3-Chloro-4-hydroxybenzohydrazide → HCID 131724060, compound

HRID 1166750Notes

Reaction equation

HRID 1166750 reaction equation
[CH:1]([C:3]1[C:12]2[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=2)[C:6]([C:13](=[C:17]([CH2:20][CH3:21])[CH2:18][CH3:19])[C:14]([NH2:16])=[O:15])=[CH:5][CH:4]=1)=O.[Cl:22][C:23]1[CH:24]=[C:25]([CH:30]=[CH:31][C:32]=1[OH:33])[C:26]([NH:28][NH2:29])=[O:27]>>[Cl:22][C:23]1[CH:24]=[C:25]([CH:30]=[CH:31][C:32]=1[OH:33])[C:26]([NH:28][N:29]=[CH:1][C:3]1[C:12]2[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=2)[C:6]([C:13](=[C:17]([CH2:20][CH3:21])[CH2:18][CH3:19])[C:14]([NH2:16])=[O:15])=[CH:5][CH:4]=1)=[O:27]

Participants

3

Reactant 2

HCID 109542683-Chloro-4-hydroxybenzohydrazideHCID 131724061HCID 131724061, compound

Product 1

HCID 131724060HCID 131724060, compound

Procedure

The compound was prepared according to the general procedure for the synthesis of alkylidene hydrazones from the condensation of 4-formyl-1-naphthyl diethylacrylamide (from step D) and 3-chloro-4-hydroxy benzoic acid hydrazide.

Workup

  1. customThe compound was prepared

Sources & evidence

ORD record
ord-2af47d0d02d5402db1cab4c53471766a
Source dataset
uspto-grants-2003_09
Patent number
US06613942B1

Reaction notes

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