Reaction #43547

ord-3963630d9c554d238c06beab53f216e6

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    Washthe solution was washed with 1M NaHSO4 (2×100 mL)
  2. 2
    OtherThe solvent was removed in vacuo
  3. 3
    Otherthe crude material was purified by silica gel chromatography (hexanes/EtOAc)

Procedure

To a stirring suspension of (S)-cyclohexyl lactic acid (558 mg, 3.42 mmol) in CH2Cl2 was added 2-(5-fluoro-2,3-dihydro-indol-1-yl)-ethylamine (616 mg, 3.42 mmol), HATU (1.429 g, 3.76 mmol), and DIEA (1.79 mL, 10.3 mmol). The reaction mixture was stirred at room temperature for several hours until the starting material had disappeared by LCMS. Ethyl acetate (100 mL) was added and the solution was washed with 1M NaHSO4 (2×100 mL), sat'd aq NaHCO3 (2×100 mL) and brine (1×100 mL). The solvent was removed in vacuo and the crude material was purified by silica gel chromatography (hexanes/EtOAc) to afford 320 mg of 3-Cyclohexyl-N-[2-(5-fluoro-2,3-dihydro-indol-1-yl)-ethyl]-2-(S)-hydroxy-propionamide as a white powder.

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07732449B2uspto-grants-2010_06