Reacción #3201

ord-80b7e4ba59954100866003a993d7b735

Ecuación de reacción

COC(=O)c1c(N)cc(Cl)cc1Cl
methyl 2-amino-4,6-dichlorobenzoate
COC(=O)C#CC(=O)OC
dimethyl acetylenedicarboxylate
CC(C)(C)[O-].[K+]
potassium t-butoxide
COC(=O)c1nc2cc(Cl)cc(Cl)c2c(O)c1C(=O)OC
title compound
Rendimiento 59.0%
COC(=O)c1nc2cc(Cl)cc(Cl)c2c(O)c1C(=O)OC
Dimethyl 5,7-dichloro-4-hydroxyquinoline-2,3-dicarboxylate
Rendimiento 59.0%

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otroformed
  2. 2
    TemperaturaAfter refluxing for 1.5 hr
  3. 3
    Temperaturathe reaction mixture was cooled to room temperature
  4. 4
    Filtraciónfiltered
  5. 5
    Otroto separate the precipitated solids
  6. 6
    LavadoThe solids were washed with t-butanol
  7. 7
    workup.DISSOLUTIONdissolved in water
  8. 8
    Otrothe resulting precipitate was collected
  9. 9
    Lavadowashed thoroughly with water
  10. 10
    Otrodried

Procedimiento

A solution of methyl 2-amino-4,6-dichlorobenzoate (1.30 g, 5.91 mM) and dimethyl acetylenedicarboxylate (0.96 g, 6.78 mM) in t-butanol (14 mL) was refluxed for 18 hr under a nitrogen atmosphere. The reaction mixture was cooled to room temperature and potassium t-butoxide (0.76 g, 6.8 mM) was added to the stirred mixture whereupon a precipitate formed. After refluxing for 1.5 hr, the reaction mixture was cooled to room temperature and filtered to separate the precipitated solids. The solids were washed with t-butanol and then dissolved in water. The resulting solution was acidified with 1N H2SO4 and the resulting precipitate was collected, washed thoroughly with water and dried to give the title compound as a light green solid (1.15 g, 59%). An analytical sample was obtained by recrystallization of a portion from toluene to provide the title compound as a light tan solid, mp 109.5°-111° C. (d); MS(CI): 330 (M+H).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05733910uspto-grants-1998_03