4-Methoxybenzaldehyde → HCID 178469136, compound
Reaction equation
[CH3:1][O:2][C:3]1[CH:10]=[CH:9][C:6]([CH:7]=O)=[CH:5][CH:4]=1.[NH2:11][C:12]1[CH:16]=[CH:15][NH:14][N:13]=1.[F:17][C:18]([F:28])([F:27])[C:19](=O)[CH2:20][C:21]([O:23][CH2:24][CH3:25])=[O:22]>>[CH3:1][O:2][C:3]1[CH:10]=[CH:9][C:6]([CH:7]2[C:20]([C:21]([O:23][CH2:24][CH3:25])=[O:22])=[C:19]([C:18]([F:17])([F:27])[F:28])[NH:11][C:12]3=[N:13][NH:14][CH:15]=[C:16]23)=[CH:5][CH:4]=1Participants
4
Procedure
The title compound was prepared from 4-methoxybenzaldehyde, 3-aminopyrazole and ethyl trifluoroacetoacetate in the same manner as in Example 1.
Sources & evidence
- ORD record
- ord-9e0135bb186e4d719482f8ac9bff925b
- Source dataset
- uspto-grants-2005_12
- Patent number
- US06977262B2
Reaction notes
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