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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 862278생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/862278

반응식

참여 물질

역할이름HCID투입량
반응물BenzhydrylamineHCID 7036—
반응물TriethylamineHCID 8471—
반응물Diethyl cyanophosphonateHCID 76257—
반응물3-Cyanoandrosta-3,5-diene-17beta-carboxylic acidHCID 15380254—
용매DichloromethaneHCID 6344—
생성물N-diphenylmethyl-3-cyanoandrosta-3,5-diene-17beta-carboxamideHCID 15380255—

반응 단계

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 hydrogen-carbonate 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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05717088
출처 데이터셋uspto-grants-1998_02
ORD IDord-52ff906006db4e26a0dccd90ca175c9c
출처 메모uspto-grants-1998_02