反応式
[H-].[Na+].[N+:3]([C:6]1[CH:7]=[CH:8][C:9]([C:13]#[C:14][CH3:15])=[C:10]([NH2:12])[CH:11]=1)([O-:5])=[O:4].ClC(OCC)=O.[O-]CC.[Na+].C(O)C>CN(C=O)C.C(OCC)(=O)C>[CH3:15][C:14]1[NH:12][C:10]2[C:9]([CH:13]=1)=[CH:8][CH:7]=[C:6]([N+:3]([O-:5])=[O:4])[CH:11]=2参加物
実験手順
Cool a mixture of sodium hydride (60% dispersion in oil, 0.33 g, 8.19 mmol) in anhydrous DMF to 0° C. under inert atmosphere. Add 5-nitro-2-prop-1-ynyl-phenylamine 17 (1.31 g, 7.44 mmol) in 10 mL DMF and stir 5 minutes. Add ethyl chloroformate (0.78 mL, 8.19 mmol), warm to ambient temperature, and stir 2 hours. Quench the reaction with saturated aqueous sodium bicarbonate, add ethyl acetate, and wash with saturated aqueous sodium bicarbonate followed by saturated aqueous brine. Dry the organic layer over sodium sulfate, filter, and concentrate in vacuo. Add to the residue a solution of sodium ethoxide in ethanol (0.6 M, 50 mL, 0.30 mmol) and reflux 14 hours. Cool to ambient temperature and concentrate in vacuo. Redissolve the residue in diethyl ether and wash with saturated aqueous sodium bicarbonate followed by saturated aqueous brine. Dry the organic layer over sodium sulfate, filter, concentrate in vacuo, and chromatograph the residue over silica gel, eluting with hexanes/ethyl acetate (9:1) to afford the title compound, 0.79 g (60%). LRMS (API ES−)=175.0 (M−H).
後処理
- temperatureCool
- customQuench
- customthe reaction with saturated aqueous sodium bicarbonate
- washwash with saturated aqueous sodium bicarbonate
- dry with materialDry the organic layer over sodium sulfate
- filtrationfilter
- concentrationconcentrate in vacuo
- temperaturereflux 14 hours
- concentrationconcentrate in vacuo
- dissolutionRedissolve the residue in diethyl ether
- washwash with saturated aqueous sodium bicarbonate
- dry with materialDry the organic layer over sodium sulfate
- filtrationfilter
- concentrationconcentrate in vacuo, and chromatograph the residue over silica gel
- washeluting with hexanes/ethyl acetate (9:1)
出典と根拠
- ORDレコード
- ord-b7443fbb105549c2ac2a8095ee759b5e
- 出典データセット
- uspto-grants-2011_04
- 特許番号
- US07932284B2
関連ノート
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