Reacción #91310

ord-693f9bedb57c4f69bf39d51a4643c9ad

Ecuación de reacción

O=C(O)c1ccncc1F
3-Fluoroisonicotinic acid
NCc1ccccc1F
2-fluorobenzylamine
O=C(O)c1ccncc1NCc1ccccc1F
title compound
Rendimiento 10.3%
O=C(O)c1ccncc1NCc1ccccc1F
3-[(2-fluorobenzyl)amino]pyridine-4-carboxylic acid
Rendimiento 10.3%

Disolventes

Condiciones de reacción

Temperatura
158°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    ConcentraciónThe solution was concentrated in vacuo
  2. 2
    Otropurified by silica gel chromatography (10% to 20% MeOH/DCM)
  3. 3
    ConcentraciónThe semi-pure fractions were concentrated
  4. 4
    Otroto give a white precipitate, which
  5. 5
    Filtraciónwas collected by filtration
  6. 6
    Otrodried under vacuum

Procedimiento

3-Fluoroisonicotinic acid (100 mg, 0.71 mmol) and 2-fluorobenzylamine (308 μL, 2.84 mmol) were combined in ACN (3 mL) and the solution was stirred at 158° C. in a microwave for 1 h. The solution was concentrated in vacuo and purified by silica gel chromatography (10% to 20% MeOH/DCM). The semi-pure fractions were concentrated and then taken up in water to give a white precipitate, which was collected by filtration and dried under vacuum to give 18 mg (10%) of the title compound. 1H NMR (500 MHz, DMSO-d6): δ 8.18 (s, 1H), 7.99 (br s, 1H), 7.84 (d, 1H, J=5.0 Hz), 7.58 (d, 1H, J=5.0 Hz), 7.31-7.41 (m, 2H), 7.15-7.23 (m, 2H), 4.62 (s, 2H). [M+H] calc'd for C13H11FN2O2, 247. found 247.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US09447045B2uspto-grants-2016_09