded to each other to form a ring optionally having substituent (s) ;

X is a hydrogen atom, an acyclic hydrocarbon group optionally having substituent (s) , or a saturated cyclic group optionally having substituent (s) ;

Y ¹ , Y ² and Y ³ are each independently a hydrogen atom, a

hydrocarbon group optionally having substituent (s) , or a heterocyclic group optionally having substituent (s) ;

X and Y ¹ , and Y ¹ and Y ² , are each optionally bonded to each other to form a ring optionally having substituent (s) ; and Z ¹ , Z ² and Z ³ are each independently a hydrogen atom or a substituent.

[0033]

WO 2012/013727 (patent document 11) discloses, as an LSD1 inhibitor, the compound of the following formula or a salt thereof.

[

(

(II)

[0036]

wherein each symbol is as defined in patent document 11.

[0037]

WO 2013/057322 (patent document 12) discloses, as an LSD1 inhibitor, the compound of the following formula or a salt thereof. [0038]

[0039]

wherein each symbol is as defined in patent document 12.

[0040]

WO 2013/057320 (patent document 13) discloses, as an LSD1 inhibitor, the compound of the following formula or a salt thereof .

[0041]

I

[0042]

wherein each symbol is as defined in patent document 13.

[0043]

WO 2014/058071 (patent document 14) discloses, as an LSD1 inhibitor, the compound of the following formula or a salt thereof.

[0044]

[0045]

wherein ,each symbol is as defined in patent document 14.

[0046]

The Journal of Neuroscience, October 17, 2007, 27(42) 11254-11262 (non-patent document 2) discloses that a decrease in histone H3K4 methylation and a decrease in Gadl mRNA

expression are observed in the brain of schizophrenia patients. In addition, Nature Neuroscience, Feb. 2015, 18, 199-209 (non- patent document 3) discloses that H3K4 methylation pathway is deeply involved in mental diseases such as schizophrenia and the like.

[0047]

MOLECULAR AND CELLULAR BIOLOGY, Aug. 2011, 31(16), 3298- 3311 (non-patent document 4) discloses that LSD1 is a

component of a protein complex that regulates transcription of beta globin and potentially involved in the suppression of transcription of beta globin. Activation of beta globin

transcription is known to be useful for the treatment of

sickle cell anaemia and beta thalassemia, from which it is assumed that LSD1 inhibition results in disinhibition of beta globin transcription, and provides a treatment effect.-

Document List

patent documents

[0048]

patent document 1: WO 2010/084160

patent document 2: WO 2010/043721

patent document 3: WO 2011/035941

patent document 4: WO 2011/042217

patent document 5: US 2010/0324147

patent document 6: WO 2010/143582

patent document 7: WO 2012/156531

patent document 8: WO 2012/156537

patent document 9: WO 2012/135113

patent document 10 : WO 2013/022047

patent document 11 : WO 2012/013727

patent document 12 : WO 2013/057322

patent document 13 : WO 2013/057320

patent document 14 : WO 2014/058071 non-patent documents

[0049]

non-patent document 1: J. Am. Chem. Soc. 2010, 132, 6827-6833 non-patent document 2: The Journal of Neuroscience, October 17, 5 2007, 27 (42) .11254-11262

non-patent document 3: Nature Neuroscience, Feb. 2015, 18, 199-209

non-patent document 4: MOLECULAR AND CELLULAR BIOLOGY, Aug.

2011, 31(16), 3298-3311

0 Summary of the Invention

Problems to be Solved by the Invention

[0050]

An object of the present invention is to provide a cyclopropanamine compound having a superior LSDl inhibitory

5 action and high LSDl selectivity, and useful as a medicament

such as a prophylactic or therapeutic agent for cancer,

schizophrenia, developmental disorders, particularly diseases having intellectual disability (e.g., autistic spectrum

disorders, Rett syndrome, Down's syndrome, Kabuki syndrome,0 fragile X syndrome, Kleefstra syndrome, neurofibromatosis type 1, Noonan syndrome, tuberous sclerosis), neurodegenerative diseases (e.g., Alzheimer's disease, Parkinson's disease, spinocerebellar degeneration (e.g., dentatorubural

pallidoluysian atrophy) and Huntington's disease (Huntington5 chorea)), epilepsy (e.g., Dravet syndrome) or drug dependence such as concaine dependence, and the like.

Means of Solving the Problems

[0051]

The present inventors have conducted intensive studies in0 an attempt to solve the aforementioned problems and found that a compound represented by the following formula (I) has a superior LSDl inhibitory action and high LSDl selectivity, which resulted in the completion of the present invention.

[0052]

5 Accordingly, the present invention relates to the following.

[1] A compound represented by the formula

[0053]

[0054]

wherein

A is an optionally substituted heterocyclic group, or an optionally substituted hydrocarbon group;

B is a ring selected from

(1) a 5- or 6-membered aromatic heterocycle optionally fused with an optionally substituted 5- or 6-membered ring, and (2) a benzene ring fused with an optionally substituted 5- or 6-membered ring,

wherein the ring represented by B is optionally substituted, and binds, via two adjacent carbon atoms with one atom in between, to a group represented by the formula

[0055]

[0056]

a group represented by the formula

[0057]

[0058]

R ¹ , R ² , R ³ and R ⁴ are each independently a hydrogen atom, an optionally substituted hydrocarbon group or an optionally substituted heterocyclic group;

A and R ¹ are optionally bonded with each other to form, together with the adjacent nitrogen atom, an optionally substituted cyclic group; and

R ² and R ³ are optionally bonded with each other to form, together with the adjacent nitrogen atom, an optionally substituted cyclic group,

or a salt thereof (hereinafter to be also referred to as compound ( I ) ) .

[0059]

[2] The compound of [1] , wherein A is

(1) an optionally substituted heterocyclic group, or

(2) an optionally substituted C3-10 cycloalkyl group,

or a salt thereof.

[0060]

[3] The compound of [1] or [2], wherein B is a ring selected from

(1) a 5- or 6-membered aromatic heterocycle, and

(2) a benzene ring fused with an optionally substituted 5- or 6-membered ring,

wherein the ring represented by B is optionally substituted, and binds, via two adjacent carbon atoms with one atom in between, to a group represented by the formula (II) , and a group represented by the formula (III) ,

or a salt thereof.

[0061]

[4] The compound of [1], [2] or [3], wherein, in the formula [0062]

[0063]

B is a ring selected from

[0064]

[0065]

wherein

X ¹ , X ² , X ³ and X ⁴ are each independently a carbon atom or a nitrogen atom;

at least one of X ¹ , X ² , X ³ and X ⁴ is a nitrogen atom;

Y ¹ , Y ² and Y ³ are each independently a carbon atom, a nitrogen atom, an oxygen atom or a sulfur atom;

at least one of Y ¹ , Y ² and Y ³ is a nitrogen atom, an oxygen atom or a sulfur atom; and

Z ¹ , Z ² , Z ³ and Z ⁴ are each independently a carbon atom or a nitrogen atom, which ring is optionally substituted, or a salt thereof.

[0066]

[5] The compound of [1], [2], [3] or [4], wherein R ¹ , R ² and R ⁴ are each independently a hydrogen atom or an optionally substituted Ci-6 alkyl group,

or a salt thereof.

[0067]

[6] The compound of [1], [2], [3], [4] or [5], wherein R ³ is

(1) a hydrogen atom,

(2) an optionally substituted Ci-6 alkyl group,

(3) an optionally substituted C3-10 cycloalkyl group, or

(4) an optionally substituted heterocyclic group,

or a salt thereof.

[0068] [7] The compound of [1], wherein, in the formula

[0069]

[0070]

A is

(1) (i) a 5- or 6-membered aromatic heterocyclic group or (ii) a 4- to 6-membered non-aromatic heterocyclic group, each of which is optionally substituted by Ci-6 alkyl group (s)

optionally substituted by halogen atom(s), or

(2) a C3-10 cycloalkyl group optionally substituted by halogen atom(s) ;

B is a ring selected from

[0071]

[0072]

wherein

X ¹ , X ² , X ³ and X ⁴ are each independently a carbon atom or a nitrogen atom;

at least one of X ¹ , X ² , X ³ and X ⁴ is a nitrogen atom; .

Y ¹ , Y ² and Y ³ are each independently a carbon atom, a nitrogen atom, an oxygen atom or a sulfur atom;

at least one of Y ¹ , Y ² and Y ³ is a nitrogen atom, an oxygen atom or a sulfur atom; and Z ¹ , Z ² , Z ³ and Z ⁴ are each independently a carbon atom or a nitrogen atom, which ring is optionally substituted by Ci-6 alkyl group (s) ;

R ¹ is a hydrogen atom;

R ² is a hydrogen atom;

R ³ is

(1) a hydrogen atom,

(2) a Ci-6 alkyl group optionally substituted by substituent ( s ) selected from

(a) a C3-10 cycloalkyl group,

(b) a Ce-14 aryl group optionally substituted by carboxy group (s) ,

(c) a 4- to 6-membered non-aromatic heterocyclic group optionally substituted by Ci-e alkyl group (s) optionally substituted by substituent (s) selected from a carboxy group, and a Ce-14 aryl group optionally substituted by carboxy group (s) , and

(d) a 5- or 6-membered aromatic heterocyclic group optionally substituted by amino group (s),

(3) a C3-10 cycloalkyl group optionally substituted by

substituent (s) selected from an amino group and a halogen atom or

(4) a 4- to 6-membered non-aromatic heterocyclic group

optionally substituted by substituent (s) selected from

(a) a Ci-6 alkyl group optionally substituted by halogen atom(s) ,

(b) a C3-10 cycloalkyl group,

(c) a Ci-6 alkyl-carbonyl group, and

(d) a C3-10 cycloalkyl-carbonyl group; and

R ⁴ is a hydrogen atom,

or a salt thereof.

[0073]

[7A] The compound of [1], wherein A is

(1) (i) a 5- or 6-membered aromatic heterocyclic group or (ii) a 4- to 6-membered non-aromatic heterocyclic group, each of which is optionally substituted by Ci-6 alkyl group (s) optionally substituted by halogen atoin(s), or

(2) a C3-10 cycloalkyl group optionally substituted by halogen atom (s) ;

B is a ring selected from

thiophene, thiazole, pyrazole, pyridine, naphthalene and 2,3- dihydrobenzofuran, wherein the ring is optionally substituted by Ci-6 alkyl group (s);

R ¹ is a hydrogen atom;

R ² is a hydrogen atom;

R ³ is

(1) a hydrogen atom,

(2) a Ci-6 alkyl group optionally substituted by substituent (s ) selected from

(a) a C3-10 cycloalkyl group,

(b) a Ce-14 aryl group optionally substituted by carboxy group (s),

(c) a 4- to 6-membered non-aromatic heterocyclic group optionally substituted by Ci-6 alkyl group (s) optionally substituted by substituent (s) selected from a carboxy group, and a Ce-i4 aryl group optionally substituted by carboxy group (s) , and

(d) a 5- or 6-membered aromatic heterocyclic group optionally substituted by amino group (s),

(3) a C3-10 cycloalkyl group optionally substituted by

substituent (s) selected from an amino group and a halogen atom or

(4) a 4- to 6-membered non-aromatic heterocyclic group

optionally substituted by substituent (s) selected from

(a) a Ci-6 alkyl group optionally substituted by halogen atom (s) ,

(b) a C3-10 cycloalkyl group,

(c) a Ci-6 alkyl-carbonyl group, and

(d) a C3-10 cycloalkyl-carbonyl group; and

R ⁴ is a hydrogen atom, or a salt thereof.

[0074]

[8] The compound of [1], wherein A is

(1) a piperidinyl group, an isoxazolyl group, a pyrazolyl group, a thiadiazolyl group, a thiazolyl group, a

tetrahydropyranyl group, an oxetanyl group, an oxadiazolyl group, a thienyl group, a pyridyl group or an oxazolyl group, each of which is optionally substituted by Ci-6 alkyl group (s) optionally substituted by halogen atom(s), or

(2) a C3-10 cycloalkyl group optionally substituted by halogen atom (s) ;

B is a ring selected from

thiophene, thiazole, pyrazole, pyridine, naphthalene and 2,3- dihydrobenzofuran, wherein the ring is optionally substituted by Ci-6 alkyl group (s);

R ¹ is a hydrogen atom;

R ² is a hydrogen atom;

R ³ is

(1) a hydrogen atom,

(2) a Ci-6 alkyl group optionally substituted by substituent (s) selected from

(a) a C3-10 cycloalkyl group,

(b) a C6-1 aryl group optionally substituted by carboxy group (s),

(c) a tetrahydropyranyl group or a piperidinyl group each optionally substituted by Ci-6 alkyl group (s) optionally substituted by substituent (s) selected from a carboxy group, and a C6-14 aryl group optionally substituted by carboxy group (s) , and

(d) an oxadiazolyl group optionally substituted by an amino group,

(3) a C3-10 cycloalkyl group optionally substituted by

substituent (s) selected from an amino group and a halogen atom or

(4) a tetrahydropyranyl group or a piperidinyl group . each optionally substituted by substituent (s) selected from

(a) a Ci-6 alkyl group optionally substituted by halogen atdm(s) ,

(b) a C3-10 cycloalkyl group,

(c) a Ci-6 alkyl-carbonyl group, and

(d) a C3-10 cycloalkyl-carbonyl group; and

R ⁴ is a hydrogen atom,

or a salt thereof.

[0075]

[8A] The compound of [1], wherein A is

(1) a piperidinyl group, an isoxazolyl group, a pyrazolyl group, a thiadiazolyl group, a thiazolyl group, a

tetrahydropyranyl group, an oxetanyl group, an oxadiazolyl group, a thienyl group, a pyridyl group or an oxazolyl group, each of which is optionally substituted by Ci-6 alkyl group (s) (preferably, 1 or 2 Ci-6 alkyl groups) optionally substituted by halogen atom(s) (preferably, 1 to 3 halogen atoms), or

(2) a cyclopropyl group, a cyclobutyl group, a cyclopentyl group or a cyclohexyl group, each of which is optionally substituted by halogen atom(s) (preferably, 1 or 2 halogen atoms) ;

B is a ring selected from

thiophene, thiazole, pyrazole, pyridine, naphthalene and 2,3- dihydrobenzofuran, wherein the ring is optionally substituted by Ci-6 alkyl group (s) (preferably, one Ci-6 alkyl group);

R ¹ is a hydrogen atom;

R ² is a hydrogen atom;

R ³ is

(1) a hydrogen atom,

(2) a Ci-6 alkyl group optionally substituted by substituent (s) (preferably, one substituent) selected from

(a) a cyclopropyl group or cyclobutyl group,

(b) a phenyl group optionally substituted by carboxy group (s) (preferably, one carboxy group),

(c) a tetrahydropyranyl group or a piperidinyl group each optionally substituted by Ci-6 alkyl group (s) (preferably, one Ci-6 alkyl group) optionally substituted by substituent ( s) (preferably, one substituent) selected from a carboxy group, and a phenyl group optionally substituted by carboxy group (s) (preferably, one carboxy group) , and

(d) an oxadiazolyl group optionally substituted by an amino group (one amino group) ,

(3) a cyclobutyl group or a cyclohexyl group each optionally substituted by substituent (s) (preferably, 1 or 2

substituents) selected from an amino group and a halogen atom, or

(4) a tetrahydropyranyl group or a piperidinyl group each optionally substituted by substituent (s) (preferably, one substituent) selected from

(a) a Ci-6 alkyl group optionally substituted by halogen atom(s) (preferably, 1 to 3 halogen atoms),

(b) a cyclopropyl group,

(c) a Ci-6 alkyl-carbonyl group, and

(d) a cyclopropyl-carbonyl group; and

R ⁴ is a hydrogen atom,

or a salt thereof.

[0076]

[9] The compound of [1], wherein A is

(1) a pyrazolyl group, a thiadiazolyl group or a

tetrahydropyranyl group, each optionally substituted by Ci-6 alkyl group(s) (preferably, 1 or 2 Ci-6 alkyl groups), or

(2) a cyclohexyl group optionally substituted by halogen atom(s) (preferably, 1 or 2 halogen atoms);

B is

a thiophene ring, which ring is optionally substituted by Ci-6 alkyl group (s) (preferably, one Ci-6 alkyl group);

R ¹ is a hydrogen atom;

R ² is a hydrogen atom;

R ³ is a cyclopropylmethyl group, a tetrahydropyranylmethyl group, a cyclobutylmethyl group, a cyclobutyl group or a tetrahydropyranyl group; and

R ⁴ is a hydrogen atom,

or a salt thereof.

[0077]

[9A] The compound of [1], wherein A is

a pyrazolyl group, a thiadiazolyl group or a tetrahydropyranyl group, each optionally substituted by Ci-6 alkyl group (s) (preferably, one Ci-6 alkyl group) ,

B is

a thiophene ring, which ring is optionally substituted by Ci-6 alkyl group (s) (preferably, one Ci-6 alkyl group);

R ¹ is a hydrogen atom;

R ² is a hydrogen atom;

R ³ is a cyclopropylmethyl group, a tetrahydropyranylmethyl group or a cyclobutyl group; and

R ⁴ is a hydrogen atom,

or a salt thereof.

[0078]

[10] The compound of [1], wherein A is

a pyrazolyl group, a thiadiazolyl group or a tetrahydropyranyl group, each optionally substituted by Ci-6 alkyl group (s)

(preferably, one Ci-6 alkyl group) ,

B is

a thiophene ring, which ring is optionally substituted by Ci-6 alkyl group (s) (preferably, one Ci-6 alkyl group);

R ¹ is a hydrogen atom;

R ² is a hydrogen atom;

R ³ is a cyclopropylmethyl group or. a cyclobutyl group; and R ⁴ is a hydrogen atom,

or a salt thereof.

[0079]

[11] 5- ( (1R, 2R) -2- ( (Cyclopropylmethyl) amino) cyclopropyl) -N- (tetrahydro-2H-pyran-4-yl) thiophene-3-carboxamide or a salt thereof.

[0080] [12] 4- ( (IS, 2R) -2- (Cyclobutylamino) cyclopropyl) -N- (5-methyl- 1, 3, 4-thiadiazol-2-yl) thiophene-2-carboxamide or a salt thereof.

[0081]

[13] 4- ( (IS, 2R) -2- (Cyclobutylamino) cyclopropyl) -5-methyl-N- (1- methyl-lH-pyrazol-4-yl) thiophene-2-carboxamide or a salt thereof .

[0082]

[14] A medicament comprising the compound of any one of [1] to [13], [7A], [8A] and [9A] or a salt thereof.

[0083]

[15] The medicament of [14], which is an LSDl inhibitor.

[0084]

[15A] The medicament of [14], which is a prophylactic or therapeutic agent for schizophrenia, Alzheimer's disease, Parkinson' s disease or Huntington' s disease (Huntington chorea) .

[0085]

[16] The medicament of [14] , which is a prophylactic or therapeutic agent for schizophrenia, developmental disorders, autistic spectrum disorders, Rett syndrome, Down's syndrome, Kabuki syndrome, fragile X syndrome, Kleefstra syndrome, neurofibromatosis type 1, Noonan syndrome, tuberous sclerosis, Alzheimer's disease, Parkinson's disease, spinocerebellar degeneration, Huntington' s disease, epilepsy or drug

dependence.

[0086]

[17] The compound of any one of [1] to [13], [7A] , [8A] and [9A] or a salt thereof for use in the prophylaxis or treatment of schizophrenia, developmental disorders, autistic spectrum disorders, Rett syndrome, Down's syndrome, Kabuki syndrome, fragile X syndrome, Kleefstra syndrome, neurofibromatosis type 1, Noonan syndrome, tuberous sclerosis, Alzheimer's disease, Parkinson's disease, spinocerebellar degeneration,

Huntington's disease, epilepsy or drug dependence. [0087]

[18] A method of inhibiting LSD1 in a mammal, comprising administering an effective amount of the compound of any one of [1] to [13], [7A], [8A] and [9A] or a salt thereof to the mammal .

[0088]

[19] A method for the prophylaxis or treatment of

schizophrenia, developmental disorders, autistic spectrum disorders, Rett syndrome, Down's syndrome, Kabuki syndrome, fragile X syndrome, Kleefstra syndrome, neurofibromatosis type 1, Noonan syndrome, tuberous sclerosis, Alzheimer's disease, Parkinson's disease, spinocerebellar degeneration,

Huntington's disease, epilepsy or drug dependence in a mammal, comprising administering an effective amount of the compound of any one of [1] to [13], [7A] , [8A] and [9A] or a salt thereof to the mammal.

[0089]

[20] Use of the compound of any one of [1] to [13], [7A] , [8A] and [9A] or a salt thereof in the production of a prophylactic or therapeutic agent for schizophrenia, developmental

disorders, autistic spectrum disorders, Rett syndrome, Down's syndrome, Kabuki syndrome, fragile X syndrome, Kleefstra syndrome, neurofibromatosis type 1, Noonan syndrome, tuberous sclerosis, Alzheimer's disease, Parkinson's disease,

spinocerebellar degeneration, Huntington's disease, epilepsy or drug dependence.

[0090]

[7B] The compound of [4], wherein B is a ring represented by the formula

[0091]

[0092]

wherein Y ¹ , Y ² and Υ ³ are each independently a carbon atom, a nitrogen atom, an oxygen atom or a sulfur atom; and

at least one of Y ¹ , Y ² and Y ³ is a nitrogen atom, an oxygen atom or a sulfur atom, which ring is optionally substituted, or a salt thereof.

[0093]

[8B] The compound of [1], wherein B is a ring selected from thiophene and thiazole, and the ring is optionally substituted, or a salt thereof.

[0094]

[9B] The compound of [1], [7B] or [8B] , wherein R ² is a

hydrogen atom and R ³ is a cyclopropylmethyl group, or a salt thereof .

[0095]

[10B] The compound of [1], [7B] or [8B] , wherein R ² is a

hydrogen atom and R ³ is a cyclobutyl group, or a salt thereof.

[0096]

[11B] The compound of [1], [7B] or [8B], wherein R ² is a

hydrogen atom and R ³ is a tetrahydropyranyl group, or a salt thereof.

[0097]

[12B] The compound of [1], [7B] or [8B] , wherein R ² is a

hydrogen atom and R ³ is a tetrahydropyranylmethyl group, or a salt thereof.

[0098]

[13B] The compound of [1], [7B] or [8B], wherein R ² is a

hydrogen atom and R ³ is an optionally substituted piperidinyl group (preferably, a piperidinyl group optionally substituted by one Ci-6 alkyl group optionally substituted by 1 to 3 halogen atoms), or a salt thereof.

[0099]

[14B] The compound of any one of [1] and [7B] to [13B],

wherein R ¹ is a hydrogen atom, or a salt thereof.

[0100]

[15B] The compound of any one of [1] and [7B] to [14B],. wherein A is

(1) a piperidinyl group, an isoxazolyl group, a pyrazolyl group, a thiadiazolyl group, a thiazolyl group or a

tetrahydropyranyl group, each optionally substituted by Ci-6 alkyl group (s) (preferably, one Ci-6 alkyl group) optionally substituted by halogen atom(s) (preferably, 1 to 3 halogen atoms) , or

(2) a cyclopentyl group or a cyclohexyl group, each optionally substituted by halogen atom(s) (preferably, 1 or 2 halogen atoms), or a salt thereof.

[0101]

The definition of each substituent used in the present specification is described in detail in the following. Unless otherwise specified, each substituent has the following definition.

In the present specification, examples of the "halogen ^~ atom" include fluorine, chlorine, bromine and iodine.

In the present specification, examples of the "Ci-6 alkyl group" include methyl, ethyl, propyl, isopropyl, butyl, isobutyl, sec-butyl, tert-butyl, pentyl, isopentyl, neopentyl, 1-ethylpropyl, hexyl, isohexyl, 1, 1-dimethylbutyl, 2,2- dimethylbutyl, 3, 3-dimethylbutyl and 2-ethylbutyl .

In the present specification, examples of the "optionally halogenated Ci-6 alkyl group" include a Ci-6 alkyl group

optionally having 1 to 7, preferably 1 to 5, halogen atoms. Specific examples thereof include methyl, chloromethyl, difluoromethyl, trichloromethyl, trifluoromethyl , ethyl, 2- bromoethyl, 2 , 2 , 2-trifluoroethyl, tetrafluoroethyl,

pentafluoroethyl, propyl, 2, 2-difluoropropyl, 3,3,3- trifluoropropyl, isopropyl, butyl, 4, 4, 4-trifluorobutyl, isobutyl, sec-butyl, tert-butyl, pentyl, isopentyl, neopentyl, 5, 5, 5-trifluoropentyl, hexyl and 6, 6, 6-trifluorohexyl .

In the present specification, examples of the "C2-6 alkenyl group" include ethenyl, 1-propenyl, 2-propenyl, 2- methyl-l-propenyl, 1-butenyl, 2-butenyl, 3-butenyl, 3-methyl- 2-butenyl, 1-pentenyl, 2-pentenyl, 3-pentenyl, 4-pentenyl, 4- methyl-3-pentenyl, 1-hexenyl, 3-hexenyl and 5-hexenyl.

In the present specification, examples of the "C2-6

alkynyl group" include ethynyl, 1-propynyl, 2-propynyl, 1- butynyl, 2-butynyl, 3-butynyl, 1-pentynyl, 2-pentynyl, 3- pentynyl, 4-pentynyl, 1-hexynyl, 2-hexynyl, 3-hexynyl, 4- hexynyl, 5-hexynyl and 4-methyl-2-pentynyl .

In the present specification, examples of the "C3-10

cycloalkyl group" include cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl, bicyclo [2.2.1] heptyl, bicyclo [2.2.2] octyl, bicyclo [3.2.1] octyl and adamantyl.

In the present specification, examples of the "optionally halogenated C3-10 cycloalkyl group" include a C3-10 cycloalkyl group optionally having 1 to 7, preferably 1 to 5, halogen atoms. Specific examples thereof include cyclopropyl, 2,2- difluorocyclopropyl, 2, 3-difluorocyclopropyl, cyclobutyl, difluorocyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl and cyclooctyl .

In the present specification, examples of the "C3-10

cycloalkenyl group" include cyclopropenyl, cyclobutenyl, cyclopentenyl, cyclohexenyl, cycloheptenyl and cyclooctenyl .

In the present specification, examples of the "C6-1 aryl group" include phenyl, 1-naphthyl, 2-naphthyl, 1-anthryl, 2- anthryl and 9-anthryl.

In the present specification, examples of the "C7-16

aralkyl group" include benzyl, phenethyl, naphthylmethyl and phenylpropyl .

[0102]

In the present specification, examples of the "Ci-6 alkoxy group" include methoxy, ethoxy, propoxy, isopropoxy, butoxy, isobutoxy, sec-butoxy, tert-butoxy, pentyloxy and hexyloxy.

In the present specification, examples of the "optionally halogenated Ci-6 alkoxy group" include a Ci-e alkoxy group

optionally having 1 to 7, preferably 1 to 5, halogen atoms.

Specific examples thereof include methoxy, difluoromethoxy, trifluoromethoxy, ethoxy, 2, 2, 2-trifluoroethoxy, propoxy, isopropoxy, butoxy, 4 , 4 , -trifluorobutoxy, isobutoxy, sec- butoxy, pentyloxy and hexyloxy.

In the present specification, examples of the "C3-10

cycloalkyloxy group" include cyclopropyloxy, cyclobutyloxy, cyclopentyloxy, cyclohexyloxy, cycloheptyloxy and

cyclooctyloxy.

In the present specification, examples of the "Ci-6

alkylthio group" include methylthio, ethylthio, propylthio, isopropylthio, butylthio, sec-butylthio, tert-butylthio, pentylthio and hexylthio.

In the present specification, examples of the "optionally halogenated Ci-6 alkylthio group" include a Ci-e alkylthio group optionally having 1 to 7, preferably 1 to 5, halogen atoms.

Specific examples thereof include methylthio,

difluoromethylthio, trifluoromethylthio, ethylthio, propylthio, isopropylthio, butylthio, 4, 4, 4-trifluorobutylthio, pentylthio and hexylthio.

In the present specification, examples of the "Ci-6 alkyl- carbonyl group" include acetyl, propanoyl, butanoyl, 2- methylpropanoyl, pentanoyl, 3-methylbutanoyl, 2-methylbutanoyl, 2, 2-dimethylpropanoyl, hexanoyl and heptanoyl.

In the present specification, examples of the "optionally halogenated Ci-6 alkyl-carbonyl group" include a Ci-6 alkyl- carbonyl group optionally having 1 to 7, preferably 1 to 5, halogen atoms. Specific examples thereof include acetyl, chloroacetyl, trifluoroacetyl, trichloroacetyl, propanoyl, butanoyl, pentanoyl and hexanoyl.

In the present specification, examples of the "Ci-6

alkoxy-carbonyl group" include methoxycarbonyl, ethoxycarbonyl, propoxycarbonyl, isopropoxycarbonyl, butoxycarbonyl,

isobutoxycarbonyl, sec-butoxycarbonyl, tert-butoxycarbonyl, pentyloxycarbonyl and hexyloxycarbonyl .

In the present specification, examples of the "C6-14 aryl- carbonyl group" include benzoyl, 1-naphthoyl and 2-naphth.oyl . In the present specification, examples of the "C7-16

aralkyl-carbonyl group" include phenylacetyl and

phenylpropionyl .

In the present specification, examples of the "5- to 14- membered aromatic heterocyclylcarbonyl group" include

nicotinoyl, isonicotinoyl, thenoyl and furoyl.

In the present specification, examples of the "3- to 14- membered non-aromatic heterocyclylcarbonyl group" include morpholinylcarbonyl, piperidinylcarbonyl and

pyrrolidinylcarbonyl .

[0103]

In the present specification, examples of the "mono- or di-Ci-6 alkyl-carbamoyl group" include methylcarbamoyl,

ethylcarbamoyl, dimethylcarbamoyl, diethylcarbamoyl and N- ethyl-N-methylcarbamoyl .

In the present specification, examples of the "mono- or di-C ₇ -i6 aralkyl-carbamoyl group" include benzylcarbamoyl and phenethylcarbamoyl .

In the present specification, examples of the "Ci-6

alkylsulfonyl group" include methylsulfonyl, ethylsulfonyl, propylsulfonyl, isopropylsulfonyl, butylsulfonyl, sec- butylsulfonyl and tert-butylsulfonyl .

In the present specification, examples of the "optionally halogenated Ci-6 alkylsulfonyl group" include a Ci-6

alkylsulfonyl group optionally having 1 to 7, preferably 1 to 5, halogen atoms. Specific examples thereof include

methylsulfonyl, difluoromethylsulfonyl,

trifluoromethylsulfonyl, ethylsulfonyl, propylsulfonyl,

isopropylsulfonyl, butylsulfonyl, 4 , , -trifluorobutylsulfonyl, pentylsulfonyl and hexylsulfonyl .

In the present specification, examples of the "C6-14

arylsulfonyl group" include phenylsulfonyl, 1-naphthylsulfonyl and 2-naphthylsulfonyl .

[0104]

In the present specification, examples of the "substituent" include a halogen atom, a cyano group, a nitro group, an optionally substituted hydrocarbon group, an

optionally substituted heterocyclic group, an acyl group, an optionally substituted amino group, an optionally substituted carbamoyl group, an optionally substituted thiocarbamoyl group, an optionally substituted sulfamoyl group, an optionally substituted hydroxy group, an optionally substituted sulfanyl (SH) group and an optionally substituted silyl group.

In the present specification, examples of the

"hydrocarbon group" (including "hydrocarbon group" of

"optionally substituted hydrocarbon group") include a Ci-6 alkyl group, a C2-6 alkenyl group, a C2-6 alkynyl group, a C3-10

cycloalkyl group, a C3-10 cycloalkenyl group, a C6-1 aryl group and a C7-16 aralkyl group.

[0105]

In the present specification, examples of the "optionally substituted hydrocarbon group" include a hydrocarbon group optionally having substituent (s) selected from the following substituent group A.

[substituent group A]

(1) a halogen atom,

(2) a nitro group,

(3) a cyano group,

(4) an oxo group,

(5) a hydroxy group,

(6) an optionally halogenated C1-6 alkoxy group,

(7) a C6-14 aryloxy group (e.g., phenoxy, naphthoxy) ,

(8) a C7-16 aralkyloxy group (e.g., benzyloxy) ,

(9) a 5- to 14-membered aromatic heterocyclyloxy group (e.g., pyridyloxy) ,

(10) a 3- to 14-membered non-aromatic heterocyclyloxy group (e.g., morpholinyloxy, piperidinyloxy) ,

(11) a Ci-6 alkyl-carbonyloxy group (e.g., acetoxy,

propanoyloxy) ,

(12) a C6-1 aryl-carbonyloxy group (e.g., benzoyloxy, 1- naphthoyloxy, 2-naphthoyloxy) ,

(13) a Ci-6 alkoxy-carbonyloxy group (e.g., methoxycarbonyloxy, ethoxycarbonyloxy, propoxycarbonyloxy, butoxycarbonyloxy) ,

(14) a mono- or di-Ci-6 alkyl-carbamoyloxy group (e.g.,

methylcarbamoyloxy, ethylcarbamoyloxy, dimethylcarbamoyloxy, diethylcarbamoyloxy) ,

(15) a C6-1 aryl-carbamoyloxy group (e.g., phenylcarbamoyloxy, naphthylcarbamoyloxy) ,

(16) a 5- to 14-membered aromatic heterocyclylcarbonyloxy group (e.g., nicotinoyloxy) ,

(17) a 3- to 14-membered non-aromatic heterocyclylcarbonyloxy group (e.g., morpholinylcarbonyloxy, piperidinylcarbonyloxy) ,

(18) an optionally halogenated Ci-6 alkylsulfonyloxy group (e.g., methylsulfonyloxy, trifluoromethylsulfonyloxy) ,

(19) a C6-14 arylsulfonyloxy group optionally substituted by a Ci-6 alkyl group (e.g., phenylsulfonyloxy, toluenesulfonyloxy) ,

(20) an optionally halogenated Ci-6 alkylthio group,

(21) a 5- to 14-membered aromatic heterocyclic group,

(22) a 3- to 14-membered non-aromatic heterocyclic group,

(23) a formyl group,

(24) a carboxy group,

(25) an optionally halogenated Ci-6 alkyl-carbonyl group,

(26) a C6-1 aryl-carbonyl group,

(27) a 5- to 14-membered aromatic heterocyclylcarbonyl group, (28) a 3- to 14-membered non-aromatic heterocyclylcarbonyl group,

(29) a Ci-6 alkoxy-carbonyl group,

(30) a C6-1 aryloxy-carbonyl group (e.g., phenyloxycarbonyl, 1- naphthyloxycarbonyl, 2-naphthyloxycarbonyl) ,

(31) a C7-16 aralkyloxy-carbonyl group (e.g., benzyloxycarbonyl, phenethyloxycarbonyl) ,

(32) a carbamoyl group,

(33) a thiocarbamoyl group,

(34) a mono- or di-Ci-6 alkyl-carbamoyl group,

(35) a C6-14 aryl-carbamoyl group (e.g., phenylcarbamoyl) , (36) a 5- to 14-membered aromatic heterocyclylcarbamoyl group (e.g., pyridylcarbamoyl, thienylcarbamoyl) ,

(37) a 3- to 14-membered non-aromatic heterocyclylcarbamoyl group (e.g., morpholinylcarbamoyl, piperidinylcarbamoyl) ,

(38) an optionally halogenated Ci-e alkylsulfonyl group,

(39) a C6-1 arylsulfonyl group,

(40) a 5- to 14-membered aromatic heterocyclylsulfonyl group (e.g., pyridylsulfonyl, thienylsulfonyl) ,

(41) an optionally halogenated Ci-6 alkylsulfinyl group,

(42) a C6-1 arylsulfinyl group (e.g., phenylsulfinyl, 1- naphthylsulfinyl, 2-naphthylsulfinyl ) ,

(43) a 5- to 14-membered aromatic heterocyclylsulfinyl group (e.g., pyridylsulfinyl, thienylsulfinyl) ,

(44) an amino group,

(45) a mono- or di-Ci-e alkylamino group (e.g., methylamino, ethylamino, propylamino, isopropylamino, butylamino,

dimethylamino, diethylamino, dipropylamino, dibutylamino, N- ethyl-N-methylamino) ,

(46) a mono- or di-Ce-14 arylamino group (e.g., phenylamino) , (47) a 5- to 14-membered aromatic heterocyclylamino group

(e.g., pyridylamino) ,

(48) a C ₇ -i6 aralkylamino group (e.g., benzylamino) ,

(49) a formylamino group,

(50) a Ci-6 alkyl-carbonylamino group (e.g., acetylamino, propanoylamino, butanoylamino) ,

(51) a (Ci-6 alkyl) (Ci-6 alkyl-carbonyl) amino group (e.g., N- acetyl-N-methylamino) ,

(52) a Ce-1 aryl-carbonylamino group (e.g., phenylcarbonylamino, naphthylcarbonylamino) ,

(53) a Ci-6 alkoxy-carbonylamino group (e.g.,

methoxycarbonylamino, ethoxycarbonylamino,

propoxycarbonylamino, butoxycarbonylamino, tert- butoxycarbonylamino) ,

(54) a C7-16 aralkyloxy-carbonylamino group (e.g.,

benzyloxycarbonylamino) , (55) a Ci-6 alkylsulfonylamino group (e.g., methylsulfonylamino, ethylsulfonylamino) ,

(56) a C6-1 arylsulfonylamino group optionally substituted by a Ci-6 alkyl group (e.g., phenylsulfonylamino,

toluenesulfonylamino) ,

(57) an optionally halogenated Ci-6 alkyl group,

(58) a C2-6 alkenyl group,

(59) a C2-6 alkynyl group,

(60) a C3-10 cycloalkyl group,

(61) a C3-10 cycloalkenyl group and

(62) a C6-1 aryl group.

[0106]

The number of the above-mentioned substituents in the "optionally substituted hydrocarbon group" is, for example, 1 to 5, preferably 1 to 3. When the number of the substituents is two or more, the respective substituents may be the same or different .

In the present specification, examples of the

"heterocyclic, group" (including "heterocyclic group" of

"optionally substituted heterocyclic group") include (i) an aromatic heterocyclic group, (ii) a non-aromatic heterocyclic group and (iii) a 7- to 10-membered bridged heterocyclic group, each containing, as a ring-constituting atom besides carbon atom, 1 to 4 hetero atoms selected from a nitrogen atom, a sulfur atom and an oxygen atom.

[0107]

In the present specification, examples of the "aromatic heterocyclic group" (including "5- to 14-membered aromatic heterocyclic group") include a 5- to 14-membered (preferably 5- to 10-membered) aromatic heterocyclic group containing, as a ring-constituting atom besides carbon atom, 1 to 4 hetero atoms selected from a nitrogen atom, a sulfur atom and an oxygen atom.

Preferable examples of the "aromatic heterocyclic group" include 5- or 6-membered monocyclic aromatic heterocyclic groups such as thienyl, furyl, pyrrolyl, imidazolyl, pyrazolyl, thiazolyl, isothiazolyl, oxazolyl, isoxazolyl, pyridyl,

pyrazinyl, pyrimidinyl, pyridazinyl, 1, 2, 4-oxadiazolyl, 1,3,4- oxadiazolyl, 1, 2, 4-thiadiazolyl, 1, 3, 4-thiadiazolyl, triazolyl, tetrazolyl, triazinyl and the like; and

8- to 1 -membered fused polycyclic (preferably bi or

tricyclic) aromatic heterocyclic groups such as

benzothiophenyl, benzofuranyl, benzimidazolyl, benzoxazolyl, benzisoxazolyl, benzothiazolyl, benzisothiazolyl,

benzotriazolyl, imidazopyridinyl, thienopyridinyl,

furopyridinyl, pyrrolopyridinyl, pyrazolopyridinyl,

oxazolopyridinyl, thiazolopyridinyl, imidazopyrazinyl,

imidazopyrimidinyl, thienopyrimidinyl, furopyrimidinyl,

pyrrolopyrimidinyl, pyrazolopyrimidinyl, oxazolopyrimidinyl, thiazolopyrimidinyl, pyrazolotriazinyl, naphtho [2 , 3-b] thienyl , phenoxathiinyl, indolyl, isoindolyl, lH-indazolyl, purinyl, isoquinolyl, quinolyl, phthalazinyl, naphthyridinyl,

quinoxalinyl, quinazolinyl, cinnolinyl, carbazolyl, β- carbolinyl, phenanthridinyl, acridinyl, phenazinyl,

phenothiazinyl, phenoxazinyl and the like.

[0108]

In the present specification, examples of the "non- aromatic heterocyclic group" (including "3- to 14-membered non-aromatic heterocyclic group") include a 3- to 14-membered (preferably 4- to 10-membered) non-aromatic heterocyclic group containing, as a ring-constituting atom besides carbon atom, 1 to 4 hetero atoms selected from a nitrogen atom, a sulfur atom and an oxygen atom.

Preferable examples of the "non-aromatic heterocyclic group" include 3- to 8-membered monocyclic non-aromatic

heterocyclic groups such as aziridinyl, oxiranyl, thiiranyl, azetidinyl, oxetanyl, thietanyl, tetrahydrothienyl,

tetrahydrofuranyl, pyrrolinyl, pyrrolidinyl, imidazolinyl , imidazolidinyl, oxazolinyl, oxazolidinyl, pyrazolinyl,

pyrazolidinyl, thiazolinyl, thiazolidinyl, tetrahydroisothiazolyl, tetrahydrooxazolyl,

tetrahydroisooxazolyl, piperidinyl, piperazinyl,

tetrahydropyridinyl, dihydropyridinyl, dihydrothiopyranyl, tetrahydropyrimidinyl, tetrahydropyridazinyl, dihydropyranyl, tetrahydropyranyl, tetrahydrothiopyranyl, morpholinyl,

thiomorpholinyl, azepanyl, diazepanyl, azepinyl, oxepanyl, azocanyl, diazocanyl and the like; and

9- to 14-membered fused polycyclic (preferably bi or

tricyclic) non-aromatic heterocyclic groups such as

dihydrobenzofuranyl, dihydrobenzimidazolyl,

dihydrobenzoxazolyl, dihydrobenzothiazolyl,

dihydrobenzisothiazolyl, dihydronaphtho [2, 3-b] thienyl,

tetrahydroisoquinolyl, tetrahydroquinolyl, 4H-quinolizinyl, indolinyl, isoindolinyl, tetrahydrothieno [2, 3-c] pyridinyl, tetrahydrobenzazepinyl, tetrahydroquinoxalinyl,

tetrahydrophenanthridinyl, hexahydrophenothiazinyl,

hexahydrophenoxazinyl, tetrahydrophthalazinyl,

tetrahydronaphthyridinyl, tetrahydroquinazolinyl,

tetrahydrocinnolinyl, tetrahydrocarbazolyl, tetrahydro-β- carbolinyl, tetrahydroacrydinyl, tetrahydrophenazinyl,

tetrahydrothioxanthenyl, octahydroisoquinolyl and the like.

[0109]

In the present specification, preferable examples of the "7- to 10-membered bridged heterocyclic group" include

quinuclidinyl and 7-azabicyclo [2.2.1] heptanyl .

In the present specification, examples of the "nitrogen- containing heterocyclic group" include a "heterocyclic group" containing at least one nitrogen atom as a ring-constituting atom.

In the present specification, examples of the "optionally substituted heterocyclic group" include a heterocyclic group optionally having substituent (s) selected from the

aforementioned substituent group A.

The number of the substituents in the "optionally substituted heterocyclic group" is, for example, 1 to 3. When the number of the substituents is two or more, the respective substituents may be the same or different.

[0110]

In the present specification, examples of the "acyl group" include a formyl group, a carboxy group, a carbamoyl group, a thiocarbamoyl group, a sulfino group, a sulfo group, a sulfamoyl group and a phosphono group, each optionally having "1 or 2 substituents selected from a Ci-6 alkyl group, a C2-6 alkenyl group, a C3-10 cycloalkyl group, a C3-10 cycloalkenyl group, a C6-14 aryl group, a C7-16 aralkyl group, a 5- to 14- membered aromatic heterocyclic group and a 3- to 14-membered non-aromatic heterocyclic group, each of which optionally has 1 to 3 substituents selected from a halogen atom, an

optionally halogenated Ci-6 alkoxy group, a hydroxy group, a nitro group, a cyano group, an amino group and a carbamoyl group" .

Examples of the "acyl group" also include a hydrocarbon- sulfonyl group, a heterocyclylsulfonyl group, a hydrocarbon- sulfinyl group and a heterocyclylsulfinyl group.

Here, the hydrocarbon-sulfonyl group means a hydrocarbon group-bonded sulfonyl group, the heterocyclylsulfonyl group means a heterocyclic group-bonded sulfonyl group, the

hydrocarbon-sulfinyl group means a hydrocarbon group-bonded sulfinyl group and the heterocyclylsulfinyl group means a heterocyclic group-bonded sulfinyl group.

Preferable examples of the "acyl group" include a formyl group, a carboxy group, a Ci-6 alkyl-carbonyl group, a C2-6

alkenyl-carbonyl group (e.g., crotonoyl) , a C3-10 cycloalkyl- . carbonyl group (e.g., cyclobutanecarbonyl,

cyclopentanecarbonyl, cyclohexanecarbonyl,

cycloheptanecarbonyl) , a C3-10 cycloalkenyl-carbonyl group (e.g., 2-cyclohexenecarbonyl) , a Ce-u aryl-carbonyl group, a C7-16

aralkyl-carbonyl group, a 5- to 14-membered aromatic

heterocyclylcarbonyl group, a 3- to 14-membered non-aromatic heterocyclylcarbonyl group, a Ci-6 alkoxy-carbonyl group, a Ce-u aryloxy-carbonyl group (e.g., phenyloxycarbonyl,

naphthyloxycarbonyl) , a C ₇ -i6 aralkyloxy-carbonyl group (e.g., benzyloxycarbonyl, phenethyloxycarbonyl) , a carbamoyl group, a mono- or di-Ci-6 alkyl-carbamoyl group, a mono- or di-C2-6

alkenyl-carbamoyl group (e.g., diallylcarbamoyl) , a mono- or di-C3-io cycloalkyl-carbamoyl group (e.g., cyclopropylcarbamoyl) , a mono- or di-C6-i ₄ aryl-carbamoyl group (e.g., phenylcarbamoyl) , a mono- or di-C ₇ -i6 aralkyl-carbamoyl group, a 5- to 14-membered aromatic heterocyclylcarbamoyl group (e.g., pyridylcarbamoyl) , a thiocarbamoyl group, a mono- or di-Ci-6 alkyl-thiocarbamoyl group (e.g., methylthiocarbamoyl, N-ethyl-N- methylthiocarbamoyl) , a mono- or di-C2-6 alkenyl-thiocarbamoyl group (e.g., diallylthiocarbamoyl) , a mono- or di-C3-io

cycloalkyl-thiocarbamoyl group (e.g., cyclopropylthiocarbamoyl, cyclohexylthiocarbamoyl) , a mono- or di-C6-i4 aryl-thiocarbamoyl group (e.g., phenylthiocarbamoyl) , a mono- or di-C ₇ -i6 aralkyl- thiocarbamoyl group (e.g., benzylthiocarbamoyl,

phenethylthiocarbamoyl) , a 5- to 14-membered aromatic

heterocyclylthiocarbamoyl group (e.g., pyridylthiocarbamoyl) , a sulfino group, a Ci-6 alkylsulfinyl group (e.g.,

methylsulfinyl, ethylsulfinyl) , a sulfo group, a Ci-6

alkylsulfonyl group, a C6-1 arylsulfonyl group, a phosphono group and a mono- or di-Ci-6 alkylphosphono group (e.g.,

dimethylphosphono, diethylphosphono, diisopropylphosphono, dibutylphosphono) .

[0111]

In the present specification, examples of the "optionally substituted amino group" include an amino group optionally having "1 or 2 substituents selected from a Ci-6 alkyl group, a C ₂ -6 alkenyl group, a C3-10 cycloalkyl group, a C6-H aryl group, a C7-16 aralkyl group, a Ci-6 alkyl-carbonyl group, a C6-1 aryl- carbonyl group, a C7-16 aralkyl-carbonyl group, a 5- to 14- membered aromatic heterocyclylcarbonyl group, a 3- to 14- membered non-aromatic heterocyclylcarbonyl group, a Ci-6 alkoxy- carbonyl group, a 5- to 14-membered aromatic heterocyclic group, a carbamoyl group, a mono- or di-Ci-6 alkyl-carbamoyl group, a mono- or di-C ₇ -i6 aralkyl-carbamoyl group, a Ci-6

alkylsulfonyl group and a Ce-u arylsulfonyl group, each of which optionally has 1 to 3 substituents selected from

substituent group A".

Preferable examples of the optionally substituted amino group include an amino group, a mono- or di- (optionally halogenated Ci-6 alkyl) amino group (e.g., methylamino,

trifluoromethylamino, dimethylamino, ethylamino, diethylamino, propylamino, dibutylamino) , a mono- or di-C ₂ -6 alkeriylamino group (e.g., diallylamino) , a mono- or di-C3-io cycloalkylamino group (e.g., cyclopropylamino, cyclohexylamino) , a mono- or di-C6-i arylamino group (e.g., phenylamino) , a mono- or di-C ₇ -i6 aralkylamino group (e.g., benzylamino, dibenzylamino) , a mono- or di- (optionally halogenated Ci-6 alkyl) -carbonylamino group (e.g., acetylamino, propionylamino) , a mono- or di-C6-i4 aryl- carbonylamino group (e.g., benzoylamino) , a mono- or di-C ₇ -ie aralkyl-carbonylamino group (e.g., benzylcarbonylamino) , a mono- or di-5- to 14-membered aromatic

heterocyclylcarbonylamino group (e.g., nicotinoylamino, isonicotinoylamino) , a mono- or di-3- to 14-membered non- aromatic heterocyclylcarbonylamino group (e.g.,

• piperidinylcarbonylamino) , a mono- or di-Ci-6 alkoxy- carbonylamino group (e.g., tert-butoxycarbonylamino) , a- 5- to 14-membered aromatic heterocyclylamino group (e.g.,

pyridylamino) , a carbamoylamino group, a (mono- or di-Ci-6 alkyl-carbamoyl) amino group (e.g., methylcarbamoylamino) , a (mono- or di-C ₇ -i6 aralkyl-carbamoyl ) amino group (e.g.,

benzylcarbamoylamino) , a Ci-6 alkylsulfonylamino group (e.g., methylsulfonylamino, ethylsulfonylamino) , a C6-1

, arylsulfonylamino group (e.g., phenylsulfonylamino) , a (Ci-6 alkyl) (Ci-6 alkyl-carbonyl ) amino group (e.g., N-acetyl-N- methylamino) and a (Ci-6 alkyl) (C6-1 aryl-carbonyl) amino group (e.g. , N-benzoyl-N-methylamino) .

[0112] In the present specification, examples of the "optionally substituted carbamoyl group" include a carbamoyl group

optionally having "1 or 2 substituents selected from a Ci-6 alkyl group, a C2-6 alkenyl group, a C3-10 cycloalkyl group, a Ce- 1 aryl group, a C ₇ -i6 aralkyl group, a Ci-6 alkyl-carbonyl group, a Ce-1 aryl-carbonyl group, a C ₇ -i6 aralkyl-carbonyl group, a 5- to 14-membered aromatic heterocyclylcarbonyl group, a 3- to 14-membered non-aromatic heterocyclylcarbonyl group, a Ci-6 alkoxy-carbonyl group, a 5- to 14-membered aromatic

heterocyclic group, a carbamoyl group, a mono- or di-Ci-6 alkyl- carbamoyl group and a mono- or di-C ₇ -i6 aralkyl-carbamoyl group, each of which optionally has 1 to 3 substituents selected from substituent group A".

Preferable examples of the optionally substituted

carbamoyl group include a carbamoyl group, a mono- or di-Ci-6 alkyl-carbamoyl group, a mono- or di-C2-6 alkenyl-carbamoyl group (e.g., diallylcarbamoyl) , a mono- or di-C ₃ -io cycloalkyl- carbamoyl group (e.g., cyclopropylcarbamoyl,

cyclohexylcarbamoyl) , a mono- or di-C6-i4 aryl-carbamoyl group (e.g., phenylcarbamoyl) , a mono- or di-C ₇ -i6 aralkyl-carbamoyl group, a mono- or di-Ci-6 alkyl-carbonyl-carbamoyl group (e.g., acetylcarbamoyl, propionylcarbamoyl) , a mono- or di-C6-i4 aryl- carbonyl-carbamoyl group (e.g., benzoylcarbamoyl ) and a 5- to 14-membered aromatic heterocyclylcarbamoyl group (e.g., pyridylcarbamoyl) .

[0113]

In the present specification, examples of the "optionally substituted thiocarbamoyl group" include a thiocarbamoyl group optionally, having "1 or 2 substituents selected from a Ci-6 alkyl group, a C2-6 alkenyl group, a C3-10 cycloalkyl group, a Ce- 14 aryl group, a C ₇ -i6 aralkyl group, a Ci-6 alkyl-carbonyl group, a C6-14 aryl-carbonyl group, a C ₇ -i6 aralkyl-carbonyl group, a 5- to 14-membered aromatic heterocyclylcarbonyl group, a 3- to 14-membered non-aromatic heterocyclylcarbonyl group, a Ci-6 alkoxy-carbonyl group, a 5- to 14-membered aromatic heterocyclic group, a carbamoyl group, a mono- or di-Ci-6 alkyl- carbamoyl group and a mono- or di-C ₇ -i6 aralkyl-carbamoyl group, each of which optionally has 1 to 3 substituents selected from substituent group A".

Preferable examples of the optionally substituted thiocarbamoyl group include a thiocarbamoyl group, a mono- or di-Ci-6 alkyl-thiocarbamoyl group (e.g., methylthiocarbamoyl, ethylthiocarbamoyl, dimethylthiocarbamoyl,

diethylthiocarbamoyl, N-ethyl-N-methylthiocarbamoyl) , a monoor di-C ₂ -6 alkenyl-thiocarbamoyl group (e.g.,

diallylthiocarbamoyl) , a mono- or di-C3-io cycloalkyl- thiocarbamoyl group (e.g., cyclopropylthiocarbamoyl,

cyclohexylthiocarbamoyl) , a mono- or di-Ce-i4 aryl-thiocarbamoyl group (e.g., phenylthiocarbamoyl) , a mono- or di-C ₇ -i6 aralkyl- thiocarbamoyl group (e.g., benzylthiocarbamoyl,

phenethylthiocarbamoyl) , a mono- or di-Ci-6 alkyl-carbonyl- thiocarbamoyl group (e.g., acetylthiocarbamoyl ,

propionylthiocarbamoyl) , a mono- or di-C6-i4 aryl-carbonyl- thiocarbamoyl group (e.g., benzoylthiocarbamoyl) and a 5- to. 14-membered aromatic heterocyclylthiocarbamoyl group (e.g., pyridylthiocarbamoyl) .

[0114]

In the present specification, examples of the "optionally substituted sulfamoyl group" include a sulfamoyl group

optionally having "1 or 2 substituents selected from a Ci-6 alkyl group, a C2-6 alkenyl group, a C3-10 cycloalkyl group, a C6- 14 aryl group, a C-i6 aralkyl group, a Ci-6 alkyl-carbonyl group, a C6-14 aryl-carbonyl group, a C ₇ -i6 aralkyl-carbonyl group, a 5- to 14-membered aromatic heterocyclylcarbonyl group, a 3- to 14-membered non-aromatic heterocyclylcarbonyl group, a Ci-6 alkoxy-carbonyl group, a 5- to 14-membered aromatic

heterocyclic group, a carbamoyl group, a mono- or di-Ci-6 alkyl- carbamoyl group and a mono- or di-C ₇ -i6 aralkyl-carbamoyl group, each of which optionally has 1 to 3 substituents selected from substituent group A". Preferable examples of the optionally substituted sulfamoyl group include a sulfamoyl group, a mono- or di-Ci-6 alkyl-sulfamoyl group (e.g., methylsulfamoyl, ethylsulfamoyl, dimethylsulfamoyl, diethylsulfamoyl, N-ethyl-N- 5 methylsulfamoyl) , a mono- or di-C2-6 alkenyl-sulfamoyl group

(e.g., diallylsulfamoyl) , a mono- or di-C ₃ -io cycloalkyl- sulfamoyl group (e.g., cyclopropylsulfamoyl,

cyclohexylsulfamoyl) , a mono- or di-C6-i4 aryl-sulfamoyl group (e.g., phenylsulfamoyl) , a mono- or di-C ₇ -i6 aralkyl-sulfamoyl

10 group (e.g., benzylsulfamoyl, phenethylsulfamoyl ) , a mono- or di-Ci-6 alkyl-carbonyl-sulfamoyl group (e.g., acetylsulfamoyl, propionylsulfamoyl) , a mono- or di-C6-i aryl-carbonyl-sulfamoyl group (e.g., benzoylsulfamoyl ) and a 5- to 14-membered

aromatic heterocyclylsulfamoyl group (e.g., pyridylsulfamoyl) .

