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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2290586Generated: October 26, 2026

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

https://huagongshe.com/reaction/2290586

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethyl 2-methyl-5-sulfamoyl-2,3-dihydrobenzofuran-7-carboxylateHCID 13420574—
Reactant[1-(2-Methylpropyl)pyrrolidin-2-yl]methanamineHCID 14709035—
SolventDiethylene GlycolHCID 8117—
ProductN-(1-isobutyl-2-pyrrolidinylmethyl)-2-methyl-5-sulfamoyl-2,3-dihydrobenzofuran-7-carboxamideHCID 13420581—

Reaction Steps

A suspension of 5.2 g of methyl 2-methyl-5-sulfamoyl-2,3-dihydrobenzofuran-7-carboxylate and 4.5 g of 1-isobutyl-2-aminomethylpyrrolidine in 20 ml of diethylene glycol is heated at 130°-140° C. and stirred for 18-19 hours. The reaction solution is cooled to room temperature and poured into 150-200 ml of water while stirring. Under ice-cooling crystals are deposited thoroughly and collected by suction filtration. The crude crystals are washed with cold water, dissolved in chloroform and separated on a column of silica gel (developing solvent: methanol/chloroform=1/9). Crystals obtained are recrystallized from about 35 ml of methanol to give crystals of N-(1-isobutyl-2-pyrrolidinylmethyl)-2-methyl-5-sulfamoyl-2,3-dihydrobenzofuran-7-carboxamide, m.p. 182°-184° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04617314
Source datasetuspto-grants-1986_10
ORD IDord-5afa806ec4f44f17b8a70f45c2ae6c65
Source noteuspto-grants-1986_10