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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 330157Generated: October 30, 2026

2-Methylbenzenesulfonamide → HCID 14882520, compound

https://huagongshe.com/reaction/330157

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MethylbenzenesulfonamideHCID 6924—
ReactantCarbodiimideHCID 160435—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantHCID 14882511HCID 14882511—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductHCID 14882520HCID 1488252071%

Reaction Steps

A mixture of E-4-[6-[2-(propylcarbamoyl)vinyl]indol-1-ylmethyl]-3-methoxybenzoic acid (0.76 g), 4-dimethylaminopyridine (0.26 g), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (0.41 g), and 2-methylbenzenesulfonamide (0.36 g) in methylene chloride (20 ml) was stirred under an atmosphere of nitrogen for 18 hr. Further quantities of 4-dimethylaminopyridine (0.026 g), the carbodiimide (0.041 g), and the sulfonamide (0.036 g) were added, and stirring was continued for a further 5 hr. The mixture was diluted with methylene chloride (40 ml); washed with 1M hydrochloric acid, water (twice) and brine; dried (MgSO4); and evaporated to give a foam. Crystallization from hot acetonitrile provided the title compound (0.75 g, 71%) as an off-white solid; mp 240°-242°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04894386
Source datasetuspto-grants-1990_01
ORD IDord-be9a5c9b8f71428496a293e60c7ccaf2
Source noteuspto-grants-1990_01