15 [0115]

In the present specification, examples of the "optionally substituted hydroxy group" include a hydroxyl group optionally having "a substituent selected from a Ci-6 alkyl group, a C2-6 alkenyl group, a C3-10 cycloalkyl group, a C6-14 aryl group, a C ₇ -

20 16 aralkyl group, a Ci-6 alkyl-carbonyl group, a C6-14 aryl- carbonyl group, a C ₇ -i6 aralkyl-carbonyl group, a 5- to 14- membered aromatic heterocyclylcarbonyl group, a 3- to 14- membered non-aromatic heterocyclylcarbonyl group, a Ci-6 alkoxy- carbonyl group, a 5- to 14-membered aromatic heterocyclic

25 group, a carbamoyl group, a mono- or di-Ci-6 alkyl-carbamoyl

group, a mono- or di-C ₇ -i6 aralkyl-carbamoyl group, a Ci-6

alkylsulfonyl group and a Ce-14 arylsulfonyl group, each of which optionally has 1 to 3 substituents selected from

substituent group A".

30 Preferable examples of the optionally substituted hydroxy group include a hydroxy group, a Ci-6 alkoxy group, a C2-6

alkenyloxy group (e.g., allyloxy, 2-butenyloxy, 2-pentenyloxy, 3-hexenyloxy) , a C3-10 cycloalkyloxy group (e.g., cyclohexyloxy) , a C6-1 aryloxy group (e.g., phenoxy, naphthyloxy) , a C ₇ -i6

35 aralkyloxy group (e.g., benzyloxy, phenethyloxy) , a Ci-6 alkyl- carbonyloxy group (e.g., acetyloxy, propionyloxy, butyryloxy, isobutyryloxy, pivaloyloxy) , a C6-1 aryl-carbonyloxy group

(e.g., benzoyloxy) , a C ₇ -i6 aralkyl-carbonyloxy group (e.g., benzylcarbonyloxy) , a 5- to 14-membered aromatic

heterocyclylcarbonyloxy group (e.g., nicotinoyloxy) , a 3- to 14-membered non-aromatic heterocyclylcarbonyloxy group (e.g., piperidinylcarbonyloxy) , a Ci-6 alkoxy-carbonyloxy group (e.g., tert-butoxycarbonyloxy) , a 5- to 14-membered aromatic

heterocyclyloxy group (e.g., pyridyloxy) , a carbamoyloxy group, a Ci-6 alkyl-carbamoyloxy group (e.g., methylcarbamoyloxy) , a

C ₇ -i6 aralkyl-carbamoyloxy group (e.g., benzylcarbamoyloxy) , a Ci-6 alkylsulfonyloxy group (e.g., methylsulfonyloxy,

ethylsulfonyloxy) and a Ce-14 arylsulfonyloxy group (e.g., phenylsulfonyloxy) .

[0116]

In the present specification, examples of the "optionally substituted sulfanyl group" include a sulfanyl group

optionally having "a substituent selected from a Ci-6 alkyl group, a C2-6 alkenyl group, a C3-10 cycloalkyl group, a C6-1

aryl group, a C7-16 aralkyl group, a Ci-6 alkyl-carbonyl group, a Ce-1 aryl-carbonyl group and a 5- to 14-membered aromatic heterocyclic group, each of which optionally has 1 to 3

substituents selected from substituent group A" and a

halogenated sulfanyl group.

Preferable examples of the optionally substituted

sulfanyl group include a sulfanyl (-SH) group, a Ci-6 alkylthio group, a C2-6 alkenylthio group (e.g., allylthio, 2-butenylthio, 2-pentenylthio, 3-hexenylthio) , a C3-10 cycloalkylthio group (e.g., cyclohexylthio) , a C6-1 arylthio group (e.g., phenylthio, naphthylthio) , a C7-16 aralkylthio group (e.g., benzylthio, phenethylthio) , a Ci-6 alkyl-carbonylthio group (e.g.,

acetylthio, propionylthio, butyrylthio, isobutyrylthio,

pivaloylthio) , a C6-1 aryl-carbonylthio group (e.g.,

benzoylthio) , a 5- to 14-membered aromatic heterocyclylthio group (e.g., pyridylthio) and a halogenated thio group (e.g., pentafluorothio) .

[0117]

In the present specification, examples of the "optionally substituted silyl group" include a silyl group optionally having "1 to 3 substituents selected from a Ci-6 alkyl group, a C2-6 alkenyl group, a C3-10 cycloalkyl group, a Ce-1 aryl group and a C ₇ -i6 aralkyl group, each of which optionally has 1 to 3 substituents selected from substituent group A".

Preferable examples of the optionally substituted silyl group include a tri-Ci-6 alkylsilyl group (e.g., trimethylsilyl, tert-butyl (dimethyl) silyl) .

[0118]

In the present specification, examples of the "5- or 6- membered aromatic heterocycle" include a 5- or 6-membered aromatic heterocycle containing, as a ring-constituting atom besides carbon atoms, 1 to 4 hetero atoms selected from a nitrogen atom, a sulfur atom and an oxygen atom. Preferable examples of the "5- or 6-membered aromatic heterocycle" include 5- or 6-membered aromatic heterocycles such as

thiophene, furan, pyrrole, imidazole, pyrazole, thiazole, isothiazole, oxazole, isoxazole, pyridine, pyrazine,

pyrimidine, pyridazine, 1, 2, 4-oxadiazole, 1, 3, 4-oxadiazole, 1, 2, 4-thiadiazole, 1, 3, 4-thiadiazole, triazole, triazine and the like.

[0119]

A is an optionally substituted heterocyclic group, or an optionally substituted hydrocarbon group.

[0120]

A is preferably

(1) an optionally substituted heterocyclic group, or

(2) an optionally substituted C3-10 cycloalkyl group.

[0121]

A is more preferably

(1) a heterocyclic group (preferably, (i) a 5- or 6-membered aromatic heterocyclic group or (ii) a 4- to 6-membered non- aromatic heterocyclic group, each containing, as a ring- constituting atom besides carbon atoms, 1 to 4 hetero atoms selected from a nitrogen atom, a sulfur atom and an oxygen atom) (e.g., piperidinyl group, isoxazolyl group, pyrazolyl group, thiadiazolyl group, thiazolyl group, tetrahydropyranyl group, oxetanyl group, oxadiazolyl group, thienyl group, pyridyl group, oxazolyl group) optionally substituted by Ci-6 alkyl group (s) (preferably, 1 or 2 Ci-6 alkyl groups) optionally substituted by halogen atom(s) (preferably, 1 to 3 halogen atoms) , or

(2) a C3-10 cycloalkyl group (e.g., cyclopropyl group,

cyclobutyl group, cyclopentyl group, cyclohexyl group)

optionally substituted by halogen atom(s) (preferably, 1 or 2 halogen atoms) .

[0122]

A is more preferably

(1) a piperidinyl group, an isoxazolyl group, a pyrazolyl group, a thiadiazolyl group, a thiazolyl group or a

tetrahydropyranyl group, each optionally substituted by Ci-6 alkyl group (s) (preferably, one Ci-6 alkyl group) optionally substituted by halogen atom(s) (preferably, 1 to 3 halogen atoms) , or

(2) a cyclopentyl group or a cyclohexyl group, each optionally substituted by halogen atom(s) (preferably, 1 or 2 halogen atoms) .

[0123]

A is particularly preferably

(1) a pyrazolyl group, a thiadiazolyl group or a

tetrahydropyranyl group, each optionally substituted by Ci-e alkyl group (s) . (preferably, one Ci-6 alkyl group), or

(2) a cyclopentyl group or a cyclohexyl group, each optionally substituted by halogen atom(s) (preferably, 1 or 2 halogen atoms) .

[0124]

B is a ring selected from (1) a 5- or 6-membered aromatic heterocycle optionally fused with an optionally substituted 5- or 6-membered ring, and

(2) a benzene ring fused with an optionally substituted 5- or 6-membered ring,

and the ring represented by B is optionally substituted and binds, via two adjacent carbon atoms with one atom in between, to a group represented by the formula

[0125]

[0126]

and a group represented by the formula

[0127]

Examples of the "optionally substituted 5- or 6-membered ring" include a 5- or 6-membered ring optionally having substituent (s) selected from the aforementioned substituent group A.

[0129]

The number of the substituents for the "optionally substituted 5- or 6-membered ring" is, for example, 1 to 3. When the number of the substituents is two or more, respective substituents may be the same or different.

[0130]

The substituent that B optionally has is, for example, a substituent selected from the aforementioned substituent group A.

[0131] The number of the substituents that B optionally has is, for example, 1 to 3, preferably 1 or 2, more preferably 1. When the number of the substituents is two or more, respective substituents may be the same or different.

[0132]

B is preferably a ring selected from

(1) a 5- or 6-membered aromatic heterocycle, and

(2) a benzene ring fused with an optionally substituted 5- or 6-membered ring,

and the ring represented by B is optionally substituted, via two adjacent carbon atoms with one atom in between, and binds to a group represented by the formula (II) , and a group represented by the formula (III) .

[0133]

In the formula

[0134]

[0135]

B is more preferably, a ring selected from

[0136]

[0137] wherein

X ¹ , X ² , X ³ and X ⁴ are each independently a carbon atom or a nitrogen atom;

at least one of X ¹ , X ² , X ³ and X ⁴ is a nitrogen atom;

Y ¹ , Y ² and Y ³ are each independently a carbon atom, a nitrogen atom, an oxygen atom or a sulfur atom;

at least one of Y ¹ , Y ² and Y ³ is a nitrogen atom, an oxygen atom or a sulfur atom; and

Z ¹ , Z ² , Z ³ and Z ⁴ are each independently a carbon atom or a nitrogen atom, which ring is optionally substituted.

[0138]

Preferable examples of B include a ring selected from

[0139]

[0140]

The ring is optionally substituted by 1 or 2 (preferably 1) Ci-6 alkyl groups.

[0141]

B is more preferably a ring represented by the formula [0142]

[0143]

wherein

Y ¹ , Y ² and Υ ³ are each independently a carbon atom, a nitrogen atom, an oxygen atom or a sulfur atom; and

at least one of Y ¹ , Y ² and Y ³ is a nitrogen atom, an oxygen atom or a sulfur atom, and the ring is optionally substituted.

[0144]

B is particularly preferably a ring selected from

thiophene and thiazole, and the ring is optionally substituted.

[0145]

Another preferable embodiment of B is thiophene or

thiazole each optionally substituted by 1 or 2 (preferably 1) Ci-6 alkyl groups.

[0146]

A still another preferable embodiment of B is thiophene optionally substituted by one Ci-6 alkyl group.

[0147]

A yet another preferable embodiment of B is

[0148]

[0149]

wherein R ⁷ is a hydrogen atom or a Ci-6 alkyl group.

[0150]

R ¹ , R ² , R ³ and R ⁴ are each independently a hydrogen atom, an optionally substituted hydrocarbon group or an optionally substituted heterocyclic group.

[0151]

R ¹ is preferably a hydrogen atom or an optionally substituted Ci-6 alkyl group, more preferably, a hydrogen atom or a Ci-6 alkyl group, particularly preferably a hydrogen atom.

[0152]

A and R ¹ are optionally bonded with each other to form, together with the adjacent nitrogen atom optionally

substituted cyclic group.

[0153]

Examples of the "cyclic group" of the "optionally

substituted cyclic group", which is formed, together with the adjacent nitrogen atom, by A and R ¹ bonded to each other

include a 4- to 10-membered heterocyclic group containing one nitrogen atom as a ring-constituting atom besides carbon atom, and optionally further containing one hetero atom selected from a nitrogen atom, a sulfur atom and an oxygen atom, and the like. Examples of the "4- to 10-membered heterocyclic group" include azetidin-l-yl, pyrrolidin-l-yl, pyrrolin-l-yl, pyrazolin-l-yl, imidazolin-l-yl, thiazolidin-3-yl, oxazolidin-

3-yl, isothiazolidin-2-yl, isoxazolidin-2-yl, thiazolin-3-yl, oxazolin-3-yl, isothiazolin-2-yl, isoxazolin-2-yl, piperidin- 1-yl, piperazin-l-yl, morpholin-4-yl , thiomorpholin-4-yl, azepan-l-yl, diazepan-l-yl, 1, 4-oxazepan-4-yl, 1 , 4-thiazepan-

4-yl, 5, 7-dihydro-6H-pyrrolo [3, -b] pyridin-6-yl and the like.

Examples of the substituent of the "optionally

substituted cyclic group", which is formed, together with the adjacent nitrogen atom, by A and R ¹ bonded to each other, include substituents selected from the aforementioned

substituent group A.

The number of the substituents in "optionally substituted cyclic group", which is formed, together with the adjacent nitrogen atom, by A and R ¹ bonded to each other, is, for

example, 1 to 3. When the number of the substituents is two or more, the respective substituents may be the same or different.

[0154]

Preferable examples of the "optionally substituted cyclic group", which is formed, together with the adjacent nitrogen atom, by A and R ¹ bonded to each other include a 4 to 10- membered heterocyclic group containing one nitrogen atom as a ring-constituting atom besides carbon atoms, and optionally further containing one hetero atom selected from a nitrogen atom, a sulfur atom and an oxygen atom (e.g., azetidin-l-yl, pyrrolidin-l-yl, piperidin-l-yl , 5, 7-dihydro-6H-pyrrolo [3, 4- b] pyridin-6-yl) , and the heterocyclic group is optionally substituted by 1 to 3 substituents selected from a hydroxy group and a cyano group, .

[0155]

As regards -IS^R ¹ ) (A) moiety,

R ¹ is preferably a hydrogen atom.

A is preferably

(1) a piperidinyl group, an isoxazolyl group, a pyrazolyl group, a thiadiazolyl group, a thiazolyl group or a

tetrahydropyranyl group each optionally substituted by Ci-6 alkyl group (s) (preferably, one Ci-6 alkyl group) optionally substituted by halogen atom(s) (preferably, 1 to 3 halogen atoms) , or

(2) a cyclopentyl group or a cyclohexyl group each optionally substituted by halogen atom(s) (preferably, 1 or 2 halogen atoms) .

[0156]

R ² is preferably a hydrogen atom or an optionally substituted Ci-6 alkyl group, more preferably, a hydrogen atom or a Ci-6 alkyl group, particularly preferably a hydrogen atom.

[0157]

R ³ is preferably

(1) a hydrogen atom,

(2) an optionally substituted Ci-6 alkyl group,

(3) an optionally substituted C3-10 cycloalkyl group, or

(4) an optionally substituted heterocyclic group.

[0158]

R ³ is more preferably

(1) a hydrogen atom, (2) a Ci-6 alkyl group substituted by one C3-10 cycloalkyl group (e.g., cyclopropylmethyl group),

(3) a Ci-6 alkyl group substituted by one 4- to 6-membered non- aromatic heterocyclic group (preferably, a 4- to 6-membered non-aromatic heterocyclic group containing, as a ring- constituting atom besides carbon atoms, 1 or 2 hetero atoms selected from a nitrogen atom, a sulfur atom and an oxygen atom) (e.g., tetrahydropyranylmethyl group),

(4) a C3-10 cycloalkyl group (e.g., cyclobutyl group, cyclohexyl group) optionally substituted by one amino group, or

(5) a 4- to 6-membered non-aromatic heterocyclic group

(preferably, a 4- to 6-membered non-aromatic heterocyclic group containing, as a ring-constituting atom besides carbon atoms, 1 or 2 hetero atoms selected from a nitrogen atom, a sulfur atom and an oxygen atom) (e.g., tetrahydropyranyl group, piperidinyl group), and the heterocyclic group is optionally substituted by one substituent selected from

(a) a Ci-6 alkyl group optionally substituted by halogen atom(s) (preferably, 1 to 3 halogen atoms), and

(b) a C3-10 cycloalkyl group (e.g., cyclopropyl group).

[0159]

R ³ is more preferably a hydrogen atom, a

cyclopropylmethyl group, a tetrahydropyranylmethyl group, a cyclobutyl group or a tetrahydropyranyl group.

[0160]

R ³ is particularly preferably a cyclopropylmethyl group, a tetrahydropyranylmethyl group, a cyclobutyl group or a tetrahydropyranyl group.

[0161]

R ² and R ³ are optionally bonded with each other to form, together with the adjacent nitrogen atom, an optionally, substituted cyclic group.

[0162]

Examples of the "cyclic group" of the "optionally

substituted cyclic group", which is formed, together with the adjacent nitrogen atom, by R ² and R ³ bonded to each other include a 4- to 10-membered heterocyclic group containing one nitrogen atom as a ring-constituting atom besides carbon atom, and optionally further containing one hetero atom selected from a nitrogen atom, a sulfur atom and an oxygen atom, and the like. Examples of the "4- to 10-membered heterocyclic group" include azetidin-l-yl, pyrrolidin-l-yl, pyrrolin-l-yl, pyrazolin-l-yl , imidazolin-l-yl, thiazolidin-3-yl, oxazolidin-

3-yl, isothiazolidin-2-yl, isoxazolidin-2-yl, thiazolin-3-yl, oxazolin-3-yl, isothiazolin-2-yl, isoxazolin-2-yl, piperidin-

1-yl, piperazin-l-yl, morpholin-4-yl , thiomorpholin-4-yl, azepan-l-yl, diazepan-l-yl, 1, 4-oxazepan-4-yl, 1, 4-thiazepan-

4-yl, 5, 7-dihydro-6H-pyrrolo [3, 4-b] pyridin-6-yl and the like.

Examples of the substituent of the "optionally

substituted cyclic group", which is formed, together with the adjacent nitrogen atom, by R ² and R ³ bonded to each other include substituents selected from the aforementioned

substituent group A.

The number of the substituents in "optionally substituted cyclic group", which is formed, together with the adjacent nitrogen atom, by R ² and R ³ bonded to each other is, for

example, 1 to 3. When the number of the substituents is two or more, the respective substituents may be the same or different.

[0163]

Preferable examples of the "optionally substituted cyclic group", which is formed, together with the adjacent nitrogen atom, by R ² and R ³ bonded to each other include a 4- to 10- membered heterocyclic group containing one nitrogen atom as a ring-constituting atom besides carbon atom, and optionally further containing one hetero atom selected from a nitrogen atom, a sulfur atom and an oxygen atom (e.g., pyrrolidin-l-yl, piperidin-l-yl, morpholin-4-yl, thiomorpholin-4-yl) , and the heterocyclic group is optionally substituted by 1 to 3 oxo groups .

[0164] A preferable combination of R ² and R ³ is

a hydrogen atom and a cyclopropylmethyl group,

a hydrogen atom and a cyclobutyl group,

a hydrogen atom and a tetrahydropyranyl group,

a hydrogen atom and a tetrahydropyranylmethyl group, or a hydrogen atom and an optionally substituted piperidinyl group (preferably, a piperidinyl group optionally substituted by one Ci-6 alkyl group optionally substituted by 1 to 3 halogen atoms) .

[0165]

R ⁴ is preferably a hydrogen atom or an optionally

substituted Ci-6 alkyl group, more preferably, a hydrogen atom or a Ci-6 alkyl group, particularly preferably a hydrogen atom.

[0166]

In the formula (I) , the relative configuration of the substituent represented by the formula (R ¹ ) (A)N-CO-B- and the substituent represented by the formula -N(R ² ) (R ³ ) on the cyclopropane ring is cis or trans, preferably trans.

[0167]

A compound of the formula (I) having a preferable relative configuration is shown by the following formula (IA) .

[0168]

relative configuration

[0169]

wherein A, B, R ¹ , R ² , R ³ and R ⁴ are as defined above.

Compound (I) encompasses a compound having the absolute configuration represented by the following formula (IB) or (IC), and a mixture thereof at any ratio.

[0170]

absolute configuration

[0171]

wherein A, B, R ¹ , R ² , R ³ and R ⁴ are as defined above.

[0172]

Preferable examples of compound (I) include the following compounds .

[Compound A]

Compound (I) wherein

B is a ring selected from thiophene, thiazole, pyrazole, pyridine, naphthalene and 2 , 3-dihydrobenzofuran, and the ring is optionally substituted by Ci-6 alkyl group (s) (preferably, one Ci-6 alkyl group) ;

A is

(1) a heterocyclic group (preferably, (i) a 5- or 6-membered aromatic heterocyclic group or (ii) a 4- to 6-membered non- aromatic heterocyclic group, each containing, as a ring- constituting atom besides carbon atoms, 1 to 4 hetero atoms selected from a nitrogen atom, a sulfur atom and an oxygen atom) (e.g.,. piperidinyl group, isoxazolyl group, pyrazolyl group, thiadiazolyl group, thiazolyl group, tetrahydropyranyl group, oxetanyl group, oxadiazolyl group, thienyl group, pyridyl group, oxazolyl group) optionally substituted by Ci-6 alkyl group (s) (preferably, 1 or 2 Ci-6 alkyl groups) optionally substituted by halogen atom(s) (preferably, 1 to 3 halogen atoms) or

(2) a C3-10 cycloalkyl group (e.g., cyclopropyl group, cyclobutyl group, cyclopentyl group, cyclohexyl group) optionally substituted by halogen atom(s) (preferably, 1 or 2 halogen atoms) ;

R ¹ is a hydrogen atom;

R ² is a hydrogen atom;

R ³ is

(1) a hydrogen atom,

(2) a Ci-6 alkyl group substituted by one C3-10 cycloalkyl group (e.g., cyclopropylmethyl group),

(3) a Ci-6 alkyl group substituted by one 4- to 6-membered non- aromatic heterocyclic group (preferably, a 4- to 6-membered non-aromatic heterocyclic group containing, as a ring- constituting atom besides carbon atoms, 1 or 2 hetero atoms selected from a nitrogen atom, a sulfur atom and an oxygen atom) (e.g., tetrahydropyranylmethyl group),

(4) a C3-10 cycloalkyl group (e.g., cyclobutyl group, cyclohexyl group) optionally substituted by one amino group, or

(5) a 4- to 6-membered non-aromatic heterocyclic group

(preferably, a 4- to 6-membered non-aromatic heterocyclic group containing, as a ring-constituting atom besides carbon atoms, 1 or 2 hetero atoms selected from a nitrogen atom, a sulfur atom and an oxygen atom) (e.g., tetrahydropyranyl group, piperidinyl group) optionally substituted by one substituent selected from

(a) a Ci-6 alkyl group optionally substituted by halogen atom(s) (preferably, 1 to 3 halogen atoms), and

(b) a C3-10 cycloalkyl group (e.g., cyclopropyl group); and

R ⁴ is a hydrogen atom.

[0173]

[Compound B]

Compound (I) wherein

B is a ring selected from

thiophene, thiazole, pyrazole, pyridine, naphthalene and 2,3- dihydrobenzofuran, wherein the ring is optionally substituted by Ci-6 alkyl group (s) (preferably, one Ci-6 alkyl group);

A is

(1) a pyrazolyl group, a thiadiazolyl group or a

tetrahydropyranyl group, each optionally substituted by Ci-6 alkyl group (s) (preferably, one Ci-6 alkyl group), or

(2) a cyclopentyl group or a cyclohexyl group, each optionally substituted by halogen atom(s) (preferably, 1 or 2 halogen atoms) ;

R ¹ is a hydrogen atom;

R ² is a hydrogen atom;

R ³ is a hydrogen atom, a cyclopropylmethyl group, a

tetrahydropyranylmethyl group, a cyclobutyl group or a tetrahydropyranyl group; and

R ⁴ is a hydrogen atom.

[0174]

[Compound C]

Compound (I) wherein

B is a ring selected from thiophene and thiazole, and the ring is optionally substituted by Ci-6 alkyl group (s) (preferably, one Ci- 6 alkyl group) ;

A is

(1) a pyrazolyl group, a thiadiazolyl group or a

tetrahydropyranyl group, each optionally substituted by Ci-6 alkyl group (s) (preferably, one Ci-6 alkyl group, or

(2) a cyclopentyl group or a cyclohexyl group, each optionally substituted by halogen atom(s) (preferably, 1 or 2 halogen atoms) ;

R ¹ is a hydrogen atom;

R ² is a hydrogen atom;

R ³ is a cyclopropylmethyl group, a tetrahydropyranylmethyl group, a cyclobutyl group or a tetrahydropyranyl group; and R ⁴ is a hydrogen atom.

[0175]

[Compound D]

A compound represented by the formula (IA) [0176]

[0177]

wherein A, B, R ¹ , R ² , R ³ and R ⁴ are as defined for compound A, and the steric configuration shows a relative configuration, or a salt thereof.

[0178]

[Compound E]

A compound represented by the formula (IA)

[0179]

[0180]

wherein A, B, R ¹ , R ² , R ³ and R ⁴ are as defined for compound B, and the steric configuration shows a relative configuration, or a salt thereof.

[0181]

[Compound F]

A compound represented by the formula (IA)

[0182]

[0183]

wherein A, B, R ¹ , R ² , R ³ and R ⁴ are as defined for compound C, and the steric configuration shows a relative configuration, or a salt thereof.

[0184]

The salt of compound (I) is preferably a

pharmacologically acceptable salt. Examples of such salt include salts with inorganic bases, salts with organic bases, salts with inorganic acids, salts with organic acids, and salts with basic or acidic amino acids.

Preferable examples of salts with inorganic bases include alkali metal salts such as sodium salts, potassium salts and the like; alkali earth metal salts such as calcium salts, magnesium salts and the like; aluminum salts; and ammonium salts .

Preferable examples of salts with organic bases include salts with trimethylamine, triethylamine, pyridine, picoline, ethanolamine, diethanolamine, triethanolamine,

dicyclohexylamine, N, -dibenzylethylenediamine and the like.

Preferable examples of salts with inorganic acids include salts with hydrochloric acid, hydrobromic acid, nitric acid, sulfuric acid, phosphoric acid and the like.

Preferable examples of salts with organic acids include salts with formic acid, acetic acid, trifluoroacetic acid, fumaric acid, oxalic acid, tartaric acid, maleic acid, citric acid, succinic acid, malic acid, methanesulfonic acid,

benzenesulfonic acid, p-toluenesulfonic acid and the like.

Preferable examples of salts with basic amino acids include salts with arginine, lysine, ornithine and the like.

Preferable examples of salts with acidic amino acids include salts with aspartic acid, glutamic acid and the like.

The salt of compound (I) is preferably a salt with an inorganic acid (preferably, hydrochloric acid) or an organic acid (preferably, trifluoroacetic acid) .

[0185]

Compound (I) may also be used as a prodrug. A prodrug of compound (I) means a compound which is converted to compound (I) due to a reaction due to an enzyme, gastric acid, etc. under the physiological condition in the living body, that is, a compound which is converted to compound (I) with oxidation, reduction, hydrolysis, and the like according to an enzyme; a compound which is converted to compound (I) by hydrolysis etc. due to gastric acid, and the like. A prodrug for compound (I) may be a compound obtained by subjecting an amino group in compound (I) to an acylation, alkylation or phosphorylation (e.g., a compound obtained by subjecting an amino group in compound (I) to an eicosanoylation, alanylation,

pentylaminocarbonylation, (5-methyl-2-oxo-l, 3-dioxolen-4- yl) methoxycarbonylation, tetrahydrofuranylation,

pyrrolidylmethylation, pivaloyloxymethylation and tert- butylation, etc.); a compound obtained by subjecting a hydroxy group in compound (I) to an acylation, alkylation,

phosphorylation or boration (e.g., a compound obtained by subjecting a hydroxy group in compound (I) to an acetylation, palmitoylation, propanoylation, pivaloylation, succinylation, fumarylation, alanylation and

dimethylaminomethylcarbonylation) ; a compound obtained by subjecting a carboxyl group in compound (I) to an

esterification or amidation (e.g., a compound obtained by subjecting a carboxyl group in compound (I) to an ethyl esterification, phenyl esterification, carboxymethyl

esterification, dimethylaminomethyl esterification,

pivaloyloxymethyl esterification, ethoxycarbonyloxyethyl esterification, phthalidyl esterification, ( 5-methyl-2-oxo- 1, 3-dioxolen-4~yl) methyl esterification,

cyclohexyloxycarbonylethyl esterification and methylamidation) and. the like. Any of these compounds can be produced from compound (I) by a method known per se.

[0186]

The prodrug of compound (I) may be a compound that converts to compound (I) under physiological conditions as described in Development of Pharmaceutical Products, vol. 7, Molecular Design, 163-198, Hirokawa Shoten (1990). Compound (I) may be labeled with an isotope (e.g., ² H, ³ H, ¹⁴ C, ³⁵ S, ¹²⁵ I, C, ¹⁸ F) and the like.

Compound (I) labeled with or substituted by an isotope can be used, for example, as a tracer used for Positron

Emission Tomography (PET) (PET tracer) , and is useful in the field of medical diagnosis and the like.

Compound (I) may be an anhydrate or a hydrate. Compound (I) may be a solvate or a non-solvate. Furthermore, compound (I) may be a deuterated compound.

Compound (I) may be a crystal, and both a single crystal and crystal mixtures are encompassed in compound (I) . Crystals can be produced by crystallization according to

crystallization methods known per se.

In addition, compound (I) may be a pharmaceutically acceptable cocrystal or cocrystal salt. Here, the cocrystal or cocrystal salt means a crystalline substance consisting of two or more particular substances which are solids at room

temperature, each having different physical properties (e.g., structure, melting point, heat of melting, hygroscopicity, and stability) . The cocrystal and cocrystal salt can be produced by cocrystallization method known per se.

When compound (I) includes isomers such as optical isomers, stereoisomers, regioisomers, rotational isomers, geometrical isomers, and the like, one of the isomers and mixture are also encompassed in compound (I) .

[0187]

Compound (I) or a prodrug thereof (hereinafter sometimes to be simply abbreviated as the compound of the present

invention) has low toxicity (e.g., acute toxicity, chronic . toxicity, genetic toxicity, reproductive toxicity,

cardiotoxicity, carcinogenicity) , and can be used as it is or in the form of a pharmaceutical composition (in the present specification, sometimes to be abbreviated as "medicament of the present invention") after mixing with a pharmacologically acceptable carrier etc. to mammals (e.g., human, mouse, rat, rabbit, dog, cat, bovine, horse, swine, monkey) as an agent for the prophylaxis or treatment of various diseases mentioned below.

[0188]

As a pharmaceutical acceptable carrier here, common organic or inorganic carrier substances are used as

formulation raw materials. Carriers are added as vehicles, lubricants, binders and disintegrants in the solid

formulations; and as solvents, solubilizing agents, suspending agents, isotonization agents, buffering agents, soothing agents etc. in the liquid formulations. If desired,

formulation additives such as preservatives, antioxidants, colorants, sweeteners, etc. can be used.

[0189]

Preferable examples of the vehicles are as follows:

lactose, sucrose, D-mannitol, D-sorbitol, starch, oc-starch, dextrin, crystalline cellulose, low-substituted hydroxypropyl cellulose, sodium carboxymethylcellulose, gum Arabic, pullulan, light anhydrous silicic acid, synthetic aluminum silicate, and magnesium metasilicic aluminate.

[0190]

Preferable examples of the lubricant include magnesium stearate, calcium stearate, talc, colloidal silica, and the like .

[0191]

Preferable examples of the binders are as follows: oc- starch, sucrose, gelatin, gum Arabic, methylcellulose,

carboxymethylcellulose, sodium carboxymethylcellulose,

crystalline cellulose, sucrose, D-mannitol, trehalose, dextrin, pullulan, hydroxypropylcellulose, hydroxypropyl

methylcellulose, and polyvinylpyrrolidone.

[0192]

Preferable examples of the disintegrants are as follows.: lactose, sucrose, starch, carboxymethylcellulose, calcium carboxymethylcellulose, croscarmellose sodium, sodium carboxymethyl starch, light anhydrous silicic acid, and low- substituted hydroxypropylcellulose .

[0193]

Preferable examples of the solvents are as follows: water for injection, physiological saline, Linger solution, alcohol, propylene glycol, polyethylene glycol, sesame oil, corn oil, olive oil, and cottonseed oil.

[0194]

Preferable examples of the solubilizing agents are as follows: polyethylene glycol, propylene glycol, D-mannitol, trehalose, benzyl benzoate, ethanol, tris-aminomethane,

cholesterol, triethanolamine, sodium carbonate, sodium citrate, sodium salicylate, and sodium acetate.

[0195]

Preferable examples of the suspending agent include surfactants such as stearyl triethanolamine, sodium lauryl sulfate, laurylaminopropionic acid, lecithin, benzalkonium chloride, benzetonium chloride, glycerin monostearate and the like; hydrophilic polymers such as polyvinyl alcohol,

polyvinylpyrrolidone, carboxymethylcellulose sodium,

methylcellulose, hydroxymethylcellulose, hydroxyethylcellulose, hydroxypropylcellulose and the like; polysorbates, and

polyoxyethylene hydrogenated castor oil.

[0196]

Preferable examples of the isotonization agents include sodium chloride, glycerin, D-mannitol, D-sorbitol, and glucose.

[0197]

Preferable examples of the buffering agent include buffer solutions such as phosphates, acetates, carbonates, and

citrates.

[0198]

Preferable examples of the soothing agent include benzyl alcohol.

[0199]

Preferable examples of the preservative include p- hydroxybenzoates, chlorobutanol, benzyl alcohol, phenethyl alcohol, dehydroacetic acid, and sorbic acid.

[0200]

Preferable examples of antioxidants include sulfites and ascorbates.

[0201]

Preferable examples of the colorants include water

soluble edible tar dyes (e.g., edible dyes such as Food Red No. 2 and No. 3, Food Yellow No. 4 and No. 5, Food Blue No. 1 and 2, etc.); water insoluble lake dyes (e.g., aluminum salts of the aforementioned water soluble edible tar dyes) , and natural dyes (e.g., β-carotene, chlorophyll, ferric oxide red).

[0202]

Preferable examples of the sweeteners include sodium saccharin, dipotassium glycyrrhizinate, aspartame and stevia.

[0203]

Examples of the dosage form of the medicament of the present invention include oral preparations such as tablet

(including sublingual tablet, orally disintegrating tablet) , capsule (including soft capsule, microcapsule) , granule, powder, troche, syrup, emulsion, suspension and the like; and . parenteral agents such as injection (e.g., subcutaneous

injection, intravenous injection, intramuscular injection, intraperitoneal injection, drip infusion) , external

preparation (e.g., dermal preparation^ ointment), suppository (e.g., rectal suppository, vaginal suppository), pellet, nasal preparation, pulmonary preparation (inhalant) , eye drop and the like, which can be respectively safely administered orally or parenterally.

[0204]

These preparations may be a release control preparation (e.g., sustained-release microcapsule) such as an immediate- release preparation, a sustained-release preparation and the like.

[0205] The medicament of the present invention can be manufactured by the common methods in the field of formulation technology, for example, methods listed in the Japanese

Pharmacopoeia, and the like.

[0206]

The content of the compound of the present invention in the medicament of the present invention varies based on the dosage forms, dosages of the compound of the present invention, and the like. For example, it is approximately about 0.1 to 100 wt%.

[0207]

The compound of the present invention has a superior LSD1 inhibitory action and can be used as a prophylactic or

therapeutic agent for various diseases in mammals (e.g., human, mouse, rat, rabbit, dog, cat, bovine, horse, swine, monkey) . Moreover, since the compound of the present invention shows low monoamine oxidase A (MAO-A) and monoamine oxidase B (MAO- B) inhibitory activity and high LSD1 selectivity, it causes fewer side effects.

[0208]

In addition, the compound of the present invention is expected to show, after transfer into the brain, suppression of a decrease in histone H3K4 methylation and suppression of a decrease in Gadl mRNA expression, which are derived from the inhibition of LSD1. As a result, it is also useful as a

medicament based on superior actions such as neuronal function, enhancement of neural plasticity, promotion of neurogenesis, and promotion of BDNF production.

In addition, the compound of the present invention can, after transfer into the brain, suppress a decrease in histone H3K9 methylation derived from LSD1 inhibition. As a result, it is effective for the treatment of some diseases associated with a decrease in the methylation of H3K9.

[0209]

The compound of the present invention can be used as a prophylactic or therapeutic agent for cancer. Examples of the cancer include breast cancer, prostate cancer, pancreatic cancer, gastric cancer, lung cancer, colorectal cancer, rectal cancer, esophagus cancer, duodenal cancer, tongue cancer, pharyngeal cancer, brain tumor, schwannoma, non-small cell lung cancer, small cell lung cancer, liver cancer, kidney cancer, bile duct cancer, uterine body cancer, cervical cancer, ovarian cancer, urinary bladder cancer, skin cancer,

hemangioma, malignant lymphoma, malignant melanoma, thyroid cancer, bone tumor, angiofibroma, retinoblastoma, penile cancer, childhood solid cancer, Kaposi's sarcoma, AIDS-related Kaposi's sarcoma, tumor of maxillary sinus, fibrous

histiocytoma, leiomyosarcoma, rhabdomyosarcoma, and leukemia. Among these, the compound can be preferably used for prostate cancer, leukemia, and malignant lymphoma.

[0210]

It is known that the level of H3K4me2, which is a

substrate of LSDl, and memory improvement are correlated

(Nature 2007, Vol. 447, page 175), and the compound of the present invention having a superior LSDl inhibitory action can also be used as a prophylactic or therapeutic agent for

neurodegenerative diseases.

[0211]

The compound of the present invention can be used as a therapeutic agent for anemia.. Examples of anemia include sickle cell anaemia and beta thalassemia.

[0212]

The compound of the present invention can be used as a prophylactic or therapeutic agent for central nervous system diseases. It is useful as a prophylactic or therapeutic agent for diseases such as

(1) psychiatric diseases [e.g., depression, major depression, bipolar depression, dysthymic disorder, emotional disorder

(seasonal affective disorder and the like), recurrent

depression, postpartum depression, stress disorder, depression symptom, mania, anxiety, generalized anxiety disorder, anxiety syndrome, mood disorder, panic disorder, phobia, social phobia, social anxiety disorder, obsessive disorder, post-traumatic stress syndrome, post-traumatic stress disorder, Tourette syndrome, adjustment disorder, bipolar disorder, neurosis, schizophrenia (e.g., positive symptom, negative symptom, cognitive impairment) , chronic fatigue syndrome, anxiety neurosis, compulsive neurosis, panic disorder, anxiety symptom, anxious mental state, emotional abnormality, cyclothymia, nervous erethism, faint, addiction, low sex drive, attention deficit hyperactivity disorder (ADHD), psychotic major

depression, refractory major depression, treatment-resistant depression] ,

(2) neurodegenerative diseases [e.g., Alzheimer's disease, Alzheimer-type senile dementia, Parkinson's disease,

Huntington's disease (Huntington chorea), multi-infarct

dementia, frontotemporal dementia, frontotemporal dementia with Parkinsonism, progressive supranuclear palsy, Pick' s syndrome, Niemann-Pick syndrome, corticobasal degeneration, vascular dementia, postencephalitic parkinsonism, dementia with Lewy body, HIV dementia, amyotrophic lateral sclerosis (ALS) , motor neurogenesis disease (MND) , Creutzfeldt-Jakob disease or prion disease, cerebral palsy, progressive

supranuclear palsy, multiple sclerosis, spinocerebellar

degeneration (e.g., dentatorubural pallidoluysian atrophy)],

(3) developmental disorders, particularly, diseases with

intellectual disability (e.g., autistic spectrum disorders, Rett syndrome, Down's syndrome, Kabuki syndrome, fragile X syndrome, Kleefstra syndrome, neurofibromatosis type 1, Noonan syndrome, tuberous sclerosis) ,

(4) age-related cognition and memory disorders [e.g., age-, related memory disorders, senile dementia] ,

(5) sleep disorders [e.g., intrinsic sleep disorders (e.g., psychophysiological insomnia and the like) , extrinsic sleep disorder, circadian rhythm disorders (e.g., time zone change syndrome (jet lag) , shift work sleep disorder, irregular sleep-wake pattern, delayed sleep phase syndrome, advanced sleep phase syndrome, non-24-hour sleep-wake disorder and the like) , parasomnia, sleep disorders associated with internal medical or psychiatric disorder (e.g., chronic obstructive pulmonary disease, Alzheimer's disease, Parkinson's disease, cerebrovascular dementia, schizophrenia, depression, anxiety neurosis) , stress insomnia, insomnia, insomniac neurosis, sleep apnea syndrome] ,

(6) respiratory depression caused by anesthetics, traumatic disease, or neurodegenerative disease and the like,

(7) epilepsy (e.g., Dravet syndrome), traumatic brain injury, cerebral apoplexy, neurotic anorexia, eating disorder,

anorexia nervosa, hyperorexia, other eating disorder, alcohol dependence, alcohol abuse, alcoholic amnesia, alcohol paranoia, alcohol preference, alcohol withdrawal, alcoholic insanity, alcohol intoxication, alcoholic jealousy, alcoholic mania, alcohol-dependent psychiatric disorder, alcoholic insanity, drug dependence, drug intoxication, pharmacophilia,

pharmacophobia, pharmacomania, drug withdrawal, migraine, stress headache, catatonic headache, diabetic neuropathy, obesity, diabetes, muscular spasm, Meniere's disease,

autonomic ataxia, alopecia, glaucoma, hearing loss,

hypertension, cardiac disease, tachycardia, congestive cardiac failure, hyperventilation, bronchial asthma, apnea, sudden infant death syndrome, inflammatory disease, allergic disease, impotence, climacteric disorder, infertility, cancer, .

immunodeficiency syndrome caused by HIV infection,

immunodeficiency syndrome caused by stress, cerebrospinal meningitis, acromegaly, incontinence, metabolic syndrome, osteoporosis, peptic ulcer, irritable bowel syndrome, .

inflammatory bowel disease, ulcerative colitis, Crohn's

disease, stress gastrointestinal disorder, stress vomiting, stress ulcer, diarrhea, constipation, postoperative ileus, and the like. [0213]

The compound of the present invention is particularly useful as an agent for the prophylaxis or treatment of

diseases such as schizophrenia, developmental disorders, particularly diseases having intellectual disability (e.g., autistic spectrum disorders, Rett syndrome, Down's syndrome, Kabuki syndrome, fragile X syndrome, Kleefstra syndrome, neurofibromatosis type 1, Noonan syndrome, tuberous sclerosis) , neurodegenerative diseases (e.g., Alzheimer's disease,

Parkinson's disease, spinocerebellar degeneration (e.g., dentatorubural pallidoluysian atrophy) and Huntington's

disease (Huntington chorea)), epilepsy (e.g., Dravet syndrome) or drug dependence, and the like.

[0214]

Since the compound of the present invention has a

superior LSD1 inhibitory activity, it is expected to show a superior treatment effects for the above-mentioned diseases.

[0215]

The dosage of the compound of the present invention varies depending on the administration subjects,

administration routes, target diseases, symptoms, and the like. For example, for oral administration to adult patients with cancer, generally a single dose is about 0.01 to 100 mg/kg body weight, preferably 0.1 to 50 mg/kg body weight, further preferably 0.5 to 20 mg/kg body weight, and this dosage is preferably . administered 1 to 3 times daily.

[0216]

The compound of the present invention can be used in combination with a medicament such as chemotherapeutic agent, immunotherapeutic agent, medicament inhibiting actions of cell growth factor and receptor thereof (hereinafter to be

abbreviated as a concomitant drug) .

By combining the compound of the present invention and a concomitant drug, a superior effect such as

(1) the dose can be reduced as compared to single administration of the compound of the present invention or a concomitant drug,

(2) the drug to be combined with the compound of the present invention can be selected according to the condition of patients (mild case, severe case and the like) ,

(3) the period of treatment can be set longer by selecting a concomitant drug having different action and mechanism from the compound of the present invention,

(4) a sustained treatment, effect can be designed by selecting a concomitant drug having different action and mechanism from the compound of the present invention,

(5) a synergistic effect can be afforded by a combined use of the compound of the present invention and a concomitant drug, and the like, can be achieved.

[0217]

Hereinafter the compound of the present invention and a concomitant drug used in combination are referred to as the "combination agent of the present invention".

When using the combination agent of the present invention, the administration time of the compound of the present

invention and the concomitant drug is not restricted, and the compound of the present invention or a pharmaceutical

composition thereof and the concomitant drug or a

pharmaceutical composition thereof can be administered to an administration subject simultaneously, . or may be administered at different times. The dosage of the concomitant drug may be determined according to the dose clinically used, and can be appropriately selected depending on an administration subject, administration route, disease, combination and the. like.

The administration mode of the combination agent of the present invention is not particularly restricted, and it is sufficient that the compound of the present invention and the concomitant drug are combined in administration. Examples of such administration mode include the following methods:

(1) administration of a single preparation obtained by simultaneously processing the compound of the present invention and the concomitant drug, (2) simultaneous

administration of two kinds of preparations of the compound of the present invention and the concomitant drug, which have been separately produced, by the same administration route, (3) administration of two kinds of preparations of the

compound of the present invention and the concomitant drug, which have been separately produced, by the same

administration route in a staggered manner, (4) simultaneous administration of two kinds of preparations of the compound of the present invention and the concomitant drug, which have been separately produced, by different administration routes, (5) administration of two kinds of preparations of the

compound of the present invention and the concomitant drug, which have been separately produced, by different

administration routes in a staggered manner (e.g.,

administration in the order of the compound of the present invention and the concomitant drug, or in the reverse order) and the like.

The dose of the concomitant drug can be appropriately determined based on the dose employed in clinical situations. The mixing ratio of the compound of the present invention and a concomitant drug can be appropriately determined depending on the administration subject, administration route, target disease, symptom, combination and the like.

For example, the content of the compound of the present invention in the combination agent of the present invention differs depending on the form of a preparation, and usually from _^ about 0.01 to about 100 wt%, preferably from about 0.1 to about 50 wt%, further preferably from about 0.5 to about 20. wt%, based on the preparation.

The content of the concomitant drug in the combination agent of the present invention differs depending on the form of a preparation, and usually from about 0.01 to about 100 wt%, preferably from about 0.1 to about 50 wt%, further preferably from about 0.5 to about 20 wt%, based on the preparation.

The content of additives such as a carrier and the like in the combination agent of the present invention differs depending on the form of a preparation, and usually from about 1 to about 99.99 wt%, preferably from about 10 to about 90 wt%, based on the preparation.

When the compound of the present invention and a

concomitant drug are separately formulated into preparations, the contents thereof are similar to the above.

[0218]

Examples of the chemotherapeutic agent include alkylating agents (e.g., nitrogen mustard, nitrogen mustard-N-oxide hydrochloride, chlorambutyl, cyclophosphamide, ifosfamide, thiotepa, carboquone, improsulfan tosylate, busulfan,

nimustine hydrochloride, mitobronitol, melphalan, dacarbazine, ranimustine, estramustine phosphate sodium,

triethylenemelamine, carmustine, lomustine, streptozocin, pipobroman, etoglucid, carboplatin, cisplatin, miboplatin, nedaplatin, oxaliplatin, altretamine, ambamustine,

dibrospidium hydrochloride, fotemustine, prednimustine,

pumitepa, ^' ribomustin, temozolomide, treosulphan,

trophosphamide, zinostatin stimalamer, adozelesin,

cystemustine, bizelesin) , metabolic antagonists (e.g.,

mercaptopurine, 6-mercaptopurine riboside, thioinosine,

methotrexate, pemetrexed, enocitabine, cytarabine, cytarabine ocfosfate, ancitabine hydrochloride, 5-FU drug (e.g.,

fluorouracil, tegafur, UFT, doxifluridine, carmofur,

gallocitabine, emitefur, capecitabine) , aminopterin,

nelzarabine, leucovorin calcium, tabloid, butocine, folinate calcium, levofolinate calcium, cladribine, emitefur,

fludarabine, gemcitabine, hydroxycarbamide, pentostatin, piritrexim, idoxuridine, mitoguazone, tiazofurin, ambamustine, bendamustine) , antitumor antibiotics (e.g., actinomycin D, actinomycin C, mitomycin C, chromomycin A3, bleomycin

hydrochloride, bleomycin sulfate, peplomycin sulfate, daunorubicin hydrochloride, doxorubicin hydrochloride,

aclarubicin hydrochloride, pirarubicin hydrochloride,

epirubicin hydrochloride, neocarzinostatin, mithramycin, sarkomycin, carzinophilin, mitotane, zorubicin hydrochloride, mitoxantrone hydrochloride, idarubicin hydrochloride) , and plant-derived antitumor agents (e.g., etoposide, etoposide phosphate, vinblastine sulfate, vincristine sulfate, vindesine sulfate, teniposide, paclitaxel, docetaxel, vinorelbine) .

[0219]

Examples of the immunotherapeutic agent include picibanil, krestin, schizophyllan, lentinan, ubenimex, interferon, interleukin, macrophage colony stimulating factor, granulocyte colony stimulating factor, erythropoietin, lymphotoxin, BCG vaccine, corynebacterium parvum, levamisole, polysaccharide K, procodazole and anti-CTLA4 antibody.

[0220]

Examples of the "medicament inhibiting actions of cell growth factor and receptor thereof" include anti-VEGF antibody (e.g., Bevacizumab) , anti-HER2 antibody (e.g., Trastuzumab, Pertuzumab) , anti-EGFR antibody (e.g., Cetuximab, Panitumumab, Matuzumab, Nimotuzumab) , anti-VEGFR antibody, anti-HGF

antibody, Imatinib mesylate, Erlotinib, Gefitinib, Sorafenib, Sunitinib, Dasatinib, Lapatinib, Vatalanib, 4- (4-fluoro-2- methyl-lH-indol-5-yloxy) -6-methoxy-7- [3- (1- pyrrolidinyl) propoxy] quinazoline (AZD-2171) , Lestaurtinib, Pazopanib, Canertinib, Tandutinib, 3- ( 4-bromo-2 , 6- difluorobenzyloxy) -5- [3- [4- (1- pyrrolidinyl) butyl] ureido] isothiazole-4-carboxamide (CP- 547632), Axitinib, N- (3, 3-dimethyl-2 , 3-dihydro-lH-indol-6-yl) - 2- (pyridin-4-ylmethylamino) pyridine-3-carboxamide (A G-706) , Nilotinib, 6- [4- (4-ethylpiperazin-l-ylmethyl) phenyl] -N- [1 (R) - phenylethyl] -7H-pyrrolo [2, 3-d] pyrimidin-4-amine (AEE-788) , Vandetanib, Temsirolimus, Everolimus, Enzastaurin, N-[4-[4-(4- methylpiperazin-l-yl) -6- ( 3-methyl-lH-pyrazol-5- ylamino) pyrimidin-2-ylsulfanyl] phenyl] cyclopropanecarboxamide (VX-680) , 2- [N- [3- [4- [5- [N- (3-fluorophenyl) carbamoylmethyl] - lH-pyrazol-3-ylamino] quinazolin-7-yloxy] propyl] -N- ethylamino] ethyl phosphate (AZD-1152), 4- [ 9-chloro-7- (2 , 6- difluorophenyl) -5H-primido [5, 4-d] [2 ] benzazepin-2- ylamino] benzoic acid (MLN-8054), N- [2-methoxy-5- [ (E) -2- (2, 4 , 6- trimethoxyphenyl) vinylsulfonylmethyl] phenyl] glycine sodium salt (ON-1910Na), 4- [ 8-cyclopentyl-7 (R) -ethyl-5-methyl-6-oxo- 5,6,7, 8-tetrahydropteridin-2-ylamino] -3-methoxy-N- (1- methylpiperidin-4-yl) benzamide (BI-2536) , 5- (4-bromo-2- chlorophenylamino) -4-fluoro-l-methyl-lH-benzimidazole-6- carbohydroxamic acid 2-hydroxyethyl ester (AZD-6244), N- [2 (R) , 3-dihydroxypropoxy] -3, 4-difluoro-2- (2-fluoro-4- iodophenylamino) benzamide (PD-0325901) and everolimus (RAD001) .

[0221]

Examples of the concomitant drug for the central nervous system diseases include the following,

benzodiazepine (chlordiazepoxide, diazepam, potassium

clorazepate, lorazepam, clonazepam, alprazolam etc.), L-type calcium channel inhibitor (pregabalin etc.), tricyclic or tetracyclic antidepressant (imipramine hydrochloride,

amitriptyline hydrochloride, desipramine hydrochloride,

clomipramine hydrochloride etc.), selective serotonin reuptake inhibitor (fluvoxamine maleate, fluoxetine hydrochloride, citalopram hydrobromide, sertraline hydrochloride, paroxetine hydrochloride, escitalopram oxalate etc.), serotonin- noradrenaline reuptake inhibitor (venlafaxine hydrochloride, duloxetine hydrochloride, desvenlafaxine hydrochloride etc.), noradrenaline reuptake inhibitor (reboxetine . mesylate etc.), mirtazapine, trazodone . hydrochloride, nefazodone hydrochloride, bupropion hydrochloride,, setiptiline maleate, 5-HTi _A agonist, (buspirone hydrochloride, tandospirone citrate, osemozotan hydrocloride etc.), 5-HT ₃ antagonist (cyamemazine etc.), non- cardioselective β blocker (propranolol hydrochloride,

oxprenolol hydrochloride etc.), histamine Hi antagonist

(hydroxyzine hydrochloride etc.), therapeutic drug for schizophrenia (chlorpromazine, haloperidol, sulpiride, clozapine, trifluoperazine hydrochloride, fluphenazine

hydrochloride, olanzapine, quetiapine fumarate, risperidone, aripiprazole etc.) , CRF antagonist, other antianxiety drug (meprobamate etc.) , tachykinin antagonist (MK-869, saredutant etc.), medicament that acts on metabotropic glutamate receptor, CCK antagonist, β3 adrenaline antagonist (amibegron

hydrochloride etc.), GAT-1 inhibitor (tiagabine hydrochloride etc.), N-type calcium channel inhibitor, carbonic anhydrase II inhibitor, N DA glycine site agonist, NMDA antagonist

(memantine etc.), peripheral benzodiazepine receptor agonist, vasopressin antagonist, vasopressin Vlb antagonist,

vasopressin Via antagonist, phosphodiesterase inhibitor, opioid antagonist, opioid agonist, uridine, nicotinic acid receptor agonist, thyroid hormone (T3, T4), TSH, TRH (Hirtonin, Ceredist), MAO inhibitor (phenelzine sulfate, tranylcypromine sulfate, moclobemide etc.), 5-HT _2A antagonist, 5-HT _2A inverse agonist, COMT inhibitor (entacapone etc.), therapeutic drug for bipolar disorder (lithium carbonate, sodium valproate, lamotrigine, riluzole, felbamate etc.), cannabinoid CBl

antagonist (rimonabant etc.), FAAH inhibitor, sodium channel inhibitor, anti-ADHD drug (methylphenidate hydrochloride, methamphetamine hydrochloride etc.), therapeutic drug for alcohol dependence, therapeutic drug for autism, therapeutic drug for chronic fatigue syndrome, therapeutic drug for spasm, therapeutic drug for fibromyalgia syndrome, therapeutic drug . for headache, therapeutic drug for insomnia (etizolam,

zopiclone, triazolam, Zolpidem, ramelteon, indiplon etc . ) , therapeutic drug for quitting smoking, therapeutic drug for myasthenia gravis, therapeutic drug for cerebral infarction, therapeutic drug for mania, therapeutic drug for hypersomnia, therapeutic drug for pain, therapeutic drug for dysthymia, therapeutic drug for autonomic ataxia, therapeutic drug for male and female sexual dysfunction, therapeutic drug for

migraine, therapeutic drug for pathological gambler, therapeutic drug for restless legs syndrome, therapeutic drug for substance dependence (varenicline etc.), therapeutic drug for alcohol-related syndrome, therapeutic drug for irritable bowel syndrome, therapeutic drug for Alzheimer's disease

(donepezil, galanthamine, memantine etc.), therapeutic drug for Parkinson's disease, therapeutic drug for Huntington's disease (Huntington chorea) , therapeutic drug for ALS

(riluzole etc., neurotrophic factor etc . ) , · antiepileptic drug (phenobarbital, phenytoin, valproic acid, clonazepam,

topiramate, gabapentin, phenobarbital ethosuximide etc.), therapeutic drug for lipid abnormality such as cholesterol- lowering drug (statin series (pravastatin sodium, atrovastatin, simvastatin, rosuvastatin etc.), fibrate (clofibrate etc.), squalene synthetase inhibitor) , therapeutic drug for abnormal behavior or suppressant of dromomania due to dementia

(sedatives, antianxiety drug etc.), apoptosis inhibitor, antiobesity drug, therapeutic drug for diabetes, therapeutic drug for hypertension, therapeutic drug for hypotension, therapeutic drug for rheumatism (DMARD) , anti-cancer agent, therapeutic drug for parathyroid (PTH) , calcium receptor

antagonist, sex hormone or a derivative thereof (progesterone, estradiol, estradiol benzoate etc.), neuronal differentiation promoter, nerve regeneration promoter, non-steroidal antiinflammatory drug (meloxicam, tenoxicam, indomethacin,

ibuprofen, celecoxib, rofecoxib, aspirin, indomethacin etc.), steroid (dexamethasone, cortisone acetate etc.), anti-cytokine drug (TNF inhibitor, MAP kinase inhibitor etc.), antibody medicament, nucleic acid or nucleic acid derivative, aptamer drug, and the like.

[0222]

The above-mentioned concomitant drug may be used in a combination of two or more kinds at an appropriate ratio.

When the compound of the present invention is used in combination with a concomitant drug, the respective dosages can be reduced within a safe range in consideration of the opposite effects of the respective drugs. As a result, the opposite effect caused by these agents can be prevented safely.

The compound of the present invention can also be used in combination with a non-medication therapy. Specific examples of the non-medication therapy include (1) operation; (2) hypertensive chemical therapy using angiotensin II and the like; (3) gene therapy; (4) hyperthermic therapy; (5)

cryotherapy; (6) laser ablation method; (7) radiation therapy; and (8) immunotherapy.

[0223]

[Production method]

The production method of the compound of the present invention is explained below. Those of ordinary skill in the art can produce compound (I) according to the methods shown in each step of the following production methods and Examples, or a method analogous thereto.

