Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Diethyl Ether → 17beta,19-Di-(1-methoxy-1-cyclopentyloxy)-androst-4-en-3beta-ol
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Diethyl Ether | HCID 3283 | — |
| 반응물 | 19-Hydroxytestosterone | HCID 150968 | — |
| 반응물 | Aluminium lithium hydride | HCID 21226445 | — |
| 반응물 | 17beta,19-Di-(1-methoxy-1-cyclopentyloxy)-androst-4-en-3-one | HCID 86735678 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 17beta,19-Di-(1-methoxy-1-cyclopentyloxy)-androst-4-en-3beta-ol | HCID 86735677 | — |
반응 단계
The compound 17β,19-dihydroxyandrost-4-en-3-one is similarly etherified to form the 17β-OR4, 19-OR1, derivatives of androst-4-en-3-one. Reduction as previously described yields the corresponding 3-hydroxy analogues. For example, 17β,19-dihydroxyandrost-4-en-3-one is converted to 17β,19-di-triphenylsiloxyandrost-4-en-3-one and 17β,19-di-(1-methoxy-1-cyclopentyloxy)-androst-4-en-3-one as previously described. These compounds are then reduced using lithium aluminum hydride in an ether or tetrahydrofuran solution to produce 17β,19-di-triphenylsiloxyandrost-4-en-3β-ol and 17β,19-di-(1-methoxy-1-cyclopentyloxy)-androst-4-en-3β-ol, respectively.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US04087524 |
| 출처 데이터셋 | uspto-grants-1978_05 |
| ORD ID | ord-c843252dc8e045bd9c6a786e7333510e |
| 출처 메모 | uspto-grants-1978_05 |