Water → [(3S,6R)-6-(tert-butyl-dimethyl-silanyloxy)-2-oxo-1-pyridin-3-ylmethyl-azepan-3-yl]-carbamic acid tert-butyl ester
反応式
[C:1]([O:5][C:6](=[O:24])[NH:7][C@H:8]1[CH2:14][CH2:13][C@@H:12]([O:15][Si:16]([C:19]([CH3:22])([CH3:21])[CH3:20])([CH3:18])[CH3:17])[CH2:11][NH:10][C:9]1=[O:23])([CH3:4])([CH3:3])[CH3:2].Cl.Cl[CH2:27][C:28]1[CH:29]=[N:30][CH:31]=[CH:32][CH:33]=1.O>C1COCC1>[C:1]([O:5][C:6](=[O:24])[NH:7][C@H:8]1[CH2:14][CH2:13][C@@H:12]([O:15][Si:16]([C:19]([CH3:22])([CH3:21])[CH3:20])([CH3:18])[CH3:17])[CH2:11][N:10]([CH2:27][C:28]2[CH:29]=[N:30][CH:31]=[CH:32][CH:33]=2)[C:9]1=[O:23])([CH3:4])([CH3:2])[CH3:3]参加物
反応物 3
生成物 1
試薬・触媒・溶媒 1
実験手順
To a stirred solution of [(3S,6R)-6-(tert-butyl-dimethyl-silanyloxy)-2-oxo-azepan-3-yl]-carbamic acid tert-butyl ester (4.0 g, 11.1 mmol) in THF (30 mL) at −78° C. is added KN(Si(CH3)3)2 (45.0 mL 1M THF, 45.0 mmol) slowly. The mixture is stirred at room temperature for 20 min, cooled to −78° C., and 3-chloromethyl-pyridine hydrochloride (2.75 g, 16.7 mmol) is added in portions. The reaction is warmed to room temperature and stirred for 16 h, H2O (20 mL) is added and the mixture is partitioned with H2O/ether, the organic layer is separated, dried with Na2SO4 and evaporated to give a white solid, 5.0 g (quantitative) of [(3S,6R)-6-(tert-butyl-dimethyl-silanyloxy)-2-oxo-1-pyridin-3-ylmethyl-azepan-3-yl]-carbamic acid tert-butyl ester. MS (ESI) 899.3 (2M+H)+
後処理
- temperaturecooled to −78° C.
- temperatureThe reaction is warmed to room temperature
- stirringstirred for 16 h
- customthe mixture is partitioned with H2O/ether
- customthe organic layer is separated
- dry with materialdried with Na2SO4
- customevaporated
出典と根拠
- ORDレコード
- ord-d3d6753766854c0fa0aa228f1dcc9db3
- 出典データセット
- uspto-grants-2008_05
- 特許番号
- US07378410B2
反応ノート
読み込み中…