2,4-Dichlorobenzyl bromide → 1-((2,4-Dichlorophenyl)methyl)-1H-pyrazol-3-amine
Reaction equation
[NH2:1][C:2]1[CH:6]=[CH:5][NH:4][N:3]=1.[Cl:7][C:8]1[CH:15]=[C:14]([Cl:16])[CH:13]=[CH:12][C:9]=1[CH2:10]Br>>[Cl:7][C:8]1[CH:15]=[C:14]([Cl:16])[CH:13]=[CH:12][C:9]=1[CH2:10][N:4]1[CH:5]=[CH:6][C:2]([NH2:1])=[N:3]1Participants
3
Procedure
Prepared in analogy to example 10a) starting with 3-amino-1H-pyrazole and 2,4-dichlorobenzyl bromide. The title compound was obtained as a light yellow solid (Yield=52%). MS ISP (m/e): 242.2 (100) [(M+H)+].
Workup
- customPrepared in analogy to example 10a)
Sources & evidence
- ORD record
- ord-d2a4b2efdd2b4f4fa08951f8926f1f1f
- Source dataset
- uspto-grants-2012_10
- Patent number
- US08288403B2
Reaction notes
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