Reacción #67779

ord-33b761c65db04d79ba5693157d6cd85b

Ecuación de reacción

Cc1cc(I)ccc1N
4-Iodo-2-methylaniline
O=C(O)c1ccncc1F
3-fluoropyridine-4-carboxylic acid
C[Si](C)(C)[N-][Si](C)(C)C.[Li+]
LiHMDS
Cc1cc(I)ccc1Nc1cnccc1C(=O)O
desired product
Rendimiento 59.0%
Cc1cc(I)ccc1Nc1cnccc1C(=O)O
3-[(4-Iodo-2-methylphenyl)amino]isonicotinic acid
Rendimiento 59.0%

Disolventes

Condiciones de reacción

Temperatura
-78°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturato warm to ambient temperature
  2. 2
    OtroAfter 36 h the reaction was quenched
  3. 3
    workup.ADDITIONby adding solid NH4Cl
  4. 4
    FiltraciónAfter filtration the volatiles
  5. 5
    Otrowere removed in vacuo
  6. 6
    Otrothe crude material was purified by flash chromatography

Procedimiento

4-Iodo-2-methylaniline (233 mg, 1.00 mmol) and 3-fluoropyridine-4-carboxylic acid (141 mg, 1.00 mmol) were dissolved in dry THF (6.0 ml) under argon and the mixture was cooled to −78° C. A solution of LiHMDS (1.0M in THF, 3.5 ml) was added and the reaction mixture was allowed to warm to ambient temperature. After 36 h the reaction was quenched by adding solid NH4Cl. After filtration the volatiles were removed in vacuo and the crude material was purified by flash chromatography using silica gel and a gradient of 0-10% methanol in DCM as eluent to give 208 mg (588 μmol; 59% yield) of pure desired product.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08524911B2uspto-grants-2013_09