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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Acetate | HCID 175 | — |
| Edukt | 1-(Allyl)pyrrolidine-2-methylamine | HCID 117296 | — |
| Edukt | Methyl-7-sulfamoyl-1,4-benzodioxane-5-carboxylate | HCID 20544687 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | N-(1-allyl-2-pyrrolidylmethyl)-7-sulfamoyl-1,4-benzodioxane-5-carboxamide | HCID 24834927 | 64,8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04255580 |
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| Quelldatensatz | uspto-grants-1981_03 |
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| ORD ID | ord-d432ac23ca704fcdb426b3353b672908 |
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| Quellennotiz | uspto-grants-1981_03 |
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