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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1807637Generated: November 1, 2026

Methyl 3-cyclohexyl-1-methyl-2-{2-[2-(methyl {4-[methyl(sulfamoyl)amino]butyl}amino)-2-oxoethoxy]phenyl}-1H-indole-6-carboxylate → 3-cyclohexyl-1-methyl-2-{2-[2-(methyl {4-[methyl(sulfamoyl)amino]butyl}amino)-2-oxoethoxy]phenyl}-1H-indole-6-carboxylic acid

https://huagongshe.com/reaction/1807637

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 3-cyclohexyl-1-methyl-2-{2-[2-(methyl {4-[methyl(sulfamoyl)amino]butyl}amino)-2-oxoethoxy]phenyl}-1H-indole-6-carboxylateHCID 58317795—
Reactant3-cyclohexyl-1-methyl-2-(2-{2-[methyl(2-{2-[methyl(sulfamoyl)amino]ethoxy}ethyl)amino]-2-oxoethoxy}phenyl)-1H-indole-6-carboxylic acidHCID 58317827—
Product3-cyclohexyl-1-methyl-2-{2-[2-(methyl {4-[methyl(sulfamoyl)amino]butyl}amino)-2-oxoethoxy]phenyl}-1H-indole-6-carboxylic acidHCID 5831782178%

Reaction Steps

3-cyclohexyl-1-methyl-2-{2-[2-(methyl {4-[methyl(sulfamoyl)amino]butyl}amino)-2-oxoethoxy]phenyl}-1H-indole-6-carboxylic acid 13 was synthesized in 78% yield from intermediate 12 following the procedure reported for the synthesis of intermediate 8: m/z=585 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08357687B2
Source datasetuspto-grants-2013_01
ORD IDord-b0a124e1b2464f7e8b39cc9af67c59d8
Source noteuspto-grants-2013_01