1,3-Cyclohexanedione, 4,4-dimethyl- → HCID 135449983, compound

HRID 1862383Notes

Reaction equation

HRID 1862383 reaction equation
[CH3:1][C:2]1([CH3:10])[CH2:7][CH2:6][C:5](=O)[CH2:4][C:3]1=[O:9].[Br:11][C:12]1[C:13]([OH:21])=[C:14]([CH:17]=[C:18]([Cl:20])[CH:19]=1)[CH:15]=O.[NH2:22][C:23]1[CH:27]=[CH:26][NH:25][N:24]=1>>[Br:11][C:12]1[C:13]([OH:21])=[C:14]([CH:15]2[C:4]3[C:3](=[O:9])[C:2]([CH3:10])([CH3:1])[CH2:7][CH2:6][C:5]=3[NH:22][C:23]3=[CH:27][CH:26]=[N:25][N:24]23)[CH:17]=[C:18]([Cl:20])[CH:19]=1

Participants

4

Reactant 3

HCID 1363601,3-Cyclohexanedione, 4,4-dimethyl-HCID 5196763-Bromo-5-chloro-2-hydroxybenzaldehydeHCID 178418806HCID 178418806, compound

Product 1

HCID 135449983HCID 135449983, compound

Procedure

4,4-Dimethyl-1,3-cyclohexanedione, 3-bromo-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-d08b02fed71a4ce79b5aa53f960c436a
Source dataset
uspto-grants-2003_03
Patent number
US06538000B1

Reaction notes

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