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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 127403Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/127403

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetateHCID 175—
Edukt1-(Allyl)pyrrolidine-2-methylamineHCID 117296—
EduktMethyl-7-sulfamoyl-1,4-benzodioxane-5-carboxylateHCID 20544687—
LösungsmittelWaterHCID 962—
ProduktN-(1-allyl-2-pyrrolidylmethyl)-7-sulfamoyl-1,4-benzodioxane-5-carboxamideHCID 2483492764,8%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04255580
Quelldatensatzuspto-grants-1981_03
ORD IDord-d432ac23ca704fcdb426b3353b672908
Quellennotizuspto-grants-1981_03