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.
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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 |
代理机构 |
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代理人 |
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地址 |
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