Acetonitrile → HCID 86639521, 화합물
반응식
Cl[C:2]1[N:11]=[C:10]([C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)[C:9]2[C:4](=[CH:5][CH:6]=[C:7]([Cl:18])[CH:8]=2)[N:3]=1.C(#N)C.Cl.[CH3:23][O:24][NH2:25].C(N(CC)CC)C>O>[Cl:18][C:7]1[CH:8]=[C:9]2[C:4](=[CH:5][CH:6]=1)[N:3]=[C:2]([NH:25][O:24][CH3:23])[N:11]=[C:10]2[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1참가 물질
실험 절차
To a mixture of 275 mg of 2,6-dichloro-4-phenylquinazoline (compound No. Ia1-3), 10 ml of acetonitrile and 334 mg of methoxyamine hydrochloride was added dropwise 506 mg of triethylamine at room temperature to obtain a mixture. The mixture was charged in a pressure-resistant reaction vessel made of stainless steel and the reaction was carried out at 105° C. for 3.5 hours. After cooling, the reaction solution was poured into 100 ml of water. The mixture was extracted with ethyl acetate and the resultant extract was washed with water and then concentrated. The resulting residue was purified by silica gel column chromatography (hexane:ethyl acetate=3:1) to obtain 156 mg of crude crystals. The crude crystals were recrystallized from ethyl acetate to obtain 55 mg of the titled compound. Mp.173.9° C. 1H NMR (CDCl3): 3.98 (3H, s), 7.47-7.72 (6H, m), 7.87 (1H, d, J=9.0 Hz), 7.89 (1H, d, J=2.2 Hz), 8.03 (1H, br. s).
후처리
- customto obtain a mixture
- additionThe mixture was charged in a pressure-resistant reaction vessel
- temperatureAfter cooling
- extractionThe mixture was extracted with ethyl acetate
- extractionthe resultant extract
- washwas washed with water
- concentrationconcentrated
- customThe resulting residue was purified by silica gel column chromatography (hexane:ethyl acetate=3:1)
- customto obtain 156 mg of crude crystals
- customThe crude crystals were recrystallized from ethyl acetate
출처 및 근거
- ORD 기록
- ord-b4cda63bc41d4228991113abf29b0927
- 출처 데이터셋
- uspto-grants-2014_05
- 특허 번호
- US08722580B2
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