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m-Toluidine → HCID 178425535, compound

HRID 24733
Notes
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Reaction equation

HRID 24733 reaction equation
C([N:4]1[C:12]2[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=2)[C:6](=[C:13](Cl)[C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[C:5]1=[O:21])(=O)C.[NH2:22][C:23]1[CH:28]=[CH:27][CH:26]=[C:25]([CH3:29])[CH:24]=1.[OH-].[Na+]>ClCCl.CO>[CH3:29][C:25]1[CH:24]=[C:23]([NH:22]/[C:13](=[C:6]2\[C:5](=[O:21])[NH:4][C:12]3[C:7]\2=[CH:8][CH:9]=[CH:10][CH:11]=3)/[C:14]2[CH:15]=[CH:16][CH:17]=[CH:18][CH:19]=2)[CH:28]=[CH:27][CH:26]=1
ParticipantsProcedureSources & evidenceReaction notes

Participants

6

Reactant 3

HCID 7934m-ToluidineHCID 14798Sodium HydroxideHCID 697436571-Acetyl-3-(1-chloro-1-phenyl-methylidene)-2-indolinone

Product 1

HCID 178425535HCID 178425535, compound

Reagents, catalysts & solvents 2

HCID 887MethanolSolventHCID 6344
Dichloromethane
Solvent

Procedure

Prepared analogously to Example 2 from 1-acetyl-3-(1-chloro-1-phenyl-methylidene)-2-indolinone and m-toluidine in dichloromethane and subsequent treatment with sodium hydroxide solution in methanol.

Sources & evidence

ORD record
ord-dd3b3f82cfd04632a2e14883b865cadd
Source dataset
uspto-grants-2005_02
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US06855710B2

Reaction notes

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On this pageParticipantsProcedureSources & evidenceReaction notes