Triethylamine → 3-(2-Fluoro-4-iodophenyl)-4-fluoro-8-methyl-1H-imidazo[4,5-g]quinazolin-2(3H)-one
반응식
[F:1][C:2]1[CH:7]=[C:6]([I:8])[CH:5]=[CH:4][C:3]=1[NH:9][C:10]1[C:19]([F:20])=[C:18]2[C:13]([C:14]([CH3:21])=[N:15][CH:16]=[N:17]2)=[CH:12][C:11]=1C(O)=O.C([N:27]([CH2:30]C)CC)C.C1(P(N=[N+]=[N-])(C2C=CC=CC=2)=[O:39])C=CC=CC=1>C1(C)C=CC=CC=1>[F:1][C:2]1[CH:7]=[C:6]([I:8])[CH:5]=[CH:4][C:3]=1[N:9]1[C:10]2[C:11](=[CH:12][C:13]3[C:14]([CH3:21])=[N:15][CH:16]=[N:17][C:18]=3[C:19]=2[F:20])[NH:27][C:30]1=[O:39]참가 물질
5
실험 절차
To a suspension of 7-(2-fluoro-4-iodophenylamino)-8-fluoro-4-methylquinazoline-6-carboxylic acid (190 mg, 0.47 mmol) in toluene (10 ml) was added triethylamine (0.19 ml, 1.41 mmol) and diphenylphosphoryl azide (0.20 ml, 0.94 mmol). The reaction was heated at reflux for 4 h. The mixture was cooled to room temperature and concentrated to dryness. Silica gel chromatography (EtOAc:Hexane=75:25) yields 143 mg (75%) of the title compound as a tan solid.
후처리
- temperatureThe reaction was heated
- temperatureat reflux for 4 h
- concentrationconcentrated to dryness
출처 및 근거
- ORD 기록
- ord-09ca919c796d4f5c8c31f888592a63ca
- 출처 데이터셋
- uspto-grants-2010_10
- 특허 번호
- US07820664B2
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