Reacción #1319

ord-314d43ab585348f7bd5e6d904c0e5adc

Ecuación de reacción

O=C(O)c1ccc(Cl)nc1
6-chloronicotinic acid
CCO
ethanol
C(=NC1CCCCC1)=NC1CCCCC1
dicyclohexylcarbodiimide
CN(C)c1ccccn1
dimethylaminopyridine
CCOC(=O)c1ccc(Cl)nc1
title compound
CCOC(=O)c1ccc(Cl)nc1
Ethyl 6-chloronicotinate

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturawas heated
  2. 2
    Temperaturaat reflux for 2 hours
  3. 3
    Temperaturato cool
  4. 4
    Otrosolvent removed in vacuo

Procedimiento

A mixture of 15.75 g (0.1 mol) 6-chloronicotinic acid, 6.9 g (0.15 mol) ethanol, 22.7 g (0.11 mol) dicyclohexylcarbodiimide and 3.7 g dimethylaminopyridine in 200 ml methylene chloride was heated at reflux for 2 hours. The mixture was allowed to cool, solvent removed in vacuo and the residue subjected to flash chromatography to give the title compound as a low-melting white solid. PMR (CDCl3): & 1.44 (3H, t, J~6.2 Hz) 4.44 (2H, q, J~4.4 Hz), 7.44 (1H, d, J~8.1 Hz), 8.27 (1H, dd, J~8.1 Hz, 3 Hz), 9.02 (1H, d, J~3 Hz).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05723620uspto-grants-1998_03