Reacción #607478

ord-d77f39abfd45434e9bb9cbd64d4bf720

Ecuación de reacción

O=C(O)C1CCC1
cyclobutanecarboxylic acid
CN(C)C(On1nnc2cccnc21)=[N+](C)C.F[P-](F)(F)(F)(F)F
HATU
CCN(C(C)C)C(C)C
DIPEA
Cn1cc(Br)cc(N)c1=O
3-amino-5-bromo-1-methylpyridin-2(1H)-one
Cn1cc(Br)cc(NC(=O)C2CCC2)c1=O
101a
Rendimiento 54.0%
Cn1cc(Br)cc(NC(=O)C2CCC2)c1=O
N-(5-bromo-1-methyl-2-oxo-1,2-dihydropyridin-3-yl)cyclobutanecarboxamide
Rendimiento 54.0%

Disolventes

Condiciones de reacción

Temperatura
25°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroThe resulting mixture was evaporated under reduced pressure
  2. 2
    Otrothe residue was purified on a silica-gel column
  3. 3
    Lavadoeluting with 20:1 DCM/methanol

Procedimiento

To a mixture or cyclobutanecarboxylic acid (200 mg, 2.0 mmol), HATU (1.14 g, 3.0 mmol) and DIPEA (516 mg, 4.0 mmol) in DCM (8 mL) was added 3-amino-5-bromo-1-methylpyridin-2(1H)-one (330 mg, 1.62 mmol). The reaction mixture was stirred at 25° C. for 5 hours. The resulting mixture was evaporated under reduced pressure and the residue was purified on a silica-gel column eluting with 20:1 DCM/methanol to afford 101a (230 mg, 54%). MS-ESI: [M+H]+ 285.1

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US09326985B2uspto-grants-2016_05