Propanamide, 2-chloro-N,N-dimethyl- → HCID 20370453, compound
Reaction equation
Cl[CH:2]([CH3:8])[C:3]([N:5]([CH3:7])[CH3:6])=[O:4].[Br:9][C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][C:11]=1[C:16]1[C:20]([CH3:21])=[CH:19][NH:18][N:17]=1.[CH3:22]C1C(C2C=CC=CC=2)=NNC=1>>[Br:9][C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][C:11]=1[C:16]1[C:20]([CH3:21])=[CH:19][N:18]([CH:2]([CH2:8][CH3:22])[C:3]([N:5]([CH3:7])[CH3:6])=[O:4])[N:17]=1Participants
4
Procedure
Using the procedure of Example 1, but substituting 2-bromo-N,N-dimethylbutyramide for 2-chloro-N,N-dimethylpropionamide and 3-(o-bromophenyl)-4-methylpyrazole for 4-methyl-3-phenylpyrazole, there was obtained 3-(o-bromophenyl)-α-ethyl-N,N,4-trimethylpyrazole-1acetamide, b.p. 188°-190° C./0.12 mm.
Sources & evidence
- ORD record
- ord-acaf406e2b2b4e9a982bb935099232ff
- Source dataset
- uspto-grants-1978_02
- Patent number
- US04072498
Reaction notes
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