2-(Trifluoromethyl)aniline → 1-(2-trifluoromethyl-phenyl)-1H-[1,2,4]triazol-3-ylamine
Reaction equation
C1([C:7]2O[N:10]=[C:9]([NH2:12])[N:8]=2)C=CC=CC=1.[NH2:13][C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][C:15]=1[C:20]([F:23])([F:22])[F:21]>>[F:23][C:20]([F:21])([F:22])[C:15]1[CH:16]=[CH:17][CH:18]=[CH:19][C:14]=1[N:13]1[CH:7]=[N:8][C:9]([NH2:12])=[N:10]1Participants
3
Procedure
Prepared in analogy to example 18a), starting with 5-phenyl-[1,2,4]oxadiazol-3-ylamine and 2-aminobenzotrifluoride. The title compound was obtained as brownish solid in a yield of 94%. MS ISP (m/e): 229.2 (64) [(M+H)+].
Workup
- customPrepared in analogy to example 18a),
Sources & evidence
- ORD record
- ord-8bf32df4eb42479c8ab6b17b8ffe72e6
- Source dataset
- uspto-grants-2012_10
- Patent number
- US08288403B2
Reaction notes
Loading…