发明名称 |
PROCESS FOR PRODUCING CARBAPENEM COMPOUND FOR ORAL ADMINISTRATION |
摘要 |
<p>A process for efficiently producing a 1beta-methylcarbapenem compound for oral administration. The process, which is for producing a 1beta-methylcarbapenem compound represented by the general formula (2), is characterized by reacting a beta-lactam compound represented by the general formula (1) as a starting material with a thiol compound (R3-SH) in the presence of a base and optionally eliminating the protective group R1. (1) (2) (In the formulae, R1 represents hydrogen, trimethylsilyl, or triethylsilyl; R2 represents C1-10 alkyl or C3-10 cycloalkyl; R3 represents an organic group; and R4 represents hydrogen, trimethylsilyl, or triethylsilyl.)</p> |
申请公布号 |
WO2004043961(A1) |
申请公布日期 |
2004.05.27 |
申请号 |
WO2003JP14420 |
申请日期 |
2003.11.13 |
申请人 |
KANEKA CORPORATION;NISHINO, KEITA;KOGA, TERUYOSHI |
发明人 |
NISHINO, KEITA;KOGA, TERUYOSHI |
分类号 |
C07D477/06;C07F7/18;(IPC1-7):C07D477/06 |
主分类号 |
C07D477/06 |
代理机构 |
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代理人 |
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主权项 |
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地址 |
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