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Bicyclic compounds with nitrogen content assets in chronic pain conditions

机译:慢性疼痛条件下具有氮含量资产的双环化合物

摘要

The compounds are active in chronic pain conditions of different Origins; they may be used alone or with other drugs. Also included is a process for preparing such compounds and Pharmaceutical compositions suitable for delivery to a patient.Claim 1: compounds of the formula (1) in which the R groups are independently C1 - 6 h, alkyl, aryl, CF3 and CH2, c = o, X is link, c = o, SO2, c = N - CN, M is 0, 1, N is 0 1; is a Heterocyclic Group, or a formula (2) in which R1, R2, R4 and R5 are independently h, h Allogenic, alkyl alkoxy C1 C1 - 6, 6 -, cyano, amino, Hydroxy, aryl, alquiloamino C1 - 6Di (alkyl amino aminoc1 C1 - 6), 6alquilo C1 - alkyl -, 6 - aminoc1 - 6aiquiio, di (alkyl C1 - 6) 6alquilo aminoc1 - Carboxy - or perhaloc1 6alquilo; R3 is perhaloc1 - 6alquilo h, alkyl, halogen, alkoxy C1 C1 - 6, 6 -, cyano, carboxy, hydroxy alquiloamino C1, 6 - di (alkyl, amino, aminoc1 C1 - 6) 6alquilo C1 -, alkyl - 6 - 6alquilo aminoc1 -, or di (alquiio C1 - 6) aminoc1 - 6alquilo; or two adjacent groups chosen from R1,R2, R3, R4, R5, Can form a methylenedioxy group or ethylenedioxy, provided that: (i) when, simultaneously, and X is CH2, is c = o or SO2, M is 1, N is 0 and R1, R2, R4 and R5 are all then R3 is Hydrogen, h, F CL, OCH3, CH3,; (ii) when simultaneously, and X is CH2, is c = 0, month 1, N is 0 OR 1, And R1, R4 and R5 (R1, R2 and R5) are all hydrogens,Then with R3 (R2 or R3 to R4) do not form a methylenedioxy or ethylenedioxy Group; (iii) when simultaneously, and is CH2 and M and N are both 1 - X, then the Group took jointly is not a 4 - or benzoyl benzoyl fluorobencenosulfonil insustituido.
机译:这些化合物在不同来源的慢性疼痛病情中具有活性;它们可以单独使用或与其他药物一起使用。权利要求1:式(1)的化合物,其中R基团独立地为C1-6h,烷基,芳基,CF3和CH2,c = o,X为链,c = o,SO 2,c = N-CN,M为0,1,N为0 1;是杂环基或式(2),其中R1,R2,R4和R5独立地为h,h同种异体烷基烷氧基C1-6-6,氰基,氨基,羟基,芳基,烷氨基C1-6Di(烷基氨基氨基C1-6),6烷基C1-烷基-,6-氨基C1-6-烷基,二(烷基C1-6)6烷基氨基C1-羧基-或全卤代6烷基; R3是全卤代1-6烷基,烷基,卤素,烷氧基C1-6,6-,氰基,羧基,羟基氨基氨基C1,6-二(烷基,氨基,氨基C1-6)6烷基C1-,烷基-6-6烷基aminoc1-或di(alquiio C1-6)aminoc1-6 aquilo;或选自R1,R2,R3,R4,R5的两个相邻基团可形成亚甲二氧基或亚乙二氧基,条件是:(i)同时X为CH2,c = o或SO2时,M为1, N为0且R1,R2,R4和R5全部为R3,则R3为氢,h,F CL,OCH 3,CH 3; (ii)当同时且X为CH2,c = 0,第1个月,N为0或1,且R1,R4和R5(R1,R2和R5)均为氢时,则与R3(R2或R3 R4)不形成亚甲二氧基或亚乙二氧基; (iii)当同时为CH 2且M和N均为1-X时,则说明该基团合起来不是4-或苯甲酰基苯甲酰基氟苯磺磺腈。

著录项

  • 公开/公告号AR070465A1

    专利类型

  • 公开/公告日2010-04-07

    原文格式PDF

  • 申请/专利权人 NEUROTUNE AG;

    申请/专利号AR2009P100617

  • 申请日2009-02-20

  • 分类号C07D487/04;A61K31/4188;A61K31/4985;A61P25/06;C07D487/04;C07D221/00;C07D241/00;

  • 国家 AR

  • 入库时间 2022-08-21 18:47:34

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