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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 862321생성일: 2026년 10월 24일

Benzhydrylamine → 17beta-(N-Diphenylmethylcarbamoyl)androsta-4-ene-3-one

https://huagongshe.com/ko/reaction/862321

반응식

참여 물질

역할이름HCID투입량
반응물BenzhydrylamineHCID 7036—
반응물TriethylamineHCID 8471—
반응물Trifluoromethanesulfonyl chlorideHCID 79000—
반응물(17beta)-3-Oxoandrost-4-ene-17-carboxylic acidHCID 99472—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매DichloromethaneHCID 6344—
생성물17beta-(N-Diphenylmethylcarbamoyl)androsta-4-ene-3-oneHCID 2286242089%

반응 단계

0.108 ml of benzhydrylamine was added to a solution of 100 mg of androsta-4-ene-3-one-17β-carboxylic acid, a catalytic amount of 4-dimethylaminopyridine and 0.132 ml of triethylamine in 4 ml of methylene chloride. 0.050 ml of trifluoromethanesulfonyl chloride was divided into three portions and added to this reaction mixture at intervals of 30 minutes at room temperature, whilst stirring. One hour after finishing the addition of trifluoromethanesulfonyl chloride, the reaction mixture was diluted with methylene chloride, 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. It was then dried over anhydrous magnesium sulfate, and concentrated by evaporation under reduced pressure. The resulting residue was crystallized from acetone to give 135.2 mg (yield 89%) of the title compound, having the same properties as the product of Preparation 17.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05717088
출처 데이터셋uspto-grants-1998_02
ORD IDord-a7e6ac32d1f64e65a08bc902b7ef9752
출처 메모uspto-grants-1998_02