Réaction #7914
ord-793139195a0c4d8191a85ccb7a10382e
Équation de réaction
Réactifs
Solvants
Conditions de réaction
Traitement
- 1Températureto warm to room temperature
- 2workup.STIRRINGAfter stirring at room temperature overnight
- 3Concentrationthe reaction was concentrated
- 4workup.ADDITIONconcentrated hydrochloric acid (10 mL) was added
- 5TempératureThe reaction was heated to 95° C.
- 6workup.STIRRINGwith stirring for 1 h
- 7Températureto cool to room temperature
- 8Extractionwas extracted with dichloromethane
- 9ExtractionThe basic solution was extracted with dichloromethane
- 10Lavagewashed with brine
- 11Séchagedried with anhydrous sodium sulfate
- 12Filtrationfiltered
- 13Concentrationconcentrated
- 14workup.ADDITIONThe mixture was diluted with diethyl ether
- 15Filtrationfiltered
Mode opératoire
To a suspension of potassium thiocyanate (2.02 g, 20.8 mmol) in acetone (10.7 mL) at 0° C. was slowly added pivolyl chloride (2.6 mL, 21.1 mmol). The mixture was stirred at 0° C. for 3 h. Dimethylpyrrolidin-3-yl-amine (2.44 g, 21.3 mmol) was added slowly at 0° C., and the reaction was allowed to warm to room temperature. After stirring at room temperature overnight, the reaction was concentrated, and concentrated hydrochloric acid (10 mL) was added. The reaction was heated to 95° C. with stirring for 1 h. The mixture was allowed to cool to room temperature, and was extracted with dichloromethane. The aqueous layer was made basic with 20% aqueous sodium hydroxide. The basic solution was extracted with dichloromethane. The organics were combined, washed with brine, dried with anhydrous sodium sulfate, filtered, and concentrated. The mixture was diluted with diethyl ether and filtered to provide pure 3-dimethylamino-pyrrolidine-1-carbothioic acid amide (135) (0.863 g, 23.3%) as a white solid.