3,5-Dimethoxybenzoic Acid → HCID 178493450, compound

HRID 347978

Reaction equation

HRID 347978 reaction equation
[C:1]([N:4]1[C:12]2[C:7](=[CH:8][C:9]([C:13](=[O:15])[CH3:14])=[CH:10][CH:11]=2)[CH2:6][C:5]1=[O:16])(=[O:3])[CH3:2].[CH3:17][O:18][C:19]1[CH:20]=[C:21]([CH:25]=[C:26]([O:28][CH3:29])[CH:27]=1)[C:22](O)=[O:23]>>[C:1]([N:4]1[C:12]2[C:7](=[CH:8][C:9]([C:13](=[O:15])[CH3:14])=[CH:10][CH:11]=2)[C:6](=[C:22]([C:21]2[CH:25]=[C:26]([O:28][CH3:29])[CH:27]=[C:19]([O:18][CH3:17])[CH:20]=2)[OH:23])[C:5]1=[O:16])(=[O:3])[CH3:2]

Participants

3

Reactant 2

HCID 143323,5-Dimethoxybenzoic AcidHCID 210845601,5-Diacetyl-2-indolinone

Product 1

HCID 178493450HCID 178493450, compound

Procedure

Prepared from 1,5-diacetyl-2-indolinone and 3,5-dimethoxybenzoic acid

Sources & evidence

ORD record
ord-dedea04ff3164ca28af9f858369fbf6b
Source dataset
uspto-grants-2007_02
Patent number
US07176231B2

Linked notes

Loading…