Reaktion #332840

Reaktionsgleichung

acetic acid

N-((3-chloropyrazin-2-yl)methyl)-4-oxocyclohexanecarboxamide

benzyl 1-piperazinecarboxylate

sodium cyanoborohydride

→

title compound

Ausbeute 134.6%

benzyl 4-[4-[(3-chloropyrazin-2-yl)methylcarbamoyl]cyclohexyl]piperazine-1-carboxylate

Ausbeute 134.6%

Lösungsmittel

dichloromethane

Reaktionsbedingungen

Aufarbeitung

1. 1
   SonstigeReaction
2. 2
   Sonstigewas quenched with an aqueous sodium hydrogencarbonate solution
3. 3
   Extraktionextracted twice with dichloromethane
4. 4
   SonstigeThe combined organic layers were dried over phase separation
5. 5
   Filtrationfilter
6. 6
   Einengenconcentrated under reduced pressure
7. 7
   Sonstigepurified

Vorschrift

N-((3-chloropyrazin-2-yl)methyl)-4-oxocyclohexanecarboxamide (3.7 mmol, 1 g) was dissolved in dichloromethane (10 mL) and acetic acid (0.1 mL) was added. To this solution benzyl 1-piperazinecarboxylate (11.2 mmol, 2.16 mL) and sodium cyanoborohydride (7.47 mmol, 0.47 g) were added subsequently. The mixture was stirred overnight at room temperature. Reaction was quenched with an aqueous sodium hydrogencarbonate solution and extracted twice with dichloromethane. The combined organic layers were dried over phase separation filter, concentrated under reduced pressure and purified using column chromatography (silica gel; dichloromethane/methanol) to yield 2.35 g of the title compound as a mixture of cis and trans isomers which was used in the next step without further purification.

Quelle