Hydrochloric Acid → (3S,6S,10aS)-6-amino-5-oxo-1,2,3,5,6,7,10,10a-octahydro-pyrrolo[1,2-a]azocine-3-carboxylic acid
反応式
C[O:2][C:3]([CH:5]1[N:9]2[C:10](=[O:17])[CH:11]([NH2:16])[CH2:12][CH:13]=[CH:14][CH2:15][CH:8]2[CH2:7][CH2:6]1)=[O:4].[Li+].[OH-].Cl>C1COCC1.O>[NH2:16][C@@H:11]1[C:10](=[O:17])[N:9]2[C@H:5]([C:3]([OH:4])=[O:2])[CH2:6][CH2:7][C@H:8]2[CH2:15][CH:14]=[CH:13][CH2:12]1参加物
5
反応物 3
生成物 1
試薬・触媒・溶媒 1
実験手順
To a solution of 6-amino-5-oxo-1,2,3,5,6,7,10,10a-octahydro-pyrrolo[1,2-a]azocine-3-carboxylic acid methyl ester, 8, (1.4 g, 5.2 mmol) in THF/water (3:1) is added LiOH (1.1 eq) and the solution is stirred overnight. The reaction is treated with 1 N HCl to pH 4. The mixture is then frozen and lyophilized to a pale yellow powder, which can be used directly in the next step.
後処理
- temperatureThe mixture is then frozen
出典と根拠
- ORDレコード
- ord-d165c1a2325b46768aeebb89839745fb
- 出典データセット
- uspto-grants-2006_05
- 特許番号
- US07041696B2
反応ノート
読み込み中…