phenyl 4-aminobenzenesulfonate → HCID 178517094, compound

HRID 2213227Notes

Reaction equation

HRID 2213227 reaction equation
O[CH:2]=[C:3]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[NH:5][C:4]1=[O:12].[NH2:13][C:14]1[CH:19]=[CH:18][C:17]([S:20]([O:23][C:24]2[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=2)(=[O:22])=[O:21])=[CH:16][CH:15]=1>>[C:24]1([O:23][S:20]([C:17]2[CH:16]=[CH:15][C:14]([NH:13][CH:2]=[C:3]3[C:11]4[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=4)[NH:5][C:4]3=[O:12])=[CH:19][CH:18]=2)(=[O:21])=[O:22])[CH:25]=[CH:26][CH:27]=[CH:28][CH:29]=1

Participants

3

Reactant 2

HCID 4426510phenyl 4-aminobenzenesulfonateHCID 1784187413-(hydroxymethylidene)-1H-indol-2-one

Product 1

HCID 178517094HCID 178517094, compoundYield 23%

Procedure

The title compound was prepared in 23% yield from 3-hydroxymethylene-1,3-dihydro-indol-2-one and phenyl 4-aminobenzenesulfonate according to

Sources & evidence

ORD record
ord-a330a9f1ac5a411598aec865c98683d3
Source dataset
uspto-grants-2006_09
Patent number
US07105529B2

Reaction notes

Loading…