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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 969735생성일: 2026년 10월 26일

Potassium Iodide → DES(6-fluoro-1,2-benzoxazole)-2,4-difluorobenzoyl risperidone

https://huagongshe.com/reaction/969735

반응식

참여 물질

역할이름HCID투입량
반응물Potassium IodideHCID 4875—
반응물Sodium BicarbonateHCID 516892—
반응물3-(2-Chloroethyl)-2-methyl-6,7,8,9-tetrahydro-4hpyrido(1,2-a)pyrimidin-4-oneHCID 2763079—
반응물(2,4-Difluorophenyl)(piperidin-4-yl)methanone hydrochlorideHCID 18759874—
용매WaterHCID 962—
용매AcetonitrileHCID 6342—
생성물DES(6-fluoro-1,2-benzoxazole)-2,4-difluorobenzoyl risperidoneHCID 29941101—

반응 단계

A suspension of 29.2 g (0.1116 mole) of 4-(2,4-difluoro-benzoyl)-piperidine-hydrochloride, 25.3 g (0.1117 mole) of 3-(2-chloroethyl)-6,7,8,9-tetrahydro-2-methyl-4H-pyrido[1,2-a]pyrimidin-4-one, 500 ml of acetonitrile, 19.6 g (0.2333 mole) of sodium hydrogencarbonate and 0.25 g (0.0015 mole) of potassium iodide is heated to boiling for 10 hours with stirring. The reaction mixture is cooled to room temperature, to the residue 200 ml of water are added. The mixture is stirred for 30 minutes and extracted with 200 ml of dichloromethane. The organic phase is separated, dried over magnesium sulfate, filtered and the filtrate is evaporated. The oily residue thus obtained is purified as follows:

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07307168B2
출처 데이터셋uspto-grants-2007_12
ORD IDord-12fc39fc25a4411fbc84b164281c31d8
출처 메모uspto-grants-2007_12