[0224]

The starting materials and reagents used in each step of the following production methods, as well as the obtained compounds may each form a salt. Examples of such salt include those similar to the salts of the aforementioned compounds of the present invention and the like.

[0225]

When the compound obtained in each step is a free

compound, it can be converted to a desired salt by a method known per se. Conversely, when the compound obtained in each step is a salt, it can be converted to a free form or a

desired other kind of salt by a method known per se.

[0226]

While the compounds obtained in each step can be directly used for the next reaction in the form of a reaction mixture or as a crude product, the compound obtained in each step can be isolated and/or purified according to a conventional method from the reaction mixture by separation means such as

concentration, crystallization, recrystallization, distillation, solvent extraction, fractionation,

chromatography and the like.

[0227]

When the compound of a starting material or a reagent for each step is commercially available, the commercially

available product can be directly used.

[0228]

In the reaction of each step, while the reaction time varies depending on the reagents and solvents to be used, unless particularly indicated, it is generally 1 min to 72 hr, preferably 10 min to 8 hr.

[0229]

In the reaction of each step, while the reaction

temperature varies depending on the reagents and solvents to be used, unless particularly indicated, it is generally -78°C to 300°C, preferably -78°C to 150°C.

[0230]

In the reaction of each step, while the pressure varies depending on the reagents and solvents to be used, unless particularly indicated, it is generally 1 atm to 20 atm, preferably 1 atm to 3 atm.

[0231]

In the reaction of each step, microwave synthesizers such as Initiator manufactured by Biotage and the like are

sometimes used. While the reaction temperature varies

depending on the reagents and solvents to be used, unless particularly indicated, it is generally room temperature to

300°C, preferably 50°C to 250°C. While the reaction time varies depending on the reagents and solvents to be used, unless particularly indicated, it is generally 1 min to 48 hr, preferably 1 min to 8 hr.

[0232]

In the reaction of each step, . unless particularly indicated, the reagents are used in 0.5 equivalent to 20 equivalents, preferably 0.8 equivalent to 5 equivalents, relative to the substrate. When a reagent is used as a catalyst, the reagent is used in 0.001 equivalent to 1

equivalent, preferably 0.01 equivalent to 0.2 equivalent, relative to the substrate. When the reagent is also used as a reaction solvent, the reagent is used in a solvent amount.

[0233]

In the reaction of each step, unless particularly indicated, the reaction is performed without solvent, or by dissolving or suspending a starting material in a suitable solvent. Specific examples of the solvent include the solvents described in Examples, and the following,

alcohols: methanol, ethanol, tert-butyl alcohol, 2- methoxyethanol and the like;

ethers: diethyl ether, diphenyl ether, tetrahydrofuran, 1,2- dimethoxyethane and the like;

aromatic hydrocarbons: chlorobenzene, toluene, xylene and the like;

saturated hydrocarbons: cyclohexane, hexane and the like ;

amides: N, N-dimethylformamide, N-methylpyrrolidone and the like;

hydrocarbon halides: dichloromethane, carbon tetrachloride and the like;

nitriles: acetonitrile and the like;

sulfoxides: dimethyl sulfoxide and the like;

aromatic organic bases: pyridine and the like;

acid anhydrides: acetic anhydride and the like;

organic acids: formic acid, acetic acid, trifluoroacetic acid and the like;

inorganic acids: hydrochloric acid, sulfuric acid and the like;

esters: ethyl acetate and the like;

ketones: acetone, methyl ethyl ketone and the like;

water .

Two or more kinds of the above-mentioned solvents may be mixed and used at appropriate ratios. [0234]

When a base is used in the reaction of each step, for example, the bases shown below or the bases described in the Examples are used.

inorganic bases: sodium hydroxide, magnesium hydroxide,

lithium hydroxide and the like;

basic salts: sodium carbonate, calcium carbonate, sodium

hydrogen carbonate and the like;

organic bases: triethylamine, diethylamine, pyridine, 4- dimethylaminopyridine, N, N-dimethylaniline, 1,4- diazabicyclo [2.2.2] octane, 1, 8-diazabicyclo [5.4.0] -7-undecene, imidazole, piperidine and the like;

metal alkoxides: sodium ethoxide, potassium tert-butoxide and the like;

alkali metal hydrides: sodium hydride and the like;

metal amides: sodium amide, lithium diisopropylamide, lithium hexamethyldisilazide and the like;

organic lithiums: n-butyllithium and the like.

[0235]

When an acid or an acidic catalyst is used in the

reaction of each step, for example, the acids or acidic

catalysts shown below or those described in the Examples are used.

inorganic acids: hydrochloric acid, sulfuric acid, nitric acid, hydrobromic acid, phosphoric acid and the like;

organic acids: acetic acid, trifluoroacetic acid, citric acid, . p-toluenesulfonic acid, 10-camphorsulfonic acid and the like;

Lewis acids: boron trifluoride diethyl ether complex, zinc iodide, anhydrous aluminum chloride, anhydrous zinc chloride, anhydrous iron chloride and the like.

[0236]

Unless otherwise specified, the reaction of each step is performed by a method known per se, for example, the methods described in Jikken Kagaku Koza (Courses in Experimental

Chemistry) , 5th Edition, Volumes 13-19 (The Chemical Society of Japan ed.) Shin Jikken Kagaku Koza (New Experimental

Chemistry Course) , Volumes 14-15 (The Chemical Society of Japan ed. ) ; Seimitsu Yuki Gosei (Reactions and Syntheses: In the Organic Chemistry Laboratory) , Revised 2nd Edition (L. F. Tietze, Th. Eicher, Nankodo Co., Ltd.); Revised Edition

Organic Name Reactions; The Reaction Mechanism and Essence (Hideo Togo, Kodansha Ltd.); ORGANIC SYNTHESES Collective Volumes I-VII (John Wiley & Sons, Inc.); Modern Organic

Synthesis in the Laboratory A Collection of Standard

Experimental Procedures (Jie Jack Li, OXFORD UNIVERSITY

PRESS); Comprehensive Heterocyclic Chemistry III, Vol.1 - Vol.14 (Elsevier Japan KK) ; Strategic Applications of Named Reactions in Organic Synthesis (translated by Kiyoshi Tomioka, Kagaku-Dojin Publishing Company, INC); Comprehensive Organic Transformations (VCH Publishers Inc.) 1989 and the like, or the methods described in. the Examples.

[0237]

In each step, protection or deprotection of functional groups is performed according to a method known per se, for example, the methods described in Wiley-Interscience, 2007, "Protective Groups in Organic Synthesis, 4th Ed." (Theodora W. Greene, Peter G. M. Wuts) ; Thieme, 2004, "Protecting Groups 3rd Ed." (P. J. Kocienski) and the like, or the methods described in the Examples.

Examples of the protecting group for hydroxyl group of alcohol and the like and phenolic hydroxyl · group include ether-type protecting groups such as methoxymethyl ether, benzyl ether, t-butyldimethylsilyl ether, tetrahydropyranyl . ether and the like; carboxylate-type protecting groups such as acetate and the like; sulfonate-type protecting groups such as methanesulfonate and the like; carbonate-type protecting groups such as t-butyl carbonate and the like; and the like.

Examples of the protecting group for carbonyl group of aldehyde include acetal-type protecting groups such as

dimethyl acetal and the like; cyclic acetal-type protecting groups such as cyclic 1,3-dioxane and the like; and the like.

Examples of the protecting group for carbonyl group of ketone include ketal-type protecting groups such as dimethyl - ketal and the like; cyclic ketal-type protecting groups such as cyclic 1,3-dioxane and the like; oxime-type protecting groups such as O-methyloxime and the like; hydrazone-type protecting groups such as N, -dimethylhydrazone and the like; and the like.

Examples of the protecting group for carboxyl group include ester-type protecting groups such as methyl ester and the like; amide-type protecting groups such as N,N- dimethylamide and the like; and the like.

Examples of the protecting group for thiol include ether- type protecting groups such as benzyl thioether and the like; ester-type protecting groups such as thioacetate,

thiocarbonate, thiocarbamate and the like; and the like.

Examples of the protecting group for amino group, and aromatic heterocycle such as imidazole, pyrrole, indole and the like include carbamate-type protecting groups such as benzyl carbamate, tert-butyl carbamate and the like; amide- type protecting groups such as acetamide and the like;

alkylamine-type protecting groups such as N- triphenylmethylamine and the like; sulfonamide-type protecting groups such as methanesulfonamide and the like; and the like.

Protecting groups can be removed by a method known per se, for example, methods using acid, base, ultraviolet rays, hydrazine, phenylhydrazine, sodium N-methyldithiocarbamate, tetrabutylammonium fluoride, palladium acetate, trialkylsilyl halide (e.g., trimethylsilyl iodide, trimethylsilyl bromide), reduction methods and the like.

[0238]

When a reduction reaction is performed in each step, the reducing agent to be used includes metal hydrides such as lithium aluminum hydride, sodium triacetoxyborohydride, sodium cyanoborohydride, diisobutylaluminum hydride (DIBAL-H) , sodium borohydride, tetramethylammonium triacetoxyborohydride and the like; boranes such as borane-tetrahydrofuran complex and the like; Raney-nickel; Raney-cobalt; hydrogen; formic acid and the like. When a carbon-carbon double bond or triple bond is reduced, a method using a catalyst such as palladium-carbon, Lindlar catalyst and the like can be used.

[0239]

When oxidation reaction is performed in each step, the oxidizing agent to be used includes peracids such as m- chloroperbenzoic acid (MCPBA) , hydrogen peroxide, t-butyl hydroperoxide and the like; perchlorates such as

tetrabutylammonium perchlorate and the like; chlorates such as sodium chlorate and the like; chlorites such as sodium

chlorite and the like; periodic acids such as sodium periodate and the like; hypervalent iodine reagents such as

iodosylbenzene and the like; reagents having manganese such as manganese dioxide, potassium permanganate and the like; lead compounds such as lead tetraacetate and the like; reagents having chrome such as pyridinium chlorochromate (PCC) , pyridinium dichromate (PDC) , Jones reagent and the like;

halogen compounds such as N-bromosuccinimide (NBS) and the like; oxygen; ozone; sulfur trioxide-pyridine complex; osmium tetroxide; selenium dioxide; 2, 3-dichloro-5, 6-dicyano-l, 4- benzoquinone (DDQ) and the like.

[0240]

When radical cyclization reaction is performed in each, step, the radical initiator to be used includes azo compounds such as azobisisobutyronitrile (AIBN) and the like; water- soluble radical initiators such as 4 , 4 ' -azobis-4- cyanopentanoic acid (ACPA) and the like; triethylboron in the presence of air or oxygen; benzoyl peroxide and the like. The radical reaction reagent to be used includes tributylstannane, tris (trimethylsilyl ) silane, 1 , 1 , 2 , 2-tetraphenyldisilane, .

diphenylsilane, samarium iodide and the like.

[0241] When the Wittig reaction is performed in each step, the Wittig reagent to be used includes alkylidene phosphoranes and the like. Alkylidene phosphoranes can be prepared by a method known per se, for example, by reacting a phosphonium salt with a strong base.

[0242]

When the Horner-Emmons reaction is performed in each step, the reagent to be used includes phosphonoacetates such as methyl dimethylphosphonoacetate, ethyl diethylphosphonoacetate, tert-butyl diethylphosphonoacetate and the like; bases such as alkali metal hydrides, organic lithiums, 1,8- diazabicyclo [5.4.0] ndec-7-ene and the like; lithium chloride, sodium iodide and the like.

[0243]

When the Friedel-Crafts reaction is performed in each step, the reagent to be used includes Lewis acid and acid chloride or alkylating agents (e.g., alkyl halides, alcohol, olefins and the like) . Alternatively, organic acid and

inorganic acid can also be used instead of Lewis acid, and acid anhydrides such as acetic anhydride and the like can also be used instead of acid chloride.

[0244]

When an aromatic nucleophilic substitution reaction is performed in each step, nucleophilic agents (e.g., amines, imidazole and the like) and bases (e.g., basic salts, organic bases and the like) are used as the reagents.

[0245]

When a nucleophilic addition reaction by a nucleophilic agent, a nucleophilic addition reaction by carbanion, a

nucleophilic 1,4-addition reaction by carbanion (Michael addition) or a nucleophilic substitution reaction by carbanion is performed in each step, a base used to generate carbanion includes organic lithiums, metal alkoxides, inorganic bases, organic bases and the like.

[0246] When the Grignard reaction is performed in each step, the Grignard reagent includes arylmagnesium halides such as

phenylmagnesium bromide and the like; alkylmagnesium halides such as methylmagnesium bromide and the like. Grignard

reagents can be prepared by a method known per se, for example, by reacting alkyl halide or aryl halide with metal magnesium in ether or tetrahydrofuran as a solvent.

[0247]

When the Knoevenagel condensation is performed in each step, active methylene compounds (e.g., malonic acid, diethyl malonate, malononitrile and the like) and bases (e.g., organic bases, metal alkoxides, inorganic bases) sandwiched between two electron withdrawing groups are used as the reagents.

[0248]

When the Vilsmeier-Haack reaction is performed in each step, phosphoryl chloride and amide derivative (e.g., N,N- dimethylformamide and the like) are used as the reagents.

[0249]

When an azidation reaction of alcohols, alkyl halides or sulfonates is performed in each step, the azidating agent to be used includes diphenylphosphoryl azide (DPPA) ,

trimethylsilyl azide, sodium azide and the like. For example, when alcohols are azidated, a method using diphenylphosphoryl azide and 1, 8-diazabicyclo [5.4.0] undec-7-ene (DBU) , a method using trimethylsilyl azide and Lewis acid, and the like can be used.

[0250]

When a reductive amination reaction is performed in each step, the reducing agent to be used includes sodium

triacetoxyborohydride, sodium cyanoborohydride, hydrogen, formic acid, sodium borohydride, 2-picoline-borane complex and. the like. When the substrate is an amine compound, a carbonyl compound to be used includes paraformaldehyde, aldehydes such as acetaldehyde and the like, and ketones such as

cyclohexanone and the like. When the substrate is a carbonyl compound, amines to be used includes primary amines such as ammonia, methylamine and the like; secondary amines such as dimethylamine and the like, and the like. An additive such as trimethyl orthoformate and the like may be added to the reaction.

[0251]

When the Mitsunobu reaction is performed in each step, azodicarboxylates (e.g., diethyl azodicarboxylate (DEAD), diisopropyl azodicarboxylate (DIAD) and the like) and

triphenylphosphine are used as the reagents.

[0252]

When an esterification reaction, an amidation reaction or a ureation reaction is performed in each step, the reagent to be used includes acyl halides such as acid chloride, acid bromide and the like; and activated carboxylic acids such as acid anhydride, active ester form, sulfuric acid ester form and the like. An activator of carboxylic acid includes

carbodiimide-type condensing agents such as l-ethyl-3- ( 3- dimethylaminopropyl) carbodiimide hydrochloride (WSCD) and the like; triazine-type condensing agents such as 4- (4, 6- dimethoxy-1, 3, 5-triazin-2-yl) -4-methylmorpholinium chloride-n- hydrate (DMT-MM) and the like; carbonate-type condensing agents such as 1, 1-carbonyldiimidazole (CDI) and the like;

diphenylphosphoryl azide (DPPA) ; benzotriazol-l-yloxy- trisdimethylaminophosphonium salt (BOP reagent) ; 2-chloro-l- methyl-pyridinium iodide (Mukaiyama reagent); thionyl

chloride; lower alkyl haloformates such as ethyl chloroformate and the like; 0- (7-azabenzotriazol-l-yl) -N, N, N' , N' - tetramethyluronium hexafluorophosphate (HATU) ; sulfuric acid; or combinations of these and the like. When a carbodiimide- type condensing agent is used, an additive such as 1- hydroxybenzotriazole (HOBt) , N-hydroxysuccinimide (HOSu) , dimethylaminopyridine (DMAP) and the like may be further added to the reaction.

[0253] When a coupling reaction is performed in each step, the metal catalyst to be used includes palladium compounds such as palladium (II) acetate,

tetrakis (triphenylphosphine) palladium (0) ,

dichlorobis (triphenylphosphine) palladium (II) ,

dichlorobis (triethylphosphine) palladium ( II ) ,

tris (dibenzylideneacetone) dipalladium ( 0) , 1,1'- bis (diphenylphosphino) ferrocene palladium ( II ) chloride, palladium ( II) acetate and the like; nickel compounds such as tetrakis (triphenylphosphine) nickel (0) and the like; rhodium compounds such as tris (triphenylphosphine) rhodium ( III )

chloride and the like; cobalt compound; copper compounds such as copper oxide, copper (I) iodide and the like; platinum compound and the like. Furthermore, a base may be added to the reaction, and examples of such base include inorganic bases, basic salts and the like.

[0254]

When a thiocarbonylation reaction is performed in each step, diphosphorus penfasulfide is typically used as a

thiocarbonylating agent. However, a reagent having a 1,3,2,4- dithiadiphosphetane-2 , 4-disulfide structure such as 2,4-bis(4- methoxyphenyl-1, 3,2, 4-dithiadiphosphetane-2 , 4-disulfide

(Lawesson' s reagent) and the like may be used besides

diphosphorus pentasulfide .

[0255]

When the Wohl-Ziegler reaction is performed in each step, the halogenating agent to be used includes N-iodosuccinimide, N-bromosuccinimide (NBS), N-chlorosuccinimide (NCS) , bromine, sulfuryl chloride and the like. Furthermore, the reaction can. be accelerated by adding a radical initiator such as heat, light, benzoyl peroxide, azobisisobutyronitrile and the like to the reaction.

[0256]

When halogenation of hydroxy group is performed in each step, the halogenating agent to be used includes hydrohalic acid and acid halide of inorganic acid, specifically, hydrochloric acid, thionyl chloride, phosphorus oxychloride and the like for chlorination, and 48% hydrobromic acid and the like for bromination. In addition, a method for obtaining alkyl halide from alcohol by a reaction of triphenylphosphine and carbon tetrachloride or carbon tetrabromide and the like may be used. Alternatively, a method for synthesizing alkyl halide by a two-step reaction including converting alcohol to sulfonate and reacting same with lithium bromide, lithium chloride or sodium iodide may be used.

[0257]

When the Arbuzov reaction is performed in each step, the reagent to be used includes alkyl halides such as ethyl bromoacetate and the like; and phosphites such as triethyl phosphite, tri (isopropyl) phosphite and the like.

[0258]

When a sulfonylation reaction is performed in each step, the sulfonylating agent to be used includes methanesulfonyl chloride, p-toluenesulfonyl chloride, methanesulfonic

anhydride, p-toluenesulfonic anhydride and the like.

[0259]

When hydrolysis is performed in each step, an acid or a base is used as a reagent. When acid hydrolysis of t-butyl ester is performed, formic acid, triethylsilane and the like are sometimes added to reductively trap the by-produced t- butyl cation.

[0260]

When a dehydration reaction is performed in each step, the dehydrating agent to be used. includes sulfuric acid, .. phosphorus pentoxide, phosphorus oxychloride, Ν,Ν'- dicyclohexylcarbodiimide, alumina, polyphosphoric .acid and the like.

[0261]

When the Corey-Chaykovsky cyclopropanation reaction is · performed in each step, the reagent to be used includes trimethylsulfoxonium iodide, potassium tert-butoxide, sodium hydride and the like.

[0262]

When a carbon monoxide insertion reaction and a

subsequent nucleophilic substitution reaction by alcohol are performed in each step, the metal catalyst to be used includes palladium compounds such as palladium (II) acetate,

tetrakis (triphenylphosphine) palladium ( 0) ,

dichlorobis (triphenylphosphine) palladium ( II ) ,

dichlorobis (triethylphosphine)palladium(II) ,

tris (dibenzylideneacetone) dipalladium ( 0 ) , 1,1'- bis (diphenylphosphino) ferrocene palladium(II) chloride, palladium (II) acetate and the like; and examples of the phosphine ligand include triphenylphosphine, 2,2'- bis (diphenylphosphino) -1, 1' -binaphthyl, 2- (di-tert- butylphosphino) biphenyl, 2- (dicyclohexylphosphino) biphenyl, 2- (dicyclohexylphosphino) -2' , 6' -dimethoxy-1, 1' -biphenyl, 2- (dicyclohexylphosphino) -2' , 4' , 6' -triisopropyl-1, 1' -biphenyl, 2- (dicyclohexylphosphino) -2' - (N, -dimethylamino) biphenyl, 1, 1' -bis (diphenylphosphino) ferrocene, tri-tert-butylphosphine, tricyclohexylphosphine, (9, 9-dimethyl-9H-xanthene- , 5- diyl) bis (diphenylphosphine) and the like.

Examples of the alcohol include methanol, ethanol, 2- propanol, benzyl alcohol and the like.

This reaction is performed using, as necessary, a phosphine ligand generally under a carbon monoxide atmosphere from normal pressure to about 10 atm in an inert solvent.

[0263]

When the Curtius rearrangement reaction is performed in each step, the reagents to be used includes diphenylphosphoryl azide and tert-butyl alcohol and the like. As reagents, ethyl chloroformate, a base, sodium azide, tert-butyl alcohol and the like can also be used.

When a diastereomeric salt resolution method is performed in each step, the optically active organic base to be used includes, for example, ( (1R, 4aS, lOaR) -7-isopropyl-l, 4a- dimethyl-1, 2, 3, 4, 4a, 9, 10, lOa-octahydrophenanthren-1- yl)methanamine, (R) -2-amino-3-phenylpropan-l-ol and the like.

The compound obtained in each step may be used after optical resolution by a known means such as chiral column chromatography, optical fractional crystallization,

diastereomer derivatization and the like.

[0264]

In the schemes, R ⁵ and R ⁶ are alkyl groups such as methyl group, ethyl group, tert-butyl group and the like, and other symbols are each as defined above. Compound (la) to compound (Ik) , compound (Iaa) and compound (Iga) are included in the aforementioned compound (I), and each of them shows a compound group of compound (I) wherein R ³ =H. The thiophene ring, pyrazole ring, naphthalene ring, dihydrobenzofuran ring, pyridine ring and thiazole ring each optionally has

substituent ( s ) on the ring.

[0265]

<Reaction scheme 1>

Compound (la) can be produced from compound (1) by the following method.

[0266]

[0267]

<Reaction scheme 2>

Compound (lb) can be produced from compound (10) by the following method.

[0269]

Compound (11) can be produced by reacting compound (10) with N-phenylbis (trifluoromethanesulfonimide) and a base.

Examples of the base include sodium hydroxide, potassium hydroxide, sodium carbonate, potassium carbonate, cesium carbonate, tripotassium phosphate, sodium methoxide, sodium ethoxide, triethylamine, diisopropylethylamine, pyridine, 1,8- diazabicyclo [5.4.0] undec-7-ene and the like.

Compound (12) can be produced by reacting compound (11) with acrylates. This reaction is performed using a base and a palladium catalyst and, where necessary, a phosphine ligand may also be used. The acrylate to be used includes tert-butyl acrylate, methyl acrylate, ethyl acrylate and the like. The palladium catalyst to be used includes palladium(II) acetate, tetrakis (triphenylphosphine) palladium (0) ,

dichlorobis (triphenylphosphine) palladium(II) ,

dichlorobis (triethylphosphine)palladium(II) ,

tris (dibenzylideneacetone) dipalladium(O) , 1,1'- bis (diphenylphosphino) ferrocene palladium ( II ) chloride, palladium (II) acetate and the like. Examples of the phosphine ligand include triphenylphosphine, 2,2'- bis (diphenylphosphino) -1, 1' -binaphthyl, 2- (di-tert- butylphosphino) biphenyl, 2- (dicyclohexylphosphino) biphenyl, 2- (dicyclohexylphosphino) -2' , 6' -dimethoxy-1, 1' -biphenyl, 2- (dicyclohexylphosphino) -2' , 4' , 6' -triisopropyl-1, 1' -biphenyl, 2- (dicyclohexylphosphino) -2' - (N, N-dimethylamino) biphenyl,

1, 1' -bis (diphenylphosphino) ferrocene, tri-tert-butylphosphine, tricyclohexylphosphine, (9, 9-dimethyl-9H-xanthene-4, 5- diyl) bis (diphenylphosphine) , tri (o-tolyl) phosphine and the like. Examples of the base include sodium hydroxide, potassium hydroxide, sodium carbonate, potassium carbonate, cesium carbonate, tripotassium phosphate, sodium methoxide, sodium ethoxide, triethylamine, diisopropylethylamine, pyridine, 1,8- diazabicyclo [5.4.0] undec-7-ene and the like. In this step, for example, a microwave synthesizer such as Initiator

manufactured by Biotage and the like may also be used.

[0270]

<Reaction scheme 3>

Compound (Ic) can be produced from compound (19) by the following method.

[0271]

[0272]

<Reaction scheme 4>

Compound (Id) can be produced from compound (31) by the following method.

[0273]

[0274]

Compound (32) can be produced by reacting compound (31) with acrylates. This reaction is performed using a base and a palladium catalyst, as necessary, and a phosphine ligand may also be used. The acrylate to be used includes tert-butyl acrylate, methyl acrylate, ethyl acrylate and the like. The palladium catalyst to be used includes palladium (II) acetate, tetrakis (triphenylphosphine) palladium (0) ,

dichlorobis (triphenylphosphine) palladium (II) ,

dichlorobis (triethylphosphine) palladium(II) ,

tris (dibenzylideneacetone) dipalladium ( 0 ) , 1,1'- bis (diphenylphosphino) ferrocene palladium ( II ) chloride, palladium (II) acetate and the like. Examples of the phosphine ligand include triphenylphosphine, 2,2'- bis (diphenylphosphino) -1, 1' -binaphthyl, 2- (di-tert- butylphosphino) biphenyl, 2- (dicyclohexylphosphino) biphenyl, 2- (dicyclohexylphosphino) -2' , 6' -dimethoxy-1, 1' -biphenyl, 2- (dicyclohexylphosphino) -2' , 4' , 6' -triisopropyl-1, 1' -biphenyl, 2- (dicyclohexylphosphino) -2' - (N, -dimethylamino) biphenyl, 1,1' -bis (diphenylphosphino) ferrocene, tri-tert-butylphosphine, tricyclohexylphosphine, (9, 9-dimethyl-9H-xanthene-4 , 5- diyl) bis (diphenylphosphine) , tri (o-tolyl) phosphine and the like. Examples of the base include sodium hydroxide, potassium hydroxide, sodium carbonate, potassium carbonate, cesium carbonate, tripotassium phosphate, sodium methoxide, sodium ethoxide, triethylamine, diisopropylethylamine, pyridine, 1,8- diazabicyclo [5.4.0] undec-7-ene and the like. In this step, for example, a microwave synthesizer such as Initiator

manufactured by Biotage and the like may also be used.

[0275]

<Reaction scheme 5>

Compound (Ie) can be produced from compound (40) by the following method.

[

[0277]

<Reaction scheme 6>

Compound (If) can be produced from compound (49) by the following method.

[0278]

[0279]

<Reaction scheme 7>

Compound (Ig) can be produced from compound (58) by the following method.

5 [0280]

[0281]

<Reaction scheme 8>

Compound (Ih) can be produced from compound (71) by the I D following method.

[0282]

[0283]

<Reaction scheme 9> Compound (Ii) can be produced from compound (81) by the following method.

[0284]

[0285]

<Reaction scheme 10>

Compound (Ij) can be produced from compound (70) by the following method.

[0287]

<Reaction scheme 11>

Compound (Ik) can be produced from compound (89) by the following method.

0288]

(92)

[0289] <Reaction scheme 12>

Compound (Iaa) can be produced from compound (6) or compound (4) by the following method.

[0290]

[0291]

<Reaction scheme 13>

Compound (Iga) can be produced from compound (61) or compound (63) by the following method.

[0292]

Examples

[0293]

The present invention is explained in detail in the following by referring to Examples, Experimental Examples and Formulation Examples. However, the examples do not limit the present invention and the present invention can be modified within the scope of the present invention.

[0294]

The "room temperature" in the following Examples is generally about 10°C to about 35°C. The ratio for a mixed solvent is, unless otherwise specified, a volume mixing ratio and % means wt% unless otherwise specified.

[0295]

In silica gel column chromatography, the indication of NH means use of aminopropylsilane-bonded silica gel. In HPLC

(high performance liquid chromatography) , the indication of C18 means use of octadecyl-bonded silica gel. Unless otherwise, specified, the ratio of elution solvents is a volume mixing ratio.

[0296]

In the following Examples, the following abbreviations are used.

mp: melting point

MS: mass spectrum

[M+H] ⁺ , [M-H] ^~ : molecular ion peak

M: molar concentration

N: normality

CDCI3: deuterated chloroform

DMSO-d6: deuterated dimethyl sulfoxide

¹ H NMR: proton nuclear magnetic resonance

LC/MS: liquid chromatography mass spectrometer

ESI: ElectroSpray Ionization

APCI : Atmospheric Pressure Chemical Ionization

THF: tetrahydrofuran

DMF: N, N-dimethylformamide

DMSO: dimethyl sulfoxide

TFA: trifluoroacetic acid

SFC: supercritical fluid chromatography

TEA: triethylamine

AA: acetic acid

DMAP: 4-dimethylaminopyridine

[0297]

1H NMR was measured by Fourier-transform NMR. For the analyses, ACD/SpecManager (trade name) and the like were used. A peak showing very mild proton of hydroxyl group, amino group or the like is not described.

[0298]

MS was measured by LC/MS. As the ionization method, ESI method or APCI method was used. The data indicates measured ■ values (found). Generally, a molecular ion peak is observed. However, when a compound has a tert-butoxycarbonyl group, a peak free of a tert-butoxycarbonyl group or tert-butyl group may be observed as a fragment ion. When a compound has a hydroxyl group, a peak free of H2O may be observed as a

fragment ion. In the case of a salt, a molecular ion peak or a fragment ion peak of a free form is generally observed.

[0299]

The unit of the sample concentration (c) in optical rotation ( [0£]D) is g/100 mL.

As the elemental analytical values (Anal.), Calculated (Calcd) and measured values (Found) are described.

[0300]

Example 1

4- (trans-2-aminocyclopropyl ) -5-methyl-N- (5-methyl-l, 3, 4- thiadiazol-2-yl) thiophene-2-carboxamide dihydrochloride

A) (E) -ethyl 3- (5-bromo-2-methylthiophene-3-yl) acrylate

To a mixture of potassium tert-butoxide (4.59 g) and dry THF (60 mL) was added ethyl diethylphosphonoacetate (7.5 mL) at -5°C, and the mixture was stirred for 20 min. To the reaction mixture was added a mixture of 5-bromo-2- methylthiophene-3-carbaldehyde (7.0 g) and dry THF (10 mL) at -5°C, and the mixture was stirred for 30 min. To the reaction mixture was added water (100 mL) , and the mixture was

extracted twice with ethyl acetate (100 mL each) . The extracts were combined, dried over anhydrous sodium sulfate, and concentrated under reduced pressure to give the title compound (7.2 g) .

¾ NMR (400 MHz, DMSO-d ₆ ) δ 1.17-1.35 (3H, m) , 2.45 (3H, s) , 4.19 (2H, q, J = 5.8 Hz), 6.40 (1H, d, J = 15.7 Hz), 7.48 (1H, d, J = 15.7 Hz) , 7.78 (1H, s) .

[0301]

B) ethyl trans-2- ( 5-bromo-2-methylthiophen-3- yl) cyclopropanecarboxylate

To a suspension of sodium hydride (50% in oil, 2.26 g) in DMSO (50 mL) was added trimethylsulfoxonium iodide (10.4 g) , and the mixture was stirred at room temperature for 1 hr. To the reaction mixture was added a mixture of ethyl (E) -ethyl 3- (5-bromo-2-methylthiophen-3-yl) acrylate (6.5 g) and DMSO (30 mL) , and the mixture was stirred at room temperature for 4 hr. To the reaction mixture was added ice water (200 mL) , and the mixture was extracted with ethyl acetate (100 mL, twice) . The extracts were combined, washed with saturated brine (100 mL) , dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to give the title compound (3.5 g) .

¾ NMR (400 MHz, DMSO-d ₆ ) δ 1.23 (3H, t, J = 5.2 Hz), 1.24-1.29 (1H, m) , 1.30-1.40 (1H, m) , 1.86-1.90 (1H, m) , 2.23-2.28 (1H, m) , 2.33 (3H, s) , 4.09 (2H, q , J = 7.1 Hz), 6.82 (1H, s) .

[0302]

C) trans-2- ( 5-bromo-2-methylthiophen-3- yl) cyclopropanecarboxylic acid

Ethyl trans-2- (5-bromo-2-methylthiophen-3- yl) cyclopropanecarboxylate (500 mg) was dissolved in methanol (8 mL) , a mixture of sodium hydroxide (138 mg) and water (2 mL) was added at 0°C, and the mixture was stirred at room temperature for 2 hr. The reaction mixture was concentrated under reduced pressure, and adjusted to pH 6 with 2 mol/L hydrochloric acid at an inside temperature of not more than 10°C. The precipitated solid was collected by filtration and dried under reduced pressure to give the title compound (350 mg) .

¾ NMR (400 MHz, DMSO-d ₆ ) δ 1.22-1.27 (1H, m) , 1.31-1.36 (1H, m) , 1.72-1.76 (1H, m) , 2.19-2.24 (1H, m) , 2.34 (3H, s) , 6.79 (1H, s) , 12.31 (1H, brs) .

[0303]

D) tert-butyl (trans-2- (5-bromo-2-methylthiophen-3- yl) cyclopropyl ) carbamate

To a mixture of trans-2- ( 5-bromo-2-methylthiophen-3- yl) cyclopropanecarboxylic acid (1.5 g) and tert-butyl alcohol (70 mL) were added triethylamine (8.3 mL) and

diphenylphosphoryl azide (3.7 mL) at room temperature, and the mixture was stirred at 90°C for 16 hr. The reaction mixture was cooled to room temperature, and concentrated under reduced pressure. To the residue was added water (100 mL) , and the mixture was extracted twice with ethyl acetate (200 mL each) . The extracts were combined, washed with saturated brine (100 mL) , dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to give the title compound (0.75 g).

¾ NMR (400 MHz, DMSO-de) δ 0.99-1.05 (2H, m) , 1.38 (9H, s) , 1.72-1.76 (1H, m) , 2.35 (3H, s) , 2.52-2.54 (1H, m) , 6.72 (1H, s) , 7.20 (1H, s) .

[0304]

E) methyl 4- (trans-2- ( (tert-butoxycarbonyl) amino) cyclopropyl) - 5-methylthiophene-2-carboxylate

A mixture of tert-butyl (trans-2- (5-bromo-2- methylthiophen-3-yl) cyclopropyl) carbamate (1.3 g) ,

diisopropylethylamine (3.42 mL) , dichloro ( 1, 1' - bis (diphenylphosphino) ferrocene) palladium (0.96 g) and

methanol (45 mL) was heated under a carbon monoxide atmosphere (10 atm) at 80°C for 16 hr. After cooling to room temperature, the insoluble material was filtered off, and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to give the title compound (0.90 g) .

¾ NMR (400 MHz, DMSO-de) δ 1.05-1.15 (2H, m) , 1.36 (9H, s) , 1.73-1.78 (1H, m) , 2.47 (3H, s) , 2.50-2.55 (1H, m) , 3.76 (3H, s), 7.25 (1H, brs) , 7.34 (1H, s) .

[0305]

F) 4- (trans-2- ( (tert-butoxycarbonyl) amino) cyclopropyl) -5- methylthiophene-2-carboxylic acid

Methyl 4- (trans-2- ( (tert- butoxycarbonyl) amino) cyclopropyl) -5-methylthiophene-2- carboxylate (900 mg) was. dissolved in methanol (45 mL) , a mixture of sodium hydroxide (1160 mg) and water (15 mL) was added at 0°C, and the mixture was stirred at room temperature for 16 hr. The reaction mixture was concentrated under reduced pressure, and water (10 mL) was added to the residue. The mixture was adjusted to pH 6 with 2 mol/L hydrochloric acid at an inside temperature of not more than 10°C, and extracted with 20% methanol-dichloromethane solution (100 mL each) . The extracts were combined, dried over anhydrous sodium sulfate, and concentrated under reduced pressure to give the title compound (660 mg) .

^X H NMR (400 MHz, DMSO-d ₆ ) δ 1.02-1.07 (2H, m) , 1.38 (9H, s) , 1.72-1.76 (1H, m) , 2.45 (3H, s) , 2.49-2.54 (1H, m) , 7.24 (2H, s) , 12.79 (1H, s) .

[0306]

G) tert-butyl (trans-2- (2-methyl-5- ( (5-methyl-l, 3, 4- thiadiazol-2-yl) carbamoyl) thiophen-3-yl) cyclopropyl) carbamate 4- (trans-2- ( (tert-Butoxycarbonyl) amino) cyclopropyl) -5- methylthiophene-2-carboxylic acid (100 mg) , 5-methyl-l, 3, - thiadiazol-2-amine (44.8 mg) and triethylamine (0.187 mL) were dissolved in DMF (3.0 mL) , and the mixture was cooled to 0°C. 0- (7-Azabenzotriazol-l-yl) -N, , N' , N' -tetramethyluronium hexafluorophosphate (153 mg) was added, and the mixture was stirred at room temperature overnight. The reaction mixture was poured into water, and the mixture was extracted with ethyl acetate. The extract was successively washed with saturated aqueous sodium hydrogen carbonate solution and saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane/ethyl acetate) and concentrated under reduced pressure. The obtained residue was diluted with ethyl acetate-THF, successively washed with water and saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure to give the title compound (64 mg) .

MS: [M+H] ⁺ 395.2.

[0307]

H) 4- (trans-2-aminocyclopropyl) -5-methyl-N- (5-methyl-l, 3, 4- thiadiazol-2-yl) thiophene-2-carboxamide dihydrochloride

To a mixture of tert-butyl (trans-2- (2-methyl-5- ( (5- methyl-1, 3, -thiadiazol-2-yl) carbamoyl) thiophen-3- yl) cyclopropyl) carbamate (64 mg) , ethyl acetate (5 mL) and methanol (2 mL) was added 4 mol/L hydrogen chloride/ethyl acetate solution (0.811 mL) at room temperature, and the

mixture was stirred at room temperature for 3 days. The

precipitated solid was collected by filtration and dried under reduced pressure to give the title compound (45 mg) .

[0308]

Example 2

4- (trans-2- ( (.cyclopropylmethyl) amino) cyclopropyl) -5-methyl-N- (5-methyl-l, 3, 4-thiadiazol-2-yl ) thiophene-2-carboxamide

dihydrochloride

To a mixture of 4- (trans-2-aminocyclopropyl) -5-methyl-N-

( 5-methyl-l, 3, 4-thiadiazol-2-yl) thiophene-2-carboxamide

dihydrochloride (42 mg) , sodium hydrogen carbonate (38.4 mg) , THF (0.5 mL) and methanol (0.5 mL) was added

cyclopropanecarbaldehyde (13 L) at room temperature. Under a nitrogen atmosphere, the reaction mixture was stirred at 50°C for 1.5 hr and at room temperature for 1 hr. To the reaction mixture was added cyclopropanecarbaldehyde (8.8 μL) at room temperature, and the mixture was stirred at 50°C for 1.5 hr under a nitrogen atmosphere and at room temperature for 30 min. Sodium borohydride (8.7 mg) was added under ice-cooling and the reaction mixture was stirred for 30 min under a nitrogen atmosphere. Under ice-cooling, to the reaction mixture were added ethyl acetate (5 mL) , water and saturated aqueous sodium hydrogen carbonate solution, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, and the aqueous layer was extracted with a mixture of ethyl acetate and THF. The combined organic layer was dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. The residue was washed with a mixture of ethyl acetate and diisopropyl ether, and dissolved in methanol. A 2 mol/L hydrogen chloride/methanol solution (2 mL) was added, and the mixture was concentrated under reduced pressure. The residue was crystallized from

ethanol/diisopropyl ether to give the title compound (25.9 mg) . ^X H NMR (300 MHz, DMSO-d ₆ ) δ 0.33-0.43 (2H, m) , 0.55-0.65 (2H, m) , 1.06-1.14 (1H, m) , 1.16-1.27 (1H, m) , 1.53-1.62 (1H, m) , 2.40-2.47 (1H, m) , 2.52 (3H, s) , 2.62 (3H, s) , 2.85-3.02 (3H, m) , 7.85 (1H, brs) , 9.24 (2H, brs) , 12.66 (1H, brs) .

[0309]

Example 3

5- (trans-2- ( (cyclopropylmethyl) amino) cyclopropyl) -N- (4,4- difluorocyclohexyl) -l-methyl-lH-pyrazole-3-carboxamide

hydrochloride

A) methyl l-methyl-5- ( ( (trifluoromethyl) sulfonyl) oxy) -1H- pyrazole-3-carboxylate

To a mixture of methyl 5-hydroxy-l-methyl-lH-pyrazole-3- carboxylate (2.404 g) , diisopropylethylamine (5.38 mL) and DMF (24 mL) was added N-phenyIbis (trifluoromethanesulfonimide) (6.05 g) at 0°C, and the mixture was stirred at room

temperature overnight under a nitrogen atmosphere. The

reaction mixture was poured into water, extracted with ethyl acetate, washed with saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The. obtained residue was purified by silica gel column

chromatography (hexane/ethyl acetate) and concentrated under reduced pressure to give the title compound (3.92 g) .

!H NMR (300 MHz, CDC1 ₃ ) δ 3.92 (3H, s) , 3.94 (3H, s) , 6.69 (1H, s) .

[0310] .

B) methyl 5- ( (IE) -3-tert-butoxy-3-oxoprop-l-en-l-yl) -1-methyl- lH-pyrazole-3-carboxylate

A mixture of methyl l-methyl-5- ( ( (trifluoromethyl) sulfonyl) oxy) -lH-pyrazole-3-carboxylate

(890 mg) , tert-butyl acrylate (1.35 mL) , tri (o-tolyl ) phosphine (188 mg) , palladium acetate (69.3 mg) , triethylamine (1.29 mL) and DMF (8 rtiL) was stirred at 80°C for 3 hr under a nitrogen atmosphere. The reaction mixture was poured into water at room temperature, and the mixture was extracted with ethyl acetate, washed with saturated brine, dried over anhydrous sodium

sulfate, and concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography

(hexane/ethyl acetate) and concentrated under reduced pressure to give the title compound (144 mg) .

^X H NMR (300 MHz, CDC1 ₃ ) δ 1.53 (9H, s) , 3.93 (3H, s) , 4.02 (3H, s), 6.34 (1H, d, J = 15.9 Hz), 7.07 (1H, s) , 7.45 (1H, d, J = 15. Hz) .

[0311]

C) methyl 5- (trans-2- ( (tert-butoxycarbonyl) amino) cyclopropyl) - 1-methyl-lH-pyrazole-3-carboxylate

By a method similar to that of Example 1, step B, the title compound was obtained.

MS: [M+H] ⁺ 281.2.

[0312]

D) 2- (3- (methoxycarbonyl) -l-methyl-lH-pyrazol-5- yl ) cyclopropanecarboxylic acid

To methyl 5- (trans-2- ( (tert- butoxycarbonyl ) amino) cyclopropyl) -l-methyl-lH-pyrazole-3- carboxylate (135 mg) was added trifluoroacetic acid (2 mL) at

0°C, and the mixture was stirred at room temperature for 4 hr and concentrated under reduced pressure. Water was added to the residue, and the mixture was extracted with ethyl acetate, successively washed with water and saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The obtained residue was diluted with ethyl acetate and saturated aqueous sodium hydrogen carbonate solution. The aqueous layer was separated, acidified with 2 mol/L

hydrochloric acid, and extracted with ethyl acetate. The extract was successively washed with water and saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was diluted with toluene and concentrated under reduced pressure to give the title compound (100 mg) .

MS: [M+H] ⁺ 225.1.

[0313]

E) 5- (trans-2- ( (cyclopropylmethyl) amino) cyclopropyl) -N- (4,4- difluorocyclohexyl) -l-methyl-lH-pyrazole-3-carboxamide hydrochloride

By a method similar to that of Example 1, steps D, F, G and H and Example 2, the title compound was obtained.

[0314]

Example 4

5- (trans-2-aminocyclopropyl) -N- (4, 4-difluorocyclohexyl) -1- methyl-lH-pyrazole-3-carboxamide hydrochloride

By a method similar to that of Example 3, steps A, B, C and D and Example 1, steps D, F, G and H, the title compound was obtained.

[0315]

Example 5

4- (trans-2-aminocyclopropyl) -N- (5-methyl-l, 3, 4-thiadiazol-2- yl) -2-naphthamide dihydrochloride

A) 3-bromo-N-methoxy-N-methyl-l-naphthamide

3-Bromo-l-naphthoic acid (3.00 g) , N,0- dimethylhydroxylamine hydrochloride (1.32 g) , l-ethyl-3- ( 3- dimethylaminopropyl) carbodiimide hydrochloride (2.80 g) and anhydrous 1-hydroxybenzotriazole (1.94 g) were dissolved in anhydrous DMF (60.0 mL) , triethylamine (4.16 mL) was added, and the mixture was stirred at room temperature for 16 hr. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The extract was successively washed with water and saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to give the title compound (2.69 g) . MS: [M+H] ⁺ 293.9.

[0316] B) 3-bromo-l-naphthaldehyde

To a solution of 3-bromo-N-methoxy-N-methyl-l-naphthamide (2.69 g) in THF (50.0 mL) was slowly added 1.5 mol/L

diisobutylaluminum hydride toluene solution (9.15 mL) at 0°C, and the mixture was stirred at 0°C for 2 hr under a nitrogen atmosphere. To the reaction mixture was added 1 mol/L

hydrochloric acid at 0°C, and the mixture was extracted with ethyl acetate. The extract was successively washed with water and saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane/ethyl acetate) to give the title compound (1.52 g) .

^! H NMR (300 MHz, CDC1 ₃ )5 7.57-7.66 (1H, m) , 7.67-7.74 (1H, m) , 7.84 (1H, d, J = 8.3 Hz), 8.06 (1H, d, J = 2.3 Hz), 8.26 (1H, s), 9.16 (1H, d, J = 8.7 Hz), 10.36 (1H, s).

[0317]

C) (E) -tert-butyl 3- ( 3-bromonaphthalen-l-yl ) acrylate

Lithium chloride (0.28 g) was dried in vacuo, and acetonitrile (20.0 mL) was added. To the mixture were added 3- bromo-l-naphthaldehyde (1.52 g) and tert-butyl

diethylphosphonoacetate (1.71 g) at 0°C, and the mixture was stirred at 0°C for 5 min under a nitrogen atmosphere. To the reaction mixture was added 1, 8-diazabicyclo [5.4.0] ndec-7-ene

(1.02 mL) at 0°C, and the mixture was stirred at room

temperature for 18 hr under a nitrogen atmosphere. Water was added to the reaction mixture at room temperature, and the mixture was extracted with ethyl acetate. The extract was successively washed with water and saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to give the title compound (1.93 g).

^X H NMR (300 MHz, CDC1 ₃ ) : δ 1.57 (9H, s) , 6.46 (1H, d, J = 15.9 Hz), 7.51-7.61 (2H, m) , 7.75-7.82 (2H, m) , 8.02 (1H, d, J = ^■ 1.5 Hz), 8.10-8.16 (1H, m) , 8.32 (1H, d, J = 15.9 Hz). [0318]

D) 4- (trans-2-aminocyclopropyl) -N- (5-methy1-1, 3, 4-thiadiazol- 2-yl) -2-naphthamide dihydrochloride

By a method similar to that of Example 1, steps B, D, E, F, G and H and Example 3, step D, the title compound was obtained.

[0319]

Example 6

N- (5-methyl-l, 3, -thiadiazol-2-yl) -4- (trans-2- ( (tetrahydro-2H- pyran-4-ylmethyl) amino) cyclopropyl) -2-naphthamide

hydrochloride

A) tert-butyl (trans-2- (3- ( (5-methyl-l, 3, 4-thiadiazol-2- yl) carbamoyl) naphthalen-l-yl) cyclopropyl) ( (tetrahydro-2H- pyran-4-yl) methyl) carbamate

4- (trans-2-Aminocyclopropyl) -N- (5-methyl-l, 3, 4- thiadiazol-2-yl) -2-naphthamide dihydrochloride (56.6 mg) and sodium hydrogen carbonate (35.9 mg) were dissolved in THF (5.00 mL) /methanol (5.00 mL) , and tetrahydro-2H-pyran-4- carbaldehyde (19.5 mg) was added. Under a nitrogen atmosphere, the reaction mixture was stirred at 60°C for 3 hr, and sodium borohydride (10.8 mg) was added at 0°C. The ^' reaction mixture was stirred at room temperature for 2 hr, to the reaction mixture was added di-tert-butyl dicarbonate (0.099 mL) , and the mixture was stirred at room temperature for 16 hr. Water was added to the reaction mixture, and the mixture was

extracted with ethyl acetate. The extract was successively washed with water and saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography

(hexane/ethyl acetate) to give the title compound (33.5 mg) . MS: [M+H] ⁺ 523.1.

[0320]

B) N- (5-methyl-l, 3, 4-thiadiazol-2-yl) -4- (trans-2- ( (tetrahydro- 2H-pyran-4-ylmethyl) amino) cyclopropyl) -2-naphthamide

hydrochloride By a method similar to that of Example 1, step H, the title compound was obtained.

Anal. Calcd for C23H26N4O2S HC1: C, 60.19; H, 5.93; N, 12.21. Found: C, 59.52; H, 5.87; N, 11.88.

[0321]

Example 7

4- (trans-2- ( (cyclopropylmethyl) amino) cyclopropyl) -N- (5-methyl- 1, 3, 4-thiadiazol-2-yl) -2-naphthamide dihydrochloride

By a method similar to that of Example 6, the title compound was obtained.

Anal. Calcd for C21H22N4OS 2HC1: C, 55.88; H, 5.36; N, 12.41. Found: C, 56.60; H, 5.56; N, 12.39.

[0322]

Example 8

N- (4 , 4-difluorocyclohexyl) -5-methyl-4- (trans-2- ( (tetrahydro- 2H-pyran-4-ylmethyl) amino) cyclopropyl) thiophene-2-carboxamide hydrochloride

A) tert-butyl (trans-2- (5- ( (4, 4-difluorocyclohexyl) carbamoyl) - 2-methylthiophen-3-yl) cyclopropyl) carbamate

4- (trans-2- ( (tert-Butoxycarbonyl) amino) cyclopropyl) -5- methylthiophene-2-carboxylic acid (100 mg) , 4,4- difluorocyclohexanamine hydrochloride (63.5 mg) and

triethylamine (0.187 mL) were dissolved in DMF (1.0 mL) , 0-(7- azabenzotriazol-l-yl) -Ν,Ν,Ν' ,Ν' -tetramethyluronium

hexafluorophosphate (153 mg) was added at room temperature, and the mixture was stirred overnight. Water was added to the reaction mixture, and the resulting precipitate was collected by filtration to give the title compound (140 mg) .

MS: [M+H] ⁺ 415.3.

[0323]

B) 4- (trans-2-aminocyclopropyl) -N- (4, 4-difluorocyclohexyl ) -5- methylthiophene-2-carboxamide hydrochloride

To a solution (2.0 mL) of tert-butyl (trans-2- (5- ( (4, 4- difluorocyclohexyl) carbamoyl) -2-methylthiophen-3- yl) cyclopropyl) carbamate (140 mg) in ethyl acetate was added 4 mol/L hydrogen chloride/ethyl acetate solution (2.0 mL) at room temperature, and the mixture was stirred at room

temperature for 3 days. The resulting precipitate was

collected by filtration to give the title compound (90 mg) . MS: [M-HC1+HP 315.2.

[0324]

C) N- (4, 4-difluorocyclohexyl) -5-methyl-4- (trans-2- ( (tetrahydro-2H-pyran-4-ylmethyl) amino) cyclopropyl) thiophene- 2-carboxamide hydrochloride

To a mixture of 4- (trans-2-aminocyclopropyl) -N- ( 4 , 4- difluorocyclohexyl) -5-methylthiophene-2-carboxamide

hydrochloride (48.9 mg) , sodium hydrogen carbonate (46.8 mg) , THF (1 mL) and methanol (1 mL) was added tetrahydro-2H-pyran- 4-carbaldehyde (19.1 mg) at room temperature. The reaction mixture was stirred at 60°C for 1.5 hr and at room temperature for 30 min, and sodium borohydride (7.91 mg) was added at 0°C. Under a nitrogen atmosphere, the reaction mixture was stirred at room temperature for 1 hr. To the reaction mixture were added ethyl acetate, water and saturated aqueous sodium hydrogen carbonate solution under ice-cooling, and the mixture was extracted with ethyl acetate. The extract was washed with water and saturated brine. The organic layer was dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography (ethyl acetate/methanol) . To the obtained fraction was added 4 mol/L hydrogen chloride/ethyl acetate solution and the mixture was concentrated under reduced pressure to give the title compound (42.3 mg) .

lR NMR (300 MHz, DMSO-de) δ 1.11-1.34 (3H, m) , 1.54-2.12 (13H, m) , 2.83-3.04 (4H, m) , 3.21-3.34 (2H, m) , 3.86 (3H, dd, J = 11.3, 2.3 Hz)., 7.40 (1H, s) , 8.12 (1H, d, J = 7.9 Hz)., 8.56 (1H, brs) , 9.39 (2H, brs) .

[0325]

Example 9

7- (trans-2-aminocyclopropyl) -N- (5-methyl-l, 3, 4-thiadiazol-2- yl) -2, 3-dihydro-l-benzofuran-5-carboxamide dihydrochloride

By a method similar to that of Example 1, the title compound was obtained.

[0326]

Example 10

7- (trans-2- ( (cyclopropylmethyl) amino) cyclopropyl) -N- (5-methyl- ¹ 1, 3, 4-thiadiazol-2-yl) -2, 3-dihydro-l-benzofuran-5-carboxamide dihydrochloride

By a method similar to that of Example 2, the title compound was obtained.

[0327]

Example 11

7- (trans-2- ( (cyclopropylmethyl) amino) cyclopropyl) -N- (4, 4- difluorocyclohexyl) -2, 3-dihydro-l-benzofuran-5-carboxamide hydrochloride

By a method similar to that of Example 1, steps G and H and Example 2, the title compound was obtained.

[0328]

Example 12

N- (4 , 4-difluorocyclohexyl) -7- (trans-2- ( (tetrahydro~2H-pyran-4- ylmethyl) amino) cyclopropyl) -2, 3-dihydro-l-benzofuran-5- carboxamide hydrochloride

By a method similar to that of Example 2, the title compound was obtained.

[0329]

•Example 13

5- (trans-2-aminocyclopropyl) -N- (4, 4-difluorocyclohexyl) -6- methylnicotinamide dihydrochloride

By a method similar to that of Example 1, the title compound was obtained.

[0330]

Example 14

5- (trans-2- ( (cyclopropylmethyl) amino) cyclopropyl) -N- (4, 4- difluorocyclohexyl) -6-methylnicotinamide dihydrochloride

By a method similar to that of Example 2, the title compound was obtained.

[0331]

Example 15

3- (trans-2-aminocyclopropyl) -N- (5-methyl-l, 3, 4-thiadiazol-2- yl) -1-naphthamide dihydrochloride

A) (E) -methyl 3- (3- (tert-butoxy) -3-oxoprop-l-en-l-yl ) -1- naphthoate

A mixture of methyl 3-bromo-l-naphthoate (500 mg) , tert- butyl acrylate (0.422 mL) , tri (o-tolyl) phosphine (114 mg) , palladium acetate (43.2 mg) , triethylamine (0.781 mL) and anhydrous DMF (3.00 mL) was heated at 100°C for 1 hr under microwave irradiation. The reaction mixture was poured into water and the mixture was extracted with ethyl acetate. The extract was washed with water and saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced

pressure. The obtained residue was purified by silica gel column chromatography (hexane/ethyl acetate) and concentrated under reduced pressure to give the title compound (575 mg) .

XH NMR (300 MHz, CDC1 ₃ )51.56 (9H, s) , 4.03 (3H, s) , 6.55 (1H, d, J = 15.8 Hz), 7.52-7.59 (1H, m) , 7.60-7.67 (1H, m) , 7.74 (1H, d, J = 15.8 Hz), 7.89 (1H, d, J = 7.5 Hz), 8.07 (1H, s) , 8.37 (1H, d, J = 1.9 Hz), 8.87 (1H, d, J = 8.7 Hz).

[0332]

B) 3- (trans-2-aminocyclopropyl) -N- (5-methyl-l, 3, 4-thiadiazol- 2-yl) -1-naphthamide dihydrochloride

By a method similar to that of Example 1, steps B, D, F, G and H and Example 3, step D, the title compound was obtained. Anal. Calcd for Ci ₇ Hi ₆ N ₄ OS 2HC1 H ₂ 0: C, 49.16; H, 4.85; N, 13.49. Found: C, 49.12; H, 5.47; N, 13.12.

[0333]

Example 16

N- (5-methyl-l, 3, -thiadiazol-2-yl ) -3- (trans-2- ( (tetrahydro-2H- pyran-4-ylmethyl) amino) cyclopropyl) -1-naphthamide

dihydrochloride

By a method similar to that of Example 6, the title compound was obtained.

Anal. Calcd for C23H26N4O2S 2HC1 1.4H ₂ 0: C, 53.06; H, 5.96; N, 10.76. Found: C, 52.93; H, 5.96; N, 10.31.

