WO1999021555A2

WO1999021555A2 - Adenosine a3 receptor antagonists

Info

Publication number: WO1999021555A2
Application number: PCT/JP1998/004837
Authority: WO
Inventors: Shigenori Ohkawa; Hiroyuki Kimura; Naoyuki Kanzaki
Original assignee: Takeda Chemical Industries, Ltd.
Priority date: 1997-10-27
Filing date: 1998-10-26
Publication date: 1999-05-06
Also published as: US6620825B1; WO1999021555A3; US6436966B1; EP1027050B1; DE69821132D1; DE69821132T2; ATE257703T1; EP1027050A2; CA2302417A1; JPH11193281A; AU9648098A

Abstract

A pharmaceutical composition for antagonizing adenosine at adenosine A3 receptors which comprises a 1,3-azole compound substituted on the 4- or 5- position, or both, by a pyridyl which may be substituted is provided and can be used as a prophylactic and therapeutic agent for asthma, allergosis, inflammation, and so on.

Description

DESCRIPTION Adenosine A₃ Receptor Antagonists

TECHNICAL FIELD The present invention relates to an agent for antagonizing adenosine at adenosine A3 receptors and a novel thiazole compound having a superior antagonistic activity at adenosine A3 receptor.

BACKGROUND ART

As subtypes of adenosine receptors, A-^ , A_2a, ^2^ and A3 are known. Adenosine induces bronchial constriction in asthma patients, while theophylline , which is known as an antiasthmatic, antagonizes adenosine. Recently several reports showed that activation of adenosine A3 receptors in rats promotes degranulation of mast cells [ Journal of Biological Chemistry, 268. 16887-16890 (1993)], that adenosine A3 receptors exist on peripheral blood eosinophils and that the stimulation of adenosine A₃ receptors activates phospholipase C and elevates intracellular calcium [Blood, 88, 3569-3574 (1996)].

Currently, as selective A3 adenosine receptor antagonists, xanthine derivatives are reported in GB-A- 2288733 and WO 95/11681, and the following compounds are reported in Journal of Medicinal Chemistry, 40. 2596-2608(1997) .

The following thiazole compounds are known. 1) A thiazole derivative of the formula:

wherein R¹ represents i) cycloalkyl, ii) cyclic amino, iii) amino which may be substituted by 1 or 2 substituents selected from the group consisting of lower alkyl, phenyl, acetyl and lower alkoxycarbonylacetyl, iv) alkyl which may be substituted by a substituent selected from the group consisting of hydroxy, carboxy and lower alkoxycarbonyl or v) phenyl which may be substituted by a substituent selected from the group consisting of carboxy, 2- carboxyethenyl and 2-carboxy-1-propenyl; R² represents pyridyl which may be substituted by a lower alkyl; and

R³ represents phenyl which may be substituted by a substituent selected from the group consisting of lower alkoxy, lower alkyl, hydroxy, halogen and methylenedioxy, or a salt thereof, which has analgesic, anti-pyretic, anti-inflammatory, anti-ulcer. thromboxane A₂ (TXA₂) synthetase inhibitory and platelet aggregation inhibiting actions ( JP-A-60-58981) . 2) A 1,3-thiazole derivative of the formula:

wherein R¹ represents an optionally substituted alkyl, alkenyl, aryl, aralkyl, cycloalkyl, heterocyclic group having carbon as the attachment point or amino; R² represents pyridyl which may be substituted by an alkyl; and R³ represents phenyl which may be substituted, or a salt thereof, which has analgesic, anti-pyretic, anti-inflammatory, anti-ulcer, thromboxane A₂ (TXA₂) synthetase inhibitory and platelet aggregation inhibiting actions (JP-A-61-10580) 3) A 1,3-thiazole derivative of the formula:

wherein R¹ represents an optionally substituted alkyl, alkenyl, aryl, aralkyl, cycloalkyl, heterocyclic group having carbon as the attachment point or amino; R² represents pyridyl which may be substituted by an alkyl; and R³ represents aryl which may be substituted, or a salt thereof, which has analgesic, anti-pyretic, anti-inflammatory, anti-ulcer, thromboxane A₂ (TXA₂) synthetase inhibitory and platelet aggregation inhibiting actions (USP 4,612,321). 4) A compound of the formula:

wherein R¹ is an optionally substituted phenyl, R² is C_1-6 alkyl or (CH₂)_nAr, n is 0-2, Ar is an optionally substituted phenyl, R³ is hydrogen or C_1-4 alkyl, R⁴ is hydrogen, C_1-4 alkyl, etc, R^: is hydrogen or C^- _^ alkyl.

R^b is hydrogen, ^- _^ alkyl, etc, or salt thereof, which has an activity of inhibiting gastric acid secretion ( JP-A-07-503023, WO 93/15071). 5) A compound of the formula:

wherein R¹ is pyridyl, etc, R² is phenyl, etc, R³ and

R⁴ are hydrogen or methyl, R⁵ is methyl, etc, R⁶ is hydrogen or methyl, etc, or a salt thereof, which is useful as anti-inflammatory and anti-allergic agents (DE-A-3601411) . 6) A compound of the formula:

wherein R- is lower alkyl substituted by halogen, R² is pyridyl, etc, R³ is phenyl, etc, or a salt thereof, which has anti-inflammatory, antipyretic, analgesic and anti-allergic activities ( JP-A-5-70446) .

From the prior art described above, it is thought that adenosine causes asthma through its binding to adenosine A₃ receptor, therefore 3 adenosine receptor antagonists are expected to become a new type of antiasthma drug. Accordingly, an agent for antagonizing adenosine at adenosine A3 receptors which has potent antagonistic activity, good bioavailability on per os administration and good metabolical stability are expected to have potent therapeutic effects for asthma, inflammation, Addison's diseases, autoallergic hemolytic anemia, Crohn's diseases, psoriasis, rheumatism and diabetes. However, as a prophylactic and therapeutic agent for adenosine A₃ receptor-related diseases , no good agent for antagonising adenosine at adenosine A₃ receptors are known in terms of potency, safety, bioavailability, and metabolic stability.

Therefore a good agent for antagonising adenosine at adenosine A₃ receptor is expected to be developed.

DISCLOSURE OF INVENTION We, the present inventors, have studied various compounds having an antagonistic activity at adenosine A₃ receptors, and as a result, have found for the first time that a 1,3-azole compound substituted on the 4- or 5-position, or both, by a pyridyl which may be substituted [hereinafter sometimes referred to briefly as compound (I)], has an unexpected, excellent selective affinity to adenosine A₃ receptor, antagonistic activity at adenosine A₃ receptor and high stability, and is therefore satisfactory as a medicine. Compound (I) comprises, for example, a compound of the formula:

wherein R¹ represents a hydrogen atom, a hydrocarbon group which may be substituted, a heterocyclic group which may be substituted, an amino which may be substituted or an acyl; at least one of R² and R³ represents a hydrogen atom, a pyridyl which may be substituted or an aromatic hydrocarbon group which may be substituted, and the other represents a pyridyl which may be substituted; and X represents a sulfur atom which may be oxidized, an oxygen atom or a group of the formula: NR⁴ wherein R⁴ represents a hydrogen atom, a hydrocarbon group which may be substituted or an acyl; or a salt thereof, which may be N-oxidized [hereinafter sometimes referred to briefly as compound (la)], and a novel compound of the formula:

wherein R^la represents (i) an aromatic heterocyclic group which may be substituted, (ii) an amino which may be substituted by substituent (s) selected from the group consisting of a substituted carbonyl and a hydrocarbon group which may be substituted, (iii) a cyclic amino which may be substituted or (iv) an acyl;

R^2a represents an aromatic hydrocarbon group which may be substituted; and

R^3a represents a pyridyl which may be substituted, or a salt thereof [hereinafter sometimes referred to briefly as compound (lb)] being within a scope of compound (la). On the basis of these findings, the inventors have completed the present invention.

Specifically, the present invention relates to: (1) A pharmaceutical composition for antagonizing adenosine at adenosine A₃ receptors which comprises compound ( I ) ;

(2) a composition of the above (1), wherein the 1,3- azole compound is compound (la);

(3) a composition of the above (2), wherein R¹ is (i) a hydrogen atom,

(ii) a C_λ _₈ alkyl, C₂_₆ alkenyl, C₂_₆ alkynyl, C₃_₆ cycloalkyl, C₆_₁₄ aryl or C₇_₁₆ aralkyl group which may be substituted by 1 to 5 substituents ,

(iii) a 5- to 14-membered heterocyclic group containing 1 to 4 hetero atoms selected from the group consisting of nitrogen, sulfur and oxygen atoms in addition to carbon atoms , which group may be substituted by 1 to 5 substituents,

(iv) an amino which may be substituted by 1 or 2 substituents selected from the group consisting of

(a) a C_λ _ ₆ alkyl, C₂_₆ alkenyl, C₂_₆ alkynyl, C₃_₆ cycloalkyl, C₆_₁₄ aryl or C₇_₁₆ aralkyl group which may be substituted by 1 to 5 substituents,

(b) a C^.g alkylidene group which may be substituted by 1 to 5 substituents,

(c) a 5- to 14-membered heterocyclic group containing 1 to 4 hetero atoms selected from the group consisting of nitrogen, sulfur and oxygen atoms in addition to carbon atoms , which group may be substituted by 1 to 5 substituents, and

(d) an acyl of the formula: -(C=0)-R⁵, -(C=0)-0R⁵, -(C=0)-NR⁵R⁶, -(C=S)-NHR⁵ or -S0₂-R⁷ wherein R⁵ is (i¹) a hydrogen atom, (ii') a C_1-6 alkyl, C₂_₆ alkenyl, C₂_₆ alkynyl, C₃_₆ cycloalkyl, C₆_₁₄ aryl or C₇_₁g aralkyl group which may be substituted by

1 to 5 substituents or (iii') a 5- to 14-membered heterocyclic group containing 1 to 4 hetero atoms selected from the group consisting of nitrogen, sulfur and oxygen atoms in addition to carbon atoms, which group may be substituted by 1 to 5 substituents; R° is a hydrogen atom or C-^.g alkyl; and R⁷ is (i' ) a C-^.g alkyl, C₂_₆ alkenyl, C₂_g alkynyl, C₃_g cycloalkyl, Cg_₁₄ aryl or C-.^g aralkyl group which may be substituted by 1 to 5 substituents or (ii') a 5- to 14-membered heterocyclic group containing 1 to 4 hetero atoms selected from the group consisting of nitrogen, sulf r and oxygen atoms in addition to carbon atoms , which group may be substituted by 1 to 5 substituents, (v) a 5- to 7-membered non-aromatic cyclic amino optionally containing 1 to 4 hetero atoms selected from the group consisting of nitrogen, sulfur and oxygen atoms in addition to carbon atoms and at least one nitrogen atom, which may be substituted by 1 to 3 substituents selected from the group consisting of C^_g alkyl, Cg_₁₄ aryl, C_1-6 alkyl-carbonyl, 5- to 10- membered aromatic heterocyclic group and oxo, or (vi) an acyl of the formula: -(C=0)-R⁵, -(C=0)-OR⁵, -(C=0)-NR⁵R⁶, -(C=S)-NHR⁵ or -S0₂-R⁷ wherein each symbol is as defined above; at least one of R² and R³ is (i) a hydrogen atom, (ii) a pyridyl which may be substituted by 1 to 5 substituents or (iii) a Cg_₁₄ aryl which may be substituted by 1 to 5 substituents in which a substituent can form, together with a neighboring substituent, a 4- to 7-membered non-aromatic carbocyclic ring; and the other is a pyridyl which may be substituted by 1 to 5 substituents; and X is a sulfur atom which may be oxidized, an oxygen atom or a group of the formula: NR⁴ wherein R⁴ is (i) a hydrogen atom, (ii) a C_1-6 alkyl, C _₆ alkenyl, C₂_₆ alkynyl, C₃_g cycloalkyl, Cg_₁₄ aryl or C₇_₁₆ aralkyl group which may be substituted by 1 to 5 substituents or (iii) an acyl of the formula: -(C=0)-R⁵,

-(C=0)-OR⁵, -(C=0)-NR⁵R⁶, -(C=S)-NHR⁵ or -S0₂-R⁷ wherein each symbol is as defined above, wherein the above "substituents" are selected from the group consisting of (1) halogen atoms, (2) C_j_3 alkylenedioxy, (3) nitro, (4) cyano, (5) optionally halogenated C^.g alkyl, (6) optionally halogenated C₂_g alkenyl, (7) carboxy C₂_g alkenyl, (8) optionally halogenated C₂_g alkynyl, (9) optionally halogenated ^c3-6 cycloalkyl, (10) Cg_₁₄ aryl, (11) optionally halogenated _ _Q alkoxy, (12) C^.g alkoxy-carbonyl-C-^.g alkoxy, (13) hydroxy, (14) Cg_₁₄ aryloxy, (15) C₇_₁₆ aralkyloxy, ( 16) mercapto, (17) optionally halogenated C_±_₆ alkylthio, (18) C₆_₁₄ arylthio, (19) C₇_₁₆ aralkylthio, (20) amino, (21) mono-C^.g alkylamino, (22) mono-Cg_₁₄ arylamino, (23) di-C-^.g alkylamino,

(24) di-Cg_ι arylamino, (25) formyl, (26) carboxy,

(27) C^g alkyl-carbonyl, (28) C₃_g cycloalkyl-carbonyl,

(29) C_j_g alkoxy-carbonyl, (30) Cg_₁₄ aryl-carbonyl,

(31) C₇_₁₆ aralkyl-carbonyl, (32) Cg_₁₄ aryloxy- carbonyl, (33) C₇_₁₆ aralkyloxy-carbonyl, (34) 5- or 6- membered heterocycle carbonyl, (35) carbamoyl, (36) mono-C-L.g alkyl-carbamoyl, (37) i-C-^g alkyl-carbamoyl,

(38) Cg_₁₄ aryl-carbamoyl, (39) 5- or 6-membered heterocycle carbamoyl, (40) Cτ_g alkylsulfonyl, (41) ^c6-14 arylsulfonyl, (42) formylamino, (43) C^_^.g alkyl- carbonylamino , (44) Cg_₁₄ aryl-carbonylamino, (45) C^.g alkoxy-carbonylamino, (46) C^.g alkylsulfonylamino,

(47) Cg_₁₄ arylsulfonylamino , (48) C_1-6 alkyl- carbonyloxy, (49) Cg_₁ aryl-carbonyloxy, (50) C-^.g alkoxy-carbonyloxy, (51) mono-C^_^.g alkyl-carbamoyloxy, (52) di-C-_j^g alkyl-carbamoyloxy, (53) Cg_₁₄ aryl- carbamoyloxy, (54) nicotinoyloxy, (55) 5- to 7-membered saturated cyclic amino which may be substituted by 1 to 3 substituents selected from the group consisting of C^.g alkyl, Cg_₁ aryl, C_π_g alkyl-carbonyl, 5- to 10- membered aromatic heterocyclic group and oxo, (56) 5- to 10-membered aromatic heterocyclic group and (57) sulfo;

(4) a composition of the above (2), wherein R¹ is an amino which may be substituted; (5) a composition of the above (3), wherein R~ is an amino which may be substituted by 1 or 2 acyl of the formula: -(C=0)-R⁵, -(C=0)-OR⁵, - (C=0) -NR⁵R⁶ ,

-(C=S)-NHR⁵ or -S0₂-R⁷;

(6) a composition of the above (3), wherein R-*- is an amino which may be substituted by 1 or 2 acyl of the formula: -(C=0)-R⁵ or - (C=0) -NR⁵R⁶;

(7) a composition of the above (3), wherein R¹ is a 5- to 7-membered non-aromatic cyclic amino optionally containing 1 to 4 hetero atoms selected from the group consisting of nitrogen, sulfur and oxygen atoms in addition to carbon atoms and at least one nitrogen atom, which may be substituted by 1 to 3 substituents selected from the group consisting of C^. alkyl, Cg_₁₄ aryl, C-^_g alkyl-carbonyl, 5- to 10-membered aromatic heterocyclic group and oxo;

(8) a composition of the above (2), wherein X is S;

(9) a composition of the above (2), wherein R² is a pyridyl which may be substituted; (10) a composition of the above (2), wherein R³ is a ^c6-14 ^arY¹ which may be substituted;

(11) a composition of the above (3), wherein R¹ is an amino which may be substituted by 1 or 2 acyl of the formula: -(C=0)-R⁵ or - (C=0) -NR⁵R⁶;

R² is a pyridyl which may be substituted by 1 to 5 C-^.g alkyl;

R^J s a Cg_ ₄ aryl which may be substituted by 1 to 5 substituents selected from the group consisting of halogen atoms, optionally halogenated C^_g alkyl, optionally halogenated C^_g alkoxy and carboxy; and

X is S;

(12) a composition of the above (2), wherein R¹ is (i) a C-L__Q alkyl, C₃_g cycloalkyl or Cg_₁₄ aryl group which may be substituted by 1 to 5 substituents selected from the group consisting of halogen atoms, optionally halogenated Cη.g alkyl, carboxy C₂_g alkenyl, optionally halogenated C^.g alkoxy, C^.g alkoxy- carbonyl-C-L_g alkoxy, hydroxy, amino, mono-C₁_g alkylamino, carboxy, C-^.g alkoxy-carbonyl, mono-C^.g alkyl-carbamoyl and Cg_₁₄ aryl-carbonylamino,

(ii) a 5-membered heterocyclic group, (iii) an amino which may be substituted by 1 or 2 substituents selected from the group consisting of (1) C_λ _ ₆ alkyl, (2) Cg_₁₄ aryl, (3) C_?_₁₆ aralkyl, (4) 6- membered heterocyclic group, (5) a C^.g alkyl-carbonyl, ^c3-6 cycloalkyl-carbonyl, Cg_₁₄ aryl-carbonyl, C₇_₁₆ aralkyl-carbonyl, C-^.g alkyl-carbamoyl or 5- or 6- membered heterocycle carbonyl group which may be substituted by 1 to 3 substituents selected from the group consisting of halogen atoms, C^_g alkyl, Cη_g alkoxy, carboxy and Cη_^.g alkoxy-carbonyl, and (6) di-

C"L_ alkylamino-C^.g alkylidene,

(iv) a 5- or 6-membered non-aromatic cyclic amino which may be substituted by C^.g alkyl-carbonyl or oxo, or (v) carboxy;

R² is a pyridyl which may be substituted by 1 to 3 C^_

₆ alkyl;

R³ is a Cg_₁₀ aryl which may be substituted by 1 to 3 substituents selected from the group consisting of halogen atoms, C-L_₃ alkylenedioxy, optionally halogenated C-^.g alkyl, carboxy C₂_g alkenyl, optionally halogenated C^. alkoxy, hydroxy, C₇_₁₆ aralkyloxy and C^_g alkyl-carbonyloxy, in which the alkyl group can form, together with a neighboring alkyl group, a 5-membered non-aromatic carbocyclic ring; and X is S;

(13) an adenosine A3 receptor antagonist which comprises a 1,3-azole compound substituted on the 4- or 5-position, or both, by a pyridyl which may be substituted;

(14) a composition of the above (1), which is for preventing and/or treating asthma or allergosis;

(15) compound (lb); (16) a compound of the above (15), wherein R^la is an amino which may be substituted by 1 or 2 substituents selected from the group consisting of C^.g alkyl, Cη.g alkyl-carbonyl, Cg_₁₄ aryl-carbonyl and Cτ_g alkyl- carbamoyl ; R^2a is a phenyl which may be substituted by 1 to 3 substituents selected from the group consisting of halogen atoms, optionally halogenated Cη_g alkyl and optionally halogenated C-^.g alkoxy; and

R^3a is a pyridyl;

(17) a process for producing of compound (lb), which comprises reacting a compound of the formula:

2a ₃a

R -CH-COR I Hal wherein Hal represents halogen atoms and other symbols are as defined above, or a salt thereof with a compound of the formula:

R -C-NH

II ² s wherein R^la is as defined above, or a salt thereof, optionally in the presence of a base;

(18) a pharmaceutical composition which comprises compound (lb);

(19) a composition of the above (18) which is an agent for antagonizing adenosine at adenosine A₃ receptors;

(20) a composition of the above (18) which is for preventing and/or treating asthma or allergosis;

(21) a method for preventing and/or treating diseases related to adenosine A₃ receptor in mammal, which comprises administering to said mammal an effective amount of a compound of the above ( 1 ) or a pharmaceutically acceptable salt thereof with a pharmaceutically acceptable excipient , carrier or diluent ; and (22) use of a compound of the above (1) or a salt thereof for manufacturing a pharmaceutical composition for preventing and/or treating diseases related to adenosine A₃ receptor, and so forth.

In this specification, the "acyl" includes, for example, an acyl of the formula: -(C=0)-R⁵, -(C=0)-OR⁵, -(C=0)-NR⁵R⁶, -(C=S)-NHR⁵ or -S0₂-R⁷ wherein R⁵ represents a hydrogen atom, a hydrocarbon group which may be substituted or a heterocyclic group which may be substituted; R⁶ represents a hydrogen atom or C^.g alkyl; and R⁷ represents a hydrocarbon group which may be substituted or a heterocyclic group which may be substituted.

In the above formulae, the "hydrocarbon group" of the "hydrocarbon group which may be substituted" for R⁵ includes, for example, an acyclic or cyclic hydrocarbon group such as alkyl, alkenyl, alkynyl, cycloalkyl, aryl, aralkyl, etc. Among them, Cη.^g acyclic or cyclic hydrocarbon group is preferable.

The preferred "alkyl" is for example C-^g alkyl such as methyl, ethyl, propyl, isopropyl, butyl, isobutyl, sec-butyl, tert-butyl, pentyl, hexyl, etc. The preferred "alkenyl" is for example C₂_g alkenyl such as vinyl, allyl, isopropenyl, 1-butenyl, 2-butenyl, 3-butenyl, 2-methyl-2-propenyl, l-methyl-2- propenyl, 2-methyl- 1-propenyl, etc.

The preferred "alkynyl" is for example C₂_g alkynyl such as ethynyl, propargyl, 1-butynyl, 2- butynyl, 3-butynyl, 1-hexynyl, etc.

The preferred "cycloalkyl" is for example C₃_g cycloalkyl such as cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, etc.

The preferred "aryl" is for example Cg_^₄ aryl such as phenyl, 1-naphthyl, 2-naphthyl, 2-biphenylyl, 3-biphenylyl, 4-biphenylyl, 2-anthryl, etc. The preferred "aralkyl" is for example C₇_₁₆ aralkyl such as benzyl, phenethyl, diphenylmethyl , 1- naphthylmethyl , 2-naphthylmethyl, 2, 2-diphenylethyl, 3- phenylpropyl , 4-phenylbutyl, 5-phenylpentyl, etc.

