HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 374173Erstellt: 24. Oktober 2026
Isopropyl N-cyano-4-pyridinecarboximidate → N-cyano-N'-(3-nitroxypropyl)-4-pyridinecarboximidamide
https://huagongshe.com/de/reaction/374173
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Isopropyl N-cyano-4-pyridinecarboximidate | HCID 10012715 | — |
| Edukt | Sodium Methoxide | HCID 10942334 | — |
| Edukt | 3-Nitroxypropylamine nitrate | HCID 22014591 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | N-cyano-N'-(3-nitroxypropyl)-4-pyridinecarboximidamide | HCID 10037676 | 41,5% |
Reaktionsschritte
Isopropyl N-cyano-4-pyridinecarboximidate (0.50 g, 2.6 mmol) was dissolved in methanol (10 ml), and 3-nitroxypropylamine nitrate (0.53 g, 2.9 mmol) and sodium methoxide (0.22 g, 4.1 mmol) were added. The mixture was stirred at room temperature for 18 hours. After the reaction was completed, the reaction solution was concentrated under reduced pressure. The residual concentrate was extracted with chloroform (50 ml×3). The chloroform layer was washed with water (100 ml), dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residual concentrate was subjected to chromatography on a silica gel column (WAKO GEL C-200, 50 g) eluting with chloroform-methanol (60:1). The eluted fractions were concentrated under reduced pressure and crystallized from methanol-diethyl ether to give the title compound (0.27 g, 1.08 mmol, yield: 41%) as colorless crystals.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05166347 |
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| Quelldatensatz | uspto-grants-1992_11 |
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| ORD ID | ord-af49dd18063e4be799d543e2d517d44b |
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| Quellennotiz | uspto-grants-1992_11 |
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