Acetate → Galeterone
反応式
C([O-])(=O)C.C([O:8][C@H:9]1[CH2:26][CH2:25][C@@:24]2([CH3:27])[C:11](=[CH:12][CH2:13][C@@H:14]3[C@@H:23]2[CH2:22][CH2:21][C@@:19]2([CH3:20])[C@H:15]3[CH2:16][CH:17]=[C:18]2[N:28]2[C:32]3[CH:33]=[CH:34][CH:35]=[CH:36][C:31]=3[N:30]=[CH:29]2)[CH2:10]1)(=O)C.[OH-].[K+]>CO>[OH:8][C@H:9]1[CH2:26][CH2:25][C@@:24]2([CH3:27])[C:11](=[CH:12][CH2:13][C@@H:14]3[C@@H:23]2[CH2:22][CH2:21][C@@:19]2([CH3:20])[C@H:15]3[CH2:16][CH:17]=[C:18]2[N:28]2[C:32]3[CH:33]=[CH:34][CH:35]=[CH:36][C:31]=3[N:30]=[CH:29]2)[CH2:10]1参加物
5
実験手順
Compound 5 prepared by following general method C, treating acetate solution of 15 (1 g 3.02 mmol) in methanol (15 mL) with 10% methanolic KOH (5 mL) for 1.5 h. Purification by FCC over short column provided pure 5 with identical spectral and analytical data as we previously reported.
後処理
- customPurification by FCC over short column
- customprovided pure 5 with identical spectral and analytical data as we
出典と根拠
- ORDレコード
- ord-219de467e34b4d72ad05d9e2ef510967
- 出典データセット
- uspto-grants-2016_09
- 特許番号
- US09439912B2
反応ノート
読み込み中…