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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 893682생성일: 2026년 10월 24일

Hydrochloric Acid → 6-(2-chloroethyl)-7-methyl-5H-(1,3)thiazolo(3,2-a)pyrimidin-5-one

https://huagongshe.com/ko/reaction/893682

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물2-AminothiazoleHCID 2155—
반응물2-AcetylbutyrolactoneHCID 10601—
반응물Phosphorus oxychlorideHCID 24813—
용매WaterHCID 962—
용매TolueneHCID 1140—
생성물6-(2-chloroethyl)-7-methyl-5H-(1,3)thiazolo(3,2-a)pyrimidin-5-oneHCID 817872—

반응 단계

A mixture of 50 parts of 2-thiazolamine, 76 parts of 3-acetyl-4,5-dihydro-2(3H)-furanone, 1.2 parts of concentrated hydrochloric acid and 270 parts of methylbenzene was stirred and refluxed for 2 hours using a water-separator. The reaction mixture is cooled and 340 parts of phosphoryl chloride were added at a temperature between 20° and 30° c. The whole was heated slowly to 100°-110° C. and stirring was continued for 2 hours at this temperature. The reaction mixture was evaporated and the residue was poured onto a mixture of crushed ice and ammonium hydroxide. The product was extracted with trichloromethane. The extract was dried, filtered and evaporated. The residue was purified by column chromatography over silica gel using a mixture of trichloromethane and methanol (95:5 by volume) as eluent. The pure fractions were collected and the eluent was evaporated. The residue was crystallized from a mixture of 2-propanol and 1,1'-oxybisethane, yielding 36 parts of 6-(2-chloroethyl)-7-methyl-5H-thiazolo[3,2-a]pyrimidin-5-one (intermediate 172).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05126339
출처 데이터셋uspto-grants-1992_06
ORD IDord-4e87cf8d775e4199b275e6f618d73dcf
출처 메모uspto-grants-1992_06