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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 840182생성일: 2026년 10월 24일

Acetic Acid → 4-Methyl-4-aza-androst-5-ene-3,17-dione

https://huagongshe.com/ko/reaction/840182

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물AndrostenedioneHCID 6128—
반응물Methanamine, hydrochloride (1:1)HCID 11637—
용매Ethyl AcetateHCID 8857—
생성물4-Methyl-4-aza-androst-5-ene-3,17-dioneHCID 10063447—

반응 단계

Androst-4-ene-3,17-dione is oxidized into 5-oxo-4-nor-3,5-seco-androstane-5,17-dione as in Example 16A (seco-acid). The seco-acid (9.000 g, 31.423 mmol) is slurried with methylammonium chloride (19.5000 g, 288.80 mmol) into acetic acid (75 mL) and heated to reflux under an inert atmosphere. After 3 days, the reaction mixture is allowed to cool to room temperature and diluted with ethyl acetate (EtOAc, 500 mL). The organic solution is washed with water (3×200 mL), saturated aqueous NaHCO3 (2×200 mL) and brine (200 mL), then dried over magnesium sulfate (MgSO4), filtered, concentrated and purified by flash chromatography (1:1:2 EtOAc/CH2Cl2) to afford 4-methyl-4-aza-androst-5-ene-3,17-dione (aza-dione).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06365597B1
출처 데이터셋uspto-grants-2002_04
ORD IDord-5646ca0d3e0443e79f977e76764b1bf1
출처 메모uspto-grants-2002_04