Реакция #1709955

ord-ff81785239c5466f96cb90ed0191d21a

Уравнение реакции

Cc1cnc(N)c(Br)n1
3-bromo-5-methylpyrazin-2-amine
OB(O)c1ccc(OC2CCCCC2)cc1
4-(cyclohexyloxy)phenylboronic acid
O.O.O.O.O.O.O.O.O.O.O=C([O-])[O-].[Na+].[Na+]
sodium carbonate decahydrate
Cc1cnc(N)c(-c2ccc(OC3CCCCC3)cc2)n1
title compound
Выход 99.5%
Cc1cnc(N)c(-c2ccc(OC3CCCCC3)cc2)n1
3-(4-(cyclohexyloxy)phenyl)-5-methylpyrazin-2-amine
Выход 99.5%

Растворители

Условия реакции

Температура
80°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ДругоеThe insoluble material was removed by filtration (eluted with EtOAc), and silica-gel
  2. 2
    workup.ADDITIONwas added
  3. 3
    Другоеthe volatiles were removed in vacuo
  4. 4
    Другоеwas purified by column chromatography (silica gel, eluted with EtOAc in hexane)

Методика

Tetrakis(triphenylphosphine)palladium(0) (0.922 g) was added to a suspension of 3-bromo-5-methylpyrazin-2-amine (5 g), 4-(cyclohexyloxy)phenylboronic acid (7.61 g) and sodium carbonate decahydrate (15.2 g) in DME (200 mL) and water (40 mL) and the mixture was stirred at 80° C. under nitrogen overnight. The insoluble material was removed by filtration (eluted with EtOAc), and silica-gel was added and the volatiles were removed in vacuo. The mixture supported on silica-gel was purified by column chromatography (silica gel, eluted with EtOAc in hexane) to give the title compound (7.5 g) as a pale orange solid.

Источник

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