Water → HCID 52951272, Verbindung
Reaktionsgleichung
[NH2:1][C:2]1[CH:6]=[C:5]([C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=2)[N:4]([C:13]2[CH:18]=[CH:17][C:16]([S:19]([NH2:22])(=[O:21])=[O:20])=[CH:15][CH:14]=2)[N:3]=1.[F:23][C:24]([F:35])([F:34])[C:25]1[CH:26]=[C:27]([N:31]=[C:32]=[O:33])[CH:28]=[CH:29][CH:30]=1.C(N(CC)CC)C.O>CN(C=O)C>[C:7]1([C:5]2[N:4]([C:13]3[CH:18]=[CH:17][C:16]([S:19]([NH2:22])(=[O:20])=[O:21])=[CH:15][CH:14]=3)[N:3]=[C:2]([NH:1][C:32]([NH:31][C:27]3[CH:28]=[CH:29][CH:30]=[C:25]([C:24]([F:23])([F:34])[F:35])[CH:26]=3)=[O:33])[CH:6]=2)[CH:8]=[CH:9][CH:10]=[CH:11][CH:12]=1Komponenten
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
To a solution of amine 6 (0.1 g, 0.32 mmol) in 5 mL of DMF was added 3-(trifluoromethyl)phenyl isocyanate (0.12 g, 0.62 mmol) followed by triethylamine (0.05 mL, 0.32 mmol) at 0° C. The reaction mixture was warmed up to room temperature and stirred overnight. The reaction mixture was poured into water, and the resulting precipitates were collected and washed with water. The crude product was purified by column chromatography by dry loading method to give the titled compound (0.13 g, 81% yield). mp 195.1-197.0° C. 1H NMR (300 MHz, DMSO-d6): δ 9.48 (s, 1H), 9.21 (s, 1H), 8.07 (s, 1H), 7.80 (d, J=9 Hz, 2H), 7.61-7.26 (m, 12H), 6.81 (s, 1H). MS (ESI) m/z: 502.12 (M+H+). Anal. Calcd for C23H18F3N5O3S.0.36CH4O: C, 54.69; H, 3.82; N, 13.65. Found: C, 54.69; H, 3.70; N, 13.44.
Aufarbeitung
- customthe resulting precipitates
- customwere collected
- washwashed with water
- customThe crude product was purified by column chromatography
- customby dry loading method
Quellen und Nachweise
- ORD-Eintrag
- ord-5c682b22891e4bd895909b27dd4c393a
- Quelldatensatz
- uspto-grants-2015_08
- Patentnummer
- US09096532B2
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