摘要
目的合成盐酸沙格雷酯杂质Ⅲ。方法以2-[2-(3-甲氧基苯基)乙烯基]苯酚为原料,经过亲核取代、加成、酰化、环氧化、还原等5步反应制备盐酸沙格雷酯杂质Ⅲ。结果用廉价原料合成了盐酸沙格雷酯杂质Ⅲ,总收率30%。结论该工艺简单可行,产品质量符合对照品要求。
Objective To synthesize impurity III of the sarpogrelate hydrochloride. Methods The impurity III of the sarpogrelate hydrochloride was synthesized with 2-[2-(3-methoxyphenyl) vinyl] phenol by substitution reaction, addition reaction, acylation reaction, epoxidation reaction. Results The impurity III of sarpogrelate hydrochloride was synthesized with inexpensive and readily available catalyst and the total yield of the target compound was 30%. Conclusion This technology is simple, possible and the quality of the produce meets the national standard.
出处
《中国抗生素杂志》
CAS
CSCD
北大核心
2016年第7期538-540,共3页
Chinese Journal of Antibiotics
关键词
盐酸沙格雷酯
杂质
抗血栓
Sarpogrelate hydrochloride
Impurity
Antithrombotic