Reaktion #156830

Reaktionsgleichung

triphenyl phosphite

Methyl 6-(benzyl(2-ethoxy-2-oxoethyl)amino)-5-nitronicotinate

hydrogen

→

title compound

Ausbeute 71.0%

Methyl 4-benzyl-2-oxo-1,2,3,4-tetrahydropyrido[2,3-b]pyrazine-7-carboxylate

Ausbeute 71.0%

Lösungsmittel

dichloromethane

dichloromethane

Reaktionsbedingungen

Aufarbeitung

1. 1
   Temperaturwas then refluxed for 30 min
2. 2
   FiltrationThe hot solution was filtered through a pad of celite
3. 3
   Waschenwashed with hot dichloromethane (3×10 mL)
4. 4
   EinengenThe filtrate was concentrated

Vorschrift

Methyl 6-(benzyl(2-ethoxy-2-oxoethyl)amino)-5-nitronicotinate (445 mg g, 1.19 mmol) was dissolved in dichloromethane (5 mL). To the yellow solution was added ammonium metavanadate (10.0 mg, 0.085 mmol), triphenyl phosphite (aprox 10 ul, 0.032 mmol), and Pt/C (50 mg, 5% w/w). The reaction mixture was pressurized with hydrogen gas (75 psi) and stirred at room temperature for 48 h. The reaction was then depressurized and diluted with dichloromethane (20 mL) which was then refluxed for 30 min. The hot solution was filtered through a pad of celite and washed with hot dichloromethane (3×10 mL). The filtrate was concentrated to yield the title compound (250 mg, 71%) as a white solid. [M+H] calc'd for C16H15N3O3, 298; found, 298.

Quelle