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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 437038Erstellt: 25. Oktober 2026

Hexane → 1,5-Naphthyridine

https://huagongshe.com/reaction/437038

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHexaneHCID 8058—
Edukt3-AminopyridineHCID 10009—
Edukt1,5-NaphthyridineHCID 136070—
KatalysatorAdams' catalystHCID 345198—
LösungsmittelEthanolHCID 702—
Produkt1,5-NaphthyridineHCID 136070—
Produkt1,2,3,4-Tetrahydro-1,5-naphthyridineHCID 6917495—

Reaktionsschritte

1,5-Naphthyridine was prepared from 3-aminopyridine according to the method descried in J. Org. Chem., 1963, 1757 and was isolated as colorless needles from n-hexane m.p. 69° C. (lit. 74°). 1,5-Naphthyridine 2.6 g.) was hydrogenated in 95% ethanol over PtO2 catalyst under atmospheric conditions to give 1,2,3,4-tetrahydro-1,5-naphthyridine as colourless needles (2.51 g.).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04029667
Quelldatensatzuspto-grants-1977_06
ORD IDord-fa7af60bef8c427a8e61f1b155672687
Quellennotizuspto-grants-1977_06