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3,3-Diphenylacrolein → 4-(4-(3,3-Diphenyl-2-propenyl)-1-piperazinyl)benzonitrile
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 3,3-Diphenylacrolein | HCID 71027 | — |
| 反応物 | Diisopropylethylamine | HCID 81531 | — |
| 反応物 | Cyano-borohydride | HCID 498716 | — |
| 反応物 | 4-(Piperazin-1-yl)benzonitrile hydrochloride | HCID 2733994 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 4-(4-(3,3-Diphenyl-2-propenyl)-1-piperazinyl)benzonitrile | HCID 59186611 | 84.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07585858B2 |
| 出典データセット | uspto-grants-2009_09 |
| ORD ID | ord-0b4095b6d8be45d7a5f7dc22995109e0 |
| 出典メモ | uspto-grants-2009_09 |