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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 484736생성일: 2026년 10월 25일

Sodium Carbonate → 6-[2-[4-[bis(4-fluorophenyl)methylene]-1-piperidinyl]ethyl]-3,7-dimethyl-5H-thiazolo[3,2-a]pyrimidin-5-one

https://huagongshe.com/reaction/484736

반응식

참여 물질

역할이름HCID투입량
반응물Sodium CarbonateHCID 10340—
반응물4-(Bis(4-fluorophenyl)methylene)piperidineHCID 2724436—
반응물Sodium MethoxideHCID 10942334—
반응물6-(2-Bromoethyl)-3,7-dimethyl-5H-thiazolo[3,2-A]pyrimidin-5-one monohydrobromideHCID 13983077—
용매WaterHCID 962—
용매Methyl Isobutyl KetoneHCID 7909—
생성물6-[2-[4-[bis(4-fluorophenyl)methylene]-1-piperidinyl]ethyl]-3,7-dimethyl-5H-thiazolo[3,2-a]pyrimidin-5-oneHCID 1336319472.8%

반응 단계

A mixture of 5.6 parts of 6-(2-bromoethyl)-3,7-dimethyl-5H-thiazolo[3,2-a]pyrimidin-5-one monohydrobromide, 3.5 parts of 4-[bis(4-fluorophenyl)methylene]piperidine, 1 part of a sodium methoxide solution 30%, 8 parts of sodium carbonate and 240 parts of 4-methyl-2-pentanone was stirred and refluxed for 20 hours using a water-separator. The reaction mixture was filtered while hot and the filtrate was 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 acetonitrile, yielding 4.3 parts (72.8%) of 6-[2-[4-[bis(4-fluorophenyl)methylene]-1-piperidinyl]ethyl]-3,7-dimethyl-5H-thiazolo[3,2-a]pyrimidin-5-one; mp. 183.8° C. (compound 112).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04533665
출처 데이터셋uspto-grants-1985_08
ORD IDord-3c1761841dc94f6a9c07fffd9f7451c0
출처 메모uspto-grants-1985_08