[0334]

Example 17

4- (trans-2- (cyclobutylamino) cyclopropyl) -5-methyl-N- (5-methyl- 1, 3, 4-thiadiazol-2-yl) thiophene-2-carboxamide 1/2 fumarate

To a mixture of 4- (trans-2-aminocyclopropyl) -5-methyl-N- (5-methyl-l, 3, 4-thiadiazol-2-yl) thiophene-2-carboxamide

dihydrochloride (45 mg) , triethylamine (0.034 mL) , trimethyl orthoformate (0.027 mL) and methanol (2.0 mL) was added

cyclobutanone (0.014 mL) at room temperature, and the mixture was stirred at room temperature overnight. Sodium borohydride (9.3 mg) was added under ice-cooling, and the reaction mixture was stirred at 0°C for 10 min. After stirring, water was added under ice-cooling, and the mixture was extracted with ethyl acetate. The extract was washed with water and saturated brine. The organic layer was dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column

chromatography (ethyl acetate/methanol) and concentrated under reduced pressure. The obtained residue was suspended in ethyl acetate, and a solution of fumaric acid (14.2 mg) in ethanol was added at room temperature. The reaction mixture was

stirred for 30 min, and the resulting precipitate was

collected by filtration to give the title compound (23 mg) .

¾ NMR (300 MHz, DMSO-d ₆ ) δ 0.78-0.88 (1H, m) , 0.91-1.02 (1H, m) , 1.52-1.83 (5H, m) , 2.05-2.19 (2H, m), 2.20-2.30 (2H, m) , 2.47 (3H, s), 2.61 (3H, s) , 6.57-6.62 (1H, m) , 7.70-7.77 (1H, m) .

[0335]

Example 18

4- (trans-2- ( (cyclopropylmethyl) amino) cyclopropyl) -N- (4,4- difluorocyclohexyl) -5-methylthiophene-2-carboxamide fumarate

By a method similar to that of Example 19, the title compound was synthesized.

[0336]

Example 19

4- (trans-2- ( (cyclopropylme.thyl) amino) cyclopropyl) -5-methyl-N- (tetrahydro-2H-pyran-4-yl) thiophene-2-carboxamide fumarate

A) tert-butyl (trans-2- (2-methyl-5- ( (tetrahydro-2H-pyran-4- yl) carbamoyl) thiophen-3-yl) cyclopropyl) carbamate

4- (trans-2- ( (tert-Butoxycarbonyl) amino) cyclopropyl) -5- methylthiophene-2-carboxylic acid (100 mg) , tetrahydro-2H- pyran-4-amine (37.4 mg) and triethylamine (0.187 mL) were dissolved in DMF (1.0 mL) , 0- (7-azabenzotriazol-l-yl) - Ν,Ν,Ν' ,Ν' -tetramethyluronium hexafluorophosphate (153 mg) was added at room temperature, and the mixture was stirred

overnight. The reaction mixture was poured into water, and the resulting precipitate was collected by filtration to give the title compound (122 mg) .

MS: [M+H] ⁺ 381.2.

[0337]

B) 4- (trans-2-aminocyclopropyl) -5-methyl-N- (tetrahydro-2H- pyran-4-yl) thiophene-2-carboxamide hydrochloride

To a mixture of tert-butyl (trans-2- (2-methyl-5- ( (tetrahydro-2H-pyran-4-yl) carbamoyl) thiophen-3- yl ) cyclopropyl ) carbamate (122 mg) and ethyl acetate (2 mL) was added 4 mol/L hydrogen chloride/ethyl acetate solution (1.60 mL) at room temperature, and the mixture was stirred at room temperature overnight. The resulting precipitate was collected by filtration to give the title compound (95 mg) .

MS: [M-HC1+H] ⁺ 281.2.

[0338]

C) 4- (trans-2- ( (cyclopropylmethyl) amino) cyclopropyl) -5-methyl- N- (tetrahydro-2H-pyran-4-yl) thiophene-2-carboxamide fumarate

To a mixture of 4- (trans-2-aminocyclopropyl) -5-methyl-N- (tetrahydro-2H-pyran-4-yl).thiophene-2-carboxamide

hydrochloride (45 mg) , triethylamine (0.040 mL) and methanol (2.0 mL) was added cyclopropanecarbaldehyde (14.9 mg) at room temperature, and the reaction mixture was stirred at room temperature overnight. Sodium borohydride (10.8 mg) was added under ice-cooling, and the reaction mixture was stirred at 0°C for 10 min. After stirring, water was added under ice-cooling, and the mixture was extracted with ethyl acetate. The extract was washed with water and saturated brine. The organic layer was dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography (ethyl acetate/methanol) and concentrated under reduced pressure. The obtained residue was suspended in ethyl acetate, a solution of fumaric acid (13.5 mg) in ethanol was added at room

temperature, and the reaction mixture was stirred for 30 min. After stirring, the resulting precipitate was collected by filtration to give the title compound (40 mg) .

^X H NMR (300 MHz, -DMSO-d ₆ ) δ 0.09-0.18 (2H, m) , 0.38-0.47 (2H, m) , 0.82-0.98 (2H, m) , 1.02-1.13 (1H, m) , 1.41-1.59 (2H, m) , 1.66-1.77 (2H, m) , 1.79-1.90 (1H, m) , 2.36-2.45 (4H, m) , 2.57 (2H, dd, J = 6.82, 1.89 Hz), 3.28-3.42 (2H, m) , 3.80-3.96 (3H, m) , 6.57 (2H, s) , 7.26 (1H, s) , 8.04 (1H, d, J = 7.57 Hz).

[0339]

Example 20

5-methyl-N- (5-methyl-l, 3, 4-thiadiazol-2-yl) -4- (trans-2- ( (tetrahydro-2H-pyran-4-ylmethyl) amino) cyclopropyl) thiophene- 2-carboxamide dihydrochloride

By a method similar to that of Example 2, the title compound was synthesized.

[0340]

Example 21

N- (4 , 4-difluorocyclohexyl) -5-methyl-4- (trans-2- (tetrahydro-2H- pyran-4-ylamino) cyclopropyl) thiophene-2-carboxamide fumarate

4- (trans-2-Aminocyclopropyl) -N- (4 , 4-difluorocyclohexyl) - 5-methylthiophene-2-carboxamide hydrochloride (49 mg) and borane-2-methylpyridine complex (44.8 mg) were dissolved in methanol (2.0 mL) /acetic acid (0.20 mL) , tetrahydro-4H-pyran- 4-one (21.0 mg) was added, and the mixture was stirred at room temperature overnight. Under ice-cooling, to the reaction mixture was added saturated aqueous sodium hydrogen carbonate solution, and the mixture was extracted with ethyl acetate. The extract was washed with water and saturated brine, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) and concentrated under reduced pressure. The obtained residue was dissolved in ethyl acetate, a solution of fumaric acid (9.32 mg) in ethanol was added at room temperature, and the reaction mixture was stirred for 30 min. After stirring, the mixture was

concentrated under reduced pressure to give the title compound (12 mg) .

¾ NMR (300 MHz, METHANOL-d ₄ ) δ 1.04-1.15 (1H, m) , 1.21-1.33 (1H, m) , 1.41-2.16 (14H, m) , 2.40 (3H, s) , 2.64-2.74 (1H, m) , 3.30-3.42 (2H, m) , 3.77-3.96 (3H, m) , 6.58-6.64 (2H, m) , 7.14- 7.17 (1H, m) .

[0341]

Example 22

4- (trans-2- (cyclobutylamino) cyclopropyl) -5-methyl-N- ( 1-methyl- lH-pyrazol-4-yl) thiophene-2-carboxamide dihydrochloride

To a mixture of 4- (trans-2-aminocyclopropyl) -5-methyl-N- (l-methyl-lH-pyrazol-4-yl) thiophene-2-carboxamide

dihydrochloride (50 mg) , triethylamine (0.040 mL) , trimethyl orthoformate (0.032 mL) and methanol (2.0 mL) was added cyclobutanone (15.1 mg) at room temperature, and the mixture was stirred at room temperature overnight. Sodium borohydride (10.8 mg) was added under ice-cooling, and the reaction mixture was stirred for 10 min. Water was added under ice- cooling, and the mixture was extracted with ethyl acetate. The extract was washed with water and saturated brine. The organic layer was dried over anhydrous magnesium, sulfate, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography (ethyl acetate/methanol) . To the obtained fraction was added 4 mol/L hydrogen chloride/ethyl acetate solution and the

reaction mixture was concentrated under reduced pressure. The obtained residue was crystallized from ethanol/heptane to give the title compound (10 mg) .

¾ NMR (300 MHz, DMSO-d ₆ ) δ 1.12-1.22 (1H, m) , 1.47-1.58 (1H, m) , 1.75-1.91 (2H, m) , 2.14-2.32 (4H, m) , 2.35-2.44 (1H, m) , 2.47-2.49 (3H, m) , 2.71-2.85 (1H, m) , 3.80 (3H, s) , 3.82-3.92 (1H, m) , 7.47-7.50 (1H, m) , 7.50-7.53 (1H, m) , 7.89-7.95 (1H, m) , 9.47-9.67 (2H, m) 10.25-10.32 (1H, m) .

[0342]

Example 23

5- (trans-2- ( (cyclopropylmethyl) amino) cyclopropyl) -N- (5-methyl- 1, 3, 4-thiadiazol-2-yl) thiophene-3-carboxamide dihydrochloride A) ethyl (2E) -3- (4-bromothiophen-2-yl) acrylate

Lithium chloride (453 mg) was dried in high vacuo, and acetonitrile (40 mL) was added. To this mixture were added 4- bromothiophene-2-carbaldehyde (2.00 g) and ethyl

diethylphosphonoacetate (2.46 g) at 0°C, and the mixture was stirred at 0°C for 5 min under a nitrogen atmosphere. To the reaction mixture was added 1, 8-diazabicyclo [5.4.0] undec-7-ene

(1.66 mL) at 0°C, and the mixture was stirred at room

temperature overnight under a nitrogen atmosphere. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The extract was successively washed with water and saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to give the title compound (2.52 g) .

iH NMR (300 MHz, DMSO-de) δ 1.18-1.31 (3H, m) , 4.18 (2H, q, J = 7.07 Hz), 6.37 (1H, d, J = 15.90 Hz), 7.58-7.89 (3H, m) .

[0343]

B) ethyl trans-2- (4-bromothiophen-2-yl) cyclopropanecarboxylate To a suspension of trimethylsulfoxonium iodide (2.54 g) in DMSO (20 mL) was added sodium hydride (60% in oil, 461 mg) , and the mixture was stirred at room temperature for 30 min. To the reaction mixture was added a solution of ethyl (2E)-3-(4- bromothiophen-2-yl) acrylate (2.51 g) in DMSO (10 mL) , and the mixture was stirred at room temperature overnight under a nitrogen atmosphere. Water was added to the reaction mixture at 0°C, and the mixture was extracted with ethyl acetate. The extract was successively washed with water and saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to give the title compound (1.27 g) .

¾ NMR (300 MHz, DMSO-de) δ 1.20 (3H, t, J = 7.19 Hz), 1.35- 1.54 (2H, m) , 1.97 (1H, ddd, J = 8.42, 5.40, 3.98 Hz), 2.58- 2.67 (1H, m) , 4.05-4.16 (2H, m) , 6.98 (1H, dd, J = 1.51, 0.76 Hz), 7.46 (1H, d, J = 1.51 Hz).

[0344]

C) trans-2- (4-bromothiophen-2-yl) cyclopropanecarboxylic acid

Ethyl trans-2- ( 4-bromothiophen-2- yl) cyclopropanecarboxylate (1.27 g) was dissolved in THF (5 mL) and ethanol (5 mL) , 8 mol/L aqueous sodium hydroxide

solution (1.44 mL) was added at 0°C, and the mixture was.

stirred at room temperature overnight. The reaction mixture was acidified with 1 mol/L hydrochloric acid at 0°C, and

extracted with ethyl acetate. The extract was successively washed with water and saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The . residue was purified by silica gel column chromatography

(hexane/ethyl acetate) to give the title compound (1.11 g) .

^! H NMR (300 MHz, DMSO-de) δ 1.29-1.50 (2H, m) , 1.78-1.87 (1H, m) , 2.54-2.63 (1H, m) , 6.97 (1H, dd, J = 1.51, 0.76 Hz), 7.45

(1H, d, J = 1.51 Hz), 12.49 (1H, brs) .

[0345]

D) tert-butyl (trans-2- (4-bromothiophen-2- yl ) cyclopropyl ) carbamate

To a mixture of trans-2- (4-bromothiophen-2- yl) cyclopropanecarboxylic acid (1.10 g) and tert-butyl alcohol (10 mL) were added triethylamine (0.745 mL) and

diphenylphosphoryl azide (1.15 mL) at room temperature, and the mixture was stirred at room temperature for 2 hr, and then at 80°C overnight. The reaction mixture was cooled to room temperature, water was added, and the mixture was extracted with ethyl acetate. The extract was successively washed with water and saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to give the title compound (930 mg) .

¾ NMR (300 MHz, DMSO-d ₆ ) δ 1.04-1.23 (2H, m) , 1.38 (9H, s) ,

2.07 (1H, ddd, J = 9.09, 6.06, 3.03 Hz),.2.61 (1H, brs) , 6.80 (1H, d, J = 0.76 Hz), 7.22-7.34 (1H, m) , 7.38 (1H, d, J = 1.51 Hz) .

[0346]

E) methyl 5- (trans-2- ( (tert- butoxycarbonyl) amino) cyclopropyl) thiophene-3-carboxylate

A mixture of tert-butyl (trans-2- (4-bromothiophen-2- yl) cyclopropyl) carbamate (925 mg) , triethylamine (0.810 mL) , dichloro (1,1' -bis (diphenylphosphino) ferrocene) palladium (425 mg) and methanol (100 mL) was stirred at 90°C for 8 hr under a carbon monoxide atmosphere (3 atm) . The insoluble material was filtered off and washed with methanol, and the filtrate was concentrated under reduced pressure. The residue was extracted with ethyl acetate and water, and the organic layer was washed with saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to give the title compound (813 mg) .

¾ NMR (300 MHz, DMSO-de) δ 1.08-1.23 (2H, m) , 1.39 (9H, s) ,

2.08 (1H, ddd, J = 9.18, 6.34, 3.03 Hz), 2.60 (1H, brs), 3.76 (3H, s), 7.08-7.15 (1H, m) , 7.29 (1H, brs), 8.07 (1H, d, J = 1.51 Hz) .

[0347] F) methyl 5- (trans-2-aminocyclopropyl) thiophene-3-carboxylate hydrochloride

To a mixture of methyl 5- (trans-2- ( (tert- butoxycarbonyl) amino) cyclopropyl) thiophene-3-carboxylate (450 mg) and ethyl acetate (5 mL) was added 4 mol/L hydrogen

chloride/ethyl acetate solution (3.78 mL) at 0°C, and the mixture was stirred at room temperature overnight. The

reaction mixture was concentrated under reduced pressure, the residue was dissolved in methanol, and ethyl acetate was added. The precipitated solid was collected by filtration and washed with ethyl acetate to give the title compound (320 mg) .

¾ NMR (300 MHz, DMSO-d ₆ ) δ 1.29 (1H, dt, J = 7.76, 6.15 Hz), 1.47 (1H, ddd, J = 10.13, 5.96, 4.73 Hz), 2.56 (1H, ddd, J = 9.75, 6.15, 3.79 Hz), 2.81-2.94 (1H, m) , 3.73-3.80 (3H, m) , 7.23 (1H, d, J = 0.76 Hz), 8.12-8.18 (1H, m) , 8.51 (3H, brs) .

[0348]

G) methyl 5- (trans-2- ( (tert- butoxycarbonyl) (cyclopropylmethyl) amino) cyclopropyl) thiophene- 3-carboxylate

A mixture of methyl 5- (trans-2- aminocyclopropyl) thiophene-3-carboxylate hydrochloride (50.0 mg) , sodium hydrogen carbonate (44.9 mg) , THF (2 mL) and

methanol (2 mL) was stirred at room temperature for 30 min, and cyclopropanecarbaldehyde (18.0 mg) was added. Under a nitrogen atmosphere, the reaction mixture was stirred at 60°C for 2 hr, and sodium borohydride (12.1 mg) was added at 0°C.

Under a nitrogen atmosphere, the reaction mixture was stirred at room temperature for 1.5 hr, and to the reaction mixture were added ethyl acetate and water under ice-cooling. The mixture was extracted with ethyl acetate, and the extract was washed with water and saturated brine and dried over anhydrous sodium sulfate. The solvent was evaporated under- reduced pressure, and the obtained residue was dissolved in THF (3 mL) . Triethylamine (0.037 mL) and di-tert-butyl dicarbonate (0.077 mL) were added, and the reaction mixture was stirred at room temperature overnight. Water was added, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography

(hexane/ethyl acetate) to give the title compound (75.7 mg) . ¾ NMR (300 MHz, DMSO-d ₆ ) δ 0.09-0.30 (2H, m) , 0.34-0.52 (2H, m) , 0.91-1.01 (1H, m) , 1.20-1.28 (1H, m) , 1.28-1.43 (10H, m) , 2.23-2.38 (1H, m) , 2.70-2.81 (1H, m) , 2.92 (1H, dd, J = 14.39, 7.19 Hz), 3.22 (1H, dd, J = 14.20, 7.00 Hz), 3.73-3.80 (3H, m) , 7.19 (1H, dd, J = 1.51, 0.76 Hz), 8.08 (1H, d, J = 1.51 Hz).

[0349]

H) 5- (trans-2- ( (tert- butoxycarbonyl) (cyclopropylmethyl) amino) cyclopropyl) thiophene- 3-carboxylic acid

Methyl 5- (trans-2- ( (tert- butoxycarbonyl) (cyclopropylmethyl) amino) cyclopropyl) thiophene- 3-carboxylate (73.0 mg) was dissolved in THF (1.5 mL) and methanol (1.5 mL) , 2 mol/L aqueous sodium hydroxide solution (0.260 mL) was added at 0°C, and the mixture was stirred at room temperature overnight. The reaction mixture was acidified with 1 mol/L hydrochloric acid, and extracted with ethyl acetate. The extract was successively washed with water and saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure to give the title compound ( 66.5 mg) .

MS: [M+2H-Boc] ⁺ 238.2.

[0350]

I) tert-butyl (cyclopropylmethyl) (trans-2- (4- ( (5-methyl-l, 3, 4- thiadiazol-2-yl) carbamoyl) thiophen-2-yl) cyclopropyl) carbamate

5- (trans-2- ( (tert- Butoxycarbonyl) (cyclopropylmethyl) amino) cyclopropyl) thiophene- 3-carboxylic acid (33.0 mg) , 5-methyl-l, 3, 4-thiadiazol-2-amine (12.4 mg) and triethylamine (0.027 mL) were dissolved in DMF (2 mL) , 0- (7-azabenzotriazol-l-yl) -Ν,Ν,Ν' ,Ν' - tetramethyluronium hexafluorophosphate (44.6 mg) was added, and the mixture was stirred at room temperature overnight.

Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to give the title compound (27.4 mg) .

MS: [M+H] ⁺ 435.3.

[0351]

J) 5- (trans-2- ( (cyclopropylmethyl) amino) cyclopropyl) -N- (5- methyl-1, 3, 4-thiadiazol-2-yl) thiophene-3-carboxamide

dihydrochloride

To a mixture of tert-butyl (cyclopropylmethyl) (trans-2- (4- ( (5-methyl-l, 3, -thiadiazol-2-yl ) carbamoyl) thiophen-2- yl) cyclopropyl) carbamate (27.0 mg) and ethyl acetate (2 mL) was added 4 mol/L hydrogen chloride/ethyl acetate solution

(0.310 mL) at 0°C, and the mixture was stirred at room

temperature overnight. The reaction mixture was concentrated under reduced pressure, and the residue was fractionated with LC/MS (C18, mobile phase: water/acetonitrile (containing 0.1% TFA) ) . The obtained fraction was extracted with ethyl acetate and saturated aqueous sodium hydrogen carbonate solution. The organic layer was successively washed with water and saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was dissolved in ethyl acetate, 4 mol/L hydrogen chloride/ethyl acetate solution was added, and the mixture was stirred at room temperature for 2 nr. The precipitated solid was collected by filtration and washed with ^" ethyl acetate to give the title compound (22.9 mg) . ¾ NMR. (300 MHz, DMSO-d ₆ ) δ 0.35-0.44 (2H, m) , 0.53-0.64 (2H, m) , 1.28-1.39 (1H, m) , 1.63-1.75 (1H, m) , 2.63 (3H, s) , 2.80 (1H, ddd, J = 9.75, 6.15, 3.79 Hz), 2.90-2.99 (2H, m) , 7.51 (1H, s), 8.45 (1H, d, J = 1.51 Hz), 9.57 (2H, brs) , 10.08 (1H, brs), 12.36-13.00 (1H, m) . [0352]

Example 24

N- (4 , 4-difluorocyclohexyl) -5- (trans-2- ( (tetrahydro-2H-pyran-4- ylmethyl) amino) cyclopropyl) thiophene-3-carboxamide

hydrochloride

A) 5- (trans-2- ( (tert- butoxycarbonyl) amino) cyclopropyl) thiophene-3-carboxylic acid

Methyl 5- (trans-2- ( (tert- butoxycarbonyl) amino) cyclopropyl) thiophene-3-carboxylate (450 mg) was dissolved in methanol (5 mL) and THF (5 mL) , 2 mol/L aqueous sodium hydroxide solution (1.89 mL) was added at 0°C, and the mixture was stirred at room temperature overnight. The reaction mixture was acidified with 1 mol/L hydrochloric acid at 0°C and extracted with ethyl acetate. The extract was washed with saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure to give the title compound (385 mg) .

¾ NMR (300 MHz, DMSO-d ₆ ) δ 1.02-1.23 (2H, m) , 1.39 (9H, s) , 2.07 (1H, ddd, J = 9.09, 6.25, 3.22 Hz), 2.59 (1H, brs) , 7.07 (1H, d, J = 0.76 Hz), 7.28 (1H, brs), 7.97 (1H, d, J = 1.51 Hz) , 12.61 (1H, brs) .

[0353]

B) N- (4, 4-difluorocyclohexyl) -5- (trans-2- ( (tetrahydro-2H- pyran-4-ylmethyl) amino) cyclopropyl) thiophene-3-carboxamide hydrochloride

By a method similar to that of Example 1, steps G and H and Example 2, the title compound was obtained.

[0354]

Example 25

4- (trans-2-aminocyclopropyl) -5-methyl-N- ( 1-methyl-lH-pyrazol- 4-yl) thiophene-2-carboxamide dihydrochloride

4- (trans-2- ( (tert-Butoxycarbonyl) amino) cyclopropyl) -5- methylthiophene-2-carboxylic acid (50 mg) , 1-methyl-lH- pyrazol-4-amine hydrochloride (27 mg) and triethylamine (0.094 mL) were dissolved in DMF (1.0 mL) , 0- ( 7-azabenzotriazol-l- yl) -Ν,Ν, N' ,Ν' -tetramethyluronium hexafluorophosphate (77 mg) was added at room temperature, and the mixture was stirred at room temperature overnight. The reaction mixture was poured into water, extracted with ethyl acetate, washed with water and saturated brine, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. To a mixture of the obtained residue and ethyl acetate (2.0 mL) was added 4 mol/L hydrogen chloride/ethyl acetate solution (2.0 mL) at room temperature, and the mixture was stirred at room temperature overnight. The resulting precipitate was collected by

filtration to give the title compound (55 mg) .

MS: [M-2HC1+H] ⁺ 277.1.

[0355]

Example 26

4- (trans-2- ( (cyclopropylmethyl) amino) cyclopropyl) -5-methyl-N- (5-methyl-l, 3, 4-thiadiazol-2-yl ) thiophene-2-carboxamide fumarate

To a mixture of 4- (trans-2- ( (cyclopropylmethyl) amino) cyclopropyl) -5-methyl-N- (5-methyl- 1,3, 4-thiadiazol-2-yl) thiophene-2-carboxamide dihydrochloride (15 mg) and ethyl acetate was added saturated aqueous sodium hydrogen carbonate solution, and the mixture was extracted with ethyl acetate. The extract was washed with water and saturated brine, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. To a mixture of the obtained residue and ethyl acetate was added a solution of fumaric acid (4.13 mg) in ethanol at room temperature, and the reaction mixture was stirred for 30 min. The resulting precipitate was collected by filtration to give the title compound (9.0 mg) .

¹ H NMR (30:0 MHz, METHANOL-d ₄ ) δ 0.26-0.36 (2H, m) , 0.58-0.69 (2H, m) , 1.01-1.12 (1H, m) , 1.13-1.22 (1H, m) , 1.30-1.40 (1H, m) , 2.10-2.20 (1H, m) , 2.55 (3H, s), 2.67 (3H, s) , 2.72-2.79 (1H, m) , 2.83-2.90 (2H, m) , 6.63-6.72 (1H, m) , 7.52-7.65 (1H, m) . [0356]

Example 27

4- (trans-2- ( (cyclopropylmethyl) amino) cyclopropyl) -N- (5-methyl- 1,3, 4-thiadiazol-2-yl) thiophene-2-carboxamide dihydrochloride A) ethyl (E) -3- (5-bromothiophen-3-yl) acrylate

To a suspension of lithium chloride (174 mg) and

acetonitrile (15 mL) were added 5-bromothiophene-3- carbaldehyde (770 mg) and ethyl diethylphosphonoacetate (0.840 mL) at 0°C, and the mixture was stirred at 0°C for 10 min. To the reaction mixture was added 1, 8-diazabicyclo [5.4.0] undec-7- ene (0.638 mL) , and the mixture was stirred at room

temperature overnight. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The extract was successively washed with water and saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column

chromatography (hexane/ethyl acetate) to give the title

compound (1.01 g) .

¾ NMR (300 MHz, DMSO-de) δ 1.19-1.29 (3H, m) , 4.11-4.23 (2H, m) , 6.48 (1H, d, J = 15.90 Hz), 7.53 (1H, d, J = 15.0 Hz), 7.74 (1H, d, J = 1.51 Hz), 7.98 (1H, d, J = 1.51 Hz).

[0357]

B) ethyl trans-2- (5-bromothiophen-3-yl) cyclopropanecarboxylate To a suspension of trimethylsulfoxonium iodide (1.01 g) in DMSO (10 mL) was added sodium hydride (60% in oil, 184 mg) under a nitrogen atmosphere, and the mixture was stirred at room temperature for 30 min. To the reaction mixture was added a mixture of ethyl (E) -3- (5-bromothiophen-3-yl) acrylate (1.00 g) and DMSO (5 mL) , and the mixture was stirred at room

temperature overnight under a nitrogen atmosphere. Water was added to the reaction mixture at room temperature, and the .. mixture was extracted with ethyl acetate. The extract was successively washed with water and saturated brine, dried, over anhydrous sodium sulfate, and concentrated under reduced

pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to give the title compound (263 mg) .

¹ H NMR (300 MHz, DMSO-d ₆ ) δ 1.16-1.24 (3H, m) , 1.27-1.42 (2H, m) , 1.92 (1H, ddd, J = 8.33, 5.30, 4.16 Hz), 2.44 (1H, ddd, J = 9.18, 6.72, 4.16 Hz), 4.03-4.14 (2H, m) , 7.09 (1H, d, J = 1.89 Hz), 7.32 (1H, d, J = 1.51 Hz).

[0358]

C) trans-2- (5-bromothiophen-3-yl) cyclopropanecarboxylic acid

Ethyl trans-2- (5-bromothiophen-3- yl ) cyclopropanecarboxylate (260 mg) was dissolved in THF (2 mL) and ethanol (2 mL) , 2 mol/L aqueous sodium hydroxide solution (1.18 mL) was added at 0°C, and the mixture was

stirred at room temperature overnight. The reaction mixture was acidified with 1 mol/L hydrochloric acid, and extracted with ethyl acetate. The extract was successively washed with water and saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure to give the title compound (215 mg) .

¾ NMR (300 MHz, DMSO-d ₆ ) δ 1.22-1.40 (2H, m) , 1.78 (1H, ddd, J = 8.33, 5.30, 4.16 Hz), 2.39 (1H, ddd, J = 9.09, 6.44, 4.16 Hz), 7.08 (1H, d, J = 1.51 Hz), 7.30 (1H, d, J = 1.51 Hz), 12.35 (1H, brs) .

[0359]

D) tert-butyl (trans-2- (5-bromothiophen-3- yl) cyclopropyl) carbamate

To a mixture of trans-2- ( 5-bromothiophen-3- yl) cyclopropanecarboxylic acid (230 mg) and tert-butyl alcohol (3 mL) were added triethylamine (0.156 mL) and

diphenylphosphoryl azide (0.241 mL) at room temperature, and the mixture was stirred at room temperature for 2 hr and then at 80°C overnight. The reaction mixture was cooled to room temperature, water was added, and the mixture was extracted with ethyl acetate. The extract was successively washed with water and saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to give the title compound (205 mg) .

¾ NMR (300 MHz, DMSO-d ₆ ) δ 0.92-1.10 (2H, m) , 1.34-1.41 (9H, m) , 1.87 (1H, ddd, J = 9.28, 6.25, 3.41 Hz), 2.53-2.65 (1H, m) , 7.00 (1H, d, J = 1.51 Hz), 7.12 (1H, d, J = 1.51 Hz), 7.20 (1H, brs) .

[0360]

E) methyl 4- (trans-2- ( (tert- butoxycarbonyl) amino) cyclopropyl) thiophene-2-carboxylate

A mixture of tert-butyl (trans-2- (5-bromothiophen-3- yl) cyclopropyl) carbamate (330 mg) , triethylamine (0.289 mL) , dichloro (1,1' -bis (diphenylphosphino) ferrocene) palladium (152 mg) and methanol (30 mL) was stirred at 90°C for 8 hr under a carbon monoxide atmosphere (3 atm) . The insoluble material was filtered off, and the filtrate was concentrated under reduced pressure. The residue was extracted with ethyl acetate and water, and the organic layer was washed with saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to give the title compound (253 mg) .

¾ NMR (300 MHz, DMSO-d ₆ ) δ 0.99-1.12 (2H, m) , 1.38 (,9H, s) , 1.88-1.98 (1H, m) , 2.60 (1H, brs), 3.80 (3H, s) , 7.22 (1H, brs), 7.50 (1H, d, J = 1.51 Hz), 7.59 (1H, d, J = 1.51 Hz).

[0361]

F) 4- (trans-2- ( (tert- butoxycarbonyl) amino) cyclopropyl) thiophene-2-carboxylic acid

Methyl 4- (trans-2- ( (tert- butoxycarbonyl) amino) cyclopropyl) thiophene-2-carboxylate (250 mg) was dissolved in THF (4 mL) and methanol (4 mL) , 2 mol/L aqueous sodium hydroxide solution (1.05 mL) was added at 0°C, and the mixture was stirred at room temperature overnight. The reaction mixture was acidified with 1 mol/L hydrochloric acid at 0°C, and the mixture was extracted with ethyl acetate. The extract was successively washed with water and saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure to give the title compound (235 mg) .

¾ N R (300 MHz, DMSO-d ₆ ) δ 0.96-1.12 (2H, m) , 1.38 (9H, s) , 1.92 (1H, ddd, J = 9.18, 6.34, 3.03 Hz), 2.58 (1H, brs) , 7.22 (1H, brs), 7.39-7.46 (1H, m) , 7.50 (1H, d, J = 1.51 Hz), 12.99 (1H, brs) .

[0362]

G) tert-butyl (trans-2- (5- ( (5-methyl-l, 3, 4-thiadiazol-2- yl) carbamoyl) thiophen-3-yl) cyclopropyl) carbamate

4- (trans-2- ( (tert-

Butoxycarbonyl) amino) cyclopropyl) thiophene-2-carboxylic acid (80.0 mg) , 5-methyl-l, 3, 4-thiadiazol-2-amine (35.8 mg) and triethylamine (0.079 mL) were dissolved in DMF (3 mL) , 0-(7- azabenzotriazol-l-yl) -Ν,Ν,Ν' ,Ν' -tetramethyluronium

hexafluorophosphate (129 mg) was added, and the mixture was stirred at room temperature overnight. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to give the title compound (58.2 mg) .

MS: [M+H] ⁺ 381.2.

[0363]

H) 4- (trans-2-aminocyclopropyl) -N- (5-methyl-l, 3, 4-thiadiazol- 2-yl) thiophene-2-carboxamide dihydrochloride

To a mixture of tert-butyl (trans-2- (5- ( (5-methyl-l, 3, 4- thiadiazol-2-yl) carbamoyl) thiophen-3-yl) cyclopropyl) carbamate (55.0 mg) and ethyl acetate (3 mL) was added 4 mol/L hydrogen chloride/ethyl acetate solution (0.361 mL) at 0°C, and the mixture was stirred at room temperature overnight. The precipitated solid was collected by filtration and washed with ethyl acetate to give the title compound (26.3 mg) .

λΗ NMR (300 MHz, DMSO-de) δ 1.11-1.23 (1H, m) , 1.44 (1H, ddd, J = 10.03, 5.87, 4.54 Hz), 2.43 (1H, ddd, J = 9.75, 6.15, 3.41 Hz), 2.62 (3H, s), 2.81 (1H, dd, J = 7.76, 3.98 Hz), 7.73 (1H, s), 7.92-8.19 (1H, m) , 8.54 (3H, brs) .

[0364]

I) 4- (traris-2- ( (cyclopropylmethyl) amino) cyclopropyl) -N- (5- methyl-1, 3, -thiadiazol-2-yl) thiophene-2-carboxamide

dihydrochloride

To a mixture of 4- (trans-2-aminocyclopropyl) -N- (5-methyl- 1, 3, 4-thiadiazol-2-yl) thiophene-2-carboxamide dihydrochloride (24.0 mg) , sodium hydrogen carbonate (14.3 mg) , THF (1.5 mL) and methanol (1.5 mL) was added cyclopropanecarbaldehyde (5.71 mg) at room temperature. Under a nitrogen atmosphere, the reaction mixture was stirred at 60°C for 1.5 hr and at room temperature for 30 min, and sodium borohydride (3.86 mg) was added at 0°C. The reaction mixture was stirred at room

temperature for 1 hr, and ethyl acetate, water and saturated aqueous sodium hydrogen carbonate solution were added to the reaction mixture. The mixture was extracted with ethyl acetate, and the extract was successively washed with water and

saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure and the residue was purified by silica gel column chromatography (ethyl, acetate/methanol) . To the obtained fraction was added 4 mol/L hydrogen chloride/ethyl acetate solution and the reaction mixture was stirred at room temperature overnight. The

precipitated solid was collected by filtration and washed with ethyl acetate to give the title compound (17.6 mg) .

¾ N R (300 MHz, DMSO-d ₆ ) δ 0.30-0.44 (2H, m) , 0.50-0.68 (2H, m) , 1.05-1.17 (1H, m) , 1.19-1.32 (1H, m) , 1.52-1.66 (1H, m) , 2.55-2.67 (4H, m) , 2.86-3.00 (3H, m) , 7.75 ( 1H, s ) , .8.07 (1H, brs) , 9.37-9.60 (2H, m) .

[0365]

Example 28

4- (trans-2- ( (cyclopropylmethyl) amino) cyclopropyl) -N- (4,4- difluorocyclohexyl ) thiophene-2-carboxamide hydrochloride

A) tert-butyl (trans-2- (5- ( (4 , 4- difluorocyclohexyl) carbamoyl) thiophen-3- yl ) cyclopropyl ) carbamate

4- (trans-2- ( (tert- Butoxycarbonyl) amino) cyclopropyl) thiophene-2-carboxylic acid (150 mg) , 4 , -difluorocyclohexanamine hydrochloride (100 mg) and triethylamine (0.295 mL) were dissolved in DMF (6 mL) , 0- (7-azabenzotriazol-l-yl) -N, , ' , N' -tetramethyluronium

hexafluorophosphate (242 mg) was added at room temperature, and the mixture was stirred overnight. To the reaction mixture were added ethyl acetate and water, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to give the title compound (211 mg) .

¾ N R (300 MHz, DMSO-d ₆ ) δ 0.92-1.12 (2H, m) , 1.33-1.42 (9H, m) , 1.48-1.69 (2H, m) , 1.79-2.14 (7H, m) , 2.62 (1H, brs) , 3.92 (1H, d, J = 7.57 Hz), 7.22 (1H, brs), 7.31 (1H, s) , 7.55 (1H, d, J = 1.14 Hz) , 8.20 (1H, d, J = 7.95 Hz) .

[0366]

B) 4- (trans-2-aminocyclopropyl) -N- (4,4- difluorocyclohexyl) thiophene-2-carboxamide hydrochloride

To a mixture of tert-butyl (trans-2- (5- ( (4, - difluorocyclohexyl ) carbamoyl) thiophen-3- yl) cyclopropyl) carbamate (210 mg) and ethyl acetate (3 mL) was added 4 mol/L hydrogen chloride/ethyl acetate solution (1.31 mL) at 0°C, and the mixture was stirred at room temperature overnight. The precipitated solid was collected by filtration, washed with ethyl acetate, and dried under reduced pressure to. give the title compound (108 mg) .

MS: [M-HC1+H] ⁺ 301.2.

[0367]

C) 4- (trans-2- ( (cyclopropylmethyl) amino) cyclopropyl) -N- (4,4- difluorocyclohexyl) thiophene-2-carboxamide hydrochloride

To a mixture of 4- (trans-2-aminocyclopropyl) -N- ( 4 , 4- . difluorocyclohexyl) thiophene-2-carboxamide hydrochloride (30.0 mg) , sodium hydrogen carbonate (18.7 mg) , THF (1.5 mL) and methanol (1.5 mL) was added cyclopropanecarbaldehyde (7.49 mg) at room temperature. Under a nitrogen atmosphere, the reaction mixture was stirred at 60°C for 1.5 hr and at room temperature for 30 min, and sodium borohydride (5.05 mg) was added at 0°C. The reaction mixture was stirred at room temperature for 1 hr, and ethyl acetate, water and saturated aqueous sodium hydrogen carbonate solution were added to the reaction mixture. The mixture was extracted with ethyl acetate, and the extract was successively washed with water and saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) , and to the obtained fraction was added 4 mol/L hydrogen chloride/ethyl acetate solution. The reaction mixture was stirred at room temperature overnight, and the precipitated solid was

collected by filtration, washed with ethyl acetate and dried under reduced pressure to give the title compound (18.1 mg) . ^! H NMR (300 MHz, DMSO-ds) δ 0.36 (2H, brs) , 0.59 (2H, brs) , 0.97-1.34 (2H, m) , 1.45-1.68 (3H, m) , 1.80-2.13 (6H, m) , 2.94 (3H, d, J = 7.57 Hz), 3.92 (2H, brs), 7.44-7.75 (2H, m) , 8.23 (1H, d, J = 8.33 Hz), 9.19 (1H, brs).

[0368]

Example 29

N- (4, 4-difluorocyclohexyl) -4- (trans-2- (tetrahydro-2H-pyran-4- ylamino) cyclopropyl ) thiophene-2-carboxamide hydrochloride

To a mixture of 4- (trans-2-aminocyclopropyl) -N- (4, 4- difluorocyclohexyl) thiophene-2-carboxamide hydrochloride (30.0 mg) , sodium hydrogen carbonate (18.7 mg) , THF (1.5 mL) and methanol (1.5 mL) was added dihydro-2H-pyran-4 (3H) -one (10.7 mg) . Under a nitrogen atmosphere, the reaction mixture was stirred at 60°C for 1.5 hr and at room temperature for 30 min, and sodium borohydride (5.05 mg) was added at 0°C. The

reaction mixture was stirred at room temperature for 1 hr, and ethyl acetate, water and saturated aqueous sodium hydrogen carbonate solution were added to the reaction mixture. The mixture was extracted with ethyl acetate, and the extract was successively washed with water and saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (methanol/ethyl acetate) , and to the obtained fraction was added 4 mol/L hydrogen chloride/ethyl acetate solution. The reaction mixture was stirred at room temperature overnight, and the precipitated solid was

collected by filtration, and washed with ethyl acetate to give the title compound (14.8 mg) .

^X H N R (300 MHz, DMSO-d ₆ ) δ 1.11-1.33 (1H, m) , 1.42-2.20 (15H, m) , 2.93 (1H, brs) , 3.38-3.55 (2H, m) , 3.92 (3H, d, J = 10.60 Hz), 7.43-7.71 (2H, m) , 8.23 (1H, d, J = 6.82 Hz), 9.43 (1H, brs) .

[0369]

Example 30

5- (trans-2- ( (cyclopropylmethyl) amino) cyclopropyl) -N- (4, 4- difluorocyclohexyl) thiophene-3-carboxamide hydrochloride

A) tert-butyl (trans-2- ( 4- ( ( 4 , 4- difluorocyclohexyl) carbamoyl) thiophen-2- yl) cyclopropyl) carbamate

5- (trans-2- ( (tert- Butoxycarbonyl) amino) cyclopropyl) thiophene-3-carboxylic acid (100 mg) , 4, 4-difluorocyclohexanamine hydrochloride (66.6 mg) and triethylamine (0.197 mL) were dissolved in DMF (4 mL) , 0- (7-azabenzotriazol-l-yl) -Ν,Ν,Ν' ,Ν' -tetramethyluronium

hexafluorophosphate (161 mg) was added, . and the mixture was stirred at room temperature overnight. To the reaction mixture were added ethyl acetate and water, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to give the title compound (92.1 mg) .

MS: [M+H] ⁺ 401.2.

[0370]

B) 5- (trans-2-aminocyclopropyl) -N- (4, 4- difluorocyclohexyl) thiophene-3-carboxamide hydrochloride

To a mixture of tert-butyl (trans-2- (4- ( (4, 4- difluorocyclohexyl) carbamoyl) thiophen-2- yl) cyclopropyl) carbamate (90.0 mg) and ethyl acetate (3 mL) was added 4 mol/L hydrogen chloride/ethyl acetate solution (0.562 mL) at 0°C, and the mixture was stirred at room

temperature overnight. The precipitated solid was collected by filtration and washed with ethyl acetate to give the title compound (76.8 mg) .

MS: [M-HC1+H] ⁺ 301.2.

[0371]

C) 5- (trans-2- ( (cyclopropylmethyl) amino) cyclopropyl) -N- (4,4- difluorocyclohexyl) thiophene-3-carboxamide hydrochloride

To a mixture of 5- (trans-2-aminocyclopropyl) -N- ( 4 , 4- difluorocyclohexyl ) thiophene-3-carboxamide hydrochloride (30.0 mg) , sodium hydrogen carbonate (18.7 mg) , THF (1.5 mL) and methanol (1.5 mL) was added cyclopropanecarbaldehyde (7.49 mg) at room temperature. Under a nitrogen atmosphere, the reaction mixture was stirred at 60°C for 1.5 hr and at room temperature for 30 min, and sodium borohydride (5.05 mg) was added at 0°C. Under a nitrogen atmosphere, the reaction mixture was stirred at room temperature for 1 hr, and ethyl acetate, water and saturated aqueous sodium hydrogen carbonate solution were added to the reaction mixture. The mixture was extracted with , ethyl acetate, and the extract was successively washed with water and saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate), and to the obtained fraction was added 4 mol/L hydrogen chloride/ethyl acetate solution. The reaction mixture was stirred at room temperature overnight, and. the precipitated solid was collected by filtration, and washed with ethyl acetate to give the title compound (14.6 mg) .

*Η NMR (300 MHz, DMSO-de) δ 0.38 (2H, m, J = 3.41 Hz), 0.58 (2H, d, J = 6.44 Hz), 1.07 (1H, brs) , 1.20-1.38 (1H, m) , 1.45-1.68 (3H, m) , 1.86 (3H, m) , 2.03 (3H, m) , 2.69 (2H, m), 2.95 (2H, d, J = 7.19 Hz), 3.93 (1H, brs), 7.28 (1H, s) , 7.95 (1H, s) , 8.05 (1H, d, J = 7.95 Hz), 9.26 (2H, brs) .

[0372]

Example 31

N- (4, 4-difluorocyclohexyl) -5- (trans-2- ( tetrahydro-2H-pyran-4- ylamino) cyclopropyl) thiophene-3-carboxamide hydrochloride

To a mixture of 5- (trans-2-aminocyclopropyl) -N- (4, 4- difluorocyclohexyl) thiophene-3-carboxamide hydrochloride (30.0 mg) , sodium hydrogen carbonate (18.7 mg) , THF (1.5 mL) and methanol (1.5 mL) was added dihydro-2H-pyran- (3H) -one (10.7 mg) at room temperature. Under a nitrogen atmosphere, the reaction mixture was stirred at 60°C for 1.5 hr and at room temperature for 30 min, and sodium, borohydride (5.05 mg) was added at 0°C. The reaction mixture was stirred at room

temperature for 1 hr, and ethyl acetate, water and saturated aqueous sodium hydrogen carbonate solution were added to the reaction mixture. The mixture was extracted with ethyl acetate, and the extract was successively washed with water and

saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (methanol/ethyl acetate) , and to the obtained fraction was added 4 mol/L

hydrogen chloride/ethyl acetate solution. The reaction mixture was stirred at room temperature overnight, and the

precipitated solid was collected by filtration, and washed with ethyl acetate to give the title compound (18.1 mg) .

¾ NMR (300 MHz, DMSO-de) δ 1.25-1.41 (1H, m) , 1.62 (5H, d, J = 10.60 Hz), 1.77-2.15 (9H, m) , 2.62-2.80 (1H, m) , 2.89-3.08 (1H, m) , 3.39-3.59 (1H, m) , 3.92 (3H, d, J = 9.47 Hz), 7.28 (1H, s) , 7.95 (1H, s), 8.04 (1H, d, J = 7.95 Hz), 9.44 (2H, brs) . [0373]

Example 32

5- (trans-2- ( (cyclopropylmethyl) amino) cyclopropyl) -N- (tetrahydro-2H-pyran-4-yl) thiophene-3-carboxamide

hydrochloride

A) tert-butyl (2- ( 4- ( (tetrahydro-2H-pyran-4- yl) carbamoyl) thiophen-2-yl) cyclopropyl) carbamate

5- (trans-2- ( (tert- Butoxycarbonyl) amino) cyclopropyl) thiophene-3-carboxylic acid (50.0 mg) , tetrahydro-2H-pyran-4-amine (19.6 mg) and

triethylamine (0.049 mL) were dissolved in D F (2 mL) , 0- (7- azabenzotriazol-l-yl) -Ν,Ν,Ν' ,Ν' -tetramethyluronium

hexafluorophosphate (81.0 mg) was added at room temperature, and the mixture was stirred overnight. To the reaction mixture were added ethyl acetate and water, and the mixture was

extracted with ethyl acetate. The extract was washed with saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to give the title compound (61.8 mg) .

^X H NMR (300 MHz, DMSO-d ₆ ) δ 0.99-1.11 (1H, m) , 1.12-1.21 (1H, m) , 1.39 (9H, s) , 1.44-1.62 (2H, m) , 1.72 (2H, dd, J = 12.49, 2.27 Hz), 2.06 (1H, ddd, J = 8.99, 5.77, 3.41. Hz), 2.62 (1H, brs), 3.33-3.42 (2H, m) , 3.80-4.00 (3H, m) , 7.17 (1H, s) , 7.28 (1H, brs), 7.83 (1H, d, J = 1.51 Hz), 8.00 (1H, d, J = 7.95 Hz) .

[0374]

B) 5- (trans-2-aminocyclopropyl) -N- (tetrahydro-2H-pyran-4- yl) thiophene-3-carboxamide hydrochloride

To a mixture of tert-butyl (2- ( - ( (tetrahydro-2H-pyran-4- yl) carbamoyl) thiophen-2-yl) cyclopropyl) carbamate (59.0 mg) and ethyl acetate (3 mL) was added 4 mol/L hydrogen chloride/ethyl acetate solution (0.402 mL) at 0°C, and the mixture was stirred at room temperature overnight. The precipitated solid was collected by filtration and washed with ethyl acetate to give . the title compound (45.5 mg) .

^! H NMR (300 MHz, DMSO-d ₆ ) δ 1.17-1.31 (1H, m) , 1.40-1.62 (3H, m) , 1.64-1.79 (2H, m) , 2.55 (1H, td, J = 6.44, 3.41 Hz), 2.75- 2.88 (1H, m) , 3.29-3.45 (2H, m) , 3.79-4.01 (3H, m) , 7.24-7.32 (1H, m) , 7.94 (1H, d, J = 1.51 Hz), 8.08 (1H, d, J = 7.95 Hz), 8.55 (3H, d, J = 2.65 Hz) .

[0375]

C) 5- (trans-2- ( (cyclopropylmethyl) amino) cyclopropyl) -N- (tetrahydro-2H-pyran-4-yl) thiophene-3-carboxamide

hydrochloride

To a mixture of 5- (trans-2-aminocyclopropyl) -N- (tetrahydro-2H-pyran-4-yl) thiophene-3-carboxamide

hydrochloride (43.0 mg) , sodium hydrogen carbonate (29.8 mg) , THF (2 mL) and methanol (2 mL) was added

cyclopropanecarbaldehyde (11.9 mg) . Under a nitrogen

atmosphere, the reaction mixture was stirred at 60°C for 1.5 hr and at room temperature for 30 min, and sodium borohydride

(8.06 mg) was added at 0°C. Under a nitrogen atmosphere, the reaction mixture was stirred at room temperature for 1 hr, and ethyl acetate, water and saturated aqueous sodium hydrogen carbonate solution were added to the reaction mixture. The mixture was extracted with ethyl acetate, and the extract was washed successively with water and saturated brine. The extract was dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel colum chromatography (hexane/ethyl . acetate) , and to the obtained fraction was added 4 mol/L hydrogen chloride/ethyl acetate solution under ice-cooling. The reaction mixture was. stirred at room temperature for 2 hr. The precipitated solid was collected by filtration and washed with ethyl acetate to give the title compound (29.8 mg) .

¾ NMR (300 MHz, DMSO-de) δ 0.31-0.44 (2H, m) , 0.51-0.66 (2H, m) , 0.98-1.15 (1H, m) , 1.21-1.38 (1H, m) , 1.42-1.66 (3H, m) , 1.66-1.81 (2H, m) , 2.70 (1H, ddd, J = 9.66, 6.25, 3.41 Hz), 2.91-3.01 (3H, m), 3.33-3.45 (2H, m) , 3.78-4.04 (3H, m). , 7.28 (1H, s), 7.95 (1H, d, J = 1.51 Hz), 8.06 (1H, d, J - 7.57 Hz),

9.30 (2H, brs) .

[0376]

Example 33

5- (trans-2- (cyclobutylamino) cyclopropyl) -N- ( 5-methyl-l, 3, 4~ thiadiazol-2-yl) thiophene-3-carboxamide dihydrochloride

A) methyl 5- (trans-2- ( (te ^' rt- butoxycarbonyl) (cyclobutyl) amino) cyclopropyl) thiophene-3- carboxylate

To a mixture of methyl 5- (trans-2- aminocyclopropyl) thiophene-3-carboxylate hydrochloride (100 mg) , sodium hydrogen carbonate (90.0 mg) , THF (4 mL) and methanol (4 mL) was added cyclobutanone (36.0 mg) . Under a nitrogen atmosphere, the reaction mixture was stirred at 60°C for 1.5 hr and at room temperature for 30 min, and sodium borohydride (24.3 mg) was added at 0°C. The reaction mixture was stirred at room temperature for 1 hr, and ethyl acetate, water and saturated aqueous sodium hydrogen carbonate solution were added to the reaction mixture. The mixture was extracted with ethyl acetate, and the extract was successively washed with water and saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure. The obtained residue was dissolved in THF (3 mL) , and triethylamine (0.090 mL) and di-tert-butyl dicarbonate (0.120 mL) were added. The reaction mixture was stirred at room temperature overnight, and the mixture was extracted with ethyl acetate and water. The organic layer was washed with saturated brine, and dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to give the title compound (98.9 mg) .

XH NMR (300 MHz, DMSO-d ₆ ) δ 1.23-1.33 (2H, m) , 1.37 (9H, s) , 1.45-1.68 (2H, m) , 2.01-2.32 (5H, m) , 2.62 (1H, ddd, J = 7.10, . 5.02, 3.41 Hz), 3.77 (3H, s) , 3.92-4.09 (1H, m) , 7.14-7.21 (1H, m) , 8.08 (1H, d, J = 1.51 Hz). [0377]

B) 5- (trans-2- ( (tert- butoxycarbonyl) (cyclobutyl) amino) cyclopropyl) thiophene-3- carboxylic acid

Methyl 5- (trans-2- ( (tert- butoxycarbonyl) (cyclobutyl) amino) cyclopropyl) thiophene-3- carboxylate (95.0 mg) -was dissolved in THF (2 mL) and methanol (2 mL) , 2 mol/L aqueous sodium hydroxide solution (0.338 mL) was added at 0°C, and the mixture was stirred at room

temperature overnight. The reaction mixture was acidified with 1 mol/L hydrochloric acid at 0°C, and extracted with ethyl acetate. The extract was successively washed with water and saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure to give the title compound (90.1 mg) .

¾ NMR (300 MHz, DMSO-d ₆ ) δ 1.22-1.32 (2H, m) , 1.38 (9H, s) , 1.48-1.67 (2H, m) , 2.04-2.30 (5H, m) , 2.61 (1H, ddd, J = 7.29, 4.45, 3.41 Hz), 3.94-4.07 (1H, m) , 7.11-7.15 (1H, m) , 7.99 (1H, d, J = 1.51 Hz), 12.60 (1H, brs) .

[0378]

C) tert-butyl cyclobutyl (trans-2- (4- ( (5-methyl-l, 3, 4- thiadiazol-2-yl) carbamoyl) thiophen-2-yl) cyclopropyl) carbamate

5- (trans-2- ( (tert- Butoxycarbonyl) (cyclobutyl) amino) cyclopropyl) thiophene-3- carboxylic acid (45.0 mg) , 5-methyl-l, 3, 4-thiadiazol-2-amine (18.4 mg) and triethylamine (0.028 mL) were dissolved in DMF (3 mL), 0- (7-azabenzotriazol-l-yl) -Ν,Ν,Ν' ,Ν' - tetramethyluronium hexafluorophosphate (60.8 mg) was added, and the mixture was stirred at room temperature overnight. The reaction mixture was extracted with ethyl acetate and water, and the organic layer was washed with saturated brine, dried . over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column

chromatography (hexane/ethyl acetate) to give the title

compound (38.3 mg). ¾ N R (300 MHz, DMSO-d ₆ ) δ 1.14-1.43 (11H, m) , 1.48-1.69 (2H, m) , 2.04-2.34 (5H, m) , 2.58-2.67 (4H, m) , 4.03 (1H, quin, J = 8.52 Hz), 7.47 (1H, s) , 8.36 (1H, d, J = 1.14 Hz), 12.64 (1H, brs) .

[0379]

D) 5- (trans-2- (cyclobutylamino) cyclopropyl) -N- (5-methyl-l, 3, 4- thiadiazol-2-yl) thiophene-3-carboxamide dihydrochloride

To a mixture of tert-butyl cyclobutyl (trans-2- (4- ( (5- methyl-1, 3, 4-thiadiazol-2-yl) carbamoyl) thiophen-2- yl) cyclopropyl) carbamate (36.0 mg) and ethyl acetate (2 mL) was added 4 mol/L hydrogen chloride/ethyl acetate solution

(0.207 mL) at 0°C, and the mixture was stirred at room

temperature overnight.. The precipitated solid was collected by filtration and washed with ethyl acetate to give the title compound (26.5 mg) .

^X H NMR (300 MHz, DMSO-d ₆ ) δ 1.17 (1H, t, J = 7.00 Hz), 1.26- 1.42 (1H, m), 1.56-1.68 (1H, m) , 1.74-1.92 (2H, m) , 2.29 (4H, d, J = 13.63), 2.69-3.11 (3H, m) , 3.60-4.26 (2H, m) , 7.42 (1H, s) , 8.45 (1H, brs), 9.67-10.18 (1H, m) , 13.03 (1H, brs).

[0380]

Example 34

5- (trans-2- (cyclobutylamino) cyclopropyl) -N- ( 1-methyl-lH- pyrazol-4-yl) thiophene-3-carboxamide hydrochloride

A) tert-butyl cyclobutyl (trans-2- ( 4- (( l-methyl-lH-pyrazol-4- yl) carbamoyl) thiophen-2-yl) cyclopropyl) carbamate

5- (trans-2- ( (tert- Butoxycarbonyl) (cyclobutyl) amino) cyclopropyl) thiophene^3- carboxylic acid (45.0 mg) , l-methyl-lH-pyrazol-4-amine (15.5 mg) and triethylamine (0.028 mL) were dissolved in DMF (3 mL) , 0- (7-azabenzotriazol-l-yl) -Ν,Ν,Ν' ,Ν' -tetramethyluronium

hexafluorophosphate (60.8 mg) was added, and the mixture, was stirred at room temperature overnight. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to give the title compound (24.0 mg) .

¾ NMR (300 MHz, DMSO-d ₆ ) δ 1.20-1.35 (2H, m) , 1.36-1.42 (9H, m) , 1.47-1.70 (2H, m) , 2.01-2.34 (5H, m) , 2.57-2.67 (1H, m) , 3.76-3.85 (3H, m) , 3.93-4.15 (1H, m) , 7.30 (1H, d, J = 0.76 Hz), 7.50 (1H, s), 7.93 (2H, s) , 10.11 (1H, s) .

