Réaction #719655

ord-cebe5f0af8654e32bfbe31811e2ffc75

Équation de réaction

Cl
HCl
O=C(O)c1ccc(B(O)O)cc1F
4-borono-2-fluorobenzoic acid
CN(C)C(On1nnc2cccnc21)=[N+](C)C.F[P-](F)(F)(F)(F)F
HATU
C1COCCN1
morpholine
O=C(c1ccc(B(O)O)cc1F)N1CCOCC1
crude compound
Rendement 87.3%
O=C(c1ccc(B(O)O)cc1F)N1CCOCC1
(3-Fluoro-4-(morpholine-4-carbonyl)phenyl) boronic acid
Rendement 87.3%

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    workup.ADDITIONThe reaction mixture was poured into ice cold water
  2. 2
    Extractionextracted with EtOAc (2×50 mL)
  3. 3
    LavageThe organic layer was washed with brine solution (20 mL)
  4. 4
    Séchagedried over anhydrous Na2SO4 and solvent
  5. 5
    Autrewas evaporated under reduced pressure

Mode opératoire

To a solution of 4-borono-2-fluorobenzoic acid (1.0 g, 5.43 mmol) and HATU (2.0 g, 5.43 mmol) in DMF (20.0 mL) was added morpholine (0.9 g, 10.87 mmol) at room temperature. The reaction mixture was stirred at room temperature for 18 h. The reaction mixture was poured into ice cold water, acidified with 1N HCl, extracted with EtOAc (2×50 mL). The organic layer was washed with brine solution (20 mL), dried over anhydrous Na2SO4 and solvent was evaporated under reduced pressure to afford 1.2 g of crude compound as a colourless gum. Crude compound was directly used for the next step without any further purification.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US09321748B2uspto-grants-2016_04