Reacción #433798

ord-ea0c48814e0b45288a2ca660b98531d3

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otroto come to room temperature
  2. 2
    Otrothe solids formed
  3. 3
    Filtraciónwere filtered
  4. 4
    LavadoThe solids were washed by excess water
  5. 5
    Otrodried
  6. 6
    Otrorecrystallized by ethyl acetate

Procedimiento

2-Furoyl chloride (148 μL, 1.5 mmol) was added to a stirred solution of Compound 48 (363 mg, 1 mmol) in pyridine (5 mL) under argon at 0° C. The solution was allowed to come to room temperature and further stirred overnight. The solution was poured into ice water and the solids formed were filtered. The solids were washed by excess water, dried, and recrystallized by ethyl acetate to yield 332 mg (73%) of white solids. M.P. 209° C. 1H NMR (DMSO-d6): δ 3.69 (m, 4H), 3.97 (m, 4H), 5.49 (s, 2H), 6.66 (m, 1H), 7.09 (d, J=3.3 Hz, 1H), 7.22 (m, 3H), 7.32 (m, 2H), 7.45 (dd, J=4.7, 9.5 Hz, 1H), 7.55 (m, 1H), 7.69 (dd, J=2.8, 9.7 Hz, 1H), 7.88 (s, 1H). EIMS m/z 479 (M+23). Anal. (C26H21FN4O3) C, H, N.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07173036B2uspto-grants-2007_02