HCID 69133284, 화합물 → 6beta-Methoxymethylandrostane-3,17-dione
반응식
[CH2:1]1COC23OCCOC2([C@]2(CC[C@H]4[C@@H](C[C@@H](COC)C5[C@]4(C)CCCC5)[C@@H]2C3)C)[O:2]1.[C:31]([C@@H:33]1[CH:50]2[C@:45]([CH3:52])([CH2:46][CH2:47][C:48](=[O:51])[CH2:49]2)[C@@H:44]2[C@H:35]([C@H:36]3[C@@:40]([CH2:42][CH2:43]2)([CH3:41])[C:39](=[O:53])[CH2:38][CH2:37]3)[CH2:34]1)#N>>[CH3:1][O:2][CH2:31][C@H:33]1[CH:50]2[C@:45]([CH3:52])([CH2:46][CH2:47][C:48](=[O:51])[CH2:49]2)[C@@H:44]2[C@H:35]([C@H:36]3[C@@:40]([CH2:42][CH2:43]2)([CH3:41])[C:39](=[O:53])[CH2:38][CH2:37]3)[CH2:34]1참가 물질
3
실험 절차
The title compound II-aj was prepared in 90% yield from 3,3:17,17-bis(ethylendioxy)-6β-methoxymethylandrostane by the procedure described above for the preparation of 6α-cyanoandrostane-3,17-dione (II-ac, Prepn. 3). The combined organic extracts were washed with H2O, dried over Na2SO4 and evaporated to dryness. The residue was purified by flash chromatography (SiO2, n-hexane/CH2Cl2/acetone 70/10/20). 1H-NMR (300 MHz, acetone-d6, ppm from TMS): δ 3.45 (m, 2H), 3.27 (s, 3H), 2.80-0.80 (m, 21H), 1.10 (s, 3H), 0.89 (s, 3H).
후처리
- washThe combined organic extracts were washed with H2O
- dry with materialdried over Na2SO4
- customevaporated to dryness
- customThe residue was purified by flash chromatography (SiO2, n-hexane/CH2Cl2/acetone 70/10/20)
출처 및 근거
- ORD 기록
- ord-5838251eb4da40749e7fa205593aa84f
- 출처 데이터셋
- uspto-grants-2013_12
- 특허 번호
- US08609644B2
반응 노트
불러오는 중…