Reaction #325109

ord-34f9b4ba363a485c8b439229d8ff7386

Solvents

Conditions

Temperature
60°CELSIUS
Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    ConcentrationThe reaction was concentrated by reduced pressure
  2. 2
    Otherproviding a light yellow oil to which
  3. 3
    ExtractionThe reaction mixture was extracted by ethyl acetate 3×20 mL
  4. 4
    Dryingdried (MgSO4)
  5. 5
    Filtrationfiltered
  6. 6
    Concentrationconcentrated to dryness
  7. 7
    workup.ADDITIONEther was added
  8. 8
    Otherthe mixture was sonicated
  9. 9
    Filtrationfiltered

Procedure

2-(tetrahydro-2H-pyran-4-ylamino)acetic acid (0.2 g, 1.256 mmol) F44 was dissolved in DMF (22.5 mL) and Et3N (2.5 mL, 17.94 mmol). After 5 minutes BOC2O (0.583 mL, 2.51 mmol) was added and the reaction solution was heated to 60° C. for 1 h. The reaction was concentrated by reduced pressure providing a light yellow oil to which was added 20 mL HCl/H2O which was adjusted to PH3 at 0° C. and stirred for 10 minutes. The reaction mixture was extracted by ethyl acetate 3×20 mL, dried (MgSO4), filtered, and concentrated to dryness. Ether was added and the mixture was sonicated and filtered providing a white solid F45 2-(tert-butoxycarbonyl(tetrahydro-2H-pyran-4-yl)amino)acetic acid (0.14 g, 0.540 mmol, 43.0% yield).

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08642025B2uspto-grants-2014_02