Hydroxyamine hydrochloride → tert-butyl (1R,3S,4S,6E)-3-[(2S)-2-cyanopyrrolidine-1-carbonyl]-6-hydroxyimino-2-azabicyclo[2.2.1]heptane-2-carboxylate
反応式
[C:1]([C@@H:3]1[CH2:7][CH2:6][CH2:5][N:4]1[C:8]([C@@H:10]1[C@H:15]2[CH2:16][C@H:12]([C:13](=O)[CH2:14]2)[N:11]1[C:18]([O:20][C:21]([CH3:24])([CH3:23])[CH3:22])=[O:19])=[O:9])#[N:2].Cl.[NH2:26][OH:27].C([O-])(=O)C.[Na+]>C(O)C.O>[C:1]([C@@H:3]1[CH2:7][CH2:6][CH2:5][N:4]1[C:8]([C@@H:10]1[C@H:15]2[CH2:16][C@H:12](/[C:13](=[N:26]/[OH:27])/[CH2:14]2)[N:11]1[C:18]([O:20][C:21]([CH3:23])([CH3:22])[CH3:24])=[O:19])=[O:9])#[N:2]参加物
6
反応物 3
生成物 1
試薬・触媒・溶媒 2
反応条件
- 温度
- 80 °C
実験手順
To a solution of tert-butyl (1R,3S,4S)-3-{[(2S)-2-cyano-1-pyrrolidinyl]carbonyl}-6-oxo-2-azabicyclo[2.2.1]heptane-2-carboxylate obtained in Example 22-1 (296 mg) in ethanol (5 mL) and water (1 mL),were added hydroxylamine hydrochloride (123 mg) and sodium acetate (153 mg). The mixture was stirred at 80° C. for 20 minutes.
出典と根拠
- ORDレコード
- ord-ac2a8ff429ed4b26a185ddbb10bb8372
- 出典データセット
- uspto-grants-2007_03
- 特許番号
- US07186731B2
反応ノート
読み込み中…