首页> 外国专利> NEW 4- (2-FUROYL) -AMINO-PIPERIDINES, INTERMEDIATE PRODUCTS FOR THE SYNTHESIS, METHOD FOR THE PRODUCTION THEREOF AND THEIR MEDICAL USE

NEW 4- (2-FUROYL) -AMINO-PIPERIDINES, INTERMEDIATE PRODUCTS FOR THE SYNTHESIS, METHOD FOR THE PRODUCTION THEREOF AND THEIR MEDICAL USE

机译:新的4-(2-呋喃基)-氨基哌啶类化合物,用于合成的中间产物,其生产方法及其医学用途

摘要

There are provided novel 4-(2-furoyl)aminopiperidines represented by the general formula (I), their synthetic intermediates, processes for their preparation and medicaments containing them. CHEM In the above formula, X is CH or N, and Y is a group of the following general formula (II), formula (II-a) or formula (III): CHEM CHEM CHEM wherein a, b and c are each an integer of 0-6; Z is CH2 or NH; W is O or S; T is O or N-R15 wherein R15 is H, a C1-C6 alkyl group, a benzyl group or a phenethyl group; and R1 is H, a C1-C6 alkoxycarbonyl group, a benzyloxycarbonyl group, or the like. ??The 4-(2-furoyl) aminopiperidine derivatives according to this invention possess opioid mu antagonistic activity and are useful for the treatment or prevention of side effects which are caused by mu receptors agonist and which are selected from constipation, nausea/emesis or itch, or for the treatment or prevention of idiopathic constipation, postoperative ileus, paralytic ileus, irritable bowel syndrome or chronic pruritus.
机译:提供了由通式(I)表示的新颖的4-(2-呋喃基)氨基哌啶,它们的合成中间体,其制备方法和包含它们的药物。 <化学式>在上式中,X为CH或N,且Y为以下通式(II),式(II-a)或式(III)的基团: a,b和c均为0-6的整数; Z为CH 2或NH; W是O或S; T为O或N-R 15,其中R 15为H,C 1 -C 6烷基,苄基或苯乙基; R 1为H,碳原子数1〜6的烷氧羰基,苄氧羰基等。根据本发明的4-(2-糠酰基)氨基哌啶衍生物具有阿片样物质mu拮抗活性,可用于治疗或预防由mu受体激动剂引起的副作用,所述副作用选自便秘,恶心/呕吐或瘙痒,或用于治疗或预防特发性便秘,术后肠梗阻,麻痹性肠梗阻,肠易激综合征或慢性瘙痒症。

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