Reaction #172006

ord-6ddd994d2a3144a28adac0cd99d653ec

Solvents

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    OtherThe organic phase was separated
  2. 2
    Washwashed with 1N HCl
  3. 3
    Dryingdried over Na2SO4
  4. 4
    Concentrationconcentrated in vacuo
  5. 5
    OtherThe residue was purified by a silica gel column
  6. 6
    Washeluted with 0-70% EtOAc in hexane

Procedure

A solution of 2-bromo-4-fluorobenzonitrile (200 mg, 1.00 mmol), (R)-2-amino-3-cyclohexylpropanamide (280 mg, 1.64 mmol) and DIEA (0.500 mL, 2.87 mmol) in DMSO (3 mL) was stirred at 120 C for 18 h. Water and EtOAc were added. The organic phase was separated, washed with 1N HCl, dried over Na2SO4, concentrated in vacuo. The residue was purified by a silica gel column, eluted with 0-70% EtOAc in hexane to give (R)-2-(3-bromo-4-cyanophenylamino)-3-cyclohexylpropanamide (222 mg).

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08846928B2uspto-grants-2014_09