Examples of the "substituents" of the "hydrocarbon group which may be substituted" for R⁵ include halogen atoms (e.g., fluoro, chloro, bromo, iodo, etc.),

alkylenedioxy (e.g., methylenedioxy, ethylenedioxy, etc.), nitro, cyano, optionally halogenated Cη_^.g alkyl, optionally halogenated C₂_g alkenyl, carboxy C₂_g alkenyl (e.g., 2-carboxyethenyl, 2-carboxy-2- methylethenyl , etc.), optionally halogenated C₂_₆ alkynyl, optionally halogenated C₃_g cycloalkyl, Cg_^₄ aryl (e.g., phenyl, 1-naphthyl, 2-naphthyl, 2- biphenylyl, 3-biphenylyl, 4-biphenylyl, 2-anthryl, etc.), optionally halogenated C-L_₈ alkoxy, C^.g alkoxycarbonyl-C^.g alkoxy (e.g., ethoxycarbonylmethyloxy, etc.), hydroxy, Cg_₁₄ aryloxy (e.g., phenyloxy, 1- naphthyloxy, 2-naphthyloxy, etc.), C₇_₁₆ aralkyloxy (e.g., benzyloxy, phenethyloxy, etc.), mercapto, optionally halogenated C^_ alkylthio, C _^₄ arylthio

(e.g., phenylthio, 1-naphthylthio, 2-naphthylthio, etc.), C₇_₁₆ aralkylthio (e.g., benzylthio, phenethylthio, etc.), amino, mono-C₁_g alkylamino (e.g. methylamino, ethylamino, etc.), mono-Cg_₁₄ arylamino

(e.g., phenylamino, 1-naphthylamino, 2-naphthylamino, etc.), di-C-^g alkylamino (e.g., dimethylamino , diethylamino , ethylmethylamino , etc.), di-Cg_₁₄ arylamino (e.g., diphenylamino , etc.), formyl, carboxy, ^ci-6 alkyl-carbonyl (e.g., acetyl, propionyl, etc.), ^c3-6 cycloalkyl-carbonyl (e.g., cyclopropylcarbonyl , cyclopentylcarbonyl, cyclohexylcarbonyl, etc.), C^.g alkoxy-carbonyl (e.g. , methoxycarbonyl , ethoxycarbonyl , propoxycarbonyl , tert-butoxycarbonyl, etc.), Cg_₁₄ aryl-carbonyl (e.g., benzoyl, 1-naphthoyl, 2-naphthoyl, etc.), C₇_ιg aralkyl-carbonyl (e.g., phenylacetyl , 3- phenylpropionyl , etc.), C₆_ι₄ aryloxy-carbonyl (e.g.. phenoxycarbonyl, etc.), C-y.^g aralkyloxy-carbonyl (e.g., benzyloxycarbonyl, phenethyloxycarbonyl , etc.), 5- or 6-membered heterocycle carbonyl (e.g., nicotinoyl, isonicotinoyl, thenoyl, furoyl, morpholinocarbonyl , thiomorpholinocarbonyl , piperazin-1-ylcarbonyl, pyrrolidin-1-ylcarbonyl, etc.), carbamoyl, mono-C^g alkyl-carbamoyl (e.g. , methylcarbamoyl , ethylcarbamoyl , etc.), di-C^.g alkyl-carbamoyl (e.g., dimethylcarbamoyl, diethylcarbamoyl , ethylmethylcarbamoyl , etc.), C₆_₁₄ aryl-carbamoyl (e.g., phenylcarbamoyl , 1- naphthylcarbamoyl , 2-naphthylcarbamoyl, etc.), 5- or 6- membered heterocycle carbamoyl (e.g., 2- pyridylcarbamoyl , 3-pyridylcarbamoyl, 4- pyridylcarbamoyl , 2-thienylcarbamoyl, 3- thienylcarbamoyl , etc.), C^.g alkylsulfonyl (e.g., methylsulfonyl , ethylsulfonyl , etc.), Cg_₁₄ arylsulfonyl (e.g., phenylsulfonyl, 1-naphthylsulfonyl, 2-naphthylsulfonyl, etc.), formylamino, C_1-6 alkyl- carbonylamino (e.g., acetylamino, etc.), Cg_₁₄ aryl- carbonylamino (e.g., benzoylamino, naphthoylamino , etc.), CL_g alkoxy-carbonylamino (e.g., methoxycarbonylamino , ethoxycarbonylamino , propoxycarbonylamino , butoxycarbonylamino , etc.), C^.g alkylsulfonylamino (e.g., methylsulfonylamino , ethylsulfonylamino, etc.), Cg_₁₄ arylsulfonylamino

(e.g., phenylsulfonylamino , 2-naphthylsulfonylamino, 1- naphthylsulfonylamino , etc.), C^_₆ alkyl-carbonyloxy

(e.g., acetoxy, propionyloxy, etc.), Cg_₁₄ aryl- carbonyloxy (e.g., benzoyloxy, naphthylcarbonyloxy, etc.), C-L_g alkoxy-carbonyloxy (e.g., methoxycarbonyloxy, ethoxycarbonyloxy, propoxycarbonyloxy, butoxycarbonyloxy, etc.), mono-C-^.g alkyl-carbamoyloxy (e.g., methylcarbamoyloxy. ethylcarbamoyloxy, etc.), di-C-^_g alkyl-carbamoyloxy

(e.g., dimethylcarbamoyloxy, diethylcarbamoyloxy, etc.), Cg_₁₄ aryl-carbamoyloxy (e.g., phenylcarbamoyloxy, naphthylcarbamoyloxy, etc.), nicotinoyloxy, 5- to 7- membered saturated cyclic amino which may be substituted, 5- to 10-membered aromatic heterocyclic group (e.g., 2-thienyl, 3-thienyl, 2-pyridyl, 3-pyridyl, 4-pyridyl, 2-quinolyl, 3-quinolyl, 4-quinolyl, 5- quinolyl, 8-quinolyl, 1-isoquinolyl, 3-isoquinolyl, 4- isoquinolyl, 5-isoquinolyl, 1-indolyl, 2-indolyl, 3- indolyl, 2-benzothiazolyl, 2-benzo[b] thienyl, 3- benzo[b]thienyl, 2-benzo[b]furanyl, 3-benzo[b]furanyl, etc.), sulfo, and so forth.

The "hydrocarbon group" may have 1 to 5, preferably 1 to 3 substituents as mentioned above at possible positions of the hydrocarbon group and, when the number of substituents is two or more, those substituents may be the same as or different from one another. The above-mentioned "optionally halogenated C^.g alkyl" includes, for example, C_1-6 alkyl (e.g., methyl, ethyl, propyl, isopropyl, butyl, isobutyl, sec-butyl, tert-butyl, pentyl, hexyl, etc.) which may have 1 to 5, preferably 1 to 3 halogen atoms (e.g., fluoro, chloro, bromo, iodo, etc.). Concretely mentioned is methyl, chloromethyl , difluoromethyl , trichloromethyl , trifluoromethyl, ethyl, 2-bromoethyl, 2,2,2- trifluoroethyl, pentafluoroethyl, propyl, 3,3,3- trifluoropropyl, isopropyl, butyl, 4 , 4 , 4-trifluorobutyl, isobutyl, sec-butyl, tert-butyl, pentyl, isopentyl, neopentyl, 5, 5, 5-trifluoropentyl, hexyl, 6,6,6- trifluorohexyl, etc.

The above-mentioned "optionally halogenated C₂_₆ alkenyl" includes, for example, C₂_₆ alkenyl (e.g., vinyl, propenyl, isopropenyl, 2-buten-l-yl, 4-penten-l- yl, 5-hexen-l-yl, etc.) which may have 1 to 5, preferably 1 to 3 halogen atoms (e.g., fluoro, chloro, bromo , iodo , etc . ) .

The above-mentioned "optionally halogenated C₂_g alkynyl" includes, for example, C₂_g alkynyl (e.g., 2- butyn-1-yl, 4-pentyn-l-yl, 5-hexyn-l-yl, etc.) which may have 1 to 5, preferably 1 to 3 halogen atoms (e.g., fluoro, chloro, bromo, iodo, etc.).

The above-mentioned "optionally halogenated C₃_₆ cycloalkyl" includes, for example, C₃_ cycloalkyl

(e.g. , cyclopropyl , cyclobutyl , cyclopentyl , cyclohexyl , etc . ) which may have 1 to 5 , preferably 1 to 3 halogen atoms (e.g., fluoro, chloro, bromo, iodo, etc.). Concretely mentioned is cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, 4 , 4-dichlorocyclohexyl,

2,2, 3, 3-tetrafluorocyclopentyl, 4-chlorocyclohexyl, etc. The above-mentioned "optionally halogenated C-L_₈ alkoxy" includes, for example, C_1-8 alkoxy (e.g., methoxy, ethoxy, propoxy, isopropoxy, butoxy, isobutoxy, sec-butoxy, pentyloxy, hexyloxy, etc.) which may have 1 to 5, preferably 1 to 3 halogen atoms (e.g., fluoro, chloro, bromo, iodo, etc.). Concretely mentioned is methoxy, difluoromethoxy, trifluoromethoxy, ethoxy, 2,2, 2-trifluoroethoxy, propoxy, isopropoxy, butoxy, 4, 4, 4-trifluorobutoxy, isobutoxy, sec-butoxy, pentyloxy, hexyloxy, etc.

The above-mentioned "optionally halogenated Cη_.g alkylthio" includes, for example, C^.g alkylthio (e.g., methylthio, ethylthio, propylthio, isopropylthio, butylthio, sec-butylthio, tert-butylthio, etc.) which may have 1 to 5, preferably 1 to 3 halogen atoms (e.g., fluoro, chloro, bromo, iodo, etc.). Concretely mentioned is methylthio, difluoromethylthio, trifluoromethylthio, ethylthio, propylthio, isopropylthio, butylthio, 4 , 4 , 4-trifluorobutylthio. pentylthio, hexylthio, etc.

The above-mentioned "5- to 7-membered saturated cyclic amino" of the "5- to 7-membered saturated cyclic amino which may be substituted" includes, for example, 5- to 7-membered saturated cyclic amino optionally containing 1 to 4 hetero atoms selected from the group consisting of nitrogen, sulfur and oxygen atoms in addition to carbon atoms and at least one nitrogen atom, such as pyrrolidin-1-yl, piperidino, piperazin-1-yl, morpholino, thiomorpholino , tetrahydroazepin-1-yl, etc.

The "substituents" of the "5- to 7-membered saturated cyclic amino which may be substituted" include, for example, 1 to 3 substituents selected from the group consisting of C-^.g alkyl (e.g., methyl, ethyl, propyl, isopropyl, butyl, isobutyl, sec-butyl, tert- butyl, pentyl, hexyl, etc.), C₆_₁₄ aryl (e.g., phenyl,

1-naphthyl, 2-naphthyl, 2-biphenylyl, 3-biphenylyl, 4- biphenylyl, 2-anthryl, etc.), C_π_₆ alkyl-carbonyl (e.g., acetyl, propionyl, etc.), and 5- to 10-membered aromatic heterocyclic group (e.g., 2-thienyl, 3-thienyl, 2-pyridyl, 3-pyridyl, 4-pyridyl, 2-quinolyl, 3-quinolyl, 4-quinolyl, 5-quinolyl, 8-quinolyl, 1-isoquinolyl, 3- isoquinolyl, 4-isoquinolyl, 5-isoquinolyl, 1-indolyl, 2-indolyl, 3-indolyl, 2-benzothiazolyl, 2- benzo[b]thienyl, 3-benzo[b] thienyl, 2-benzo[b]furanyl, 3-benzo[b]furanyl, etc.), oxo, and so forth.

The "heterocyclic group" of the "heterocyclic group which may be substituted" for R⁵ includes, for example, a monovalent group formed by removing an optional hydrogen atom from a 5- to 14-membered

(monocyclic, bicyclic or tricyclic) heterocyclic ring containing 1 to 4 hetero atoms of 1 or 2 species selected from the group consisting of nitrogen, sulfur and oxygen atoms in addition to carbon atoms, preferably, (i) a 5- to 14-membered, preferably, 5- to 10-membered aromatic heterocyclic ring, (ii) a 5- to 10-membered non-aromatic heterocyclic ring and (iii) a 7- to 10-membered bridged heterocyclic ring, etc.

The above-mentioned "5- to 14-membered, preferably 5- to 10-membered aromatic heterocyclic ring" includes, for example, an aromatic heterocyclic ring such as thiophene, benzofb] thiophene, benzo[b]furan, benzimidazole, benzoxazole, benzothiazole, benzisothiazole, naphtho[2, 3-b] thiophene, furan, pyrrole, imidazole, pyrazole, pyridine, pyrazine, pyrimidine, pyridazine, indole, isoindole, IH-indazole, purine, 4H-quinolidine, isoquinoline, quinoline, phthalazine, naphthyridine, quinoxaline, quinazoline, cinnoline, carbazole, β-carboline, phenanthridine, acridine, phenazine, thiazole, isothiazole, phenothiazine, isoxazole, furazan, phenoxazine, etc.; and a ring as formed through condensation of those rings, preferably a monocyclic ring, with one or more, preferably one or two aromatic rings (e.g., benzene ring, etc.), etc.

The above-mentioned "5- to 10-membered non- aromatic heterocyclic ring" includes, for example, pyrrolidine, imidazoline, pyrazolidine, pyrazoline, piperidine, piperazine, morpholine, thiomorpholine, dioxazole, oxadiazoline, oxathiazole, thiadiazoline, triazoline, thiadiazole, dithiazole, etc.

The above-mentioned "7- to 10-membered bridged heterocyclic ring" includes, for example, quinuclidine , 7-azabicyclo[2.2.1]heptane, etc. Preferable examples of the "heterocyclic group" include, for example, a 5- to 14-membered (preferably 5- to 10-membered) (monocyclic or bicyclic) heterocyclic group containing 1 to 4 hetero atoms of 1 or 2 species selected from the group consisting of nitrogen, sulfur and oxygen atoms in addition to carbon atoms. Concretely mentioned are an aromatic heterocyclic group such as 2-thienyl, 3-thienyl, 2- furyl, 3-furyl, 2-pyridyl, 3-pyridyl, 4-pyridyl, 2- quinolyl, 3-quinolyl, 4-quinolyl, 5-quinolyl, 8- quinolyl, 1-isoquinolyl, 3-isoquinolyl, 4-isoquinolyl, 5-isoquinolyl, pyrazinyl, 2-pyrimidinyl, 4-pyrimidinyl, 3-pyrrolyl, 2-imidazolyl, 3-pyridazinyl, 3-isothiazolyl, 3-isoxazolyl, 1-indolyl, 2-indolyl, 3-indolyl, 2- benzothiazolyl, 2-benzo[b] thienyl, 3-benzo[b] thienyl, 2-benzo[b]furanyl, 3-benzo[b]furanyl, etc; and a non- aromatic heterocyclic group such as 1-pyrrolidinyl, 2- pyrrolidinyl , 3-pyrrolidinyl, 2-imidazolinyl, 4- imidazolinyl, 2-pyrazolidinyl, 3-pyrazolidinyl, 4- pyrazolidinyl, piperidino, 2-piperidyl, 3-piperidyl, 4- piperidyl, 1-piperazinyl, 2-piperazinyl, morpholino, thiomorpholino , etc.

Among these groups, a 5- or 6-membered heterocyclic group containing 1 to 3 hetero atoms selected from the group consisting of nitrogen, sulfur and oxygen atoms in addition to carbon atoms . Concretely mentioned are 2-thienyl, 3-thienyl, 2- pyridyl, 3-pyridyl, 4-pyridyl, 2-furyl, 3-furyl, pyrazinyl, 2-pyrimidinyl, 3-pyrrolyl, 3-pyridazinyl, 3- isothiazolyl, 3-isoxazolyl, 1-pyrrolidinyl, 2- pyrrolidinyl , 3-pyrrolidinyl, 2-imidazolinyl, 4- imidazolinyl, 2-pyrazolidinyl, 3-pyrazolidinyl, 4- pyrazolidinyl , piperidino, 2-piperidyl, 3-piperidyl, 4- piperidyl, 1-piperazinyl, 2-piperazinyl, morpholino, thiomorpholino, etc.

The "substituents" of the "heterocyclic group which may be substituted" are the same as those mentioned above for the "substituents" of the

"hydrocarbon group which may be substituted" for R⁵.

The "heterocyclic group" may have 1 to 5, preferably 1 to 3 substituents as mentioned above at possible positions of the heterocyclic group and, when the number of substituents is two or more, those substituents may be the same as or different from one another.

The "Cι_ alkyl" for R⁶ includes, for example, methyl, ethyl, propyl, isopropyl, butyl, isobutyl, sec- butyl, tert-butyl, pentyl, hexyl, etc.

The "hydrocarbon group which may be substituted" and the "heterocyclic group which may be substituted" for R⁷ include, for example, the "hydrocarbon group which may be substituted" and the "heterocyclic group which may be substituted" for R⁵ above, respectively. The "1,3-azole compound" of the "1,3-azole compound substituted on the 4- or 5-position, or both, by a pyridyl which may be substituted" in the above compound (I) includes, for example, 1, 3-thiazole, 1,3- oxazole, 1 , 3-imidazole, and so forth.

The "substituents" of the "pyridyl which may be substituted" in the "1,3-azole compound substituted on the 4- or 5-position, or both, by a pyridyl which may be substituted" are, for example, the same as those mentioned above for the "substituents" of the

"hydrocarbon group which may be substituted" for R .

The "pyridyl" may have 1 to 5, preferably 1 to 3 substituents as mentioned above at possible positions thereof and, when the number of substituents is two or more, those substituents may be the same as or different from one another. The ring-constituting nitrogen atom in the "pyridyl" may be oxidized (N- oxidized) .

The above-mentioned "1,3-azole compound substituted on the 4- or 5-position, or both, by a pyridyl which may be substituted" may further have 1 to 4, preferably 1 to 3 substituents. When the number of substituents is two or more, those substituents may be the same as or different from one another. Such "substituents" include, for example, a hydrocarbon group which may be substituted, a heterocyclic group which may be substituted, amino which may be substituted, acyl, and so forth.

The above-mentioned "hydrocarbon group which may be substituted" and the "heterocyclic group which may be substituted" includes, for example, the "hydrocarbon group which may be substituted" and the "heterocyclic group which may be substituted" for R^ above, respectively. The above-mentioned "amino which may be substituted" includes, for example, (1) an amino which may be substituted by 1 or 2 substituents and (2) a cyclic amino which may be substituted.

The "substituents" of the above (1) "amino which may be substituted by 1 or 2 substituents" include, for example, a hydrocarbon group which may be substituted, a heterocyclic group which may be substituted, acyl, alkylidene which may be substituted, and so forth. The "hydrocarbon group which may be substituted" and the "heterocyclic group which may be substituted", include, for example, the "hydrocarbon group which may be substituted" and the "heterocyclic group which may be substituted" for R⁵ above, respectively.

The above-mentioned "alkylidene" of the "alkylidene which may be substituted" include, for example, C^_ alkylidene such as methylidene, ethylidene, propylidene, etc. The "substituents" of the "alkylidene which may be substituted" includes, for example, the same as those mentioned above for the "substituents" of the "hydrocarbon group which may be substituted" for R⁵. The number of such substituent is 1 to 5 , preferably 1 to 3.

When the number of substituents of the above "amino which may be substituted by 1 or 2 substituents" is two, those substituents may be the same as or different from one another.

The "cyclic amino" of the above-mentioned (2) "cyclic amino which may be substituted" includes, for example, 5- to 7-membered non-aromatic cyclic amino optionally containing 1 to 4 hetero atoms selected from the group consisting of nitrogen, sulfur and oxygen atoms in addition to carbon atoms and at least one nitrogen atom, such as pyrrolidin-1-yl, piperidino, piperazin-1-yl, morpholino, thiomorpholino, tetrahydroazepin-1-yl, imidazolidin-1-yl, 2,3-dihydro- lH-imidazol-1-yl, tetrahydro-l(2H) -pyrimidinyl, 3,6- dihydro-1 ( 2H) -pyrimidinyl , 3,4-dihydro-1 ( 2H) - pyrimidinyl, etc. The "substituents" of the "cyclic amino which may be substituted" include, for example, 1 to 3 of the "substituents" of the "5- to 7-membered saturated cyclic amino which may be substituted" described in detail in the foregoing referring to the "substituents" of the "hydrocarbon group which may be substituted" for R⁵. Examples of the 5- to 7-membered non-aromatic cyclic amino substituted by an oxo are 2- oxoimidazolidin-1-yl, 2-oxo-2 , 3-dihydro-lH-imidazol-l- yl, 2-oxotetrahydro-l(2H) -pyrimidinyl, 2-oxo-3, 6- dihydro- 1 ( 2H) -pyrimidinyl , 2-oxo-3 , 4-dihydro- 1 ( 2H) - pyrimidinyl, etc.

Preferable example of compound ( I ) is compound (la).

The ring-constituting nitrogen atom in the 1,3- azole in compound (la) may be oxidized (N-oxidized). The "hydrocarbon group which may be substituted" , the "heterocyclic group which may be substituted" and the "amino which may be substituted" for R¹, include, for example, the "hydrocarbon group which may be substituted" , the "heterocyclic group which may be substituted" and the "amino which may be substituted" which the above compound (I) may have, respectively. R¹ is preferably an amino which may be substituted. More preferred is an amino which may be substituted by

1 or 2 acyl of the formula: -(C=0)-R⁵, -(C=0)-OR⁵,

-(C=0)-NR⁵R⁶, -(C=S)-NHR⁵ or -S0₂-R⁷ (more preferably, -(C=0)-R⁵ or -(C=0)-NR⁵R⁶) wherein each symbol is as defined above . Among others , especially preferred is a 5- to 7-membered non-aromatic cyclic amino optionally containing 1 to 4 hetero atoms selected from the group consisting of nitrogen, sulfur and oxygen atoms in addition to carbon atoms and at least one nitrogen atom, which may be substituted by 1 to 3 substituents selected from the group consisting of C^_g alkyl, C _^₄ aryl, C^_^.g alkyl-carbonyl, 5- to 10-membered aromatic heterocyclic group and oxo. The "pyridyl which may be substituted" for R² or

R³ includes, for example, the "pyridyl which may be substituted" which the above compound ( I ) has .

The "aromatic hydrocarbon group" of the "aromatic hydrocarbon group which may be substituted" for R² or R³ includes, for example, a Cg_₁₄ monocyclic or fused polycyclic (e.g., bi- or tri-cyclic) aromatic hydrocarbon group, etc. Concretely mentioned is Cg_₁₄ aryl such as phenyl, 1-naphthyl, 2-naphthyl, 2- biphenylyl, 3-biphenylyl, 4-biphenylyl, 2-anthryl, etc. The "substituents" of the "aromatic hydrocarbon group which may be substituted" include, for example, the same as those mentioned above for the "substituents" of the "hydrocarbon group which may be substituted" for R⁵. The number of such substituent is 1 to 5 , preferably 1 to 3. When the number of substituents is two or more, those substituents may be the same as or different from one another. The two substituents (preferably alkyl groups) can form. together with a neighboring substituent, a 4- to 7- membered (preferably, 5-membered) non-aromatic carbocyclic ring.

It is preferred case that at least one of R² and R³ is a pyridyl which may be substituted or an aromatic hydrocarbon group which may be substituted, and the other is a pyridyl which may be substituted.

R² is preferably a pyridyl which may be substituted. R³ is preferably a Cg_₁₄ (preferably Cg_₁₀) aryl which may be substituted.

The "sulfur atom which may be oxidized" for X includes S, SO and S0₂.

The "hydrocarbon group which may be substituted" for R⁴ includes, for example, the "hydrocarbon group which may be substituted" for R⁵ above.

X is preferably a sulfur atom which may be oxidized. More preferred is S.

In compound (la), preferred is a compound wherein R¹ is an amino which may be substituted, preferably a monoacylamino; at least one of R² and R³ is a pyridyl which may be substituted or an aromatic hydrocarbon group which may be substituted, and the other is a pyridyl which may be substituted; and X is S.

More preferred is a compound wherein

R¹ is an amino which may be substituted by 1 or 2 acyl of the formula: -(C=0)-R⁵ or -(C=0)-NR⁵R⁶ wherein each symbol is as defined above;

R² is a pyridyl which may be substituted by 1 to 5 C^_ alkyl;

R³ is a C₆_₁₄ aryl which may be substituted by 1 to 5 substituents selected from the group consisting of halogen atoms, optionally halogenated C^.g alkyl, optionally halogenated Cτ_g alkoxy and carboxy; and

X is S. Another preferred example is a compound, wherein

R¹ is (i) a CT._Q alkyl, C₃_g cycloalkyl or Cg_₁₄ aryl group which may be substituted by 1 to 5 substituents selected from the group consisting of halogen atoms, optionally halogenated C-^g alkyl, carboxy C₂_g alkenyl, optionally halogenated C^.g alkoxy, C-^_g alkoxycarbonyl-C₁_₆ alkoxy, hydroxy, amino, mono-C^.g alkylamino, carboxy, C-^.g alkoxy-carbonyl, mono-C^_g alkyl-carbamoyl and Cg_₁₄ aryl-carbonylamino,

(ii) a 5-membered heterocyclic group, (iii) an amino which may be substituted by 1 or 2 substituents selected from the group consisting of (1) C_± _ ₆ alkyl, (2) Cg_₁₄ aryl, (3) C₇_₁₆ aralkyl, (4) 6- membered heterocyclic group, (5) a Cη.g alkyl-carbonyl, ^c3-6 cycloalkyl-carbonyl, Cg_₁₄ aryl-carbonyl, C-y.^g aralkyl-carbonyl, C^.g alkyl-carbamoyl or 5- or 6- membered heterocycle carbonyl group which may be substituted by 1 to 3 substituents selected from the group consisting of halogen atoms, C_1-6 alkyl, C_1-6 alkoxy, carboxy and C^_g alkoxy-carbonyl, and (6) di- ^ci-6 alkylamino-C^_g alkylidene,

(iv) a 5- or 6-membered non-aromatic cyclic amino which may be substituted by C^_g alkyl-carbonyl or oxo, or

(v) carboxy;

R- is a pyridyl which may be substituted by 1 to 3 C^. g alkyl;

R³ is a C₆_₁₀ aryl which may be substituted by 1 to 3 substituents selected from the group consisting of halogen atoms, C_1-3 alkylenedioxy, optionally halogenated C_1-6 alkyl, carboxy C₂_g alkenyl, optionally halogenated C-^.g alkoxy, hydroxy, C₇_₁₆ aralkyloxy and C-^.g alkyl-carbonyloxy, and the alkyl group can form, together with the neighboring alkyl group, a 5-membered non-aromatic carbocyclic ring; and X is S.

