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HRID 2097872Erstellt: 26. Oktober 2026

Triphenyl phosphite → Methyl 4-isopropyl-2-oxo-1,2,3,4-tetrahydropyrido[2,3-b]pyrazine-7-carboxylate

https://huagongshe.com/reaction/2097872

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriphenyl phosphiteHCID 7540—
EduktMethyl 6-((2-ethoxy-2-oxoethyl)(isopropyl)amino)-5-nitronicotinateHCID 58324358—
EduktHCID 178418361HCID 178418361—
KatalysatorPlatinumHCID 23939—
KatalysatorAmmonium metavanadateHCID 516859—
LösungsmittelDichloromethaneHCID 6344—
ProduktMethyl 4-isopropyl-2-oxo-1,2,3,4-tetrahydropyrido[2,3-b]pyrazine-7-carboxylateHCID 5832444793%

Reaktionsschritte

Methyl 6-((2-ethoxy-2-oxoethyl)(isopropyl)amino)-5-nitronicotinate (2.39 g, 7.35 mmol) was dissolved in dichloromethane (10 mL). To the yellow solution was added ammonium metavanadate (15.0 mg, 1.13 mmol), triphenyl phosphite (aprox 10 ul, 0.032 mmol), and Pt/C (240 mg, 5% w/w). The reaction mixture was pressurized with hydrogen gas (110 psi) and stirred at room temperature for 16 h. The reaction was then depressurized and diluted with dichloromethane (80 mL) which was then refluxed for 30 min. The hot solution was filtered through a pad of celite and washed with hot dichloromethane (3×20 mL). The filtrate was concentrated to yield the title compound (1.70 g, 93%) as a white solid. [M+H] calc'd for C, 12; H, 15; N, 3; O, 3, 250; found, 250.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08450323B2
Quelldatensatzuspto-grants-2013_05
ORD IDord-9b4af75eef554ce499a154c3b2d13bbf
Quellennotizuspto-grants-2013_05