1-(4-Fluorophenyl)-4-methyl-5-piperidino-4,5-dihydro-1,2,3-triazole → 1-(2-Fluorophenyl)-4-methyl-1H-1,2,3-triazole
Reaction equation
[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[N:8]1[CH:12](N2CCCCC2)[CH:11]([CH3:19])[N:10]=[N:9]1.FC1C=CC(N2C(N3CCCCC3)C(C)N=N2)=CC=1>>[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[N:8]1[CH:12]=[C:11]([CH3:19])[N:10]=[N:9]1Participants
3
Procedure
As described for example 60c, 1-(1-(2-fluorophenyl)-4-methyl-4,5-dihydro-1H-1,2,3-triazol-5-yl)piperidine (1.32 g, 5.32 mmol), instead of 1-[3-(4-fluoro-phenyl)-5-methyl-4,5-dihydro-3H-[1,2,3]triazol-4-yl]-piperidine, was converted to the title compound (616 mg, 65%) which was obtained as a colourless liquid. MS: m/e=178.1 [M+H]+.
Sources & evidence
- ORD record
- ord-c5dc034016824e3fa866d6202887e33a
- Source dataset
- uspto-grants-2014_06
- Patent number
- US08742097B2
Reaction notes
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