Reaction #325109
ord-34f9b4ba363a485c8b439229d8ff7386
Reaction equation
Reagents
Solvents
Conditions
Workup
- 1ConcentrationThe reaction was concentrated by reduced pressure
- 2Otherproviding a light yellow oil to which
- 3ExtractionThe reaction mixture was extracted by ethyl acetate 3×20 mL
- 4Dryingdried (MgSO4)
- 5Filtrationfiltered
- 6Concentrationconcentrated to dryness
- 7workup.ADDITIONEther was added
- 8Otherthe mixture was sonicated
- 9Filtrationfiltered
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).