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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1413156Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/1413156

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
Edukt1-Methylpyrrolidine-2-methylamineHCID 117300—
Edukt7-Methylsulfamoyl-1,4-benzodioxane-5-carbonyl chlorideHCID 20544720—
LösungsmittelChloroformHCID 6212—
ProduktN-(1-methyl-2-pyrrolidylmethyl)-7-methylsulfamoyl-1,4-benzodioxane-5-carboxamideHCID 2483493678,5%

Reaktionsschritte

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%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04248885
Quelldatensatzuspto-grants-1981_02
ORD IDord-86195d134c864bc18be0f97dc3bf147a
Quellennotizuspto-grants-1981_02