发明申请
WO1998005674A1 PROCESS FOR THE PRODUCTION OF SALTS OF ERYTHROMYCIN, ROXITHROMYCIN, CLARITHROMYCIN AND AZITHROMYCIN
审中-公开
基本信息:
- 专利标题: PROCESS FOR THE PRODUCTION OF SALTS OF ERYTHROMYCIN, ROXITHROMYCIN, CLARITHROMYCIN AND AZITHROMYCIN
- 专利标题(中):生产红霉素,罗红霉素,克拉霉素和阿奇霉素的方法
- 申请号:PCT/IE1997000056 申请日:1997-08-07
- 公开(公告)号:WO1998005674A1 公开(公告)日:1998-02-12
- 发明人: RUSSINSKY LIMITED
- 申请人: RUSSINSKY LIMITED , SCHICKANEDER, Helmut , NIKOLOPOULOS, Aggelos
- 专利权人: RUSSINSKY LIMITED,SCHICKANEDER, Helmut,NIKOLOPOULOS, Aggelos
- 当前专利权人: RUSSINSKY LIMITED,SCHICKANEDER, Helmut,NIKOLOPOULOS, Aggelos
- 优先权: IE960568 19960807
- 主分类号: C07H17/08
- IPC分类号: C07H17/08
摘要:
N-acetylcysteine, carboxymethylcysteine and thiazolidincarboxylic acid salts of erythromycin-2-propionate are produced by charging erythromycin-2-propionate and the sulphur-containing acid into a reactor. The reactants are homogenised and milled under nitrogen for 1 - 2 hours at 10 - 20 DEG C. To this mixture purified water is added under nitrogen and the resultant aqueous mixture is further homogenised and milled for 1 to 2 hours at 10 - 30 DEG C under nitrogen to produce a suspension of the desired salt. The suspension is dried under vacuum to produce a high yield of the desired salt at high levels of purity. Carboxymethylcysteine, N-acetylcysteine and thiazolidin-carboxylic acid salt of erythromycin, clarithromycin, roxithromycin and azithromycin may be produced in a similar manner.
摘要(中):
通过将红霉素-2-丙酸酯和含硫酸装入反应器中制备红霉素-2-丙酸的N-乙酰半胱氨酸,羧甲基半胱氨酸和噻唑烷羧酸盐。 将反应物均化并在10-20℃下在氮气下研磨1-2小时。向该混合物中加入纯化水,并将所得含水混合物进一步均化并在10-30℃下研磨1至2小时 在氮气下产生所需盐的悬浮液。 将悬浮液在真空下干燥以产生高纯度的所需盐的高产率。 红霉素,克拉霉素,罗红霉素和阿奇霉素的羧甲基半胱氨酸,N-乙酰半胱氨酸和噻唑烷 - 羧酸盐可以以类似的方式制备。
IPC结构图谱:
C | 化学;冶金 |
--C07 | 有机化学 |
----C07H | 糖类;及其衍生物;核苷;核苷酸;核酸 |
------C07H17/00 | 含有直接连在糖化物基团的杂原子上的杂环基的化合物 |
--------C07H17/04 | .仅含有氧作为杂环原子的杂环基 |
----------C07H17/08 | ..含有八元或更多元的杂环,如红霉素 |