Reacción #164624

ord-315f4008d95f4cddbbd565fc70894b6d

Ecuación de reacción

NCc1ccc(Cl)c(Cl)c1
(3,4-dichlorophenyl)methanamine
COC(=O)c1ccc(Cl)nc1
methyl 6-chloronicotinate
COC(=O)c1ccc(NCc2ccc(Cl)c(Cl)c2)nc1
methyl 6-(3,4-dichlorobenzylamino)nicotinate
Rendimiento 33.0%

Disolventes

Condiciones de reacción

Temperatura
120°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    TemperaturaThe reaction mixture was further heated at 100° C. for 54 h
  2. 2
    Concentraciónconcentrated
  3. 3
    OtroThe residue was purified by flash chromatography on silica gel using 5-35% ethyl acetate in hexanes
  4. 4
    ConcentraciónThe desired fractions were concentrated

Procedimiento

A mixture of (3,4-dichlorophenyl)methanamine (1.010 mL, 7.58 mmol), TEA (1.218 mL, 8.74 mmol), and methyl 6-chloronicotinate (1 g, 5.83 mmol) in ethanol (29 mL) was heated at 120° C. for 5 min in a microwave oven. The reaction mixture was further heated at 100° C. for 54 h, then concentrated. The residue was purified by flash chromatography on silica gel using 5-35% ethyl acetate in hexanes. The desired fractions were concentrated to give methyl 6-(3,4-dichlorobenzylamino)nicotinate as a pale yellow solid (0.55 g, 33%). 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 8.77 (1H, s), 8.01 (1H, dd, J=8.78, 2.01 Hz), 7.33-7.52 (2H, m), 7.19 (1H, d, J=8.03 Hz), 6.37 (1H, d, J=8.78 Hz), 5.37 (1H, br. s.), 4.58 (2H, d, J=6.02 Hz), 3.88 (3H, s). LCMS: R.T.=2.81; [M+H]+=311.18.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08841301B2uspto-grants-2014_09