反応式
[CH2:1]([NH2:4])[CH2:2][NH2:3].C([Li])CCC.[Cl:10][C:11]1[CH:17]=[C:16]([Cl:18])[CH:15]=[C:14]([C:19](F)(F)F)[C:12]=1[NH2:13].O>C(OCC)C>[Cl:10][C:11]1[CH:17]=[C:16]([Cl:18])[CH:15]=[C:14]([C:19]2[NH:3][CH2:2][CH2:1][N:4]=2)[C:12]=1[NH2:13]参加物
6
実験手順
To a solution of ethylene diamine (1.2 mL, 18 mmol) in ethyl ether (50 mL) at −20° C. was added n-butyl lithium (6.4 mL, 2.5 M in hexanes, 16 mmol). The mixture was stirred at 0° C. for 0.3 hour before the addition of 2,4-dichloro-6-trifluoromethyl aniline (0.92 g, 4.2 mmol). The mixture was stirred at 0° C. for an additional 1.5 hours, at which point water (0.36 mL, 20 mmol) was added and the solvent was removed under reduced pressure. Purification by flash column chromatography (silica gel, 1% to 10% methanol in dichloromethane) to give the title compound of Step A (0.35 g) as a yellow solid.
後処理
- additionwas added
- customthe solvent was removed under reduced pressure
- customPurification by flash column chromatography (silica gel, 1% to 10% methanol in dichloromethane)
出典と根拠
- ORDレコード
- ord-108abbfac5ef4efa9ff9a1344a16d7e8
- 出典データセット
- uspto-grants-2008_02
- 特許番号
- US07326704B2
関連ノート
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