反応式
[CH3:1][N:2]1[C:19](=[O:20])[CH2:18][CH2:17][C@@:16]2([CH3:21])[C:3]1=[CH:4][CH2:5][C@@H:6]1[C@@H:15]2[CH2:14][CH2:13][C@@:11]2([CH3:12])[C@H:7]1[CH2:8][CH2:9][C@@H:10]2[C:22](O)=[O:23].[CH3:25][C:26]([NH2:33])([C:28]1[S:29][CH:30]=[CH:31][CH:32]=1)[CH3:27]>>[CH3:25][C:26]([NH:33][C:22]([C@H:10]1[CH2:9][CH2:8][C@H:7]2[C@H:6]3[C@H:15]([CH2:14][CH2:13][C@:11]12[CH3:12])[C@:16]1([CH3:21])[C:3]([N:2]([CH3:1])[C:19](=[O:20])[CH2:18][CH2:17]1)=[CH:4][CH2:5]3)=[O:23])([C:28]1[S:29][CH:30]=[CH:31][CH:32]=1)[CH3:27]参加物
3
実験手順
The title compound was prepared in a yield of 50% in a similar manner to that described in Example 2 by reacting 4-methyl-3-oxo-4-azaandrost-5-ene-17β-carboxylic acid (prepared as described in Preparation 5) and 1-methyl-1-(2-thienyl)ethylamine.
出典と根拠
- ORDレコード
- ord-759b35d22a3b41b88d63b25c78671dde
- 出典データセット
- uspto-grants-1994_04
- 特許番号
- US05302621
関連ノート
読み込み中…