Potassium trimethylsilanolate → (1R)-2-(6-(2-((2,6-dichlorophenyl)methoxy)ethoxy)hexylamino)-1-(2,2-dimethyl-4H-1,3-benzodioxin-6-yl)ethanol
反応式
[Cl:1][C:2]1[CH:36]=[CH:35][CH:34]=[C:33]([Cl:37])[C:3]=1[CH2:4][O:5][CH2:6][CH2:7][O:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][N:15]1[CH2:19][C@@H:18]([C:20]2[CH:31]=[CH:30][C:23]3[O:24][C:25]([CH3:29])([CH3:28])[O:26][CH2:27][C:22]=3[CH:21]=2)[O:17]C1=O.C[Si](C)(C)[O-].[K+]>C1COCC1>[Cl:1][C:2]1[CH:36]=[CH:35][CH:34]=[C:33]([Cl:37])[C:3]=1[CH2:4][O:5][CH2:6][CH2:7][O:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][NH:15][CH2:19][C@@H:18]([C:20]1[CH:31]=[CH:30][C:23]2[O:24][C:25]([CH3:28])([CH3:29])[O:26][CH2:27][C:22]=2[CH:21]=1)[OH:17]参加物
4
反応物 2
生成物 1
試薬・触媒・溶媒 1
実験手順
A solution of (5R)-3-(6-{2-[(2,6-dichlorobenzyl)oxy]ethoxy}hexyl)-5-(2,2-dimethyl-4H-1,3-benzodioxin-6-yl)-1,3-oxazolidin-2-one (140 mg) in THF (7 ml) under nitrogen was treated with potassium trimethylsilanolate (130 mg) and the mixture was heated (oil bath temperature 80°) with stirring for 3 h. The mixture was cooled to 20° and was partitioned between phosphate buffer solution (20 ml, pH6.5) and EtOAc (20 ml). The organic phase was separated, dried (NaSO4) and the solvent evaporated in vacuo to give the title compound (130 mg). LCMS RT=3.00 min.
後処理
- temperaturethe mixture was heated (oil bath temperature 80°)
- temperatureThe mixture was cooled to 20°
- customwas partitioned between phosphate buffer solution (20 ml, pH6.5) and EtOAc (20 ml)
- customThe organic phase was separated
- dry with materialdried (NaSO4)
- customthe solvent evaporated in vacuo
出典と根拠
- ORDレコード
- ord-94f74a6e85da45edabf9fef562d1a2aa
- 出典データセット
- uspto-grants-2010_08
- 特許番号
- US07776895B2
反応ノート
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