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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1660006Generated: October 26, 2026

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

https://huagongshe.com/reaction/1660006

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-aminomethyl-pyrrolidine, 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 numberUS04306072
Source datasetuspto-grants-1981_12
ORD IDord-51d2c7a9e84e487bb91f78a01101f37f
Source noteuspto-grants-1981_12