HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 127449Erstellt: 23. Oktober 2026
Water → N-(4-methyl-1-piperazinyl)-7-nitro-1,4-benzodioxane-5-carboxamide
https://huagongshe.com/de/reaction/127449
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Water | HCID 962 | — |
| Edukt | 1-Amino-4-methylpiperazine | HCID 81349 | — |
| Edukt | 7-Nitro-1,4-benzodioxane-5-carbonyl chloride | HCID 20544745 | — |
| Lösungsmittel | Methyl Ethyl Ketone | HCID 6569 | — |
| Produkt | N-(4-methyl-1-piperazinyl)-7-nitro-1,4-benzodioxane-5-carboxamide | HCID 20544699 | 55,8% |
Reaktionsschritte
33 g of 1-amino-4-methylpiperazine were dissolved in 630 ml of methyl ethyl ketone. The mixture was cooled to 10° C. and 61 g of 7-nitro-1,4-benzodioxane-5-carbonyl chloride were introduced by portions. The mixture was stirred for two hours and then the solid was filtered off and washed with 150 ml of methyl ethyl ketone. The obtained product was purified by transformation into the base (M.P.: 212° C.) and recystallized by treatment with hydrochloric ethanol. 45 g of N-(4-methyl-1-piperazinyl)-7-nitro-1,4-benzodioxane-5-carboxamide were obtained (M.P.: 210° C. with one mole of water). The structure was confirmed by nuclear magnetic resonance and infrared analyses.
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-15a0016f5e2a4643903fc71c61d06e76 |
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| Quellennotiz | uspto-grants-1981_03 |
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