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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2285490Generated: October 30, 2026

Ethylene Glycol → N-(1-ethyl-2-pyrrolidyl-methyl)-8-methoxy-7-sulfamoyl-1,4-benzodioxane-5-carboxamide

https://huagongshe.com/reaction/2285490

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene GlycolHCID 174—
ReactantWaterHCID 962—
Reactant2-Aminomethyl-1-ethylpyrrolidineHCID 117295—
ReactantMethyl-8-methoxy-7-sulfamoyl-1,4-benzodioxane-5-carboxylateHCID 20544706—
SolventAcetic AcidHCID 176—
ProductN-(1-ethyl-2-pyrrolidyl-methyl)-8-methoxy-7-sulfamoyl-1,4-benzodioxane-5-carboxamideHCID 2029364973%

Reaction Conditions

Temperature50 °C

Reaction Steps

150 g of methyl-8-methoxy-7-sulfamoyl-1,4-benzodioxane-5-carboxylate and 750 cm3 of ethylene glycol were introduced into a balloon flask. After dissolution, 127 g of 1-ethyl-2-aminomethylpyrrolidine was added and the mixture was heated at 50° C. The resulting solution was dissolved with 2 liters of water and acidified by means of 120 cm3 of acetic acid. The precipitate formed was dried off, washed with water and then dried. The precipitate was then redissolved in 915 cm3 of hot water. The solution was filtered and then the base was precipitated with ammonia. The precipitate was dried off, washed with water and then dried. 144 g of N-(1-ethyl-2-pyrrolidyl-methyl)-8-methoxy-7-sulfamoyl-1,4-benzodioxane-5-carboxamide was produced (M.P.: 110°-115° C.; yield: 73%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04323503
Source datasetuspto-grants-1982_04
ORD IDord-a79ce2e50ac94ba686aaca6d29ee8238
Source noteuspto-grants-1982_04