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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 703532Generated: October 30, 2026

Triethylamine → N-[4-[2-(Dimethylamino)ethoxy]benzyl]-5-dimethylaminosulfonyl 2-methoxybenzamide

https://huagongshe.com/reaction/703532

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl chloroformateHCID 10928—
Reactantp-(2-(Dimethylamino)ethoxy)benzylamineHCID 88349—
Reactant5-(N,N-dimethylsulfamoyl)-2-methoxybenzoic acidHCID 13576895—
SolventTetrahydrofuranHCID 8028—
ProductN-[4-[2-(Dimethylamino)ethoxy]benzyl]-5-dimethylaminosulfonyl 2-methoxybenzamideHCID 1562278891.4%

Reaction Steps

To a cooled suspension of 3.20 g of 5-dimethylaminosulfonyl-2-methoxybenzoic acid in 10 ml of tetrahydrofuran were successively added dropwise 1.25 g of triethylamine and 1.34 g of ethyl chloroformate with stirring. The mixture was stirred at the same temperature for 30 minutes and then a solution of 2.00 g of 4-[2-(dimethylamino)ethoxy]benzylamine in 10 ml of tetrahydrofuran was added dropwise with stirring. The mixture was stirred at room temperature for 2 hours and the solvent was evaporated. Hydrochloric acid (10%) was added to the residue and the aqueous solution was washed with ethyl acetate. The aqueous layer was made alkaline with potassium carbonate and was extracted with ethyl acetate. The extract was dried and evaporated. The residue was washed with isopropyl ether to give 4.10 g of colorless crystals, which were recrystallized from a mixture of ethyl acetate and ether to give colorless needles, m.p. 99.5°-100.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04983633
Source datasetuspto-grants-1991_01
ORD IDord-0998027b0f7c46eb9408bc62bd472629
Source noteuspto-grants-1991_01