HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 432797Erstellt: 25. Oktober 2026
Methyl Isocyanate → Ethyl 1-(n-methylaminocarbonyl)-4-oxo-3-piperidinecarboxylate
https://huagongshe.com/reaction/432797
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Methyl Isocyanate | HCID 12228 | — |
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Edukt | 3-Piperidinecarboxylic acid, 4-oxo-, ethyl ester, hydrochloride (1:1) | HCID 107315 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | Ethyl 1-(n-methylaminocarbonyl)-4-oxo-3-piperidinecarboxylate | HCID 18760282 | — |
Reaktionsschritte
Commercially available ethyl 4-piperidone-3-carboxylate hydrochloride (203.2 mg; 0.98 mmol) was suspended in dichloromethane (7 ml), diisopropylethylamine (180 μl; 0.99 mmol) was added, followed by commercially available methyl isocyanate and (57 μl; 0.98 mmol). This mixture was stirred at ambient temperature for approximately 3 hours, and then diluted with fresh dichloromethane and washed with water. The dichloromethane solution was dried with anhydrous potassium carbonate and evaporated at ambient temperature under reduced pressure, giving ethyl 1-(N-methylaminocarbonyl)-4-oxo-3-piperidinecarboxylate (74.4 mg) as a white solid. MS m/z (positive ion) 479 (dimer+Na+; 40), 457 (dimer+; 25), 251 (M+Na+; 100), 229 (MH+; 90), 205 (25), 130 (25).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06664271B1 |
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| Quelldatensatz | uspto-grants-2003_12 |
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| ORD ID | ord-5c25927d6f514dd4815de0cb4cd844aa |
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| Quellennotiz | uspto-grants-2003_12 |
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