Reacción #85801

ord-9a28bae1fc6a40d8874fa0fae747a213

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    ConcentraciónIt was then concentrated under reduced pressure
  2. 2
    workup.ADDITIONthe residue was treated in EtOAc
  3. 3
    OtroThe insoluble solid was removed by filtration
  4. 4
    Concentraciónthe organic solution was concentrated under reduced pressure

Procedimiento

A mixture of 2-chloro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine (200 mg, 0.84 mmol), methanamine (277 mg, 8.4 mmol), and DIPEA (0.35 mL, 2.01 mmol) in dioxane (5 mL) was stirred at room temperature for 16 hours. It was then concentrated under reduced pressure, and the residue was treated in EtOAc. The insoluble solid was removed by filtration, and the organic solution was concentrated under reduced pressure to give the title compound.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US09434726B2uspto-grants-2016_09