反応式
[NH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[C:3]([C:10]([O:12][CH3:13])=[O:11])=[CH:2]1.CN1CCN(C)CC1.ClN1C(=O)CCC1=O.[Cl:30][CH2:31][CH2:32][CH2:33][OH:34].ClC(Cl)(Cl)C(O)=O>ClCCl>[Cl:30][CH2:31][CH2:32][CH2:33][O:34][C:2]1[NH:1][C:9]2[C:4]([C:3]=1[C:10]([O:12][CH3:13])=[O:11])=[CH:5][CH:6]=[CH:7][CH:8]=2参加物
反応条件
- 温度
- 0 °C
実験手順
A mixture of methyl indole-3-carboxylate and dichloromethane is cooled to 0° C. 1,4-dimethylpiperazine (0.55 eq.) and N-chlorosuccinimide (1.1 eq) are added and the mixture left to stir for two hours to give a slurry containing the compound of formula (C) above. The resulting slurry is added to a solution of 3-chloropropanol (1.1 eq) and trichloroacetic acid (0.12 eq) in dichloromethane, maintaining the temperature below 0° C. The reaction mixture is left to stir for half an hour, then washed with 10% aqueous sodium carbonate, 0.5 M hydrochloric acid and water. The organic solution is dried over sodium sulphate, filtered and the solvent evaporated. Toluene is added and the mixture stirred at 0-5° C. for one hour. The product is then filtered, washed with toluene and dried to give the title product in 83% yield.
後処理
- waitthe mixture left
- customto give a slurry
- temperaturemaintaining the temperature below 0° C
- waitThe reaction mixture is left
- stirringto stir for half an hour
- washwashed with 10% aqueous sodium carbonate, 0.5 M hydrochloric acid and water
- dry with materialThe organic solution is dried over sodium sulphate
- filtrationfiltered
- customthe solvent evaporated
- additionToluene is added
- stirringthe mixture stirred at 0-5° C. for one hour
- filtrationThe product is then filtered
- washwashed with toluene
- customdried
出典と根拠
- ORDレコード
- ord-a22556098eba400f8396a5a1c34c3d64
- 出典データセット
- uspto-grants-2005_09
- 特許番号
- US06946565B2
関連ノート
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