反応式
[Cl-].[Cl-].[Cl-].[Al+3].[CH3:5][N:6]1[C:14]2[C:13](=[O:15])[NH:12][C:11]([C:16]3[CH:21]=[CH:20][CH:19]=[CH:18][C:17]=3[O:22][CH2:23][CH2:24][CH3:25])=[N:10][C:9]=2[C:8]([CH2:26][CH2:27][CH3:28])=[N:7]1.[Br:29][CH2:30][C:31](Cl)=[O:32].O>ClCCl>[Br:29][CH2:30][C:31]([C:20]1[CH:19]=[CH:18][C:17]([O:22][CH2:23][CH2:24][CH3:25])=[C:16]([C:11]2[NH:12][C:13](=[O:15])[C:14]3[N:6]([CH3:5])[N:7]=[C:8]([CH2:26][CH2:27][CH3:28])[C:9]=3[N:10]=2)[CH:21]=1)=[O:32]参加物
反応物 4
生成物 1
試薬・触媒・溶媒 1
実験手順
Aluminium trichloride (6.0 g, 0.045 mol) was added portionwise to a stirred solution of 1-methyl-5-(2-n-propoxyphenyl)-3-n-propyl-1,6-dihydro-7H-pyrazolo[4,3-d]pyrimidin-7-one (5.0 g, 0.0153 mol) and 2-bromoacetyl chloride (2.5 ml, 0.0303 mol) in dichloromethane (100 ml) at 0° C. The reaction mixture was allowed to warm to room temperature, stirred for 18 hours, heated under reflux for 3 hours and then added cautiously to ice and water (100 g). The resulting mixture was stirred for 1 hour and extracted with dichloromethane (2×50 ml). The combined organic extracts were washed with brine (2×50 ml), dried (Na2SO4), then evaporated under vacuum to give an off-white solid, which was triturated with ether to give the title compound as a white solid (4.1 g, 60%). A small sample was crystallised from ethyl acetate-hexane to give the pure product, m.p. 136°-137° C. Found: C,53.82; H,5.24; N,12.57. C20H23BrN4O3 requires C,53.70; H,5.18; N,12.52%.
後処理
- temperatureheated
- temperatureunder reflux for 3 hours
- stirringThe resulting mixture was stirred for 1 hour
- extractionextracted with dichloromethane (2×50 ml)
- washThe combined organic extracts were washed with brine (2×50 ml)
- dry with materialdried (Na2SO4)
- customevaporated under vacuum
- customto give an off-white solid, which
- customwas triturated with ether
出典と根拠
- ORDレコード
- ord-ac6e5907089a45fd8fa2861c6cec197c
- 出典データセット
- uspto-grants-1995_06
- 特許番号
- US05426107
関連ノート
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