戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 655011作成日:2026年10月26日

Water → 3-[4-(2-propenyl)-1-piperazinyl]-1-phenyl-1H-indazole

https://huagongshe.com/reaction/655011

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Allyl bromideHCID 7841—
反応物Potassium CarbonateHCID 11430—
反応物1-phenyl-3-(1-piperazinyl)-1H-indazoleHCID 9795644—
溶媒DimethylformamideHCID 6228—
生成物3-[4-(2-propenyl)-1-piperazinyl]-1-phenyl-1H-indazoleHCID 15117074—

反応条件

温度70 °C

反応手順

To a stirred suspension of 5.0 g of 1-phenyl-3-(1-piperazinyl)-1H-indazole and 2.7 g of potassium carbonate in 50 ml of dimethylformamide was added 2.4 g of allyl bromide. The reaction mixture was stirred at 70° C. for 16 hours, poured into water and extracted with ethyl acetate. The extract was washed with water, dried over anhydrous magnesium sulfate, and concentrated to yield 3-[4-(2-propenyl)-1-piperazinyl]-1-phenyl-1H-indazole as an oil. The oil was diluted with diethyl ether and filtered. Treatment of the filtrate with ethereal hydrogen chloride precipitated the hydrochloride salt. Recrystallization from ethanol/diethyl ether gave 2.0 g (21%) of 3-[4-(2-propenyl)-1-piperazinyl]-1-phenyl-1H-indazole hydrochloride, mp 234°-236°.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05134236
出典データセットuspto-grants-1992_07
ORD IDord-c218bbc84a4f446285108113f05214c3
出典メモuspto-grants-1992_07