Boron tribromide → 4-Acetyl-1-ethyl-2-(4-hydroxyphenyl)-6-methoxypyrrolo[2,1,5-cd]indolizine
反応式
[C:1]([C:4]1[CH:5]=[C:6]2[N:14]3[C:9](=[CH:10][C:11]([O:15][CH3:16])=[CH:12][C:13]=13)[C:8]([CH2:17][CH3:18])=[C:7]2[C:19]1[CH:24]=[CH:23][C:22]([O:25]C)=[CH:21][CH:20]=1)(=[O:3])[CH3:2].B(Br)(Br)Br.[O-2].[Al+3].[O-2].[O-2].[Al+3]>ClCCl.ClCCl.CO>[C:1]([C:4]1[CH:5]=[C:6]2[N:14]3[C:9](=[CH:10][C:11]([O:15][CH3:16])=[CH:12][C:13]=13)[C:8]([CH2:17][CH3:18])=[C:7]2[C:19]1[CH:20]=[CH:21][C:22]([OH:25])=[CH:23][CH:24]=1)(=[O:3])[CH3:2]参加物
反応物 3
生成物 1
試薬・触媒・溶媒 2
実験手順
A solution of 4-acetyl-1-ethyl-6-methoxy-2-(4-methoxyphenyl)pyrrolo[2,1,5-cd]indolizine (0.3 g, 0.85 mmol) in 7 ml of dry dichloromethane was cooled to -65° C. and stirred in a nitrogen atmosphere while 1.2 ml of a 1 M boron tribromide solution in dichloromethane was added. Stirring was continued for one hour and the cooling source was removed. The reaction mixture was allowed to reach room temperature and then poured into a stirred medium of dichloromethane (100 ml) and a saturated sodium hydrogen carbonate solution (100 ml). The usual work up afforded 200 mg of a substance which was submitted to column chromatography (aluminium oxide) with dichloromethane/methanol (20:1) as eluent. The fractions having RF 0.4 (silica gel 60, dichloromethane/methanol (20:1)) was collected and evaporated to afford 160 mg (58%) of the title compound. M.p. 245-46° C. 1H-NMR (DMSO-d6, 200 MHz) δ: 1.37 (t, 3H), 2.62 (s, 3H), 3.13 (q, 2H), 4.07 (s, 3H), 7.00 (d, 2H), 7.70 (d, 2H), 7.79 (d, 1H), 7.87 (d, 1H), 8.12 (s, 1H), 9.87 (s, 1H). (Compound 7).
後処理
- additionwas added
- customthe cooling source was removed
- customto reach room temperature
- additionpoured into a stirred medium of dichloromethane (100 ml)
- customThe usual work up afforded 200 mg of a substance which
- customwas collected
- customevaporated
出典と根拠
- ORDレコード
- ord-9c62228dec544e90a5f977f2d2fbeed6
- 出典データセット
- uspto-grants-2000_06
- 特許番号
- US06075036
反応ノート
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