Nitroethane → Ethyl 2-(3,5-dihydroxyphenyl)-8,9-dimethoxy-3-methyl-5,6-dihydro-pyrrolo[2,1-a]-isoquinoline-1-carboxylate
反応式
[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][C:12]=1[O:13][CH3:14])[C:9](=[CH:15][C:16]([O:18][CH2:19][CH3:20])=[O:17])[NH:8][CH2:7][CH2:6]2.[OH:21][C:22]1[CH:23]=[C:24]([CH:27]=[C:28]([OH:30])[CH:29]=1)[CH:25]=O.[N+]([CH2:34][CH3:35])([O-])=O.N1CCCCC1>C(O)C.C(O)(C)C.C(O)(C)C>[OH:21][C:22]1[CH:23]=[C:24]([C:25]2[C:15]([C:16]([O:18][CH2:19][CH3:20])=[O:17])=[C:9]3[C:10]4[C:5](=[CH:4][C:3]([O:2][CH3:1])=[C:12]([O:13][CH3:14])[CH:11]=4)[CH2:6][CH2:7][N:8]3[C:34]=2[CH3:35])[CH:27]=[C:28]([OH:30])[CH:29]=1参加物
7
反応物 4
生成物 1
試薬・触媒・溶媒 2
反応条件
- 温度
- 80 °C
実験手順
A mixture of 500 mg (1.8 mmol) of ethyl (6,7-dimethoxy-3,4-dihydro-1(2H)-isoquinolinylidene)-ethanoate (Example III.1), 499 mg (3.61 mmol) of 3,5-dihydroxybenzaldehyde, 281 mg (3.61 mmol) of nitroethane and 61.4 mg (0.72 mmol) of piperidine in 10 mL of an ethanol/isopropanol 1:1 mixture was stirred at 80° C. overnight. 40 mL of isopropanol were added, the mixture was cooled to 0° C., and the resulting precipitate was filtered off. The solid was washed with ethanol and dried in vacuo to give the title compound as a white solid which was readily recrystallized from ethyl acetate to furnish white needles.
後処理
- temperaturethe mixture was cooled to 0° C.
- filtrationthe resulting precipitate was filtered off
- washThe solid was washed with ethanol
- customdried in vacuo
出典と根拠
- ORDレコード
- ord-aa8fd636a9504701a856c152ff2eaebb
- 出典データセット
- uspto-grants-2005_08
- 特許番号
- US06930114B2
反応ノート
読み込み中…