Hydrochloric Acid → HCID 67436541、化合物
反応式
Cl.[O:2]=[C:3]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[C:5](=[O:12])[N:4]1[CH2:13][CH2:14][C:15]1[CH:22]=[CH:21][C:18]([C:19]#[N:20])=[CH:17][CH:16]=1.[CH2:23](N)[CH2:24][NH2:25]>C(O)C>[NH:20]1[CH2:23][CH2:24][N:25]=[C:19]1[C:18]1[CH:17]=[CH:16][C:15]([CH2:14][CH2:13][N:4]2[C:3](=[O:2])[C:11]3[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=3)[C:5]2=[O:12])=[CH:22][CH:21]=1参加物
実験手順
Dry hydrogen chloride gas was bubbled through an ice cold solution of 4-[2-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-ethyl]-benzonitrile (7.83 g, 28.3 mmol) in ethanol (400 mL) for 3 h, then the so obtained mixture was kept at 8° C. overnight. The reaction mixture was concentrated in vacuo, the residue was dissolved in dry ethanol (400 mL), ethylenediamine (2.0 mL, 29.7 mmol) was added and the reaction mixture was stirred at room temperature overnight. The mixture was concentrated in vacuo, the residue was partitioned between dichloromethane (400 mL) and concentrated ammonium hydroxide (400 mL), the phases were separated and the water phase was extracted with dichloromethane (2×200 mL). The combined organic layers were dried over sodium sulfate, filtered and concentrated. The crude product was recrystallized from 2-propanol to yield 5.58 g (62%) of the title compound as a white solid.
後処理
- concentrationThe reaction mixture was concentrated in vacuo
- dissolutionthe residue was dissolved in dry ethanol (400 mL)
- concentrationThe mixture was concentrated in vacuo
- customthe residue was partitioned between dichloromethane (400 mL) and concentrated ammonium hydroxide (400 mL)
- customthe phases were separated
- extractionthe water phase was extracted with dichloromethane (2×200 mL)
- dry with materialThe combined organic layers were dried over sodium sulfate
- filtrationfiltered
- concentrationconcentrated
- customThe crude product was recrystallized from 2-propanol
出典と根拠
- ORDレコード
- ord-b77423716e3645508e69277aa65255f9
- 出典データセット
- uspto-grants-2011_10
- 特許番号
- US08034827B2
反応ノート
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