Reacción #2329043

ord-d8c2b5d9c88244998d9dbeba44ae60ea

Ecuación de reacción

COc1ccc(-c2nnc3c4ccccc4c(Cl)nn23)cc1
6-chloro-3-(4-methoxy-phenyl)-[1,2,4]triazolo[3,4-a]phthalazine
COc1ccc(-c2nnc3c4ccccc4c(Cl)nn23)cc1
compound B1
COc1ccc(-c2nnc3c4ccccc4c(Cl)nn23)cc1
6-chloro-3-(4-methoxy-phenyl)-[1,2,4]triazolo[3,4-a]phthalazine
COc1ccc(N)cc1
p-anisidine
COc1ccc(Nc2nn3c(-c4ccc(OC)cc4)nnc3c3ccccc23)cc1
title compound
Rendimiento 81.3%
COc1ccc(Nc2nn3c(-c4ccc(OC)cc4)nnc3c3ccccc23)cc1
(4-Methoxyphenyl)-[3-(4-methoxyphenyl)-[1,2,4]triazolo[3,4-a]phthalazin-6-yl]-amine
Rendimiento 81.3%

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Filtraciónthe precipitate is filtered with suction
  2. 2
    OtroThe solid is recrystallized from N,N-dimethylformamide

Procedimiento

5.0 g of 6-chloro-3-(4-methoxy-phenyl)-[1,2,4]triazolo[3,4-a]phthalazine (compound B1), and 20 g p-anisidine are stirred at 170° C. for 5 h. The reaction mixture is diluted with 40 ml ethanol and the precipitate is filtered with suction. The solid is recrystallized from N,N-dimethylformamide to yield 5.2 g of the title compound. M.p.: 301-304° C.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07671050B2uspto-grants-2010_03