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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 963044Generated: October 30, 2026

2-Naphthalenesulfonyl chloride → HCID 67727807, compound

https://huagongshe.com/reaction/963044

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Naphthalenesulfonyl chlorideHCID 7125—
ReactantTriethylamineHCID 8471—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 22439190HCID 22439190—
SolventDimethylformamideHCID 6228—
ProductHCID 67727807HCID 6772780770.3%

Reaction Steps

3-Aminomethyl-4-(3-(2-chlorobenzoyl)-5-ethylthiophen-2-yl) [1,2,4]triazole di-p-toluenesulfonate (5.0 g) was dissolved in dimethylformamide (20 ml). 2-Naphthalenesulfonyl chloride (1.8 g) and triethylamine (5.0 ml) were added under ice-cooling, and the mixture was stirred at room temperature for 5 hours. A saturated aqueous sodium hydrogencarbonate solution was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with an aqueous citric acid solution and then saturated brine, and dried over magnesium sulfate. The solvent was evaporated, and the residue was recrystallized from ethyl acetate to give 2.73 g of N-(4-(3-(2-chlorobenzoyl)-5-ethylthiophen-2-yl) [1,2,4]triazol-3-ylmethyl)naphthalene-2-sulfonamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05760032
Source datasetuspto-grants-1998_06
ORD IDord-058d8d7f6ea944788697a67dd2f74ca6
Source noteuspto-grants-1998_06