More preferred examples of compound (la) are

N- [ 4- ( 4-methoxyphenyl) -5- 3-pyridyl) -1 , 3-thiazol-2- yl]acetamide,

N- [ 4- ( 4-methoxyphenyl ) -5- 4-pyridyl) -1 , 3-thiazol-2- yl]acetamide,

N- [ 4- ( 4-methoxyphenyl ) -5- 4-pyridyl ) - 1 , 3-thiazol-2- yl]propionamide ,

N- [ 4- ( 4-methoxyphenyl ) -5- 4-pyridyl ) - 1 , 3-thiazol-2-yl]

2-methylpropionamide ,

N- [ 4- ( 4-methoxyphenyl ) -5- 4-pyridyl ) -1 , 3-thiazol-2- yl]butyramide ,

N- [ 4- ( 4-methoxyphenyl ) -5- 4-pyridyl) -1, 3-thiazol-2- yl]benzamide,

N- [4- (4-methoxyphenyl) -5- 4-pyridyl) -1,3-thiazol-2- yl]nicotinamide ,

N- [4- (4-methoxyphenyl) -5- 4-pyridyl) -1 , 3-thiazol-2-yl]

N¹ -ethylurea,

N- [ 4- ( 4-methoxyphenyl ) -5- 4-pyridyl ) -1 , 3-thiazol-2-yl ]

N ' -propylurea,

4- (4-methoxyphenyl) -2- ( 2-oxoimidazolidin-l-yl) -5- ( 4- pyridyl) -1, 3-thiazole,

4- ( 4-methoxyphenyl) -2- ( 2-oxo-2 , 3-dihydro-lH-imidazol-l- yl) -5- ( 4-pyridyl) -1 , 3-thiazole,

4-(4-methoxyphenyl) -2- [2-oxotetrahydro-l(2H) - pyrimidinyl) -5- (4-pyridyl) -1, 3-thiazole,

4- ( 4-methoxyphenyl ) -2- ( 2-oxopyrrolidin- 1-yl ) - 5- ( 4- pyridyl) -1 , 3-thiazole,

N- [ 4- ( 4-ethylphenyl ) - 5- ( 4-pyridyl ) - 1 , 3-thiazol-2- yl] acetamide ,

N- [ 4- ( 4-ethylphenyl ) -5- ( 4-pyridyl ) - 1 , 3-thiazol-2- yl ]propionamide ,

N-[4-[4-(l,l-dimethylethyl )phenyl ] -5- ι ( 3-pyridyl) -1,3- thiazol-2-yl] acetamide,

N- [ 4- [ 4- ( 1 , 1-dimethylethyl )phenyl ] -5• (4-pyridyl)-l,3- thiazol-2-yl] acetamide ,

N- [ 4- [4- ( 1 , 1-dimethylethyl)phenyl] -5- ( 4-pyridyl) -1,3- thiazol-2-yl]propionamide , N- [ 4- [ 4- ( 1 , 1-dimethylethyl)phenyl] -5- (ι 4-pyridyl) -1,3- thiazol-2-yl] -2-methylpropionamide ,

N-[4-[4-(l,l- imethylethyl )phenyl ] -5- ι(4-pyridyl)-l,3- thiazol-2-yl ] butyramide ,

N-[4-[4-(l,l- imethylethyl)phenyl ] -5- ι( 4-pyridyl ) - 1 , 3- thiazol-2-yl]benzamide,

N-[4-[4-(l,l-dimethylethyl)phenyl ] (4-pyridyl)-l,3- thiazol-2-yl ]nicotinamide ,

N-[4-[4-(l,l-dimethylethyl)phenyl] ( 4-pyridyl) -1,3- thiazol-2-yl] -N' -ethylurea, N-[4-[4-(l,l- imethylethyl)phenyl ] -5- ι(4-pyridyl)-l,3- thiazol-2-yl] -N' -propylurea,

4- [4- ( 1, 1- imethylethyl)phenyl] -2- ( 2-oxoimidazolidin-l- yl) -5- (4-pyridyl) -1 , 3-thiazole,

4- [ 4- ( 1 , 1- imethylethyl)phenyl] -2- ( 2-oxo-2,3-dihydro- lH-imidazol-1-yl) -5- ( 4-pyridyl) -1 , 3-thiazole,

4- [4- ( 1, 1- imethylethyl)phenyl] -2- [ 2-oxotetrahydro-

1(2H)-pyrimidinyl] -5- ( 4-pyridyl) -1 , 3-thiazole,

4- [ 4- ( 1 , 1- imethylethyl)phenyl ] -2- ( 2-oxopyrrolidin- 1- yl) -5- (4-pyridyl) -1,3-thiazole, N-[4-(3,5-dimethylphenyl ) -5- ( 3-pyridyl ) - 1 , 3-thiazol-2- yl] acetamide,

N- [ 4- ( 3 , 5- imethylphenyl) - 5- ( 4-pyridyl) -1 , 3-thiazol-2- yl] acetamide,

N- [ 4- ( 3 , 5-dimethylphenyl ) -5- ( 4-pyridyl ) - 1 , 3-thiazol-2- yl]propionamide ,

N- [ 4- ( 3 , 5-dimethylphenyl ) -5- ( 4-pyridyl ) - 1 , 3-thiazol-2- yl] -2-methylpropionamide ,

N- [ 4- ( 3 , 5-dimethylphenyl) -5- ( 4-pyridyl) -1 , 3-thiazol-2- yl]butyramide ,

N- [ 4- ( 3 , 5-dimethylphenyl) -5- ( 4-pyridyl) -1 , 3-thiazol-2- yl]benzamide,

N- [4- (3, 5-dimethylphenyl) -5- (4-pyridyl)- 1,3-thiazol-2- yl]nicotinamide ,

N- [ 4- ( 3 , 5-dimethylphenyl ) -5- ( 4-pyridyl ) - 1 , 3-thiazol-2- yl] -N' -ethylurea, N- [ 4- ( 3 , 5-dimethylphenyl) -5- ( 4-pyridyl) -1 , 3-thiazol-2- yl ] -N ' -propylurea,

4- (3, 5-dimethylphenyl) -2- ( 2-oxoimidazolidin-l-yl) -5- (4- pyridyl ) - 1 , 3-thiazole ,

4- ( 3 , 5-dimethylphenyl) -2- ( 2-oxo-2,3-dihydro-1H- imidazol-1-yl) -5- ( 4-pyridyl) -1 , 3-thiazole,

4- ( 3 , 5-dimethylphenyl) -2- [ 2-oxotetrahydro-1 ( 2H) - pyrimidinyl] -5- ( 4-pyridyl) - 1 , 3-thiazole ,

4- (3, 5-dimethylphenyl) -2- ( 2-oxopyrrolidin-l-yl) -5- (4- pyridyl) - 1 , 3-thiazole , N-[5-(4-pyridyl ) -4- ( 4-trifluoromethylphenyl ) - 1 , 3- thiazol-2-yl] acetamide ,

N- [5- (4-pyridyl) -4- ( 4-trifluoromethylphenyl) -1,3- thiazol-2-yl]propionamide ,

N- [5- (4-pyridyl) -4- ( 4-trifluoromethylphenyl) -1,3- thiazol-2-yl] -2-methylpropionamide,

N- [5- (4-pyridyl) -4- ( 4-trifluoromethylphenyl) -1,3- thiazol-2-yl ]benzamide ,

N- [ 5- ( 4-pyridyl) -4- ( 4-trifluoromethylphenyl) -1,3- thiazol-2-yl]nicotinamide , N-[5-(4-pyridyl ) -4- ( 4-trifluoromethylphenyl ) - 1 , 3- thiazol-2-yl] -N' -ethylurea,

N- [5- ( 4-pyridyl) -4- ( 4-trifluoromethylphenyl) -1,3- thiazol-2-yl ] -N¹ -propylurea, salts thereof, and so forth.

In compound (la), compound (lb) is novel compound. The "aromatic heterocyclic group" of the "aromatic heterocyclic group which may be substituted" for R -^a includes , for example , a monovalent group formed by removing an optional hydrogen atom from a 5- to 14- membered preferably 5- to 10-membered (monocyclic, bicyclic or tricyclic) aromatic heterocyclic ring containing 1 to 4 hetero atoms of 1 or 2 species selected from the group consisting of nitrogen, sulfur and oxygen atoms in addition to carbon atoms , etc . Concretely mentioned are a monovalent group formed by removing an optional hydrogen atom from an aromatic heterocyclic ring such as thiophene, benzo[b] thiophene, benzo[b] furan, benzimidazole, benzoxazole, benzothiazole, benzisothiazole, naphthof 2 , 3-b] thiophene, furan, pyrrole, imidazole, pyrazole, pyridine, pyrazine, pyrimidine, pyridazine, indole, IH-indazole, purine, 4H-quinolidine, isoquinoline, quinoline, phthalazine, naphthyridine , quinoxaline, quinazoline, cinnoline, carbazole, β-carboline, phenanthridine , acridine, phenazine, isothiazole, phenothiazine, isoxazole, furazan, phenoxazine, etc.; and a ring as formed through condensation of those rings , preferably a monocyclic ring, with one or more, preferably one or two aromatic rings (e.g., benzene ring, etc.), etc. The preferred example of the "aromatic heterocyclic group" is a 5- or 6-membered aromatic heterocyclic group which may be fused with one benzene ring. Concretely mentioned are 2-thienyl, 3-thienyl, 2-furyl, 3-furyl, 2-pyridyl, 3-pyridyl, 4-pyridyl, 2- quinolyl, 3-quinolyl, 4-quinolyl, 5-quinolyl, 8- quinolyl, 1-isoquinolyl, 3-isoquinolyl, 4-isoquinolyl, 5-isoquinolyl, pyrazinyl, 2-pyrimidinyl, 4-pyrimidinyl, 3-pyrrolyl, 2-imidazolyl, 3-pyridazinyl, 3-isothiazolyl, 3-isoxazolyl, 1-indolyl, 2-indolyl, 3-indolyl, 2- benzothiazolyl, 2-benzo[b] thienyl, 3-benzo[b] thienyl, 2-benzo[b]furanyl, 3-benzo[b]furanyl, etc. More preferred are 2-thienyl, 3-thienyl, 2-pyridyl, 3- pyridyl, 4-pyridyl, 2-quinolyl, 3-quinolyl, 1- isoquinolyl, 1-indolyl, 2-benzothiazolyl, etc.

The "substituents" of the "aromatic heterocyclic group which may be substituted" and their number are the same as those mentioned above for the "substituents" of the "hydrocarbon group which may be substituted" for R⁵.

The "amino" of the "amino which may be substituted by substituent (s) selected from the group consisting of a substituted carbonyl and a hydrocarbon group which may be substituted" for R^la includes an amino which may be substituted by 1 or 2 substituents selected from the group consisting of a substituted carbonyl and a hydrocarbon group which may be substituted. When the number of substituents is two, those substituents may be the same as or different from one another.

The "substituted carbonyl" of the "amino which may be substituted by substituent (s) selected from the group consisting of a substituted carbonyl and a hydrocarbon group which may be substituted" includes, for example, a group of the formula: -(C=0)-R^5a,

-(C=0)-OR⁵ or -(C=0)-NR⁵ R^6a wherein R^5a represents a hydrogen atom, a hydrocarbon group which may be substituted or a heterocyclic group which may be substituted, and R^6a represents a hydrogen atom or a C₁_₆ alkyl.

The "hydrocarbon group which may be substituted" and the "heterocyclic group which may be substituted" for R^5a include, for example, the "hydrocarbon group which may be substituted" and the "heterocyclic group which may be substituted" for R⁵ above, respectively.

The "C^.g alkyl" for R^6a includes, for example. the "C₁_₆ alkyl" for R⁶ above. The examples of the "substituted carbonyl" are formyl, carboxy, C-^g alkyl-carbonyl (e.g., acetyl, propionyl, etc.), C₃_g cycloalkyl-carbonyl (e.g., cyclopropylcarbonyl , cyclopentylcarbonyl , cyclohexylcarbonyl , etc.), C-^.g alkoxy-carbonyl (e.g., methoxycarbonyl, ethoxycarbonyl, propoxycarbonyl, tert- butoxycarbonyl , etc.), Cg_₁₄ aryl-carbonyl (e.g., benzoyl, 1-naphthoyl, 2-naphthoyl, etc.), C₇_₁₆ aralkyl-carbonyl (e.g., phenylacetyl , 3-phenylpropionyl, etc.), Cg_₁₄ aryloxy-carbonyl (e.g., phenoxycarbonyl, etc.), C₇_₁₆ aralkyloxy-carbonyl (e.g., benzyloxycarbonyl, phenethyloxycarbonyl , etc.), 5- or 6-membered heterocycle carbonyl (e.g., nicotinoyl, isonicotinoyl, thenoyl, furoyl, morpholinocarbonyl , thiomorpholinocarbonyl , piperazin-1-ylcarbonyl, pyrrolidin-1-ylcarbonyl, etc.), carbamoyl, mono-C_]__g alkyl-carbamoyl (e.g. , methylcarbamoyl , ethylcarbamoyl , etc.), di-C^.g alkyl-carbamoyl (e.g., dimethylcarbamoyl, diethylcarbamoyl , ethylmethylcarbamoyl , etc.), C₆_₁₄ aryl-carbamoyl (e.g., phenylcarbamoyl , 1- naphthylcarbamoyl , 2-naphthylcarbamoyl, etc.), 5- or 6- membered heterocycle carbamoyl (e.g., 2- pyridylcarbamoyl , 3-pyridylcarbamoyl , 4- pyridylcarbamoyl , 2-thienylcarbamoyl, 3- thienylcarbamoyl , etc.), etc.

The "hydrocarbon group which may be substituted" of the "amino which may be substituted by substituent (s) selected from the group consisting of a substituted carbonyl and a hydrocarbon group which may be substituted" for R^la includes, for example, the

"hydrocarbon group which may be substituted" for R⁵. The "cyclic amino which may be substituted" for

R^la includes, for example, the "cyclic amino which may be substituted" described in the "amino which may be substituted" for R- .

R^l is preferably an amino which may be substituted by substituent (s) selected from the group consisting of a substituted carbonyl and a hydrocarbon group which may be substituted.

The "aromatic hydrocarbon group which may be substituted" for R^2a includes, for example, the "aromatic hydrocarbon group which may be substituted" for R² or R³ above. The "pyridyl which may be substituted" for R^3a includes, for example, the "pyridyl which may be substituted" which the above compound (I) has.

Preferred example of compound ( lb ) is a compound wherein R^la is an amino which may be substituted by 1 or 2 substituents selected from the group consisting of C^.g alkyl, C-^.g alky1-carbonyl , Cg_₁₄ aryl-carbonyl and C^. g alkyl-carbamoyl ;

R^2a is a phenyl which may be substituted by 1 to 3 substituents selected from the group consisting of halogen atoms, optionally halogenated C^.g alkyl and optionally halogenated C^g alkoxy; and

R^3a is a pyridyl.

The examples of compound (lb) are N-methyl[5-phenyl-4-(3-pyridyl) -1, 3-thiazol-2-yl] amine,

[5-phenyl-4- ( 3-pyridyl) thiazol-2-yl] amine,

N- [ 5-phenyl-4- ( 3-pyridyl) thiazol-2-yl]acetoamide,

N-[5-[4-(l,l-dimethylethyl )phenyl ] -4- ( 4-pyridyl) - 1 , 3- thiazol-2-yl] acetamide , N-[5-[4-(l,l-dimethylethyl ) phenyl ] -4- ( 4-pyridyl) -1 , 3- thiazol-2-yl]propionamide ,

N-[5-[4-(l,l-dimethylethyl)phenyl]-4-(4-ρyridyl)-l,3- thiazol-2-yl ]nicotinamide , N- [ 5- ( 3 , 5-dimethylphenyl) -4- ( 4-pyridyl) -1 , 3-thiazol-2- yl]acetamide,

N- [ 5- ( 3 , 5-dimethylphenyl) -4- ( 4-pyridyl) -1 , 3-thiazol-2- yl]propionamide,

N- [ 5- ( 3 , 5-dimethylphenyl) -4- ( 4-pyridyl) -1 , 3-thiazol-2- yl]nicotinamide, salts thereof, and so forth.

A novel compound of the formula:

wherein R^lD represents a hydrogen atom, a hydrocarbon group which may be substituted, a heterocyclic group which may be substituted, an amino which may be substituted or an acyl;

_R ^2b represents a N-oxidized pyridyl which may be substituted; and

R^3b represents a hydrogen atom, a pyridyl which may be substituted or an aromatic hydrocarbon group which may be substituted; or a salt thereof, [hereinafter sometimes referred to briefly as compound (lc)] is also within a scope of compound (la).

The "hydrocarbon group which may be substituted" , the "heterocyclic group which may be substituted" , the "amino which may be substituted" and the "acyl" for

R^lD include, for example, the "hydrocarbon group which may be substituted" , the "heterocyclic group which may be substituted", the "amino which may be substituted" and the "acyl" for R¹ above, respectively.

R^lD is preferably an amino which may be substituted. More preferred is an amino which may be substituted by 1 or 2 acyl of the formula: -(C=0)-R⁵, -

(C=0)-OR⁵, -(C=0)-NR⁵R⁶, -(C=S)-NHR⁵ or -S0₂-R⁷ (more preferably, -(C=0)-R⁵ or - (C=0) -NR⁵R⁶) wherein each symbol is as defined above.

The "substituents" of the "N-oxidized pyridyl which may be substituted" are the same as those mentioned above for the "substituents" of the "hydrocarbon group which may be substituted" for R⁵ above. The "N-oxidized pyridyl" may have 1 to 4, preferably 1 to 3 substituents as mentioned above at possible positions of the pyridyl and, when the number of substituents is two or more, those substituents may be the same as or different from one another.

The "pyridyl which may be substituted" and the "aromatic hydrocarbon group which may be substituted" for R^3t> include, for example, the "pyridyl which may be substituted" and the "aromatic hydrocarbon group which may be substituted" for R³ above, respectively.

R^3D is preferably a C₆_₁₄ (preferably Cg_₁₀) aryl which may be substituted.

Preferred example of compound (lc) is a compound wherein R^lb is an amino which may be substituted by 1 or 2 acyl of the formula: -(C=0)-R⁵ or -(C=0)-NR⁵R⁶ wherein each symbol is as defined above;

R^2b is a N-oxidized pyridyl which may be substituted by 1 to 3 C^g alkyl; and R^3b is a Cg_₁₀ aryl which may be substituted by 1 to 5 substituents selected from the group consisting of halogen atoms, optionally halogenated C^_ alkyl, optionally halogenated C-^.g alkoxy and carboxy.

The examples of compound (lc) are 3- [ 2-acetylamino-4- ( 4-methoxyphenyl) -1 , 3-thiazol-5- yl]pyridine 1-oxide,

4- [2-acetylamino-4- (4-methoxyphenyl) -1 , 3-thiazol-5- yl]pyridine 1-oxide. 4- [ 4- ( 4-methoxyphenyl) -2-propionylamino-1,3-thiazol-5- yl]pyridine 1-oxide,

4- [ 4- ( 4-methoxyphenyl ) -2- ( 2-methylpropionyl) amino-1,3- thiazol-5-yl]pyridine 1-oxide, 4- [ 2-butyrylamino-4- ( 4-methoxyphenyl) -1 , 3-thiazol-5- yl]pyridine 1-oxide,

4- [ 2-benzoylamino-4- ( 4-methoxyphenyl) -1 , 3-thiazol-5- yl] yridine 1-oxide,

4- [ 4- ( 4-methoxyphenyl) -2-nicotinoylamino-1,3-thiazol-5- yl]pyridine 1-oxide,

4- [ 2- (N ' -ethylureido ) -4- ( 4-methoxyphenyl ) -1 , 3-thiazol-

5-yl]pyridine 1-oxide,

4- [ 4- (4-methoxyphenyl) -2-(N' -propylureido) -1 , 3-thiazol-

5-yl] yridine 1-oxide, 4- [ 2-acetylamino-4- ( 4-ethylphenyl) -1 , 3-thiazol-5- yl]pyridine 1-oxide,

4- [4- (4-ethylphenyl) -2-propionylamino-1 , 3-thiazol-5- yl]pyridine 1-oxide,

3- [2-acetylamino-4- [4-(l, 1-dimethylethyl)phenyl] -1,3- thiazol-5-yl]pyridine 1-oxide,

4- [2-acetylamino-4- [4- (1, 1-dimethylethyl)phenyl] -1,3- thiazol- 5-yl]pyridine 1-oxide,

4-[4-[4-(l,l-dimethylethyl)phenyl ] -2-propionylamino-

1,3-thiazol-5-yl] yridine 1-oxide , 4-[4-[4-(l,l-dimethylethyl)phenyl]-2-(2- methylpropionyl ) amino- 1 , 3-thiazol-5-yl]pyridine 1-oxide,

4- [2-butyrylamino-4- [4-(l, 1-dimethylethyl)phenyl] -1,3- thiazol-5-yl]pyridine 1-oxide,

4- [2-benzoylamino-4- [4- (1, 1-dimethylethyl)phenyl] -1,3- thiazol-5-yl]pyridine 1-oxide,

4- [4- [4- ( 1 , 1-dimethylethyl)phenyl] -2-nicotinoylamino-

1,3-thiazol-5-yl]pyridine 1-oxide ,

4-[4-[4-(l,l-dimethylethyl )phenyl ] -2- (N ' -ethylureido ) -

1,3-thiazol-5-yl ]pyridine 1-oxide , 4-[4-[4-(l,l-dimethylethyl )phenyl ] -2- (N ' -propylureido) -

1, 3-thiazol-5-yl]pyridine 1-oxide, 3- [ 2-acetylamino-4- ( 3 , 5-dimethylphenyl) -1 , 3-thiazol-5- yl]pyridine 1-oxide,

4- [2-acetylamino-4- (3 , 5-dimethylphenyl) -1, 3-thiazol-5- yl] pyridine 1-oxide, 4- [ 4- ( 3 , 5-dimethylphenyl) -2-propionylamino- 1 , 3-thiazol-

5-yl]pyridine 1-oxide,

4- [ 4- ( 3 , 5-dimethylphenyl ) -2- ( 2-methylpropionyl)amino-

1,3-thiazol-5-yl ]pyridine 1-oxide ,

4- [ 2-butyrylamino-4- ( 3 , 5-dimethylphenyl ) - 1 , 3-thiazol-5- yl]pyridine 1-oxide,

4- [ 2-benzoylamino-4- ( 3 , 5-dimethylphenyl ) -1 , 3-thiazol-5- y1] pyridine 1-oxide ,

4- [4- (3, 5-dimethylphenyl) -2-nicotinoylamino-1 , 3- thiazol-5-yl]pyridine 1-oxide, 4-[4-(3,5-dimethylphenyl)-2-(N' -ethylureido) -1 , 3- thiazol-5-yl]pyridine 1-oxide,

4- [ 4- ( 3 , 5-dimethylphenyl ) -2- (N ' -propylureido ) -1 , 3- thiazol-5-yl]pyridine 1-oxide,

4- [ 2-acetylamino-4- ( 4-trifluoromethylphenyl ) - 1 , 3- thiazol-5-yl]pyridine 1-oxide,

4- [ 2-propionylamino-4- ( 4-trifluoromethylphenyl) - 1 , 3- thiazol-5-yl]pyridine 1-oxide,

4- [2- (2-methylpropionyl) amino-4- (4- trifluoromethylphenyl) -1 , 3-thiazol-5-yl ]pyridine 1- oxide,

4- [ 2-butyrylamino-4- ( 4-trifluoromethylphenyl ) -1 , 3- thiazol-5-yl]pyridine 1-oxide,

4- [ 2-benzoylamino-4- ( 4-trifluoromethylphenyl ) - 1 , 3- thiazol-5-yl]pyridine 1-oxide, 4- [ 2-nicotionylamino-4- ( 4-trifluoromethylphenyl) - 1 , 3- thiazol-5-yl] pyridine 1-oxide,

4- [ 2- (N ' -ethylureido ) -4- ( 4-trifluoromethylphenyl ) - 1 , 3- thiazol-5-yl]pyridine 1-oxide,

4- [2-(N* -propylureido) -4- ( 4-trifluoromethylphenyl) -1,3- thiazol-5-yl]pyridine 1-oxide, and so forth. Salts of compound (I), compound (la), compound (lb) or compound (lc) include, for example, metal salts, ammonium salts, salts with organic bases, salts with inorganic acids, salts with organic acids, salts with basic or acidic amino acids, etc. Preferred examples of metal salts include alkali metal salts such as sodium salts, potassium salts; alkaline earth metal salts such as calcium salts, magnesium salts, barium salts; aluminium salts, etc. Preferred examples of salts with organic bases include salts with trimethylamine, triethylamine, pyridine, picoline, 2,6- lutidine, ethanolamine, diethanolamine , triethanolamine, cyclohexylamine, dicyclohexylamine, N,N'- dibenzylethylenediamine, etc. Preferred examples of salts with inorganic acids include hydrochlorides , hydrobromides , nitrates, sulfates, phosphates, etc. Preferred examples of salts with organic acids include formates , acetates , trifluoroacetates , fumarates , oxalates , tartrates, maleates, citrates, succinates, malates, methanesulfonates , benzenesulfonates, p- toluenesulfonates, etc. Preferred examples of salts with basic amino acids include salts with arginine, lysine, ornithine, etc. Preferred examples of salts with acidic amino acids include aspartates , glutamates , etc.

