2,3-Dichloro-5,6-dicyano-1,4-benzoquinone → Dimethyl 4-ethyl-6-methoxy-3-(4-methoxyphenyl)pyrrolo[2,1,5-cd]indolizine-1,2-dicarboxylate
反応式
[CH2:1]([C:3]1[C:4]([C:14]2[CH:19]=[CH:18][C:17]([O:20][CH3:21])=[CH:16][CH:15]=2)=[CH:5][N:6]2[C:11]=1[CH:10]=[C:9]([O:12][CH3:13])[CH:8]=[CH:7]2)[CH3:2].[C:22]([C:28]([O:30][CH3:31])=[O:29])#[C:23][C:24]([O:26][CH3:27])=[O:25].ClC1C(=O)C(C#N)=C(C#N)C(=O)C=1Cl>C1(C)C=CC=CC=1>[CH2:1]([C:3]1[C:11]2[N:6]3[C:7]([CH:8]=[C:9]([O:12][CH3:13])[CH:10]=2)=[C:23]([C:24]([O:26][CH3:27])=[O:25])[C:22]([C:28]([O:30][CH3:31])=[O:29])=[C:5]3[C:4]=1[C:14]1[CH:19]=[CH:18][C:17]([O:20][CH3:21])=[CH:16][CH:15]=1)[CH3:2]参加物
実験手順
A solution of 1-ethyl-7-methoxy-2-(4-methoxyphenyl)indolizine (25.0 g, 0.089 mol) in 800 ml of toluene was stirred in an ice bath, while dimethyl acetylenedicarboxylate (12.6 ml, 0.103 mol) was added dropwise. When the starting material had been consumed according to TLC, 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (21.18 g, 0.093 mol) was added in portions. When the addition was complete, the mixture was refluxed for one hour. The resulting hydroquinone was filtered off, and the filtrate was concentrated to dryness. The residue was triturated with petroleum ether (40-60) and isolated to afford 33.8 g (92%) of the title compound. M.p. 153-5° C. 1H-NMR (DMSO-d6, 200 MHz) δ: 1.36 (t, 3H), 3.07 (q, 2H), 3.76 (s, 3H), 3.86 (s, 3H), 3.89 (s, 3H), 4.10 (s, 3H), 7.15 (d, 2H), 7.53 (d, 2H), 7.84 (d, 1H), 8.00 (d, 1H). (Compound 1).
後処理
- additionwas added dropwise
- customWhen the starting material had been consumed
- additionwas added in portions
- additionWhen the addition
- temperaturethe mixture was refluxed for one hour
- filtrationThe resulting hydroquinone was filtered off
- concentrationthe filtrate was concentrated to dryness
- customThe residue was triturated with petroleum ether (40-60)
- customisolated
出典と根拠
- ORDレコード
- ord-090fe8e5960b4846bf0b59ae15177ac6
- 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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