Ammonia → N,N-Dimethyl-2-(4-methyl-3-phenyl-1H-pyrazol-1-yl)-2-phenylacetamide
Reaction equation
[CH3:1][CH:2]([N:6]1[CH:10]=[C:9]([CH3:11])[C:8]([C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)=[N:7]1)[C:3]([OH:5])=O.[CH3:18][NH:19][CH3:20].N>>[CH3:18][N:19]([CH3:20])[C:3](=[O:5])[CH:2]([C:1]1[CH:13]=[CH:12][CH:8]=[CH:9][CH:10]=1)[N:6]1[CH:10]=[C:9]([CH3:11])[C:8]([C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)=[N:7]1Participants
4
Procedure
Following the procedure of Example 68, but substituting 4-methyl-α,3-diphenylpyrazole-1-acetic acid for α,4-dimethyl-3-phenylpyrazole-1-acetic acid and dimethylamine for aqueous ammonia, there was obtained N,N,4-trimethyl-α,3-diphenylpyrazole-1-acetamide having a melting point of 135.5°-138° C.
Sources & evidence
- ORD record
- ord-1b061fee49e441ce8074f3055a569f03
- Source dataset
- uspto-grants-1978_02
- Patent number
- US04072498
Reaction notes
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