Reacción #44237

ord-2a38b22f978247a88c8d9e78908eb208

Ecuación de reacción

COC(=O)c1nn(C)c(=O)cc1Cl
methyl 4-chloro-1-methyl-6-oxo-1,6-dihydropyridazine-3-carboxylate
CSc1ccc(N)c(F)c1
2-fluoro-4-methylthioaniline
c1ccc(P(c2ccccc2)c2ccc3ccccc3c2-c2c(P(c3ccccc3)c3ccccc3)ccc3ccccc23)cc1
BINAP
O=C([O-])[O-].[Cs+].[Cs+]
Cs2CO3
N#N
N2
COC(=O)c1nn(C)c(=O)cc1Nc1ccc(SC)cc1F
desired product
Rendimiento 42.4%
COC(=O)c1nn(C)c(=O)cc1Nc1ccc(SC)cc1F
methyl 4-(2-fluoro-4-(methylthio)phenylamino)-1-methyl-6-oxo-1,6-dihydropyridazine-3-carboxylate
Rendimiento 42.4%

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturaheated at 80° C. for 16 hours
  2. 2
    workup.STIRRINGwith stirring
  3. 3
    TemperaturaThe reaction mixture was cooled to room temperature
  4. 4
    FiltraciónThe precipitate was filtered off
  5. 5
    Lavadowashed with EtOAc
  6. 6
    LavadoThe filtrate was washed with water
  7. 7
    OtroThe organic layer was separated
  8. 8
    Extracciónthe aqueous layer was extracted with EtOAc
  9. 9
    SecadoThe combined organic layers were dried over MgSO4
  10. 10
    Filtraciónfiltered
  11. 11
    Concentraciónconcentrated
  12. 12
    Otroto give the crude material that
  13. 13
    Otrowas purified by silica gel flash column chromatography (100% CH2Cl2 to 1% MeOH in CH2Cl2)

Procedimiento

A mixture solution of methyl 4-chloro-1-methyl-6-oxo-1,6-dihydropyridazine-3-carboxylate (72 mg, 0.35 mmol), 2-fluoro-4-methylthioaniline (69 mg, 0.44 mmol), Pd(OAc)2 (10 mg, 0.044 mmol), BINAP (40 mg, 0.064 mmol), and Cs2CO3 (197 mg, 0.60 mmol) in toluene (1.5 mL) was sealed in a vial under N2 atmosphere. It was stirred for 10 minutes at room temperature and then heated at 80° C. for 16 hours with stirring. The reaction mixture was cooled to room temperature and diluted with EtOAc. The precipitate was filtered off and washed with EtOAc. The filtrate was washed with water. The organic layer was separated and the aqueous layer was extracted with EtOAc. The combined organic layers were dried over MgSO4, filtered, concentrated to give the crude material that was purified by silica gel flash column chromatography (100% CH2Cl2 to 1% MeOH in CH2Cl2) followed by additional silica gel flash column chromatography (10 to 15 to 20% EtOAc in CH2Cl2) to afford 48 mg (42%) of the desired product.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07732616B2uspto-grants-2010_06