发明名称 Pyrrolidinyl hydroxamic acid compounds and their production process
摘要 <p>A compound of the formula: and it pharmaceutically acceptable salt, wherein A is hydrogen, hydroxy or OY, where Y is a hydroxy protecting group; Ar is phenyl optionally substituted with one or more substituents selected from halo, hydroxy, C1-C4 alkyl, C1-C4 alkoxy, CF3, C1-C4 alkyloxy, and carboxy-C1-C4 alkyloxy; X is phenyl, naphthyl, biphenyl, indanyl, benzofuranyl, benzothiopheny, 1-tetralone-6-yl, C1-C4 alkylenedioxy, pyridyl, furyl and thienyl, these groups optionally being substituted with up to three substituents selected from halo, C1-C4 alkyl, C1-C4 alkoxy, hydroxy, NO2, CF3 and SO2CH3; and R is hydrogen, C1-C4 alkyl or a hydroxy protecting group. These compounds and pharmaceutical compositions containing them are useful as analgesic, antiinflammatory, diuretic, anesthetic or neuroprotective agents, or an agent for stroke or treatment of functional bowel diseases such as abdominal pain, for the treatment of a mammalian subject, especially a human subject. Further, the present invention provides processes for producing the hydroxamic compounds of formula (I) and their intermediate compounds of formula (II).</p>
申请公布号 OA10518(A) 申请公布日期 2002.04.22
申请号 OA19970070091 申请日期 1997.09.30
申请人 PFIZER INC. 发明人 FUMITAKA ITO
分类号 C07D295/12;A61K31/40;A61K31/4025;A61K31/44;A61K31/4427;A61K31/443;A61K31/4433;A61P1/00;A61P7/00;A61P7/10;A61P23/00;A61P25/00;A61P25/04;A61P25/28;A61P29/00;A61P43/00;C07D;C07D207/12;C07D213/54;C07D295/13;C07D307/79;C07D401/06;C07D401/12;C07D405/06;C07D405/12;C07D405/14;C07D409/12;(IPC1-7):C07D207/12;A61K3/40 主分类号 C07D295/12
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