戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 962672作成日:2026年10月26日

Benzhydrylamine → N-diphenylmethyl-3-cyanoandrosta-3,5-diene-17beta-carboxamide

https://huagongshe.com/reaction/962672

反応式

関与物質

役割名称HCID仕込み量
反応物BenzhydrylamineHCID 7036—
反応物TriethylamineHCID 8471—
反応物Diethyl cyanophosphonateHCID 76257—
反応物3-Cyanoandrosta-3,5-diene-17beta-carboxylic acidHCID 15380254—
溶媒DichloromethaneHCID 6344—
生成物N-diphenylmethyl-3-cyanoandrosta-3,5-diene-17beta-carboxamideHCID 15380255—

反応手順

1.0 g of 3-cyanoandrosta-3,5-diene-17β-carboxylic acid [prepared as described in step (b) above], 1.0 ml of diphenylmethylamine and 1.0 ml of triethylamine were dissolved in 10 ml of dry methylene chloride, and 0.75 ml of diethyl cyanophosphate was added to the resulting solution at room temperature. The reaction mixture was stirred at room temperature overnight, after which it was diluted with 100 ml of methylene chloride, and then washed with 1N aqueous hydrochloric acid, with water, with an aqueous solution of sodium hydrogencarbonate and with a saturated aqueous solution of sodium chloride, in that order. The solution was then dried over anhydrous magnesium sulfate, after which it was concentrated by evaporation under reduced pressure. The resulting residue was subjected to column chromatography through 40 g of silica gel using a gradient elution method, with mixtures of acetone and methylene chloride in ratios ranging from 1:99 to 4:96 by volume as the eluent, to give 0.85 g of the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05760025
出典データセットuspto-grants-1998_06
ORD IDord-483f3600b6994defb1e85a142e6e0457
出典メモuspto-grants-1998_06