Reacción #67777

ord-1896779e9c5746ddb0e468683b4bf7d2

Ecuación de reacción

Nc1ccc(Cl)cc1Cl
2,4-Dichloraniline
O=C(O)c1ccncc1F
3-fluoropyridine-4-carboxylic acid
C[Si](C)(C)[N-][Si](C)(C)C.[Li+]
LiHMDS
O=C(O)c1ccncc1Nc1ccc(Cl)cc1Cl
desired product
Rendimiento 72.0%
O=C(O)c1ccncc1Nc1ccc(Cl)cc1Cl
3-[(2,4-Dichlorophenyl)amino]isonicotinic acid
Rendimiento 72.0%

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 18 h the reaction was quenched
  3. 3
    workup.ADDITIONby adding a solution of HCl in dioxane (4.0M, 2.0 ml)
  4. 4
    OtroThe volatiles were removed in vacuo
  5. 5
    Otrothe crude material was purified by flash chromatography

Procedimiento

2,4-Dichloraniline (162 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 18 h the reaction was quenched by adding a solution of HCl in dioxane (4.0M, 2.0 ml). 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 204 mg (721 μmol; 72% yield) of pure desired product.

Fuente

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