5-Chloro-salicylaldehyde → HCID 135407023, compound

HRID 1862380Notes

Reaction equation

HRID 1862380 reaction equation
[CH3:1][C:2]1([CH3:10])[CH2:7][CH2:6][C:5](=O)[CH2:4][C:3]1=[O:9].[Cl:11][C:12]1[CH:13]=[CH:14][C:15]([OH:20])=[C:16]([CH:19]=1)[CH:17]=O.[NH2:21][C:22]1[CH:26]=[CH:25][NH:24][N:23]=1>>[Cl:11][C:12]1[CH:13]=[CH:14][C:15]([OH:20])=[C:16]([CH:17]2[C:4]3[C:3](=[O:9])[C:2]([CH3:10])([CH3:1])[CH2:7][CH2:6][C:5]=3[NH:21][C:22]3=[CH:26][CH:25]=[N:24][N:23]23)[CH:19]=1

Participants

4

Reactant 3

HCID 124815-Chloro-salicylaldehydeHCID 1363601,3-Cyclohexanedione, 4,4-dimethyl-HCID 178418806HCID 178418806, compound

Product 1

HCID 135407023HCID 135407023, compound

Procedure

4,4-Dimethyl-1,3-cyclohexanedione, 5-chloro-2-hydroxybenzaldehyde and 3-aminopyrazole were processed as described in General Procedure A to provide the title compound.

Sources & evidence

ORD record
ord-7ece792a3a9346338e26e2d77853fc83
Source dataset
uspto-grants-2003_03
Patent number
US06538000B1

Reaction notes

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