Phenylhydrazine → 1-(4-Chlorophenyl)-3-methyl-1H-pyrazole
Reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([NH:8][NH2:9])=[CH:4][CH:3]=1.[C:10]1(NN)[CH:15]=CC=[CH:12][CH:11]=1>>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([N:8]2[CH:15]=[CH:10][C:11]([CH3:12])=[N:9]2)=[CH:4][CH:3]=1Participants
3
Procedure
This compound was prepared by the same methodology described for EXAMPLE 8 with 4-chlorophenyl hydrazine · HCl substituted for phenyl hydrazine and 2-amino-5-(2-N-t-butylaminosulfonylphenyl)pyridine was used in the coupling step. There was obtained the title compound; HRMS (M+H)+ : calc. 468.089714; found 468.088873.
Workup
- customThis compound was prepared by the same methodology
Sources & evidence
- ORD record
- ord-aceddcd41e9842d6bbb76c3ad1c2d59d
- Source dataset
- uspto-grants-1999_12
- Patent number
- US05998424
Reaction notes
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