Among others , more preferred are pharmaceutically acceptable salts. For example, for the compound having an acidic functional group in the molecule, mentioned are their inorganic salts , such as alkali metal salts (e.g., sodium salts, potassium salts, etc.), and alkaline earth metal salts (e.g., calcium salts, magnesium salts, barium salts, etc.), ammonium salts, etc.; and for the compound having a basic functional group in the molecule, mentioned are their inorganic salts such as hydrobromides, nitrates, sulfates, phosphates, etc., and organic salts such as acetates. maleates , fumarates , succinates , citrates , tartrates , methanesulfonates, p-toluenesulfonates, etc.

Process for producing compound (I) (including compounds (la), (lb) and (lc)) is mentioned below.

Compound ( I ) can be produced in any per se known manner, for example, according to the methods of the following processes 1 to 3 or analogous methods thereto as well as the methods disclosed in WO 95/13067 or analogous methods thereto in case that compound (I) is 1,3-oxazole compounds, the methods disclosed in USP 3,940,486, WO 88/01169, WO 93/14081, WO 95/02591, WO 97/12876 or analogous methods thereto in case that compound (I) is 1, 3-imidazole compounds, and the methods disclosed in JP-A-60-58981, JP-A-61-10580 , JP- A-7-503023, WO 93/15071, DE-A-3601411 , JP-A-5-70446 or analogous methods thereto in case that compound ( I ) is 1,3-thiazole.

Each symbol in the compounds in the following processes 1 to 3 is same as defined above. The compounds described in the following processes include their salts. For their salts, for example, referred to are the same as the salts of compound (I).

Process 1

3 8

R COR

R²-C ₁H-COR³

Hal

(IX)

( la )

Compounds (II), (III), (V), (VII), (XI), (XIII) and (XIV) may be purchased from commercial sources if they are available on the market or can be produced in any per se known manner.

Compound (IV) is produced by subjecting compound (II) to condensation with compound (III) in the presence of a base. In compound (III), R⁸ represents, for example, (i) ~ι__β alkoxy (e.g., methoxy, ethoxy, etc.), (ii) di-C-^g alkylamino (e.g. , dimethylamino, diethylamino , etc . ) , (iii) N-C₆_₁₀ aryl-N-C-L_g alkylamino (e.g., N-phenyl-N- methylamino, etc.), (iv) 3- to 7-membered cyclic amino (e.g., pyrrolidino, morpholino, methylaziridin-1-yl, etc.) which may be substituted by

g alkyl, etc. The amount of compound (III) to be used is 0.5 to 3.0 mols or so, preferably 0.8 to 2.0 mols or so, relative to one mol of compound (II).

The amount of the base to be used is 1.0 to 30 mols or so, preferably 1.0 to 10 mols or so, relative to one mol of compound (II).

The "base" includes, for example, basic salts such as sodium carbonate, potassium carbonate, cesium carbonate, etc. ; inorganic bases such as sodium hydroxide, potassium hydroxide, etc.; aromatic amines such as pyridine, lutidine, etc.; tertiary amines such as triethylamine, tripropylamine, tributylamine , cyclohexyldimethylamine , 4-dimethylaminopyridine, N,N- dimethylaniline, N-methylpiperidine, N- methylpyrrolidine, N-methylmorpholine, etc.; alkali metal hydrides such as sodium hydride, potassium hydride , etc. ; metal amides such as sodium amide, lithium diisopropylamide, lithium hexamethyldisilazide, etc.; metal alkoxides such as sodium methoxide, sodium ethoxide, potassium tert-butoxide, etc.

This reaction is advantageously carried out in the absence of a solvent or in an inert solvent . There is no particular limitation on the kind of solvent that can be used unless the reaction is interfered with. Preferred are halogenated hydrocarbons, aliphatic hydrocarbons, aromatic hydrocarbons, ethers, amides, alcohols, water, and mixtures of those solvents.

The reaction temperature is generally -5 to 200 °C or so, preferably 5 to 150 °C or so. The reaction time is generally about 5 minutes to 72 hours, preferably about 0.5 to 30 hours.

The product as produced in the manner mentioned above may be applied to the next reaction while it is still crude in the reaction mixture, or may be isolated from the reaction mixture in any ordinary manner. This can be easily purified through separation means such as recrystallization, distillation, chromatography and the like.

Compound (VIII) is produced by treating compound (IV) with an acid.

The amount of the acid to be used is 1.0 to 100 mols or so, preferably 1.0 to 30 mols or so, relative to one mol of compound (IV).

The "acids" include, for example, mineral acids such as hydrochloric acid, hydrobromic acid, sulfuric acid, etc.

This reaction is advantageously carried out in an inert solvent. There is no particular limitation on the kind of solvent that can be used unless the reaction is interfered with. Preferred are water, mixtures of water and amides , mixtures of water and alcohols, etc.

The reaction temperature is generally 20 to 200 ° C or so, preferably 60 to 150 °C or so. The reaction time is generally about 30 minutes to 72 hours, preferably about 1 to 30 hours.

Compound (VIII) is also produced by treating compound (V) with a base followed by subjecting the resultant compound (VI) to condensation with compound (VII).

In compound (VI), M represents, for example, an alkali metal such as lithium, sodium, potassium, etc.

In compound (VII), R⁹ represents, for example. same as those mentioned above for R° .

The amount of the base to be used is 1.0 to 30 mols or so, preferably 1.0 to 10 mols or so, relative to one mol of compound (V) . The "base" includes, for example, metal amides such as sodium amide, lithium diisopropylamide, lithium hexamethyldisilazide, etc.

This reaction is advantageously carried out in the absence of a solvent or in an inert solvent . There is no particular limitation on the kind of solvent that can be used unless the reaction is interfered with. Preferred are aliphatic hydrocarbons , aromatic hydrocarbons, ethers, and mixtures of those solvents.

The reaction temperature is generally -78 to 60 °C or so, preferably -78 to 20 ^CC or so. The reaction time is generally about 5 minutes to 24 hours, preferably about 0.5 to 3 hours .

Compound (IX) is produced by treating compound (VIII) with a halogen. If desired, this reaction is carried out in the presence of a base or a basic salt. The amount of the halogen to be used is 1.0 to 5.0 mols or so, preferably 1.0 to 2.0 mols or so, relative to one mol of compound (VIII).

The "halogen" includes, for example, bromine, chlorine, iodine, etc.

The amount of the base to be used is 1.0 to 10.0 mols or so, preferably 1.0 to 3.0 mols or so, relative to one mol of compound (VIII). The "base" includes, for example, aromatic amines such as pyridine, lutidine, etc.; tertiary amines such as triethylamine, tripropylamine , tributylamine , cyclohexyldimethylamine , 4-dimethylaminopyridine, N,N- dimethylaniline , N-methylpiperidine, N- methylpyrrolidine , N-methylmorpholine, etc.

The amount of the basic salt to be used is 1.0 to 10.0 mols or so, preferably 1.0 to 3.0 mols or so, relative to one mol of compound (VIII). The "basic salt" includes, for example, sodium carbonate, potassium carbonate, cesium carbonate, sodium hydrogencarbonate , sodium acetate, potassium acetate, etc.

This reaction is advantageously carried out in the absence of a solvent or in an inert solvent. There is no particular limitation on the kind of solvent that can be used unless the reaction is interfered with. Preferred are ethers , aromatic hydrocarbons , aliphatic hydrocarbons , amides , halogenated hydrocarbons , nitriles, sulfoxides , organic acids, aromatic amines and mixtures of those solvents.

The reaction temperature is -20 to 150 ° C or so, preferably 0 to 100 °C or so. The reaction time is generally 5 minutes to 24 hours, preferably about 10 minutes to 5 hours.

Compound (la) is produced by subjecting compound (IX) to condensation with compound (X). If desired. this reaction is carried out in the presence of a base or a basic salt.

In compound (IX), Hal represents halogens. Compound (X) may be purchased from commercial sources if they are available on the market or can be produced according to any per se known methods or analogous methods thereto as well as the methods disclosed in the following process 2.

The amount of compound (X) to be used is 0.5 to 3.0 mols or so, preferably 0.8 to 2.0 mols or so, relative to one mol of compound (IX).

The amount of the base to be used is 1.0 to 30 mols or so, preferably 1.0 to 10 mols or so, relative to one mol of compound (IX). The "base" includes, for example, basic salts such as sodium carbonate, potassium carbonate, cesium carbonate, sodium hydrogencarbonate , etc.; aromatic amines such as pyridine, lutidine, etc.; tertiary amines such as triethylamine, tripropylamine , tributylamine , cyclohexyldimethylamine , 4- dimethylaminopyridine , N,N-dimethylaniline, N- methylpiperidine , N-methylpyrrolidine, N- methylmorpholine , etc .

This reaction is advantageously carried out in the absence of a solvent or in an inert solvent. There is no particular limitation on the kind of solvent that can be used unless the reaction is interfered with. Preferred are halogenated hydrocarbons , aliphatic hydrocarbons , aromatic hydrocarbons , ethers , amides , alcohols, nitriles and mixtures of those solvents.

The reaction temperature is -5 to 200 °C or so, preferably 5 to 150 °C or so. The reaction time is generally 5 minutes to 72 hours, preferably about 0.5 to 30 hours. The product as produced in the manner mentioned above may be applied to the next reaction while it is still crude in the reaction mixture, or may be isolated from the reaction mixture in any ordinary manner. This can be easily purified through separation means such as recrystallization, distillation, chromatography and the like.

Process 2

R^1XH 10 II 11

R¹⁰CONCS R CONH-C-R

(XI) (XII)

Hydrolysis

R^XCONH₂ R -C-NH (XIV) P₄S₁₀ or (X)

Lawesson reagent

Compound (XII) is produced by subjecting compound (XI) to condensation with an amine of the formula: R-^H. R¹¹ represents the "amine which may be substituted" for R¹ above.

In compound (XI), R ,10 represents an alkoxy. The "alkoxy" includes, for example, a C^.g alkoxy such as methoxy, ethoxy, propoxy, isopropoxy, butoxy, etc.

The amount of the "amine" to be used is 1.0 to 30 mols or so, preferably 1.0 to 10 mols or so, relative to one mol of compound (XI).

This reaction is advantageously carried out in the absence of a solvent or in an inert solvent . There is no particular limitation on the kind of solvent that can be used unless the reaction is interfered with. Preferred are halogenated hydrocarbons , aliphatic hydrocarbons , aromatic hydrocarbons , ethers , amides , alcohols, nitriles, ketones and mixtures of those solvents.

The reaction temperature is -5 to 200 °C or so, preferably 5 to 120 °C or so. The reaction time is generally 5 minutes to 72 hours, preferably about 0.5 to 30 hours.

Compound (X) is produced by subjecting compound (XII) to hydrolysis using an acid or a base.

The amount of the "acid" or "base" to be used is 0.1 to 50 mols or so, preferably 1 to 20 mols or so, relative to one mol of compound (XII), respectively. The "acid" includes, for example, mineral acids such as hydrochloric acid, hydrobromic acid, sulfuric acid, etc; Lewis acids such as boron trichloride, boron tribromide, etc; thiols or sulfides in combination with Lewis acids; organic acids such as trifluoroacetic acid, p-toluenesulfonic acid, etc.

The "base" includes, for example, metal hydroxides such as sodium hydroxide, potassium hydroxide, barium hydroxide, etc.; metal alkoxides such as sodium methoxide, sodium ethoxide, potassium tert-butoxide, etc; organic bases such as triethylamine, imidazole, formamidine, etc .

This reaction is advantageously carried out in the absence of a solvent or in an inert solvent . There is no particular limitation on the kind of solvent that can be used unless the reaction is interfered with. Preferred are alcohols, ethers, aromatic hydrocarbons, aliphatic hydrocarbons, halogenated hydrocarbons, sulfoxides , water and mixtures of those solvents .

The reaction time is generally 10 minutes to 50 hours, preferably about 30 minutes to 12 hours. The reaction temperature is 0 to 200 ^βC or so, preferably 20 to 120 ° C or so.

Compound (X) is also produced by treating compound (XIII) with a hydrogen sulfide in the presence of a base.

The amount of the hydrogen sulfide to be used is 1 to 30 mols or so, relative to one mol of compound

(XIII) . The amount of the "base" to be used is 1.0 to 30 mols or so, preferably 1.0 to 10 mols or so, relative to one mol of compound (XIII).

The "base" includes, for example, aromatic amines such as pyridine, lutidine, etc.; tertiary amines such as triethylamine, tripropylamine , tributylamine, cyclohexyldimethylamine, 4-dimethylaminopyridine, N,N- dimethylaniline, N-methylpiperidine, N- methylpyrrolidine , N-methylmorpholine, etc.

This reaction is advantageously carried out in the absence of a solvent or in an inert solvent. There is no particular limitation on the kind of solvent that can be used unless the reaction is interfered with.

Preferred are halogenated hydrocarbons , aliphatic hydrocarbons , aromatic hydrocarbons , ethers , aromatic amines and mixtures of those solvents.

This reaction is carried out under atmospheric pressure or pressurized condition. The reaction temperature is -20 to 80 °C or so, preferably -10 to 30

°C or so. The reaction time is generally 5 minutes to 72 hours, preferably about 0.5 to 30 hours. The product as produced in the manner mentioned above may be applied to the next reaction while it is still crude in the reaction mixture, or may be isolated from the reaction mixture in any ordinary manner. This can be easily purified through separation means such as recrystallization, distillation, chromatography and the like.

Compound (X) is also produced by treating compound (XIV) with a phosphorous pentasulfide or Lawesson's reagent .

The amount of the "phosphorous pentasulfide" or "Lawesson's reagent" to be used is 0.5 to 10 mols or so, preferably 0.5 to 3 mols or so, relative to one mol of compound (XIV) .

This reaction is advantageously carried out in the absence of a solvent or in an inert solvent . There is no particular limitation on the kind of solvent that can be used unless the reaction is interfered with. Preferred are ethers, aromatic hydrocarbons, aliphatic hydrocarbons , halogenated hydrocarbons and mixtures of those solvents .

The reaction time is generally 10 minutes to 50 hours, preferably about 30 minutes to 12 hours. The reaction temperature is 0 to 150 °C or so, preferably 20 to 120 ° C or so.

The product (X) may be applied to the next reaction while it is still crude in the reaction mixture, or may be isolated from the reaction mixture in any ordinary manner. This can be easily purified through separation means such as recrystallization, distillation, chromatography and the like.

In case that compound (la) is an acylamino derivative, the desired product can be also obtained by subjecting the corresponded amine compound to any per se known acylation method.

For example, compound (la) wherein R¹ is an acylamino which may be substituted is produced by reacting a corresponding 2-thiazolyl amine with an acylating agent optionally in the presence of a base or an acid.

The amount of the "acylating agent" to be used is 1.0 to 5.0 mols or so, preferably 1.0 to 2.0 mols or so, relative to one mol of compound (la). The "acylating agent" includes, for example, carboxylic acid or a reactive derivative thereof (e.g., acid halides, acid anhydrides, esters, etc.) correspond to the desired product .

The amount of the "base" or "acid" to be used is 0.8 to 5.0 mols or so, preferably 1.0 to 2.0 mols or so, relative to one mol of compound (la).

The "base" includes, for example, triethylamine, pyridine, N,N-dimethylaminopyridine, etc.

The "acid" includes, for example, methanesulfonic acid, p-toluenesulfonic acid, camphor-sulfonic acid etc. This reaction is advantageously carried out in the absence of a solvent or in an inert solvent . There is no particular limitation on the kind of solvent that can be used unless the reaction is interfered with. Preferred are ethers, aromatic hydrocarbons, aliphatic hydrocarbons , amides , halogenated hydrocarbons , nitriles , sulfoxides , aromatic amines and mixtures of those solvents .

The reaction temperature is -20 to 150 ° C or so, preferably 0 to 100 °C or so. The reaction time is generally 5 minutes to 24 hours, preferably about 10 minutes to 5 hours .

The product may be applied to the next reaction while it is still crude in the reaction mixture, or may be isolated from the reaction mixture in any ordinary manner. This can be easily purified through separation means such as recrystallization, distillation, chromatography and the like.

Compound (lc) can be also produced according to the methods of the following process 3 or analogous methods thereto .

Process 3

(XV)

Compound (XV) can be produced according to any per se known methods or analogous methods thereto.

Compound (lc) is produced by treating compound (XV) with a peroxy acid.

In compound (XV) , R^2D represents a pyridyl which may be substituted. The "pyridyl which may be substituted" includes, for example, the "pyridyl which may be substituted" for R² above.

The amount of the "peroxy acid" to be used is 0.8 to 10 mols or so, preferably 1.0 to 3.0 mols or so, relative to one mol of compound (XV) .

The "peroxy acid" includes, for example, peracetic acid, trifluoroperacetic acid, m-chloroperbenzoic acid, etc.

Preferred are halogenated hydrocarbons , aliphatic hydrocarbons , aromatic hydrocarbons , organic acids , ethers, amides, sulfoxides, alcohols, nitriles, ketones and mixtures of those solvents . The reaction temperature is -20 to 130 ° C or so, preferably 0 to 100 °C or so. The reaction time is generally 5 minutes to 72 hours, preferably about 0.5 to 12 hours.

Compound (lc) is also produced by treating compound (XV) with a hydrogen peroxide or an alkylhydroperoxide , in the presence of a base, an acid or a metal oxides if desired. The amount of the "hydrogen peroxide" or the

"alkylhydroperoxide" to be used is 0.8 to 10 mols or so, preferably 1.0 to 3.0 mols or so, relative to one mol of compound (XV) .

The "alkylhydroperoxide" includes, for example, tert-butylhydroperoxide, cumene hydroperoxide , etc.

The amount of the "base", the "acid" or the "metal oxides" to be used is 0.1 to 30 mols or so, preferably 0.8 to 5 mols or so, relative to one mol of compound (XV). The "base" includes, for example, inorganic bases such as sodium hydroxide and potassium hydroxide, basic salts such as sodium carbonate and potassium carbonate, etc.

The "acid" includes, for example, mineral acids such as hydrochloric acid, sulfuric acid and perchloric acid, Lewis acids such as boron trifluoride and aluminum (III) chloride, titanium(IV) chloride, organic acids such as formic acid and acetic acid, etc.

The "metal oxides" includes, for example, vanadium oxide (V₂0₅), osmium oxide (Os0₄) , tungsten oxide (W0₃), molybdenum oxide (Mo0₃), selenium oxide (Se0₂), chromium oxide (Cr0₃), etc.

This reaction is advantageously carried out in the absence of a solvent or in an inert solvent. There is no particular limitation on the kind of solvent that can be used unless the reaction is interfered with. Preferred are halogenated hydrocarbons , aliphatic hydrocarbons , aromatic hydrocarbons , organic acids , ethers, amides, sulfoxides, alcohols, nitriles, ketones and mixtures of those solvents .

The reaction temperature is -20 to 130 "C or so, preferably 0 to 100 °C or so. The reaction time is generally 5 minutes to 72 hours, preferably about 0.5 to 12 hours. The product may be applied to the next reaction while it is still crude in the reaction mixture, or may be isolated from the reaction mixture in any ordinary manner. This can be easily purified through separation means such as recrystallization, distillation, chromatography and the like.

In the above-mentioned reactions where the starting compounds are substituted by any of amino, carboxy or hydroxy, those groups may be protected by ordinary protective groups which are generally used in peptide chemistry. The protective groups may be removed after the reaction to give the disired products.

The amino-protecting group includes, for example, formyl, C-^.g alkyl-carbonyl (e.g., acetyl, propionyl, etc.) which may be substituted, phenylcarbonyl which may be substituted, C-^g alkoxy-carbonyl (e.g., methoxycarbonyl, ethoxycarbonyl, etc.) which may be substituted, phenyloxycarbonyl which may be substituted, ^c7-1₀ aralkyloxy-carbonyl (e.g., benzyloxycarbonyl, etc.) which may be substituted, trityl which may be substituted, phthaloyl which may be substituted, etc. These substituents include, for example, halogen atoms (e.g., fluoro, chloro, bromo, iodo, etc.), -^_ alkyl- carbonyl (e.g. , acetyl, propionyl , valeryl , etc . ) , nitro, etc. The number of those substituents is 1 to 3. The carboxy-protecting group includes, for example, C-L_g alkyl (e.g., methyl, ethyl, propyl, isopropyl, butyl, tert-butyl, etc.) which may be substituted, phenyl which may be substituted, trityl which may be substituted, silyl which may be substituted, etc.

These substituents includes, for example, halogen atoms (e.g., fluoro, chloro, bromo, iodo, etc.), formyl, C^_g alkyl-carbonyl (e.g. , acetyl, propionyl, butylcarbonyl, etc.), nitro, C_1-6 alkyl (e.g., methyl, ethyl, tert- butyl, etc.), Cg_₁₀ aryl (e.g., phenyl, naphthyl, etc.), etc. The number of those substituents is 1 to 3.

The hydroxy-protecting group includes, for example, C^_g alkyl (e.g., methyl, ethyl, propyl, isopropyl, butyl, tert-butyl, etc.) which may be substituted, phenyl which may be substituted, ^~η- aralkyl (e.g., benzyl, etc.) which may be substituted, formyl which may be substituted, C^.g alkyl-carbonyl (e.g., acetyl, propionyl, etc.) which may be substituted, phenyloxycarbonyl which may be substituted, ^~η - _{\ \} aralkyloxy-carbonyl (e.g., benzyloxycarbonyl, etc.) which may be substituted, tetrahydropyranyl which may be substituted, tetrahydrofuranyl which may be substituted, silyl which may be substituted, etc. Those substituents include, for example, halogen atoms (e.g., fluoro, chloro, bromo, iodo, etc.), C^_g alkyl

(e.g., methyl, ethyl, tert-butyl, etc.), ^~η - i_\ aralkyl

(e.g., benzyl, etc.), C₆_₁₀ aryl (e.g., phenyl, naphthyl, etc.), nitro, etc. The number of those substituents is 1 to 4. Those protective groups may be removed by any per se known methods or analogous methods thereto, such as methods using acids, bases, ultraviolet rays, hydrazine, phenylhydrazine, sodium N-methyldithiocarbamate, tetrabutylammonium fluoride, palladium acetate, etc.; and reduction, etc.

In any case, products formed in the reaction mixtures may be subjected to deprotection, acylation, alkylation, hydrogenation, oxidation, reduction, chain extension, substituents-exchange reaction and combined reactions thereof, to obtain compound (I). These methods include, for example, the methods described in "Shin Jikken Kagaku Kouza (New Edition of Lectures of Experimental Chemistry)" L4, 15_ (1977) edited by Maruzen .

The above "alcohols" include, for example, methanol, ethanol, propanol, isopropanol, tert-butanol, etc.

The above "ethers" include, for example, diethyl ether, diisopropyl ether, diphenyl ether, tetrahydrofuran, dioxane , 1,2-dimethoxyethane , etc.

The above "halogenated hydrocarbons" include, for example, dichloromethane, chloroform, 1,2- dichloroethane, carbon tetrachloride, etc.

The above "aliphatic hydrocarbons" include, for example, hexane , pentane , cyclohexane, etc .

The above "aromatic hydrocarbons" include, for example, benzene, toluene, xylene, chlorobenzene, etc. The above "aromatic amines" include, for example, pyridine, lutidine, quinoline, etc.

The above "amides" include, for example, N,N- dimethylformamide , N,N-dimethylacetamide, hexamethylphosphoric triamide, etc.

The above "ketones" include, for example, acetone, methyl ethyl ketone, etc.

The above "sulfoxides" include, for example, dimethylsulfoxide, etc. The above "nitriles" include, for example, acetonitrile, propionitrile, etc. The above "organic acids" include, for example, acetic acid, propionic acid, trifluoroacetic acid, etc.

Where the products are formed in their free form in the reaction, they may be converted into their salts in any ordinary manner. Where they are formed in the form of their salts , they may be converted into free compounds or other salts in any ordinary manner. The thus-obtained compound (I) may be isolated and purified from the reaction mixtures through any ordinary means of, for example, trans-solvation, concentration, solvent extraction, fractionation, crystallization, recrystallization, chromatography and the like.

Where compound (I), (la), (lb) or (lc) exists in the reaction mixtures in the form of its configurational isomers , diastereomers , conformers or the like, they may be optionally isolated into single isomers through the separation and isolation means mentioned above. Where compound (I), (la), (lb) or (lc) is in the form of its racemates , they may be resolved into S- and R-forms through any ordinary optical resolution.

Compound (I), (la), (lb) or (lc) includes stereoisomers, depending on the type of the substituents therein, and both single isomers and mixtures of different isomers are within the scope of the present invention.

Compounds (I), (la), (lb) and (lc) may be in any form of their hydrates and non-hydrates.

