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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 484708생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/484708

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 concentrate hydrochloric acid and 270 parts of methylbenzene was stirred and refluxed for 2 hours using a water-separator. The reaction mixture was 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 5).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04533665
출처 데이터셋uspto-grants-1985_08
ORD IDord-6a6bb6747b0f430b8b5d9dff5992a315
출처 메모uspto-grants-1985_08