Reacción #8758

ord-0edf5ca02a324a7d8ed1899271441890

Ecuación de reacción

BrCCOc1cccc(-c2noc3ccsc23)c1
3-[3-(2-bromo-ethoxy)-phenyl]-thieno[2,3-d]isoxazole
O=C([O-])[O-].[K+].[K+]
potassium carbonate
NCc1ccc(Cl)c(Cl)c1
3,4-dichlorobenzylamine
Clc1ccc(CNCCOc2cccc(-c3noc4ccsc34)c2)cc1Cl
title compound
Clc1ccc(CNCCOc2cccc(-c3noc4ccsc34)c2)cc1Cl
(3,4-dichloro-benzyl)-[2-(3-thieno[2,3-d]isoxazol-3-yl-phenoxy)-ethyl]-amine

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Lavadois eluted
  2. 2
    workup.ADDITIONa graded solvent mixture of 40% ethyl acetate in heptane

Procedimiento

The title compound is prepared from 3-[3-(2-bromo-ethoxy)-phenyl]-thieno[2,3-d]isoxazole, potassium carbonate, 3,4-dichlorobenzylamine and acetonitrile essentially as described above in example 18 except that the column is eluted using a graded solvent mixture of 40% ethyl acetate in heptane, to 100% ethyl acetate. Purity by LC/MS (APCI)=100%, [M+H]+=419.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07091199B1uspto-grants-2006_08