The agent (pharmaceutical composition) of the present invention comprising compound (I), (la), (lb) or (lc) shows a high affinity for adenosine receptor, especially for adenosine A₃ receptor, while having low toxicity and few side effects. The agent is useful as a safe medicine. The agent (pharmaceutical composition) of the present invention comprising compound (I), (la), (lb) or (lc) has a potent antagonistic activity on mammals (e.g., mouse, rat, hamster, rabbit, feline, canine, bovine, sheep, monkey, human, etc.), a good bioavailability on per os administration, a good metabolical stability, and therefore, it can be used for preventing and/or treating diseases that may be related to adenosine A₃ receptor, for example, asthma, allergosis, inflammation, Addison's disease, autoallergic hemolytic anemia, Crohn's disease, psoriasis, rheumatism, diabetes, and so on. Among others, preferred is for asthma, allergosis, etc. The agent (pharmaceutical composition) of the present invention comprising compound (I), (la), (lb) or (lc) has low toxicity, and therefore, compound (I), (la), (lb) or (lc) is, either directly as it is or after having been formulated into pharmaceutical compositions along with pharmaceutically acceptable carriers in any per se known manner, for example, into tablets (including sugar-coated tablets, film-coated tablets), powders, granules, capsules (including soft capsules), liquid preparations, injections, suppositories, sustained release preparations, etc., safely administered orally or parenterally (e.g., locally, rectally, intravenously, etc.). In the pharmaceutical composition of the present invention, the amount of compound (I), (la), (lb) or (lc) is from 0.01 to 100 % by weight or so of the total weight of the composition. The dose of the composition varies, depending on the subject to which the composition is administered, the administration route employed, the disorder of the subject, etc. For example, as an adenosine A₃ receptor antagonist , oral composition for treating asthma, its dose for adults (body weight ca.

60 kg) may be from 0.1 to 30 mg/kg of body weight or so. preferably from 1 to 20 mg/kg of body weight or so, in terms of the active ingredient of compound (I), (la), (lb) or (lc), and this may be administered once or several times a day. Any ordinary organic and inorganic carrier substances that are generally used in formulating medicines are usable as the carriers for formulating the pharmaceutical compositions of the present invention. For example, employable are ordinary excipients, lubricants, binders, disintegrators, etc. for formulating solid preparations; and solvents, solubilizers, suspending agents, isotonizing agents, buffers, soothing agents, etc. for formulating liquid preparations. If desired, further employable are other additives such as preservatives, antioxidants, colorants, sweeteners, adsorbents, wetting agents, etc.

The excipients include, for example, lactose, white sugar, D-mannitol, starch, corn starch, crystalline cellulose, light silicic anhydride, etc. The lubricants include, for example, magnesium stearate, calcium stearate, talc, colloidal silica, etc.

The binders include, for example, crystalline cellulose, white sugar, D-mannitol, dextrin, hydroxypropyl cellulose, hydroxypropylmethyl cellulose, polyvinyl pyrrolidone, starch, sucrose, gelatin, methyl cellulose, carboxymethyl cellulose sodium, etc.

The disintegrators include, for example, starch, carboxymethyl cellulose, carboxymethyl cellulose calcium, croscarmellose sodium, carboxymethyl starch sodium, L-hydroxypropyl cellulose, etc.

The solvents include, for example, water for injections, alcohol, propylene glycol, macrogol, sesame oil, corn oil, olive oil, etc.

The solubilizers include, for example, polyethylene glycol, propylene glycol, D-mannitol, benzyl benzoate, ethanol, trisaminomethane, cholesterol, triethanolamine, sodium carbonate, sodium citrate, etc.

The suspending agents include, for example, surfactants such as stearyl triethanolamine, sodium lauryl sulfate, lauryl aminopropionic acid, lecithin, benzalkonium chloride, benzethonium chloride, glycerin monostearate, etc.; hydrophilic polymers such as polyvinyl alcohol, polyvinyl pyrrolidone, carboxymethyl cellulose sodium, methyl cellulose, hydroxymethyl cellulose, hydroxyethyl cellulose, hydroxypropyl cellulose, etc.

The isotonizing agents include, for example, glucose, D-sorbitol, sodium chloride, glycerin, D- mannitol, etc. The buffers include, for example, liquid buffers of phosphates, acetates, carbonates, citrates, etc.

The soothing agents include, for example, benzyl alcohol, etc.

The preservatives include, for example, parahydroxybenzoates , chlorobutanol, benzyl alcohol, phenethyl alcohol, dehydroacetic acid, sorbic acid, etc.

The antioxidants include, for example, sulfites, ascorbic acid, etc.

BEST MODE FOR CARRYING OUT THE INVENTION

The invention will be described in more detail hereinunder, with reference to the following Reference Examples, Examples, Formulation Examples and Experimental Examples, which, however, are to concretely illustrate some embodiments of the invention and are not intended to restrict the scope of the invention. Various changes and modifications can be made within the range that does not deviate the scope of the invention. "Room temperature" as referred to in the following Reference Examples and Examples is meant to indicate a temperature falling between 10° C and 35° C. Unless otherwise specifically indicated, "%" is by weight. The yield indicates mol/mol %.

The meanings of the abbreviations used hereinunder are as follows: s : singlet d: doublet t : triplet q : quartet dd: double doublet ddd: double double doublet dt : double triplet br : broad

J: coupling constant Hz: Hertz

CDCI3 : deuterated chloroform

-"-H-NMR: proton nuclear magnetic resonance spectrum Me : methyl

Reference Example 1

1- ( 4-Methoxyphenyl ) -2- ( 3-pyridyl ) ethanone

To a stirred solution of diisopropylamine (33.2 mL) in dry tetrahydrofuran (300 mL) cooled at -78 °C, was added a solution of 1.6 M n-butyllithium in hexane (148 mL) dropwise. After addition, the resulting mixture was stirred for 10 min at the same temperature, followed by the addition of β-picoline (20 g) . The resulting mixture was allowed to warm up to -10 - 0 °C. After an additional 20 min stirring, a solution of ethyl p-anisate (19.4 g) in dry tetrahydrofuran (40 mL) was added. After addition the mixture was stirred for another 1 h at ambient temperature, and water (100 mL) was added to the mixture . The solvent was removed under reduced pressure and the oily product was extracted with ethyl acetate. The extracts were washed with water, dried, and concentrated under reduced pressure. The crystalline residue was recrystallized from ethyl acetate - isopropyl ether to afford the title compound (20.8 g, yield 85 %). mp 71-72 ^βC.

Reference Example 2

Using ethyl benzoate, ethyl 3, 4-dimethoxybenzoate, ethyl 3,4,5-trimethoxybenzoate, ethyl 4-

(methoxymethoxy)benzoate, ethyl 4-fluorobenzoate, ethyl 4-ethylbenzoate, ethyl 3, 4-methylenedioxybenzoate, methyl 5-indanecarboxylate, methyl 5,6, 7,8-tetrahydro-

2-naphthoic acid, methyl 1, 4-benzodioxane-6-carboxylate, and methyl 2-naphthoic acid instead of using ethyl p- anisate, the below Reference Example Compounds 2-1 to 2-11 were obtained in the same manner as described in the above Reference Example 1.

Reference Example Compound 2-1:

1-Phenyl-2- ( 3-pyridyl )ethanone mp 44.5-45.5°C. Reference Example Compound 2-2:

1- ( 3 , 4-Dimethoxyphenyl) -2- ( 3-pyridyl ) ethanone mp 114-115°C.

Reference Example Compound 2-3:

2- ( 3-Pyridyl) -1- ( 3 , 4 , 5-trimethoxyphenyl ) ethanone mp 104-105° C.

Reference Example Compound 2-4:

1- ( 4-Methoxymethoxyphenyl ) -2- ( 3-pyridyl ) ethanone mp 43-44° C.

Reference Example Compound 2-5: l-(4-Fluorophenyl) -2- ( 3-pyridyl)ethanone oil.

Reference Example Compound 2-6:

1- ( 4-Ethylphenyl ) -2- ( 3-pyridyl ) ethanone mp 80-81° C. Reference Example Compound 2-7:

1- ( 3 , 4-Methylenedioxyphenyl) -2- ( 3-pyridyl)ethanone mp 98 - 99° C .

Reference Example Compound 2-8: 1- ( 5-Indanyl) -2- ( 3-pyridyl ) ethanone mp 55-56° C. Reference Example Compound 2-9:

2- ( 3-Pyridyl)-l-(5,6,7,8-tetrahydro-2-naphthyl ) ethanone mp 65-66° C.

Reference Example Compound 2-10: 1- ( 1 , 4-Benzodioxan-6-yl ) -2- ( 3-pyridyl) ethanone mp 89-90° C.

Reference Example Compound 2-11:

1- ( 2-Naphtyl ) -2- ( 3-pyridyl )ethanone mp 69-70° C.

Reference Example 3

Using -picoline, γ-picoline, and 3,5-lutidine instead of using β-picoline, the below Reference

Example Compounds 3-1 to 3-5 were obtained in the same manner as described in the above Reference Example 2. Reference Example Compound 3-1:

1-Phenyl-2- ( 2-pyridyl ) ethanone mp 59-60° C.

Reference Example Compound 3-2:

1- ( 4-Methoxyphenyl) -2- ( 2-pyridyl) ethanone mp 77-78° C.

Reference Example Compound 3-3: l-Phenyl-2- ( 4-pyridyl) ethanone mp 109-110° C.

Reference Example Compound 3-4: 1- (4-Methoxyphenyl) -2- ( 4-pyridyl) ethanone mp 103-104°C.

Reference Example Compound 3-5:

2-(5-Methyl-3-pyridyl) -1-phenylethanone mp 53-54° C.

Reference Example 4 2-Cyano-2-phenyl- 1- (3-pyridyl) ethanone

To a solution of ethyl nicotinate (10 g) and phenylacetonitrile (5.1 g) in tert-butyl alcohol (30 mL), was added potassium tert-butoxide (6.4 g) , and the mixture was stirred at 100° C for 3 h. After cooling, the resulting mixture was dissolved in water and washed with isopropyl ether. The aqueous phase was adjusted to pH 7.0 with 2 N hydrochloric acid and extracted with ethyl acetate. The extracts were washed with water, dried, and the solvent was evaporated. The crystalline residue was recrystallized from ethyl acetate-isopropyl ether to obtain the title compound (6.0 g, yield 62 %). mp 148-149° C.

Reference Example 5

2-Phenyl-l- ( 3-pyridyl)ethanone

2-Cyano-2-phenyl- 1- ( 3-pyridyl) ethanone (5.0 g) was dissolved in 48 % hydrobromic acid (50 mL) and the solution was stirred at 140° C for 5 h. After the mixture was cooled, the mixture was neutralized with an aqueous saturated solution of sodium hydrogen carbonate and the product was extracted with ethyl acetate . The extracts were washed with water, dried, and the solvent was evaporated. The crystalline residue was recrystallized from isopropyl ether to obtain the title compound (3.9 g, yield 88 %). mp 61-62° C.

Reference Example 6 2-Bromo- 1- ( 4-methoxyphenyl) -2- (3-pyridyl) ethanone hydrobromide l-( 4-Methoxyphenyl) -2- (3-pyridyl) ethanone (6.85 g) was dissolved in acetic acid (36 mL), bromine (1.7 mL) was added to the solution and the resulting mixture was stirred at 80° C for 3 h. After the mixture was cooled with ice-water, the crude crystalline mass was collected by filtration. The crude crystalline was recrystallized from ethanol-ethyl ether to afford the title compound (10.4 g, yield 89 %). mp 188-195° C.

Reference Example 7

Using 1-phenyl-2- ( 3-pyridyl) ethanone, l-(3,4- dimethoxyphenyl ) -2- ( 3-pyridyl) ethanone, 2- (3-pyridyl) - 1- ( 3 , 4 , 5-trimethoxyphenyl ) ethanone , 1- ( 4- methoxymethoxyphenyl) -2- (3-pyridyl) ethanone, l-(4- fluorophenyl) -2- (3-pyridyl) ethanone, 1-phenyl-2- (2- pyridyl ) ethanone , 1- ( 4-methoxyphenyl) -2- ( 2- pyridyl ) ethanone , 1-phenyl-2- (4-pyridyl) ethanone, l-(4- methoxyphenyl ) -2- ( 4-pyridyl) ethanone, 2- ( 5-methyl-3- pyridyl) -1-phenylethanone, 1- (4-ethylphenyl) -2- (3- pyridyl ) ethanone , 1- ( 3 , 4-methylenedioxyphenyl) -2- ( 3- pyridyl ) ethanone , 1- (5-indanyl) -2- (3-pyridyl)ethanone, 2- ( 3-pyridyl )-l-(5,6,7,8-tetrahydro-2-naphthyl) ethanone , 1- ( 1 , 4-benzodioxan-6-yl) -2- ( 3-pyridyl ) ethanone , 1- ( 2- naphthyl) -2- (3-pyridyl) ethanone, 1- ( 4-methoxyphenyl) -2- (2-pyridyl) ethanone and 2-phenyl-l- ( 3-pyridyl) ethanone instead of using 1- (4-methoxyphenyl) -2- (3- pyridyl )ethanone , the below Reference Example Compounds 7-1 to 7-18 were obtained in the same manner as described in the above Reference Example 6. Reference Example Compound 7-1:

2-Bromo-1-phenyl-2- ( 3-pyridyl ) ethanone hydrobromide mp 208-215°C. Reference Example Compound 7-2: 2-Bromo-l- ( 3 , 4-dimethoxyphenyl) -2- ( 3-pyridyl) ethanone hydrobromide mp 191-193°C.

Reference Example Compound 7-3: 2-Bromo-2- ( 3-pyridyl ) - 1- ( 3 , 4 , 5- trimethoxyphenyl ) ethanone hydrobromide mp 184-186° C. Reference Example Compound 7-4:

2-Bromo-1- (4-hydroxyphenyl) -2- ( 3-pyridyl) ethanone hydrobromide

The crude mixture without purification was used to next reaction.

Reference Example Compound 7-5:

2-Bromo- 1- ( 4-fluorophenyl ) -2- ( 3-pyridyl ) ethanone hydrobromide mp 189-191° C. Reference Example Compound 7-6:

2-Bromo- 1-phenyl-2- ( 2-pyridyl ) ethanone hydrobromide mp 180-181° C.

Reference Example Compound 7-7:

2-Bromo-1- (4-methoxyphenyl) -2- ( 2-pyridyl)ethanone hydrobromide mp 170-171°C.

Reference Example Compound 7-8:

2-Bromo-1-phenyl-2- ( 4-pyridyl) ethanone hydrobromide mp 230-232° C. Reference Example Compound 7-9:

2-Bromo-1- ( 4-methoxyphenyl ) -2- ( 4-pyridyl ) ethanone hydrobromide mp 207-209° C.

Reference Example Compound 7-10: 2-Bromo-2-(5-methyl-3-pyridyl) -1-phenylethanone hydrobromide mp 189-193°C.

Reference Example Compound 7-11:

2-Bromo-l-(4-ethylphenyl) -2- ( 3-pyridyl)ethanone hydrobromide mp 145-146° C.

Reference Example Compound 7-12:

2-Bromo- 1-(3,4-me hylenedioxyphenyl ) -2- ( 3- pyridyl)ethanone hydrobromide mp 174-175°C.

Reference Example Compound 7-13: 2-Bromo- l - ( 5-indanyl ) -2- ( 3 -pyridyl ) ethanone hydrobromide mp 177 - 178° C .

Reference Example Compound 7-14: 2-Bromo-2- ( 3-pyridyl)-l-(5,6,7,8-tetrahydro-2- naphthyl)ethanone hydrobromide mp 160-162° C.

Reference Example Compound 7-15:

1- (1, 4-Benzodioxan-6-yl) -2-bromo-2- ( 3-pyridyl) ethanone hydrobromide oil.

Reference Example Compound 7-16:

2-Bromo-l- ( 2-naphthyl) -2- ( 3-pyridyl) ethanone hydrobromide mp 197-199° C.

Reference Example Compound 7-17:

2-Bromo- 1- ( 4-methoxyphenyl ) -2- ( 2-pyridyl ) ethanone hydrobromide mp 170-171° C. Reference Example Compound 7-18:

2-Bromo-2-phenyl- 1- ( 3-pyridyl)ethanone hydrobromide mp 213-218° C.

Reference Example 8 [ - ( 4-Methoxyphenyl) -5- ( 3-pyridyl ) -1 , 3-thiazol-2- yl ] amine

To a suspension of thiourea (516 mg) in acetonitrile (40 mL) , was added 2-bromo-l- ( 4- methoxyphenyl ) -2- ( 3-pyridyl ) ethanone hydrobromide (2.5 g), and then triethylamine (0.95 mL) was added slowly dropwise to the mixture with stirring. After addition, the mixture was stirred at reflux for 3 h. After cooling, the crude crystalline was collected by filtration. The crystalline was washed with an aqueous saturated solution of sodium hydrogen carbonate, water, ethanol, and ethyl ether, in that order, and dried. The obtained crude crystalline was recrystallized from tetrahydrofuran to give the title compound (1.5 g, yield 90 %) . mp 265-266° C.

Reference Example 9

N-Methyl [ 4- ( 4-methoxyphenyl ) -5- ( 3-pyridyl) -1 , 3-thiazol-

2-yl] amine

To a suspension of N-methylthiourea (242 mg) in acetonitrile (18 mL), was added 2-bromo-l- (4- methoxyphenyl ) -2- ( 3-pyridyl) ethanone hydrobromide (1.0 g) and then triethylamine (0.4 mL) was added slowly dropwise to the mixture. After addition, the resulting mixture was stirred at reflux for 3 h, and the solvent was evaporated. An aqueous saturated solution of sodium hydrogen carbonate was added to the residue and extracted with ethyl acetate. The extracts were washed with water, dried, and the solvent was evaporated. The crystalline residue was recrystallized from ethyl acetate-isopropyl ether to afford the title compound (650 mg, yield 85 %) . mp 158-159° C.

Reference Example 10 N- [ 4- ( 4-Methoxyphenyl ) - 5- ( 3-pyridyl) - 1 , 3-thiazol-2- yl] acetamide

Using [ (4-methoxyphenyl) -5- (3-pyridyl) -1,3- thiazol-2-yl]amine as starting material, the title compound was obtained in the same manner as described in below Example 3. Yield 82 %. mp 208-210° C.

Reference Example 11

2- ( 4-Acetylpiperazin-1-yl ) -4- ( 4-methoxyphenyl) -5- ( 3- pyridyl) -1, 3-thiazole

To a solution of 1-piperazinecarbothioamide (387 mg) in acetonitrile (15 mL), was added 2-bromo-l- (4- methoxyphenyl) -2- ( 3-pyridyl ) ethanone hydrobromide (1.0 g), and then triethylamine (0.4 mL) was added slowly dropwise to the resulting mixture . After addition the mixture was stirred at reflux for 3 h and the solvent was evaporated. An aqueous saturated solution of sodium hydrogen carbonate was added to the residue and extracted with ethyl acetate. The extracts were washed with water, dried and the solvent was evaporated. The residue was dissolved in pyridine (2 mL) and acetyl chloride (0.3 mL) was added to the solution under ice cooling. The resulting mixture was stood at room temperature for 1 h. The reaction mixture was poured into ice-water and the product was extracted with ethyl acetate. The extracts were washed with water , dried, and the solvent was evaporated. The residue was purified using silica-gel column chromatography (ethyl acetate-methanol, 9:1) to give the title compound (300 mg, yield 28 %) . oil.

Reference Example 12

[4- (4-Methoxyphenyl) -5- (3-pyridyl) -1 , 3-thiazol-2- yl] amine hydrochloride [ 4- ( 4-Methoxyphenyl ) - 5- ( 3-pyridyl ) - 1 , 3-thiazol-2- yl] amine (200 mg) was dissolved in 1 % methanol solution of hydrogen chloride (3.2 mL), and the solvent was evaporated. The crude crystalline was recrystallized from methanol-ethyl acetate to give the title compound (180 mg, yield 80 %). mp 145-150° C.

The chemical structures of the compounds obtained in the Reference Examples 8 to 12 are shown in Table 1. Table 1

Ref. Ex. Compd. R_a Rb e Additive

11 -N N-COMe fy- MeO-^>—

Reference Example 13

The following Reference Example Compounds 13-1 to 13-106 shown in Tables 2 to 7 were obtained in the same manner as described in the above References 8 to 12, JP-A-61-10580 and USP 4,612,321.

Table 2

Ref. Ex. Compd I. R_a R_b Re mp/°C

13-1 -NHMe 168-169

N=/ o-

13-2 -NH₂ - o- 253-254

13-5 -NHMe fy- 7 157-158

13-8 -NHCOCH₂COOCH₂Me MeO- ^" — 201-202

N=/

13-9 -NHCOCH₂COOMe f 85-186

Ny=/- o- 1

13-10 -NH₂ ^~ — o- 236-237

13-11 -NHMe

^N o- 215-216

13-12 -NHMe f^~%— MeO-^~%— 214-215

13-13 -NH₂ MeO- ^~S— 217-218

\=N

13-15 -NH₂ ^■o- o- 248-250

13-16 -NHMe ^»€ MeO- — 177-178

Table 3

Ref. Ex. Compd Ra Rb e mp/°C

MeO

13-19 -CH₂Me ry- MeO-s ^~ — 84-84.5 MeO

13-20 -CH₂Me

^{Me0-< >—} 59-60

13-22 -Me MeO-^^>— 113-114

13-23 -CH₂Me O" o- 83-84

13-24 -o o- 135-136

13-27 →72 Me0- — 195-196

MeO

13-28 -K> MeO- ^~ ~ 211-213 MeO

13-30 X ry- o- 100-101

13-31 ^2 93 N^ ^{Meo-< >—} 92-

MeO

13-32 - fy- ^e0- — 111-112

MeO

13-33 — ^" cOOH - 264-265

13-35 — ^"V-COOH 247-248

Table 4

Ref. Ex. Compd. R_a Rb R_c mp / °C

13-39 -(CH₂)₃COOH 43-144

13-40 -(CH₂)₃COOH 63-164

Me

13-41 -(CH₂)₃COOH ^ ^~~ 134-135 N=/

13-42 -(CH₂)₈COOH 112-113

13-43 -(CH₂)₄OH 51-52

13-44 -NHCH₂Me fy- ^Me0- !χ 154-155

13-45 -NHMe fy- ^ X 187-188

N=/

13-46 -NHMe fy- MeCH₂-<^>— 124-125

13-47 -NHMe o- ^~V"^~ 191-192

13-49 -NMe₂

N=/ ^{Me0→ >— oii}

13-51 -CH₂Me fy- ^{~ oii}

13-52 -(CH₂)₃Me f Ny=/- ^{~ oii}

Table 5

Ref. Ex. Compd. R_a Rb Re mp / °C

13-54 -o N^ ^MeO-^ - 104-105

13-55 -CH₂COOH oil

N=/ o-

13-56 -(CH₂)₃COOMe oil

N=/ -

13-57 -(CH₂)₅COOH

o- oil

13-61 -(CH₂)₂Me

^Me0" ^— oil

13-64 -N(CH₂Me)₂ 97-98

N^

13-65 -NHMe ^■O- ^b- 234-235

13-66 -NMe₂ O- °^ 144-145

13-69 -NHMe ^•O -O- 205-206

13-70 -NHMe <0^~ α- - 224-225

13-71 -NHMe Ό- ^B-O- 206-207 Table 6

Ref Ex Compd R_a Rb R_c Additive mp/°C

13-72 -NHMe o- o- 191-192

13-74 -NHMe 172-173

13-76 -^K-Q ^{Me0→ >_} 222-223

13-77 XD Wi O- y— 132-133

13-79 -O^cι N=/ ^{Me0-< >—} 148-149

13-84 -N(CH₂Me)₂ <b- 56-57

13-85 -CH₂NH₂

^Me°^{→ >—} oil

13-86 -CH₂NHMe MeO- ^~V- oil

N=/

13-87 -NHCOMe

^{e0-< >— HCI} 214-217

13-88 -NHCOMe 228-231

13-89 -NHCOMe ^<D^~ HCl 275-278

13-90 -NHCOCH₂Me 0^{~~ HCi} 248-251

Table 7

Rb s

Ref. Ex. Compd I. Ra Rb Re mp / °C

13-91 -NHCOCH₂Me 196-199

13-92 -NHCOCHMe₂

^Me0_O^~ 213-216

13-94 -NHCOMe Me(H₂C)₃0-Q)— 230-233

13-96 -NHCOMe 230-234

13-97 -NHCO- MeO- 275-278

13-98 -NHCOMe fy- ^HO - 287-292

13-99 -NMeCOMe •o- ^Me0~^ ^— 169-172

13-100 -NHCOMe X- o- 222-224

13-101 -NHCOMe 175-178

13-102 -N=CHNMe₂ 118-120

Reference Example 14

N- ( 4-Chlorobenzoyl)propyleneimine

A solution of propyleneimine (12.3 mL) in tetrahydrofuran (160 mL) was added to an IN aqueous sodium hydroxide solution. To the mixture was added dropwise 4-chlorobenzoyl chloride (25 g) at 0°C. After addition, the mixture was stirred for additional 30 min. The reaction mixture was extracted with ethyl acetate. The extract was dried, concentrated under reduced pressure to afford the title compound (24.9 g, yield 89 %) . oil. ^XH-NMR (CDC1₃) δ: 1.39 (3H, d, J= 5.5 Hz), 2.15 (IH, d, J= 2.9 Hz), 2.51-2.66 (2H, m) , 7.39-7.47 (2H, m) , 7.93- 8.01 (2H, m).

