首页> 外国专利> ANTAGONIST REPLACED IMIDAZOLS OF THE Y5 NEUROPEPTIDE Y.

ANTAGONIST REPLACED IMIDAZOLS OF THE Y5 NEUROPEPTIDE Y.

机译:拮抗剂取代了Y5神经肽Y的咪唑。

摘要

A compound having the structural formula: or one of its pharmaceutically acceptable salts, solvates or N-oxides, in which: X is = CH; Y represents 1 to 3 substituents independently selected from the group consisting of H, halogen, trihaloalkyl, C1-C6 alkyl, C2-C6 alkenyl, C3-C7 cycloalkyl, C1-C6 alkyl, substituted with C3-C7 cycloalkyl, -OH,, -O-C1-C6 alkyl, -SH, -S-C1-C6 alkyl, or CN. R is R4 is hydrogen or C1-C6 alkyl; R5 is C1-C6 alkyl, aryl or heteroaryl; with the proviso that R4 and R5 are not both C1-C6 alkyl, and with the proviso that when R4 is hydrogen, R5 is not C1-C6 alkyl; or, R4 and R5 together are C3-C6 alkylene and together with the nitrogen atom to which they are attached form a 4- to 7-membered ring; or, R4 and R5 together with the nitrogen to which they are attached, form a 5, 6 or 7 member ring, in which 1 or 2 ring members are independently selected
机译:结构式为:的化合物或其药学上可接受的盐,溶剂化物或N-氧化物之一,其中:X为CH; Y代表1-3个独立地选自H,卤素,三卤代烷基,C 1 -C 6烷基,C 2 -C 6烯基,C 3 -C 7环烷基,C 1 -C 6烷基,被C 3 -C 7环烷基,-OH 、、 -O-C1-C6烷基,-SH,-S-C1-C6烷基或CN。 R是R4是氢或C1-C6烷基; R5是C1-C6烷基,芳基或杂芳基;其中R4和R5都不都是C1-C6烷基,并且当R4是氢时,R5不是C1-C6烷基。或者,R4和R5一起是C3-C6亚烷基,并且与它们所连接的氮原子一起形成4至7元环;或者,R 4和R 5与它们所连接的氮一起形成5、6或7元环,其中1或2个环元独立地选择

著录项

  • 公开/公告号ES2243337T3

    专利类型

  • 公开/公告日2005-12-01

    原文格式PDF

  • 申请/专利权人 SCHERING CORPORATION;

    申请/专利号ES20000986362T

  • 申请日2000-12-14

  • 分类号C07D233/54;C07D413/10;C07D401/10;C07D401/04;C07D401/12;C07D403/12;C07D401/06;A61K31/415;

  • 国家 ES

  • 入库时间 2022-08-21 21:36:05

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