HCID 459269, compound → HCID 15410728, compound

HRID 2396558Notes

Reaction equation

HRID 2396558 reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[N:7]([CH3:11])[C:6]([CH2:12][C:13]([OH:15])=O)=[C:5]2[C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][C:17]=1[O:22][CH3:23].[CH2:24]([O:26][C:27]1[CH:33]=[CH:32][CH:31]=[C:30]([O:34][CH2:35][CH3:36])[C:28]=1[NH2:29])[CH3:25]>>[Cl:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[N:7]([CH3:11])[C:6]([CH2:12][C:13]([NH:29][C:28]1[C:30]([O:34][CH2:35][CH3:36])=[CH:31][CH:32]=[CH:33][C:27]=1[O:26][CH2:24][CH3:25])=[O:15])=[C:5]2[C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][C:17]=1[O:22][CH3:23]

Participants

3

Reactant 2

HCID 459269HCID 459269, compoundHCID 15410732HCID 15410732, compound

Product 1

HCID 15410728HCID 15410728, compound

Procedure

5-Chloro-3-(2-methoxyphenyl)-1-methylindole-2-acetic acid was reacted with 2,6-diethoxyaniline by a method similar to Example 6 to give the title compound as colorless crystals.

Sources & evidence

ORD record
ord-348849ee915e43a087d66f49dbae1933
Source dataset
uspto-grants-1996_02
Patent number
US05492929

Reaction notes

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