摘要 |
<p>Anti-infective compound, preparation method thereof and use thereof. The present invention disclosed a crystal of 6-fluoro-1-methyl-4-oxo-7-(1-piperazinyl)-4H-[1,3]thiazeto[3,2-a]quinoline-3-carboxylic acid (II) methanesulfonate, which is separated out by solvent crystallization following the reaction of compound (II) with pharmaceutical methanesulfonic acid using water or water containing organic solvent as solvents. The obtained compound has a definitive structure. It is stable and has confirmed anti-bacterial effect. The water solubility of compound (II) has been improved by this way, and it is convenient to make appropriate dosage forms for clinic use to expand the extension of clinic use. By preparing the methanesulfonate of compound (II), the toxicity of the active compound (II) has been reduced and the safety of its clinic use has been improved.</p> |
申请人 |
GUANGZHOU BAIYUNSHAN PHARMACEUTICAL CO., LTD. GUANGZHOU BAIYUNSHAN PHARMACEUTICAL FACTORY;GUANGZHOU PHARMACEUTICAL INDUSTRIAL RESEARCH INSTITUTE;GUANGZHOU BAIYUNSHAN PHARMACEUTICAL CO., LTD. GUANGZHOU BAIYUNSHAN CHEMICAL PHARMACEUTICAL FACTORY;CHEN, MAO;ZHU, SHAOXUAN;LIU, XUEBIN;ZHENG, LIZHEN;XU, SHUWEN;LIU, DANQING |
发明人 |
CHEN, MAO;ZHU, SHAOXUAN;LIU, XUEBIN;ZHENG, LIZHEN;XU, SHUWEN;LIU, DANQING |