반응식
[N+:1]([C:4]1[CH:5]=[C:6]2[C:11](=[CH:12][CH:13]=1)[NH:10][C:9](=O)[NH:8][C:7]2=O)([O-:3])=[O:2].P(Cl)(Cl)([Cl:18])=O.C(N(C(C)C)C=O)(C)C.[C:30]12([NH2:40])[CH2:39][CH:34]3[CH2:35][CH:36]([CH2:38][CH:32]([CH2:33]3)[CH2:31]1)[CH2:37]2.C(N(CC)CC)C>O>[C:30]12([NH:40][C:7]3[C:6]4[C:11](=[CH:12][CH:13]=[C:4]([N+:1]([O-:3])=[O:2])[CH:5]=4)[N:10]=[C:9]([Cl:18])[N:8]=3)[CH2:37][CH:36]3[CH2:35][CH:34]([CH2:33][CH:32]([CH2:38]3)[CH2:31]1)[CH2:39]2참가 물질
실험 절차
To 250 mg (1.21 mmol) of 6-nitroquinazoline-2,4(1H,3H)-dione were added 5.00 ml (53.64 mmol) of phosphorus oxychloride and 0.18 ml (1.21 mmol) of diisopropylformamide, and the resulting mixture was subjected to heating under reflux for 24 hours. After phosphorus oxychloride was removed in vacuo, the mixture was dissolved in 5 ml of acetonitrile, followed by addition of 183 mg (1.21 mmol) of 1-adamantylamine and 0.84 ml (6.05 mmol) of triethylamine under ice cooling and stirring under ice cooling for 30 minutes. To the reaction solution was added water, followed by extraction with ethyl acetate, washing with brine and drying over anhydrous sodium sulfate. After the solvent was distilled off, the residue was purified by a silica gel column to give 90 mg (20.7%) of the title compound.
후처리
- temperatureto heating
- temperatureunder reflux for 24 hours
- customAfter phosphorus oxychloride was removed in vacuo
- dissolutionthe mixture was dissolved in 5 ml of acetonitrile
- extractionfollowed by extraction with ethyl acetate
- washwashing with brine
- dry with materialdrying over anhydrous sodium sulfate
- distillationAfter the solvent was distilled off
- customthe residue was purified by a silica gel column
출처 및 근거
- ORD 기록
- ord-f77c119c947f45b7bbc8fb01093600d6
- 출처 데이터셋
- uspto-grants-2002_01
- 특허 번호
- US06339089B2
연결된 노트
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