反応式
[CH3:1][O:2][C:3](=[O:24])[C:4]([O:10][CH2:11][C:12]([N:21]=[N+]=[N-])([C:14]1[CH:19]=[CH:18][CH:17]=[C:16]([Br:20])[CH:15]=1)[CH3:13])([CH3:9])[C:5]([F:8])([F:7])[F:6].[In].Cl.C([O-])([O-])=O.[K+].[K+]>C1COCC1.O>[CH3:1][O:2][C:3](=[O:24])[C:4]([O:10][CH2:11][C:12]([NH2:21])([C:14]1[CH:19]=[CH:18][CH:17]=[C:16]([Br:20])[CH:15]=1)[CH3:13])([CH3:9])[C:5]([F:8])([F:7])[F:6]参加物
反応物 4
生成物 1
試薬・触媒・溶媒 1
反応条件
- 温度
- 25 °C
実験手順
To a solution of the 2-[2-azido-2-(3-bromo-phenyl)-propoxy]-3,3,3-trifluoro-2-methyl-propionic acid methyl ester (4.2 g, 9.22 mmol) in THF-H2O 3:1 (48 ml) was added indium (2.116 g, 18.43 mmol) followed by 4N aqueous HCl over a period of 20 min and stirring for 1 h at 25° C. The reaction mixture was added to a 10% aqueous K2CO3 solution and the product was extracted with EtOAc. The combined organic layers were washed with brine, dried over MgSO4, filtered and evaporated. The crude product was purified by flash-chromatography on NEt3 deactivated silica gel (hexane/EtOAc 2:1 to EtOAc) to provide a diastereomeric mixture of the title compound as a yellow oil: TLC (EtOAc): Rf=0.46; HPLC RtH5=0.999 min; 1H NMR (360 MHz, CDCl3): δ 7.73 (s, 1H), 7.47 (d, 1H), 7.41 (d, 1H), 7.24 (t, 1H), 3.84 and 3.83 (s, 3H), 3.59 (s, 2H), 1.61 and 1.59 (s, 3H), 1.52 and 1.51 (s, 3H); ESIMS: 384, 386 [(M+H)+].
後処理
- extractionthe product was extracted with EtOAc
- washThe combined organic layers were washed with brine
- dry with materialdried over MgSO4
- filtrationfiltered
- customevaporated
- customThe crude product was purified by flash-chromatography on NEt3 deactivated silica gel (hexane/EtOAc 2:1 to EtOAc)
- customto provide
出典と根拠
- ORDレコード
- ord-887923ae8f0649e8bfb999fb14fb4cde
- 出典データセット
- uspto-grants-2012_06
- 特許番号
- US08207164B2
関連ノート
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