反応式
Cl[C:2]1[CH:7]=[C:6]([Cl:8])[N:5]=[C:4]([NH:9][CH2:10][CH3:11])[N:3]=1.[K].[S:13]([C:17]1[CH:22]=[CH:21][C:20]([NH:23][C:24](=[O:26])[CH3:25])=[CH:19][CH:18]=1)(=[O:16])(=[O:15])[NH2:14]>CN1CCCC1=O>[Cl:8][C:6]1[N:5]=[C:4]([NH:9][CH2:10][CH3:11])[N:3]=[C:2]([NH:14][S:13]([C:17]2[CH:18]=[CH:19][C:20]([NH:23][C:24](=[O:26])[CH3:25])=[CH:21][CH:22]=2)(=[O:15])=[O:16])[CH:7]=1参加物
実験手順
2.0 g (0.011 mol) of (4,6-dichloropyrimidin-2-yl)-ethylamine and 5.67 g (0.022 mol) of N-(4-sulfamoyl-phenyl)-acetamide potassium salt were stirred in 10 ml of 1-methyl-2-pyrrolidone at 140° C. for 8 hours. Then, the solvent was distilled off in a high vacuum, the residue was partitioned in ethyl acetate/water, the inorganic phase was saturated with sodium chloride and the residual ethyl acetate dissolved in the aqueous phase was distilled off on a rotary evaporator. The aqueous phase was made acid with 1N HCl, the crystals which separated were filtered off under suction and washed with water. After drying there were obtained 2.88 g (75%) of N-[4-(6-chloro-2-ethylamino-pyrimidin-4-ylsulfamoyl)-phenyl]-acetamide as beige crystals, which were used directly in the next step.
後処理
- distillationThen, the solvent was distilled off in a high vacuum
- customthe residue was partitioned in ethyl acetate/water
- dissolutionthe residual ethyl acetate dissolved in the aqueous phase
- distillationwas distilled off on a rotary evaporator
- customthe crystals which separated
- filtrationwere filtered off under suction
- washwashed with water
- customAfter drying there
出典と根拠
- ORDレコード
- ord-03f8f475c4c34d3fa3d84e67c1a8c125
- 出典データセット
- uspto-grants-1999_12
- 特許番号
- US05998665
関連ノート
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