Sodium → Methyl 1-(3-pyridylmethyl)-2,4-dioxopiperidine-3-carboxylate

HRID 977964Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 977964
[Na].[N:2]1[CH:7]=[CH:6][CH:5]=[C:4]([CH2:8][N:9]([CH2:18][CH2:19][C:20]([O:22]C)=O)[C:10]([CH2:12][C:13]([O:15][CH2:16]C)=[O:14])=[O:11])[CH:3]=1>CO.C1C=CC=CC=1>[N:2]1[CH:7]=[CH:6][CH:5]=[C:4]([CH2:8][N:9]2[CH2:18][CH2:19][C:20](=[O:22])[CH:12]([C:13]([O:15][CH3:16])=[O:14])[C:10]2=[O:11])[CH:3]=1

Komponenten

5

Versuchsvorschrift

Sodium (0.77 g) is dissolved in methanol (30 ml), and thereto is added dropwise a solution of ethyl [N-(3-pyridylmethyl)-N-(methoxycarbonylethyl)carbamoyl]acetate (10.0 g) in benzene (170 ml) at 3°-8° C. The mixture is stirred at the same meperature for 2 hours. The mixture is distilled to remove the solvent, and the residue is dissolved in water. The aqueous solution is extracted with benzene, and the aqueous layer is neutralized with 10% HCl, and extracted with chloroform. The extract is dried and distilled to remove the solvent to give methyl 1-(3-pyridylmethyl)-2,4-dioxopiperidine-3-carboxylate (8.50 g, quantitative) as oil.

Aufarbeitung

  1. distillationThe mixture is distilled
  2. customto remove the solvent
  3. dissolutionthe residue is dissolved in water
  4. extractionThe aqueous solution is extracted with benzene
  5. extractionextracted with chloroform
  6. customThe extract is dried
  7. distillationdistilled
  8. customto remove the solvent

Quellen und Nachweise

ORD-Eintrag
ord-3c8b492233f447a5b3d01e1f05db6dd9
Quelldatensatz
uspto-grants-1987_05
Patentnummer
US04663319

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