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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1413144Generated: October 26, 2026

Acetate → N-(1-allyl-2-pyrrolidylmethyl)-7-sulfamoyl-1,4-benzodioxane-5-carboxamide

https://huagongshe.com/reaction/1413144

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetateHCID 175—
Reactant1-(Allyl)pyrrolidine-2-methylamineHCID 117296—
ReactantMethyl-7-sulfamoyl-1,4-benzodioxane-5-carboxylateHCID 20544687—
SolventWaterHCID 962—
ProductN-(1-allyl-2-pyrrolidylmethyl)-7-sulfamoyl-1,4-benzodioxane-5-carboxamideHCID 2483492764.8%

Reaction Steps

145 g of methyl-7-sulfamoyl-1,4-benzodioxane-5-carboxylate, 48 g of water and 89 g of 1-allyl-2-aminomethyl-pyrrolidine were introduced into a balloon flask provided with a condenser. The mixture was heated on a water bath until a test sample was soluble in dilute acids and then 1 liter of water was added. The precipitated carboxamide was redissolved by acetate formation. The solution formed was filtered on carbon black and then the base was precipitated by the addition of 20% ammonia. The resulting crystals were dried off, washed with water, dried and purified by passing over hydrochloride (M.P.: 228°-230° C.) followed by transformation into a base by treatment with 20% ammonia. 131 g of N-(1-allyl-2-pyrrolidylmethyl)-7-sulfamoyl-1,4-benzodioxane-5-carboxamide was produced (M.P.: 143°-144° C.; yield: 64.8%). The structure was confirmed by nuclear magnetic resonance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04248885
Source datasetuspto-grants-1981_02
ORD IDord-547ab528f7f444e894b67be42e7d75c1
Source noteuspto-grants-1981_02