[0381]

B) 5- (trans-2- (cyclobutylamino) cyclopropyl) -N- (1-methyl-lH- pyrazol-4-yl) thiophene-3-carboxamide hydrochloride

To a mixture of tert-butyl cyclobutyl (trans-2- (4- ( (1- methyl-lH-pyrazol-4-yl) carbamoyl) thiophen-2- yl) cyclopropyl) carbamate (22.0 mg) and ethyl acetate (1 mL) was added 4 mol/L hydrogen chloride/ethyl acetate solution

(0.132 mL) at 0°C, and the mixture was stirred at room

temperature overnight. The precipitated solid was collected by filtration and washed with ethyl acetate to give the title compound (11.2 mg) .

¾ NMR (300 MHz, DMSO-de) δ 1.24-1.38 (1H, m) , 1.51-1.66 (1H, m) , 1.72-1.90 (2H, m) , 2.12-2.40 (4H, m) , 2.74 (1H, ddd, J = 9.94, 6.15, 3.22 Hz), 2.82-2.96 (1H, m) , 3.75-3.95 (4H, m) , 7.29-8.12 (4H, m) , 9.76 (2H, brs) , 10.26 (1H, s) .

[0382]

Example 35

4- (trans-2- ( (cyclopropylmethyl) amino) cyclopropyl) -N- (4, 4- difluorocyclohexyl) thiazole-2-carboxamide hydrochloride

A) ethyl (E) -3- (2-bromothiazol-4-yl) acrylate

To a suspension of lithium chloride (450 mg) in

acetonitrile (30 mL) were added 2-bromothiazole-4-carbaldehyde (2.00 g) and ethyl diethylphosphonoacetate (2.17 mL) at 0°C, and the mixture was stirred under a nitrogen atmosphere at 0°C for 5 min. To the reaction mixture was added 1,8- diazabicyclo [5.4.0] undec-7-ene (1.65 mL) at 0°C, and the

mixture was stirred under a nitrogen atmosphere at room

temperature overnight. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The extract was successively washed with water and saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column

chromatography (hexane/ethyl acetate) to give the title

compound (2.34 g) .

¾ NMR (300 MHz, DMSO-de) δ 1.25 (3H, t, J = 7.00 Hz), 4.19 (2H, q, J = 6.94 Hz), 6.54 (1H, d, J = 15.52 Hz), 7.60 (1H, d, J = 15.52 Hz) , 8.14 (1H, s) .

[0383]

B) ethyl trans-2- (2-bromothiazol-4-yl) cyclopropanecarboxylate

To a suspension of trimethylsulfoxonium iodide (2.35 g) in DMSO (20 mL) was added sodium hydride (50% in oil, 512 mg) under a nitrogen atmosphere, and the mixture was stirred at room temperature for 30 min. To the reaction mixture was added a mixture of ethyl (E) -3- (2-bromothiazol-4-yl) acrylate (2.33 g) and DMSO (10 mL) , and the mixture was stirred at room

temperature overnight. Water was added to the reaction mixture at 0°C, and the mixture was extracted with ethyl acetate. The extract was successively washed with water and saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to give the title compound (912 mg) .

!H NMR (300 MHz, DMSO-de) δ 1.16-1.23 (3H, m) , 1.39-1.48 (2H, m) , 1.93-2.03 (1H, m) , 2.56-2.65 (1H, m)., 4.09 (2H, q, J =

6.94 Hz) , 7.56 (1H, s) . .

[0384]

C) trans-2- (2-bromothiazol-4-yl) cyclopropanecarboxylic acid

Ethyl trans-2- (2-bromothiazol-4- yl) cyclopropanecarboxylate (905 mg) was dissolved. in THF (5 mL) and ethanol (5mL) , 2 mol/L aqueous sodium hydroxide

solution (4.10 mL) was added at 0°C,. and the mixture was

stirred at room temperature overnight. The reaction mixture was acidified with 1 mol/L hydrochloric. acid, and extracted with ethyl acetate. The extract was successively washed with water and saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure to give the title compound (809 mg) .

XH NMR (300 MHz, DMSO-d ₆ ) δ 1.32-1.45 (2H, m) , 1.88 (1H, ddd, J = 8.24, 5.40, 4.16 Hz), 2.53-2.60 (1H, m) , 7.54 (1H, s) , 12.42 (1H, brs) .

[0385]

D) tert-butyl (trans-2- (2-bromothiazol-4- yl) cyclopropyl) carbamate

To a mixture of trans-2- (2-bromothiazol-4- yl) cyclopropanecarboxylic acid (805 mg) and tert-butyl alcohol (10 mL) were added triethylamine (0.543 mL) and

diphenylphosphoryl azide (0.838 mL) at room temperature, and the mixture was stirred at room temperature for 2 hr and then at 80°C overnight. The reaction mixture was cooled to room temperature, water was added, and the mixture was extracted with ethyl acetate. The extract was successively washed with water and saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to give the title compound (514 mg) .

¾ NMR (300 MHz, DMSO-d ₆ ) δ 1.05-1.14 (2H, m) , 1.37 (9H, s) , 2.06 (lH, td, J = 7.57, 3.03 Hz), 2.79 (1H, brs), 7.24 (1H, brs) , 7.36 (1H, s) .

[0386]

E) trans-2- (2-bromothiazol-4-yl) cyclopropanamine hydrochloride

To a mixture of tert-butyl (trans-2- (2-bromothiazol-4- yl) cyclopropyl) carbamate (200 mg) and ethyl acetate (3 mL) was added 4 mol/L hydrogen chloride/ethyl acetate solution (1.57 mL) at 0°C, and the mixture was stirred at room temperature overnight. The precipitated solid was collected by filtration and washed with ethyl acetate to give the title compound (158 mg) .

!H NMR (300 MHz, DMSO-de) δ 1.24 (1H, dt, J = 7.95, 6.06 Hz), 1.36-1.46 (1H, m) , 2.56 (1H, ddd, J = 9.75, 6.15, 3.41 Hz), 2.81-2.95 (1H, m) , 7.56 (1H, s) , 8.54 (3H, brs) .

[0387]

F) trans-2- (2-bromothiazol-4-yl) -N- (cyclopropylmethyl) cyclopropanamine

A mixture of trans-2- (2-bromothiazol-4- yl) cyclopropanamine hydrochloride (100 mg) , sodium hydrogen carbonate (131 mg) , THF (3 ml) and methanol (3 mL) was stirred at room temperature for 30 min, and cyclopropanecarbaldehyde (32.9 mg) was added. Under a nitrogen atmosphere, the reaction mixture was stirred at 60°C for 2 hr, and sodium borohydride (22.2 mg) was added at 0°C. Under a nitrogen atmosphere, the reaction mixture was stirred at room temperature for 1.5 hr, and ethyl acetate and water were added to the reaction mixture under ice-cooling. The mixture was extracted with ethyl

acetate, and the extract was successively washed with water and saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (NH,

hexane/ethyl acetate) to give the title compound (84.4 mg) .

!H NMR (300 MHz, DMSO-d ₆ ) δ 0.02-0.09 (2H, m) , 0.33-0.41 (2H, m) , 0.76-0.89 (1H, m) , 0.90-1.03 (2H, m) , 1.87-2.02 (1H, m) , 2.36-2.47 (4H, m) , 7.27 (1H, s) .

[0 ^' 388]

G) tert-butyl (trans-2- (2-bromothiazol-4- yl ) cyclopropyl ) (cyclopropylmethyl) carbamate

trans-2- (2-Bromothiazol-4-yl) -N- (cyclopropylmethyl) cyclopropanamine (81.0 mg) was dissolved in THF (4 mL) , and triethylamine (0.062 mL) and di-tert-butyl dicarbonate (0.103 mL) were added. The reaction mixture was stirred at room temperature overnight, and extracted with ethyl acetate and water. The organic layer was washed with water and saturated brine, dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure, . The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to give the title compound (106 mg) .

¾ NMR (300 MHz, DMSO-d ₆ ) δ 0.06-0.28 (2H, m) , 0.33-0.53 (2H, m) , 0.87-1.03 (1H, m) , 1.24 (2H, dd, J = 7.57, 6.44 Hz), 1.35 (9H, s), 2.18-2.33 (1H, m) , 2.79-2.99 (2H, m) , 3.21 (1H, dd, J = 14.39, 6.82 Hz), 7.44 (1H, s) .

[0389]

H) methyl 4- (trans-2- ( (tert- butoxycarbonyl ) (cyclopropylmethyl) amino) cyclopropyl) thiazole- 2-carboxylate

A mixture of tert-butyl (trans-2- (2-bromothiazol-4- yl) cyclopropyl) (cyclopropylmethyl) carbamate (80.0 mg) ,

triethylamine (0.060 mL) , dichloro (1, 1' - bis (diphenylphosphino) ferrocene) palladium (31.4 mg) and

methanol (15 mL) was stirred at 90°C for 8 hr under a carbon monoxide atmosphere (3 atm) . After cooling to room temperature, the insoluble material was filtered off, and the filtrate was concentrated under reduced pressure. The residue was extracted with ethyl acetate and water, and the organic layer was washed with saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to give the title compound (76.0 mg) .

^X H NMR (300 MHz, DMSO-de) δ 0.05-0.28 (2H, m) , 0.32-0.53 (2H, m) , 0.87-1.05 (1H, m) , 1.27-1.37 (11H, m) , 2.36 (1H, td, J = 7.86, 3.22 Hz), 2.87-3.03 (2H, m) , 3.22 (1H, dd, J = 14.39, 6.82 Hz), 3.82-3.93 (3H, m) , 7.85 (1H, s) .

[0390]

I) 4- (trans-2- ( (tert- butoxycarbonyl) (cyclopropylmethyl) amino) cyclopropyl) thiazole- 2-carboxylic acid

-Methyl ^■ 4- (trans-2- ( (tert- butoxycarbonyl) (cyclopropylmethyl) amino) cyclopropyl) thiazole- 2-carboxylate (93.0 mg) was dissolved in methanol (5 mL) , 2 mol/L aqueous sodium hydroxide solution (0.330 mL) was added at 0°C, and the mixture was stirred at room temperature for 1 hr. The reaction mixture was acidified with 1 mol/L hydrochloric acid at 0°C, and extracted with ethyl acetate. The extract was successively washed with water and saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure to give the title compound (78.9 mg) . MS: [M+H] ⁺ 339.2.

[0391]

J) tert-butyl (cyclopropylmethyl) (trans-2- (2- ( (4, 4- difluorocyclohexyl) carbamoyl) thiazol-4- yl) cyclopropyl) carbamate

4- (trans-2- ( (tert- Butoxycarbonyl) (cyclopropylmethyl) amino) cyclopropyl) thiazole- 2-carboxylic acid (38.0 mg) , 4 , 4-difluorocyclohexanamine hydrochloride (21.2 mg) and triethylamine (0.063 mL) were dissolved in DMF (3 mL) , 0- ( 7-azabenzotriazol-l-yl ) -N, N, ' , ' - tetramethyluronium hexafluorophosphate (51.2 mg) was added, and the mixture was stirred at room temperature overnight. To the reaction mixture were added ethyl acetate and water, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to give the title compound (17.6 mg) .

1H NMR (300 MHz, DMSO-de) δ .0.07-0.28 (2H, m) , 0.32-0.54 (2H, m) , 0.90-1.04 (1H, m) , 1.23-1.42 (11H, m) , 1.64-1.95 (5H, m) , 1.99-2.12 (3H, m) , 2.29 (1H, ddd, J = 9.47, 6.25, 3.22 Hz), 2.94-3.07 (2H, m) , 3.10-3.25 (1H, m) , 3.96 (1H, d, J = 7.95 Hz), 7.66 (1H, s), 8.54 (1H, d, J = 8.71 Hz).

[0392]

K) 4- (trans-2- ( (cyclopropylmethyl) amino) cyclopropyl) -N- (4,4- difluorocyclohexyl) thiazole-2-carboxamide hydrochloride

To a mixture of tert-butyl (cyclopropylmethyl) (trans-2- (2- ( ( , -difluorocyclohexyl) carbamoyl) thiazol-4- yl) cyclopropyl) carbamate (16.0 mg) and ethyl acetate (1.5 mL) was added 4 mol/L hydrogen chloride/ethyl acetate solution. (0.088 mL) at 0°C, and the mixture was stirred at room temperature overnight. The precipitated solid was collected by filtration and washed with ethyl acetate to give the title compound (10.1 mg) .

iH N R (300 MHz, DMSO-d ₆ ) δ 0.36 (2H, d, J = 4.16 Hz) , 0.57 (2H, d, J = 6.44 Hz), 1.00-1.18 (1H, m) , 1.33-1.49 (1H, m) , 1.55- 1.67 (1H, m) , 1.68-1.87 (4H, m) , 2.05 (3H, brs) , 2.76-2.85 (1H, m) , 2.94 (2H, d, J = 6.44 Hz), 3.13 (1H, brs), 3.97 (2H, brs), 7.78 (1H, s), 8.59 (1H, d, J = 8.71 Hz), 9.33-9.67 (2H, m) .

[0393]

Example 36

5- (trans-2- ( (cyclopropylmethyl) amino) cyclopropyl) -N- (4,4- difluorocyclohexyl) thiophene-2-carboxamide hydrochloride

A) trans-2- (5-bromothiophen-2-yl) cyclopropanecarboxylic acid

To a mixture of lithium hydroxide monohydrate (12.7 g) , water (100 mL) and methanol (100 mL) was added ethyl trans-2- (5-bromothiophen-2-yl) cyclopropanecarboxylate (16.7 g) at room temperature. After stirring at room temperature for 24 hr, methanol was evaporated under reduced pressure. The aqueous layer was washed with dichloromethane, acidified with 2 mol/L hydrochloric acid, and extracted with ethyl acetate. The extract was dried over anhydrous sodium sulfate, and

concentrated under reduced pressure to give the title compound (14.7 g) .

¾ NMR (400 MHz, CDC1 ₃ ) δ 1.35-1.40 (1H, m) , 1.65-1.69 (1H, m) , 1.90-1.94 (1H, m) , 2.67-2.72 (1H, m) , 6.61 (1H, d, J = 3.6 Hz), 6.87 (1H, d, J = 3.6 Hz).

[0394]

B) tert-butyl (2- (5-bromothiophen-2-yl) cyclopropyl) carbamate

trans-2- (5-Bromothiophen-2-yl) cyclopropanecarboxylic acid

(14.7 g) was dissolved in acetone (150 mL) , triethylamine

(9.03 g) was added, and then ethyl chloroformate (9.68 g) was added at -20°C. After stirring at -10°C to -20°C for 2 hr, a mixture of sodium azide (6.57 g) and water (20 mL) was added, and the mixture was stirred at -10°C to -20°C for 3 hr. Acetone was evaporated by concentration under reduced pressure, and water (150 rtiL) and toluene (150 itL) were added. The

aqueous layer was extracted twice with toluene (100 mL) . The combined extract was dried over anhydrous sodium sulfate and concentrated to 150 mL under reduced pressure. To the obtained mixture was added tert-butyl alcohol (25 mL) , and the mixture was heated under reflux for 18 hr. The mixture was

concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (petroleum

ether/ethyl acetate) to give the title compound (8.66 g) .

¾ NMR (400 MHz, CDC1 ₃ ) δ 1.15 (2H, t, J = 6.8 Hz), 1.46 (9H, s), 2.08-2.13 (1H, m) , 2.67-2.74 (1H, m) , 4.81 (1H, s) , 6.57 (1H, d, J = 3.2 Hz), 6.82 (1H, d, J = 3.2 Hz).

[0395]

C) trans-2- ( 5-bromothiophen-2-yl) cyclopropanamine

hydrochloride

To a mixture of tert-butyl (2- (5-bromothiophen-2- yl ) cyclopropyl ) carbamate (200 mg) and ethyl acetate (5 mL) was added 4 mol/L hydrogen chloride/ethyl acetate solution (1.57 mL) at 0°C, and the mixture was stirred at room temperature overnight. The precipitated solid was collected by filtration and washed with ethyl acetate to give the title compound (135 mg) .

^X H NMR (300 MHz, DMSO-d ₆ ) δ 1.23 (1H, dt, J = 7.95, 6.25 Hz), 1.36-1.51 (1H, m) , 2.47-2.54 (1H, m) , 2.73-2.85 (1H, m), 6.75 (1H, dd, J = 3.79, 1.14 Hz), 6.99-7.10 (1H, m) , 8.50 (2H, brs) .

[0396]

D) tert-butyl (2-trans- (5-bromothiophen-2- yl) cyclopropyl) (cyclopropylmethyl) carbamate

To a mixture of trans-2- ( 5-bromothiophen-2- yl) cyclopropanamine hydrochloride (130 mg) , sodium hydrogen carbonate (107 mg) , THF (4 mL) and methanol (4 mL) was added cyclopropanecarbaldehyde. (43.0 mg) at room temperature. Under a nitrogen atmosphere, the reaction mixture was stirred at 60°C for 1.5 hr and then at room temperature for 30 min, and sodium borohydride (29.0 mg) was added at 0°C. The reaction mixture was stirred at room temperature for 1 hr, and ethyl acetate, water and saturated aqueous sodium hydrogen carbonate solution were added to the reaction mixture. The mixture was extracted with ethyl acetate, and the extract was successively washed with water and saturated brine and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure.

The obtained residue was dissolved in THF (5 mL) ,

triethylamine (0.094 mL) and di-tert-butyl dicarbonate (0.156 mL) were added, and the mixture was stirred at room

temperature overnight. To the reaction mixture were added ethyl acetate and water, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to give the title compound (160 mg) .

¾ NMR (300 MHz, DMSO-d ₆ ) δ 0.08-0.27 (2H, m) , 0.35-0.52 (2H, m) , 0.88-1.06 (1H, m) , 1.14-1.24 (1H, m) , 1.25-1.34 (1H, m) , 1.39 (9H, s), 2.20-2.32 (1H, m) , 2.65-2.77 (1H, m) , 2.93 (1H, dd, J = 14.39, 6.82 Hz), 3.18 (1H, dd, J = 14.39, 6.82 Hz), 6.71 (1H, dd, J = 3.79, 0.76 Hz), 7.02 (1H, d, J = 3.79 Hz).

[0397]

E) methyl 5- (trans-2- ( (tert- butoxycarbonyl) (cyclopropylmethyl) amino) cyclopropyl) thiophene- 2-carboxylate

A mixture of tert-butyl (2-trans- (5-bromothiophen-2- yl) cyclopropyl) (cyclopropylmethyl) carbamate (155 mg) ,

triethylamine (0.116 mL), dichloro (1, 1' - bis (diphenylphosphino) ferrocene) palladium (60.9 mg) and

methanol (15 mL) was stirred at 90°C for 8 hr under a carbon monoxide atmosphere (3 atm) . After cooling to room temperature, the insoluble material was filtered off, and the filtrate was concentrated under reduced pressure. The residue was extracted with ethyl acetate and water, and the organic layer was washed with saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to give the title compound (138 mg) .

XH NMR (300 MHz, DMSO-d ₆ ) δ 0.06-0.30 (2H, m) , 0.33-0.52 (2H, m) , 0.84-1.05 (1H, m) , 1.23-1.33 (1H, m) , 1.35-1.49 (10H, m) , 2.39 (1H, ddd, J = 9.47, 6.25, 3.22 Hz), 2.76-2.87 (1H, m) , 2.88-3.02 (1H, m) , 3.20 (1H, dd, J = 14.20, 7.00 Hz), 3.73- 3.82 (3H, m) , 6.96 (1H, d, J = 3.79 Hz), 7.63 (1H, d, J = 3.79 Hz) .

[0398]

F) 5- (trans-2- ( (tert- butoxycarbonyl ) (cyclopropylmethyl) amino) cyclopropyl) thiophene- 2-carboxylic acid

Methyl 5- (trans-2- ( (tert- butoxycarbonyl) (cyclopropylmethyl) amino) cyclopropyl) thiophene- 2-carboxylate (130 mg) was dissolved in methanol (5 mL) , 2 mol/L aqueous sodium hydroxide solution (0.462 mL) was added at 0°C, and the mixture was stirred at room temperature overnight. The reaction mixture was acidified with 1 mol/L hydrochloric acid at 0°C, and extracted with ethyl acetate. The extract was successively washed with water and saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure to give the title compound (125 mg) . MS: [M+2H- (Boc) ] ⁺ 238.2.

[0399]

G) tert-butyl (cyclopropylmethyl) (trans-2- (5- ( (4, 4- difluorocyclohexyl) carbamoyl) thiophen-2- yl ) cyclopropyl ) carbamate

5- (trans-2- ( (tert-

Butoxycarbonyl ) (cyclopropylmethyl) amino) cyclopropyl) thiophene- 2-carboxylic acid (35.0 mg) , 4 , 4-difluorocyclohexanamine hydrochloride (19.6 mg) and triethylamine (0.058 mL) were dissolved in DMF (3 mL) , 0- (7-azabenzotriazol-l-yl) -Ν,Ν,Ν' ,Ν' - tetramethyluronium hexafluorophosphate (47.3 mg) was added, and the mixture was stirred at room temperature overnight. To the reaction mixture were added ethyl acetate and water, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to give the title compound (42.3 mg) .

¾ NMR (300 MHz, DMSO-d ₆ ) δ 0.08-0.28 (2H, m) , 0.34-0.52 (2H, m) , 0.88-1.04 (1H, m) , 1.18-1.27 (1H, m) , 1.32-1.42 (10H, m) , 1.50-1.69 (2H, m) , 1.77-1.96 (3H, m) , 1.97-2.13 (3H, m) , 2.32 (1H, m) , 2.70-2.80 (1H, m) , 2.89-3.04 (1H, m) , 3.10-3.26 (1H, m) , 3.91 (1H, d, J = 7.57 Hz), 6.86 (1H, d, J = 3.79 Hz), 7.58 (1H, d, J = 3.79 Hz), 8.16 (1H, d, J = 7.57 Hz).

[0400]

H) 5- (trans-2- ( (cyclopropylmethyl) amino) cyclopropyl) -N- (4, 4- difluorocyclohexyl) thiophene-2-carboxamide hydrochloride

tert-Butyl (cyclopropylmethyl) (trans-2- ( 5- ( (4, 4- difluorocyclohexyl) carbamoyl) thiophen-2- yl) cyclopropyl) carbamate (40.0 mg) was dissolved in ethyl acetate (3 mL) , 4 mol/L hydrogen chloride/ethyl acetate solution (0.220 mL) was added at 0°C, and the mixture was stirred at room temperature for 4 hr. The precipitated solid was collected by filtration and washed with ethyl acetate to give the title compound (22.1 mg) .

¾ NMR (300 MHz, DMSO-de) δ 0.31-0.44 (2H, m) , 0.51-0.64 (2H, m) , 0.97-1.15 (1H, m) , 1.23-1.40 (1H, m) , 1.50-1.72 (3H, m) , 1.78-2.10 (6H, m) , 2.74 (1H, ddd, J = 9.84, 6.25, 3.60 Hz), 2.87-3.05 (3H, m) , 3.82-4.00 (1H, m) , 6.93 (1H, d, J = 3.79 Hz), 7.63 (1H, d, J = 3.79 Hz), 8.25 (1H, d, J = 7.95 Hz), 9.39 (2H, brs) .

[0401]

Example 37

5- (trans-2- ( (cyclopropylmethyl) amino) cyclopropyl) -N- (5-methyl- 1, 3, 4-thiadiazol-2-yl) thiophene-2-carboxamide dihydrochloride A) tert-butyl (cyclopropylmethyl) (trans-2- (5- ( (5-methyl-l, 3, 4- thiadiazol-2-yl) carbamoyl) thiophen-2-yl) cyclopropyl) carbamate

5- (trans-2- ( (tert- Butoxycarbonyl ) (cyclopropylmethyl) amino) cyclopropyl) thiophene- 2-carboxylic acid (35.0 mg) , 5-methyl-l, 3, 4-thiadiazol-2-amine (13.1 mg) and triethylamine (0.029 mL) were dissolved in DMF (3 mL) , 0- (7-azabenzotriazol-l-yl) -Ν,Ν,Ν' ,Ν' - tetramethyluronium hexafluorophosphate (47.3 mg) was added, and the mixture was stirred at room temperature overnight. To the reaction mixture were added ethyl acetate and water, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to give the title compound (23.7 mg) .

¾ NMR (300 MHz, DMSO-d ₆ ) δ 0.08-0.31 (2H, m) , 0.35-0.53 (2H, m) , 0.90-1.07 (1H, m) , 1.20-1.50 (11H, m) , 2.33-2.45 (1H, m) , 2.62 (3H, s), 2.7.8-2.88 (1H, m) , 2.90-3.07 (1H, m) , 3.19 (1H, dd, J = 14.39, 6.82 Hz), 6.98 (1H, d, J = 3.79 Hz), 8.08 (1H, brs) , 12.85 (1H, brs) .

[0402]

B) 5- (trans-2- ( (cyclopropylmethyl) amino) cyclopropyl) -N- (5- methyl-1, 3, 4-thiadiazol-2-yl ) thiophene-2-carboxamide

dihydrochloride

To a mixture of tert-butyl (cyclopropylmethyl) (trans-2- (5- ( (5-methyl-l, 3, 4-thiadiazol-2-yl) carbamoyl) thiophen-2- yl) cyclopropyl) carbamate (22.0 mg) and ethyl acetate (2 mL) was added 4 mol/L hydrogen chloride/ethyl acetate solution (0.127 mL) at 0°C, and the mixture was stirred at room

temperature overnight. The precipitated solid was collected by filtration, and washed with ethyl acetate and methanol to give the title compound (10.2 mg) .

¾ NMR (300 MHz, DMSO-de) - δ 0.32-0.44 (2H, m) , 0.51-0.65 (2H, m) , 0.97-1.19 (1H, m) , 1.30-1.45 (1H, m) , 1.65-1.81 (1H, m) , 2.62 (3H, s), 2.78-2.90 (1H, m) , 2.96 (2H, d, J = 5.68 Hz), 3.01-3.11 (1H, m) , 3.86 (2H, s) , 7.06 (1H, d, J = 3.79 Hz), 8.09 (1H, s), 9.55 (2H, brs) .

[0403]

Example 38

N-cyclopentyl-5- (trans-2- (tetrahydro-2H-pyran-4- ylamino) cyclopropyl) thiophene-3-carboxamide hydrochloride

[optical isomer, compound derived from methyl 5- (trans-2- ( (tert-butoxycarbonyl) amino) cyclopropyl) thiophene-3- carboxylate (optical isomer, retention time long) ]

A) methyl 5- (trans-2- ( (tert- butoxycarbonyl) amino) cyclopropyl) thiophene-3-carboxylate

(optical isomer, retention time long)

B) methyl 5- (trans-2- ( (tert- butoxycarbonyl) amino) cyclopropyl) thiophene-3-carboxylate

(optical isomer, retention time short)

A racemate (16.9 g) of methyl 5- (trans-2- ( (tert- butoxycarbonyl ) amino) cyclopropyl) thiophene-3-carboxylate was fractionated by SFC (column: CHIRALPAK AD, 20 mmIDx250 mmL, manufactured by Daicel Corporation, mobile phase: carbon dioxide/methanol = 820/180) , and the obtained fraction was concentrated under reduced pressure to give the title compound (7.23 g) having a short retention time and the title compound (7.39 g) having a long retention time.

[0404]

methyl 5- (trans-2- ( (tert- butoxycarbonyl) amino) cyclopropyl) thiophene-3-carboxylate

(optical isomer, retention time long)

NMR (300 MHz, DMSO-d ₆ ) δ 1.07-1.25 (2H, m) , 1.39 (9H, s) , 2.08 (1H, ddd, J = 9.09, 6.25, 3.22 Hz), 2.60 (1H, d, J = 5.30 Hz), 3.76 (3H,. s), 7.08-7.14. ( 1H, m) , 7.29 (1H, brs), 8.07 (1H, d, J = 1.14 Hz) .

HPLC retention time 2.859 min (column: CHIRALPAK ADH (trade name), 4.6 mmIDxl50 mmL, mobile phase: carbon dioxide/methanol = 820/180, flow rate: 4.0 mL/min, temperature: 35°C, detection: UV 220 nm, concentration: 0.5 mg/mL, injection volume: 0.005 mL) . [0405]

methyl 5- (trans-2- ( (tert- butoxycarbonyl) amino) cyclopropyl) thiophene-3-carboxylate

(optical isomer, retention time short)

xti NMR (300 MHz, DMSO-d ₆ ) δ 1.08-1.24 (2H, m) , 1.39 (9H, s) , 2.08 (1H, ddd, J = 8.99, 6.15, 3.03 Hz), 2.60 (1H, brs) , 3.77 (3H, s), 7.12 (1H, dd, J = 1.51, 0.76 Hz), 7.29 (1H, brs), 8.07 (1H, d, J = 1.14 Hz) .

HPLC retention time 1.950 min (column: CHIRALPAK ADH (trade name), 4.6 mmIDxl50 mmL, mobile phase: carbon dioxide/methanol

= 820/180, flow rate: 4.0 mL/min, temperature: 35°C, detection: UV 220 nm, concentration: 0.5 mg/mL, injection volume: 0.005 mL) .

Methyl 5- (trans-2- ( (tert- butoxycarbonyl) amino) cyclopropyl) thiophene-3-carboxylate

(optical isomer, retention time long) was clarified to be methyl 5- ( ( 1R, 2R) -2- ( (tert- butoxycarbonyl) amino) cyclopropyl) thiophene-3-carboxylate .

Methyl 5- (trans-2- ( (tert- butoxycarbonyl) amino) cyclopropyl) thiophene-3-carboxylate

(optical isomer, retention time short) was clarified to be methyl 5- ( (IS, 2S) -2- ( (tert- butoxycarbonyl ) amino) cyclopropyl) thiophene-3-carboxylate .

[0406]

C) 5- (trans-2- ( (tert- butoxycarbonyl ) amino) cyclopropyl) thiophene-3-carboxylic acid [optical isomer, compound derived from methyl 5- (trans-2- ( (tert-butoxycarbonyl) amino) cyclopropyl) thiophene-3- carboxylate (optical isomer, retention time long) ]

Methyl 5- (trans-2- ( (tert- butoxycarbonyl ) amino) cyclopropyl) thiophene-3-carboxylate

(optical isomer, retention time long) (458 mg) was dissolved in methanol (5 mL) , 2 mol/L aqueous sodium hydroxide solution (1.93 mL) was added at 0°C, and the mixture was stirred at room temperature overnight. The reaction mixture was acidified with 1 mol/L hydrochloric acid at 0°C, and extracted with ethyl acetate. The extract was successively washed with water and saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure to give the title compound (435 mg) .

^X H NMR (300 MHz, DMSO-de) δ 1.05-1.22 (2H, m) , 1.39 (9H, s) , 2.07 (1H, ddd, J = 9.09, 6.06, 3.03 Hz), 2.59 (1H, d, J = 7.57 Hz), 7.05-7.09 (lH,.m), 7.28 (1H, brs) , 7.97 (1H, d, J = 1.51 Hz) , 12.61 (1H, brs) .

5- (trans-2- ( (tert- butoxycarbonyl ) amino) cyclopropyl) thiophene-3-carboxylic acid [optical isomer, compound derived from methyl 5- (trans-2- ( (tert-butoxycarbonyl) amino) cyclopropyl) thiophene-3- carboxylate (optical isomer, retention time long) ] was clarified to be 5- (( 1R, 2R) -2- ( (tert- butoxycarbonyl) amino) cyclopropyl) thiophene-3-carboxylic acid.

[0407]

D) tert-butyl (trans-2- (4- (cyclopentylcarbamoyl) thiophen^2- yl ) cyclopropyl ) carbamate [optical isomer, compound derived from methyl 5- (trans-2- ( (tert- butoxycarbonyl ) amino) cyclopropyl) thiophene-3-carboxylate (optical isomer, retention time long)]

5- (trans-2- ( (tert- Butoxycarbonyl ) amino) cyclopropyl) thiophene-3-carboxylic acid [optical isomer, compound derived from methyl 5- (trans-2- ( (tert-butoxycarbonyl) amino) cyclopropyl) thiophene-3- carboxylate (optical isomer, retention time long)] (70.0 mg) , cyclopentanamine (23.1 mg) and triethylamine (0.069 mL) were dissolved in DMF (3 mL) , 0- (7-azabenzotriazol-l-yl) -Ν,Ν,Ν' ,Ν' - tetramethyluronium hexafluorophosphate (113 mg) was added, and the mixture was stirred at room temperature overnight. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was

successively washed with water and saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to give the title compound (77.8 mg) .

MS: [M+H] ⁺ 351.3.

tert-Butyl (trans-2- (4- (cyclopentylcarbamoyl) thiophen-2- yl) cyclopropyl) carbamate [optical isomer, compound derived from methyl 5- (trans-2- ( (tert- butoxycarbonyl) amino) cyclopropyl) thiophene-3-carboxylate (optical isomer, retention time long) ] was clarified to be tert-butyl ( (1R, 2R) -2- (4- (cyclopentylcarbamoyl) thiophen-2- yl ) cyclopropyl) carbamate .

[0408]

E) 5- (trans-2-aminocyclopropyl) -N-cyclopentylthiophene-3- carboxamide hydrochloride [optical isomer, compound derived from methyl 5- (trans-2- ( (tert- butoxycarbonyl) amino) cyclopropyl) thiophene-3-carboxylate (optical isomer, retention time long) ]

To a mixture of tert-butyl (trans-2- (4- (cyclopentylcarbamoyl) thiophen-2-yl ) cyclopropyl) carbamate

[optical isomer, compound derived from methyl 5- (trans-2- ( (tert-butoxycarbonyl) amino) cyclopropyl) thiophene-3- carboxylate (optical isomer, retention time long)] (75.0 mg) and ethyl acetate (2 mL) was added 4 mol/L hydrogen

chloride/ethyl acetate solution (0.535 mL) at 0°C, and the mixture was stirred at room temperature overnight. The precipitated solid was collected by filtration and washed with ethyl acetate to give the title compound (56.2 mg) .

MS: [M+H- (HC1) ] ⁺ 251.2.

5- (trans-2-Aminocyclopropyl) -N-cyclopentylthiophene-3- carboxamide hydrochloride [optical isomer, compound derived from methyl 5- (trans-2- ( (tert- butoxycarbonyl) amino) cyclopropyl) thiophene-3-carboxylate

(optical isomer, retention time long) ] was clarified to be 5- ( (1R,2R) -2-aminocyclopropyl) -N-cyclopentylthiophene-3- carboxamide hydrochloride. [0409]

F) N-cyclopentyl-5- (trans-2- (tetrahydro-2H-pyran-4- ylamino) cyclopropyl) thiophene-3-carboxamide hydrochloride . [optical isomer, compound derived from methyl 5- (trans-2- ( (tert-butoxycarbonyl) amino) cyclopropyl) thiophene-3- carboxylate (optical isomer, retention time long) ]

To a mixture of 5- (trans-2-aminocyclopropyl) -N- cyclopentylthiophene-3-carboxamide hydrochloride [optical isomer, compound derived from methyl 5- (trans-2- ( (tert- butoxycarbonyl) amino) cyclopropyl) thiophene-3-carboxylate

(optical isomer, retention time long)] (53.0 mg) , sodium hydrogen carbonate (38.8 mg) , THF (3 mL) and methanol (3 mL) was added dihydro-2H-pyran-4 (3H) -one (22.2 mg) at room

temperature. Under a nitrogen atmosphere, the reaction mixture was stirred at 60°C for 1.5 hr and at room temperature for 30 min, and sodium borohydride (10.5 mg) was added at 0°C. The reaction mixture was stirred at room temperature for 1 hr, and ethyl acetate, water and saturated aqueous sodium hydrogen carbonate solution were added to the reaction mixture. The. mixture was extracted with ethyl acetate, and the extract was successively washed with water and saturated brine and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/methanol) , and to the obtained fraction was added 4 mol/L hydrogen chloride/ethyl acetate solution. The reaction mixture was stirred at room temperature overnight, and the precipitated solid was

collected by filtration, and washed with ethyl acetate to give the title compound (38.9 mg) .

λΕ NMR (300 MHz, DMSO-d ₆ ) δ 1.28-1.39 (1H, m) , 1.39-1.75 (9H, m) , 1.78-1.92 (2H, m) , 1.93-2.06 (2H, m) , 2.73 (1H, ddd, J= 9.75, 6.34, 3.60 Hz), 2.99 (1H, brs) , 3.24-3.34 (2H, m) , 3.47 (1H, brs), 3.85-4.02 (2H, m) , 4.15 (1H, sxt, J = 6.74 Hz), 7.29 (1H, s), 7.94 (1H, d, J = 1.14 Hz), 8.02 (lH, d, J = 7.19 Hz) , 9.54 (2H, brs) . N-Cyclopentyl-5- (trans-2- (tetrahydro-2H-pyran-4- ylamino) cyclopropyl) thiophene-3-carboxamide hydrochloride

[optical isomer, compound derived from methyl 5- (trans-2- ( (tert-butoxycarbonyl) amino) cyclopropyl) thiophene-3- carboxylate (optical isomer, retention time long) ] was

clarified to be N-cyclopentyl-5- ( (1R, 2R) -2- (tetrahydro-2H- pyran-4-ylamino) cyclopropyl ) thiophene-3-carboxamide

hydrochloride

[0410]

Example 39

N-cyclopentyl-5- (trans-2- (tetrahydro-2H-pyran-4- ylamino) cyclopropyl) thiophene-3-carboxamide hydrochloride

[optical isomer, compound derived from methyl 5- (trans-2- ( (tert-butoxycarbonyl) amino) cyclopropyl) thiophene-3- carboxylate (optical isomer, retention time short) ]

■ By a method similar to that of Example 38, the title compound was obtained.

N-Cyclopentyl-5- (trans-2- (tetrahydro-2H-pyran-4- ylamino) cyclopropyl) thiophene-3-carboxamide hydrochloride

[optical isomer, compound derived from methyl 5- (trans-2- ( (tert-butoxycarbonyl) amino) cyclopropyl) thiophene-3- carboxylate (optical isomer, retention time short) ] was clarified to be N-cyclopentyl-5- (( IS , 2S) -2- (tetrahydro-2H- pyran-4-ylamino) cyclopropyl) thiophene-3-carboxamide .

[0411]

Example 40

N- (5-methyl-l, 3, -thiadiazol-2-yl) -5- (trans-2- ( (tetrahydro-2H- pyran-4-ylmethyl) amino) cyclopropyl) thiophene-3-carboxamide dihydrochloride [optical isomer, compound derived from methyl , 5- (trans-2- ( (tert-butoxycarbonyl) amino) cyclopropyl) thiophene- 3-carboxylate (optical isomer, retention time long) ]

A) tert-butyl (trans-2- (4- ( (5-methyl-l, 3, 4-thiadiazol-2- yl) carbamoyl) thiophen-2-yl) cyclopropyl) carbamate [optical isomer, compound derived from methyl 5- (trans-2- ( (tert- butoxycarbonyl) amino) cyclopropyl) thiophene-3-carboxylate (optical isomer, retention time long) ]

5- (trans-2- ( (tert- Butoxycarbonyl) amino) cyclopropyl) thiophene-3-carboxylic acid [optical isomer, compound derived from methyl 5- (trans-2- ( (tert-butoxycarbonyl) amino) cyclopropyl) thiophene-3- carboxylate (optical isomer, retention time long)] (70.0 mg) , 5-methyl-l, 3, 4-thiadiazol-2-amine (31.3 mg) and triethylamine (0.069 mL) were dissolved in DMF (3 mL) , 0- (7-azabenzotriazol-

1-yl) -Ν,Ν,Ν' , N' -tetramethyluronium hexafluorophosphate (113 mg) was added, and the mixture was stirred at room temperature overnight. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was successively washed with water and saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to give the title compound (37.6 mg) .

MS: [M+H] ⁺ 381.2.

tert-Butyl (trans-2- (4- ( (5-methyl-l, 3, 4-thiadiazol-2- yl) carbamoyl) thiophen-2-yl) cyclopropyl) carbamate [optical isomer, compound derived from methyl 5- (trans-2- ( (tert- butoxycarbonyl ) amino) cyclopropyl) thiophene-3-carboxylate (optical isomer, retention time long) ] was clarified to be tert-butyl ( (1R, 2R) -2- (4- ( (5-methyl-l, 3, 4-thiadiazol-2- yl) carbamoyl) thiophen-2-yl) cyclopropyl) carbamate .

[0412]

B) 5- (trans-2-aminocyclopropyl) -N- (5-methyl-l, 3, 4-thiadiazol-

2-yl) thiophene-3-carboxamide dihydrochloride [optical isomer, compound derived from methyl 5- (trans-2- ( (tert- butoxycarbonyl) amino) cyclopropyl) thiophene-3-carboxylate (optical isomer, retention time long) ]

To a mixture of tert-butyl (trans-2- (4- ( (5-methyl-l, 3, 4- thiadiazol-2-yl) carbamoyl) thiophen-2-yl) cyclopropyl) carbamate [optical isomer, compound derived from methyl 5- (trans-2- ( (tert-butoxycarbonyl) amino) cyclopropyl) thiophene-3- carboxylate (optical isomer, retention time long)] (37.6 mg) , ethyl acetate (2 mL) and methanol (2 mL) was added 4 mol/L hydrogen chloride/ethyl acetate solution (0.247 mL) at 0°C, and the mixture was stirred at room temperature overnight. The precipitated solid was collected by filtration and washed with ethyl acetate to give the title compound (34.5 mg) .

MS: [M+H- (2HC1) ] ⁺ 281.1.

5- (trans-2-Aminocyclopropyl) -N- ( 5-methyl-l , 3, 4- thiadiazol-2-yl) thiophene-3-carboxamide dihydrochloride

[optical isomer, compound derived from methyl 5- (trans-2- ( (tert-butoxycarbonyl) amino) cyclopropyl) thiophene-3- carboxylate (optical isomer, retention time long) ] was

clarified to be 5- ( (1R, 2R) -2-aminocyclopropyl) -N- (5-methyl- 1, 3, 4-thiadiazol-2-yl) thiophene-3-carboxamide dihydrochloride.

[0413]

C) N- (5-methyl-l, 3, 4-thiadiazol-2-yl ) -5- (trans-2- ( (tetrahydro- 2H-pyran-4-ylmethyl) amino) cyclopropyl) thiophene-3-carboxamide dihydrochloride [optical isomer, compound derived from methyl 5- (trans-2- ( (tert-butoxycarbonyl) amino) cyclopropyl) thiophene- 3-carboxylate (optical isomer, retention time long) ]

To a mixture of 5- (trans-2-aminocyclopropyl) -N- (5-methyl- 1,3, 4-thiadiazol-2-yl) thiophene-3-carboxamide dihydrochloride [optical isomer, compound derived from methyl 5- (trans-2- ( (tert-butoxycarbonyl) amino) cyclopropyl) thiophene-3- carboxylate (optical isomer, retention time long)] (33.0 mg) , sodium hydrogen carbonate (19.6 mg) , THF (2 mL) and methanol (2 mL) was added tetrahydro-2H-pyran-4-carbaldehyde (12.8 mg) at room temperature. Under a nitrogen atmosphere, the reaction mixture was stirred at 60°C for 1.5 hr and at room temperature for 30 min, and sodium borohydride (5.30 mg) was added at 0°C. The reaction mixture was stirred at room temperature for 1 hr, and ethyl acetate, water and saturated aqueous sodium hydrogen carbonate solution were added to the reaction mixture. The . mixture was extracted with ethyl acetate, and the extract was successively washed with water and saturated brine and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure. The residue, was purified by silica gel column chromatography (ethyl acetate/methanol) , and to the obtained fraction was added 4 mol/L hydrogen chloride/ethyl acetate solution. The reaction mixture was stirred at room temperature overnight. The precipitated solid was collected by filtration and washed with ethyl acetate to give the title compound (19.6 mg) .

¾ NMR (300 MHz , DMSO-d ₆ ) δ 1.16-1.41 (3H, m) , 1.60-1.77 (3H, m) , 1.84-2.06 (1H, m) , 2.63 (3H, s) , 2.70-2.84 (1H, m) , 2.94-

3.11 (3H, m) , 3.29 (2H, t, J = 11.93 Hz), 3.90-4.00 (2H, m) ,

7.51 (1H, s), 8.46 (1H, s) , 9.26 (2H, brs) .

N- (5-Methyl-l, 3, 4-thiadiazol-2-yl) -5- (trans-2-

( (tetrahydro-2H-pyran-4-ylmethyl) amino) cyclopropyl) thiophene- 3-carboxamide dihydrochloride [optical isomer, compound derived from methyl 5- (trans-2- ( (tert- butoxycarbonyl ) amino) cyclopropyl) thiophene-3-carboxylate

(optical isomer, retention time long) ] was clarified to be N- (5-methyl-l, 3, 4-thiadiazol-2-yl) -5- ( (1R, 2R) -2- ( (tetrahydro-2H- pyran-4-ylmethyl ) amino) cyclopropyl) thiophene-3-carboxamide dihydrochloride .

[0414]

Example 41

N- (5-methyl-l, 3, 4-thiadiazol-2-yl) -5- (trans-2- ( (tetrahydro-2H- pyran-4-ylmethyl) amino) cyclopropyl) thiophene-3-carboxamide dihydrochloride [optical isomer, compound derived from methyl 5- (trans-2- ( (tert-butoxycarbonyl) amino) cyclopropyl) thiophene- 3-carboxylate (optical isomer, retention time short)]

By a method similar to that of Example 40, the title compound was obtained.

N- (5-Methyl-l, 3, 4-thiadiazol-2-yl) -5- (trans-2- ( (tetrahydro-2H-pyran-4-ylmethyl) amino) cyclopropyl) thiophene- 3-carboxamide dihydrochloride [optical isomer, compound, derived from methyl 5- (trans-2- ( (tert- butoxycarbonyl) amino) cyclopropyl) thiophene-3-carboxylate (optical isomer, retention time short) ] was clarified to be N- (5-methyl-l, 3, 4-thiadiazol-2-yl) -5- ( (1S,2S) -2- ( (tetrahydro-2H- pyran-4-ylmethyl) amino) cyclopropyl) thiophene-3-carboxamide dihydrochloride .

[0415]

Example 42

5- (trans-2- (cyclobutylamino) cyclopropyl) -N- (tetrahydro-2H- pyran-4-yl) thiophene-3-carboxamide hydrochloride [optical isomer, compound derived from methyl 5- (trans-2- ( (tert- butoxycarbonyl) amino) cyclopropyl) thiophene-3-carboxylate

(optical isomer, retention time long) ]

A) tert-butyl (trans-2- ( 4- ( (tetrahydro-2H-pyran-4- yl) carbamoyl) thiophen-2-yl) cyclopropyl) carbamate [optical isomer, compound derived from methyl 5- (trans-2- ( (tert- butoxycarbonyl) amino) cyclopropyl) thiophene-3-carboxylate

(optical isomer, retention time long) ]

5- (trans-2- ( (tert- Butoxycarbonyl) amino) cyclopropyl) thiophene-3-carboxylic acid [optical isomer, compound derived from methyl 5- (trans-2- ( (tert-butoxycarbonyl) amino) cyclopropyl) thiophene-3- carboxylate (optical isomer, retention time long)] (70.0 mg) was dissolved in DMF (3 mL) . Tetrahydro-2H-pyran-4-amine (27.5 mg) , triethylamine (0.069 mL) and 0- (7-azabenzotriazol-l-yl) - N, , N' , N' -tetramethyluronium hexafluorophosphate (113 mg) were added, and the mixture was stirred at room temperature

overnight. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was successively washed with water and saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to give the title compound (71.8 mg) .

MS: [M+H] ⁺ 367.2.

tert-Butyl (trans-2- (4- ( (tetrahydro-2H-pyran-4- yl) carbamoyl) thiophen-2-yl) cyclopropyl) carbamate [optical isomer, compound derived from methyl 5- (trans-2- ( (tert- butoxycarbonyl) amino) cyclopropyl) thiophene-3-carboxylate

(optical isomer, retention time long) ] was clarified to be tert-butyl ( (1R, 2R) -2- (4- ( (tetrahydro-2H-pyran-4- yl) carbamoyl ) thiophen-2-yl) cyclopropyl ) carbamate .

[0416]

B) 5- (trans-2-aminocyclopropyl) -N- (tetrahydro-2H-pyran-4- yl) thiophene-3-carboxamide dihydrochloride [optical isomer, compound derived from methyl 5- (trans-2- ( (tert- butoxycarbonyl) amino) cyclopropyl) thiophene-3-carboxylate

(optical isomer, retention time long) ]

To a mixture of tert-butyl (trans-2- (4- ( (tetrahydro-2H- pyran-4-yl) carbamoyl) thiophen-2-yl) cyclopropyl) carbamate

[optical isomer, compound derived from methyl 5- (trans-2- ( (tert-butoxycarbonyl) amino) cyclopropyl) thiophene-3- carboxylate (optical isomer, retention time long)] (69.5 mg) and ethyl acetate (2 mL) was added 4 mol/L hydrogen

chloride/ethyl acetate solution (0.474 mL) at 0°C, and the mixture was stirred at room temperature overnight. The precipitated solid was collected by filtration and washed with ethyl acetate to give the title compound (53.6 mg) .

MS: [M+H-(2HC1) ] ⁺ 267.2.

5- (trans-2-Aminocyclopropyl ) -N- (tetrahydro-2H-pyran-4- yl ) thiophene-3-carboxamide dihydrochloride [optical isomer, compound derived from methyl 5- (trans-2- ( (tert- butoxycarbonyl) amino) cyclopropyl) thiophene-3-carboxylate

(optical isomer, retention time long) ] was clarified to be 5- ( (1R, 2R) -2-aminocyclopropyl) -N- (tetrahydro-2H-pyran-4- yl.) thiophene-3-carboxamide dihydrochloride.

[0417]

C) 5- (trans-2- (cyclobutylamino) cyclopropyl) -N- (tetrahydro-2H- . pyran-4-yl) thiophene-3-carboxamide hydrochloride [optical isomer, compound derived from methyl 5- (trans-2- ((tert- butoxycarbonyl ) amino) cyclopropyl) thiophene-3-carboxylate

(optical isomer, retention time long) ] To a mixture of 5- (trans-2-aminocyclopropyl) -N- (tetrahydro-2H-pyran-4-yl) thiophene-3-carboxamide

dihydrochloride [optical isomer, compound derived from methyl 5- (trans-2- ( (tert-butoxycarbonyl) amino) cyclopropyl) thiophene- 3-carboxylate (optical isomer, retention time long)] (51.0 mg) , sodium hydrogen carbonate (35.4 mg) , THF (2 mL) and methanol (2 mL) was added cyclobutanone (14.2 mg) at room temperature. Under a nitrogen atmosphere, the reaction mixture was stirred . at 60°C for 1.5 hr and at room temperature for 30 min, and sodium borohydride (9.56 mg) was added at 0°C. The reaction mixture was stirred at room temperature for 1 hr, and ethyl acetate, water and saturated aqueous sodium hydrogen carbonate solution were added to the reaction mixture. The mixture was extracted with ethyl acetate, and the extract was successively washed with water and saturated brine and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure. The residue was purified by silica gel column

chromatography (ethyl acetate/methanol), and to the obtained fraction was added 4 mol/L hydrogen chloride/ethyl acetate solution. The reaction mixture was stirred at ^' room temperature overnight. The precipitated solid was collected by filtration and washed with ethyl acetate to give the title compound (28.7 mg) .

¾ NMR (300 MHz, DMSO-d ₆ ) δ 1.03 (2H, d, J = 6.06 Hz), 1.22- 1.36 (1H, m) , 1.43-1.62 (3H, m) , 1.65-1.91 (4H, m) , 2.11-2.32 (4H, m) , 2.65 (1H, brs) , 2.85 (1H, d, J = 3.41 Hz), 3.77-4.00 (4H, m) , 7.26 (1H, s) , 7.95 (1H, s) , 8.05 (1H, d, J = 7.95 Hz), 9.49 (2H, brs) .

5- (trans-2- (Cyclobutylamino) cyclopropyl) -N- (tetrahydro- 2H-pyran-4-yl) thiophene-3-carboxamide hydrochloride [optical isomer, compound . derived from methyl 5- (trans-2- ( (tert- .

butoxycarbonyl) amino) cyclopropyl) thiophene-3-carboxylate

(optical isomer, retention time long) ] was clarified to be 5- ( (1R, 2R) -2- (cyclobutylamino) cyclopropyl) -N- (tetrahydro-2H- pyran-4-yl) thiophene-3-carboxamide hydrochloride. [0418]

Example 43

5- (trans-2- (cyclobutylamino) cyclopropyl) -N- (tetrahydro-2H- pyran-4-yl) thiophene-3-carboxamide hydrochloride [optical isomer, compound derived from methyl 5- (trans-2- ( (tert- butoxycarbonyl ) amino) cyclopropyl) thiophene-3-carboxylate (optical isomer, retention time short) ]

By a method similar to that of Example 42, the title compound was obtained.

5- (trans-2- (Cyclobutylamino) cyclopropyl) -N- (tetrahydro-

2H-pyran-4-yl) thiophene-3-carboxamide hydrochloride [optical isomer, compound derived from methyl 5- (trans-2- ( (tert- butoxycarbonyl) amino) cyclopropyl) thiophene-3-carboxylate (optical isomer, retention time short) ] was clarified to be 5- ( (1S,2S) -2- (cyclobutylamino) cyclopropyl) -N- (tetrahydro-2H- pyran-4-yl) thiophene-3-carboxamide hydrochloride .

[0419]

Example 44

N- (4, 4-difluorocyclohexyl) -5- ( (1R, 2R) -2- (tetrahydro-2H-pyran- 4-ylamino) cyclopropyl) thiophene-3-carboxamide hydrochloride

A) tert-butyl ( (1R, 2R) -2- (4- ( (4, 4- difluorocyclohexyl) carbamoyl) thiophen-2- yl ) cyclopropyl ) carbamate

5- ( (1R, 2R) -2- ( (tert- Butoxycarbonyl) amino) cyclopropyl) thiophene-3-carboxylic acid

(400 mg) was dissolved in DMF (10 mL) , 4,4- difluorocyclohexanamine hydrochloride (291 mg) , triethylamine (0.59 mL) and 0- (7-azabenzotriazol-l-yl) -Ν,Ν,Ν' ,Ν' - tetramethyluronium hexafluorophosphate (644 mg) were added, and the mixture was stirred at room temperature overnight. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was

successively washed with water and saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure to give the title compound (680 mg) . The title compound was used for the next reaction without further purification .

MS: [M-tBu (C4H9) +2H] ⁺ 345.1.

[0420]

B) 5- ( (1R, 2R) -2-aminocyclopropyl) -N- (4, 4- difluorocyclohexyl) thiophene-3-carboxamide hydrochloride

tert-Butyl ( ( 1R, 2R) -2- ( 4- ( ( 4 , 4- difluorocyclohexyl) carbamoyl) thiophen-2- yl) cyclopropyl) carbamate (680 mg) and 4 mol/L hydrogen

chloride/ethyl acetate solution (1.7 mL) were stirred at room temperature overnight. The precipitated solid was collected by filtration to give the title compound (500 mg) .

MS: [M+H-(HC1) ] ⁺ 301.1.

[0421]

C) N- (4, 4-difluorocyclohexyl) -5- ( (1R, 2R) -2- (tetrahydro-2H- pyran-4-ylamino) cyclopropyl) thiophene-3-carboxamide

hydrochloride

To a mixture of 5- ( (1R, 2R) -2-aminocyclopropyl) -N- (4, 4- difluorocyclohexyl ) thiophene-3-carboxamide hydrochloride (62.0 mg) , borane-2-picoline complex (29.5 mg) , methanol (2.0 mL) and acetic acid (0.2 mL) was added dihydro-2H-pyran-4 (3H) -one (58.2 mg) at room temperature. The reaction mixture was stirred at room temperature for 18 hr, and saturated aqueous sodium hydrogen carbonate solution was added at 0°C. The mixture was extracted with ethyl acetate, and the extract was successively washed with water and saturated brine and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure. The residue was purified by NH silica gel column chromatography (ethyl acetate/hexane), and to the obtained fraction was added 4 mol/L hydrogen chloride/ethyl acetate solution. The reaction mixture was concentrated under reduced pressure, and the obtained residue was crystallized from ethanol/heptane to give the title compound (40.0 mg) .

¾ NMR (300 MHz, DMSO-de) δ 1.27-1.41 (1H, m) , 1.49-1.72 (5H, m) , 1.77-2.16 (8H, m) , 2.61-2.73 (1H, m) , 2.89-3.08 (1H, m) , 3.26-3.39 (2H, m) , 3.40-3.55 (1H, m) , 3.83-4.02 (3H, m) , 7.24- 7.31 (1H, m) , 7.92-7.98 (1H, m) , 7.99-8.08 (lH, m) , 8.99-9.48

(2H, m) .

[0422]

The compounds of Examples 45 to 59 could be produced according to the production methods described in the present specification, a method shown in the Examples, or a method analogous thereto.

