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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2081708Generated: November 1, 2026

2-Methylbenzenesulfonamide → HCID 9825050, compound

https://huagongshe.com/reaction/2081708

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MethylbenzenesulfonamideHCID 6924—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantHCID 19780392HCID 19780392—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductHCID 9825050HCID 9825050—

Reaction Steps

A mixture of the carboxylic acid (Example 33) (0.5 g), 2-methylbenzene sulphonamide (0.28 g), 1-(3-dimethylaminopropyl)-3-ethyl-carbodiimide hydrochloride (0.37 g) and 4-dimethylaminopyridine (0.05 g) in dichloromethane (6 ml) was stirred at room temperature for 72 hours. The reaction mixture was diluted with dichloromethane and washed with water and brine. The organic phase was dried over anhydrous magnesium sulphate, filtered and evaporated in vacuo. Purification by flash chromatography on silica, eluting with 0-2% ethyl acetate in dichloromethane, gave a yellow oil which, on crystallisation from methanol, afforded N-[1-(3-nitrobenzyl)indolin-5-ylcarbonyl]-2-methylbenzene sulphonamide, m.p. 159°-163° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05185361
Source datasetuspto-grants-1993_02
ORD IDord-7bbda33eddac4d6898b8d21521697d91
Source noteuspto-grants-1993_02