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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 15929Erstellt: 23. Oktober 2026

Methylamine → Ethyl 4-hydroxy-1,2,5-trimethyl-6-oxo-1,6-dihydropyridine-3-carboxylate

https://huagongshe.com/de/reaction/15929

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethylamineHCID 6329—
Edukt1,1-DiethoxyetheneHCID 137673—
EduktDiethyl 2-methyl-3-oxopentanedioateHCID 10921903—
KatalysatorSodium MethoxideHCID 10942334—
LösungsmittelDiethyl EtherHCID 3283—
ProduktEthyl 4-hydroxy-1,2,5-trimethyl-6-oxo-1,6-dihydropyridine-3-carboxylateHCID 6667346734%

Reaktionsbedingungen

Temperatur85 °C

Reaktionsschritte

A mixture of 2-methyl-3-oxo-pentanedioic acid diethyl ester (10.0 g, 46.3 mmol), 1,1-diethoxy-ethene (12.8 mL, 92.5 mmol) and sodium methoxide (0.026 mg, 0.481 mmol) was heated to 85° C. for nine hours. The reaction mixture was cooled to room temperature and concentrated. To the resulting residue was added methylamine (1.91 mL, 55.5 mmol, 40% H2O). After stirring at room temperature for 16 hours, the reaction mixture was diluted with diethyl ether and washed with water. The aqueous phase was acidified to pH 1 with 10% HCl solution and extracted with EtOAc. The organic layer was dried (MgSO4) and concentrated. Trituration of the resulting residue with diethyl ether and flash column chromatography (3% MeOH in methylene chloride) gave 3.55 g (34%) desired product.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07732616B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-4177aaa645f44dd69db93fa00123b3e9
Quellennotizuspto-grants-2010_06