2-Chlorobenzaldehyde → HCID 135584145, compound

HRID 489323Notes

Reaction equation

HRID 489323 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]=[C:14]([CH3:16])[NH:13][N:12]=1.[F:17][C:18]([F:28])([F:27])[C:19](=O)[CH2:20][C:21]([O:23][CH2:24][CH3:25])=[O:22]>>[Cl:1][C:2]1[CH:9]=[CH:8][CH:7]=[CH:6][C:3]=1[CH:4]1[C:20]([C:21]([O:23][CH2:24][CH3:25])=[O:22])=[C:19]([C:18]([F:17])([F:27])[F:28])[NH:10][C:11]2=[N:12][NH:13][C:14]([CH3:16])=[C:15]12

Participants

4

Reactant 3

HCID 69962-ChlorobenzaldehydeHCID 67793Ethyl 4,4,4-trifluoroacetoacetateHCID 931461H-Pyrazol-3-amine, 5-methyl-

Product 1

HCID 135584145HCID 135584145, compound

Procedure

The title compound was prepared from 2-chlorobenzaldehyde, 3-amino-5-methylpyrazole and ethyl trifluoroacetoacetate in the same manner as in Example 1.

Sources & evidence

ORD record
ord-f82462059ce94f0f8492c73cbc2bd918
Source dataset
uspto-grants-2005_12
Patent number
US06977262B2

Reaction notes

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