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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1582956Erstellt: 26. Oktober 2026

Sodium hydride → ethyl 4-{N-[3-(3-chlorobenzoyl)-6-methylpyridin-2-yl]-N-ethylcarbamoyl}butanoate

https://huagongshe.com/reaction/1582956

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium hydrideHCID 24758—
Edukt3-(3-Chlorobenzoyl)-2-ethylamino-6-methylpyridineHCID 11054902—
EduktMonoethyl chloroglutarateHCID 22716689—
LösungsmittelDimethylformamideHCID 6228—
Produktethyl 4-{N-[3-(3-chlorobenzoyl)-6-methylpyridin-2-yl]-N-ethylcarbamoyl}butanoateHCID 22716702—

Reaktionsschritte

A DMF solution of 3-(3-chlorobenzoyl)-2-ethylamino-6-methylpyridine was treated with 60% sodium hydride and then reacted with monoethyl chloroglutarate under heating. Thereafter, the whole was worked up and purified in a usual manner to obtain ethyl 4-{N-[3-(3-chlorobenzoyl)-6-methylpyridin-2-yl]-N-ethylcarbamoyl}butanoate. The resulting compound was reacted with sodium methoxide in ethanol under heating, then concentrated sulfuric acid was added to the reaction mixture, followed by reaction under heating for 2 days. Thereafter, the reaction mixture was worked up and purified in a usual manner to obtain ethyl 3-[4-(3-chlorophenyl)-1-ethyl-7-methyl-2-oxo-1,2-dihydro-1,8-naphthyridin-3-yl]propanoate. MS: 399.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06740662B1
Quelldatensatzuspto-grants-2004_05
ORD IDord-275262b710cf4a448b90a8a6fff1385a
Quellennotizuspto-grants-2004_05