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Patent Searching and Data


Title:
ベンゾシクロアルキルアゾールチオン誘導体
Document Type and Number:
Japanese Patent JPH09512269
Kind Code:
A
Abstract:
The present invention relates to novel benzocycloalkylazolethione compounds of formula (I) in which n is 0, 1 or 2; t is 0, 1, 2 or 3; R<1> is independently halo, hydroxy or (C1-4)alkyloxy; and R<2> is attached to the alpha , beta or gamma -position and is a group selected from formulae (a), (b) and (c) which are dopamine beta -hydroxylase inhibitors in which the benzocycloalkyl portion of the compound is selected from indanyl, 1,2,3,4-tetrahydronaphthalenyl and 6,7,8,9-tetrahydro-5H-benzocycloheptenyl (in which the benzo is optionally substituted with one to three substituents) and the azolethione portion of the compound is selected from 2-thioxo-2,3-dihydro-1H-imidazol-3-yl, 5-thioxo-4,5-dihydro-1H-[1,2,4]triazol-4-yl and 5-thioxo-4,5-dihydro-1H-[1,2,4]triazol-1-yl (each optionally substituted with one to three substituents); and the prodrugs, pharmaceutically acceptable salts, individual isomers and mixtures of isomers and the methods of using and preparing such benzocycloalkylazolethione compounds.

Inventors:
ウォーカー,キース・エイ・エム
オーヤング,カウンド
グッディング,オーウェン・ダブリュー
テイテルボーム,フィリップ・ジェイ
バンサル,レクハ・ピー
ホワイティング,ロジャー・エル
マルティネス,グレゴリー・アール
ミュールドルフ,アレキサンダー・ブイ
レプケ,デイビッド・ビー
Application Number:
JP52772795A
Publication Date:
December 09, 1997
Filing Date:
April 25, 1995
Export Citation:
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Assignee:
シンテックス(ユー・エス・エイ) インコーポレイテッド
International Classes:
A61K31/41; A61K31/415; A61P25/00; A61P43/00; C07B53/00; C07C209/42; C07C211/38; C07C213/02; C07C215/64; C07C217/74; C07D233/28; C07D233/32; C07D233/36; C07D233/42; C07D233/84; C07D233/88; C07D233/90; C07D249/12; C07D249/14; C07D257/04; C07D403/04; C07D403/10; C07D405/12; (IPC1-7): C07D233/84; C07C209/42; C07C211/38; C07C213/02; C07C215/64; C07C217/74; C07D249/12; C07D249/14; C07D257/04
Attorney, Agent or Firm:
青山 葆 (外1名)