反応式
[SH:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][N:3]=1.C(N(CC)CC)C.Br[CH2:16][CH2:17][CH2:18][CH2:19][Cl:20]>C(O)C>[Cl:20][CH2:19][CH2:18][CH2:17][CH2:16][S:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][N:3]=1参加物
5
実験手順
To a solution of 25.0 g (225 mmol) of 2-mercaptopyridine and 34.5 ml (247 mmol) of triethylamine in 300 ml of ethanol, 28.5 ml (247 mmol) of 1-bromo-4-chlorobutane was added with stirring under ice-cooling, and the mixture was stirred at room temperature for 16 hours. The solvent was distilled off and the residue was dissolved in chloroform. The solution was washed with saturated aqueous sodium bicarbonate and water, and dried. The solvent was distilled off and the residue was purified by column chromatography (eluent: ethyl acetate/hexane =1:3) to give 29.73 g of the desired compound (65.5% yield, pale yellow oil).
後処理
- temperaturecooling
- stirringthe mixture was stirred at room temperature for 16 hours
- distillationThe solvent was distilled off
- dissolutionthe residue was dissolved in chloroform
- washThe solution was washed with saturated aqueous sodium bicarbonate and water
- customdried
- distillationThe solvent was distilled off
- customthe residue was purified by column chromatography (eluent: ethyl acetate/hexane =1:3)
出典と根拠
- ORDレコード
- ord-e9a40193820a432da78afb9efd42f92a
- 出典データセット
- uspto-grants-1993_09
- 特許番号
- US05246948
関連ノート
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