Methyl 4-aminobenzoate → HCID 178498144, compound

HRID 1007390Notes

Reaction equation

HRID 1007390 reaction equation
[C:1]([O:4][N:5]1[C:13]2[C:8](=[CH:9][CH:10]=[C:11]([N+:14]([O-:16])=[O:15])[CH:12]=2)[C:7](=[C:17](OCC)[C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=2)[C:6]1=[O:27])(=[O:3])[CH3:2].[NH2:28][C:29]1[CH:38]=[CH:37][C:32]([C:33]([O:35][CH3:36])=[O:34])=[CH:31][CH:30]=1>>[C:1]([O:4][N:5]1[C:13]2[C:8](=[CH:9][CH:10]=[C:11]([N+:14]([O-:16])=[O:15])[CH:12]=2)/[C:7](=[C:17](/[NH:28][C:29]2[CH:30]=[CH:31][C:32]([C:33]([O:35][CH3:36])=[O:34])=[CH:37][CH:38]=2)\[C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=2)/[C:6]1=[O:27])(=[O:3])[CH3:2]

Participants

3

Reactant 2

HCID 12082Methyl 4-aminobenzoateHCID 545503491-Acetoxy-3-(1-ethoxy-1-phenylmethylidene)-6-nitro-2-indolinone

Product 1

HCID 178498144HCID 178498144, compound

Procedure

Prepared from 1-acetoxy-3-(1-ethoxy-1-phenyl-methylidene)-6-nitro-2-indolinone and methyl 4-aminobenzoate without subsequent hydrogenation

Sources & evidence

ORD record
ord-d9201dfee59841b8b046a820439e71bc
Source dataset
uspto-grants-2004_09
Patent number
US06794395B1

Reaction notes

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