Reaktion #6197

Reaktionsgleichung

4-(3-aminopropylthio)pyridine dihydrochloride

triethylamine

trifluoroacetic acid

→

desired compound

Ausbeute 68.4%

4-[3-(trifluoroacetylamino)propylthio]pyridine hydrochloride

Ausbeute 68.4%

Lösungsmittel

methylene chloride

Reaktionsbedingungen

Aufarbeitung

1. 1
   Temperaturcooling
2. 2
   workup.STIRRINGthe mixture was stirred for 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 )
7. 7
   Sonstigeto obtain the powder which
8. 8
   Waschenwas washed with hexane
9. 9
   Sonstigedried

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 0.70 ml (4.96 mmol) of anhydrous trifluoroacetic acid under ice-cooling with stirring and the mixture was stirred for 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 the powder which was washed with hexane and dried to obtain 750 mg of the desired compound (free base) (68.4%, pale yellow prisms).

Quelle