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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 484734생성일: 2026년 10월 26일

Potassium Iodide → Ritanserin

https://huagongshe.com/reaction/484734

반응식

참여 물질

역할이름HCID투입량
반응물Potassium IodideHCID 4875—
반응물Sodium CarbonateHCID 10340—
반응물6-(2-chloroethyl)-7-methyl-5H-(1,3)thiazolo(3,2-a)pyrimidin-5-oneHCID 817872—
반응물4-(Bis(4-fluorophenyl)methylene)piperidineHCID 2724436—
용매WaterHCID 962—
용매Methyl Isobutyl KetoneHCID 7909—
생성물RitanserinHCID 5074—

반응 단계

A mixture of 3.8 parts of 6-(2-chloroethyl)-7-methyl-5H-thiazolo[3,2-a]pyrimidin-5-one, 3.5 parts of 4-[bis(4-fluorophenyl)methylene]piperidine, 10 parts of sodium carbonate, 0.1 parts of potassium iodide and 240 parts of 4-methyl-2-pentanone was stirred and refluxed for 20 hours using a water-separator. The reaction mixture was filtered hot and the filtrate was evaporaed. 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 2.8 parts of 6-[2-[4-[bis(4-fluorophenyl)methylene]-1-piperidinyl]ethyl]-7-methyl-5H-thiazolo[3,2-a]pyrimidin-5-one; mp. 145.5° C. (compound 1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04533665
출처 데이터셋uspto-grants-1985_08
ORD IDord-0039ce3e13644395aa1bf74bb636feb5
출처 메모uspto-grants-1985_08