Propanamide, 2-chloro-N,N-dimethyl- → HCID 20370441, compound
Reaction equation
Cl[CH:2]([CH3:8])[C:3]([N:5]([CH3:7])[CH3:6])=[O:4].[CH2:9]([C:11]1[C:12]([C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=2)=[N:13][NH:14][CH:15]=1)[CH3:10].[CH3:22]C1C(C2C=CC=CC=2)=NNC=1>>[CH2:8]([CH:2]([N:14]1[CH:15]=[C:11]([CH2:9][CH3:10])[C:12]([C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=2)=[N:13]1)[C:3]([N:5]([CH3:7])[CH3:6])=[O:4])[CH3:22]Participants
4
Procedure
Using the procedure of Example 1, but substituting 2-bromo-N,N-dimethylbutyramide for 2-chloro-N,N-dimethylpropionamide and 4-ethyl-3-phenylpyrazole for 4-methyl-3-phenylpyrazole, there was obtained α,4-diethyl-N,N-dimethyl-3-phenylpyrazole-1-acetamide, m.p. 77.5°-79° C.
Sources & evidence
- ORD record
- ord-5fdeeb4c82bb43988fd99ca2f8efd91c
- Source dataset
- uspto-grants-1978_02
- Patent number
- US04072498
Reaction notes
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