박시토진

박시토진
박시토진 구조식 이미지
카스 번호:
84386-11-8
한글명:
박시토진
동의어(한글):
박시토진
상품명:
Baxitozine
동의어(영문):
RU-38086;Baxitozine;(E)-4-Oxo-4-(3,4,5-trimethoxyphenyl)-2-butenoic acid;2-Butenoic acid, 4-oxo-4-(3,4,5-trimethoxyphenyl)-, (2E)-
CBNumber:
CB01178081
분자식:
C13H14O6
포뮬러 무게:
266.25
MOL 파일:
84386-11-8.mol

박시토진 속성

안전

박시토진 C화학적 특성, 용도, 생산

Originator

Baxitozine,ZYF Pharm Chemical

Manufacturing Process

29.6 g of glyoxylic acid of 50% by weight are heated in water under reduced pressure until elimination of 80% of the water present, whereupon, after cooling, 84.1 g of 3,4,5-trimethoxy acetophenone are introduced into the reaction mixture. Heating is effected for 2 h at 95°-100°C under reduced pressure (about 50 mm/Hg), at the same time distilling off the residual water present.
After cooling of the medium, 120 ml of water containing 11.6 g of sodium carbonate and ether are introduced, the aqueous phase is decanted and washed with : ether, whereupon the aqueous phase is acidified to a pH of 1 with 50% hydrochloric acid. The desired product is extracted with ethyl acetate. After elimination of the extraction solvent 31.5 g of the 4-(3,4,5- trimethoxyphenyl)-4-oxo-2-hydroxy butanoic acid, melting point 119°-120° are obtained (recrystallization from 1,2-dichloroethane).
15.8 g of 4-(3,4,5-trimethoxyphenyl)-4-oxo-2-hydroxy butanoic acid, 20 ml of acetic acid and 20 ml of concentrated hydrochloric acid (d-1.18) are heated for 2.5 h under reflux. The reaction medium is cooled and precipitated by water. The precipitate formed is filtered off. 10.5 g of the (E)-4-(3,4,5- trimethoxyphenyl)-4-oxo-2-butenoic acid, melting point 140°C are obtained (recrystallization from ethanol-water 1:1).

Therapeutic Function

Gastric cytoprotective; Antiulcer

박시토진 준비 용품 및 원자재

원자재

준비 용품


박시토진 공급 업체

글로벌( 2)공급 업체
공급자 전화 이메일 국가 제품 수 이점
Changzhou Bojia Biomedical Technology Co., Ltd. 2122619822
czbjpharma@126.com China 18488 58

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