Reference Example 15 Using 3-chlorobenzoyl chloride, 2-chlorobenzoyl chloride, 2-methylbenzoyl chloride, 3-methylbenzoyl chloride, 4-methylbenzoyl chloride, 2-methoxybenzoyl chloride, 3-methoxybenzoyl chloride, 4-ethylbenzoyl chloride, 4- ( 1-methylethyl)benzoyl chloride, 4- (1,1- dimethylethyl)benzoyl chloride, 4-propylbenzoyl chloride, 4-butylbenzoyl chloride, 4-hexylbenzoyl chloride, 4-trifluoromethoxybenzoyl chloride, 4- trifluoromethylbenzoyl chloride, 3, 4-dimethoxybenzoyl chloride, 3 , 4-dimethylbenzoyl chloride, 3,5- dimethylbenzoyl chloride, 3 , 4-methylenedioxybenzoyl chloride and 2-naphthoyl chloride instead of using 4- chlorobenzoyl chloride , the below Reference Example Compounds 15-1 to 15-20 were obtained in the same manner as described in the above Reference Example 14. Reference Example Compound 15-1: N- ( 3-Chlorobenzoyl)propyleneimine oil.

'H-NMR (CDCI₃) δ : 1.40 (3H, d, J= 5.1 Hz), 2.17 (IH, d, J= 3.3 Hz), 2.53-2.68 (2H, m) , 7.40 (IH, dd, J= 8.1, 7.7 Hz), 7.53 (IH, ddd, J= 8.1, 2.2, 1.5 Hz), 7.90 (IH, dt, J= 7.7, 1.5 Hz), 8.00 (IH, dd, J= 2.2, 1.5 Hz). Reference Example Compound 15-2: N- ( 2-Chlorobenzoyl )propyleneimine oil. ^XH-NMR (CDCI₃) δ : 1.30 (3H, d, J= 5.1 Hz), 2.12 (IH, d, J= 3.3 Hz), 2.53 (IH, d, J= 5.5 Hz), 2.56-2.68 (IH, m) , 7.28-7.48 (3H, m) , 7.75-7.81 (IH, m) . Reference Example Compound 15-3: N- ( 2-Methylbenzoyl)propyleneimine oil. ^XH-NMR (CDC1₃) δ : 1.30 (3H, d, J= 5.5 Hz), 2.08 (IH, d, J= 3.3 Hz), 2.43-2.57 (5H, m) , 7.20-7.31 (2H, m) , 7.33- 7.43 (IH, m), 7.89 (IH, d, J= 7.7 Hz). Reference Example Compound 15-4: N- ( 3-Methylbenzoyl )propyleneimine oil.

^-NMR (CDCI₃) δ : 1.39 (3H, d, J= 5.5 Hz ) , 2.14 (IH, d, J= 3.3 Hz), 2.41 (3H, s), 2.51-2.66 (2H, m) , 7.32-7.39 (2H, m), 7.79-7.87 (2H, m) . Reference Example Compound 15-5: N- (4-Methylbenzoyl)propyleneimine oil.

'H-NMR (CDCI₃) δ : 1.39 (3H, d, J= 5.5 Hz), 2.12 (IH, d, J= 2.9 Hz), 2.42 (3H, s), 2.50-2.62 (2H, m) , 7.25 (2H, d, J= 8.1 Hz), 7.92 (2H, d, J= 8.1 Hz). Reference Example Compound 15-6:

N- ( 2-Methoxybenzoyl)propyleneimine oil.

'H-NMR (CDCI₃) δ : 1.30 (3H, d, J= 5.5 Hz ) , 2.10 (IH, d, J= 3.3 Hz), 2.50 (IH, d, J= 5.9Hz), 2.53-2.65 (IH, m) , 3.90 (3H, s), 6.95-7.05 (2H, m) , 7.41-7.52 (IH, m) 7.81-7.88 (IH, m) . Reference Example Compound 15-7: N- ( 3-Methoxybenzoyl)propyleneimine oil. 'H-NMR (CDC1₃) δ : 1.40 (3H, d, J= 5.9 Hz), 2.14 (IH, d, J= 2.9 Hz), 2.52-2.65 (2H, m) , 3.86 (3H, s), 7.10 (IH, ddd, J= 8.4, 2.6, 1.1 Hz), 7.37 (IH, dd, J= 8.4, 7.3 Hz), 7.55 (IH, dd, J= 2.6, 1.5 Hz ) , 7.63 (IH, ddd, J= 7.3, 1.5, 1.1 Hz). Reference Example Compound 15-8: N- ( 4-Ethylbenzoyl)propyleneimine oil.

^XH-NMR (CDC1₃) δ : 1.27 (3H, t, J= 7.6 Hz), 1.39 (3H, d, J= 5.5 Hz), 2.13 (IH, d, J= 3.3 Hz), 2.50-2.61 (2H, m) , 2.71 (2H, q, J= 7.6 Hz), 7.28 (2H, d, J= 7.7 Hz), 7.95 (2H, d, J= 7.7 Hz) . Reference Example Compound 15-9: N- [ 4- ( 1-Methylethyl )benzoyl] propyleneimine oil. 'H-NMR (CDCI₃) δ : 1.28 (6H, d, J= 7.0 Hz), 1.40 (3H, d, J= 5.5 Hz), 2.13 (IH, d, J= 3.3 Hz), 2.50-2.64 (2H, m) , 2.90-3.05 (IH, m), 7.31 (2H, d, J= 8.2 Hz), 7.96 (2H, d, J= 8.2 Hz) . Reference Example Compound 15-10: N- [4- (1, 1-Dimethylethyl)benzoyl]propyleneimine oil.

^XH-NMR (CDC1₃) δ : 1.35 (9H, s), 1.41 (3H, d, J= 5.5Hz), 2.12 (IH, d, J= 2.9 Hz), 2.51-2.64 (2H, m) , 7.47 (2H, d, J= 8.8 Hz), 7.96 (2H, d, J= 8.8Hz ) . Reference Example Compound 15-11: N- ( 4-Propylbenzoyl )propyleneimine oil.

'H-NMR (CDCI₃) δ : 0.96 (3H, t, J= 7.3 Hz), 1.39 (3H, d, J= 5.5 Hz), 1.57-1.75 (2H, m) , 2.12 (IH, d, J= 3.3 Hz), 2.50-2.59 (2H, m) , 2.65 (2H, t, J= 7.7 Hz), 7.26 (2H, d, J= 8.1 Hz), 7.94 (2H, d, J= 8.1 Hz). Reference Example Compound 15-12: N- ( 4-Butylbenzoyl )propyleneimine oil. 'H-NMR (CDCI₃) δ : 0.94 (3H, t, J= 7.1 Hz), 1.26-1.47 (5H, m) , 1.54-1.73 (2H, m) , 2.12 (IH, d, J= 2.9 Hz), 2.51-2.62 (2H, m) , 2.67 (2H, t, J= 7.7 Hz), 7.26 (2H, d, J= 8.1 Hz), 7.94 (2H, d, J= 8.1 Hz). Reference Example Compound 15-13: N- ( 4-Hexylbenzoyl) propyleneimine oil.

^-NMR (CDC1₃) δ : 0.89 (3H, t, J= 6.6 Hz), 1.24-1.38

(6H, m), 1.39 (3H, d, J= 5.5 Hz), 1.56-1.68 (2H, m) ,

2.12 (IH, d, J= 3.3 Hz), 2.51-2.61 (2H, m) , 2.66 (2H, t, J= 7.7 Hz), 7.26 (2H, d, J= 8.1 Hz), 7.94 (2H, d, J=

8.1 Hz) .

Reference Example Compound 15-14:

N- ( 4-Trifluoromethoxybenzoyl)propyleneimine oil. 'H-NMR (CDC1₃) δ : 1.40 (3H, d, J= 5.5 Hz), 2.16 (IH, d, J= 3.3 Hz), 2.53-2.68 (2H, m) , 7.29 (2H, d, J= 9.0 Hz), 8.08 (2H, d, J= 9.0 Hz) . Reference Example Compound 15-15: N- ( 4-Trifluoromethylbenzoyl)propyleneimine oil.

^XH-NMR (CDC1₃) δ : 1.40 (3H, d, J= 5.5 Hz), 2.19 (IH, d, J= 3.7 Hz), 2.54-2.70 (2H, ) , 7.73 (2H, d, J= 8.0 Hz),

8.13 (2H, d, J= 8.0 Hz) . Reference Example Compound 15-16: N- (3, 4-Dimethoxybenzoyl)propyleneimine oil.

'H-NMR (CDCI₃) δ : 1.41 (3H, d, J= 5.5 Hz), 2.12 (IH, d, J= 3.3 Hz), 2.51-2.63 (2H, m) , 3.94 (3H, s), 3.95 (3H, s), 6.92 (IH, d, J= 8.5 Hz), 7.56 (IH, d, J= 2.2 Hz), 7.69 (IH, dd, J= 8.5, 2.2 Hz).

Reference Example Compound 15-17:

N- (3, 4 -Dimethylbenzoyl) propyleneimine oil.

^XH-NMR (CDCI₃) δ : 1.39 (3H, d, J= 5.5 Hz ) , 2.12 (IH, d, J= 3.3 Hz), 2.32 (6H, s), 2.49-2.61 (2H, m) , 7.21 (IH, d, J= 7.7 Hz), 7.77 (IH, dd, J= 7.7, 1.8 Hz), 7.80 (IH, d, J= 1.8 Hz) .

Reference Example Compound 15-18:

N- (3, 5-Dimethylbenzoyl)propyleneimine oil. ^XH-NMR (CDC1₃) δ : 1.39 (3H, d, J= 5.5 Hz), 2.13 (IH, d, J= 3.7 Hz), 2.37 (6H, s), 2.47-2.62 (2H, m) , 7.19 (IH, s), 7.64 (2H, s).

Reference Example Compound 15-19: N- ( 3 , 4-Methylenedioxybenzoyl )propyleneimine oil.

^-NMR (CDCI₃) δ : 1.38 (3H, d, J= 4.9 Hz), 2.11 (IH, d, J= 3.1 Hz), 2.48-2.64 (2H, m) , 6.05 (2H, s), 6.86 (IH, d, J= 8.2 Hz), 7.48 (IH, d, J= 1.7 Hz), 7.65 (IH, dd, J= 8.2, 1.7 Hz) .

Reference Example Compound 15-20: N- ( 2-Naphthoyl )propyleneimine oil.

^XH-NMR (CDC1₃) δ : 1.44 (3H, d, J= 5.5 Hz), 2.22 (IH, d, J= 3.3 Hz), 2.57-2.84 (2H, m) , 7.50-7.65 (2H, m) , 7.85- 8.00 (3H, m), 8.06 (IH, dd, J= 8.6, 1.5 Hz), 8.59 (IH, s).

Reference Example 16 1- ( 2-Chlorophenyl ) -2- ( 4-pyridyl ) ethanone

To a stirred solution of diisopropylamine (15.4 mL) in dry tetrahydrofuran (100 mL) cooled at -50° C, was added a solution of 1.6 M n-butyllithium in hexane (69 mL) dropwise. After addition, the resulting mixture was stirred for 10 min at the same temperature, followed by the addition of a solution of γ-picoline (20 g) in dry tetrahydrofuran (10 mL) at -30° C. After an additional 1 h stirring, a solution of N-(2- chlorobenzoyl)propyleneimine (20 g) in dry tetrahydrofuran (10 mL) was added dropwise to the resulting mixture at -10°C. After addition the mixture was stirred for another 2 h at ambient temperature. Water (100 mL) was added to the mixture and extracted with ethyl acetate. The extract was washed with water, dried, and concentrated under reduced pressure. The residue was purified using silica-gel column chromatography (hexane-ethyl acetate, 1:1) to give the title compound (16.4 g, yield 71 %). oil. ^XH-NMR (CDC1₃) δ : 4.28 (2H, s), 7.20 (2H, d, J= 6.2 Hz), 7.28-7.39 (IH, m) , 7.41-7.48 (3H, m) , 8.56 (2H, d, J= 6.2 Hz) .

Reference Example 17 Using N- (3-chlorobenzoyl)propyleneimine, N-(4- chlorobenzoyl)propyleneimine , N- ( 2- methylbenzoyl)propyleneimine , N- ( 3- methylbenzoyl )propyleneimine , N- ( 4- methylbenzoyl) ropyleneimine , N- ( 2- methoxybenzoyl)propyleneimine, N-(3- methoxybenzoyl)propyleneimine , N- ( 4- ethylbenzoyl )propyleneimine , N- [ 4- ( 1- methylethyl)benzoyl]propyleneimine , N- [ 4- ( 1 , 1- dimethylethyl)benzoyl ]propyleneimine , N- ( 4- propylbenzoyl)propyleneimine, N-(4- butylbenzoyl )propyleneimine , N- ( 4- hexylbenzoyl)propyleneimine, N- (4- trifluoromethoxybenzoyl )propyleneimine , N- ( 4- trifluoromethylbenzoyl)propyleneimine , N- ( 3 , 4- dimethoxybenzoyl)propyleneimine, N-(3,4- dimethylbenzoyl)propyleneimine, N- (3, 5- dimethylbenzoyl )propyleneimine , N- ( 3 , 4- methylenedioxybenzoyl)propyleneimine and N-(2- naphthoyl)propyleneimine instead of using N-(2- chlorobenzoyl)propyleneimine, the below Reference

Example Compounds 17-1 to 17-20 were obtained in the same manner as described in the above Reference Example

16.

Reference Example Compound 17-1: 1- ( 3-Chlorophenyl ) -2- ( 4-pyridyl ) ethanone mp 79-80° C. Reference Example Compound 17-2: 1- ( 4-Chlorophenyl) -2- ( 4-pyridyl) ethanone mp 93-94° C.

Reference Example Compound 17-3: l-(2-Methylphenyl) -2- ( 4-pyridyl)ethanone oil.

^XH-NMR (CDC1₃) δ : 2.48 (3H, s), 4.23 (2H, s), 7.19 (2H, d, J= 6.2 Hz), 7.24-7.47 (3H, m) , 7.73 (IH, d, J= 7.7

Hz), 8.56 (2H, d, J= 6.2 Hz). Reference Example Compound 17-4:

1- ( 3-Methylphenyl ) -2- ( 4-pyridyl)ethanone mp 115-116° C.

Reference Example Compound 17-5: l- ( 4-Methylphenyl ) -2 - ( 4 -pyridyl ) ethanone mp 110- 111° C .

Reference Example Compound 17-6:

1- ( 2-Methoxyphenyl ) -2- ( 4-pyridyl)ethanone oil.

"H-NMR (CDCI₃) δ : 3.92 (3H, s), 4.30 (2H, s), 6.95-7.07 (2H, m), 7.17 (2H, d, J= 5.9 Hz), 7.50 (IH, ddd, J= 8.4,

7.3, 1.8 Hz), 7.73 (IH, dd, J= 7.7, 1.8 Hz), 8.53 (2H, d, J= 5.9 Hz) .

Reference Example Compound 17-7:

1- ( 3-Methoxyphenyl) -2- ( 4-pyridyl)ethanone oil.

^-NMR (CDCI₃) δ : 3.86 (3H, s), 4.28 (2H, s), 7.14 (IH, ddd, J= 8.1, 2.6, 1.1 Hz), 7.20 (2H, d, J= 6.2 Hz) ,

7.36 (IH, dd, J= 8.1, 7.7 Hz), 7.51 (IH, dd, J= 2.6,

1.5 Hz), 7.58 (IH, ddd, J= 7.7, 1.5, 1.1 Hz) 8.57 (2H, d, J= 6.2 Hz) .

Reference Example Compound 17-8:

1- ( 4-Ethylphenyl ) -2- ( 4-pyridyl ) ethanone mp 87-89° C.

Reference Example Compound 17-9: 1- [ 4- (1-Methylethyl)phenyl]-2- (4-pyridyl) ethanone mp 86 - 88° C .

Reference Example Compound 17-10:

1- [4-(l, 1-Dimethylethyl)phenyl] -2- ( 4-pyridyl) ethanone mp 75-76° C. Reference Example Compound 17-11:

1- (4-Propylphenyl) -2- (4-pyridyl)ethanone mp 71-72°C.

Reference Example Compound 17-12:

1- (4-Butylphenyl) -2- (4-pyridyl) ethanone mp 41-43° C.

Reference Example Compound 17-13:

1- ( 4-Hexylphenyl) -2- ( 4-pyridyl ) ethanone mp 57-58° C.

Reference Example Compound 17-14: 2- ( 4-Pyridyl) - 1- ( 4-trifluoromethoxyphenyl ) ethanone mp 65-66° C.

Reference Example Compound 17-15:

2- (4-Pyridyl) -1- ( 4-trifluoromethylphenyl)ethanone mp 94-95° C. Reference Example Compound 17-16:

1- (3, 4-Dimethoxyphenyl) -2- ( 4-pyridyl) ethanone mp 110-111° C.

Reference Example Compound 17-17:

1- ( 3 , 4-Dimethylphenyl) -2- ( 4-pyridyl ) ethanone mp 81-83° C.

Reference Example Compound 17-18:

1- ( 3 , 5-Dimethylphenyl ) -2- ( 4-pyridyl )ethanone mp 90-91° C.

Reference Example Compound 17-19: 1- (3, 4-Methylenedioxyphenyl) -2- ( 4-pyridyl) ethanone mp 126-127°C.

Reference Example Compound 17-20:

1- ( 2-Naphthyl) -2- ( 4-pyridyl ) ethanone mp 114-115°C.

Reference Example 18 Using α-picoline instead of using γ-picoline, the below Reference Example Compounds 18-1 to 18-9 were obtained in the same manner as described in the above Reference Example 17. Reference Example Compound 18-1:

1- (2-Chlorophenyl) -2- (3-pyridyl) ethanone oil.

^XH-NMR (CDC1₃) δ : 4.28 (2H, s), 7.18-7.49 (5H, m) , 7.59-7.67 (IH, m) , 8.47-8.56 (2H, m) . Reference Example Compound 18-2:

1- (3-Chlorophenyl)-2- ( 3-pyridyl)ethanone oil.

'H-NMR (CDCI₃) δ : 4.29 (2H, s), 7.25-7.34 (IH, m) , 7.44 (IH, t, J= 7.7 Hz), 7.54-7.63 (2H, m) , 7.90 (IH, dt , J= 7.7, 1.5 Hz), 8.00 (IH, dd, J= 1.8, 1.5 Hz), 8.49-8.57 (2H, m).

Reference Example Compound 18-3: 1- ( 4-Chloropheny1 ) -2- ( 3-pyridyl )ethanone H-NMR (CDCI₃) δ : 4.27 (2H, s), 7.24-7.31 (IH, m) , 7.47 (2H, d, J= 8.8 Hz), 7.55-7.63 (IH, m) , 7.96 (2H, d, J= 8.8 Hz), 8.46-8.53 (2H, m) . Reference Example Compound 18-4: 1- ( 2-Methylphenyl ) -2- ( 3-pyridyl) ethanone oil. 'H-NMR (CDC1₃) δ : 2.47 (3H, s), 4.23 (2H, s), 7.18-7.47 (5H, m), 7.73 (IH, d, J= 7.7 Hz), 8.47-8.56 (2H, m) . Reference Example Compound 18-5: 1- ( 3-Methylphenyl ) -2- ( 3-pyridyl ) ethanone oil. "H-NMR (CDCI₃) δ : 2.43 (3H, s), 4.29 (2H, s), 7.17-7.36 (IH, m) , 7.36-7.46 (2H, m) , 7.58-7.65 (IH, m) , 7.78- 7.86 (2H, m) , 8.50-8.56 (2H, m) . Reference Example Compound 18-6: 1- ( 4-Methylphenyl ) -2- ( 3-pyridyl) ethanone mp 72-74° C. Reference Example Compound 18-7:

1- (3-Methoxyphenyl) -2- (3-pyridyl) ethanone oil.

^XH-NMR (CDC1₃) δ : 3.86 (3H, s), 4.29 (2H, s), 7.14 (IH, ddd, J= 8.1, 2.6, 1.8 Hz), 7.28 (IH, dd, J= 7.3, 4.8 Hz), 7.40 (IH, dd, J= 8.1, 7.7 Hz), 7.53 (IH, dd, J= 2.6, 1.8 Hz), 7.58-7.65 (2H, m) , 8.50-8.55 (2H, m) . Reference Example Compound 18-8:

1- [4-(l, 1 -Dimethylethyl)phenyl] -2- ( 3-pyridyl) ethanone oil.

'H-NMR (CDC1₃) δ : 1.34 (9H, s), 4.28 (2H, s), 7.22-7.31 (IH, m), 7.50 (2H, d, 3= 8.4 Hz), 7.56-7.65 (IH, m) , 7.96 (2H, d, J= 8.4 Hz), 8.48-8.55 (2H, m) . Reference Example Compound 18-9: 1- (3, 5-Dimethylphenyl) -2- ( 3-pyridyl) ethanone oil.

^XH-NMR (CDCI₃) δ : 2.38 (6H, s), 4.27 (2H, s), 7.24-7.30 (2H, m) , 7.58-7.63 (3H, m) , 8.50-8.52 (2H, m) .

Reference Example 19

Using ethyl 4-dimethylaminobenzoate instead of using ethyl p-anisate, the below Reference Example Compound 19 was obtained in the same manner as described in the above Reference Example 1. Reference Example Compound 19:

1- ( 4-Dimethylaminophenyl ) -2- ( 4-pyridyl) ethanone mp 189-192° C.

Reference Example 20 2- [ 4- ( 1 , 1-Dimethylethyl)phenyl ] - 1- ( 4-pyridyl ) ethanone

To a solution of ethyl isonicotinate (12 g) and 4- (1, 1-Dimethylethyl )phenylacetonitrile (9.1 g) in tert- butyl alcohol (36 mL), was added potassium tert- butoxide (7.3 g), and the mixture was stirred at 100° C for 3 h. After cooling, the resulting mixture was dissolved in water and washed with isopropyl ether. The aqueous phase was adjusted to pH 7.0 with 2 N hydrochloric acid and extracted with ethyl acetate. The extract was washed with water, dried, and the solvent was evaporated. The crystalline residue was recrystallized from ethyl acetate-isopropyl ether to obtain 2-cyano-2-[4-(l,l-dimethylethyl )phenyl] -1- ( 4- pyridyl ) ethanone (5.09 g, yield 35 %).

2-Cyano-2-[4-(l,l-dimethylethyl)phenyl]-l-(4- pyridyl ) ethanone (5.0 g) obtained above was dissolved in 48 % hydrobromic acid (50 mL) and the solution was stirred at 140° C for 5 h. After the mixture was cooled, the mixture was neutralized with an aqueous saturated solution of sodium hydrogen carbonate and the product was extracted with ethyl acetate. The extract was washed with water, dried, and the solvent was evaporated. The residue was purified using silica-gel column chromatography (hexane-ethyl acetate, 1:1) to obtain the title compound (3.1 g, yield 68 %). oil. ^-NMR (CDC1₃) δ : 1.30 (9H, s), 4.25 (2H, s), 7.18 (2H, d, J= 8.4 Hz), 7.36 (2H, d, J= 8.4 Hz), 7.78 (2H, d, J= 6.2 Hz), 8.81 (2H, d, J= 6.2 Hz).

Reference Example 21 2- (3, 5-Dimethylphenyl) -1- ( 4-pyridyl)ethanone

Using 3 , 5-dimethylphenylacetonitrile instead of using 4- ( 1, 1-Dimethylethyl)phenylacetonitrile, the title compound was obtained in the same manner as described in the above Reference Example 20. mp 96-97° C.

