Reacción #46585

ord-c0f5acefd2d04046a1c5c95838958347

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Concentraciónthen was concentrated in vacuo
  2. 2
    workup.ADDITIONThe residue was diluted with water
  3. 3
    Extracciónthe solution was extracted with ethyl acetate
  4. 4
    LavadoThe combined organic extracts were washed with brine
  5. 5
    Secadodried over Na2SO4
  6. 6
    Concentraciónconcentrated

Procedimiento

2-Methoxyethylamine (1.49 mL, 17.16 mmole) was added to a solution of 2-amino-5-bromo-3-(bromomethyl)pyridine hydrobromide (1.49 g, 4.29 mmole) and DIEA (2.24 mL, 12.87 mmole) in CH2Cl2 (10 mL) at RT. The reaction was stirred overnight then was concentrated in vacuo. The residue was diluted with water and the solution was extracted with ethyl acetate. The combined organic extracts were washed with brine, dried over Na2SO4, and concentrated to afford the title compound (1.00 g, 90%) as a light brown liquid after drying in vacuo: MS (ES) m/e 260/262 (M+H)+.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07741339B2uspto-grants-2010_06