Reacción #6196

ord-ddf096337738401cbb2a49419e14ead6

Ecuación de reacción

Cl.Cl.NCCCSc1ccncc1
4-(3-aminopropylthio)pyridine dihydrochloride
CCN(CC)CC
triethylamine
CC(C)(C)C(=O)Cl
pivaloyl chloride
CC(C)(C)C(=O)NCCCSc1ccncc1.Cl
desired compound
Rendimiento 96.4%
CC(C)(C)C(=O)NCCCSc1ccncc1.Cl
4-[3-(pivaloylamino)propylthio]pyridine hydrochloride
Rendimiento 96.4%

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturacooling
  2. 2
    workup.STIRRINGthe mixture was stirred at room temperature for 30 minutes
  3. 3
    LavadoThe reaction mixture was washed with an aqueous saturated sodium bicarbonate solution and water
  4. 4
    Otrodried
  5. 5
    workup.DISTILLATIONThe solvent was distilled off
  6. 6
    OtroThe residue was purified by column chromatography (eluent: ethyl acetate)

Procedimiento

To a solution of 1.00 g (4.15 mmol) of 4-(3-aminopropylthio)pyridine dihydrochloride and 2.77 ml (19.8 mmol) of triethylamine in 40 ml of methylene chloride was added 0.61 ml (4.96 mmol) of pivaloyl chloride under ice-cooling with stirring and the mixture was stirred at room temperature for 30 minutes. The reaction mixture was washed with an aqueous saturated sodium bicarbonate solution and water and dried. The solvent was distilled off. The residue was purified by column chromatography (eluent: ethyl acetate) to obtain 1.01 g of the desired compound (free base) (96.4%, yellow oil).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05246948uspto-grants-1993_09