Reaktion #75338

ord-2e9252f1b37d4a8f95e6b4a6feb9158b

Reaktionsgleichung

Nc1ncccc1C=O
2-aminonicotinaldehyde
CCOC(=O)CC#N
ethyl α-cyanoacetate
C1CCNCC1
piperidine
N#Cc1cc2cccnc2nc1O
2-Hydroxy-3-cyano-1,8-naphthyridine

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturunder reflux
  2. 2
    Temperaturthe solution is cooled to 0°-4° C
  3. 3
    FiltrationThe yellow solid is filtered
  4. 4
    Sonstigedried
  5. 5
    Sonstigeto yield 2.5 g

Vorschrift

A mixture of 2-aminonicotinaldehyde (2.44 g., 0.02 m), ethyl α-cyanoacetate (4.52 g., 0.04 m.), absolute ethanol (50 ml.) and piperidine (0.5 ml) is stirred under reflux. After 1 hour, the solution is cooled to 0°-4° C. The yellow solid is filtered and dried to yield 2.5 g. (73%) of 2-hydroxy-3-cyano-1,8-naphthyridines, m.p. 300° C.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04176183uspto-grants-1979_11