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HRID 731544作成日:2026年10月25日

3,3-Diphenylacrolein → 4-(4-(3,3-Diphenyl-2-propenyl)-1-piperazinyl)benzonitrile

https://huagongshe.com/reaction/731544

反応式

関与物質

役割名称HCID仕込み量
反応物3,3-DiphenylacroleinHCID 71027—
反応物DiisopropylethylamineHCID 81531—
反応物Cyano-borohydrideHCID 498716—
反応物4-(Piperazin-1-yl)benzonitrile hydrochlorideHCID 2733994—
溶媒MethanolHCID 887—
溶媒DichloromethaneHCID 6344—
生成物4-(4-(3,3-Diphenyl-2-propenyl)-1-piperazinyl)benzonitrileHCID 5918661184.3%

反応手順

A suspension of 4-piperazin-1-ylbenzonitrile hydrochloride (1.30 g, 5.00 mmol) and 3,3-diphenylacrylaldehyde (1.56 g, 7.50 mmol)) in dichloromethane (10 mL) and methanol (10 mL) was neutralized to pH 5 with diisopropylethylamine, treated with polymer-supported cyanoborohydride (2.47 mmol/g, 6 g, 14.82 mmol), shaken at room temperature for 24 hours, and filtered. The resin was washed with 1:1 dichloromethane/methanol (10 mL×3) and the combined filtrates were concentrated. The concentrate was purified by silica gel chromatography eluting with a gradient from 10%-50% ethyl acetate/hexanes to provide the desired product (1.60 g, 84%). MS (CI) m/e 380 (M+H)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07585858B2
出典データセットuspto-grants-2009_09
ORD IDord-0b4095b6d8be45d7a5f7dc22995109e0
出典メモuspto-grants-2009_09