2-Chlorobenzaldehyde → HCID 178468519, compound

HRID 489363Notes

Reaction equation

HRID 489363 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.[CH3:16][O:17][C:18]1[CH:31]=[CH:30][C:21]([C:22]([CH2:24][C:25]([O:27][CH2:28][CH3:29])=[O:26])=O)=[CH:20][CH:19]=1>>[Cl:1][C:2]1[CH:9]=[CH:8][CH:7]=[CH:6][C:3]=1[CH:4]1[C:24]([C:25]([O:27][CH2:28][CH3:29])=[O:26])=[C:22]([C:21]2[CH:20]=[CH:19][C:18]([O:17][CH3:16])=[CH:31][CH:30]=2)[NH:10][C:11]2=[N:12][NH:13][CH:14]=[C:15]12

Participants

4

Reactant 3

HCID 69962-ChlorobenzaldehydeHCID 76150Benzenepropanoic acid, 4-methoxy-beta-oxo-, ethyl esterHCID 178418806HCID 178418806, compound

Product 1

HCID 178468519HCID 178468519, compound

Procedure

The title compound was prepared from 2-chlorobenzaldehyde, 3-aminopyrazole and ethyl (4-methoxybenzoyl)acetate in the same manner as in Example 1.

Sources & evidence

ORD record
ord-31ebb38544df4480a1e553a2dcd3b07a
Source dataset
uspto-grants-2005_12
Patent number
US06977262B2

Reaction notes

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