4-(Trifluoromethyl)benzoyl chloride → 3-(3-Bromo-thiophen-2-yl)-5-(4-trifluoromethyl-phenyl)-[1,2,4]-oxadiazole
Reaction equation
[F:1][C:2]([F:13])([F:12])[C:3]1[CH:11]=[CH:10][C:6]([C:7](Cl)=[O:8])=[CH:5][CH:4]=1.[Br:14][C:15]1[CH:19]=[CH:18][S:17][C:16]=1[C:20](=[N:22]O)[NH2:21]>>[Br:14][C:15]1[CH:19]=[CH:18][S:17][C:16]=1[C:20]1[N:22]=[C:7]([C:6]2[CH:10]=[CH:11][C:3]([C:2]([F:13])([F:12])[F:1])=[CH:4][CH:5]=2)[O:8][N:21]=1Participants
3
Procedure
The title compound was prepared from 4-trifluoromethyl-benzoyl chloride (66 μL, 0.44 mmol) and 3-bromo-thiophene-2-amidoxime (98 mg, 0.44 mmol) similar to Example 16, and yielded 130 mg (78%) of white solid. 1H NMR (CDCl3): 8.34 (d, J=8.24 Hz, 2H), 7.83 (d, J=8.51 Hz, 2H), 7.52 (d, J=5.22 Hz, 1H), 7.19 (d, J=5.21 Hz, 1H).
Sources & evidence
- ORD record
- ord-ccc2321ad5ca4e1580fe88c2f10e6157
- Source dataset
- uspto-grants-2006_05