Reference Example 22

Using 1- ( 2-chlorophenyl) -2- (3-pyridyl) ethanone, 1- ( 3-chlorophenyl) -2- ( 3-pyridyl ) ethanone , 1- ( 4- chlorophenyl) -2- (3-pyridyl) ethanone, l-(2- methylphenyl) -2- ( 3-pyridyl ) ethanone , 1- ( 3- methylphenyl) -2- ( 3-pyridyl ) ethanone , 1- ( 4- methylphenyl ) -2- ( 3-pyridyl ) ethanone , 1- ( 3- methoxyphenyl) -2-(3-pyridyl) ethanone, 1- [4-(l, 1- dimethylethyl )phenyl ] -2- ( 3-pyridyl)ethanone , 1- ( 3 , 5- dimethylphenyl) -2-(3-pyridyl) ethanone, l-(2- chlorophenyl) -2- (4-pyridyl) ethanone, 1- (3- chlorophenyl ) -2- ( 4-pyridyl ) ethanone , 1- ( 4- chlorophenyl ) -2- ( 4-pyridyl) ethanone , 1- ( 2- methylphenyl ) -2- ( 4-pyridyl ) ethanone , 1- ( 3- methylphenyl) -2- (4-pyridyl) ethanone, l-(4- methylphenyl) -2- ( 4-pyridyl) ethanone , 1- ( 2- methoxyphenyl) -2- ( 4-pyridyl) ethanone, 1- (3- methoxyphenyl ) -2- (4-pyridyl) ethanone, l-(4- ethylphenyl) -2- (4-pyridyl) ethanone, 1- [4- (1- methylethyl)phenyl] -2- (4-pyridyl) ethanone, l-[4-(l,l- dimethylethyl)phenyl] -2- ( 4-pyridyl) ethanone, l-(4- propylphenyl) -2- ( 4- yridyl ) ethanone , 1- ( 4-butylpheny1 ) - 2- ( 4-pyridyl) ethanone , 1- ( 4-hexylphenyl ) -2- ( 4- pyridyl ) ethanone , 2- (4-pyridyl) -l-(4- trifluoromethoxyphenyl ) ethanone , 2- ( 4-pyridyl) -1- ( 4- trifluoromethylphenyl) ethanone , 1- ( 4- dimethylaminophenyl) -2- ( 4-pyridyl ) ethanone hydrobromide , 1- (3, 4-dimethoxyphenyl) -2- ( 4-pyridyl) ethanone, 1- (3, 4- dimethylphenyl ) -2- ( 4-pyridyl) ethanone , 1- ( 3 , 5- dimethylphenyl) -2- (4-pyridyl) ethanone, l-(3,4- methylenedioxyphenyl ) -2- ( 4-pyridyl) ethanone , 1- ( 2- naphthyl) -2- (4-pyridyl) ethanone, 2- [4- (1,1- dimethylethyl )phenyl] -1- (4-pyridyl) ethanone and 2- (3, 5- dimethylphenyl ) -1- (4-pyridyl) ethanone instead of using 1- (4-methoxyphenyl) -2- (3-pyridyl) ethanone, the below

Reference Example Compounds 22-1 to 22-33 were obtained in the same manner as described in the above Reference Example 6. Reference Example Compound 22-1: 2-Bromo-1- ( 2-chlorophenyl) -2- (3-pyridyl) ethanone hydrobromide mp 88 - 90° C .

Reference Example Compound 22-2:

2-Bromo- 1- ( 3-chlorophenyl ) -2- ( 3-pyridyl) ethanone hydrobromide mp 164-166° C.

Reference Example Compound 22-3:

2-Bromo- 1- ( 4-chlorophenyl) -2- ( 3-pyridyl )ethanone hydrobromide

The crude mixture without purification was used to next reaction.

Reference Example Compound 22-4:

2-Bromo-1- ( 2-methylphenyl) -2- ( 3-pyridyl) ethanone hydrobromide

The crude mixture without purification was used to next reaction.

Reference Example Compound 22-5:

2-Bromo-1- (3-methylphenyl) -2- ( 3-pyridyl) ethanone hydrobromide

The crude mixture without purification was used to next reaction.

Reference Example Compound 22-6:

2-Bromo- 1- ( 4-methylphenyl ) -2- ( 3-pyridyl ) ethanone hydrobromide mp 96-98° C. Reference Example Compound 22-7:

2-Bromo- 1- ( 3-methoxyphenyl ) -2- ( 3-pyridyl ) ethanone hydrobromide

The crude mixture without purification was used to next reaction. Reference Example Compound 22-8:

2-Bromo-1- [ 4- ( 1 , 1-dimethylethyl )phenyl ] -2- ( 3- pyridyl) ethanone hydrobromide mp 190-194° C.

Reference Example Compound 22-9: 2-Bromo-l- (3, 5-dimethylphenyl) -2- ( 3-pyridyl) ethanone hydrobromide mp 195 - 197° C .

Reference Example Compound 22-10:

2-Bromo-l- (2-chlorophenyl) -2- (4-pyridyl) ethanone hydrobromide mp 157-159°C.

Reference Example Compound 22-11:

2-Bromo-l- ( 3-chlorophenyl) -2- ( 4-pyridyl) ethanone hydrobromide mp 178-181° C. Reference Example Compound 22-12:

2-Bromo- 1- ( 4-chlorophenyl) -2- ( 4-pyridyl) ethanone hydrobromide mp 189-193°C.

Reference Example Compound 22-13: 2-Bromo-l- ( 2-methylphenyl) -2- ( 4-pyridyl)ethanone hydrobromide mp 183-186° C.

Reference Example Compound 22-14:

2-Bromo- 1- ( 3-methylphenyl ) -2- ( 4-pyridyl ) ethanone hydrobromide

The crude mixture without purification was used to next reaction.

Reference Example Compound 22-15:

2-Bromo- 1- ( 4-methylphenyl ) -2- ( 4-pyridyl ) ethanone hydrobromide mp 111-113°C.

Reference Example Compound 22-16:

2-Bromo- 1- ( 2-methoxyphenyl ) -2- ( 4-pyridyl ) ethanone hydrobromide mp 168 - 171° C .

Reference Example Compound 22-17:

2-Bromo-l-(3-methoxyphenyl) -2- (4-pyridyl) ethanone hydrobromide

The crude mixture without purification was used to next reaction.

Reference Example Compound 22-18: 2-Bromo- 1- (4-ethylphenyl) -2- ( 4-pyridyl) ethanone hydrobromide mp 170-173° C.

Reference Example Compound 22-19: 2-Bromo-1- [ 4- ( 1-methylethyl)phenyl] -2- ( 4- pyridyl ) ethanone hydrobromide mp 185-188° C.

Reference Example Compound 22-20:

2-Bromo-l-[4-(l,l-dimethylethyl )phenyl] -2- ( 4- pyridyl)ethanone hydrobromide mp 209-212° C.

Reference Example Compound 22-21:

2-Bromo-1- ( 4-propyIpheny1) -2- ( 4-pyridyl ) ethanone hydrobromide mp 167-170° C.

Reference Example Compound 22-22:

2-Bromo- 1- ( 4-butyIpheny1) -2- ( 4-pyridyl) ethanone hydrobromide mp 158-161° C. Reference Example Compound 22-23:

2-Bromo- 1- ( 4-hexyIpheny1) -2- ( 4-pyridyl) ethanone hydrobromide mp 153-155° C.

Reference Example Compound 22-24: 2-Bromo-2-(4-pyridyl)-l-(4- trifluoromethoxyphenyl) ethanone hydrobromide

The crude mixture without purification was used to next reaction.

Reference Example Compound 22-25: 2-Bromo-2-(4-pyridyl)-l-(4- trifluoromethylphenyl ) ethanone hydrobromide mp 190-194°C.

Reference Example Compound 22-26:

2-Bromo-1- ( 4-dimethylaminophenyl ) -2- ( 4-pyridyl) ethanone dihydrobromide mp 163-167°C. Reference Example Compound 22-27:

2-Bromo-l- ( 3 , 4-dimethoxyphenyl) -2- ( 4-pyridyl) ethanone hydrobromide mp 174-175°C. Reference Example Compound 22-28:

2-Bromo- 1- ( 3 , 4-dimethylphenyl) -2- ( 4-pyridyl ) ethanone hydrobromide mp 196-199° C.

Reference Example Compound 22-29: 2-Bromo- 1- (3, 5-dimethylphenyl) -2- ( 4-pyridyl) ethanone hydrobromide mp 216-219° C.

Reference Example Compound 22-30:

2-Bromo-1- (3, 4-methylenedioxyphenyl) -2- (4- pyridyl) ethanone hydrobromide mp 211-214° C.

Reference Example Compound 22-31:

2-Bromo-1- ( 2-naphthyl ) -2- ( 4-pyridyl ) ethanone hydrobromide mp 149-152° C.

Reference Example Compound 22-32:

2-Bromo-2- [ 4- ( 1 , 1-dimethylethyl )phenyl ] -1- ( 4- pyridyl ) ethanone hydrobromide

The crude mixture without purification was used to next reaction.

Reference Example Compound 22-33:

2-Bromo-2- (3, 5-dimethylphenyl) -1- ( 4-pyridyl) ethanone hydrobromide mp 186-188° C.

Reference Example 23

The following Reference Example Compounds 23-1 to

23-222 shown in Tables 8 to 21 were obtained in the same manner as described in the above References 5 to 9 , JP-A-61-10580 and USP 4,612,321. Table 8

^Rb S Rc N

Ref. Ex. Compd. Ra R_b Re Additive mp / °C

23-1 -NHCOHQ fy o- HCl 260

23-2 -NHC0-<^) f Ny=/- o- HCl 244-246

23-4 -NHCO→ l

o- HCl 275

23-6 -NHCOMe 218-220

23-7 -NHCOMe

23-12 -NHCO(CH₂)₂Me fy- o- 198-200

23-13 -NHCO(CH₂)₃Me f Ny=/ o- 205-206

23-14 -NHCO(CH₂)₄Me o- 175-177

23-15 -NHCOCMe₃ f Ny=/ o- 219-220

23-16 -NHCO-<Λ ~~Λ> fy MeOH^— HCl 268-270

Table 9

^Rb _vS

Re 77^κ>

Ref. Ex. Compd. Ra Rb R_c Additive mp / °C

23-18 -NHCO-c T] o-

^HCI 237-239

23-19

^Me0~O^{>— HCI 220}-²²3

23-20 -NHCOCH₂-^~ > fy MeO- — ^■ 184-185

23-21 -NHCO(CH₂)₂- ^ fy- ^MeO-^ ^-" 214-216

23-22 -NHCO(CH₂)₂Me 197-198

23-23 -NHCO(CH₂)₃Me 188-190

23-24 -NHCO(CH₂)₄Me fy ^{Me0_< >—} 167-169

23-25 -NHCOCMe₃ f 245-246

23-26 -NHCO→ N^ o- 237-238

23-29 -NHCOCH₂-<^> φ- o- 233-234

23-30 -NHCO(CH₂)₂→ > J- o- 214-216

23-31 -NHCOCMe₃ << o- 206-208

23-33 -NHCO(CH₂)₂Me Ό- o- 212-214

23-34 -NHCO(CH₂)₃Me o- 232-234

23-35 -NHCO(CH₂)₄Me o- 245-246

Table 10

Ref. Ex. Compd. Ra Rb e mp/°C

23-36 -N CO- "3- O- 219-220

23-37 -NHCOCH₂Me ^ ^{Me0-< >—} 254-256

23-38

•O" ^Me0~3^~- 255-257

23-39 -NH₂

c- - 278-280

23-40 -NHCOMe

N=/ ^α-O 266-268

23-41 -NHCOCH₂Me

^C.- - 241-242

23-42 -NH₂ fy Me- 286-288

23-43 -NHCOMe fy Me-7Q- 260-261

N=/

23-44 -NHCOCH₂Me 226-227

Cl

23-45 -NHCOMe 217-219

N^

Cl

23-46 -NHCOCH₂Me 228-229

N=/

23-47 -NHCOMe

23-48 -NHCOCH₂Me 39-241

Cl

23-49 -NHCOMe ^■O- 290-293

23-50 -NHCOCH₂Me - 289-290

23-51 -NHCOMe Ό- 287-289

Table 11

R ^bv-S.

IIM'>-^Ra

R_C A- ~^N

Ref. Ex. Compd. Ra Rb Re mp / °C

Me

23-52 -NHCOCH₂Me »3- 258-260

23-53 -NHCOMe O- _ayy 317-320

23-54 -NHCOCH₂Me - ^o-O- 257-259

23-55 -NHCOMe N^ "•-Q- 308-309

23-56 -NHCOCH₂Me ®^~ M_*2 ~ 249-250

Cl

23-57 -NH₂ 228-230

N=/

Cl

23-59 -NH₂ J- 256-258

Me

23-60 -NH₂ >< 255-258

23-61 -NH₂ Ό- ^~- - >300

23-62 -NH₂ o- Mβ→ - 296-298

23-63 -N=C(Me)NMe₂ f Ny=/ o- 129-131

23-64 -NHCOMe o- ^Me°^{~< >—} 282-284

23-65 -NHCOMe f Ny MeO ^ O ύ- 236-239

23-66 -NHCOCH₂Me fy Me

222-224

N=/

Table 12

Ref. Ex. Compd. Ra R_b Re mp/°C

MeO

23-68 -NHCOMe N^- ό- 234-236

MeO

23-69 -NHCOCH₂Me o- 237-239

23-70 -NHCOH o- MeO

220-222

23-71 -NHCOMe o- o- 294-297

23-72 -NHCOCH₂Me 2- o- 267-269

23-73 -N(CH₂Me)COMe < - ^Me0-^ ^— 143-144

23-74 -N((CH₂)₄Me)COMe o- MeO-cζ — 111-113

23-75

MeCO H₂ ^-7 ^■O ^Me°^{~< >—} 162-164

MeO

23-76 -NH₂

N=/

MeO ύ- 206-209

23-77 -NH₂ o- 232-234

23-78 -NH₂ X 36-239

N=- Cl

2 /

Cl

23-79 -NH₂ •O 232-235

Table 13

Ref. Ex. Compd. Ra Rb Re mp / °C

23-83 -NHCO-<f~Vci O" MeO-<^^— 346-348

23-84 -NHCO-^^>-OMe »x MeO- y— 308-310

23-85 -NH₂ Ό- HO QX 323-326

23-86 -NHCOMe 59-261

Cl

23-87 -NHCOMe _"X 0- 292-293

23-90 -NHCOMe _"X MeC00- — 254-257

23-91 -NHCOCH₂-^~^ _"X ^Me0~ ^-~ 274-277

23-92 -NHCOMe <χ Me

0- 237-239

23-93 -NHCOMe 7

"^ _H0-<Q_^ 285-28

23-95 -NHCOMe 272-274

23-96 -NH₂ •o- OMe

213-215

23-97 -NHCOMe 259-261

23-98 -NHCO(CH₂)₄CI 228-229

Table 14

<b .

X XR_a

Ref. Ex. Compd. Ra R_b Re mp / °C

23-99 -NHCOMe O ?7^ 254-257

23-100 '? _ J- MeO- y~ 159-160

23-101 - co-ζ^~)> Ό- 278-281

23-102 -NHCO-<^N _"X MeO- y— 295-297

23-105 -NHCOCHMe₂ _"X MeO→^^— 227-230

23-106 -NHCOCMe₃

MeO-fy— 254-256

23-107 -NHCOCH₂CHMe₂ 261-262

23-108 -NHCONH(CH₂)₂Me 215-219

23-110 -NHCOMe o- MeCH₂-^X 294-295

23-111 -NHCOMe 206-209

23-112 -NHCOMe «x Me(CH₂)₃0-^>— 201-203

23-113 -NHCOMe _" Me(CH₂)₆0-^- 210-212

23-114 -NHCO(CH₂)₃CI MeO- 191-194

Table 15

Ref. Ex. Compd. Ra R_b Re mp / °C

23-116 -NHCO(CH₂)₅CI « ^Me0_<0^>— 223-225

23-117

MeO

23-118 -NHCOMe " MeO→χV- 265-267

23-119 -NHCOMe o- Me

248-250

23-120 -NHCOMe Me₂CH-f%— 295-297

23-121 -NHCO(CH₂)₂COOCH₂Me

MeO-fy— 261-264

23-122 -NHCO(CH₂)₂COOH 334-336

23-125 -NH₂ 248-250

23-126 -NH₂ »x o^ 273-275

23-127 -NHCOMe o^ 295-296

23-128 -NHCOMe X 284-286

23-129 -NHCOMe X 289-291

Table 16

^Rb s

Ref. Ex. Compd. Ra Rb R_c Additive mp / °C

23-130 -NHCOCHMe₂ _" Me₂CH-Q»— 284-285

23-131 -NHCOCMe₃ o- Me₂CH-^ - 293-295

23-132 -NHCONH(CH₂)₂Me Me₂CH-Q)— 287-288

23-134 -NH₂ «x ^{Me2N" >_} 309-311

23-135 -CH₂COOCH₂Me _"X MeO-<Q>— HCl 150-152

23-137 -NHCOMe _"X ^{Me3C_< h~} 280-281

23-138 -NHCOCHMe₂ »x Me₃C-^— 303-304

23-139 -NHCOCMe₃ « Me₃C-<^— 317-319

23-140 -NHCOMe o- 342-345 -

23-141 -NHCOCHMe₂ " y- 297-298

23-142 -NHCOCMe₃ « ^ - 313-315

23-143 -NH₂ " Me₃C-X— 254-257

23-144 -NH₂ " Q 261-264

23-145 -CH₂COOH N MeO→^X 135-137

23-146 -CH₂CONHMe MeO- ^" — 129-130

Table 17

<b -

Jf XR_a

R_C A-^MN

Ref. Ex. Compd. ^Ra Rb Re mp / °C

23-147 -Me O- MeO→ — 132-133

23-148 -NHCOMe _" 256-258

23-149 -NHCOCHMe₂ « Me(CH₂)₂-^— 269-272

23-150

Me(CH₂)₂→Qx 240-242

23-151 -NHCOMe »x Me(CH₂)₃-^>— 259-261

23-152 -NHCOMe N Me^(CH₂ ⁾ ₅-£3— 237-239

23-153 -NHCOMe _" 296-298

23-154 -NHCOCHMe₂ » CF₃0-^— 285-286

23-155 -NHCOCF₃ X" MeO- y~ 260-262

23-156 -NHCONHCH₂Me

MeO-χ — 224-226

23-157 -NHCONHCH₂Me _" Me₂CH- — 181-183

23-158 -NH₂ O- Me(CH₂)₂-HQ)— 240-242

23-159 -NH₂ ^N Me(CH₂)₃-<^— 204-206

23-160 -NH₂ Me(CH₂)₅-<Q>— 178-179

23-163 -NHCOCH₂Me 295-297

23-164 -NHCO-(\~)> _" Me₃C-^— 292-294

Table 18

^R°>rS.

Rc X X"

Ref. Ex. Compd. R_a ^Rb Rc mp / °C

23-166 -NHCO-^^N _" ^{Me3C→ ~~} 326-329

23-168 -NHCO→ ] _" e₃C-^— 309-311

23-169 -NHCONHCH₂Me o- Me₃C-ζy 289-292

23-170 -NHCONH(CH₂)₂Me o- ^Me3C Q^" 212-214

23-171 -NHCOCH₂OMe X Me₃C-ζ 248-249

23-172 -NHCOMe 228-230

23-173 -NHCOCH₂Me <x Me₃C-<^— 244-246

N^

23-174 -NHCOCHMe₂

Me₃C-ζy 228-229

23-176 -NHCO <x Me₃C- y 216-218

N=/

23-177 -NHCO-<

Me₃C- - 218-220

/=N

23-178 -NHCO-^> <χ N^ ^{Me3c^} ^ 251-253

23-179 -NHCO→TΛl <χ N=/ ^{Me3c- —} 271-273

23-180 -NHCONHCH₂Me <χ Me₃C-ζy 302-305

N^

23-181 -NHCONH(CH₂)₂Me Me₃C- ~ 190-192

N=/

Table 19

<_bv.s_.

Rc J >- _a ^'L I

N

Ref. Ex. Compd. Ra Rb R. mp/°C

23-184 -NHCOMe _" <-o- 328-330

23-185 -NHCOCH₂Me ~ CF₃H 284-286

23-186 -NHCOCHMe₂ o- _Cf,yy 274-275

23-189 -NHCO-<^ ^ <-o- 272-273

23-191 -NHCO-VMN _"X °κ-Q- 263-264

23-192 -NHCONHCH₂Me <-o- 206-207

23-193 -NHCONH(CH₂)₂Me

^CF-C- 208-210

23-194 -NHCOCH₂Me _" 291-293

23-195 -NHCOCHMe₂ »x

23-198 -NHCO-< ] o- 275-278

Table 20 _v -sS, y I --M '>~^Ra

Rc' n

Ref. Ex. Compd. R_a Rb R R_cc mp / °C

23-200 302-304

23-201 -NHCONHCH,Me 202-203

23-202 -NHCONH(CH₂)₂Me

23-203 -NHCOCH₂OMe N O^{' x}) —- 220-222

23-204 -NH₂ 237-240

23-205 -NHCOMe 288-289

23-206 -NHCOCH₂Me 292-293

23-207 -NHCOCHMe₂ 253-254

23-208 -NHCOCH₂-Q> C/ 235-238

Table 21

^R s

Ref. Ex. Compd. Ra R_ R_c Additive mp / °C

23-210 -NHCO 277-278

23-212 -NHCONHCH₂Me

23-213 -NHCONH(CH₂)₂Mc i

23-214 -COOCH₂Me X MeO-fy— 149-150

23-215 -NHCOCH₂NMe₂ X Me₃c2ζy 230-231

23-217 -NHCOMe 195-197

23-218 -NHCOMe 266-270

23-220 -NHCOMe " MeCH₂0C0CH₂0-<ζ — 239-244

23-221 -NHCOMe X H0C0CH₂0→ — HCl 237-242

23-222 V 0 ^NH ^■o- ^Me0_ 3^— 248-250 Example 1

N-Methyl [ 5-phenyl-4- ( 3-pyridyl ) - 1 , 3-thiazol-2-yl] amine

To a solution of N-methylthiourea (484 mg) in acetonitrile (40 mL), was added 2-bromo-2-phenyl- 1- (3- pyridyl) ethanone hydrobromide (2.0 g) , and then triethylamine (0.8 mL) was added dropwise to the mixture with stirring. After addition, the resulting mixture was stirred at reflux for 3 h and the solvent was evaporated. An aqueous saturated solution of sodium hydrogen carbonate was added to the residue and extracted with ethyl acetate. The extracts were washed with water, dried and the solvent was evaporated. The crystalline residue was recrystallized from ethyl acetate-isopropyl ether to give the title compound (1.2 g, yield 80 %) . mp 144-145°C.

Example 2

[ 5-Phenyl-4- ( 3-pyridyl ) -1 , 3-thiazol-2-yl] amine To a mixture of 2-bromo-2-phenyl- 1- (3- pyridyl ) ethanone hydrobromide (2.00 g) and thiourea (432 mg) in acetonitrile (30 mL) , was added triethylamine (0.80 mL) dropwise and the resulting mixture was stirred at 80° C for 3 h. The solvent was removed under reduced pressure and an aqueous saturated solution of sodium hydrogen carbonate was added to the residue. The mixture was extracted with ethyl acetate. The organic phases were washed with water, dried and concentrated under reduced pressure to give the amorphous title compound (1.10 g, yield 84 %).

^XH-NMR (CDC1₃) δ : 5.31 (2H, br s), 7.13-7.29 (6H, m) ,

7.76 (IH, dt, J = 7.8, 1.8 Hz), 8.46 (IH, dd, J = 5.0, 1.8 Hz), 8.70 (IH, d, J = 1.8 Hz).

Example 3

N-[5-Phenyl-4-(3-pyridyl)-l,3-thiazol-2-yl]acetamide To a solution of [ 5-phenyl-4- ( 3-pyridyl) -1 , 3- thiazol-2-yl]amine (1.10 g, 4.34 mmol) in N,N- dimethylacetamide (20 mL) was added acetyl chloride (680 mg, 8.68 mmol) and stirred at 80° C for 3 h. Water was added to the reaction mixture and extracted with ethyl acetate twice. The combined organic phases were washed with water, dried over magnesium sulfate, filtered and concentrated under reduced pressure. The residue was recrystallized from chloroform-ethyl ether to give the title compound (750 mg, yield 59 %). mp 264-267°C.

Example 4

Using 2-bromo-2- [ 4 - ( 1 , 1-dimethylethyl)phenyl ] - 1- (4-pyridyl) ethanone hydrobromide and 2-bromo-2- (3, 5- dimethylphenyl ) - 1- ( 4-pyridyl ) ethanone hydrobromide instead of using 2-bromo-2-phenyl- 1- (3-pyridyl) ethanone hydrobromide, the below Example Compounds 4-1 and 4-2 were obtained in the same manner as described in above Example 2.

Example Compound 4-1:

[ 5- [ 4- ( 1 , 1-dimethylethyl )phenyl ] -4- ( 4-pyridyl ) -1 , 3- thiazol-2-yl ] amine mp 275-277°C. Example Compound 4-2:

[ 5- ( 3 , 5-dimethylphenyl ) -4- ( 4-pyridyl) -1 , 3-thiazol-2- yl] amine mp 262-263° C.

Example 5

Using [ 5- [4- ( 1, 1-dimethylethyl)phenyl] -4- (4- pyridyl) -1,3-thiazol-2-yl] amine and [5- (3, 5- dimethylphenyl) -4- ( 4-pyridyl) -1 , 3-thiazol-2-yl]amine instead of using [ 5-phenyl-4- (3-pyridyl) -1, 3-thiazol-2- yl] amine, the below Example Compounds 5-1 and 5-2 were obtained in the same manner as described in above Example 3 .

