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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2052634Generated: October 27, 2026

Water → N-(1-methyl-2-pyrrolidylmethyl)-7-methylsulfamoyl-1,4-benzodioxane-5-carboxamide

https://huagongshe.com/reaction/2052634

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1-Methylpyrrolidine-2-methylamineHCID 117300—
Reactant7-Methylsulfamoyl-1,4-benzodioxane-5-carbonyl chlorideHCID 20544720—
SolventChloroformHCID 6212—
ProductN-(1-methyl-2-pyrrolidylmethyl)-7-methylsulfamoyl-1,4-benzodioxane-5-carboxamideHCID 2483493678.5%

Reaction Steps

61 g of dextrorotatory 1-methyl-2-aminomethylpyrrolidine, 465 ccm of chloroform and, in portions, 155 g of 7-methylsulfamoyl-1,4-benzodioxane-5-carbonyl chloride, with the temperature being maintained at 5°-10° C., were introduced into a balloon flask provided with an agitator and a thermometer. After agitation of the mixture and the addition of 1,850 cm3 of water, chloroform was distilled and the remaining solution was filtered. The base was precipitated by the addition of 65 cm3 of 20% ammonia. The crystals formed were dried off, washed and dried. 154 g of dextrorotatory-N-(1-methyl-2-pyrrolidylmethyl)-7-methylsulfamoyl-1,4-benzodioxane-5-carboxamide was produced (M.P.: 187°-188° C.; yield: 78.5%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04186135
Source datasetuspto-grants-1980_01
ORD IDord-5916faf628db4bf196a926374eb10505
Source noteuspto-grants-1980_01