Reacción #2439968

ord-15f13dd8d0ee46689474fc7d9060336f

Ecuación de reacción

CCn1nc(C)cc1C(=O)O
2-Ethyl-5-methyl-2H-pyrazole-3-carboxylic acid
O=S(Cl)Cl
thionyl chloride
Nc1ccc(C(=O)c2ccc3c(c2)NC(=O)C3)cc1
6-(4-Amino-benzoyl)-1,3-dihydro-indol-2-one
CCn1nc(C)cc1C(=O)Nc1ccc(C(=O)c2ccc3c(c2)NC(=O)C3)cc1
2-Ethyl-5-methyl-2H-pyrazole-3-carboxylic acid [4-(2-oxo-2,3-dihydro-1H-indole-6-carbonyl)-phenyl]-amide
Rendimiento 49.0%

Disolventes

Condiciones de reacción

Temperatura
79°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroThe thionyl chloride then was removed by concentration in vacuo
  2. 2
    TemperaturaThe crude acid chloride was cooled to room temperature
  3. 3
    workup.DISSOLUTIONdissolved in THF (5 mL)
  4. 4
    Temperaturato reflux for 4 h
  5. 5
    Temperaturato cool to room temperature
  6. 6
    OtroThe room temperature reaction mixture
  7. 7
    Concentraciónwas concentrated in vacuo
  8. 8
    workup.DISSOLUTIONthe crude residue was dissolved in EtOH (5 mL)
  9. 9
    workup.ADDITIONThe ethanolic solution was treated with 1M NaOH(aq) (2 mL)
  10. 10
    workup.STIRRINGstirred for 30 min
  11. 11
    Otroyielding a precipitate
  12. 12
    FiltraciónThe solids were filtered

Procedimiento

A dry 25 mL flask was charged with 2-Ethyl-5-methyl-2H-pyrazole-3-carboxylic acid (0.887 g, 5.16 mmol) and thionyl chloride (5 mL) and allowed to stir at 79° C. for 2 h. The thionyl chloride then was removed by concentration in vacuo. The crude acid chloride was cooled to room temperature, and then dissolved in THF (5 mL). 6-(4-Amino-benzoyl)-1,3-dihydro-indol-2-one (1.00 g, 3.97 mmol) was added to the THF solution of the acid chloride, and the mixture was allowed to reflux for 4 h. The reaction mixture was then allowed to cool to room temperature. The room temperature reaction mixture was concentrated in vacuo, and the crude residue was dissolved in EtOH (5 mL). The ethanolic solution was treated with 1M NaOH(aq) (2 mL) and stirred for 30 min. The basic solution was acidified to a pH of 1 with 1M HCl(aq) yielding a precipitate. The solids were filtered to afford the pure 2-Ethyl-5-methyl-2H-pyrazole-3-carboxylic acid [4-(2-oxo-2,3-dihydro-1H-indole-6-carbonyl)-phenyl]-amide (0.741 g, 1.94 mmol, 49%).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07749530B2uspto-grants-2010_07