4-Fluorobenzyl bromide → 1-[(4-fluorophenyl)methyl]pyrazol-3-amine
Reaction equation
[NH2:1][C:2]1[CH:6]=[CH:5][NH:4][N:3]=1.[F:7][C:8]1[CH:15]=[CH:14][C:11]([CH2:12]Br)=[CH:10][CH:9]=1>>[F:7][C:8]1[CH:15]=[CH:14][C:11]([CH2:12][N:4]2[CH:5]=[CH:6][C:2]([NH2:1])=[N:3]2)=[CH:10][CH:9]=1Participants
3
Procedure
Prepared in analogy to example 10a) starting with 3-amino-1H-pyrazole and 4-fluorobenzylbromide. The title compound was obtained as a colorless solid (Yield=34%). MS ISP (m/e): 192.2 (100) [(M+H)+].
Workup
- customPrepared in analogy to example 10a)
Sources & evidence
- ORD record
- ord-1eb8002a310c4f298f00498d0cff41ae
- Source dataset
- uspto-grants-2012_10
- Patent number
- US08288403B2
Reaction notes
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