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HRID 969735作成日:2026年10月27日

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

https://huagongshe.com/reaction/969735

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium IodideHCID 4875—
反応物Sodium BicarbonateHCID 516892—
反応物3-(2-Chloroethyl)-2-methyl-6,7,8,9-tetrahydro-4hpyrido(1,2-a)pyrimidin-4-oneHCID 2763079—
反応物(2,4-Difluorophenyl)(piperidin-4-yl)methanone hydrochlorideHCID 18759874—
溶媒WaterHCID 962—
溶媒AcetonitrileHCID 6342—
生成物DES(6-fluoro-1,2-benzoxazole)-2,4-difluorobenzoyl risperidoneHCID 29941101—

反応手順

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:

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07307168B2
出典データセットuspto-grants-2007_12
ORD IDord-12fc39fc25a4411fbc84b164281c31d8
出典メモuspto-grants-2007_12