Example 45

5- ( (1R, 2R) -2- (cis- ( 4-aminocyclohexyl ) amino) cyclopropyl) -N- (4, 4-difluorocyclohexyl) thiophene-3-carboxamide

dihydrochloride

or

5- ( (1R, 2R) -2- (trans- (4-aminocyclohexyl) amino) cyclopropyl) -N- (4, 4-difluorocyclohexyl) thiophene-3-carboxamide

dihydrochloride

Example 46

5- ( (1R, 2R) -2- (trans- (4-aminocyclohexyl) amino) cyclopropyl) -N- (4 , 4-difluorocyclohexyl) thiophene-3-carboxamide

dihydrochloride

or

5- ( (1R, 2R) -2- (cis- (4-aminocyclohexyl) amino) cyclopropyl) -N- ( 4 , 4-difluorocyclohexyl ) thiophene-3-carboxamide

dihydrochloride

Example 47

5- ( (1R, 2R) -2- ( ( , 4-difluorocyclohexyl) amino) cyclopropyl) -N- (tetrahydro-2H-pyran-4-yl) thiophene-3-carboxamide

hydrochloride

Example 48

5- ( (1R, 2R) -2- ( (l-cyclopropylpiperidin-4-yl) amino) cyclopropyl) - N- (5-methyl-l, 3, 4-thiadiazol-2-yl) thiophene-3-carboxamide dihydrochloride

Example 49

N- (5-methyl-l,.3, 4-thiadiazol-2-yl) -5- ( (1R, 2R) -2- (tetrahydro- 2H-pyran-4-ylamino) cyclopropyl) thiophene-3-carboxamide hydrochloride

Example 50

N- (2-methyl-l, 3-thiazol-5-yl) -5- ( (1R,2R) -2- (tetrahydro-2H- pyran-4-ylamino) cyclopropyl) thiophene-3-carboxamide

hydrochloride

Example 51

N- (4, 4-difluorocyclohexyl) -5- ( (1R, 2R) -2- ( (tetrahydro-2H-pyran-

4-ylmethyl) amino) cyclopropyl) thiophene-3-carboxamide

hydrochloride

Example 52

5- ( ( 1R, 2R) -2- ( (tetrahydro-2H-pyran-4- ylmethyl) amino) cyclopropyl) -N- (1- (2, 2, 2- trifluoroethyl) piperidin-4-yl) thiophene-3-carboxamide

hydrochloride

Example 53

N- (2-methyl-l, 3-thiazol-5-yl ) -5- ( (1R,2R) -2- ( (tetrahydro-2H- pyran-4-ylmethyl) amino) cyclopropyl) thiophene-3-carboxamide dihydrochloride

Example 54

N- (1, 3-dimethyl-lH-pyrazol-4-yl) -5- ( (1R, 2R) -2- ( (tetrahydro-2H- pyran-4-ylmethyl) amino) cyclopropyl) thiophene-3-carboxamide dihydrochloride

Example 55

N- (1, 5-dimethyl-lH-pyrazol-4-yl ) -5- ( (1R, 2R) -2- ( (tetrahydro-2H- pyran-4-ylmethyl) amino) cyclopropyl) thiophene-3-carboxamide dihydrochloride

Example 56

N-cyclopropyl-5- ( ( 1R, 2R) -2- ( (tetrahydro-2H-pyran-4- ylmethyl) amino) cyclopropyl) thiophene-3-carboxamide

hydrochloride

Example 57

4- (trans-2- (cyclobutylamino) cyclopropyl) -N- (5-methyl-l, 3, 4- thiadiazol-2-yl) thiophene-2-carboxamide hydrochloride

Example 58

N- (5-methyl-l, 3, 4-thiadiazol-2-yl ) -4- (trans-2- ( (tetrahydro-2H- pyran-4-ylmethyl) amino) cyclopropyl) thiophene-2-carboxamide hydrochloride

Example 59

4- (trans-2- ( (l-cyclopropylpiperidin-4-yl) amino) cyclopropyl) -N- (5-methyl-l, 3, 4-thiadiazol-2-yl ) thiophene-2-carboxamide dihydrochloride

[0423]

Example 60

3- (4- ( ( ( (1R, 2R) -2- (4- ( (5-methyl-l, 3, 4-thiadiazol-2- yl) carbamoyl) -2-thienyl) cyclopropyl) amino) methyl ) piperidin-1- yl) propanoic acid trihydrochloride

A) tert-butyl 4- ( ( ( (1R, 2R) -2- (4- ( (5-methyl-l, 3, 4-thiadiazol-2- yl) carbamoyl) thiophen-2- yl) cyclopropyl) amino) methyl) piperidine-l-carboxylate

By a method similar to that of Example 2, the title compound was obtained.

MS: [M+H]+ 478.3.

[0424]

B) tert-butyl 4- ( (2, 2, 2-trifluoro-N- ( (1R, 2R) -2- (4- ( (5-methyl- 1, 3, 4-thiadiazol-2-yl) carbamoyl) thiophen-2- yl) cyclopropyl ) acetamido) methyl) piperidine-l-carboxylate

To a mixture of tert-butyl 4- ( ( ( (1R, 2R) -2- (4- ( (5-methyl- 1, 3, 4-thiadiazol-2-yl) carbamoyl) thiophen-2- yl) cyclopropyl) amino) methyl) piperidine-l-carboxylate (301 mg) , triethylamine (127.0 mg) and THF (4.0 mL) was added

trifluoroacetic anhydride (355.0 mg) at room temperature. The reaction mixture was stirred at room temperature for 18 hr, and saturated aqueous sodium hydrogen carbonate solution was added at 0°C. ^' The mixture was extracted with ethyl acetate, and the extract was successively washed with water and

saturated brine and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure. The residue was purified by NH silica gel column chromatography (ethyl

acetate/hexane) to give the title compound (213.0 mg).

MS: [M+H] ⁺ 574.1.. [0425]

C) N- (5-methyl-l, 3, 4-thiadiazol-2-yl ) -5- ( (1R,2R) -2- (2,2,2- trifluoro-N- (piperidin-4- ylmethyl) acetamido) cyclopropyl) thiophene-3-carboxamide hydrochloride

By a method similar to that of Example 1, step H, the title compound was obtained.

MS: [M-HC1+H] ⁺ 474.1.

[0426]

D) tert-butyl 3-(4-( (2, 2, 2-trifluoro-N- ( ( 1R, 2R) -2- ( 4- ( (5- methyl-1, 3, 4-thiadiazol-2-yl) carbamoyl) thiophen-2- yl) cyclopropyl) acetamido) methyl) piperidin-l-yl ) propanoate

To a mixture of N- (5-methyl-l, 3, 4-thiadiazol-2-yl) -5- ( (1R, 2R) -2- (2, 2, 2-trifluoro-N- (piperidin-4- ylmethyl) acetamido) cyclopropyl) thiophene-3-carboxamide hydrochloride (50.0 mg) , triethylamine (10.9 mg) and ethanol (2.0 mL) was added tert-butyl acrylate (12.6 mg) at room temperature. The reaction mixture was stirred at room temperature overnight, and the solvent was evaporated under reduced pressure. To the residue were added ethyl acetate and saturated aqueous sodium hydrogen carbonate solution, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, and dried over anhydrous

magnesium sulfate. The solvent was evaporated under reduced pressure and the residue was purified by silica gel column chromatography (ethyl acetate/hexane) to give the title compound (44.0 mg) .

MS: [M+H] ⁺ 602.1.

[0427]

E) tert-butyl 3- (4- ((( (1R,2R) -2- (4- ( (5-methyl-l, 3, 4- thiadiazol-2-yl) carbamoyl) thiophen-2- yl) cyclopropyl) amino) methyl) piperidin-l-yl) propanoate

To a mixture of tert-butyl 3- (4- ( (2, 2, 2-trifluoro-N- ( (1R,2R) -2- (4- ( (5-methyl-l, 3, 4-thiadiazol-2- yl) carbamoyl) thiophen-2- yl ) cyclopropyl ) acetamido) methyl) piperidin-l-yl) propanoate (44.0 mg) , methanol (1.0 mL) and THF (1.0 ml) was added 1 mol/L aqueous sodium hydroxide solution (1.0 mL) at room temperature. The reaction mixture was stirred at room

temperature for 10 min, and water was added at room

temperature. The mixture was extracted with ethyl acetate, and the extract was washed with saturated brine and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure to give the title compound (30.0 mg) .

MS: [M+H] ⁺ 506.2.

[0428]

F) 3- (4- ( ( ( (1R, 2R) -2- (4- ( (5-methyl-l, 3, 4-thiadiazol-2- yl) carbamoyl) -2-thienyl) cyclopropyl) amino) methyl) piperidin-l- yl) propanoic acid trihydrochloride

A mixture of tert-butyl 3- (4- ( ( ( (1R, 2R) -2- (4- ( (5-methyl-

1,3, 4-thiadiazol-2-yl) carbamoyl) thiophen-2- yl) cyclopropyl) amino) methyl ) piperidin-l-yl ) propanoate (30.0 mg) and 4 mol/L hydrogen chloride/ethyl acetate solution (1.0 mL) was stirred at room temperature overnight, and the solvent was evaporated under reduced pressure to give the title compound (33.0 mg) .

¾ NMR (300 MHz, DMSO-de) δ 1.29-1.41 (1H, m) , 1.44-1.64 (2H, m) , 1.72 (1H, brs), 2.01 (3H, d, J = 12.49), 2.63 (3H, s) , 2.76-3.08 (7H, m), 3.17-3.35 (3H, m) , 3.42-3.56 (2H, m) , 7.51 (1H, s), 8.46 (lH, d, J = 1.14), 9.36-9.73 (2H, m) , 9.96-12.92

(2H, m) .

[0429]

The compounds of Examples 61 to 66 could be produced according to the production methods described in the present specification, a method shown in the Examples, or a method analogous thereto.

Example 61

4- (trans-2- (cyclobutylamino) cyclopropyl) -N- ( 1-methyl-lH- pyrazol-4-yl) thiophene-2-carboxamide dihydrochloride

Example 62 4- (trans-2- ( (cyclopropylmethyl) amino) cyclopropyl) -N- ( 1-methyl- lH-pyrazol-4-yl) thiophene-2-carboxamide dihydrochloride

Example 63

4- (trans-2- (cyclobutylamino) cyclopropyl) -N- (tetrahydro-2H- pyran-4-yl ) thiophene-2-carboxamide hydrochloride

Example 64

4- (trans-2- ( (cyclopropylmethyl) amino) cyclopropyl) -N- (tetrahydro-2H-pyran-4-yl) thiophene-2-carboxamide

hydrochloride

Example 65

5- (trans-2- ( (cyclopropylmethyl) amino) cyclopropyl) -N- (4, 4- difluorocyclohexyl) -2-methylthiophene-3-carboxamide

hydrochloride

Example 66

N- (4, 4-difluorocyclohexyl) -2-methyl-5- (trans-2- ( (tetrahydro- 2H-pyran-4-ylmethyl) amino) cyclopropyl) thiophene-3-carboxamide hydrochloride

[0430]

Example 67

N- (4, 4-difluorocyclohexyl) -2-methyl-5- (trans-2- (tetrahydro-2H- pyran-4-ylamino) cyclopropyl) thiophene-3-carboxamide

hydrochloride

To a mixture of 5- (trans-2-aminocyclopropyl) -N- ( 4 , 4- difluorocyclohexyl) -2-methylthiophene-3-carboxamide

hydrochloride (30.0 mg) , sodium hydrogen carbonate (10.8 mg) , THF (1.5 mL) and methanol (1.5 mL) was added dihydro-2H-pyran- 4(3H)-one (9.48 \iL) . Under a nitrogen atmosphere, the reaction mixture was stirred at 60°C for 1.5 hr and at room temperature for 30 min, and sodium borohydride (4.85 mg) was added under ice-cooling. The reaction mixture was stirred at room

temperature for 1 hr, and diluted with ethyl acetate. Water and saturated aqueous sodium hydrogen carbonate solution were added, and the mixture was extracted with ethyl acetate. The extract was successively washed with water and saturated brine, dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography (ethyl

acetate/methanol) . To the obtained fraction was added 4 mol/L hydrogen chloride/ethyl acetate solution, and the mixture was stirred overnight. The precipitated solid was collected by filtration and washed with ethyl acetate to give the title compound (15.6 mg) .

¾ NMR (300 MHz, DMSO-d ₆ ) δ 1.22-1.36 (1H, m) , 1.49-1.75 (5H, m) , 1.78-2.09 (9H, m) , 2.53 (3H, s) , 2.64 (1H, brs) , 2.89 (1H, brs), 3.45 (1H, brs), 3.93 (3H, d, J = 10.98 Hz), 7.06 (1H, s) , 7.83 (1H, d, J = 7.95 Hz), 9.50 (2H, brs).

[0431]

Example 68

5- (trans-2- ( (cyclopropylmethyl) amino) cyclopropyl) -2-methyl-N- (tetrahydro-2H-pyran-4-yl) thiophene-3-carboxamide

hydrochloride

The title compound could be produced according to the production methods described in the present specification, a method shown in the Examples, or a method analogous thereto.

[0432]

Example 69

5- (trans-2- ( (cyclopropylmethyl) amino) cyclopropyl) -2-methyl-N- (5-methyl-l, 3, 4-thiadiazol-2-yl) thiophene-3-carboxamide

dihydrochloride

To a mixture' of 5- (trans-2-aminocyclopropyl) -2-methyl-N-

(5-methyl-l, 3, 4-thiadiazol-2-yl) thiophene-3-carboxamide

dihydrochloride (30.0 mg) , sodium hydrogen carbonate (17.2 mg) , THF (1.5 mL) and methanol (1.5 mL) was added

cyclopropanecarbaldehyde (7.32 μΐ.) . Under a nitrogen

atmosphere, the reaction mixture was stirred at 60°C for 1.5 hr and at room temperature for 30 min. Sodium borohydride (4.63 mg) was added under ice-cooling, and the reaction mixture was stirred at room temperature for 1 hr and diluted with ethyl acetate. Water and saturated aqueous sodium hydrogen carbonate solution were added, and the mixture was extracted with ethyl acetate. The extract was successively washed with water and saturated brine, dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography

(ethyl acetate/methanol) . To the obtained fraction was added 4 mol/L hydrogen chloride/ethyl acetate solution, and the

mixture was stirred overnight. The precipitated solid was collected by filtration and washed with ethyl acetate to give the title compound (22.1 mg) .

1H NMR (300 MHz, DMSO-d ₆ ) δ 0.35-0.45 (2H, m) , 0.55-0.65 (2H, m) , 1.03-1.20 (1H, m) , 1.24-1.36 (1H, m) , 1.59-1.70 (1H, m) , 2.60-2.75 (8H, m) , 2.86-3.02 (3H, m) , 7.47 (1H, s) , 9.51 (2H, d, J = 4.54 Hz) .

[0433]

Example 70

2-methyl-N- (5-methyl-l, 3, 4-thiadiazol-2-yl) -5- (trans-2-

( (tetrahydro-2H-pyran-4-ylmethyl) amino) cyclopropyl) thiophene-

3-carboxamide dihydrochloride

The title compound could be produced according to the production methods described in the present specification, a method shown in the Examples, or a method analogous thereto.

[0434]

Example 71

5- ( ( 1R, 2R) -2- ( (cyclopropylmethyl) amino) cyclopropyl) -N- (tetrahydro-2H-pyran-4-yl) thiophene-3-carboxamide

hydrochloride

A) ( (1R, 4aS, lOaR) -7-isopropyl-l, 4a-dimethyl- 1,2,3,4, 4a, 9, 10, lOa-octahydrophenanthren-l-yl) methanamine

(1R, 2R) -2- (4-bromothiophen-2-yl) cyclopropanecarboxylate

( (1R, aS, lOaR) -7-Isopropyl-l, 4a-dimethyl-

1, 2,3,4, 4a, 9, 10, lOa-octahydrophenanthren-l-yl) methanamine

(1.040 g) was dissolved in methanol (3.2 mL) and diisopropyl ether (15.7 mL) at 40°C, and trans-2- ( 4-bromothiophen-2- yl) cyclopropanecarboxylic acid (900 mg) was added. The

reaction mixture was stirred for 5 min at the same temperature, and methanol (8 mL) was added. The reaction mixture was heated to 53°C to dissolve the precipitate. The reaction mixture was cooled to 46°C and stirred at 46-47°C for 2 hr. The reaction mixture was slowly cooled to room temperature (28°C) and

stirred overnight. The precipitate was collected by filtration, and the obtained solid was washed with a mixed solvent of ethyl acetate/hexane (1/5 = ethyl acetate/hexane (v/v) , 4 mL) to give the title compound (594 mg, 95.7%d.e.).

MS: [M-H- (C20H31N) ]- 245.0.

Column: CHIROBIOTIC R 4.6 mmIDx250 mmL

Eluent solvent: Methanol/TEA/AA=1000/3/l (v/v/v)

Flow rate: 1.0 mL/min

Retention time: 4.4 min.

Temperature: 30°C

Detection: UV 254 nm

Concentration: 0.5 mg/mL

Injection volume: 0.010 mL

[0435]

B) ( (1R, 4aS, lOaR) -7-isopropyl-l, 4a-dimethyl- 1,2,3, 4, 4a, 9, 10, lOa-octahydrophenanthren-l-yl) methanamine

(1R, 2R) -2- (4-bromothiophen-2-yl) cyclopropanecarboxylate

( (1R, 4aS, lOaR) -7-Isopropyl-l, 4a-dimethyl- 1,2,3,4, 4a, 9, 10, lOa-octahydrophenanthren-l-yl) methanamine

(1R, 2R) -2- (4-bromothiophen-2-yl) cyclopropanecarboxylate (290 mg, 95.7%d.e.) was dissolved in ethanol (3.77 mL) and

diisopropyl ether (1.45 mL) at 62°C, and diisopropyl ether

(8.12 mL) was further added dropwise at 62°C. The mixture was cooled to 46°C and stirred at 45-47°C for 2 hr. The mixture was slowly cooled to room temperature (28°C) and stirred

overnight. Furthermore, the mixture was stirred at 0°C for 1 hr. The precipitate was collected by filtration, and the obtained solid was washed with ethyl acetate/hexane (1/5 = ethyl acetate/hexane (v/v) , 2 mL) to give the title compound (246 mg, 99.6%d.e. ) .

iH NMR (300 MHz, DMSO-d ₆ ) δ 0.84 (3H, s) , 1.00-1.76 (19H, m) , 2.21-2.38 (2H, m) , 2.39-2.47 (2H, m) , 2.71-2.87 (2H, m) , 3.38- 3.50 (2H, m) , 6.81-6.86 (1H, m) , 6.88-6.92 (1H, m) , 6.92-6.98 (1H, m) , 7.10-7.19 (1H, m) , 7.40 (1H, d, J = 1.5 Hz).

Column: CHIROBIOTIC R 4.6 mmIDx250 mmL

Eluent solvent: Methanol/TEA/AA=1000/3/l (v/v/v)

Flow rate: 1.0 mL/min

Retention time: 4.3 min.

Temperature: 30°C

Detection: UV 254 nm

Concentration: 0.5 mg/mL

Injection volume: 0.010 mL

[0436]

C) (1R, 2R) -2- (4-bromothiophen-2-yl) cyclopropanecarboxylic acid

To a suspension of ( (1R, 4aS, lOaR) -7-isopropyl-l, 4a- dimethyl-1, 2, 3,4, 4a, 9, 10, lOa-octahydrophenanthren-1- yl) methanamine (1R, 2R) -2- (4-bromothiophen-2- yl) cyclopropanecarboxylate (26.8 g) in ethyl acetate (300 mL) were added 1 mol/L aqueous sodium hydroxide solution (60.4 mL) and water (200 mL) at room temperature, and the mixture was stirred at room temperature for 5 min. The aqueous layer was separated and washed with ethyl acetate (200 mL, twice) . To the aqueous layer was added 2 mol/L hydrochloric acid (35.2 mL) under ice-cooling at 0°C to adjust the mixture from pH 2 to pH 3, and the mixture was extracted with ethyl acetate (100 mL, twice) . The organic layer was separated, and the extract was washed with saturated brine, and dried over magnesium sulfate. The solvent was evaporated under reduced pressure to give the title compound (11.7 g) .

¾ NMR (300 MHz, CDC1 ₃ ) δ 1.39 (1H, ddd, J = 8.5, 6.4, 4,7 Hz), 1.64-1.73 (1H, m) , 1.90-1.98 (1H, m) , 2.66-2.78 (1H, m) , 6.75 (1H, dd, J = 1.5, 0.8. Hz), 7.02 (1H, d, J = 1.5 Hz) .

[0437]

D) tert-butyl ( ( 1R, 2R) -2- ( 4-bromothiophen-2- yl) cyclopr.opyl) carbamate

To a solution of (1R, 2R) -2- (4-bromothiophen-2- yl) cyclopropanecarboxylic acid (15 g) and tert-butyl alcohol (150 mL) were added triethylamine (10.15 mL) and

diphenylphosphoryl azide (13.07 mL) at room temperature, and the mixture was stirred at room temperature for 1 hr, and then at 80°C overnight. The reaction mixture was cooled to room temperature, saturated aqueous sodium hydrogen carbonate solution was added, and the mixture was extracted with ethyl acetate. The organic layer was separated, successively washed with water and saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to give the title compound (14.6 g) .

¾ NMR (300 MHz, DMSO-d ₆ ) δ 1.04-1.24 (2H, m) , 1.38 (9H, s) , 2.07 (1H, ddd, J = 9.18, 6.15, 3.22 Hz), 2.61 (1H, brs) , 6.80 (1H, d, J = 0.76 Hz), 7.27 (1H, brs), 7.38 (1H, d, J = 1.51 Hz) .

[0438]

E) methyl 5- ( ( 1R, 2R) -2- ( (tert- butoxycarbonyl) amino) cyclopropyl) thiophene-3-carboxylate

To a solution of tert-butyl ( ( 1R, 2R) -2- ( 4-bromothiophen-

2-yl) cyclopropyl) carbamate (7.2 g) in methanol (180 mL) were added triethylamine (6.31 mL) and dichloro (1, 1' - bis (diphenylphosphino) errocene) palladium (828 mg) at room temperature, and the mixture was stirred at 90°C for 6 hr under a carbon monoxide atmosphere (3 atm) . The reaction mixture was filtered through celite and washed with methanol. The filtrate was concentrated under reduced pressure, water was added to the residue, and the mixture was extracted with ethyl acetate. The contaminants in the organic layer were removed by

filtration, and the filtrate was concentrated under reduced pressure to give residue A.

To a solution of tert-butyl ( (1R, 2R) -2- ( 4-bromothiophen- 2-yl) cyclopropyl) carbamate- (7.2 g) in methanol (180 mL) were added triethylamine (6.31 mL) and dichloro (1, 1' - bis (diphenylphosphino) ferrocene) palladium (828 mg) at room temperature, and the mixture was stirred at 90°C for 6 hr under a carbon monoxide atmosphere (3 atm) . The reaction mixture was filtered through celite, and washed with methanol. The

filtrate was concentrated under reduced pressure, water was added to the residue, and the mixture was extracted with ethyl acetate. The contaminants in the organic layer were removed by filtration, and the filtrate was concentrated under reduced pressure to give residue B.

The residues A and B were combined and purified by silica gel column chromatography (hexane/ethyl acetate) to give the title compound (11.1 g).

^X H NMR (300 MHz, DMSO-d ₆ ) δ 1.05-1.25 (2H, m) , 1.35-1.42 (9H, m) , 2.08 (1H, ddd, J = 9.18, 6.34, 3.03 Hz), 2.60 (1H, brs) , 3.76 (3H, s), 7.12 (1H, d, J = 0.76 Hz), 7.28 (1H, brs), 8.07 (1H, d, J = 1.51 Hz) .

[0439]

F) 5- ( (1R, 2R) -2- ( (tert- butoxycarbonyl) amino) cyclopropyl) thiophene-3-carboxylic acid By a method similar to that of Example 38, step C, the title compound was obtained.

[0440]

G) tert-butyl ( ( 1R, 2R) -2- ( 4- ( (tetrahydro-2H-pyran-4- yl) carbamoyl) thiophen-2-yl) cyclopropyl) carbamate

By a method similar to that of Example 42, step A, the title compound was obtained.

[0441]

H) 5- ( (1R, 2R) -2-aminocyclopropyl) -N- (tetrahydro-2H-pyran-4- yl) thiophene-3-carboxamide dihydrochloride

By a method similar to that of Example 42, step B, the title compound was obtained.

[0442]

I) 5- ( (1R, 2R) -2- ( (cyclopropylmethyl) amino) cyclopropyl) -N- (tetrahydro-2H-pyran-4-yl) thiophene-3-carboxamide

hydrochloride

To a mixture of 5- ( (1R, 2R) -2-aminocyclopropyl) -N- (tetrahydro-2H-pyran-4-yl) thiophene-3-carboxamide

dihydrochloride (1.54 g), triethylamine (2.12 mL) , ^' THF (20 mL) and methanol (20 mL) was added cyclopropanecarbaldehyde (0.428 g) at room temperature. The reaction mixture was stirred at room temperature for 2 hr, and sodium borohydride (0.231 g) was added at 0°C. The reaction mixture was stirred at 0°C for 10 min and added to water. The methanol and tetrahydrofuran were evaporated under reduced pressure, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure and the residue was purified by silica gel column chromatography

(ethyl acetate/methanol) . To the obtained fraction was added 4 mol/L hydrogen chloride/ethyl acetate solution and the mixture was concentrated under reduced pressure. The obtained residue was crystallized from ethanol/heptane to give the title compound (1.04 g) .

^X H NMR (300 MHz, DMSO-d ₆ ) δ 0.33-0.43 (2H, m) , 0.51-0.64 (2H, m) , 0.99-1.15 (1H, m) , 1.24-1.37 (1H, m) , 1.42-1.65 (3H, m) , 1.67-1.78 (2H, m) , 2.64-2.75 (1H, m) , 2.90-3.04 (3H, m) , 3.32- 3.42 (2H, m) , 3.79-4.00 (3H, m) , 7.28 (1H, s) , 7.95 (1H, d, J = 1.5 Hz), 8.05 (1H, d, J = 8.0 Hz), 9.25 (2H, brs) .

[0443]

The compounds of Examples 72 to 80 could be produced according to the production methods described in the present specification, a method shown in the Examples, or a method analogous thereto.

Example 72

N- (5-methyl-l, 3, 4-thiadiazol-2-yl) -4- ( (IS, 2R) -2- ( (tetrahydro- 2H-pyran-4-ylmethyl) amino) cyclopropyl) thiophene-2-carboxamide hydrochloride

Example 73

4- ( (1R, 2S) -2- (cyclobutylamino) cyclopropyl) -N- (tetrahydro-2H- pyran-4-yl) thiophene-2-carboxamide hydrochloride

Example 74 N- (5-methyl-l, 3, -thiadiazol-2-yl) -4- ( (1R, 2S) -2- ( (tetrahydro- 2H-pyran-4-ylmethyl) amino) cyclopropyl) thiophene-2-carboxamide hydrochloride

Example 75

4- ( (1R, 2S) -2- ( (cyclopropylmethyl) amino) cyclopropyl) -N- (tetrahydro-2H-pyran-4-yl) thiophene-2-carboxamide

hydrochloride

Example 76

4- ( (IS, 2R) -2- (cyclobutylamino) cyclopropyl) -N- (tetrahydro-2H- pyran-4-yl) thiophene-2-carboxamide hydrochloride

Example 77

4- ( (IS, 2R) -2- ( (cyclopropylmethyl) amino) cyclopropyl) -N- (tetrahydro-2H-pyran-4-yl) thiophene-2-carboxamide

hydrochloride

Example 78

4- ( (IS, 2R) -2- ( (l-cyclopropylpiperidin-4-yl) amino) cyclopropyl) - N- (5-methyl-l, 3, -thiadiazol-2-yl) thiophene-2-carboxamide dihydrochloride

Example 79

4- ( (1R, 2S) -2- ( (l-cyclopropylpiperidin-4-yl) amino) cyclopropyl) - N- (5-methyl-l, 3, 4-thiadiazol-2-yl) thiophene-2-carboxamide dihydrochloride

Example 80

5- ( (1R, 2R) -2- ( (l-cyclopropylpiperidin-4-yl) amino) cyclopropyl) - N- ( 4 , 4-difluorocyclohexyl ) thiophene-3-carboxamide

hydrochloride

[0444]

Example 81

N- (5-methyl-l, 2-oxazol-3-yl) -5- ( (1R,2R) -2- ( (tetrahydro-2H- pyran-4-ylmethyl) amino) cyclopropyl) thiophene-3-carboxamide hydrochloride

A) tert-butyl ( ( 1R, 2R) -2- (4- ( (5-methylisoxazol-3- yl) carbamoyl) thiophen-2-yl) cyclopropyl) ( (tetrahydro-2H-pyran- 4-yl) methyl) carbamate

To a mixture of 5- ( (1R, 2R) -2- ( (tert- butoxycarbonyl) ( (tetrahydro-2H-pyran-4- yl ) methyl) amino) cyclopropyl) thiophene-3-carboxylic acid (50.0 mg) and THF (2 mL) was added oxalyl chloride (0.014 mL) at 0°C, and the mixture was stirred at 0°C for 1 hr. The solvent was evaporated under reduced pressure to give an acid chloride intermediate.

To a mixture of 5-methylisoxazol-3-amine (19.3 mg) , DMAP (8.01 mg) and pyridine (2 mL) was added a mixture of the aforementioned acid chloride and THF (1.5 mL) at 60°C, and the mixture was stirred at 60°C for 2 hr. The reaction mixture was neutralized with saturated aqueous sodium hydrogen carbonate solution, and extracted with ethyl acetate. The extract was successively washed with water and saturated brine, and dried over magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to give the title compound (17.2 mg) .

MS: [M-Boc+H] ⁺ 362.3.

[0445]

B) N-(5-methyl-l,2-oxazol-3-yl)-5-( (lR,2R)-2-( (tetrahydro-2H- pyran-4-ylmethyl) amino) cyclopropyl) thiophene-3-carboxamide hydrochloride

By a method similar to that of Example 1, step H, the title compound was obtained.

[0446]

Example 82

4- ( (IS, 2R) -2- ( (cyclopropylmethyl) amino) cyclopropyl) -N- (5- methyl-1, 3, 4-thiadiazol-2-yl) thiophene-2-carboxamide

dihydrochloride

A) (R) -2~amino-3-phenylpropan-l-ol ( 1R, 2R) -2- (5-bromothiophen- 3-yl) cyclopropanecarboxylate

trans-2- (5-Bromothiophen-3-yl) cyclopropanecarboxylic acid (47.8 g) and (R) -2-amino-3-phenylpropan-l-ol (29.2 g) were dissolved in ethanol (480 mL) at 57°C, diisopropyl ether (480 mL) was added, and the mixture was cooled to 53°C. The reaction mixture was stirred at 53°C for 1 hr, cooled to room temperature, and stirred overnight. The reaction mixture was cooled to 0°C and _. stirred for 1 hr. The precipitate was collected by filtration, and washed with a mixed solvent of ethyl acetate/hexane (1/2 = ethyl acetate/hexane (v/v) ) to give the title compound (32.6 g, >99% d.e.).

MS: [M-H- (C9H13NO) ]- 246.8.

[0447]

B) (R) -2-amino-3-phenylpropan-l-ol ( 1R, 2R) -2- ( 5-bromothiophen- 3-yl) cyclopropanecarboxylate

(R) -2-Amino-3-phenylpropan-l-ol (1R, 2R) -2- (5- bromothiophen-3-yl) cyclopropanecarboxylate (32.5 g) was dissolved in ethanol (430 mL) at 60°C, diisopropyl ether (850 mL) was added, and the mixture was cooled to 55°C. The reaction mixture was stirred at 55°C for 1 hr, cooled to room temperature, and stirred overnight. The reaction mixture was cooled to 0°C, stirred for 1 hr, and the precipitate was collected by filtration and washed with a mixed solvent of ethyl acetate/hexane (1/2 = ethyl acetate/hexane (v/v) ) to give the title compound (27.5 g, >99% d.e.).

MS: [M-H- (C9H13NO) ] - 246.8.

[0448]

C) (1R, 2R) -2- (5-bromothiophen-3-yl) cyclopropanecarboxylic acid

To a mixture of (R) -2-amino-3-phenylpropan-l-ol (1R,2R)- 2- (5-bromothiophen-3-yl) cyclopropanecarboxylate (26.0 g) and ethyl acetate was added 1 mol/L aqueous hydrochloric acid solution, and the mixture was extracted with ethyl acetate.

The extract was successively washed with water and saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure. Toluene was added to the residue, and the mixture was concentrated under reduced pressure to give the title compound (16.1 g) .

MS: [M-H]" 246.8.

[0449]

D) tert-butyl ( ( 1R, 2S ) -2- ( 5-bromothiophen-3- yl) cyclopropyl) carbamate

To a mixture of (1R, 2R) -2- ( 5-bromothiophen-3- yl) cyclopropanecarboxylic acid (16.0 g) and tert-butyl alcohol (200 mL) were added triethylamine (10.8 mL) and

diphenylphosphoryl azide (16.7 mL) at room temperature, and the mixture was stirred at room temperature for 2 hr and at 80°C overnight. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The extract was successively washed with water and saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (hexane/ethyl acetate) to give the title compound (18.1 g) .

¾ NMR (300 MHz, DMSO-d ₆ ) δ 0.91-1.11 (2H, m) , 1.37 (9H, s) , 1.87 (1H, ddd, J = 9.28, 6.25, 3.41 Hz), 2.56 (1H, s) , 7.00 (1H, d, J = 1.89 Hz), 7.12 (1H, d, J = 1.89 Hz), 7.18 (1H, brs) .

[0450]

E) methyl 4- ( ( IS, 2R) -2- ( (tert- butoxycarbonyl) amino) cyclopropyl) thiophene-2-carboxylate

To a mixture of tert-butyl ( (1R, 2S) -2- (5-bromothiophen-3- yl) cyclopropyl) carbamate (9.00 g) and methanol (200 mL) were added triethylamine (7.88 mL) and 1,1'- bis (diphenylphosphino) ferrocene-palladium (II) dichloride (1.04 g) , and the mixture was heated at 90°C for 6 hr under a carbon monoxide atmosphere (3 atm) . The insoluble material was filtered off by celite and washed with methanol, and the filtrate was concentrated under reduced pressure and extracted with ethyl acetate and water. The extract was washed with saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure to give residue A.

To a mixture of tert-butyl ( (1R, 2S) -2- (5-bromothiophen-3- yl) cyclopropyl) carbamate (9.00 g) and methanol (200 mL) were added triethylamine (7.88 mL) and 1,1'- bis (diphenylphosphino) ferrocene-palladium (II) dichloride (1.04 g) , and the mixture was stirred at 90°C for 6 hr under a carbon monoxide atmosphere (3 atm) . The insoluble material was

filtered off by celite and washed with methanol, and the filtrate was concentrated under reduced pressure and extracted with ethyl acetate and water. The extract and the residues A were combined, washed with 5% ammonia water (twice) , N-acetyl- L-cysteine aqueous solution (twice) , water and saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to give the title compound (15.2 g) .

MS: [M-Boc+2H] ⁺ 198.1.

[0451]

F) 4- ( (1S,2R) -2- ( (tert- butoxycarbonyl) amino) cyclopropyl) thiophene-2-carboxylic acid

To a solution of methyl 4- ( ( IS, 2R) -2- ( (tert- butoxycarbonyl) amino) cyclopropyl) thiophene-2-carboxylate (15.2 g) in THF (50 mL) /methanol (50 mL) was added 2 mol/L aqueous sodium hydroxide solution (63.9 mL) at 0°C, and the mixture was stirred at room temperature overnight. The reaction mixture was acidified with 1 mol/L hydrochloric acid at 0°C, and

extracted with ethyl acetate. The extract was successively washed with water and saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The obtained residue was washed with diisopropyl ether to give the title compound (13.4 g) .

^X H NMR (300 MHz, DMSO-d ₆ ) δ 1.00-1.11 (2H, m) , 1.34-1.42 (9H, m) , 1.92 (1H, ddd, J = 9.09, 6.25, 3.22 Hz), 2.54-2.66 (lH, m) , 7.21 (1H, br. s.), 7.42 (1H, d, J = 1.14 Hz), 7.50 (1H, d, J = 1.51 Hz) , 12.99 (1H, brs) .

[0452]

G) tert-butyl ( (1R, 2S) -2- (5- ( (5-methyl-l, 3, 4-thiadiazol-2- yl) carbamoyl) thiophen-3-yl) cyclopropyl) carbamate

To a solution of 4- ( ( IS, 2R) -2- ( (tert- butoxycarbonyl) amino) cyclopropyl) thiophene-2-carboxylic acid (13.3 g) in D F (200 mL) were added 5-methyl-l, 3, 4-thiadiazol- 2-amine (6.49 g) , triethylamine (13.08 mL) and 0-(7- azabenzotriazol-l-yl) -N, N, N' , ' -tetramethyluronium

hexafluorophosphate (21.42 g) , and the mixture was stirred at room temperature overnight. To the reaction mixture were added water and ethyl acetate, and the precipitate was collected by filtration and washed with ethyl acetate to give the title compound (12.1 g) . The filtrate was extracted with ethyl acetate. The organic layer was successively washed with 0.1 mol/L hydrochloric acid, saturated aqueous sodium hydrogen carbonate solution, water and saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. To the residue was added ethyl acetate, and the precipitate was collected by filtration. The obtained solid was washed with ethyl acetate to give the title compound (2.86 g ⁾ ·

MS: [M+H] ⁺ 381.1.

[0453]

H) 4- ( (IS, 2R) -2-aminocyclopropyl) -N- (5-methyl-l, 3, 4- thiadiazol-2-yl) thiophene-2-carboxamide dihydrochloride

To a suspension of tert-butyl ( ( 1R, 2S) -2- ( 5- ( ( 5-methyl- 1, 3, 4-thiadiazol-2-yl) carbamoyl) thiophen-3- yl) cyclopropyl) carbamate (1.67 g) in ethyl acetate (10 mL) and methanol (10 mL) was added 4 mol/L hydrogen chloride/ethyl acetate solution (10.97 mL) at 0°C, and the mixture was stirred at room temperature overnight. The precipitated solid was collected by filtration, and washed with ethyl acetate to give the title compound (1.55 g) .

MS: [M+H- (2HC1) ] ⁺ 281.0.

[0454]

I) 4- ( (IS, 2R) -2- ( (cyclopropylmethyl) amino) cyclopropyl) -N- (5- methyl-1, 3, 4-thiadiazol-2-yl) thiophene-2-carboxamide

dihydrochloride

To a mixture of 4- (( IS, 2R) -2-aminocyclopropyl) -N- ( 5- methyl-1, 3, -thiadiazol-2-yl) thiophene-2-carboxamide dihydrochloride (1.00 g) , sodium hydrogen carbonate (549 mg) , THF (15 mL) and methanol (15 mL) was added

cyclopropanecarbaldehyde (254 i ) . Under a nitrogen atmosphere, the reaction mixture was stirred at 60°C for 1.5 hr and at room temperature for 30 min. Sodium borohydride (161 mg) was added under ice-cooling, and the reaction mixture was stirred at room temperature for 1 hr. The reaction mixture was diluted with ethyl acetate, water and saturated aqueous sodium

hydrogen carbonate solution were added, and the mixture was extracted with ethyl acetate. The extract was successively washed with water and saturated brine, and dried over

anhydrous sodium sulfate. The solvent was evaporated under reduced pressure, and the obtained residue was purified by silica gel column chromatography (ethyl acetate/methanol) . To the obtained fraction was added 4 mol/L hydrogen

chloride/ethyl acetate solution, and the mixture was stirred overnight and concentrated under reduced pressure. The residue was crystallized from methanol/diisopropyl ether to give the title compound (723 mg) .

^! H NMR (300 MHz, DMSO-d ₆ ) δ 0.33-0.42 (2H, m) , 0.54-0.65 (2H, m) , 1.01-1.17 (1H, m) , 1.20-1.32 (1H, m) , 1.53-1.66 (1H, m) , 2.56-2.65 (4H, m) , 2.86-3.02 (3H, m) , 7.75 (1H, s) , 8.07 (1H, brs) , 9.26-9.56 (2H, m) .

[0455]

Example 83

4- ( (1R, 2S) -2- ( (cyclopropylmethyl) amino) cyclopropyl) -N- (5- methyl-1, 3, 4-thiadiazol-2-yl) thiophene-2-carboxamide

dihydrochloride

The title compound could be produced according to the production methods described in the present specification, a method shown in the Examples, or a method analogous thereto.

[0456]

Example 84

4- ( (IS, 2R) -2- (cyclobutylamino) cyclopropyl) -N- (5-methyl-l, 3, 4- thiadiazol-2-yl) thiophene-2-carboxamide dihydrochloride

To a mixture of (IS, 2R) -4- (2-aminocyclopropyl) -N- (5- methyl-1, 3, 4-thiadiazol-2-yl) thiophene-2-carboxamide

dihydrochloride (.3.36 g) , THF (30 mL) and methanol (30 mL) was added triethylamine (3.31 mL) , triethyl orthoformate (2.10 mL) and cyclobutanone (0.856 mL) at room temperature, and the mixture was stirred at room temperature overnight. Sodium borohydride (540 mg) was added under ice-cooling, and the reaction mixture was stirred at room temperature for 1 hr. The reaction mixture was diluted with ethyl acetate, water and saturated aqueous sodium hydrogen carbonate solution were added, and the mixture was extracted with ethyl acetate. The extract was successively washed with water and saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure and the obtained residue was purified by silica gel column chromatography (ethyl

acetate/methanol) . To the obtained fraction was added 4 mol/L hydrogen chloride/ethyl acetate solution, and the mixture was stirred overnight and concentrated under reduced pressure. The residue was crystallized from ethanol/water/ethyl acetate to give the title compound (2.17 g) .

^X H NMR (300 MHz, DMSO-de) δ 1.18-1.29 (1H, m) , 1.48-1.60 (1H, m) , 1.72-1.89 (2H, m) , 2.12-2.39 (4H, m) , 2.54-2.67 (4H, m) , 2.74-2.86 (1H, m) , 3.74-3.92 (1H, m) , 7.74 (1H, d, J = 1.14 Hz), 8.06 (1H, s), 9.79 (2H, brs) .

[0457]

The compounds of Examples 85 to 92 could be produced according to the production methods described in the present specification, a method shown in the Examples, or a method analogous thereto.

Example 85

4- ( (1R, 2S) -2- (cyclobutylamino) cyclopropyl) -N- ( 5-methyl-l, 3, 4- thiadiazol-2-yl) thiophene-2-carboxamide dihydrochloride

Example 86

N- (l-ethyl-lH-pyrazol-4-yl) -5- ( (1R,2R) -2- ( (tetrahydro-2H- pyran-4-ylmethyl) amino) cyclopropyl) thiophene-3-carboxamide dihydrochloride

Example 87

4- ( (IS, 2R) -2- ( (cyclopropylmethyl) amino) cyclopropyl) -N- (1- methyl-lH-pyrazol-4-yl) thiophene-2-carboxamide dihydrochloride Example 88

4- ( (1R, 2S) -2- ( (cyclopropylmethyl) amino) cyclopropyl) -N- (1- methyl-lH-pyrazol-4-yl) thiophene-2-carboxamide dihydrochloride Example 89

4- ( ( IS, 2R) -2- (cyclobutylamino) cyclopropyl) -N- ( 1-methyl-lH- pyrazol-4-yl) thiophene-2-carboxamide dihydrochloride

Example 90

4- ( (1R, 2S) -2- (cyclobutylamino) cyclopropyl) -N- ( 1-methyl-lH- pyrazol-4-yl ) thiophene-2-carboxamide dihydrochloride

Example 91

5- ( (1R, 2R) -2- ( (l-acetylpiperidin-4-yl) amino) cyclopropyl) -N- (4, 4-difluorocyclohexyl) thiophene-3-carboxamide hydrochloride Example 92

5- ( ( 1R, 2R) -2- ( (1- (cyclopropylcarbonyl) piperidin-4- yl) amino) cyclopropyl) -N- (4, -difluorocyclohexyl) thiophene-3- carboxamide hydrochloride

[0458]

Example 93

N- (4, 4-difluorocyclohexyl) -5-methyl-4- ( (IS, 2R) -2- (tetrahydro- 2H-pyran-4-ylamino) cyclopropyl) thiophene-2-carboxamide

fumarate

A) 4- ( (IS, 2R) -2-aminocyclopropyl) -N- (4, 4-difluorocyclohexyl ) - 5-methylthiophene-2-carboxamide hydrochloride

4- ( (IS, 2R) -2- ( (tert-Butoxycarbonyl) amino) cyclopropyl) -5- methylthiophene-2-carboxylic acid (50 mg) , 4,4- difluorocyclohexanamine (27.3 mg) and triethylamine (0.094 mL) were dissolved in DMF (1 mL) , 0- (7-azabenzotriazol-l-yl) - Ν,Ν,Ν' ,Ν' -tetramethyluronium hexafluorophosphate (77 mg) was added, and the mixture was stirred at room temperature

overnight. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was successively washed with water and saturated brine, dried over magnesium sulfate, and concentrated under reduced

pressure. The obtained residue (70.5 mg) and 4 mol/L hydrogen chloride/ethyl acetate solution (4.0 mL) were stirred at room temperature overnight. The precipitated solid was collected by filtration and washed with ethyl acetate to give the title compound (51 mg) .

MS: [M-HC1+H] ⁺ 315.1.

[0459]

B) N- (4, 4-difluorocyclohexyl) -5-methyl-4- ( (IS, 2R) -2- (tetrahydro-2H-pyran-4-ylamino) cyclopropyl) thiophene-2- carboxamide fumarate

To a mixture of 4- ( (IS, 2R) -2-aminocyclopropyl) -N- (4,4- difluorocyclohexyl) -5-methylthiophene-2-carboxamide

hydrochloride (40.0 mg) , borane-2-picoline complex (36.7 mg) , methanol (2.0 mL) and acetic acid (0.2 mL) was added dihydro- 2H-pyran-4 (3H) -one (17.1 mg) at room temperature. The reaction mixture was stirred at room temperature for 18 hr, and

saturated aqueous sodium hydrogen carbonate solution was added at 0°C. The mixture was extracted with ethyl acetate, and the extract was successively washed with water and saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/hexane) , the obtained residue was dissolved. in ethyl acetate, and a

solution of fumaric acid (9.3 mg) in ethanol was added . at room temperature. The reaction mixture was stirred at room

temperature for 30 min, and the solvent was evaporated under reduced pressure to give the title compound (40.0 mg) .

^! H NMR (300 MHz, DMSO-d6) δ 0.76-0. ^' 91 (1H, m) , 0.95-1.04 (1H, m) , 1.21-1.40 (2H, m) , 1.48-1.66 (2H, m) , 1.69-2.11 (9H, m) , . 2.26-2.34 (1H, m) , 2.40 (3H, s) , 2.75-2.87 (1H, m) , 3.23-3.34 (2H, m) , 3.76-3.96 (3H, m) , 6.60 (2H, s) , 7.21 (1H, s) , 7.94- 8.05 (1H, m) . [0460]

Example 94

N- (4, 4-difluorocyclohexyl) -5-methyl-4- ( (1R, 2S) -2- (tetrahydro- 2H-pyran-4-ylamino) cyclopropyl) thiophene-2-carboxamide fumarate

The title compound could be produced according to the production methods described in the present specification, a method shown in the Examples, or a method analogous thereto.

[0461]

Example 95

4- ( (IS, 2R) -2- ( (cyclopropylmethyl) amino) cyclopropyl) -5-methyl- N- (5-methyl-l, 3, 4-thiadiazol-2-yl ) thiophene-2-carboxamide fumarate

A) 4- ( (IS, 2R) -2-aminocyclopropyl) -5-methyl-N- (5-methyl-l, 3, 4- thiadiazol-2-yl) thiophene-2-carboxamide

4- ( (IS, 2R) -2- ( (tert-Butoxycarbonyl) amino) cyclopropyl) -5- methylthiophene-2-carboxylic acid (150 mg) , 5-methyl-l, 3, 4- thiadiazol-2-amine (69.7 mg) and triethylamine (0.281 mL) were dissolved in DMF (5 mL) , 0- ( 7-azabenzotriazol-l-yl ) -N, , N' , N' - tetramethyluronium hexafluorophosphate (230 mg) was added, and the mixture was stirred at room temperature overnight. Water was added to the reaction mixture, and the precipitate was collected by filtration to give solid A. The filtrate was extracted with ethyl acetate. The organic layer was

successively washed with water and saturated brine, dried over magnesium sulfate, and concentrated under reduced pressure to give solid B. The solid (197 mg) combined with the obtained solids A and B, and 4 mol/L hydrogen chloride/ethyl acetate solution (4 mL) were stirred at room temperature overnight. The precipitated solid was collected by filtration, and washed with ethyl acetate to give the title compound (120 mg) .

MS: [M-HC1+H] ⁺ 295.1.

[0462]

B) 4- ( (IS, 2R) -2- ( (cyclopropylmethyl) amino) cyclopropyl) -5- . methyl-N- (5-methyl-l, 3, 4-thiadiazol-2-yl) thiophene-2- carboxamide fumarate

To a mixture of 4- ( (IS, 2R) -2-aminocyclopropyl) -5-methyl- N- (5-methyl-l, 3, 4-thiadiazol-2-yl) thiophene-2-carboxamide hydrochloride (40.0 mg) , triethylamine (22.0 mg) , THF (1.0 mL) and methanol (1.0 mL) was added cyclopropanecarbaldehyde (11.8 mg) at room temperature. The reaction mixture was stirred at 50°C for 1.5 hr, and stirred at room temperature for 1 hr.

Sodium borohydride (8.2 mg) was added at 0°C, the reaction mixture was stirred at 0°C for 30 min, and ethyl acetate, water and saturated aqueous sodium hydrogen carbonate solution were added to the reaction mixture. The mixture was extracted with ethyl acetate/THF, and the extract was washed with saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (methanol/ethyl acetate) , the obtained residue was suspended in ethyl acetate, and a solution of fumaric acid (8.4 mg) in ethanol was added at room temperature. The reaction mixture was stirred at room temperature for 30 min, and the solid was collected by

filtration to give the title compound (28.0 mg) .

^X H NMR (300 MHz, DMSO-d ₆ ) δ 0.10-0.21 (2H, m) , 0.37-0.49 (2H, m) , 0.85-1.00 (2H, m) , 1.04-1.16 (1H, m) , 1.80-1.92 (1H, m) , 2.40-2.46 (1H, m) , 2.48(3H, s) , 2.56-2.60 (2H, m) , 2.61 (3H, s) , 6.58 (2H, s) , 7.76 (1H, s) .

[0463]

Example 96

4- ( (1R, 2S) -2- ( (cyclopropylmethyl) amino) cyclopropyl) -5-methyl- N- (5-methyl-l, 3, 4-thiadiazol-2-yl) thiophene-2-carboxamide fumarate

The title compound could be produced according to the production methods described in the present specification, a method shown in the Examples, or a method analogous thereto.

[0464]

Example 97

5-methyl-N- (5-methyl-l, 3, 4-thiadiazol-2-yl) -4- ( (IS, 2R) -2- ( (tetrahydro-2H-pyran-4-ylmethyl) amino) cyclopropyl) thiophene- 2-carboxamide hydrochloride

To a mixture of 4- ( (IS, 2R) -2-aminocyclopropyl) -5-methyl- N- (5-methyl-l, 3, 4-thiadiazol-2-yl ) thiophene-2-carboxamide hydrochloride (40.0 mg) , triethylamine (22.0 mg) , THF (1.0 mL) and methanol (1.0 mL) was added tetrahydro-2H-pyran-4- carbaldehyde (18.6 mg) at room temperature. The reaction mixture was stirred at room temperature overnight, sodium borohydride (8.2 mg) was added at 0°C, and the reaction mixture was stirred at 0°C for 10 min. To the reaction mixture were added ethyl acetate and water, and the mixture was extracted with ethyl acetate. The extract was dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (methanol/ethyl acetate) , and to the obtained fraction was added 4 mol/L hydrogen chloride/ethyl acetate solution. The reaction mixture was concentrated under reduced pressure, and the obtained residue was crystallized from ethanol/heptane to give the title compound (31.0 mg) .

¾ N R (300 MHz, DMSO-d ₆ ) δ 1.14-1.35 (4H, m) , 1.52-1.63 (1H, m) , 1.64-1.76 (2H, m) , 1.86-2.06 (1H, m) , 2.53 (3H, s) , 2.62 (3H, s), 2.86-3.09 (3H, m) , 3.21-3.30 (2H, m) , 3.79-3.95 (2H, m) , 7.70-8.03 (lH, m) , 8.94-9.41 (2H, m) , 12.34-12.97 (1H, m) .

[0465]

Example 98

5-methyl-N- (5-methyl-l, 3, 4-thiadiazol-2-yl) -4- ( (1R,2S) -2-

( (tetrahydro-2H-pyran-4-ylmethyl) amino) cyclopropyl) thiophene--

2-carboxamide hydrochloride

The title compound could be produced according to the production methods described in the present specification, a method shown, in the Examples, or a method analogous thereto.

[0466]

Example 99

4- ( (IS, 2R) -2- (cyclobutylamino) cyclopropyl) -5-methyl-N- (5- methyl-1, 3, 4-thiadiazol-2-yl) thiophene-2-carboxamide hydrochloride

To a mixture of 4- ( (IS, 2R) -2-aminocyclopropyl) -5-methyl- N- (5-methyl-l, 3, -thiadiazol-2-yl ) thiophene-2-carboxamide dihydrochloride (40.0 mg) , triethylamine (22.0 mg) , trimethyl orthoformate (17.3 mg) , methanol (1.0 mL) and THF (1.0 mL) was added cyclobutanone (11.8 mg) at room temperature, and the mixture was stirred at room temperature for 3 hr. Sodium borohydride (8.2 mg) was added under ice-cooling, the reaction mixture was stirred for 30 min, and ethyl acetate and

saturated aqueous sodium hydrogen carbonate solution were added. The mixture was extracted with ethyl acetate/THF, and the extract was washed with saturated brine. The organic layer was dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography (ethyl

acetate/methanol) , and to the obtained fraction was added 4 mol/L hydrogen chloride/ethyl acetate solution. The reaction mixture was concentrated under reduced pressure, and the obtained residue was washed with ethyl acetate to give the title compound (18.0 mg) .

^! H NMR (300 MHz, DMSO-d ₆ ) δ 1.12-1.24 (1H, m) , 1.45-1.57 (1H, m) , 1.74-1.92 (2H, m) , 2.17-2.31 (4H, m) , 2.34-2.46 (1H, m) , 2.62 (3H, s), 2.71-2.86 (lH,m) , 3.31 (3H, s) , 3.76-3.94 (1H, m) , 7.70-7.91 (1H, m) , 9.06-9.71 (2H, m) , 12.20-13.03 (1H, m) .

[0467]

Example 100

4- ( (1R, 2S) -2- (cyclobutylamino) cyclopropyl) -5-methyl-N- (5- methyl-1, 3, 4-thiadiazol-2-yl) thiophene-2-carboxamide

hydrochloride

The title compound could be produced according to the production methods described in the present specification, a method shown in the Examples, or a method analogous thereto.

[0468]

Example 101

4- ( (4- ( ( ( (1R,2R) -2- (4- ( (4, 4-difluorocyclohexyl) carbamoyl) -2- thienyl) cyclopropyl) amirio) methyl) piperidin-l-yl) methyl) benzoic acid dihydrochloride

The title compound could be produced according to the production methods described in the present specification, a method shown in the Examples, or a method analogous thereto.

[0469]

Example 102

4- ( (IS, 2R) -2- ( (cyclopropylmethyl) amino) cyclopropyl) -5-methyl- N- (l-methyl-lH-pyrazol-4-yl) thiophene-2-carboxamide

dihydrochloride

To a mixture of 4- (. (IS, 2R) -2-aminocyclopropyl) -5-methyl- N- (l-methyl-lH-pyrazol-4-yl) thiophene-2-carboxamide

dihydrochloride (35.0 mg) , sodium hydrogen carbonate (21.0 mg) , THF (1.5 mL) and methanol (1.5 mL) was added

cyclopropanecarbaldehyde (8.99 μΐι) . Under a nitrogen

atmosphere, the reaction mixture was stirred at 60°C for 1.5 hr and at room temperature for 30 min, sodium borohydride (5.69 mg) was added under ice-cooling, and the reaction mixture was stirred at room temperature for 1 hr. The reaction mixture was diluted with ethyl acetate, water and saturated aqueous sodium hydrogen carbonate solution were added, and the mixture was extracted with ethyl acetate. The extract was successively washed with water and saturated brine, and dried over

anhydrous sodium sulfate. The solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography (ethyl acetate/methanol) , and to the obtained fraction was added 4 mol/L hydrogen chloride/ethyl acetate solution. The mixture was stirred overnight, and the precipitated solid was collected by filtration, and washed with ethyl acetate to give the title compound (32.6 mg) .

¾ NMR (300 MHz, DMSO-de) δ 0.33-0.45 (2H, m) , 0.50-0.66 (2H, m) , 1.00-1.26 (2H, m) , 1.50-1.65 (1H, m) , 2.49 (3H, s) , 2.82- 3.05 (3H, m) , 3.80 (3H, s), 7.49-7.58 (2H, m) , 7.92 (1H, s) , 9.41 (2H, brs), 10.34 (1H, s) .

MS: [M-2HC1+H] ⁺ 331.2. [0470]

Example 103

4- ( ( 1R, 2S) -2- ( (cyclopropylmethyl) amino) cyclopropyl) -5-methyl- N- (l-methyl-lH-pyrazol-4-yl) thiophene-2-carboxamide

dihydrochloride

The title compound could be produced according to the production methods described in the present specification, a method shown in the Examples, or a method analogous thereto.

