2-Methoxybenzaldehyde → HCID 178469132, compound
Reaction equation
[CH3:1][O:2][C:3]1[CH:10]=[CH:9][CH:8]=[CH:7][C:4]=1[CH:5]=O.[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][CH:8]=[CH:7][C:4]=1[CH:5]1[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]2=[N:13][NH:14][CH:15]=[C:16]12Participants
4
Procedure
The title compound was prepared from 2-methoxybenzaldehyde, 3-aminopyrazole and ethyl trifluoroacetoacetate in the same manner as in Example 1.
Sources & evidence
- ORD record
- ord-5619992daa924677ac9616118c19c1a0
- Source dataset
- uspto-grants-2005_12
- Patent number
- US06977262B2
Reaction notes
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