Реакция #1709844

ord-067e0a9814b044838e012b7ac5b46074

Уравнение реакции

[Cl-].[NH4+]
NH4Cl
FC(F)(F)c1cc(Br)ccn1
4-bromo-2-(trifluoromethyl)pyridine
O=P([O-])([O-])[O-].[K+].[K+].[K+]
tripotassium phosphate
O=C(O)c1ccccn1
picolinic acid
Nc1ncc(Cl)cc1-c1ccc(O)cc1
4-(2-amino-5-chloropyridin-3-yl)phenol
NC1NC=C(Cl)C=C1c1ccc(Oc2ccnc(C(F)(F)F)c2)cc1
title compound
Выход 55.2%
NC1NC=C(Cl)C=C1c1ccc(Oc2ccnc(C(F)(F)F)c2)cc1
5-chloro-3-(4-{[2-(trifluoromethyl)pyridin-4-yl]oxy}phenyl)-1,2-dihydropyridin-2-amine
Выход 55.2%

Растворители

Условия реакции

Температура
140°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Экстракцияextracted with EtOAc
  2. 2
    ДругоеThe organic layer was separated
  3. 3
    Промывкаwashed with brine
  4. 4
    Сушкаdried over anhydrous magnesium sulfate
  5. 5
    Концентрированиеconcentrated in vacuo
  6. 6
    ДругоеThe residue was purified by column chromatography (NH silica gel, eluted with EtOAc in hexane)

Методика

A mixture of 4-bromo-2-(trifluoromethyl)pyridine (282 mg), tripotassium phosphate (481 mg), picolinic acid (27.9 mg), copper (I) iodide (21.58 mg) and 4-(2-amino-5-chloropyridin-3-yl)phenol (250 mg) in DMSO (5 ml) was stirred at 140° C. under N2 overnight. The mixture was poured into sat. NH4Cl aq. and extracted with EtOAc. The organic layer was separated, washed with brine, dried over anhydrous magnesium sulfate and concentrated in vacuo. The residue was purified by column chromatography (NH silica gel, eluted with EtOAc in hexane) to give the title compound (230 mg) as a pale yellow solid.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08778934B2uspto-grants-2014_07