[0471]

Example 104

4- ( (IS, 2R) -2- (cyclobutylamino) cyclopropyl) -5-methyl-N- (1- methyl-lH-pyrazol-4-yl) thiophene-2-carboxamide dihydrochloride To a mixture of 4- ( (IS, 2R) -2-aminocyclopropyl) -5-methyl- N- (l-methyl-lH-pyrazol-4-yl) thiophene-2-carboxamide

dihydrochloride (35.0 mg) , sodium hydrogen carbonate (21.0 mg) , THF (1.5 mL) and methanol (1.5 mL) was added cyclobutanone

(9.01 ] L) . Under a nitrogen atmosphere, the reaction mixture was stirred at 60°C for 1.5 hr and at room temperature for 30 min, sodium borohydride (5.69 mg) was added under ice-cooling, and the reaction mixture was stirred at room temperature for 1 hr. The reaction mixture was diluted with ethyl acetate, water and saturated aqueous sodium hydrogen carbonate solution were added, and the mixture was extracted with ethyl acetate. The extract was successively washed with water and saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography (ethyl

acetate/methanol) , and to the obtained fraction was added 4 mol/L hydrogen chloride/ethyl acetate solution. The mixture was stirred overnight, and the precipitated solid was

collected by filtration, and washed with ethyl acetate to give the title compound (29.6 mg) .

¾ NMR (300 MHz, DMSO-de) δ 1.10-1.24 (1H, m) , 1.49-1.60 (1H, m) , 1.72-1.89 (2H, m) , 2.15-2.35 (4H, m) , 2.39-2.48 (4H, m) , 2.73-2.84 (1H, m) , 3.76-3.91 (4H, m) , 7.50-7.56 (2H, m) , 7.92 (1H, s), 9.72 (2H, d, J = 3.79 Hz), 10.33 (1H, s) .

[0472]

The compounds of Examples 105 to 107 could be produced according to the production methods described in the present specification, a method shown in the Examples, or a method analogous thereto.

Example 105

4- ( (1R, 2S) -2- (cyclobutylamino) cyclopropyl) -5-methyl-N- (1- methyl-lH-pyrazol-4-yl) thiophene-2-carboxamide dihydrochloride [optical isomer, compound derived from methyl 4-(trans-2-

( (tert-butoxycarbonyl) amino) cyclopropyl) -5-methylthiophene-2- carboxylate (optical isomer, retention time long) ]

Example 106

4- ( (IS, 2R) -2- ( (cyclopropylmethyl) amino) cyclopropyl) -5-methyl- N- (tetrahydro-2H-pyran-4-yl) thiophene-2-carboxamide

hydrochloride

Example 107

4- ( (1R, 2S) -2- ( (cyclopropylmethyl) amino) cyclopropyl) -5-methyl- N- (tetrahydro-2H-pyran-4-yl) thiophene-2-carboxamide

hydrochloride

[0473]

Example 108

4- ( (IS, 2R) -2- (cyclobutylamino) cyclopropyl) -5-methyl-N- (tetrahydro-2H-pyran-4-yl) thiophene—2-carboxamide

hydrochloride

A) tert-butyl ( ( 1R, 2S) -2- (2-methyl-5- ( (tetrahydro-2H-pyran-4- yl) carbamoyl) thiophen-3-yl) cyclopropyl) carbamate

4- ( (IS, 2R) -2- ( (tert-Butoxycarbonyl) amino) cyclopropyl) -5- methylthiophene-2-carboxylic acid (100 mg) , tetrahydro-2H- pyran-4-amine (0.042 mL) and triethylamine (0.117 mL) were dissolved in DMF (5 mL) , 0- ( 7-azabenzotriazol-l-yl ) -N, , ' , ' - tetramethyluronium hexafluorophosphate (153 mg) was added, and the mixture was stirred at room temperature overnight. Water was added to the reaction mixture,, and the mixture was extracted with ethyl acetate. The organic layer was successively washed with water and saturated brine, dried over anhydrous sodium sulfate, and purified by silica gel column chromatography (ethyl acetate/hexane) to give the title

compound (114 mg) .

MS: [M-HC1+H] ⁺ 381.3.

[0474]

B) 4- ( (IS, 2R) -2-aminocyclopropyl) -5-methyl-N- (tetrahydro-2H- pyran-4-yl) thiophene-2-carboxamide hydrochloride

To a solution of tert-butyl ( (1R, 2S) -2- (2-methyl-5- ( (tetrahydro-2H-pyran-4-yl) carbamoyl) thiophen-3- yl) cyclopropyl) carbamate (110 mg) in ethyl acetate (3 mL) was added 4 mol/L hydrogen chloride/ethyl acetate solution (0.723 mL) , and the mixture was stirred at room temperature overnight. The precipitated solid was collected by filtration and washed with ethyl acetate to give the title compound (92 mg) .

MS: [M-HC1+H] ⁺ 281.2.

[0475]

C) 4- ( (IS, 2R) -2- (cyclobutylamino) cyclopropyl) -5-methyl-N- (tetrahydro-2H-pyran-4-yl) thiophene-2-carboxamide

hydrochloride

To a mixture of 4- ( (IS, 2R) -2-aminocyclopropyl) -5-methyl- N- (tetrahydro-2H-pyran-4-yl) thiophene-2-carboxamide

hydrochloride (35.0 mg) , sodium hydrogen carbonate (13.9 rag) , THF (1.5 mL) and methanol (1.5 mL) was added cyclobutanone

(9.94 pL) . Under a nitrogen atmosphere, the reaction mixture was stirred at 60°C for 1.5 hr and at room temperature for 30- min, sodium borohydride (6.27 mg) was added under ice-cooling, and the reaction mixture was stirred at room temperature for 1 hr. The reaction mixture was diluted with ethyl acetate, water and saturated aqueous sodium hydrogen carbonate solution were added, and the mixture was extracted with ethyl acetate. The extract was successively washed with water and saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography (ethyl acetate/methanol) , and to the obtained fraction was added 4 mol/L hydrogen chloride/ethyl acetate solution. The mixture was stirred overnight, and the precipitated solid was collected by filtration and washed with ethyl acetate to give the title compound (29.7 mg) .

*Η NMR (300 MHz, DMSO-d ₆ ) δ 1.10-1.19 (1H, m) , 1.43-1.59 (3H, m) , 1.67-1.87 (4H, m) , 2.14-2.30 (4H, m) , 2.3.4-2.43 (1H, m) , 2.44 (3H, s), 2.69-2.81 (1H, m) , 3.35-3.40 (1H, m) , 3.76-3.97 (4H, m) , 7.30-7.39 (1H, m) , 8.08 (1H, d, J = 7.95 Hz), 9.56 (2H, brs) .

[0476]

Example 109

4- ( (1R, 2S) -2- (cyclobutylamino) cyclopropyl) -5-methyl-N- (tetrahydro-2H-pyran-4-yl) thiophene-2-carboxamide

hydrochloride

The title compound could be produced according to the production methods described in the present specification, a method shown in the Examples, or a method analogous thereto.

[0477]

The compounds of Examples 110 and 111 could be produced according to the production methods described in the present specification, a method shown in the Examples, or a method analogous thereto.

Example 110

4- ( ( ( (1R,2R) -2- (4- ( (4, 4-difluorocyclohexyl) carbamoyl) -2- thienyl) cyclopropyl) amino)methyl) benzoic acid

Example 111

5- ( (1R, 2R) -2- ( ( (5-amino-l, 3, 4-oxadiazol-2- yl) methyl) amino) cyclopropyl) -N- (4, 4- difluorocyclohexyl) thiophene-3-carboxamide

[0478]

Example 112

5- ( (1R, 2R) -2- ( (cyclobutylmethyl) amino) cyclopropyl) -N- (tetrahydro-2H-pyran-4-yl) thiophene-3-carboxamide .

To a mixture of 5- ( (1R, 2R) -2-aminocyclopropyl) -N- (tetrahydro-2H-pyran-4-yl) thiophene-3-carboxamide

dihydrochloride (40 mg) , triethylamine (0.055 mL) , THF (1 mL) and methanol (1 mL) was added cyclobutanecarbaldehyde (13.33 mg) at room temperature. The reaction mixture was stirred at room temperature for 5 min, and sodium borohydride (7.5 mg) was added at 0°C. The reaction mixture was stirred at room temperature for 10 min. To the reaction mixture were added water, ethyl acetate and saturated aqueous sodium hydrogen carbonate solution, and the mixture was extracted with ethyl acetate. The extract was washed with water and saturated brine, and dried over anhydrous sodium sulfate. The ^' solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/methanol) , and to the obtained fraction was added 4 mol/L hydrogen

chloride/ethyl acetate solution. The reaction mixture was concentrated under reduced pressure, and the obtained residue was washed with ethyl acetate to give the title compound (31 mg) .

^X H NMR (300 MHz, DMSO-d ₆ ) δ 1.21-1.35 (1H, m) , 1.44-1.65 (3H, m) , 1.82 (6H, d, J = 7.2 Hz), 1.98-2.14 (2H, m) , 2.57-2.79 (2H, m) , 2.88-2.98 (1H, m) , 3.06-3.16 (2H, m) , 3.35-3.42 (2H, m) ,

3.80-4.00 (3H, m) , 7.28 (1H, s) , 7.95 (1H, d, J = 1.5 Hz),

8.06 (1H, d, J = 7.6 Hz), 9.01-9.34 (2H, m) .

[0479]

Example 113

5- ( (1R, 2R) -2- ( (cyclopropylmethyl) amino) cyclopropyl) -N-

(tetrahydro-2H-pyran-4-yl ) thiophene-3-carboxamide malate

To a suspension of L-(-) -malic acid (50.2 mg, 0.37 mmol) in ethyl acetate (2 mL) was added a solution of 5- ( (1R, 2R) -2- ( (cyclopropylmethyl) amino) cyclopropyl) -N- (tetrahydro-2H-pyran-

4-yl) thiophene-3-carboxamide (120 mg, 0.37 mmol) in ethanol (1 mL) at 60°C. The reaction mixture was stirred at room

temperature for 1 hr, and concentrated under reduced pressure. To the residue were added ethyl acetate (2 mL) and ethanol

(0.5 mL) , and ethyl acetate (2 mL) was further added. The precipitate was collected by filtration to give the title compound (106 mg) . The obtained title compound (106 mg) was recrystallized from ethanol (0.3 mL) and ethyl acetate (1.2 mL) to give the title compound (65.0 mg) .

¾ NMR (300 MHz, DMSO-d ₆ ) δ 0.12-0.25 (2H, m) , 0.37-0.54 (2H, m) , 0.82-1.12 (2H, m) , 1.23 (1H, dt, J = 9.6, 4.9 Hz), 1.41- 1.62 (2H, m) , 1.72 (2H, dd, J = 12.9, 2.3 Hz), 2.14-2.29 (1H, m) , 2.33-2.43 (1H, m) , 2.52-2.73 (4H, m) , 3.17-3.46 (2H, m) , 3.81-4.00 (3H, m) , 4.06 (1H, dd, J = 7.6, 6.1 Hz), 7.18 (1H, d, J = 0.8 Hz), 7.84 (1H, d, J = 1.1 Hz), 7.99 (1H, d, J = 8.0 Hz) .

[0480]

Example 114

5- ( (1R, 2R) -2- ( (cyclopropylmethyl) amino) cyclopropyl) -N- (tetrahydro-2H-pyran-4-yl) thiophene-3-carboxamide succinate

To a solution of succinic acid (36.9 mg, 0.31 mmol) in ethanol (3 mL) was added 5- ( ( 1R, 2R) -2-

( (cyclopropylmethyl) amino) cyclopropyl) -N- (tetrahydro-2H-pyran- 4-yl) thiophene-3-carboxamide (100 mg, 0.31 mmol) at 60°C. The reaction mixture was stirred at room temperature for 1 hr and concentrated under reduced pressure. To the residue were added ethyl acetate (2 mL) and ethanol (0.5 mL) , and ethyl acetate (2 mL) was further added. The precipitate was collected by filtration to give the title compound (105 mg) . The obtained title compound (105 mg) was recrystallized from ethanol (0.8 mL) and ethyl acetate (1.2 mL) to give the title compound

( 62.0 mg) .

^X H NMR (300 MHz, DMSO-ds) δ 0.06-0.19 (2H, m) , 0.34-0.49 (2H, m) , 0.78-1.15 (3H, m) , 1.41-1.61 (2H, m)., 1.64-1.78 (2H, m) , 1.97-2.07 (1H, m) , 2.32-2.43 (5H, m) , 2.50-2.54 (2H, m) , 3.30- 3.52 (2H, m) , 3.75-4.01 (3H, m) , 7.13 (1H, d, J = 0.8 Hz), 7.79 (1H, d, J = 1.1 Hz), 7.97 (1H, d, J = 8.0 Hz).

[0481]

Example 115

5- (( 1R, 2R) -2- ( (cyclopropylmethyl) amino) cyclopropyl) -N- (tetrahydro-2H-pyran-4-yl) thiophene-3-carboxamide fumarate

To a solution of fumaric acid (42.7 mg, 0.37 mmol) in ethanol (1 mL) was added a solution of 5- ( (1R, 2R) -2- ( (cyclopropylmethyl) amino) cyclopropyl) -N- (tetrahydro-2H-pyran- 4-yl) thiophene-3-carboxamide (118 mg, 0.37 mmol) in ethyl acetate (3 mL) at 60°C. To the reaction mixture was added ethyl acetate (2 mL) , the mixture was stirred at room

temperature, and the precipitate was collected by filtration to give the title compound (122 mg) . The obtained title

compound (122 mg) was recrystallized from ethanol (1.08 mL) and ethyl acetate (1.8 mL) to give the title compound (85 mg) . ¾ NMR (300 MHz, DMSO-d ₆ ) δ 0.06-0.17 (2H, m) , 0.36-0.48 (2H, m) , 0.82-1.18 (3H, m) , 1.52 (2H, qd, J = 11.9, 4.4 Hz), 1.66- 1.80 (2H, m) , 2.00-2.12 (1H, m) , 2.35-2.44 (1H, m) , 2.50-2.57 (2H, m) , 3.36 (2H, td, J = 11.5, 1.9 Hz), 3.75-4.01 (3H, m) ,

6.59 (2H, s), 7.13 (1H, s) , 7.80 (1H, d, J = 1.5 Hz), 7.98 (1H, d, J = 8.0 Hz) .

[0482]

Example 116

4- ( (IS, 2R) -2- (cyclobutylamino) cyclopropyl) -N- (5-methyl-l, 3, 4- thiadiazol-2-yl) thiophene-2-carboxamide phosphate

To a mixture of 4- ( (IS, 2R) -2- (cyclobutylamino) cyclopropyl) -N- (5-methyl-l, 3, 4-thiadiazol-2- yl) thiophene-2-carboxamide (100 mg) and ethanol (4 mL) was added 1 mol/1 aqueous phosphoric acid solution (0.329 mL) at room temperature, and the mixture was stirred at room

temperature for 3 hr. The precipitated solid was collected by filtration, and crystallized from ethanol/water/diisopropyl ether to give the title compound (97.0 mg) .

¾ NMR (300 MHz, DMSO-d ₆ ) δ 0.90-1..12 (2H, m) , 1.52-1.74 (2H, m) , 1.77-1.94 (2H, m) , 1.95-2.21 (3H, m) , 2.32-2.39 (1H, m) , 2.62 (3H, s), 3.34-3.50 (1H, m) , 7.56 (1H, s) , 7.98-8.04 (1H, m) .

[0483]

Example 117 4- ( (IS, 2R) -2- (cyclobutylamino) cyclopropyl) -N- (5-methyl-l, 3, 4- thiadiazol-2-yl) thiophene-2-carboxamide succinate

To a mixture of 4- ( (IS, 2R) -2- (cyclobutylamino) cyclopropyl) -N- (5-methyl-l, 3, 4-thiadiazol-2- yl) thiophene-2-carboxamide (100 mg) and ethyl acetate (4 mL) was added a mixture of succinic acid (35.3 mg) and ethanol (1 mL) at 70°C, and the mixture was stirred at room temperature for 2 hr. The precipitated solid was collected by filtration, and crystallized from ethanol/water/diisopropyl ether to give the title compound (78.2 mg) .

¹ H NMR (300 MHz, DMSO-d ₆ ) δ 0.83-1.02 (2H, m) , 1.49-1.82 (4H, m) , 1.82-1.91 (1H, m) , 2.03-2.19 (2H, m) , 2.20-2.30 (1H, m) , 2.40 (4H, s), 2.62 (3H, s) , 3.31 (2H, dt, J = 15.52, 7.76 Hz), 7.51 (1H, d, J = 1.14 Hz), 7.96 (1H, d, J = 1.14 Hz), 10.00 (2H, brs) .

[0484]

Example 118

4- ( (IS, 2R) -2- (cyclobutylamino) cyclopropyl) -N- (5-methyl-l, 3, 4- thiadiazol-2-yl) thiophene-2-carboxamide sulfate

A) 4- ( (IS, 2R) -2- (cyclobutylamino) cyclopropyl) -N- (5-methyl- 1,3, 4-thiadiazol-2-yl) thiophene-2-carboxamide

To a suspension of 4- ( (IS, 2R) -2-aminocyclopropyl) -N- (5- methyl-1, 3, 4-thiadiazol-2-yl) thiophene-2-carboxamide

dihydrochloride (13.3 g), THF (120 mL) and methanol (120 mL) were added triethylamine (15.7 mL) , triethyl orthoformate

(8.32 mL) and cyclobutanone (3.39 mL) at room temperature, and the mixture was stirred at room temperature overnight. Sodium borohydride (2.14 g) was added under ice-cooling, and the reaction mixture was stirred at room temperature for 1 hr. , To the reaction mixture was. added, saturated aqueous ammonium chloride solution at 0°C, and the mixture was stirred at 0°C for 30 min. The organic solvent was evaporated under reduced pressure. To the residue were added saturated aqueous sodium hydrogen carbonate solution and THF, and the mixture was extracted with ethyl acetate. The extract was successively washed with water and saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography (ethyl acetate/methanol) to give the title compound (6.35 g) .

MS: [M+H] ⁺ 335.0.

[0485]

B) 4- ( (IS, 2R) -2- (cyclobutylamino) cyclopropyl) -N- (5-methyl- 1,3, 4-thiadiazol-2-yl ) thiophene-2-carboxamide sulfate

To a mixture of 4- ( (IS, 2R) -2-

(cyclobutylamino) cyclopropyl) -N- (5-methyl-1, 3, 4-thiadiazol-2- yl) thiophene-2-carboxamide (9.51 g) and THF (150 mL) was added 10% aqueous sulfuric acid solution (27.4 mL) at room

temperature, and the mixture was stirred at room temperature overnight. To the reaction mixture was added ethyl acetate (100 mL) , and the mixture was further stirred for 1 hr. The precipitated solid was collected by filtration, and washed with ethyl acetate. The obtained solid (10.8 g) was dissolved in ethanol (100 mL) and water (65 mL) at 65°C, and the mixture was stirred at 65°C for 30 min. To the reaction mixture was added dropwise ethyl acetate (250 mL) . The reaction mixture was slowly cooled to room temperature, and stirred at room temperature overnight. The precipitated solid was collected by filtration, and washed with ethyl acetate to give the title compound (9.46 g).

NMR (300 MHz, DMSO-d ₆ ) δ 1.21-1.32 (1H, m) , 1.42 (1H, ddd, J = 10.22, 6.06, 4.5 Hz), 1.74-1.92 (2H, m) , 2.06-2.31 (4H, m) , 2.39-2.48 (1H, m) , 2.63 (3H, s) , 2.84 (1H, dt, J = 7.48, 4.02 Hz), 3.87 (1H, quin, J = 8.05 Hz), 7.74 (1H, d, J = 1.14 Hz), 8.04 (1H, d, J = 1.14 Hz) .

[0486]

Example 119

4- ( (IS, 2R) -2- (cyclobutylamino) cyclopropyl) -N- (5-methyl-l, 3, 4- thiadiazol-2-yl) thiophene-2-carboxamide

To 4- ( (IS, 2R) -2- (cyclobutylamino) cyclopropyl) -N- (5- methyl-1, 3, 4-thiadiazol-2-yl) thiophene-2-carboxamide dihydrochloride (650 mg) were added ethyl acetate and

saturated aqueous sodium hydrogen carbonate solution, and the mixture was extracted with ethyl acetate. The extract was washed with water and saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure to give the title compound (523 mg) .

¾ NMR (300 MHz, DMSO-d ₆ ) δ 0.82-1.00 (2H, m) , 1.48-1.88 (5H, m) , 2.01-2.17 (2H, m) , 2.18-2.25 (1H, m) , 2.62 (3H, s), 3.20- 3.41 (3H, m) , 7.48 (1H, d, J = 1.14 Hz), 7.94 (1H, d, J = 1.14 Hz) .

[0487]

Example 120

5- ( (1R, 2R) -2- ( (cyclopropylmethyl) amino) cyclopropyl) -N- (tetrahydro-2H-pyran-4-yl) thiophene-3-carboxamide

To 5- ( (1R, 2R) -2- ( (cyclopropylmethyl) amino) cyclopropyl) -N- (tetrahydro-2H-pyran-4-yl) thiophene-3-carboxamide

hydrochloride (600 mg) were added ethyl acetate and saturated aqueous sodium hydrogen carbonate solution, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over magnesium sulfate, and

concentrated under reduced pressure to give the title compound (520 mg) .

¾ NMR (300 MHz, CDC1 ₃ ) δ 0.06-0.17 (2H, m) , 0.42-0.55 (2H, m) , 0.86-1.04 (2H, m) , 1.10-1.22 (1H, m) , 1.44-1.57 (2H, m) , 1.91- 2.13 (3H, m) , 2.37-2.50 (1H, m) , 2.53-2.66 (2H, m) , 3.45-3.61 (2H, m) , 3.93-4.05 (2H, m) , 4.06-4.25 (1H, m) , 5.62-5.77 (1H, m) , 6.92-6.98 (1H, m) , 7.52 (1H, d, J = 1.5 Hz).

[0488]

The compounds of Examples 121 and 122 could be produced according to the production methods described in the present specification, a method shown in the Examples, or a method analogous thereto.

Example 121

4- ( (IS, 2R) -2- ( (cyclobutylmethyl) amino) cyclopropyl) -5-methyl-N- ( l-methyl-lH-pyrazol-4-yl) thiophene-2-carboxamide

dihydrochloride

Example 122

4- ( (IS, 2R) -2- ( (cyclobutylmethyl) amino) cyclopropyl) -5-methyl-N- (tetrahydro-2H-pyran-4-yl) thiophene-2-carboxamide

hydrochloride

[0489]

Example 123

4- ( (IS, 2R) -2- (cyclobutylamino) cyclopropyl) -5-methyl-N- Clmethyl-lH-pyrazol-4-yl) thiophene-2-carboxamide hydrochloride

A) methyl 4- ( (IS, 2R) -2- ( (tert- butoxycarbonyl) amino) cyclopropyl) -5-methylthiophene-2- carboxylate

Methyl 4- (trans-2- ( (tert- butoxycarbonyl) amino) cyclopropyl) -5-methylthiophene-2- carboxylate (8 g) was fractionated by SFC (column: CHIRALPAK AD, 20 mmIDx250 mmL, manufactured by Daicel Corporation, mobile phase: carbon dioxide/methanol = 900/100), and the obtained fraction was concentrated under reduced pressure to give methyl 4- ( (IS, 2R) -2- ( (tert- butoxycarbonyl) amino) cyclopropyl) -5-methylthiophene-2- carboxylate (optical isomer, retention time short) (3.68 g) and methyl 4- ( (1R, 2S) -2- ( (tert- butoxycarbonyl) amino) cyclopropyl) -5-methylthiophene-2- carboxylate (optical isomer, retention time long) (3.72 g) . methyl 4- ( (IS, 2R) -2- ( (tert-butoxycarbonyl) amino) cyclopropyl) -

5-methylthiophene-2-carboxylate (optical isomer, retention time short)

HPLC retention time 4.834 min (column: CHIRALPAK ADH, 4.6 mmIDxl50 mmL, mobile phase: carbon dioxide/methanol= 900/100, flow rate: 2.5 mL/min, temperature: 35°C, detection: UV 220 ran, concentration: 0.5 mg/mL, injection volume: 0.005 mL) .

MS: [M-tBu+2H] ⁺ 256.1.

methyl 4- ( (1R, 2S) -2- ( (tert-butoxycarbonyl) amino) cyclopropyl) - 5-methylthiophene-2-carboxylate (optical isomer, retention time long)

HPLC retention time 6.885 min (column: CHIRALPAK ADH, 4.6 mmIDxl50 mmL, mobile phase: carbon dioxide/methanol= 900/100, flow rate: 2.5 mL/min,. temperature: 35°C, detection: UV 220 nm, concentration: 0.5 mg/mL, injection volume: 0.005 mL) .

MS: [M-tBu+2H] ⁺ 256.1.

[0490]

B) 4- ( (IS, 2R) -2- ( (tert-butoxycarbonyl) amino) cyclopropyl) -5- methylthiophene-2-carboxylic acid

Methyl 4- ( (IS, 2R) -2- ( (tert- butoxycarbonyl) amino) cyclopropyl) -5-methylthiophene-2- carboxylate (3.2 g) was dissolved in methanol (20 mL) and tetrahydrofuran (10 mL) , 2 mol/L aqueous sodium hydroxide solution (12.9 mL) was added at 0°C, and the mixture was stirred at room temperature overnight. The reaction mixture was acidified with 1 mol/L hydrochloric acid, and extracted with ethyl acetate. The extract was washed with water and saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure to give the title compound (3.06 g) .

MS: [M-H]- 296.0.

[0491]

C) tert-butyl ( (1R, 2S) -2- (2-methyl-5- ( (l-methyl-lH-pyrazol-4- yl) carbamoyl) thiophen-3-yl) cyclopropyl) carbamate

4- ( (IS, 2R) -2- ( (tert-Butoxycarbonyl) amino) cyclopropyl) -5- methylthiophene-2-carboxylic acid (3.06 g) , 1-methyl.-1H- pyrazol-4-amine hydrochloride (1.37 g) and triethylamine (5.73 mL) were dissolved in DMF (30 mL) , 0- (7-azabenzotriazol-l-yl) - Ν,Ν,Ν' ,Ν' -tetramethyluronium hexafluorophosphate (4.69 g) was added, and the mixture was stirred at 40°C overnight. Water was added to the reaction mixture, and the mixture was

extracted with ethyl acetate. The extract was washed with saturated aqueous sodium hydrogen carbonate solution, water and saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate and methanol/ethyl acetate) to give the title compound (3.7 g) .

MS: [M+H] ⁺ 377.1

[0492]

D) 4- ( (IS, 2R) -2-aminocyclopropyl) -5-methyl-N- (1-methyl-lH- pyrazol-4-yl) thiophene-2-carboxamide dihydrochloride

To a suspension of tert-butyl ( (1R, 2S) -2- (2-methyl-5- ( ( 1- methyl-lH-pyrazol-4-yl) carbamoyl) thiophen-3- yl) cyclopropyl) carbamate (3.7 g) in ethyl acetate (45 mL) and methanol (25 mL) was added 4 mol/L hydrogen chloride/ethyl acetate solution (49.1 mL) at 0°C, and the mixture was stirred at room temperature overnight. The precipitated solid was collected by filtration, and washed with ethyl acetate to give the title compound (3 g) .

MS: [M+H-2HC1] ⁺ 277.1.

[0493]

E) 4- ( (IS, 2R) -2- (cyclobutylamino) cyclopropyl) -5-methyl-N- (1- methyl-lH-pyrazol-4-yl) thiophene-2-carboxamide

To a suspension of 4- ( (IS, 2R) -2-aminocyclopropyl) -5- methyl-N- (l-methyl-lH-pyrazol-4-yl) thiophene-2-carboxamide dihydrochloride (3 g) in methanol (40 mL) were added

triethylamine (2.99 mL, 21.5 mmol) , trimethoxymethane (1.90 mL, 17.2 mmol) and cyclobutanone (0.77 mL, 10.3 mmol) at room temperature. The reaction mixture was stirred at room

temperature overnight, and sodium borohydride (487 mg) was added under cooling at -40°C. The reaction mixture was stirred at -40°C for 1 hr, saturated aqueous ammonium chloride solution was added, and the mixture was concentrated under reduced pressure. To. the residue was added saturated aqueous sodium hydrogen carbonate solution, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure and the residue was purified by silica gel column chromatography (ethyl

acetate/methanol) to give the title compound (2 g) . MS: [M+H] ⁺ 331.1.

[0494]

F) 4- ( (IS, 2R) -2- (cyclobutylamino) cyclopropyl) -5-methyl-N- (1- methyl-lH-pyrazol-4-yl ) thiophene-2-carboxamide hydrochloride

4N Hydrogen chloride/ethyl acetate solution (6.08 mL,

24.33 mmol) was added to a solution of 4- ( (IS, 2R) -2- (cyclobutylamino) cyclopropyl) -5-methyl-N- (1-methyl-lH-pyrazol- 4-yl) thiophene-2-carboxamide (2.68 g, 8.11 mmol) in ethyl acetate (20 mL) at 0°C. The precipitate was collected by filtration, and washed with ethyl acetate to give a white solid. The obtained white solid was recrystallized from ethanol, water and ethyl acetate to give the title compound (1.920 g) as a white solid.

¾ NMR (300 MHz, DMSO-d ₆ ) δ 1.10-1.26 (1H, m) , 1.51-1.55 (1H, m) , 1.66-1.94 (2H, m) , 2.14-2.36 (4H, m) , 2.39-2.50 (4H, m) , 2.76-2.81 (1H, m), 3.70-3.93 (4H, m) , 7.50-7.57 (2H, m) , 7.92 (1H, s), 9.68 (2H, brs) , 10.33 (1H, s) .

[0495]

The compounds of Examples 124 and 125 could be produced according to the production methods described in the present specification, a method shown in the Examples, or a method analogous thereto.

Example 124

4- ( (IS, 2R) -2-aminocyclopropyl) -N- (5-methyl-l, 3, 4-thiadiazol-2- yl ) thiophene-2-carboxamide dihydrochloride

Example 125

5- ( (IS, 2S) -2- ( (cyclopropylmethyl).amino) cyclopropyl) -N- (tetrahydro-2H-pyran-4-yl) thiophene-3-carboxamide

hydrochloride

[0496]

Example compounds are shown in the following Tables. MS in the Tables shows measured values. [0497]

[Table 1-1] [0498] . [Table 1-2] [0499]

[Table 1-3] [0500]

[Table 1-4] [0501]

[Table 1-5] [0502]

[Table 1-6] [0503]

[Table 1-7] [0504]

[Table 1-8] [0505]

[Table 1-9] [0506]

[Table 1-10] [0507]

[Table 1-11] [0508]

[Table 1-12] [0509]

[Table 1-13] [0510]

[Table 1-14] [0511]

[Table 1-15] [0512]

[Table 1-16] [0513]

[Table 1-17] [0514]

[Table 1-18] [0515]

[Table 1-19] [0516]

[Table 1-20] [0517]

[Table 1-21] [0518]

[Table 1-22] [0519]

[Table 1-23] [0520]

Other preferable specific examples of the compound represented by the formula (I) include the following compounds shown in the Examples, an optically active form thereof, and a mixture of optically active forms thereof. The following compounds shown in the Examples, an optically active form thereof, and a mixture of optically active forms thereof can be produced according to the aforementioned production methods, a method shown in the Examples, or a method analogous thereto. The relative configuration of the substituent on the

cyclopropane ring is cis or trans, preferably trans.

[0521]

Example Al

4- (2- (cyclobutylamino) cyclopropyl) -N- (1, 3-dimethyl-lH-pyrazol- 4-yl) thiophene-2-carboxamide

Example A2

4- (2- (cyclobutylamino) cyclopropyl) -N- ( l-ethyl-lH-pyrazol-4- yl) thiophene-2-carboxamide

Example A3

4- (2- (cyclobutylamino) cyclopropyl) -N- (1, 3-dimethyl-lH-pyrazol-

5-yl) thiophene-2-carboxamide

Example A4

4- (2- (cyclobutylamino) cyclopropyl) -N- (tetrahydro-2H-pyran-4- yl) thiophene-2-carboxamide

Example A5

4- (2- (cyclobutylamino) cyclopropyl) -N-cyclopentylthiophene-2- carboxamide

Example A6

4- (2- (cyclobutylamino) cyclopropyl) -N- (4, 4- difluorocyclohexyl) thiophene-2-carboxamide

Example A7

4- (2- (cyclobutylamino) cyclopropyl) -N- (1- (2, 2, 2- trifluoroethyl) piperidin-4-yl) thiophene-2-carboxamide

Example A8

4- (2- (cyclobutylamino) cyclopropyl) -N- (5-methyl-l, 2-oxazol-3- yl) thiophene-2-carboxamide

Example A9

4- (2- (cyclobutylamino) cyclopropyl) -N- (3-methyl-l, 2-oxazol-5- yl) thiophene-2-carboxamide

Example A10

4- (2- (cyclobutylamino) cyclopropyl) -N- (2-methyl-l , 3-thiazol-5- yl) thiophene-2-carboxamide

[0522]

Example All

4- (2- ( (cyclopropylmethyl) amino) cyclopropyl) -N- ( 1-methyl-lH- pyrazol-4-yl ) thiophene-2-carboxamide

Example A12

4- (2- ( (cyclopropylmethyl) amino) cyclopropyl) -N- (1, 3-dimethyl- lH-pyrazol-4-yl) thiophene-2-carboxamide

Example A13

4- (2- ( (cyclopropylmethyl) amino) cyclopropyl) -N- (1-ethyl-lH- pyrazol-4-yl) thiophene-2-carboxamide

Example A14

4- (2- ( (cyclopropylmethyl) amino) cyclopropyl) -N- (1, 3-dimethyl- lH-pyrazol-5-yl) thiophene-2-carboxamide

Example A15

N-cyclopentyl-4- (2-

( (cyclopropylmethyl) amino) cyclopropyl) thiophene-2-carboxamide Example A16

4- (2- ( (cyclopropylmethyl) amino) cyclopropyl) -N- (1- (2, 2, 2- trifluoroethyl) piperidin-4-yl ) thiophene-2-carboxamide

Example A17

4- (2- ( (cyclopropylmethyl) amino) cyclopropyl) -N- (5-methyl-l, 2- oxazol-3-yl) thiophene-2-carboxamide

Example A18

4- (2- ( (cyclopropylmethyl) amino) cyclopropyl) -N- (3-methyl-l, 2- oxazol-5-yl) thiophene-2-carboxamide

Example A19

4- (2- ( (cyclopropylmethyl) amino) cyclopropyl) -N- (2-methyl-l, 3- thiazol-5-yl) thiophene-2-carboxamide Example A20

4- (2- ( (cyclopropylmethyl) amino) cyclopropyl) -N- (oxetan-3- yl) thiophene-2-carboxamide

[0523]

Example A21

4- (2- ( (cyclopropylmethyl) amino) cyclopropyl) -N- (3,3- difluorocyclobutyl) thiophene-2-carboxamide

Example A22

4- (2- ( (cyclopropylmethyl) amino) cyclopropyl) -N- (5-methyl-l, 3, 4- oxadiazol-2-yl) thiophene-2-carboxamide

Example A23

4- (2- ( (cyclopropylmethyl) amino) cyclopropyl) -N- (5-methyl-2- thienyl) thiophene-2-carboxamide

Example A24

4- (2- ( (cyclopropylmethyl) amino) cyclopropyl) -N- (pyridin-4- yl) thiophene-2-carboxamide

Example A25

4- (2- ( (cyclopropylmethyl) amino) cyclopropyl) -N- (2-methyl-l, 3- oxazol-5-yl) thiophene-2-carboxamide

Example A26

4- (2- ( (cyclopropylmethyl) amino) cyclopropyl) -N- (5- (trifluoromethyl) -1,3, 4-thiadiazol-2-yl) thiophene-2- carboxamide

Example A27

4- (2- ( (cyclopropylmethyl) amino) cyclopropyl) -N- ( 3-methyloxetan- 3-yl) thiophene-2-carboxamide

Example A28

N-cyclopropyl-4- (2-

( (cyclopropylmethyl) amino) cyclopropyl) thiophene-2-carboxamide Example A29

N-cyclopentyl-4- (2- (tetrahydro-2H-pyran-4- ylamino) cyclopropyl) thiophene-2-carboxamide

Example A30

N- (2-methyl-l, 3-thiazol-5-yl) -4- (2- (tetrahydro-2H-pyran-4- ylamino) cyclopropyl) thiophene-2-carboxamide [0524]

Example A31

4- (2- ( (l-cyclopropylpiperidin-4-yl) amino) cyclopropyl) -N- (5- methyl-1, 3, 4-thiadiazol-2-yl) thiophene-2-carboxamide

Example A32

4- (2- ( (l-cyclopropylpiperidin-4-yl) amino) cyclopropyl) -N- (1- ethyl-lH-pyrazol-4-yl ) thiophene-2-carboxamide

Example A33

4- (2- ( (l-cyclopropylpiperidin-4-yl) amino) cyclopropyl) -N- (1, 3- dimethyl-lH-pyrazol-5-yl) thiophene-2-carboxamide

Example A34

N-cyclopentyl-4- (2- ( ( l-cyclopropylpiperidin-4- yl) amino) cyclopropyl) thiophene-2-carboxamide

Example A35

4- (2- ( (l-cyclopropylpiperidin-4-yl) amino) cyclopropyl) -N- (4,4- difluorocyclohexyl) thiophene-2-carboxamide

Example A36

4- (2- ( (l-cyclopropylpiperidin-4-yl) amino) cyclopropyl) -N- (1- (2, 2, 2-trifluoroethyl) piperidin-4-yl) thiophene-2-carboxamide Example A37

4- (2- ( (l-cyclopropylpiperidin-4-yl) amino) cyclopropyl) -N- (5- methyl-1, 2-oxazol-3-yl) thiophene-2-carboxamide

Example A38

4- (2- ( ( l-cyclopropylpiperidin-4-yl) amino) cyclopropyl) -N- (3- methyl-1, 2-oxazol-5-yl) thiophene-2-carboxamide

Example A39

4- (2- ( (l-cyclopropylpiperidin-4-yl) amino) cyclopropyl) -N- (2- methyl-1, 3-thiazol-5-yl) thiophene-2-carboxamide

Example A40

N- (1, 3-dimethyl-lH-pyrazol-4-yl) -4- (2- ( (tetrahydro-2H-pyran-4- ylmethyl) amino) cyclopropyl) thiophene-2-carboxamide ..

[0525]

Example A41

N- (l-ethyl-lH-pyrazol-4-yl) -4- (2- ( (tetrahydro-2H-pyran-4- ylmethyl) amino) cyclopropyl) thiophene-2-carboxamide Example A42

N- (1, 3-dimethyl-lH-pyrazol-5-yl) -4- (2- ( (tetrahydro-2H-pyran-4- ylmethyl) amino) cyclopropyl) thiophene-2-carboxamide

Example A 3

N-cyclopentyl-4- (2- ( (tetrahydro-2H-pyran-4- ylmethyl) amino) cyclopropyl) thiophene-2-carboxamide

Example A44

4- (2- ( (tetrahydro-2H-pyran-4-ylmethyl) amino) cyclopropyl) -N- (1- (2,2, 2-trifluoroethyl) piperidin-4-yl ) thiophene-2-carboxamide Example A 5

N- (5-methyl-l, 2-oxazol-3-yl) -4- (2- ( (tetrahydro-2H-pyran-4- ylmethyl) amino) cyclopropyl) thiophene-2-carboxamide

Example A46

N- (3-methyl-l, 2-oxazol-5-yl) -4- (2- ( (tetrahydro-2H-pyran-4- ylmethyl) amino) cyclopropyl) thiophene-2-carboxamide

Example A47

N- (2-methyl-l, 3-thiazol-5-yl) -4- (2- ( (tetrahydro-2H-pyran-4- ylmethyl) amino) cyclopropyl) thiophene-2-carboxamide

Example A48

N- (5-methyl-l, 3, 4-thiadiazol-2-yl) -4- (2- ( (1- (2,2,2- trifluoroethyl) piperidin-4-yl) amino) cyclopropyl) thiophene-2- carboxamide

Example A49

N- (l-methyl-lH-pyrazol-4-yl) -4- (2- ( (1- (2,2,2- trifluoroethyl) piperidin-4-yl) amino) cyclopropyl) thiophene-2- carboxamide

Example A50

N- (l-ethyl-lH-pyrazol-4-yl) -4- (2- ( (1- (2,2,2- trifluoroethyl) piperidin-4-yl ) amino) cyclopropyl) thiophene-2- carboxamide

[0526]

Example A51

N- (1, 3-dimethyl-lH-pyrazol-5-yl) -4- (2- ( (1- (2,2,2- trifluoroethyl) piperidin-4-yl) amino) cyclopropyl) thiophene-2- carboxamide Example A52

N-cyclopentyl-4- (2- ( (1- (2 , 2 , 2-trifluoroethyl) piperidin-4- yl) amino) cyclopropyl) thiophene-2-carboxamide

Example A53

N- (4, 4-difluorocyclohexyl) -4- (2- ( (l-(2,2,2- trifluoroethyl) piperidin-4-yl) amino) cyclopropyl) thiophene-2- carboxamide

Example A54

N- (1- (2, 2, 2-trifluoroethyl) piperidin-4-yl ) -4- (2- ( (1- (2, 2, 2- trifluoroethyl) piperidin-4-yl) amino) cyclopropyl) thiophene-2- carboxamide

Example A55

N- (5-methyl-l, 2-oxazol-3-yl) -4- (2- ( (1- (2,2,2- trifluoroethyl) piperidin-4-yl ) amino) cyclopropyl) thiophene-2- carboxamide

Example A56

N- (3-methyl-l, 2-oxazol-5-yl ) -4- (2- ( (1- (2,2, 2- trifluoroethyl) piperidin-4-yl ) amino) cyclopropyl) thiophene-2- carboxamide

Example A57

N- (2-methyl-l, 3-thiazol-5-yl) -4- (2- ( (1- (2, 2, 2- trifluoroethyl) piperidin-4-yl) amino) cyclopropyl) thiophene-2- carboxamide

Example A58

4- (2- (cyclobutyland.no) ^· cyclopropyl) -N- (5-methyl-l, 3, 4- thiadiazol-2-yl) thiophene-2-carboxamide

Example A59

4- (2- (cyclobutylamino) cyclopropyl) -N- ( l-methyl-lH-pyrazol-4- yl) thiophene-2-carboxamide

Example A60

N- (5-methyl-l, 3, 4-thiadiazol-2-yl) -4- (2- ( (tetrahydro-2H-pyran-

4-ylmethyl) amino) cyclopropyl) thiophene-2-carboxamide

[0527]

Example A61

N- (4, 4-difluorocyclohexyl) -4- (2- ( (tetrahydro-2H-pyran-4- ylmethyl) amino) cyclopropyl) thiophene-2-carboxamide

Example A62

4- (2- ( (cyclopropylmethyl) amino) cyclopropyl) -N- (tetrahydro-2H- pyran-4-yl) thiophene-2-carboxamide

[0528]

Example Bl

4- (2- (cyclobutylamino) cyclopropyl) -N- (1, 3-dimethyl-lH-pyrazol- 4-yl ) -5-methylthiophene-2-carboxamide

Example B2

4- (2- (cyclobutylamino) cyclopropyl) -N- ( l-ethyl-lH-pyrazol-4- yl) -5-methylthiophene-2-carboxamide

Example B3

4- (2- (cyclobutylamino) cyclopropyl) -N- (1, 3-dimethyl-lH-pyrazol-

5-yl ) -5-methylthiophene-2-carboxamide

Example B4

4- (2- (cyclobutylamino) cyclopropyl) -5-methyl-N- (tetrahydro-2H- pyran-4-yl) thiophene-2-carboxamide

Example B5

4- (2- (cyclobutylamino) cyclopropyl) -N-cyclopentyl-5- methylthiophene-2-carboxamide

Example B6

4- (2- (cyclobutylamino) cyclopropyl) -N- (4, 4-difluorocyclohexyl) -

5-methylthiophene-2-carboxamide

Example B7

4- (2- (cyclobutylamino) cyclopropyl) -5-methyl-N- (1- (2, 2, 2- trifluoroethyl) piperidin-4-yl ) thiophene-2-carboxamide

Example B8

4- (2- (cyclobutylamino) cyclopropyl) -5-methyl-N- ( 5-methyl-1, 2- oxazol-3-yl) thiophene-2-carboxamide

Example B9

4- (2- (cyclobutylamino) cyclopropyl) -5-methyl-N- (3-methyl-l, 2- oxazol-5-yl) thiophene-2-carboxamide

Example BIO

4- (2- (cyclobutylamino) cyclopropyl) -5-methyl-N- (2-methyl-l, 3- thiazol-5-yl) thiophene-2-carboxamide [0529]

Example Bll

4- (2- ( (cyclopropylmethyl) amino) cyclopropyl) -5-methyl-N- (1- methyl-lH-pyrazol-4-yl) thiophene-2-carboxamide

Example B12

4- (2- ( (cyclopropylmethyl) amino) cyclopropyl) -N- (1, 3-dimethyl- lH-pyrazol-4-yl) -5-methylthiophene-2-carboxamide

Example B13

4- (2- ( (cyclopropylmethyl) amino) cyclopropyl) -N- (1-ethyl-lH- pyrazol-4-yl) -5-methylthiophene-2-carboxamide

Example B14

4- (2- ( (cyclopropylmethyl) amino) cyclopropyl) -N- (1, 3-dimethyl- lH-pyrazol-5-yl) -5-methylthiophene-2-carboxamide

Example B15

N-cyclopentyl-4- (2- ( (cyclopropylmethyl) amino) cyclopropyl) -5- methylthiophene-2-carboxamide

Example B16

4- (2- ( (cyclopropylmethyl) amino) cyclopropyl) -5-methyl-N- (1- (2,2, 2-trifluoroethyl) piperidin-4-yl) thiophene-2-carboxamide Example B17

4- (2- ( (cyclopropylmethyl) amino) cyclopropyl) -5-methyl-N- (5- methyl-1, 2-oxazol-3-yl) thiophene-2-carboxamide

Example B18

4- (2- ( (cyclopropylmethyl) amino) cyclopropyl) -5-methyl-N- (3- methyl-1, 2-oxazol-5-yl) thiophene-2-carboxamide

Example B19

4- (2- ( (cyclopropylmethyl) amino) cyclopropyl) -5-methyl-N- (2- methyl-1, 3-thiazol-5-yl) thiophene-2-carboxamide

Example B20

4- (2- ( (cyclopropylmethyl) amino) cyclopropyl) -5-methyl-N-

(oxetan-3-yl) thiophene-2-carboxamide . .

[0530]

Example B21

4- (2- ( (cyclopropylmethyl) amino) cyclopropyl) -N- (3,3- difluorocyclobutyl) -5-methylthiophene-2-carboxamide Example B22

4- (2- ( (cyclopropylmethyl) amino) cyclopropyl) -5-methyl-N- (5- methyl-1, 3, 4-oxadiazol-2-yl ) thiophene-2-carboxamide

Example B23

4- (2- ( (cyclopropylmethyl) amino) cyclopropyl) -5-methyl-N- (5- methyl-2-thienyl) thiophene-2-carboxamide

Example B24

4- (2- ( (cyclopropylmethyl) amino) cyclopropyl) -5-methyl-N- (pyridin-4-yl) thiophene-2-carboxamide

Example B25

4- (2- ( (cyclopropylmethyl) amino) cyclopropyl) -5-methyl-N- (2- methyl-1, 3-oxazol-5-yl) thiophene-2-carboxamide

Example B26

4- (2- ( (cyclopropylmethyl) amino) cyclopropyl) -5-methyl-N- (5- (trifluoromethyl) -1, 3, 4-thiadiazol-2-yl) thiophene-2- carboxamide

Example B27

4- (2- ( (cyclopropylmethyl) amino) cyclopropyl) -5-methyl-N- (3- methyloxetan-3-yl) thiophene-2-carboxamide

Example B28

N-cyclopropyl-4- (2- ( (cyclopropylmethyl) amino) cyclopropyl) -5- methylthiophene-2-carboxamide

Example B29

N-cyclopentyl-5-methyl-4- (2- (tetrahydro-2H-pyran-4- ylamino) cyclopropyl ) thiophene-2-carboxamide

Example B30

5-methyl-N- (2-methyl-l, 3-thiazol-5-yl) -4- (2- (tetrahydro-2H- pyran-4-ylamino) cyclopropyl) thiophene-2-carboxamide

[0531]

Example B31

4- (2- ( (l-cyclopropylpiperidin-4-yl) amino) cyclopropyl) -5- methyl-N- (5-methyl-l, 3, 4-thiadiazol-2-yl) thiophene-2- carboxamide

Example B32

4- (2- ( (l-cyclopropylpiperidin-4-yl) amino) cyclopropyl) -N- (1- ethyl-lH-pyrazol-4-yl) -5-methylthiophene-2-carboxamide

Example B33

4- (2- ( (l-cyclopropylpiperidin-4-yl) amino) cyclopropyl) -N- (1, 3- dimethyl-lH-pyrazol-5-yl) -5-methylthiophene-2-carboxamide Example B34

N-cyclopentyl-4- (2- ( ( l-cyclopropylpiperidin-4- yl) amino) cyclopropyl) -5-methylthiophene-2-carboxamide

Example B35

4- (2- ( (l-cyclopropylpiperidin-4-yl) amino) cyclopropyl) -N- (4, 4- difluorocyclohexyl) -5-methylthiophene-2-carboxamide

Example B36

4- (2- ( (l-cyclopropylpiperidin-4-yl) amino) cyclopropyl) -5- methyl-N- (1- (2, 2 , 2-trifluoroethyl) piperidin-4-yl) thiophene-2- carboxamide

Example B37

4- (2- ( (l-cyclopropylpiperidin-4-yl) amino) cyclopropyl) -5- methyl-N- (5-methyl-l, 2-oxazol-3-yl) thiophene-2-carboxamide Example B38

4- (2- ( (l-cyclopropylpiperidin-4-yl) amino) cyclopropyl) -5- methyl-N- ( 3-methyl-l , 2-oxazol-5-yl) thiophene-2-carboxamide Example B39

4- (2- ( ( l-cyclopropylpiperidin-4-yl) amino) cyclopropyl) -5- methyl-N- (2-methyl-l, 3-thiazol-5-yl) thiophene-2-carboxamide Example B40

N- (1, 3-dimethyl-lH-pyrazol-4-yl) -5-methyl-4- (2- ( (tetrahydro- 2H-pyran-4-ylmethyl) amino) cyclopropyl) thiophene-2-carboxamide [0532]

Example B41

N- (l-ethyl-lH-pyrazol-4-yl) -5-methyl-4- (2- ( (tetrahydro-2H- pyran-4-ylmethyl) amino) cyclopropyl) thiophene-2-carboxamide Example B42

N- (1, 3-dimethyl-lH-pyrazol-5-yl) -5-methyl-4- (2- ( (tetrahydro- . 2H-pyran-4-ylmethyl) amino) cyclopropyl) thiophene-2-carboxamide Example B43

N-cyclopentyl-5-methyl-4- (2- ( (tetrahydro-2H-pyran-4- ylmethyl) amino) cyclopropyl) thiophene-2-carboxamide Example B 4

5-methyl-4- (2- ( (tetrahydro-2H-pyran-4- ylmethyl) amino) cyclopropyl) -N- (1- (2, 2, 2- trifluoroethyl) piperidin-4-yl) thiophene-2-carboxamide

Example B 5

5-methyl-N- (5-methyl-l, 2-oxazol-3-yl) -4- (2- ( (tetrahydro-2H- pyran- -ylmethyl) amino) cyclopropyl) thiophene-2-carboxamide Example B46

5-methyl-N- (3-methyl-l, 2-oxazol-5-yl) -4- (2- ( (tetrahydro-2H- pyran-4-ylmethyl) amino) cyclopropyl) thiophene-2-carboxamide Example B47

5-methyl-N- (2-methyl-l, 3-thiazol-5-yl) -4- (2- ( (tetrahydro-2H- pyran-4-ylmethyl ) amino) cyclopropyl) thiophene-2-carboxamide Example B48

5-methyl-N- (5-methyl-l, 3, 4-thiadiazol-2-yl) -4- (2- ( (1- (2, 2, 2- trifluoroethyl ) piperidin-4-yl) amino) cyclopropyl) thiophene-2- carboxamide

Example B49

5-methyl-N- (l-methyl-lH-pyrazol-4-yl) -4- (2- ( (1- (2, 2, 2- trifluoroethyl) piperidin-4-yl) amino) cyclopropyl) thiophene-2- carboxamide

Example B50

N- (l-ethyl-lH-pyrazol-4-yl) -5-methyl-4~ (2- ( (1- (2,2,2- trifluoroethyl) piperidin-4-yl ) amino) cyclopropyl) thiophene-2- carboxamide

[0533]

Example B51

N- (1, 3-dimethyl-lH-pyrazol-5-yl) -5-methyl-4- (2- ( (1- (2,2,2- trifluoroethyl) piperidin-4-yl) amino) cyclopropyl) thiophene-2- carboxamide

Example B52

N-cyclopentyl-5-methyl-4- (2- ( (1- (2,2,2- trifluoroethyl) piperidin-4-yl) amino) cyclopropyl) thiophene-2- carboxamide Example B53

N- (4, -difluorocyclohexyl) -5-methyl-4- (2- ( (1- (2, 2, 2- trifluoroethyl) piperidin-4-yl) amino) cyclopropyl) thiophene-2- carboxamide

Example B54

5-methyl-N- (1- (2, 2, 2-trifluoroethyl) piperidin-4-yl) -4- (2- ( (1-

(2, 2, 2-trifluoroethyl) piperidin-4- yl) amino) cyclopropyl) thiophene-2-carboxamide

Example B55

5-methyl-N- (5-methyl-l, 2-oxazol-3-yl) -4- (2- ( (1- (2,2,2- trifluoroethyl) piperidin-4-yl) amino) cyclopropyl) thiophene-2- carboxamide

Example B56

5-methyl-N- ( 3-methyl-l , 2-oxazol-5-yl ) -4- (2- ( (1- (2,2,2- trifluoroethyl) piperidin-4-yl) amino) cyclopropyl) thiophene-2- carboxamide

Example B57

5-methyl-N- (2-methyl-l, 3-thiazol-5-yl) -4- (2- ( (1- (2,2, 2- trifluoroethyl) piperidin-4-yl ) amino) cyclopropyl) thiophene-2- carboxamide

[0534]

Example CI

5- (2- (cyclobutylamino) cyclopropyl) -N- (1, 3-dimethyl-lH-pyrazol-

4-yl) thiophene-3-carboxamide

Example C2

5- (2- (cyclobutylamino) cyclopropyl) -N- ( l-ethyl-lH-pyrazol-4- yl) thiophene-3-carboxamide

Example C3

5- (2- (cyclobutylamino) cyclopropyl) -N- (1, 3-dimethyl-lH-pyrazol- 5-yl) thiophene-3-carboxamide

Example C4

5- (2- (cyclobutylamino) cyclopropyl) -N- (tetrahydro-2H-pyran-4- yl) thiophene-3-carboxamide

Example C5

5- (2- (cyclobutylamino.) cyclopropyl) -N-cyclopentylthiophene-3- carboxamide

Example C6

5- (2- (cyclobutylamino) cyclopropyl) -N- (4, 4- difluorocyclohexyl) thiophene-3-carboxamide

Example C7

5- (2- (cyclobutylamino) cyclopropyl) -N- (1- (2, 2, 2- trifluoroethyl) piperidin-4-yl) thiophene-3-carboxamide

Example C8

5- (2- (cyclobutylamino) cyclopropyl) -N- (5-methyl-l, 2-oxazol-3- yl ) thiophene-3-carboxamide

Example C9

5- (2- (cyclobutylamino) cyclopropyl) -N- (3-methyl-l, 2-oxazol-5- yl) thiophene-3-carboxamide

Example CIO

5- (2- (cyclobutylamino) cyclopropyl) -N- (2-methyl-l, 3-thiazol-5- yl) thiophene-3-carboxamide

[0535]

Example Cll

5- (2- ( (cyclopropylmethyl) amino) cyclopropyl) -N- ( 1-methyl-lH- pyrazol-4-yl) thiophene-3-carboxamide

Example C12

5- (2- ( (cyclopropylmethyl) amino) cyclopropyl) -N- (1, 3-dimethyl- lH-pyrazol-4-yl) thiophene-3-carboxamide

Example C13

5- (2- ( (cyclopropylmethyl) amino) cyclopropyl) -N- (1-ethyl-lH- pyrazol-4-yl ) thiophene-3-carboxamide

Example CI4

5- (2- ( (cyclopropylmethyl) amino) cyclopropyl) -N- (1, 3-dimethyl- lH-pyrazol-5-yl) thiophene-3-carboxamide

Example C15

N-cyclopentyl-5- (2-

( (cyclopropylmethyl) amino) cyclopropyl) thiophene-3-carboxamide Example CI6

5- (2- ( (cyclopropylmethyl) amino) cyclopropyl) -N- (1- (2, 2, 2- trifluoroethyl) piperidin-4-yl) thiophene-3-carboxamide Example C17

5- (2- ( (cyclopropylmethyl) amino) cyclopropyl) -N- (5-methyl-l, 2- oxazol-3-yl) thiophene-3-carboxamide

Example CI8

5- (2- ( (cyclopropylmethyl) amino) cyclopropyl) -N- (3-methyl-l, 2- oxazol-5-yl) thiophene-3-carboxamide

Example CI9

5- (2- ( (cyclopropylmethyl) amino) cyclopropyl) -N- (2-methyl-l, 3- thiazol-5-yl ) thiophene-3-carboxamide

Example C20

5- (2- ( (cyclopropylmethyl) amino) cyclopropyl) -N- (oxetan-3- yl) thiophene-3-carboxamide

[0536]

Example C21

5- (2- ( (cyclopropylmethyl) amino) cyclopropyl) -N- (3, 3- difluorocyclobutyl ) thiophene-3-carboxamide

Example C22

5- (2- ( (cyclopropylmethyl) amino) cyclopropyl) -N- (5-methyl-l, 3, 4- oxadiazol-2-yl) thiophene-3-carboxamide

Example C23

5- (2- ( (cyclopropylmethyl) amino) cyclopropyl) -N- (5-methyl-2- thienyl) thiophene-3-carboxamide

Example C24

5- (2- ( (cyclopropylmethyl) amino) cyclopropyl) -N- (pyridin-4- yl) thiophene-3-carboxamide

Example C25

5- (2- ( (cyclopropylmethyl) amino) cyclopropyl) -N- (2-methyl-l, 3- oxazol-5-yl) thiophene-3-carboxamide

Example C26

5- (2- ( (cyclopropylmethyl) amino) cyclopropyl) -N- (5-,

(trifluoromethyl) -1,3, -thiadiazol-2-yl) thiophene-3- carboxamide

Example C27

5- (2- ( (cyclopropylmethyl) amino) cyclopropyl) -N- (3-methyloxetan- 3-yl) thiophene-3-carboxamide Example C28

N-cyclopropyl-5- (2-

( (cyclopropylmethyl) amino) cyclopropyl) thiophene-3-carboxamide Example C29

N-cyclopentyl-5- (2- (tetrahydro-2H-pyran-4- ylamino) cyclopropyl) thiophene-3-carboxamide

Example C30

N- (2-methyl-l, 3-thiazol-5-yl) -5- (2- (tetrahydro-2H-pyran-4- ylamino) cyclopropyl) thiophene-3-carboxamide

[0537]

Example C31

5- (2- ( (l-cyclopropylpiperidin-4-yl) amino) cyclopropyl) -N- (5- methyl-1, 3, 4-thiadiazol-2-yl) thiophene-3-carboxamide

Example C32

5- (2- ( (l-cyclopropylpiperidin-4-yl) amino) cyclopropyl) -N- (1- ethyl-lH-pyrazol-4-yl) thiophene-3-carboxamide

Example C33

5- (2- ( (l-cyclopropylpiperidin-4-yl) amino) cyclopropyl) -N- (1, 3- dimethyl-lH-pyrazol-5-yl ) thiophene-3-carboxamide

Example C34

N-cyclopentyl-5- (2- ( ( l-cyclopropylpiperidin-4- yl) amino) cyclopropyl) thiophene-3-carboxamide

Example C35

5- (2- ( (l-cyclopropylpiperidin-4-yl) amino) cyclopropyl) -N- (4, 4-, difluorocyclohexyl) thiophene-3-carboxamide

Example C36

5- (2- ( (l-cyclopropylpiperidin-4-yl) amino) cyclopropyl) -N- (1- (2,2, 2-trifluoroethyl) piperidin-4-yl) thiophene-3-carboxamide Example C37

5- (2- ( (l-cyclopropylpiperidin-4-yl) amino) cyclopropyl) -N- (5- methyl-1, 2-oxazol-3-yl) thiophene-3-carboxamide

Example C38 ^■

5- (2- ( (l-cyclopropylpiperidin-4-yl) amino) cyclopropyl) -N- (3- methyl-1, 2-oxazol-5-yl) thiophene-3-carboxamide

Example C39 5- (2- ( (l-cyclopropylpiperidin-4-yl) amino) cyclopropyl) -N- (2- methyl-1, 3-thiazol-5-yl) thiophene-3-carboxamide

Example C40

N- (1, 3-dimethyl-lH-pyrazol-4-yl) -5- (2- ( (tetrahydro-2H-pyran-4- ylmethyl) amino) cyclopropyl) thiophene-3-carboxamide

[0538]

Example C41

N- (l-ethyl-lH-pyrazol-4-yl) -5- (2- ( (tetrahydro-2H-pyran-4- ylmethyl) amino) cyclopropyl) thiophene-3-carboxamide

Example C42

N- (1, 3-dimethyl-lH-pyrazol-5-yl) -5- (2- ( (tetrahydro-2H-pyran-4- ylmethyl) amino) cyclopropyl) thiophene-3-carboxamide

Example C43

N-cyclopentyl-5- (.2- ( (tetrahydro-2H-pyran-4- ylmethyl) amino) cyclopropyl) thiophene-3-carboxamide

Example C44

5- (2- ( (tetrahydro-2H-pyran-4-ylmethyl) amino) cyclopropyl) -N- (1- (2,2, 2-trifluoroethyl) piperidin-4-yl) thiophene-3-carboxamide Example C45

N- (5-methyl-l, 2-oxazol-3-yl ) -5- (2- ( (tetrahydro-2H-pyran-4- ylmethyl) amino) cyclopropyl) thiophene-3-carboxamide

Example C46

N- (3-methyl-l, 2-oxazol-5-yl) -5- (2- ( (tetrahydro-2H-pyran-4- 'ylmethyl) amino) cyclopropyl) thiophene-3-carboxamide

Example C47

N- (2-methyl-l, 3-thiazol-5-yl) -5- (2- ( (tetrahydro-2H-pyran-4- ylmethyl) amino) cyclopropyl) thiophene-3-carboxamide

Example C48

N- (5-methyl-l, 3, 4-thiadiazol-2-yl) -5- (2- ( (1- (2, 2, 2- trifluoroethyl) piperidin-4-yl) amino) cyclopropyl) thiophene-3- carboxamide

Example C49

N- (l-methyl-lH-pyrazol-4-yl) -5- (2- ( (1- (2,2,2- trifluoroethyl) piperidin-4-yl ) amino) cyclopropyl) thiophene-3- carboxamide Example C50

N- (l-ethyl-lH-pyrazol-4-yl) -5- (2- ( (l-(2,2,2- trifluoroethyl) piperidin-4-yl) amino) cyclopropyl) thiophene-3- carboxamide

[0539]

Example C51

N- (1, 3-dimethyl-lH-pyrazol-5-yl) -5- (2- ( (1- (2,2,2- trifluoroethyl) piperidin-4-yl) amino) cyclopropyl) thiophene-3- carboxamide

Example C52 .

