Sodium → HCID 66968883, 화합물
반응식
[N+:1]([C:4]1[CH:9]=[CH:8][C:7]([C:10]2[CH:15]=[CH:14][N:13]=[C:12]([C:16]3[CH:21]=[CH:20][C:19]([C:22]([F:25])([F:24])[F:23])=[CH:18][CH:17]=3)[N:11]=2)=[CH:6][CH:5]=1)([O-])=O.[Na].O.O.Cl.FC(F)(F)C1C=CC(C(N)=N)=CC=1>CCO.C(Cl)(Cl)Cl.CCOC(C)=O>[F:25][C:22]([F:23])([F:24])[C:19]1[CH:18]=[CH:17][C:16]([C:12]2[N:11]=[C:10]([C:7]3[CH:8]=[CH:9][C:4]([NH2:1])=[CH:5][CH:6]=3)[CH:15]=[CH:14][N:13]=2)=[CH:21][CH:20]=1참가 물질
실험 절차
4-(4-Nitrophenyl)-2-(4-trifluoromethylphenyl)-pyrimidine. To sodium metal (82.7 mg, 3.60 mmol) dissolved in absolute EtOH (3 mL) was added 4-trifluoromethylbenzamidine hydrochloride dihydrate (938 mg, 3.60 mmol) followed by EtOH (4 mL). After 30 min, 3-dimethylamino-1-(4-nitrophenyl)-propenone (498 mg, 2.26 mmol) was added, and the mixture was heated at reflux approximately 66 h and was then allowed to cool. The mixture was concentrated to a tan solid which was triturated under saturated sodium bicarbonate. The solid was collected and air dried to give 937 mg. It was then dissolved in chloroform/EtOAc and was passed over silica gel eluting with 7:3 chloroform/EtOAc to afford the title compound (710 mg, 91%): mp 175-176.5° C.; 1H NMR δ 9.01 (d, J=5.3 Hz, 1H), 8.73 (d, J=8.2 Hz, 2H), 8.43 (s, 4H), 7.82 (d, J=8.1 Hz, 2H), 7.76 (d, J=5.2 Hz, 1H); EIMS m/z 345 (M+, 100), 299 (57). Anal. Calcd. for C17H10F3N3O2: C, 59.13; H, 2.92; N, 12.17. Found: C, 58.82; H, 2.63; N, 11.98.
후처리
- temperaturethe mixture was heated
- temperatureat reflux approximately 66 h
- temperatureto cool
- concentrationThe mixture was concentrated to a tan solid which
- customwas triturated under saturated sodium bicarbonate
- customThe solid was collected
- customair dried
- customto give 937 mg
출처 및 근거
- ORD 기록
- ord-4b8143a9711943649596353fc30d4bd7
- 출처 데이터셋
- uspto-grants-2015_01
- 특허 번호
- US08927729B2
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