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NEW DERIVATIVES OF BENZIMIDAZOLE AND IMIDAZOPYRIDINE AND THEIR APPLICATION AS MEDICINES

机译:苯并咪唑和咪唑并吡啶的新衍生物及其在药物中的应用

摘要

1,2-Disubstituted 6-(aminomethyl, aminocarbonyl or aminocarbonylalkyl)-benzimidazole derivatives (or imidazo-pyridine derivative analogs) (I) are new. Benzimidazole or imidazo-pyridine derivatives of formula (I), in the form of racemates, enantiomers or combinations of enantiomers in all proportions, and their salts are new. [Image] A : CH 2, CO or CO-CR aR b; X : N or CH; R a and R bH or R; R : 1-6C alkyl; R 1H or alkyl; R 2alkyl; or NR 1R 2heterobicycloalkyl or heterocycloalkyl, optionally substituted (os) by one or more R; R 3-(CH 2) p-Z 3, -CO-Z' 3, -CH(OH)-Z' 3 or -CONH-Z'' 3; Z 3R, OR, COR, COOR, CONHR, cycloalkyl, heterocycloalkyl, aryl or heteroaryl (where cycloalkyl and heterocycloalkyl are os by one or more R or oxy; and aryl is os by one or more of halo, NO 2 or -(CH 2) p-V 3-Y 3); or 1,3-benzodioxolyl, 1,4-benzodioxanyl or maleimido; V 3O, S, CO, COO, NHCO, CONR' 3, NHCONR' 3 or direct bond; Y 3H or R (os by one or more halo); Z' 3aryl (os by one or more of halo, NO 2 or -(CH 2) p-V' 3-Y 3); V' 3O, CO, COO, NHCO, CONR' 3 or direct bond; R' 3H, R or OR; Z'' 3H, -A 3-COOR, -A 3-CONHR or -A 3-OR; A 31-6C linear or branched hydrocarbon chain or arylene; p : 0-4; R 4-(CH 2) s-R' 4; R' 4heterocycloalkyl or heteroaryl (both containing at least one N and os by R); or -NW 4W' 4; W 4H or alkyl; W' 4-(CH 2) s-Z 4; Z 4H, alkyl or cycloalkyl; s : 0-6; and alkyl moieties have 1-8C and cycloalkyl moieties 3-7C unless specified otherwise. An independent claim is also included for the preparation of (I). ACTIVITY : Anorectic; immunomodulator; tranquilizer; antidepressant; analgesic; vasotropic; dermatological; antiinflammatory; antiseborrheic; cytostatic; neuroprotective. MECHANISM OF ACTION : Melanocortin receptor agonist or antagonist. In particular (I) are ligands for melanocortin MC4 receptors. Most compounds (I) have K i values of less than micromolar in MC4 receptor affinity assays (no specific values for individual compounds are given in the source material).
机译:1,2-二取代的6-(氨基甲基,氨基羰基或氨基羰基烷基)-苯并咪唑衍生物(或咪唑并吡啶衍生物类似物)(I)是新的。具有所有比例的外消旋物,对映异构体或对映异构体组合形式的式(I)的苯并咪唑或咪唑并吡啶衍生物及其盐是新的。 [图像] A:CH 2,CO或CO-CR aR b; X:N或CH; R a和R bH或R; R:1-6C烷基; R 1H或烷基; R 2烷基;或NR 1R 2杂双环烷基或杂环烷基,任选地被一个或多个R取代(os); R 3-(CH 2)p-Z 3,-CO-Z'3,-CH(OH)-Z'3或-CONH-Z''3 Z 3 R,OR,COR,COOR,CONHR,环烷基,杂环烷基,芳基或杂芳基(其中环烷基和杂环烷基为一个或多个R或氧基所形成的os;而芳基为一个或多个卤素,NO 2或-(CH 2)pV 3-Y 3);或1,3-苯并二氧戊基,1,4-苯并二氧杂烷基或马来酰亚胺基;或V 3O,S,CO,COO,NHCO,CONR'3,NHCONR'3或直接键; Y 3H或R(os具有一个或多个卤素); Z′3芳基(由卤素,NO 2或-(CH 2)p-V′3-Y 3中的一个或多个形成的os); V'3O,CO,COO,NHCO,CONR'3或直接键; R'3H,R或OR; Z''3H,-A 3-COOR,-A 3-CONHR或-A 3-OR; 31-6C直链或支链烃链或亚芳基; p:0-4; R 4-(CH 2)s-R'4; R′4杂环烷基或杂芳基(两者均含有至少一个N和R所含的os);或-NW 4W'4; W 4H或烷基; W'4-(CH 2)s-Z 4; Z 4H烷基或环烷基; s:0-6;除非另有说明,否则烷基部分具有1-8C和环烷基部分具有3-7C。还包括独立权利要求以制备(I)。活动:厌食;免疫调节剂镇定剂抗抑郁药止痛药促血管皮肤;消炎(药;抗脂溢性;细胞生长抑制具有神经保护作用。作用机理:黑皮质素受体激动剂或拮抗剂。特别地,(I)是黑皮质素MC4受体的配体。在MC4受体亲和力测定中,大多数化合物(I)的K i值均小于微摩尔(在源材料中未提供单个化合物的具体值)。

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