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[CH3:1][S:2][C:3]([NH:5][NH2:6])=[S:4].[F:7][C:8]([F:30])([F:29])[O:9][C:10]1[CH:15]=[CH:14][C:13]([N:16]2[CH:20]=[N:19][C:18]([C:21]3[CH:28]=[CH:27][C:24]([CH:25]=O)=[CH:23][CH:22]=3)=[N:17]2)=[CH:12][CH:11]=1>CCO.O>[F:30][C:8]([F:7])([F:29])[O:9][C:10]1[CH:15]=[CH:14][C:13]([N:16]2[CH:20]=[N:19][C:18]([C:21]3[CH:28]=[CH:27][C:24](/[CH:25]=[N:6]/[NH:5][C:3]([S:2][CH3:1])=[S:4])=[CH:23][CH:22]=3)=[N:17]2)=[CH:12][CH:11]=1참가 물질
5
반응 조건
- 온도
- 80 °C
실험 절차
To a 250 mL round-bottom flask containing hydrazinecarbodithioic acid methyl ester (2.38 g, 1.95 mmol) in EtOH (100 mL) was added 4-[1-(4-trifluoromethoxyphenyl)-1H-[1,2,4]triazol-3-yl]-benzaldehyde (5.00 g, 1.50 mmol). The vessel was heated at 80° C. for 3 h before being diluted with H2O (300 mL) and cooled to 0° C. The precipitated product was collected by vacuum filtration as an off-white solid (6.13 g, 93%): mp 204-206° C.; 1H NMR (400 MHz, DMSO-d6) δ 13.39 (s, 1H), 9.43 (s, 1H), 8.38 (s, 1H), 8.21 (d, J=8.3 Hz, 2H), 8.09 (d, J=8.4 Hz, 2H), 7.88 (d, J=8.4 Hz, 2H), 7.62 (d, J=8.3 Hz, 2H), 2.57 (s, 3H); ESIMS m/z 438 (M+H).
후처리
- temperaturecooled to 0° C
- filtrationThe precipitated product was collected by vacuum filtration as an off-white solid (6.13 g, 93%)
출처 및 근거
- ORD 기록
- ord-052140659b814bc49655f0ff5230b891
- 출처 데이터셋
- uspto-grants-2015_04
- 특허 번호
- US09018136B2
연결된 노트
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