发明申请
US20050090669A1 Aminoalcohol derivatives as beta-3 adrenergic receptor agonists
审中-公开
氨基醇衍生物作为β-3肾上腺素能受体激动剂
- 专利标题: Aminoalcohol derivatives as beta-3 adrenergic receptor agonists
- 专利标题(中): 氨基醇衍生物作为β-3肾上腺素能受体激动剂
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申请号: US10504990申请日: 2003-03-10
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公开(公告)号: US20050090669A1公开(公告)日: 2005-04-28
- 发明人: Kouji Hattori , Yasuyo Tomishima , Yutaka Nakajima , Masashi Imanishi
- 申请人: Kouji Hattori , Yasuyo Tomishima , Yutaka Nakajima , Masashi Imanishi
- 优先权: AUPS1104 20020314; AU2003900127 20030110
- 国际申请: PCT/JP03/02821 WO 20030310
- 主分类号: C07D295/14
- IPC分类号: C07D295/14 ; A61K31/18 ; A61K31/196 ; A61K31/24 ; A61K31/245 ; A61K31/27 ; A61K31/275 ; A61K31/341 ; A61K31/351 ; A61K31/381 ; A61K31/402 ; A61K31/44 ; A61K31/4406 ; A61K31/4439 ; A61K31/445 ; A61K31/455 ; A61K31/4965 ; A61K31/695 ; A61P1/04 ; A61P1/16 ; A61P1/18 ; A61P3/04 ; A61P3/06 ; A61P3/10 ; A61P5/24 ; A61P9/10 ; A61P9/12 ; A61P13/02 ; A61P13/04 ; A61P13/08 ; A61P13/10 ; A61P15/00 ; A61P15/06 ; A61P25/00 ; A61P25/02 ; A61P25/22 ; A61P25/24 ; A61P27/06 ; A61P29/00 ; C07C217/74 ; C07C219/26 ; C07C229/46 ; C07C229/50 ; C07C229/60 ; C07C229/64 ; C07C233/54 ; C07C233/55 ; C07C255/57 ; C07C255/59 ; C07C271/24 ; C07C271/28 ; C07C275/42 ; C07C311/08 ; C07C311/35 ; C07C311/37 ; C07C311/51 ; C07C317/44 ; C07C321/30 ; C07C323/62 ; C07D207/26 ; C07D207/27 ; C07D211/60 ; C07D211/62 ; C07D213/36 ; C07D213/38 ; C07D213/40 ; C07D213/61 ; C07D213/64 ; C07D213/643 ; C07D213/79 ; C07D213/80 ; C07D241/24 ; C07D307/54 ; C07D307/68 ; C07D309/12 ; C07D309/14 ; C07D333/22 ; C07D333/32 ; C07D333/38 ; C07D333/40 ; C07D401/04 ; C07D405/12 ; C07F7/18 ; C07D49/14 ; C07D43/14 ; C07D41/14
摘要:
The present invention relates to a compound formula [I] wherein R1 and R5 are each independently hydrogen, halogen, lower alkyl, etc., R2 is hydrogen or an amino protective group, x is bond, -o-o, —O—CH2—, etc., y is in which Z is bond, —O—(CH2)m— (in which m is 1 to 4), etc., R3 is lower alkanoyl, carboxy, lower alkoxycarbonyl, etc., and R4 is hydrogen, halogen, hydroxy, phenoxy, lower alkyl, lower alkoxy, etc., and n is 0, 1 or 2, or a salt thereof. The compound [I] of the present invention and pharmaceutically acceptable salts thereof are useful for the prophylactic and/or the therapeutic treatment of pollakiurea or urinary incontinence.
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