Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Acetic Acid → 4-Methyl-4-aza-androst-5-ene-3,17-dione
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Acetic Acid | HCID 176 | — |
| 반응물 | Androstenedione | HCID 6128 | — |
| 반응물 | Methanamine, hydrochloride (1:1) | HCID 11637 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | 4-Methyl-4-aza-androst-5-ene-3,17-dione | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US06365597B1 |
| 출처 데이터셋 | uspto-grants-2002_04 |
| ORD ID | ord-5646ca0d3e0443e79f977e76764b1bf1 |
| 출처 메모 | uspto-grants-2002_04 |