N-cyclopentyl-5- (2- ( (1- (2, 2, 2-trifluoroethyl) piperidin-4- yl) amino) cyclopropyl) thiophene-3-carboxamide

Example C53

N- (4, 4-difluorocyclohexyl) -5- (2- ( (1- (2,2,2- trifluoroethyl ) piperidin-4-yl) amino) cyclopropyl) thiophene-3- carboxamide

Example C54

N- (1- (2, 2, 2-trifluoroethyl) piperidin-4-yl) -5- (2- ( (1- (2, 2, 2- trifluoroethyl ) piperidin-4-yl) amino) cyclopropyl) thiophene-3- carboxamide

Example C55

N- (5-methyl-l, 2-oxazol-3-yl) -5- (2- ( (1- (2, 2, 2- trifluoroethyl) piperidin-4-yl) amino) cyclopropyl) thiophene-3- carboxamide

Example C56

N- (3-methyl-l, 2-oxazol-5-yl) -5- (2- ( (1- (2, 2, 2- trifluoroethyl) piperidin-4-yl) amino) cyclopropyl) thiophene-3- carboxamide

Example C57

N- (2-methyl-1, 3-thiazol-5-yl) -5- (2- ( (1- (2, 2, 2- trifluoroethyl)piperidin-4-yl) amino) cyclopropyl) thiophene-3- carboxamide

[0540]

Example Dl

5- (2- (cyclobutylamino) cyclopropyl) -N- (1, 3-dimethyl-lH-pyrazol- 4-yl) -2-methylthiophene-3-carboxamide

Example D2

5- (2- (cyclobutylamino) cyclopropyl) -N- (l-ethyl-lH-pyrazol-4- yl) -2-methylthiophene-3-carboxamide

Example D3

5- (2- (cyclobutylamino) cyclopropyl) -N- (1, 3-dimethyl-lH-pyrazol- 5-yl) -2-methylthiophene-3-carboxamide

Example D4

5- (2- (cyclobutylamino) cyclopropyl) -2-methyl-N- (tetrahydro-2H- pyran-4-yl) thiophene-3-carboxamide

Example D5

5- (2- (cyclobutylamino) cyclopropyl) -N-cyclopentyl-2- methylthiophene-3-carboxamide

Example D6

5- (2- (cyclobutylamino) cyclopropyl) -N- (4, 4-difluorocyclohexyl) - 2-methylthiophene-3-carboxamide

Example D7

5- (2- (cyclobutylamino) cyclopropyl) -2-methyl-N- (1- (2,2,2- trifluoroethyl) piperidin-4-yl) thiophene-3-carboxamide

Example D8

5- (2- (cyclobutylamino) cyclopropyl) -2-methyl-N- (5-methyl-l, 2- oxazol-3-yl) thiophene-3-carboxamide

Example D9

5- (2- (cyclobutylamino) cyclopropyl) -2-methyl-N- (3-methyl-l, 2- oxazol-5-yl) thiophene-3-carboxamide

Example D10

5- (2- (cyclobutylamino) cyclopropyl) -2-methyl-N- (2-methyl-l, 3- thiazol-5-yl) thiophene-3-carboxamide

[0541]

Example Dll

5- (2- ( (cyclopropylmethyl) amino) cyclopropyl) -2-methyl-N- (1- methyl-lH-pyrazol-4-yl) thiophene-3-carboxamide

Example D12

5- (2- ( (cyclopropylmethyl) amino) cyclopropyl) -N- (1, 3-dimethyl- lH-pyrazol-4-yl) -2-methylthiophene-3-carboxamide Example D13

5- (2- ( (cyclopropylmethyl) amino) cyclopropyl) -N- (1-ethyl-lH- pyrazol-4-yl) -2-methylthiophene-3-carboxamide

Example D14

5- (2- ( (cyclopropylmethyl) amino) cyclopropyl) -N- (1, 3-dimethyl- lH-pyrazol-5-yl) -2-methylthiophene-3-carboxamide

Example D15

N-cyclopentyl-5- (2- ( (cyclopropylmethyl) amino) cyclopropyl) -2- methylthiophene-3-carboxamide

Example D16

5- (2- ( (cyclopropylmethyl) amino) cyclopropyl) -2-methyl-N- (1- (2,2, 2-trifluoroethyl) piperidin-4-yl) thiophene-3-carboxamide Example D17

5- (2- ( (cyclopropylmethyl) amino) cyclopropyl) -2-methyl-N- (5- methyl-1, 2-oxazol-3-yl) thiophene-3-carboxamide

Example D18

5- (2- ( (cyclopropylmethyl) amino) cyclopropyl) -2-methyl-N- (3- methyl-1, 2-oxazol-5-yl) thiophene-3-carboxamide

Example D19

5- (2- ( (cyclopropylmethyl) amino) cyclopropyl) -2-methyl-N- (2- methyl-1, 3-thiazol-5-yl ) thiophene-3-carboxamide

Example D20

5- (2- ( (cyclopropylmethyl) amino) cyclopropyl) -2-methyl-N- (oxetan-3-yl) thiophene-3-carboxamide

[0542]

Example D21

5- (2- ( (cyclopropylmethyl) amino) cyclopropyl) -N- (3, 3- difluorocyclobutyl) -2-methylthiophene-3-carboxamide

Example D22

5- (2- ( (cyclopropylmethyl) amino) cyclopropyl) -2-methyl-N- (5- methyl-1, 3, 4-oxadiazol-2-yl) thiophene-3-carboxamide

Example D23

5- (2- ( (cyclopropylmethyl) amino) cyclopropyl) -2-methyl-N- (5- methyl-2-thienyl) thiophene-3-carboxamide

Example D24 . 5- (2- ( (cyclopropylmethyl) amino) cyclopropyl) -2-methyl-N- (pyridin-4-yl) thiophene-3-carboxamide

Example D25

5- (2- ( (cyclopropylmethyl) amino) cyclopropyl) -2-methyl-N- (2- methyl-1, 3-oxazol-5-yl) thiophene-3-carboxamide

Example D26

5- (2- ( (cyclopropylmethyl) amino) cyclopropyl) -2-methyl-N- (5- (trifluoromethyl) -1,3, -thiadiazol-2-yl) thiophene-3- carboxamide

Example D27

5- (2- ( (cyclopropylmethyl) amino) cyclopropyl) -2-methyl-N- (3- methyloxetan-3-yl) thiophene-3-carboxamide

Example D28

N-cyclopropyl-5- (2- ( (cyclopropylmethyl) amino) cyclopropyl) -2- methylthiophene-3-carboxamide

Example D29

N-cyclopentyl-2-methyl-5- (2- (tetrahydro-2H-pyran-4- ylamino) cyclopropyl) thiophene-3-carboxamide

Example D30

2-methyl-N- (2-methyl-l, 3-thiazol-5-yl) -5- (2- (tetrahydro-2H- pyran-4-ylamino) cyclopropyl) thiophene-3-carboxamide

[0543]

Example D31

5- (2- ( (l-cyclopropylpiperidin-4-yl) amino) cyclopropyl) -2- methyl-N- (5-methyl-l, 3, 4-thiadiazol-2-yl) thiophene-3- carboxamide

Example D32

5- (2- ( (l-cyclopropylpiperidin-4-yl) amino) cyclopropyl) -N- (1- ethyl-lH-pyrazol-4-yl) -2-methylthiophene-3-carboxamide

Example D33

5- (2- ( (l-cyclopropylpiperidin-4-yl).amino) cyclopropyl) -N- (1, 3- dimethyl-lH-pyrazol-5-yl) -2-methylthiophene-3-carboxamide Example D34

N-cyclopentyl-5- (2- ( ( l-cyclopropylpiperidin-4- yl) amino) cyclopropyl) -2-methylthiophene-3-carboxamide Example D35

5- (2- ( (l-cyclopropylpiperidin-4-yl) amino) cyclopropyl) -N- (4,4- difluorocyclohexyl) -2-methylthiophene-3-carboxamide

Example D36

5- (2- ( (l-cyclopropylpiperidin-4-yl) amino) cyclopropyl) -2- methyl-N- (1- (2, 2, 2-trifluoroethyl ) piperidin-4-yl) thiophene-3- carboxamide

Example D37

5- (2- ( (l-cyclopropylpiperidin-4-yl) amino) cyclopropyl) -2- methyl-N- (5-methyl-l, 2-oxazol-3-yl) thiophene-3-carboxamide Example D38

5- (2- ( (l-cyclopropylpiperidin-4-yl) amino) cyclopropyl) -2- methyl-N- (3-methyl-l, 2-oxazol-5-yl) thiophene-3-carboxamide Example D39

5- (2- ( (l-cyclopropylpiperidin-4-yl) amino) cyclopropyl) -2- methyl-N- (2-methyl-l, 3-thiazol-5-yl) thiophene-3-carboxamide Example D40

N- (1, 3-dimethyl-lH-pyrazol-4-yl) -2-methyl-5- (2- ( (tetrahydro- 2H-pyran-4-ylmethyl) amino) cyclopropyl) thiophene-3-carboxamide [0544]

Example D41

N- (l-ethyl-lH-pyrazol-4-yl) -2-methyl-5- (2- ( (tetrahydro-2H- pyran-4-ylmethyl) amino) cyclopropyl) thiophene-3-carboxamide Example D 2

N- (1, 3-dimethyl-lH-pyrazol-5-yl) -2-methyl-5- (2- ( (tetrahydro- 2H-pyran-4-ylmethyl) amino) cyclopropyl) thiophene-3-carboxamide Example D43

N-cyclopentyl-2-methyl-5- (2- ( (tetrahydro-2H-pyran-4- ylmethyl) amino) cyclopropyl) thiophene-3-carboxamide

Example D44

2-methyl-5- (2- ( (tetrahydro-2H-pyran-4- .

ylmethyl) amino) cyclopropyl) -N- (1- (2, 2, 2- trifluoroethyl) piperidin-4-yl) thiophene-3-carboxamide

Example D45

2-methyl-N- (5-methyl-l, 2-oxazol-3-yl ) -5- (2- ( (tetrahydro-2H- pyran-4-ylmethyl) amino) cyclopropyl) thiophene-3-carboxamide Example D46

2-methyl-N- (3-methyl-l, 2-oxazol-5-yl ) -5- (2- ( (tetrahydro-2H- pyran-4-ylmethyl) amino) cyclopropyl) thiophene-3-carboxamide Example D47

2-methyl-N- (2-methyl-l, 3-thiazol-5-yl) -5- (2- ( (tetrahydro-2H- pyran-4-ylmethyl) amino) cyclopropyl) thiophene-3-carboxamide Example D48

2-methyl-N- (5-methyl-l, 3, -thiadiazol-2-yl) -5- (2- ( (1- (2,2,2- trifluoroethyl) piperidin-4-yl) amino) cyclopropyl) thiophene-3- carboxamide

Example D49

2-methyl-N- (l-methyl-lH-pyrazol-4-yl) -5- (2- ( (1- (2, 2, 2- trifluoroethyl)piperidin-4-yl) amino) cyclopropyl) thiophene-3- carboxamide

Example D50

N- (l-ethyl-lH-pyrazol-4-yl) -2-methyl-5- (2- ( (1- (2,2,2- trifluoroethyl) piperidin-4-yl) amino) cyclopropyl) thiophene-3- carboxamide

[0545]

Example D51

N- (1, 3-dimethyl-lH-pyrazol-5-yl) -2-methyl-5- (2- ( (1- (2,2,2- trifluoroethyl) piperidin-4-yl) amino) cyclopropyl) thiophene-3- carboxamide

Example D52

N-cyclopentyl-2-methyl-5- (2- ( (1- (2,2,2- trifluoroethyl) piperidin-4-yl) amino) cyclopropyl) thiophene-3- carboxamide

Example D53

N- (4, 4-difluorocyclohexyl) -2-methyl-5- (2- ( (1- (2, 2, 2- trifluoroethyl) piperidin-4-yl) amino) cyclopropyl) thiophene-3- carboxamide

Example D54

2-methyl-N- (1- (2 , 2 , 2-trifluoroethyl) piperidin-4-yl) -5- (2- ( (1- (2, 2, 2-trifluoroethyl ).piperidin-4- yl) amino) cyclopropyl) thiophene-3-carboxamide

Example D55

2-methyl-N- (5-methyl-l, 2-oxazol-3-yl) -5- (2- ( (1- (2,2,2- trifluoroethyl) piperidin-4-yl) amino) cyclopropyl) thiophene-3- carboxamide

Example D56

2-methyl-N- (3-methyl-l, 2-oxazol-5-yl) -5- (2- ( (1- (2,2,2- trifluoroethyl ) piperidin-4-yl) amino) cyclopropyl) thiophene-3- carboxamide

Example D57

2-methyl-N- (2-methyl-l, 3-thiazol-5-yl) -5- (2- ( (1- (2,2, 2- trifluoroethyl) piperidin-4-yl) amino) cyclopropyl) thiophene-3- carboxamide

Example D58

5- (2- (cyclobutylamino) cyclopropyl) -2-methyl-N- (5-methyl-l, 3, 4- thiadiazol-2-yl) thiophene-3-carboxamide

Example D59

5- (2- ( (cyclopropylmethyl) amino) cyclopropyl) -2-methyl-N- (5- . methyl-1, 3, 4-thiadiazol-2-yl) thiophene-3-carboxamide

Example D60

2-methyl-N- (5-methyl-l, 3, 4-thiadiazol-2-yl) -5- (2- ( (tetrahydro- 2H-pyran-4-ylmethyl) amino) cyclopropyl) thiophene-3-carboxamide [0546]

Example D61

5- (2- ( (cyclopropylmethyl) amino) cyclopropyl) -N- ( , 4- difluorocyclohexyl) -2-methylthiophene-3-carboxamide

Example D62

N- (4, 4-difluorocyclohexyl) -2-methyl-5- (2- (tetrahydro-2H-pyran-

4-ylamino) cyclopropyl) thiophene-3-carboxamide

Example D63

N- (4, 4-difluorocyclohexyl ) -2-methyl-5- (2- ( (tetrahydro-2H- pyran-4-ylmethyl) amino) cyclopropyl) thiophene-3-carboxamide Example D64

5- (2- ( (cyclopropylmethyl) amino) cyclopropyl) -2-methyl-N- (tetrahydro-2H-pyran-4-yl) thiophene-3-carboxamide [0547]

Example El

4- (2- ( (3-aminocyclobutyl) amino) cyclopropyl) -N- (5-methyl-l, 3, 4- thiadiazol-2-yl) thiophene-2-carboxamide

Example E2

4- (2- ( (3-aminocyclobutyl) amino) cyclopropyl) -5-methyl-N- (5- methyl-1, 3, 4-thiadiazol-2-yl) thiophene-2-carboxamide

Example E3

5- (2- ( (3-aminocyclobutyl) amino) cyclopropyl) -2-methyl-N- (5- methyl-l, 3, 4-thiadiazol-2-yl) thiophene-3-carboxamide

Example E4

5- (2- ( (3-aminocyclobutyl) amino) cyclopropyl) -N- (5-methyl-l, 3, 4- thiadiazol-2-yl) thiophene-3-carboxamide

Example E5

4- (2- ( (4-aminocyclohexyl) amino) cyclopropyl) -N- (5-methyl-l, 3, 4- thiadiazol-2-yl) thiophene-2-carboxamide

Example E6

4- (2- ( (4-aminocyclohexyl) amino) cyclopropyl) -5-methyl-N- (5- methyl-1, 3, 4-thiadiazol-2-yl) thiophene-2-carboxamide

Example E7

5- (2- ( (4-aminocyclohexyl) amino) cyclopropyl ) -2-methyl-N- (5- methyl-1, 3, 4-thiadiazol-2-yl) thiophene-3-carboxamide

Example E8

5- (2- ( (4-aminocyclohexyl) amino) cyclopropyl) -N- (5-methyl-l, 3, 4- thiadiazol-2-yl) thiophene-3-carboxamide

Example E9

4- (2- ( (3-aminocyclobutyl) amino) cyclopropyl) -N- (1-ethyl-lH- pyrazol-4-yl ) thiophene-2-carboxamide

Example E10

4- (2- ( (3-aminocyclobutyl) amino) cyclopropyl) -N- (1-ethyl-lH- pyrazol-4-yl) -5-methylthiophene-2-carboxamide

[0548]

Example Ell

5- (2- ( (3-aminocyclobutyl) amino) cyclopropyl) -N- (1-ethyl-lH- pyrazol-4-yl) -2-methylthiophene-3-carboxamide Example E12

5- (2- ( (3-aminocyclobutyl) amino) cyclopropyl) -N- (1-ethyl-lH- pyrazol-4-yl ) thiophene-3-carboxamide

Example E13

4- (2- ( (4-aminocyclohexyl) amino) cyclopropyl) -N- (1-ethyl-lH- pyrazol-4-yl) thiophene-2-carboxamide

Example E14

4- (2- ( (4-aminocyclohexyl) amino) cyclopropyl) -N- ( 1-ethyl-lH- pyrazol-4-yl) -5-methylthiophene-2-carboxamide

Example E15

5- (2- ( (4-aminocyclohexyl) amino) cyclopropyl) -N- (1-ethyl-lH- pyrazol-4-yl) -2-methylthiophene-3-carboxamide

Example El6

5- (2- ( (4-aminocyclohexyl) amino) cyclopropyl) -N- (1-ethyl-lH- pyrazol-4-yl) thiophene-3-carboxamide

Example E17

4- (2- ( (3-aminocyclobutyl) amino) cyclopropyl) -N- ( 1-methyl-lH- pyrazol-4-yl) thiophene-2-carboxamide

Example E18

4- (2- ( (3-aminocyclobutyl) amino) cyclopropyl) -5-methyl-N- (1- methyl-lH-pyrazol-4-yl) thiophene-2-carboxamide

Example El9

5- (2- ( (3-aminocyclobutyl) amino) cyclopropyl) -2-methyl-N- (1- methyl-lH-pyrazol-4-yl) thiophene-3-carboxamide

Example E20

5- (2- ( (3-aminocyclobutyl) amino) cyclopropyl) -N- ( 1-methyl-lH- pyrazol-4-yl) thiophene-3-carboxamide

[0549]

Example E21

4- (2- ( (4-aminocyclohexyl) amino) cyclopropyl) -N- ( 1-methyl-lH- pyrazol-4-yl) thiophene-2-carboxamide

Example E22

4- (2- ( (4-aminocyclohexyl) amino) cyclopropyl) -5-methyl-N- (1- methyl-lH-pyrazol-4-yl) thiophene-2-carboxamide

Example E23 5- (2- ( (4-aminocyclohexyl) amino) cyclopropyl) -2-methyl-N- (1- methyl-lH-pyrazol-4-yl) thiophene-3-carboxamide

Example E24

5- (2- ( (4-aminocyclohexyl) amino) cyclopropyl) -N- (1-methyl-lH- pyrazol-4-yl) thiophene-3-carboxamide

Example E25

4- (2- ( (3-aminocyclobutyl) amino) cyclopropyl) -N- (1, 3-dimethyl- lH-pyrazol-4-yl) thiophene-2-carboxamide

Example E26

4- (2- ( (3-aminocyclobutyl) amino) cyclopropyl) -N- (1, 3-dimethyl- lH-pyrazol-4-yl) -5-methylthiophene-2-carboxamide

Example E27

5- (2- ( (3-aminocyclobutyl) amino) cyclopropyl) -N- (1, 3-dimethyl- lH-pyrazol-4-yl) -2-methylthiophene-3-carboxamide

Example E28

5- (2- ( (3-aminocyclobutyl) amino) cyclopropyl) -N- (1, 3-dimethyl- lH-pyrazol-4-yl) thiophene-3-carboxamide

Example E29

4- (2- ( (4-aminocyclohexyl) amino) cyclopropyl) -N- (1, 3-dimethyl- lH-pyrazol-4-yl) thiophene-2-carboxamide

Example E30

4- (2- ( (4-aminocyclohexyl) amino) cyclopropyl) -N- (1, 3-dimethyl- lH-pyrazol-4-yl) -5-methylthiophene-2-carboxamide

[0550]

Example E31

5- (2- ( (4-aminocyclohexyl) amino) cyclopropyl) -N- (1, 3-dimethyl- lH-pyrazol-4-yl) -2-methylthiophene-3-carboxamide

Example E32

5- (2- ( (4-aminocyclohexyl) amino) cyclopropyl) -N- (1, 3-dimethyl- lH-pyrazol-4-yl) thiophene-3-carboxamide

Example E33

4- (2- ( (3-aminocyclobutyl) amino) cyclopropyl) -N- (1, 3-dimethyl- lH-pyrazol-5-yl) thiophene-2-carboxamide

Example E34

4- (2- ( (3-aminocyclobutyl) amino) cyclopropyl) -N- (1, 3-dimethyl- lH-pyrazol-5-yl) -5-methylthiophene-2-carboxamide Example E35

5- (2- ( (3-aminocyclobutyl) amino) cyclopropyl) -N- (1, 3-dimethyl- lH-pyrazol-5-yl) -2-methylthiophene-3-carboxamide

Example E36

5- (2- ( (3-aminocyclobutyl) amino) cyclopropyl) -N- (1, 3-dimethyl- lH-pyrazol-5-yl) thiophene-3-carboxamide

Example E37

4- (2- ( (4-aminocyclohexyl) amino) cyclopropyl) -N- (1, 3-dimethyl- lH-pyrazol-5-yl) thiophene-2-carboxamide

Example E38

4- (2- ( (4-aminocyclohexyl) amino) cyclopropyl) -N- (1, 3-dimethyl- lH-pyrazol-5-yl ) -5-methylthiophene-2-carboxamide

Example E39

5- (2- ( (4-aminocyclohexyl) amino) cyclopropyl) -N- (1, 3-dimethyl- lH-pyrazol-5-yl) -2-methylthiophene-3-carboxamide

Example E40

5- (2- ( (4-aminocyclohexyl) amino) cyclopropyl) -N- (1, 3-dimethyl- lH-pyrazol-5-yl) thiophene-3-carboxamide

[0551]

Example E41

4- (2- ( (3-aminocyclobutyl) amino) cyclopropyl) -N- (4, 4- difluorocyclohexyl ) thiophene-2-carboxamide

Example E42

4- (2- ( (3-aminocyclobutyl) amino) cyclopropyl) -N- (4, 4- difluorocyclohexyl) -5-methylthiophene-2-carboxamide

Example E43

5- (2- ( (3-aminocyclobutyl) amino) cyclopropyl) -N- (4,4- difluorocyclohexyl) -2-methylthiophene-3-carboxamide

Example E44

5- (2- ( (3-aminocyclobutyl) amino) cyclopropyl) -N- (4,4- difluorocyclohexyl) thiophene-3-carboxamide

Example E45

4- (2- ( (4-aminocyclohexyl) amino) cyclopropyl) -N- (4,4- difluorocyclohexyl) thiophene-2-carboxamide Example E46

4- (2- ( (4-aminocyclohexyl) amino) cyclopropyl) -N- (4,4- difluorocyclohexyl) -5-methylthiophene-2-carboxamide

Example E47

5- (2- ( (4-aminocyclohexyl) amino) cyclopropyl) -N- (4, 4- difluorocyclohexyl ) -2-methylthiophene-3-carboxamide

Example _^ E48

5- (2- ( (4-aminocyclohexyl) amino) cyclopropyl) -N- (4 , 4- difluorocyclohexyl) thiophene-3-carboxamide

Example E49

4- (2- ( (3-aminocyclobutyl) amino) cyclopropyl) -N- ( 5-methyl-l , 2- oxazol-3-yl) thiophene-2-carboxamide

Example E50

4- (2- ( (3-aminocyclobutyl) amino) cyclopropyl) -5-methyl-N- (5- methyl-1, 2-oxazol-3-yl) thiophene-2-carboxamide

[0552]

Example E51

5- (2- ( (3-aminocyclobutyl) amino) cyclopropyl) -2-methyl-N- (5- methyl-1, 2-oxazol-3-yl) thiophene-3-carboxamide

Example E52

5- (2- ( (3-aminocyclobutyl) amino) cyclopropyl) -N- (5-methyl-l, 2- oxazol-3-yl) thiophene-3-carboxamide

Example E53

4- (2- ( (4-aminocyclohexyl) amino) cyclopropyl) -N- (5-methyl-l, 2- oxazol-3-yl) thiophene-2-carboxamide

Example E54

4- (2- ( (4-aminocyclohexyl) amino) cyclopropyl) -5-methyl-N- (5- methyl-1, 2-oxazol-3-yl) thiophene-2-carboxamide

Example E55

5- (2- ( (4-aminocyclohexyl) amino) cyclopropyl) -2-methyl-N- (5- methyl-1, 2-oxazol-3-yl) thiophene-3-carboxamide

Example E56

5- (2- ( (4-aminocyclohexyl) amino) cyclopropyl) -N- (5-methyl-l, 2- oxazol-3-yl) thiophene-3-carboxamide

Example E57 4- (2- ( (3-aminocyclobutyl) amino) cyclopropyl) -N- (2-methyl-l, 3- thiazol-5-yl) thiophene-2-carboxamide

Example E58

4- (2- ( (3-aminocyclobutyl) amino) cyclopropyl) -5-methyl-N- (2- methyl-1, 3-thiazol-5-yl) thiophene-2-carboxamide

Example E59

5- (2- ( (3-aminocyclobutyl) amino) cyclopropyl) -2-methyl-N- (2- methyl-1, 3-thiazol-5-yl) thiophene-3-carboxamide

Example E60

5- (2- ( (3-aminocyclobutyl) amino) cyclopropyl) -N- (2-methyl-l, 3- thiazol-5-yl) thiophene-3-carboxamide

[0553]

Example E61

4- (2- ( (4-aminocyclohexyl) amino) cyclopropyl) -N- (2-methyl-l, 3- thiazol-5-yl) thiophene-2-carboxamide

Example E62

4- (2- ( (4-aminocyclohexyl) amino) cyclopropyl) -5-methyl-N- (2- ^' methyl-1, 3-thiazol-5-yl) thiophene-2-carboxamide

Example E63

5-(2-( (4-aminocyclohexyl) amino) cyclopropyl) -2-methyl-N- (2- methyl-1, 3-thiazol-5-yl) thiophene-3-carboxamide

Example E64

5- (2- ( (4-aminocyclohexyl) amino) cyclopropyl) -N- (2-methyl-l, 3- thiazol-5-yl ) thiophene-3-carboxamide

Example E65

4- (2- ( (4, 4-difluorocyclohexyl ) amino) cyclopropyl) -N- (tetrahydro-2H-pyran-4-yl) thiophene-2-carboxamide

Example E66

4- (2- ( (4, 4-difluorocyclohexyl) amino) cyclopropyl) -5-methyl-N- (tetrahydro-2H-pyran-4-yl) thiophene-2-carboxamide

Example E67

5- (2- ( (4 , 4-difluorocyclohexyl) amino) cyclopropyl) -2-methyl-N- (tetrahydro-2H-pyran-4-yl) thiophene-3-carboxamide

Example E68

5- (2- ( (4 , 4-difluorocyclohexyl) amino) cyclopropyl) -N- (tetrahydro-2H-pyran-4-yl) thiophene-3-carboxamide

Example E69

4- (2- ( (4, 4-difluorocyclohexyl) amino) cyclopropyl) -N- (tetrahydro-2H-pyran-4-yl) thiophene-2-carboxamide

Example E70

4- (2- ( (4, 4-difluorocyclohexyl) amino) cyclopropyl) -5-methyl-N- (tetrahydro-2H-pyran-4-yl) thiophene-2-carboxamide

[0554]

Example E71

5- (2- ( (4 , 4-difluorocyclohexyl) amino) cyclopropyl) -2-methyl-N- (tetrahydro-2H-pyran-4-yl ) thiophene-3-carboxamide

Example E72

5- (2- ( (4, -difluorocyclohexyl) amino) cyclopropyl) -N- (tetrahydro-2H-pyran-4-yl) thiophene-3-carboxamide

[0555]

Experimental Example 1

The genetic engineering method described below was performed according to the method described in a book

(Maniatis et al., Molecular Cloning, Cold Spring Harbor

Laboratory, 1989) or the method described in the protocol attached to the reagent.

(1) Construction of GST-tagged expression vector having TEV Protease cleavage sequence

A GST-tagged expression vector having TEV Protease cleavage sequence was constructed by successive 2 times of PCR method. Firstly, PCR was performed using pGEX6Pl (GE

Healthcare) as a template, two primers

GST-Sw-F:

5' -AGAATCATTTAAATGGTGATCATGTAACCCATCCT-3'

[SEQ ID NO: 1]

GST-Tv-Rl:

5 ' -CGCCCTGAAAGTACAGGTTCTCATCCGATTTTGGAGGATGGTCG-3'

[SEQ ID NO: 2]

and PrimeStar GXL DNA Polymerase (Takara Bio Inc.). Template DNA 0.5 vL, PrimeStar GXL DNA Polymerase Buffer 10 vL, 2.5 mM dNTP solution 4 L, 10 μΜ primer solution each 1.5 μL, PrimeStar GXL DNA Polymerase 1 μΐ^ and sterilized distilled water 31.5 μL were mixed. After a treatment at 98°C for 1 min, the PCR was started with 35 repeats of reactions at 98°C for 10 seconds, at 65°C for 5 seconds, and at 72°C for 25 seconds, followed by a reaction at 72°C for 1 min. Then, PCR was

performed using the obtained PCR product as a template, two primers

GST-Sw-F:

5' -AGAATCATTTAAATGGTGATCATGTAACCCATCCT-3'

[SEQ ID NO: 1]

GST-TV-R2:

5' -ATAATAGGATCCGCCCTGAAAGTACAGGTTCTC-3'

[SEQ ID NO: 3]

and PrimeStar GXL DNA Polymerase. Template DNA 0.5 μΐ,,

PrimeStar GXL DNA Polymerase Buffer 10 μL, 2.5 mM dNTP

solution 4 μL, 10 μΜ primer solution each 1.5 μL, PrimeStar GXL DNA Polymerase 1 μL, and sterilized distilled water 31.5 μL were mixed. After a treatment at 98°C for 1 min, the PCR was started with 25 repeats of reactions at 98°C for 10 seconds, at 65°C for 5 seconds, and at 72°C for 25 seconds, followed by a reaction at 72°C for 1 min. The obtained PCR product was electrophoresed on agarose gel (1%), and an about 0.3 kbp DNA fragment containing a part of the GST gene was recovered from the gel. The recovered DNA fragment was cleaved with

restriction enzymes Swa I (New England Biolabs) and Bam HI (Takara Bio Inc.), and inserted into the Swa I/Bam HI site of pGEX6Pl to construct an expression vector pGEX7Vl.

[0556]

(2) Cloning of human LSDl (AOF2) cDNA

Human LSDl cDNA was cloned by PCR method using brain cDNA Library (Takara Bio Inc.) as a template, two primers

hLSDl-Nhel-ko-F:

5' -TATTATGCTAGCGCCACCATGTTATCTGGGAAGAAGGCGGCAGC-3'

[SEQ ID NO: 4] hLSDl-St-Notl-R:

5' -TATTATGCGGCCGCTCACATGCTTGGGGACTGCTGTGC-3'

[SEQ ID NO: 5]

and Pyrobest DNA Polymerase (Takara Bio Inc.)- Template DNA 0.5 μΐι, Pyrobest DNA Polymerase Buffer 5 μί, 2.5 mM dNTP solution 4 L, 10 μΜ primer solution each 2.5 μΐι, Pyrobest DNA Polymerase 0.5 μί, and sterilized distilled water 35 μL were mixed. After a reaction at 98°C for 1 min, the PCR was started with 35 repeats of reactions at 98°C for 10 seconds, at 68°C for 5 seconds, and at 72°C for 2.5 min, followed by a reaction at 72°C for 1 min. The obtained PCR product was

electrophoresed on agarose gel (1%), and an about 2.5 kbp DNA fragment containing the human LSDl cDNA was recovered from the gel. The recovered DNA fragment was cleaved with restriction enzymes Nhe I and Not I (Takara Bio Inc.), and inserted into the Nhe I/Not I site of pcDNA3.1(+) (Invitrogen) to construct an expression plasmid pcDNA3.1/hLSDl .

[0557]

(3) Construction of expression plasmid for human LSDl (172-833) in Escherichia coli

A plasmid for expression of human LSDl (172-833) in

Escherichia coli was constructed by PCR method using

pcDNA3.1/hLSDl as a template, two primers

hLSDl-172aa-Bgl2-F:

5' -ATAATAAGATCTTCGGGTGTGGAGGGCGCAGCTT-3'

[SEQ ID NO: 6]

hLSDl-833aa-St-NotI-R:

5' -ATAATAGCGGCCGCCATGGCCCCCAAAAACTGGTCTGCA-3'

[SEQ ID NO: 7]

and PrimeStar MAX DNA Polymerase (Takara Bio Inc.). Template DNA 1 μL, PrimeStar MAX DNA Polymerase Enzyme PreMix 25 μL, 10 μΜ primer solution each 1.5 ^L, and sterilized distilled water 21 μL were mixed. After a reaction at 98°C for 1 min, the PCR was started with 25 repeats of reactions at 98°C for 10 seconds and at 68°C for 8 seconds, followed by a reaction at 72°C for 1 min. The obtained PCR product was electrophoresed on agarose gel (1%) , and an about 2 kbp DNA fragment containing human LSD1 (172-833) cDNA was recovered from the gel. The recovered DNA fragment was cleaved with restriction enzymes Bgl II and Not I (Takara Bio Inc.), and inserted into the Bam Hi/Not I site of pGEX7Vl to construct an expression plasmid

pGEX7Vl/GST-hLSDl (172-833) .

[0558]

(4) Preparation of LSD1

Escherichia coli C43(DE3) pLysS was transformed with the expression plasmid pGEX7Vl/GST-hLSDl (172-833) . The obtained recombinant Escherichia coli was inoculated in a TB medium (1.2% tryptone, 2.4% yeast extract, 0.4% glycerol, 17 mM potassium dihydrogen phosphate and 72 mM dipotassium hydrogen phosphate) added with 100 mg/L ampicillin and 35 mg/L

chloramphenicol, and cultured at 37°C. When the turbidity reached 500 Klett units, the culture temperature was changed to 16°C, IPTG (Isopropyl β-D-l-thiogalactopyranoside ) having a final concentration of 0.5 mM was added to induce expression, and the cells were cultured further for 14 hr. The culture medium was centrifuged at 6,000 g for 15 min, and Escherichia coli pellets were recovered.

[0559]

Escherichia coli pellets for 12 L of the culture medium were suspended in 1000.mL of PBS (Immuno-Biological

Laboratories Co., Ltd.), 0.15 M NaCl, 5% (V/V) Glycerol (Buffer A) , and 5000 units Benzonase (Merck) , 1000 mg Lysozyme, and 10 tablets of Protease Inhibitor (Roche) were added. Using

Branson ultrasonic disintegrator, the suspension was disrupted by ultrasonication for 3 min, and centrifuged at 33,000 g for 60 min, and the supernatant was recovered. The supernatant was applied to two GSTrap 4B 5 mL columns (GE Healthcare)

equilibrated in advance with 0.1 M Tris (pH 8.0), 0.15 M NaCl, 5% (V/V) Glycerol (Buffer B) , and the columns were each washed with 30 mL of Buffer B. GST-hLSDl (172-833) was eluted from each column with Buffer B added with 13 mL of GSH with the final concentration 20 mM, applied to two HiLoad 26/60

Superdex 200 pg columns (GE Healthcare) equilibrated in advance with Buffer B, and eluted with 380 mL of Buffer B.

Total 60 mL of GST-hLSDl ( 172-833 ) -containing fraction was diluted 5-fold with 20 mM Tris (pH 8.0) (Buffer C) , applied to Mono Q 10/100 GL column (GE Healthcare) equilibrated in advance with Buffer C, and 0-500 mM NaCl gradient elution was performed to give purified GST-hLSDl (172-833) . 3.4 mg of His- TEV protease was added to about 34 mg of GST-hLSDl (172-833) , and the mixture was treated with 50 mM Tris (pH 8.0), 0.5 mM EDTA, 1 mM DTT at 4°C for 16 hr to cleave the GST tag. The reaction mixture after the cleavage reaction was applied to two series-coupled columns with Ni-NTA Superflow Cartridges 1 mL (QIAGEN) , and GSTrap 4B 5 mL column (GE Healthcare)

equilibrated in advance with Buffer A added with Imidazole at a final concentration of 20 mM, and a flow-through fraction containing hLSDl (172-833) free of GST-tag was recovered. It was concentrated to 10 mL with AmiconUltra 15 (N CO 30K)

(Millipore Japan) , and purified with HiLoad 26/60 Superdex 200 pg column (GE Healthcare) equilibrated with Buffer A to give hLSDl purified product (8.4 mg) . The protein concentration of hLSDl was measured by BCA Protein Assay Kit (Thermo Fisher Scientific K.K.) using bovine serum albumin as the standard. {0560]

(5) Measurement of LSDl inhibitory activity

A test compound dissolved in DMSO was added by to a reaction solution (50 mM Tris-HCl (pH 8.0), 0.1% BSA, 1 mM DTT) containing LSDl enzyme, and the mixture was reacted at room temperature for 60 min. Biotin-histone H3 mono methylated K4 peptide solution (NH2-ART (me-

K) QTARKSTGGKAPRKQLAGG (Biotin) -CONH2 ) was added to start the reaction. After reaction at room temperature for 5 min, 2-PCPA solution was added to terminate the reaction. A detection solution (800 mM potassium fluoride, 0.1% BSA) containing europium-labeled anti-histone H3 antibody (Wako Pure Chemical Industries, Ltd.) and Streptavidin-XL665 (Cisbio) was further added, and the mixture was left standing for 60 min. A time- resolved fluorescence (excitation 320 nm, emission 615 run, 665 5 nm) was measured by Envision (PerkinElmer) . The LSDl

inhibitory rate (%) of the test compound was calculated by the following formula.

inhibitory rate (%) = (1 - (test compound count - blank) ÷ (control - blank) ) x 100

0 The count of the LSDl enzyme reaction mixture under

compound non-addition conditions is indicated as control, and the count under compound non-addition and LSDl enzyme non- addition conditions is indicated as blank. A concentration necessary for achieving 50% inhibitory rate was taken as IC50$ value. The results are shown in Table 2.

[0561]

Experimental Example 2

(1) Measurement of MAO-A inhibitory activity

The MAO-A inhibitory activity evaluation described below0 followed the protocol of MAO-Glo (registered trademark) Assay of Promega KK.

A test compound dissolved in DMSO was added to a reaction solution (100 mM HEPES (pH 7.5), 5% glycerol) containing MAO-A enzyme (Sigma-Aldrich Co . LLC . ) , and the mixture was reacted5 at room temperature for 15 min. MAO substrate (Promega KK) was added to start the reaction. After reaction at room

temperature for 60 min, Luciferine detection reagent (Promega KK) was added to terminate the reaction. After reaction at room temperature for 20 min with stirring, the luminescence.0 was measured by Envision (PerkinElmer) . The MAO-A inhibitory rate (%) of the test compound was calculated by the following formula.

inhibitory rate (%) = (1 - (test compound count - blank) ÷ (control - blank)) x 100

5 The count of the MAO-A enzyme reaction mixture under compound non-addition conditions is indicated as control, and the count under compound non-addition and MAO-A enzyme non- addition conditions is indicated as blank. A concentration necessary for achieving 50% inhibitory rate was taken as IC50 value. The results are shown in Table 2.

[0562]

(2) Measurement of MAO-B inhibitory activity

The MAO-B inhibitory activity evaluation described below followed the protocol of MAO-Glo (registered trademark) Assay of Promega KK.

A test compound dissolved in DMSO was added to a reaction solution (100 mM HEPES (pH 7.5), 5% glycerol, 10% DMSO) containing MAO-B enzyme ( Sigma-Aldrich Co. LLC), and the mixture was reacted at room temperature for 15 min. MAO substrate (Promega KK) was added to start the reaction. After reaction at room temperature for 60 min, Luciferine detection reagent (Promega KK) (50 μL) was added to terminate the reaction. After reaction at room temperature for 20 min with stirring, the luminescence was measured by Envision

(PerkinElmer) . The MAO-B inhibitory rate (%) of the test compound was calculated by the following formula,

inhibitory rate (%) = (1 - (test compound count - blank) ÷ (control - blank)) x 100

The count of the MAO-B enzyme reaction mixture under compound non-addition conditions is indicated as control, and the count under compound non-addition and MAO-B enzyme non- addition conditions is indicated as blank. A concentration necessary for achieving 5.0% inhibitory rate was taken as IC50 value. The results are shown in Table 2. [0563]

[Table 2-1]

LSD1 MAO-A MAO-B

Example No.

IC50 value (μ ) IC50 value (μΜ) IC50 value (μΜ)

1 1.3 >100 >100

2 0.33 >100 >100

3 0.29 >100 >100

4 1.7 >100 >100

5 4.6 >100 >100

6 0.11 >100 >100

7 0.26 82 >100

8 0.25 >100 >100

9 3.0 >100 >100

10 0.23 >100 >100

11 0.18 >100 >100

12 <0.1 >100 >100

13 12 >100 93

14 2.4 >100 28

15 0.73 89 66

16 <0.1 >100 >100

17 0.22 >100 >100

18 0.26 >100 >100

19 0.65 >100 >100

20 <0.1 >100 >100

21 0.23 >100 88

22 0.14 >100 >100

23 <0.1 >100 >100

24 <0.1 >100 >100

25 3.0 >100 >100

26 0.50 >100 >100

27 0.33 >100 >100

28 <0.1 >100 >100

29 0.40 >100 >100

30 <0.1 >100 >100 [0564]

[Table 2-2]

LSD1 MAO-A MAO-B

Example No.

IC50 value (μ ) IC50 value (μΜ) IC50 value (μΜ)

31 <0.1 >100 >100

32 <0.1 >100 >100

33 <0.1 >100 >100

34 <0.1 >100 >100

35 0.68 >100 >100

36 3.8 22 6.0

37 99 85 90

38 <0.1 >100 >100

39 <0.1 23 >100

40 <0.1 >100 >100

41 <0.1 67 >100

42 <0.1 >100 >100

43 0.13 >100 >100

44 <0.1 >100 100

45 ^' <0.1 >100 >100

46 <0.1 >100 >100

47 <0.1 >100 >100

48 <0.1 31 >100

49 <0.1 >100 >100

50 <0.1 >100 >100

51 <0.1 >100 >100

52 <0.1 >100 >100

53 <0.1 61 96

54 <0.1 >100 >100

55 <0.1 >100 >100

56 <0.1 >100 >100

57 0.44 >100 >100

58 <0.1 >100 >100

59 <0.1 >100 >100

60 <0.1 >100 >100 . [0565]

[Table 2-3] [0566]

[Table 2-4] [0567]

[Table 2-5]

[0568]

As shown in Table 2, the compound of the present

invention has a superior LSDl inhibitory activity. In addition, the MAO-A inhibitory activity and MAO-B inhibitory activity of the compound of the present invention are low, and the

compound of the present invention has a selective LSDl

inhibitory activity.

[0569]

Experimental Example 3

Gadl H3 4 methylation induction activity in rat primary

culture neurons

Experimental method

Hippocampus and cerebral cortex were isolated from fetal SD rat at embryonic day 19, a cell suspension was prepared using Nerve Cell Dissociation Medium (SUMITOMO BAKELITE, MS- 0006L) , and plated on a poly L-lysine-coated 6-well plate

(SUMITOMO BAKELITE, MS-0006L) at a density of 900000

cells/well. Under the conditions of 37°C and 5% CO2, the cells were cultured in a neurobasal medium (Invitrogen, #211103049) containing B27 supplement (Invitrogen, #17504044, 1:50

dilution), 2 mM L-glutamine (Lonza, #B76053) , 100 U/mL.

penicillin/100 μg/mL streptomycin (Lonza, #17-602E) , and 20 μg/mL gentamicin sulfate (Lonza, #17-519Z) for 10 days.

[0570]

Thereafter, the compound was added to final concentrations of 10 μΜ, the cells were further cultured for 3 days, and chromatin immunoprecipitation was performed.

Chromatin immunoprecipitation was performed by using ChlP.-IT Express Enzymatic (Active Motif, #53009) and H3K4me2 antibody (Millipore, #07-030) . The culture supernatant was aspirated, ice-cold PBS was added, and the cell suspension was collected on ice using CELL SCRAPER (IWAKI) . The supernatant was removed by centrifugation at 3000 rpm, 4°C for 5 min. Lysis buffer (500 μΐ,) was added to the precipitate, and the cells were lysed by incubating for 30 min on ice. Thereafter, the

suspension was centrifuged at 2400 g, 4°C for 10 min, the supernatant was removed, the pellet was suspended in cell lysis buffer [60 mM KC1, 15 mM NaCl, 5 mM MgCl ₂ , 0.1 mM EGTA, 15 mM Tris-HCl (pH 7.6), 1.2 M sucrose, 0.5 mM DTT, protease inhibitor (Roche, #4693132) ] (500 μL) , and the suspension was centrifuged at 10000 g, 4°C for 10 min. The supernatant was removed, and the pellet was suspended in Digestion buffer (120 μL) and preincubated at 37°C for 5 min. Shearing cocktail was added, and the mixture was incubated at 37°C for 20 min. 0.5 M EDTA (2.4 μL) was added, and the mixture was incubated for 10 min on ice and centrifuged at 18000 rpm, 4°C for 10 min. The supernatant was collected as a chromatin fraction and

subjected to immunoprecipitation.

[0571]

Using the DNA obtained by the chromatin

immunoprecipitation as a template, quantitative PCR of the Gadl gene upstream genomic region was performed, and the measurement value was taken as the Gadl H3K4me2 level. The quantitative PCR was performed by ABI PRISM 7900HT Sequence Detection System (Applied Biosystems) using forward primer:

5' -TGATCTTTTCCCTGCTGTCA-3' (SEQ ID NO: 8), reverse primer: 5'-. TCCCATGAGTAATCCAGAACG-3' (SEQ ID NO: 9), and SYBR Green

Realtime PCR Master Mix-Plus- (TOYOBO, #QPK-212) . The Gadl H3K4me2 induction by the compound was expressed by the H3K4me2 level when the compound was added, as compared to the H3K4me2 level of the control (without addition of the compound) as 100%.

Gadl H3K4me2 induction activity (%) (H3K4me2 induction

5 expressed as percentage of control) = (H3K4me2 level with

addition of compound ÷ H3K4me2 level without addition of compound) xlOO

The Gadl H3K4me2 induction activity by each compound as measured by the above-mentioned method is shown in Table 3.0 [0572]

[Table 3]

[0573]

5 From the results of Table 3, it was clarified that the compound of the present invention has an inducive effect on H3K4 methylation.

[0574]

Experimental Example 4

Ό Evaluation of blood cell number in mouse

Experimental method

Male ICR mice (hereinafter mice) were acclimated for at least one week in a rearing facility. The mice were raised in a rearing room with controlled temperature and humidity under5 a 12:12 hour light-dark cycle, and allowed free ingestion of feed and water. The compounds were suspended in 0.5% methylcellulose/O .5% citric acid/distilled water and orally administered. All compounds were repeatedly administered to the mice at a dose of 1 mg/kg, 10 mg/kg or 100 mg/kg (body weight) for 7 or 9 days. One day after the final administration of the compound, the whole blood was collected.

Using Sysmex XT-1800i (Sysmex Corporation) , the white blood cell number, red blood cell number, and platelet number in the collected whole blood per unit volume were measured. The influence of each compound on each blood cell number was determined by calculating the number with the mean of each blood cell number of the mouse without administration of the compound (0 mg/kg group), and the mean of each blood cell number in the whole blood of a mouse with the administration of the compound. The values of the blood cell numbers measured by the above-mentioned method are shown in Table 4.

[0575]

[Table 4-1]

[0576]

[Table 4-2]

[0577]

[Table 4-3]

[0578]

From the results of Table 4, it was clarified that the compound of the present invention reduces an influence on the white blood cell number, red blood cell number and platelet number .

[0579]

Experimental Example 5

Evaluation of hippocampal distribution in mouse

Experimental method

Male ICR mice (hereinafter mice) were acclimated for at least one week in a rearing facility. The mice were raised in a rearing room with controlled temperature and humidity under a 12:12 hour light-dark cycle, and allowed free ingestion of feed and water.

The compounds were suspended in 0.5% methylcellulose/O .5% citric acid/distilled water and orally administered. All compounds were administered to the mice at a dose of 10 mg/kg (body weight) .

Blood samples were collected at 0.5 hr or 1 hr from compound administration, and the hippocampus was isolated simultaneously. The plasma concentration . and hippocampus concentration of each test compound were measured by the

LC/MS/MS method, the ratio (hippocampus/plasma concentration ratio) was calculated, and distribution into hippocampus was evaluated. The results are shown in Table 5.

[0580]

[Table 5]

[0581]

As shown in Table 5, the compounds of the present

invention were all confirmed to have distributed into the hippocampus .

[0582]

Formulation Example 1

A medicament containing the compound of the present invention as an active ingredient can be produced, for example, according to the following formulation.

1. capsule

(1) compound obtained in Example 1 10 mg

(2) lactose 90 mg

(3) crystalline cellulose 70 mg

(4) magnesium stearate 10 mg

1 capsule 180 mg

The total amount of the above-mentioned (1), (2) and (3) and 5 mg of (4) are blended, and the mixture is granulated.

Thereto is added the remaining 5 mg of (4), and the whole is sealed in a gelatin capsule.

[0583]

2. tablet

(1) compound obtained in Example 1 10 mg

(2) lactose 35 mg

(3) cornstarch 150 mg

(4) crystalline cellulose 30 mg

(5) magnesium stearate 5 mg

1 tablet 230 mg

The total amount of the above-mentioned (1), (2) and (3),

20 mg of (4) and 2.5 mg of (5) are blended, and the mixture is granulated. Thereto are added the remaining 10 mg of (4) and 2.5 mg of (5), and the mixture is compression-molded to give a tablet .

Industrial Applicability

[0584]

The compound of the present invention has a superior LSDl inhibitory action, and is useful as a medicament such as a prophylactic or therapeutic agent for cancer, schizophrenia, developmental disorders, particularly diseases having

intellectual disability (e.g., autistic spectrum disorders, Rett syndrome, Down's syndrome, Kabuki syndrome, fragile X syndrome, Kleefstra syndrome, neurofibromatosis type 1, Noonan syndrome, tuberous sclerosis) , neurodegenerative diseases (e.g., Alzheimer's disease, Parkinson's disease,

spinocerebellar degeneration (e.g., dentatorubural

pallidoluysian atrophy) and Huntington's disease (Huntington chorea)), epilepsy (e.g., Dravet syndrome) or drug dependence, and the like.

[0585]

This application is based on patent application No. 2014- 82057 filed in Japan, the entire contents of which are

incorporated by reference herein.