Reaktion #80334

Reaktionsgleichung

sodium hydride

N-[4-(4-piperidinomethyl-2-pyridyloxy)-cis-2-butenyl]-3-mercaptopropionamide

ethylene chlorohydrin

→

title compound

Ausbeute 65.0%

N-[4-(4-Piperidinomethyl-2 -pyridyloxy)-cis-2 -butenyl]-3-(2-hydroxyethylthio)propionamide

Ausbeute 65.0%

Lösungsmittel

dimethylformamide

Reaktionsbedingungen

Aufarbeitung

1. 1
   Temperaturcooling
2. 2
   workup.STIRRINGThe reaction mixture was stirred at room temperature for 15 minutes
3. 3
   Extraktionextracted with ethyl acetate
4. 4
   EinengenThe extract was concentrated by evaporation under reduced pressure
5. 5
   Sonstigethe residue thus obtained
6. 6
   Sonstigewas purified by column chromatography through silica gel
7. 7
   workup.ADDITIONby volume mixture of methanol and methylene chloride as the eluent

Vorschrift

105 mg of sodium hydride (as a 55% w/w dispersion in mineral oil) were added, whilst ice-cooling and in an atmosphere of nitrogen, to a solution of 0.76 g of N-[4-(4-piperidinomethyl-2-pyridyloxy)-cis-2-butenyl]-3-mercaptopropionamide (prepared as described in Preparation 3) in 24 ml of dimethylformamide, and the resulting mixture was stirred at room temperature for 30 minutes. At the end of this time, 0.16 ml of ethylene chlorohydrin were added to the reaction mixture, whilst ice-cooling. The reaction mixture was stirred at room temperature for 15 minutes, after which it was poured into ice-water and extracted with ethyl acetate. The extract was concentrated by evaporation under reduced pressure, and the residue thus obtained was purified by column chromatography through silica gel, using a 1:9 by volume mixture of methanol and methylene chloride as the eluent, to give 0.56 g of the title compound as an oil in a 65% yield.

Quelle