Reacción #1359633

ord-530ff530aed44411a635bc0f9e4a523a

Ecuación de reacción

Nc1ccccc1-c1cc2ccccc2[nH]1
2-(2-aminophenyl) indole
O=C(O)Cc1ccc(O)c(O)c1
3,4-dihydroxyphenylacetic acid
O=C(Cc1ccc(O)c(O)c1)Nc1ccccc1-c1cc2ccccc2[nH]1
2-(3,4-Dihydroxy-phenyl)-N-[2-(1H-indol-2-yl)-phenyl]-acetamide
Rendimiento 17.0%

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroThe product was chromatographed on silica
  2. 2
    Otro8, 2 Hz (1H), 6.66 d, 8 Hz (1H), 6.78 d, 2 Hz (1H), 7.03 t, 8 Hz (1H), 7.11 t, 8 Hz (1H), 7.25 t, 8 Hz (1H), 7.31–7.35 m (2H), 7.51 d, 7 Hz (1H), 7.55 dd, 8.1 Hz (1H), 7.99 d, 8 Hz (1H)

Procedimiento

Prepared from 2-(2-aminophenyl) indole and 3,4-dihydroxyphenylacetic acid in 17% yield. The product was chromatographed on silica. 100% Purity by LC/MS (230 DAD), Mass-spec [M+H+]=359, 1H NMR (MeOH-d4): 3.56 s (2H), 6.10 s (1H), 6.59 dd, 8, 2 Hz (1H), 6.66 d, 8 Hz (1H), 6.78 d, 2 Hz (1H), 7.03 t, 8 Hz (1H), 7.11 t, 8 Hz (1H), 7.25 t, 8 Hz (1H), 7.31–7.35 m (2H), 7.51 d, 7 Hz (1H), 7.55 dd, 8.1 Hz (1H), 7.99 d, 8 Hz (1H).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07208493B2uspto-grants-2007_04