Reacción #91314

ord-0d745710e5544d009a976982d437d216

Ecuación de reacción

O=C(O)c1ccncc1F
3-Fluoroisonicotinic acid
Cl.N#Cc1ccc(CN)cc1
4-(aminomethyl)-benzonitrile hydrochloride
CCN(C(C)C)C(C)C
DIEA
N#Cc1ccc(CNc2cnccc2C(=O)O)cc1
title compound
Rendimiento 18.0%
N#Cc1ccc(CNc2cnccc2C(=O)O)cc1
3-[(4-cyanobenzyl)amino]pyridine-4-carboxylic acid
Rendimiento 18.0%

Disolventes

Condiciones de reacción

Temperatura
166°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 (10-20% MeOH/DCM)
  3. 3
    ConcentraciónThe semi-pure fractions were concentrated
  4. 4
    Otroto give a pale yellow precipitate, which
  5. 5
    Filtraciónwas collected by filtration
  6. 6
    Otrodried under vacuum

Procedimiento

3-Fluoroisonicotinic acid (100 mg, 0.71 mmol), 4-(aminomethyl)-benzonitrile hydrochloride (240 mg, 1.42 mmol), and DIEA (250 μL, 1.42 mmol) were combined in DMA (2 mL) and the reaction mixture was stirred at 166° C. in a microwave for 90 min. The solution was concentrated in vacuo and purified by silica gel chromatography (10-20% MeOH/DCM). The semi-pure fractions were concentrated and then taken up in water to give a pale yellow precipitate, which was collected by filtration and dried under vacuum to give 32 mg (18%) of the title compound. 1H NMR (500 MHz, DMSO-d6): δ 8.10 (br s, 1H), 8.04 (s, 1H), 7.83 (d, 1H, J=5.0 Hz), 7.81 (d, 2H, J=8.0 Hz), 7.58 (d, 1H, J=5.0 Hz), 7.54 (d, 2H, J=8.0 Hz), 4.69 (s, 2H). [M+H] calc'd for C14H11N3O2, 254. found 254.

Fuente

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