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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 127411Generated: October 26, 2026

Chloroform → N-(1-ethyl-2-pyrrolidylmethyl)-7-methylsulfamoyl-1,4-benzodioxane-5-carboxamide

https://huagongshe.com/reaction/127411

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroformHCID 6212—
Reactant2-Aminomethyl-1-ethylpyrrolidineHCID 117295—
Reactant7-Methylsulfamoyl-1,4-benzodioxane-5-carbonyl chlorideHCID 20544720—
SolventChloroform waterHCID 22418719—
ProductN-(1-ethyl-2-pyrrolidylmethyl)-7-methylsulfamoyl-1,4-benzodioxane-5-carboxamideHCID 2483493266.1%

Reaction Steps

82 g of dextrorotatory 1-ethyl-2-aminomethylpyrrolidine, 600 ccm of chloroform and, gradually, at a temperature of from 5°-10° C., 200 g of 7-methylsulfamoyl-1,4-benzodioxane-5-carbonyl chloride were introduced into a balloon flask with an agitator and a thermometer. After the addition of a liter of water chloroform was distilled and then the remaining solution was filtered. The base was precipitated by the addition of 60 cm3 of 20% ammonia. The crystals formed were dried off, washed with water and then dried. 162 g of dextrorotatory N-(1-ethyl-2-pyrrolidylmethyl)-7-methylsulfamoyl-1,4-benzodioxane-5-carboxamide was produced (M.P.: 136°-137° C.; yield: 66%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04255580
Source datasetuspto-grants-1981_03
ORD IDord-2d1a43d94109458ca9f11b224a17d81b
Source noteuspto-grants-1981_03