Reaktion #6203

ord-afad64aa4b6845c1aa72f4e04ffcbd0e

Reaktionsgleichung

Cl.Cl.NCCCSc1ccncc1
4-(3-aminopropylthio)pyridine dihydrochloride
CCN(CC)CC
triethylamine
CC(C)(C)c1ccc(C(=O)Cl)cc1
4-t-butylbenzoyl chloride
CC(C)(C)c1ccc(C(=O)NCCCSc2ccncc2)cc1.Cl
desired compound
Ausbeute 88.0%
CC(C)(C)c1ccc(C(=O)NCCCSc2ccncc2)cc1.Cl
4-[3-(4-t-butylbenzoylamino)propylthio]pyridine hydrochloride
Ausbeute 88.0%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

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

Vorschrift

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 0.48 ml (4.96 mmol) of 4-t-butylbenzoyl 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 1.20 g of the desired compound (free base) (88.0%, yellow powder).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05246948uspto-grants-1993_09