发明名称 Production method of isoxazolidinedione compound
摘要 The present invention relates to a novel method for producing a compound of the formula [11] wherein R is an optionally substituted aromatic hydrocarbon group, an optionally substituted alicyclic hydrocarbon group, an optionally substituted heterocyclic group or an optionally substituted condensed heterocyclic group, which is useful as a therapeutic agent for diabetes. The method of the present invention is an industrially utilizable method that enables efficient production of the objective compound [11] from beta-methyl L-aspartate via an important intermediate compound [6] wherein R is as defined above, at high yield.
申请公布号 US2001039352(A1) 申请公布日期 2001.11.08
申请号 US20010839215 申请日期 2001.04.23
申请人 ANDO KOJI;SUZUKI MASANOBU 发明人 ANDO KOJI;SUZUKI MASANOBU
分类号 C07D263/32;A61K31/42;A61K31/421;A61K31/422;A61P3/10;C07C;C07C231/02;C07C233/47;C07C233/83;C07D;C07D261/12;C07D263/30;C07D413/02;C07D413/12;C07D413/14;(IPC1-7):C07D263/30 主分类号 C07D263/32
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