P-Anisidine → HCID 178492233, compound

HRID 24799Notes

Reaction equation

HRID 24799 reaction equation
C([N:4]1[C:12]2[C:7](=[CH:8][C:9]([N+:13]([O-:15])=[O:14])=[CH:10][CH:11]=2)[C:6](=[C:16](OC)[C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)[C:5]1=[O:25])(=O)C.[CH3:26][O:27][C:28]1[CH:34]=[CH:33][C:31]([NH2:32])=[CH:30][CH:29]=1>ClCCl.N>[CH3:26][O:27][C:28]1[CH:34]=[CH:33][C:31]([NH:32]/[C:16](=[C:6]2\[C:5](=[O:25])[NH:4][C:12]3[C:7]\2=[CH:8][C:9]([N+:13]([O-:15])=[O:14])=[CH:10][CH:11]=3)/[C:17]2[CH:18]=[CH:19][CH:20]=[CH:21][CH:22]=2)=[CH:30][CH:29]=1

Participants

5

Reactant 2

HCID 7732P-AnisidineHCID 541401551-Acetyl-3-(1-methoxy-1-phenyl-methylidene)-5-nitro-2-indolinone

Product 1

HCID 178492233HCID 178492233, compound

Reagents, catalysts & solvents 2

HCID 222AmmoniaSolventHCID 6344DichloromethaneSolvent

Procedure

Prepared analogously to Example 77 from 1-acetyl-3-(1-methoxy-1-phenyl-methylidene)-5-nitro-2-indolinone and 4-methoxyaniline in dichloromethane and methanolic ammonia.

Sources & evidence

ORD record
ord-f70733d128bf4738a5ceca7d7148153e
Source dataset
uspto-grants-2005_02
Patent number
US06855710B2

Reaction notes

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