Ammonia → HCID 20370526, compound

HRID 615966Notes

Reaction equation

HRID 615966 reaction equation
CN.N.[CH3:4][C:5]1[C:6]([C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)=[N:7][N:8]([CH:10]([CH2:14][CH2:15][CH3:16])[C:11](O)=[O:12])[CH:9]=1.C[CH:24]([N:28]1C=C(C)C(C2C=CC=CC=2)=N1)C(O)=O>>[CH3:24][NH:28][C:11](=[O:12])[CH:10]([CH2:14][CH2:15][CH3:16])[N:8]1[CH:9]=[C:5]([CH3:4])[C:6]([C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)=[N:7]1

Participants

5

Reactant 4

HCID 222AmmoniaHCID 6329MethylamineHCID 20370468alpha,4-Dimethyl-3-phenyl-1H-pyrazole-1-acetic acidHCID 53897824HCID 53897824, compound

Product 1

HCID 20370526HCID 20370526, compound

Procedure

Following the procedure of Example 68, but substituting aqueous methylamine for aqueous ammonia, and 4-methyl-3-phenyl-α-propylpyrazole-1-acetic acid for α,4-dimethyl-3-phenylpyrazole-1-acetic acid, there was obtained N,4-dimethyl-3-phenyl-α-propylpyrazole-1-acetamide having a melting point of 84°-86° C.

Sources & evidence

ORD record
ord-2c122e56db004dd9929d88356cedc75c
Source dataset
uspto-grants-1978_02
Patent number
US04072498

Reaction notes

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