Hydrochloric Acid → 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.Cl.[C:11]1(NN)[CH:16]=CC=[CH:13][CH:12]=1>>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([N:8]2[CH:16]=[CH:11][C:12]([CH3:13])=[N:9]2)=[CH:4][CH:3]=1Participants
4
Procedure
This compound was prepared by the same methodology described for EXAMPLE 1 with 4-chlorophenyl hydrazine.HCl substituted for phenyl hydrazine. There was obtained 1-(4′-chlorophenyl)-3-methyl-1H-pyrazole-5-[(2′-aminosulfonyl-[1,1′]-biphen-4-yl)carboxyamide; HRMS (M+H)+: calc. 467.094465; found 467.093532.
Workup
- customThis compound was prepared by the same methodology
Sources & evidence
- ORD record
- ord-c5431b08d2b94feba2fa592a2797ec16
- Source dataset
- uspto-grants-2003_08
- Patent number
- US06602895B2
Reaction notes
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