Reaktionsgleichung
C1(S([CH2:10][C:11]2[N:15]=[C:14]([C:16]3[O:17][CH:18]=[CH:19][CH:20]=3)[NH:13][N:12]=2)(=O)=O)C=CC=CC=1.[F:21][C:22]([F:38])([F:37])[C:23]1[CH:24]=[C:25]([CH:33]=[CH:34][C:35]#[N:36])[CH:26]=[C:27]([C:29]([F:32])([F:31])[F:30])[CH:28]=1>>[F:21][C:22]([F:37])([F:38])[C:23]1[CH:24]=[C:25]([C:33]2[CH:34]=[C:35]([NH2:36])[N:12]3[N:13]=[C:14]([C:16]4[O:17][CH:18]=[CH:19][CH:20]=4)[N:15]=[C:11]3[CH:10]=2)[CH:26]=[C:27]([C:29]([F:30])([F:31])[F:32])[CH:28]=1Komponenten
3
Versuchsvorschrift
The title compound, MS m/e (%): 412 (M+, 100), was prepared in accordance with the general method of example 1 from 3-benzenesulfonylmethyl-5-furan-2-yl-1H-[1,2,4]triazole and 3-[3,5-bis(trifluoromethyl)phenyl]acrylonitrile.
Quellen und Nachweise
- ORD-Eintrag
- ord-2d246282eb904ac0be9af012db8d0735
- Quelldatensatz
- uspto-grants-2002_03
- Patentnummer
- US06355653B1
Verknüpfte Notizen
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