2-Chlorobenzaldehyde → HCID 178429594, compound
Reaction equation
[Cl:1][C:2]1[CH:9]=[CH:8][CH:7]=[CH:6][C:3]=1[CH:4]=O.[NH2:10][C:11]1[CH:15]=[CH:14][NH:13][N:12]=1.[C:16]([O:22][CH2:23][C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1)(=[O:21])[CH2:17][C:18]([CH3:20])=O>>[Cl:1][C:2]1[CH:9]=[CH:8][CH:7]=[CH:6][C:3]=1[CH:4]1[C:17]([C:16]([O:22][CH2:23][C:24]2[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=2)=[O:21])=[C:18]([CH3:20])[NH:10][C:11]2=[N:12][NH:13][CH:14]=[C:15]12Participants
4
Procedure
The title compound was prepared from 2-chlorobenzaldehyde, 3-aminopyrazole and benzyl acetoacetate in the same manner as in Example 1.
Sources & evidence
- ORD record
- ord-629a99fc4e3b4b7795bebd3fdad0dae5
- Source dataset
- uspto-grants-2005_12
- Patent number
- US06977262B2
Reaction notes
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