3-Dimethylamino-3'-trifluoromethylacrylophenone → HCID 23329821, compound
Reaction equation
[NH2:1][C:2]1[C:6]([C:7]([O:9][CH2:10][CH3:11])=[O:8])=[C:5]([CH2:12][CH3:13])[NH:4][N:3]=1.CN(C)[CH:16]=[CH:17][C:18]([C:20]1[CH:25]=[CH:24][CH:23]=[C:22]([C:26]([F:29])([F:28])[F:27])[CH:21]=1)=O>>[CH2:12]([C:5]1[C:6]([C:7]([O:9][CH2:10][CH3:11])=[O:8])=[C:2]2[N:1]=[CH:16][CH:17]=[C:18]([C:20]3[CH:21]=[C:22]([C:26]([F:27])([F:28])[F:29])[CH:23]=[CH:24][CH:25]=3)[N:3]2[N:4]=1)[CH3:13]Participants
3
Procedure
As for Example 1, ethyl 3-amino-5-ethyl-pyrazole-4-carboxylate is reacted with 3-dimethylamino-3'-(trifluoromethyl)acrylophenone to give the product as crystals, m.p. 142°-143° C.
Sources & evidence
- ORD record
- ord-1b55f527f69b411b82ca285fef0684e2
- Source dataset
- uspto-grants-1980_11
- Patent number
- US04236005
Reaction notes
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