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HRID 1614769Erstellt: 25. Oktober 2026

Methanol → 2,6-Diethyl-1,4-dihydro-4-oxopyridine-3-carboxamide

https://huagongshe.com/reaction/1614769

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethanolHCID 887—
Edukt2,6-diethyl-4-hydroxy-3-Pyridinecarboxylic acid methyl esterHCID 14950476—
EduktAminodimethyl aluminiumHCID 16689643—
LösungsmittelDichloromethaneHCID 6344—
Produkt2,6-Diethyl-1,4-dihydro-4-oxopyridine-3-carboxamideHCID 15171316—

Reaktionsschritte

A 1.3M solution of aminodimethyl aluminium in dichloromethane (obtained as described in Tetrahedron Letters, 1979, 4907) (7.8 ml) was added to a solution of methyl 2,6-diethyl-1,4-dihydro-4-oxopyridine-3-carboxylate (1.05 g in dichloromethane (50 ml) and the solution was left to stand for 20 hours. Methanol (5 ml) was added and the mixture was stirred for 1 hour. The precipitated solid was removed by filtration through a bed of diatomaceous earth. The filtrate was concentrated and the residue purified by flash chromatography, eluting with methanol/dichloromethane (1:9 v/v), to give 2,6-diethyl-1,4-dihydro-4-oxopyridine-3-carboxamide (0.5 g), m.p. 254° C.; NMR (d6 -DMSO): 1.15-1.25(m,6H), 2.5(q,2H), 3.0(q,2H), 6.1(s,1H), 7.0(br s, 1H), 9.6(br s, 1H), 11.3(br s, 1H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05198439
Quelldatensatzuspto-grants-1993_03
ORD IDord-a853cc470ee044a283dbf346454c13e9
Quellennotizuspto-grants-1993_03