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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2290581Generated: October 25, 2026

Water → N-(1-ethyl-2-pyrrolidinylmethyl)-2-methyl-5-sulfamoyl-2,3-dihydrobenzofuran-7-carboxamide

https://huagongshe.com/reaction/2290581

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant2-Aminomethyl-1-ethylpyrrolidineHCID 117295—
ReactantMethyl 2-methyl-5-sulfamoyl-2,3-dihydrobenzofuran-7-carboxylateHCID 13420574—
SolventDiethylene GlycolHCID 8117—
ProductN-(1-ethyl-2-pyrrolidinylmethyl)-2-methyl-5-sulfamoyl-2,3-dihydrobenzofuran-7-carboxamideHCID 13420575—

Reaction Steps

A suspension of 10 g of methyl 2-methyl-5-sulfamoyl-2,3-dihydrobenzofuran-7-carboxylate and 7.0 g of 1-ethyl-2-aminomethylpyrrolidine in 50 ml of diethylene glycol is heated at 120°-130° C. and stirred for 18 hours. The reactant solution is cooled to room temperature and added slowly with stirring to 300-400 ml of water. Under ice-cooling crystals are thoroughly deposited. The crude crystals are collected by suction filtration and washed with cold water. The crude crystals obtained are dried and recrystallized from about 220-230 ml of ethyl acetate by the use of decolorizing charcoal to give crystals of N-(1-ethyl-2-pyrrolidinylmethyl)-2-methyl-5-sulfamoyl-2,3-dihydrobenzofuran-7-carboxamide, m.p. 167°-169° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04617314
Source datasetuspto-grants-1986_10
ORD IDord-0d92c9f9d5ad4d19a6e3a1091d7446ff
Source noteuspto-grants-1986_10