Example Compound 5- 1 :

N-[5-[4-(l,l- imethylethyl )phenyl ] -4- ( 4-pyridyl ) - 1 , 3- thiazol-2-yl] acetamide mp 245-246° C.

Example Compound 5-2:

N-[5-(3,5-dimethylphenyl)-4-(4-pyridyl)-l,3-thiazol-2- yl] acetamide mp 304-308° C.

Example 6

2-Ethyl-5-phenyl-4-(3-pyridyl)- 1,3-thiazole

Using propanethioamide instead of using N- methylthiourea, the title compound was obtained in the same manner as described in the above Example 1. mp 144-145° C

Example 7

4- [ 5-Phenyl-4- ( 3-pyridyl ) - 1 , 3-thiazol-2-yl] butyric acid A solution of methyl 4- [ 5-phenyl-4- ( 3-pyridyl) - l,3-thiazol-2-yl]butyrate (4.1 g) , which was obtained in the same manner as described in the above Example 1 using 4- (methoxycarbonyl )butanethioamide instead of using N-methylthiourea, in methanol (15 mL) was added to an 8N aqueous sodium hydroxide solution (20 mL) and stirred at 80° C for 2h. The mixture was adjusted to pH 6.0 with 2N hydrochloric acid and the product was extracted with ethyl acetate. The extract was washed with water, dried and the solvent was evaporate. The residue was recrystallized from ethyl acetate to afford the title compound (3.4 g, yield 87 %). mp 141-142° C

Example 8 4- [2-Acetylamino-4-(3, 5-dimethylphenyl) -1, 3-thiazol-5- yl] pyridine 1-oxide To a suspension of N- [4- (3, 5-dimethylphenyl) -5- (4- pyridyl)-1, 3-thiazol-2-yl] acetamide (1.0 g) in chloroform (30 mL), was added 70% m-chloroperbenzoic acid (0.80 g) , and the mixture was stirred at room temperature for 1 h. The solvent was removed under reduced pressure, and the residue was treated with an aqueous saturated solution of sodium hydrogen carbonate. The formed crystalline residue was washed with water, dried and recrystallized from ethanol to obtain the title compound (0.55 g, yield 53 %). mp 332-334° C

The chemical structures obtained in Examples 1 to 8 are shown in Table 22.

Table 22

Ex. Compd. Ra Rb Ro

2 -NH₂ o- <χ N=/

3 -NHCOMe o- <χ N^

5-1 -NHCOMe Me₃C- y~ _"

5-2 -NHCOMe

Me

8 -NHCOMe

Me fy

Formulation Example 1

(1) Reference Example Compound 13-89 50 mg

(2) Lactose 34 mg

(3) Corn starch 10.6 mg

(4) Corn starch (paste) 5 mg

(5) Magnesium stearate 0.4 mg

(6) Calcium carboxymethyl cellulose 20 mg

Total 120 mg (1) to (6) were mixed in an ordinary manner, and tabletted into tablets using a tabletting machine.

Experimental Example 1 The following procedures in this Example were carried out according to the methods described in Molecular Cloning - Cold Spring Harbor Laboratory (1989) or protocol specified by manufacturers.

(1) Cloning of human adenosine A₃ receptor Cloning of the human adenosine A₃ receptor gene was carried out by the polymerase chain reaction (PCR) from human brain cDNA. Using 1 ng of brain cDNA (Quick-Clone cDNA, TOYOBO, Osaka) as template, PCR was performed in DNA Thermal Cycler 480 (Perkin Elmer, Foster, CA) (reaction conditions: 35 cycles of 1 min at 95 °C, 1 min at 66 °C, and 2 min at 75 °C) by mixing primers (50 pmol each),

5 ' -CGCCTCTAGACAAGATGCCCAACAACAGCACTGC-3 ' [ Sequence No . 1] and 5'-CGGGGTCGACACTACTCAGAATTCTTCTCAATGC-3' [Sequence No. 2], which were designed referring to nucleotide sequence of adenosine A₃ receptor gene reported by Salvatore et. al., (Proc. Natl. Acad. Sci. U. S. A., 90:10365-10369, 1993) and TaKaRa LA PCR Kit Ver.2 (TaKaRa Shuzo Co. Ltd., Kyoto) in a Thermal cycler 480 (Parkin Elmer). The PCR product was electrophoresed and 1.0 kb DNA fragment was recovered. The DNA fragment encoding adenosine A₃ receptor was cloned using Original TA Cloning Kit (FUNAKOSHI, Tokyo) Thus obtained plasmid was digested with Xba I (TaKaRa Shuzo Co. Ltd., Kyoto), blunted with T4 DNA polymerase (TaKaRa Shuzo Co. Ltd. , Kyoto) and digested with Sal I (TaKaRa Shuzo Co. Ltd., Kyoto) to obtain adenosine A₃ receptor gene fragment .

(2) Construction of human adenosine A₃ receptor expression plasmid The SRα promoter from pTB1411 disclosed in JP-A-5- 076385 was ligated into the pCI vector (Promega, Tokyo), which was digested with Bgl II (TaKaRa Shuzo Co. Ltd., Kyoto), blunted and digested with EcoRl (TaKaRa Shuzo Co. Ltd. , Kyoto) subsequently. The resulting plasmid, designated as pCI-SRα, was then digested with Cla I (TaKaRa Shuzo Co. Ltd., Kyoto) and blunted with T4 DNA polymerase (TaKaRa Shuzo Co. Ltd., Kyoto). On the other hand, pGFP-Cl (TOYOBO, Osaka) was digested with Bsu 361 (DAIICHIKAGAKUYAKUHIN, Tokyo) and the 1.63kb fragment was recovered after the blunting with T4 DNA polymerase to ligate to the pCI-SRα vector using DNA Ligation kit (TaKaRa Shuzo Co. Ltd., Kyoto). The ligation mixture was used to transform E. coli JM109 competent cells (TaKaRa Shuzo Co. Ltd., Kyoto). The resulting plasmid thus obtained was designated as pMSRαneo. pMSRαneo was digested with EcoRΪ (TaKaRa Shuzo Co. Ltd., Kyoto), blunted with T4 DNA polymerase (TaKaRa Shuzo Co. Ltd., Kyoto) and then digested with Sal I (TaKaRa Shuzo Co. Ltd., Kyoto). After the reaction mixture was fractionated on agarose gel, the DNA at size of 5.4 kb was ligated with adenosine A₃ receptor obtained in the above (1) by using DNA Ligation kit (TaKaRa Shuzo Co. Ltd., Kyoto). The ligation mixture was used to transform E.coli JM109 competent cells (TaKaRa Shuzo Co. Ltd., Kyoto). The plasmid thus obtained was designated as pA3SRα.

(3) Transfection of adenosine A₃ receptor expression plasmid into CHO (dhfr^~) and the expression CHO (dhfr^~) cells were grown on Ham's F-12 medium (Nihon Seiyaku, Tokyo) supplement with 10 % fetal bovine serum (Life Tech Oriental; Life Technologies, Inc., Rockville, MD, USA) in a 750 ml Tissue culture flask (Becton Dickinson, Mt. View, CA) . The growing cells were treated with 0.5g/l trypsin-0.2g/l EDTA (Life Technologies, Inc., Rockville, MD, USA) to harvest, washed with PBS (Life Technologies, Inc., Rockville, MD, USA), centrifugated at 1000 rpm for 5 min, and suspended in PBS. Transfection with pA3SR into the cell was performed by electroporation using a Bio-Rad/Gene Pulser (Bio-Rad, Tokyo) at 0.25 V/960 μF

(8 x 10⁶ cells/10 μg DNA/0.4 cm electrode gap cuvette). The transfected cells were transferred into Ham's F-12 medium containing 10 % fetal bovine serum, cultivated for 24 hours, harvested, suspended in Ham's F-12 media supplement with 10 % fetal bovine serum and 500 μg/ml geneticin (Life Technologies Inc., Rockville, MD, USA) at a cell density of 10⁴ cells/ml. The cells were plated onto 96 well plates (Becton Dickinson, Mt . View, CA) containing Ham's F-12 media supplement with 10 % fetal bovine serum and 500 μg/ml geneticin (Life Technologies Inc., Rockville, MD, USA) at a cell density of 10⁴ cells/ml. The geneticin resistant cells thus obtained were further cultivated on 24 well plates (Becton Dickinson, Mt . View, CA) and the cells expressing adenosine A₃ receptor were selected from them as follows. The cells were incubated in assay buffer I (HBSS (Wako chemicals, Osaka) containing 0.1 % BSA, 0.25 mM PMSF, 1 μg/ml pepstatin, and 20 μg/ml leupeptin) to which was added 50 pM ¹²⁵I-AB-MECA (Amersham) as ligand, for 1 hour, and washed with assay buffer I . The radioactivity associated with the cell was measured in a γ-counter to select A3AR/CHO cells which specifically bind to the ligand.

(4) Cell membrane preparation of the transfectant expressing adenosine A₃ receptor

After A3AR/CH0 cells obtained in the above (3) were cultivated in Ham's F-12 medium containing 10 % fetal bovine serum for 2 days , the cells were treated with PBS plus 0.02% EDTA, centrifuged to collect, resuspended in assay buffer II (50 mM Tris-HCl (pH7.5),

1 mM EDTA, 10 mM MgCl₂, 0.25 mM PMSF, 1 μg/ml pepstatin, and 20 μg/ml leupeptin) and homogenized using Polytron homogenizer (PT-3000, KINEMATICA AG: 20,000 rpm, 20 sec, 3 times). This suspension was centrifuged at 2,000 rpm for 10 min and supernatant fraction containing cell membranes was obtained. The supernatant fraction was ultra-centrifuged at 30,000 rpm (model L8-70M, rotor 70Ti, Beckman) for 1 hour. Thus obtained pellet was resuspended in assay buffer II containing 2 unit/ml adenosine deaminase (Boehriger Mannheim, Tokyo) and incubated at 30 °C for 30 min. The suspension was ultra-centrifuged under the same condition as above and the cell membrane fraction was obtained as the pellet . (5) Binding assays with adenosine A3 receptor

10 nM of [³H]-NECA (Amersham Life Sciences, Inc., Tokyo) as ligand was added to the reaction mixture including test compound at various concentration and

100 μg/ml of membranes obtained in (4) in assay buffer II. The reaction mixture was incubated for 1 hour at room temperature and filtrated through the Unifilter GF/C (Packard Instrument Company, Tokyo) to transfer the membrane onto the filter, using Cell Harvester

(Packard Instrument Company, Tokyo). The filter was washed three times with ice-cold 50 mM Tris-HCl (pH 7.5), and dried. Then, Microscint-0 was placed on the filter and radioactivity retained on the filter was determined by Top-Count (Packard Instrument Company,

Tokyo) . Curve-fit and the concentration that inhibits

50 % specific binding (IC_5Q) to the membrane of [³H]-

NECA were calculated by program Prizm 2.01 (Graph Pad Software, San Diego). Results are shown in Table 23

Table 23

Reference Compound No. ^IC50 (^nM) 10 0.27

13-89 0.55

13-92 0.70

This result shows that the compound ( I ) has a high affinity for adenosine A3 receptor.

INDUSTRIAL APPLICABILITY Since compound (I) containing compounds (la), (lb) and (lc) has a potent A3 adenosine receptor antagonistic activity and low toxicity, it is useful as A3 adenosine receptor antagonist and can be used as a prophylactic and therapeutic agent for asthma, allergosis, inflammation, Addison's diseases, autoallergic hemolytic anemia, Crohn ' s diseases, psoriasis, rheumatism, diabetes and so on.

Claims

1. A pharmaceutical composition for antagonizing adenosine at adenosine A₃ receptors which comprises a 1,3-azole compound substituted on the 4- or 5-position, or both, by a pyridyl which may be substituted.

2. A composition of claim 1, wherein the 1,3-azole compound is a compound of the formula:

wherein R¹ represents a hydrogen atom, a hydrocarbon group which may be substituted, a heterocyclic group which may be substituted, an amino which may be substituted or an acyl; at least one of R² and R³ represents a hydrogen atom, a pyridyl which may be substituted or an aromatic hydrocarbon group which may be substituted, and the other represents a pyridyl which may be substituted; and

X represents a sulfur atom which may be oxidized, an oxygen atom or a group of the formula: NR⁴ wherein R⁴ represents a hydrogen atom, a hydrocarbon group which may be substituted or an acyl; or a salt thereof, which may be N-oxidized.

3. A composition of claim 2, wherein R¹ is (i) a hydrogen atom,

(ii) a C-^g alkyl, C₂_₆ alkenyl, C₂_g alkynyl, C₃_₆ cycloalkyl, Cg_₁₄ aryl or C₇_^ aralkyl group which may be substituted by 1 to 5 substituents,

(iii) a 5- to 14-membered heterocyclic group containing 1 to 4 hetero atoms selected from the group consisting of nitrogen, sulfur and oxygen atoms in addition to carbon atoms, which group may be substituted by 1 to 5 substituents,

(a) a C-L.g alkyl, C₂_₆ alkenyl, C₂_₆ alkynyl, C₃_₆ cycloalkyl, Cg_₁₄ aryl or C₇_₁₆ aralkyl group which may be substituted by 1 to 5 substituents,

(b) a C-L_g alkylidene group which may be substituted by 1 to 5 substituents,

(d) an acyl of the formula: -(C=0)-R⁵, -(C=0)-OR⁵, -(C=0)-NR⁵R⁶, -(C=S)-NHR⁵ or -S0₂-R⁷ wherein R⁵ is

(i') a hydrogen atom, (ii') a C^.g alkyl, C₂_g alkenyl, C₂_g alkynyl, C₃_g cycloalkyl, Cg_₁₄ aryl or C₇_₁₆ aralkyl group which may be substituted by

1 to 5 substituents or (iii') a 5- to 14-membered heterocyclic group containing 1 to 4 hetero atoms selected from the group consisting of nitrogen, sulfur and oxygen atoms in addition to carbon atoms , which group may be substituted by 1 to 5 substituents; R⁶ is a hydrogen atom or C-^.g alkyl; and R⁷ is (i') a C-^g alkyl, C₂_₆ alkenyl, C₂_₆ alkynyl, C₃_g cycloalkyl, Cg_₁₄ aryl or C₇_₁₆ aralkyl group which may be substituted by 1 to 5 substituents or (ii') a 5- to 14-membered heterocyclic group containing 1 to 4 hetero atoms selected from the group consisting of nitrogen, sulfur and oxygen atoms in addition to carbon atoms , which group may be substituted by 1 to 5 substituents , (v) a 5- to 7-membered non-aromatic cyclic amino optionally containing 1 to 4 hetero atoms selected from the group consisting of nitrogen, sulfur and oxygen atoms in addition to carbon atoms and at least one nitrogen atom, which may be substituted by 1 to 3 substituents selected from the group consisting of C^.g alkyl, Cg_₁₄ aryl, C^.g alkyl-carbonyl, 5- to 10- membered aromatic heterocyclic group and oxo, or (vi) an acyl of the formula: -(C=0)-R⁵, -(C=0)-OR⁵, -(C=0)-NR⁵R⁶, -(C=S)-NHR⁵ or -S0₂-R⁷ wherein each symbol is as defined above; at least one of R² and R³ is (i) a hydrogen atom, (ii) a pyridyl which may be substituted by 1 to 5 substituents or (iii) a Cg_₁₄ aryl which may be substituted by 1 to 5 substituents in which a substituent can form, together with a neighboring substituent, a 4- to 7-membered non-aromatic carbocyclic ring; and the other is a pyridyl which may be substituted by 1 to 5 substituents; and

X is a sulfur atom which may be oxidized, an oxygen atom or a group of the formula: NR⁴ wherein R⁴ is (i) a hydrogen atom, (ii) a C-^ alkyl, C₂_g alkenyl, C₂_g alkynyl, C₃_g cycloalkyl, Cg_₁₄ aryl or C₇_₁₆ aralkyl group which may be substituted by 1 to 5 substituents or (iii) an acyl of the formula: -(C=0)-R⁵, -(C=0)-OR⁵,

-(C=0)-NR⁵R⁶, -(C=S)-NHR⁵ or -S0₂-R⁷ wherein each symbol is as defined above, wherein the above "substituents" are selected from the group consisting of (1) halogen atoms, (2) C_1-3 alkylenedioxy, (3) nitro, (4) cyano, (5) optionally halogenated C_1-6 alkyl, (6) optionally halogenated C₂_₆ alkenyl, (7) carboxy C₂_₆ alkenyl, (8) optionally halogenated C₂_g alkynyl, (9) optionally halogenated ^c3-6 cycloalkyl, (10) Cg_₁₄ aryl, (11) optionally halogenated C-_j^ alkoxy, (12) C_1-6 alkoxy-carbonyl-C_1-6 alkoxy, (13) hydroxy, (14) C₆_₁₄ aryloxy, (15) C₇_₁₆ aralkyloxy, (16) mercapto, (17) optionally halogenated C-L.g alkylthio, (18) Cg_₁₄ arylthio, (19) C₇_₁₆ aralkylthio, (20) amino, (21) mono-C^g alkylamino,

(22) mono-Cg_₁₄ arylamino, (23) di-C₁_g alkylamino,

(24) di-Cg_₁₄ arylamino, (25) formyl, (26) carboxy, (27) C_╬╗__e alkyl-carbonyl, (28) C₃_₆ cycloalkyl-carbonyl,

(29) C"L_g alkoxy-carbonyl, (30) Cg_₁₄ aryl-carbonyl,

(31) C₇_₁₆ aralkyl-carbonyl, (32) Cg_₁₄ aryloxy- carbonyl, (33) C₇_₁₆ aralkyloxy-carbonyl, (34) 5- or 6- membered heterocycle carbonyl, (35) carbamoyl, (36) mono-C-L.g alkyl-carbamoyl, (37) di-C₁_g alkyl-carbamoyl,

(38) Cg_ ₄ aryl-carbamoyl, (39) 5- or 6-membered heterocycle carbamoyl, (40) C^.g alkylsulfonyl , (41) ^c6-14 arylsulfonyl, (42) formylamino, (43) C^.g alkyl- carbonylamino , (44) Cg_₁₄ aryl-carbonylamino, (45) C^.g alkoxy-carbonylamino, (46) C^_g alkylsulfonylamino ,

(47) Cg_₁₄ arylsulfonylamino , (48) C-^.g alkyl- carbonyloxy, (49) Cg_₁₄ aryl-carbonyloxy, (50) C-^.g alkoxy-carbonyloxy, (51) mono-C_j.g alkyl-carbamoyloxy,

(52) di-C-L_g alkyl-carbamoyloxy, (53) Cg_₁₄ aryl- carbamoyloxy, (54) nicotinoyloxy, (55) 5- to 7-membered saturated cyclic amino which may be substituted by 1 to 3 substituents selected from the group consisting of C-L_₆ alkyl, Cg_₁₄ aryl, C-^.g alkyl-carbonyl, 5- to 10- membered aromatic heterocyclic group and oxo, (56) 5- to 10-membered aromatic heterocyclic group and (57) sulfo.

4. A composition of claim 2 , wherein R¹ is an amino which may be substituted.

5. A composition of claim 3, wherein R¹ is an amino which may be substituted by 1 or 2 acyl of the formula: -(C=0)-R⁵, -(C=0)-OR⁵, -(C=0)-NR⁵R⁶, -(C=S)-NHR⁵ or

-S0₂-R⁷.

6. A composition of claim 3 , wherein R is an amino which may be substituted by 1 or 2 acyl of the formula:

-(C=0)-R⁵ or -(C=0)-NR⁵R⁶.

7. A composition of claim 3, wherein R¹ is a 5- to 7- membered non-aromatic cyclic amino optionally containing 1 to 4 hetero atoms selected from the group consisting of nitrogen, sulfur and oxygen atoms in addition to carbon atoms and at least one nitrogen atom, which may be substituted by 1 to 3 substituents selected from the group consisting of C_1-6 alkyl, Cg_₁₄ aryl, C^.g alkyl-carbonyl, 5- to 10-membered aromatic heterocyclic group and oxo.

8. A composition of claim 2, wherein X is S.

9. A composition of claim 2, wherein R² is a pyridyl which may be substituted.

10. A composition of claim 2, wherein R³ is a C _^₄ aryl which may be substituted.

11. A composition of claim 3, wherein R^ is an amino which may be substituted by 1 or 2 acyl of the formula:

-(C=0)-R⁵ or -(C=0)-NR⁵R⁶;

R² is a pyridyl which may be substituted by 1 to 5 C_1-6 alkyl ;

R³ is a Cg_₁₄ aryl which may be substituted by 1 to 5 substituents selected from the group consisting of halogen atoms, optionally halogenated C-_j^g alkyl, optionally halogenated C₁_g alkoxy and carboxy; and X is S .

12. A composition of claim 2, wherein R¹ is (i) a C-^.g alkyl, C₃_g cycloalkyl or Cg_₁₀ aryl group which may be substituted by 1 to 5 substituents selected from the group consisting of halogen atoms , optionally halogenated C^.g alkyl, carboxy C₂_g alkenyl, optionally halogenated C^_g alkoxy, C-^.g alkoxy- carbonyl-C-^.g alkoxy, hydroxy, amino, mono-C₁_g alkylamino, carboxy, C^_g alkoxy-carbonyl, mono-C^.g alkyl-carbamoyl and Cg_₁ aryl-carbonylamino,

(ii) a 5-membered heterocyclic group, (iii) an amino which may be substituted by 1 or 2 substituents selected from the group consisting of (1) C_╬╗_₆ alkyl, (2) C₆_₁₄ aryl, (3) C₇_₁₆ aralkyl, (4) 6- membered heterocyclic group, (5) a C₁_g alkyl-carbonyl, ^c ₃-₆ cycloalkyl-carbonyl, Cg_₁₄ aryl-carbonyl, C₇_₁₆ aralkyl-carbonyl, C^_g alkyl-carbamoyl or 5- or 6- membered heterocycle carbonyl group which may be substituted by 1 to 3 substituents selected from the group consisting of halogen atoms, C_1-6 alkyl, C_1-6 alkoxy, carboxy and C_1-6 alkoxy-carbonyl, and (6) di-

C _g alkylamino-C-^.g alkylidene,

(iv) a 5- or 6-membered non-aromatic cyclic amino which may be substituted by C-^.g alkyl-carbonyl or oxo, or (v) carboxy;

R² is a pyridyl which may be substituted by 1 to 3 C-L.g alkyl;

R³ is a Cg_-L_Q aryl which may be substituted by 1 to 3 substituents selected from the group consisting of halogen atoms, C₁_₃ alkylenedioxy, optionally halogenated C^_g alkyl, carboxy C₂_g alkenyl. optionally halogenated C-^.g alkoxy, hydroxy, C₇_-^g aralkyloxy and C^.g alkyl-carbonyloxy, in which the alkyl group can form, together with a neighboring alkyl group, a 5-membered non-aromatic carbocyclic ring; and X is S.

13. An adenosine A₃ receptor antagonist which comprises a 1,3-azole compound substituted on the 4- or 5-position, or both, by a pyridyl which may be substituted.

14. A composition of claim 1, which is for preventing and/or treating asthma or allergosis.

15. A compound of the formula:

_R ²a represents an aromatic hydrocarbon group which may be substituted; and

R^3a represents a pyridyl which may be substituted, or a salt thereof .

16. A compound of claim 15, wherein R^la is an amino which may be substituted by 1 or 2 substituents selected from the group consisting of C-^.g alkyl, C^_g alkyl-carbonyl, Cg_₁₄ aryl-carbonyl and C^.g alkyl- carbamoyl; R^2a is a phenyl which may be substituted by 1 to 3 substituents selected from the group consisting of halogen atoms, optionally halogenated C^_g alkyl and optionally halogenated C_j^.g alkoxy; and

R^3a is a pyridyl.

17. A process for producing of a compound of Claim 15, which comprises reacting a compound of the formula:

_2a ₃a

R -CH-COR I Hal wherein Hal represents halogen atoms and other symbols are as defined in claim 15, or a salt thereof with a compound of the formula:

ΓÇ₧la

R -C-NH

II ² s wherein R^la is as defined in claim 15, or a salt thereof, optionally in the presence of a base.

18. A pharmaceutical composition which comprises a compound of claim 15.

19. A composition of claim 18 which is an agent for antagonizing adenosine at adenosine A₃ receptors.

20. A composition of claim 18 which is for preventing and/or treating asthma or allergosis.

21. A method for preventing and/or treating diseases related to adenosine A₃ receptor in mammal, which comprises administering to said mammal an effective amount of a compound of claim 1 or a pharmaceutically acceptable salt thereof with a pharmaceutically acceptable excipient , carrier or diluent .

22. Use of a compound of claim 1 or a salt thereof for manufacturing a pharmaceutical composition for preventing and/or treating diseases related to adenosine A₃ receptor.