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HRID 353628作成日:2026年10月26日

1H-Isoindole-1,3(2H)-dione, 2-(2-bromoethyl)- → 2-[2-(4-isopropyl-1-piperidinyl)ethyl]-1H-isoindole-1,3(2H)-dione

https://huagongshe.com/reaction/353628

反応式

関与物質

役割名称HCID仕込み量
反応物1H-Isoindole-1,3(2H)-dione, 2-(2-bromoethyl)-HCID 11325—
反応物Potassium CarbonateHCID 11430—
反応物Piperidine, 4-(1-methylethyl)-HCID 140569—
溶媒AcetonitrileHCID 6342—
生成物2-[2-(4-isopropyl-1-piperidinyl)ethyl]-1H-isoindole-1,3(2H)-dioneHCID 2197825754.4%

反応手順

A solution of 4-isopropylpiperidine (3.3 g, 20.2 mmol), N-(2-bromoethyl)phthalimide (5.4 g, 21.3 mmol), potassium carbonate (5.9 g, 45.4 mmol) and acetonitrile (100 ml) and was heated under reflux for 2.5 hours then stirred at room temperature overnight. The solvent was removed under reduced pressure and the residue partitioned between ethyl acetate (100 ml) and water (100 ml). The organic layer was separated and the aqueous layer extracted with further ethyl acetate (100 ml). The combined organic extracts were dried (Na2SO4) and the solvent removed by evaporation under reduced pressure. The resulting oil was purified by column chromatography on silica gel eluting with a gradient system of dichloromethane changing to dichloromethane diethyl:ether (50:50, by volume) changing to diethyl ether to afford the title compound (3.3 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06753322B2
出典データセットuspto-grants-2004_06
ORD IDord-f65b6adc4d0848f6ad1b0bda1598dcb6
出典メモuspto-grants-2004_06