Ethyl benzoylacetate → HCID 178468499, compound
Reaction equation
[Cl:1][C:2]1[C:9]([Cl:10])=[CH:8][CH:7]=[CH:6][C:3]=1[CH:4]=O.[NH2:11][C:12]1[CH:16]=[CH:15][NH:14][N:13]=1.[C:17]([CH2:25][C:26]([O:28][CH2:29][CH3:30])=[O:27])(=O)[C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1>>[Cl:1][C:2]1[C:9]([Cl:10])=[CH:8][CH:7]=[CH:6][C:3]=1[CH:4]1[C:25]([C:26]([O:28][CH2:29][CH3:30])=[O:27])=[C:17]([C:18]2[CH:19]=[CH:20][CH:21]=[CH:22][CH:23]=2)[NH:11][C:12]2=[N:13][NH:14][CH:15]=[C:16]12Participants
4
Procedure
The title compound was prepared from 2,3-dichlorobenzaldehyde, 3-aminopyrazole and ethyl benzoylacetate in the same manner as in Example 1.
Sources & evidence
- ORD record
- ord-224f1df6dcf3422ba405cbba208d6525
- Source dataset
- uspto-grants-2005_12
- Patent number
- US06977262B2
Reaction notes
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