3-Methoxypropylamine → HCID 10432802, 화합물
반응식
[OH:1][C@H:2]1[CH2:22][CH2:21][C@@:20]2([CH3:23])[CH:4]([CH2:5][CH2:6][C:7]3[C:8]4[C@:16]([CH3:24])([CH2:17][CH2:18][C:19]=32)[C@@H:11]([C@H:12]([CH3:15])[CH:13]=O)[CH2:10][CH:9]=4)[C:3]1([CH3:26])[CH3:25].[CH3:27][O:28][CH2:29][CH2:30][CH2:31][NH2:32].C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+]>>[CH3:27][O:28][CH2:29][CH2:30][CH2:31][NH:32][CH2:15][C@H:12]([C@@H:11]1[C@:16]2([CH3:24])[C:8]([C:7]3[CH2:6][CH2:5][C@@H:4]4[C@:20]([C:19]=3[CH2:18][CH2:17]2)([CH3:23])[CH2:21][CH2:22][C@H:2]([OH:1])[C:3]4([CH3:26])[CH3:25])=[CH:9][CH2:10]1)[CH3:13]참가 물질
4
실험 절차
(20S)-3β-hydroxy-4,4,20-trimethyl-pregna-8,14-dien-21-al was treated with 3-methoxypropylamine and sodium tris(acetoxy)borohydride as described in Example 1h). (20S)-20-[N-(3-methoxypropyl)aminomethyl]-4,4-dimethyl-5α-pregna-8,14-dien-3β-ol was isolated as a white solid.
출처 및 근거
- ORD 기록
- ord-38e628b8ed8842aeb21aa98c0d528ac9
- 출처 데이터셋
- uspto-grants-2005_07