反応式
[CH2:1]([C@H:8]([NH:22]C(=O)OC(C)(C)C)[C@H:9]([OH:21])[CH2:10][NH:11][CH2:12][C:13]1[CH:18]=[CH:17][CH:16]=[C:15]([O:19][CH3:20])[CH:14]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[O:30]1[CH2:35]COCC1.[ClH:36].CC[O:39]CC>>[ClH:36].[NH2:22][C@@H:8]([CH2:1][C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1)[C@H:9]([OH:21])[CH2:10][N:11]([CH2:12][C:13]1[CH:18]=[CH:17][CH:16]=[C:15]([O:19][CH3:20])[CH:14]=1)[C:35](=[O:30])[OH:39]参加物
4
実験手順
1-tert-butyl (1S,2R)-1-benzyl-2-hydroxy-3-[(3-methoxybenzyl)amino]propylcarbamate (XXXIV, EXAMPLE 5, 5.4 g) and dioxane-hydrochloric acid (20 ml, 4 N) are mixed. The reaction mixture is stirred at 20–25° for 30 minutes then poured into stirred ether (300 ml). The product is filtered and dried under reduced pressure to give the title compound, M+H=435.
後処理
- additionthen poured
- filtrationThe product is filtered
- customdried under reduced pressure
出典と根拠
- ORDレコード
- ord-a6c5d12b119445ada3449a279e8e5e9b
- 出典データセット
- uspto-grants-2006_12
- 特許番号
- US07144897B2
関連ノート
読み込み中…