发明名称 |
METHOD FOR MANUFACTURING CEFUROXIME |
摘要 |
<p>PURPOSE: Provided is a method for easily manufacturing cefuroxime in high purity and yield by manufacturing crystalline cefuroxime sodium then treating it with inorganic acid in the presence of a mixed solvent of water and organic solvent. CONSTITUTION: The cefuroxime represented by the formula(2) is manufactured by dissolving 7-amino-3-hydroxymethylcephalosphoranic acid in inorganic salt solution, in the range of pH6-7; acylating the resultant compound with 2-(fur-2yl)-2-methoxyimino acetic chloride to obtain a cephalosporin derivative of the formula(1) as an intermediate; carbamoylating hydroxy group at C-3 of the intermediate compound with isocyanate compound of the formula(4): R-NCO in the range of less than pH 1; then hydrolyzing it to obtain cefuroxime of the formula(2). In the formula(4), R is a protecting group selected from chlorosulfonyl group, trichloroacethyl group, trimethylsilyl group, bromo sulfonyl group, dichloroacethyl group, 2,2,2-trichloroethoxycarbonyl, dihalophosphinyl group and dimethoxyphosphinyl group.</p> |
申请公布号 |
KR20020011254(A) |
申请公布日期 |
2002.02.08 |
申请号 |
KR20000044631 |
申请日期 |
2000.08.01 |
申请人 |
BORYUNG PHARMACEUTICAL CO., LTD. |
发明人 |
CHOI, IL GYUN;KIM, HO JIN;KIM, SANG RIN;LEE, IN GYU;PARK, SE CHUNG |
分类号 |
C07D501/06;(IPC1-7):C07D501/06 |
主分类号 |
C07D501/06 |
代理机构 |
|
代理人 |
|
主权项 |
|
地址 |
|