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HRID 66679作成日:2026年10月26日

Potassium Iodide → 3-[2-[4-(1H-indol-3-yl)-1-piperidinyl]ethyl]-2,8-dimethyl-4H-pyrido[1,2-a]pyrimidin-4-one

https://huagongshe.com/reaction/66679

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 CarbonateHCID 10340—
反応物3-(2-chloroethyl)-2,8-dimethyl-4H-pyrido[1,2-a]pyrimidin-4-oneHCID 100861—
反応物3-(4-Piperidinyl)-1H-indoleHCID 702235—
溶媒Methyl Isobutyl KetoneHCID 7909—
生成物3-[2-[4-(1H-indol-3-yl)-1-piperidinyl]ethyl]-2,8-dimethyl-4H-pyrido[1,2-a]pyrimidin-4-oneHCID 20530728—

反応手順

A mixture of 3.8 parts of 3-(2-chloroethyl)-2,8-dimethyl-4H-pyrido[1,2-a]pyrimidin-4-one, 3 parts of 3-(4-piperidinyl)-1H-indole, 10 parts of sodium carbonate, 0.1 parts of potassium iodide and 240 parts of 4-methyl-2-pentanone is stirred and refluxed for 20 hours. The reaction mixture is filtered hot over Hyflo and the filtrate is evaporated. The residue is purified by column-chromatography over silica gel using a mixture of trichloromethane and methanol (90:10 by volume) as eluent. The pure fractions are collected and the eluent is evaporated. The residue is crystallized from a mixture of 2-propanol, 2,2'-oxybispropane and 4-methyl-2-pentanone, yielding 4.7 parts of 3-[2-[4-(1H-indol-3-yl)-1-piperidinyl]ethyl]-2,8-dimethyl-4H-pyrido[1,2-a]pyrimidin-4-one; mp. 235.9° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04342870
出典データセットuspto-grants-1982_08
ORD IDord-a83bd7ef27d846d5a90d4576e897ecf9
出典メモuspto-grants-1982_08