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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 372829Erstellt: 25. Oktober 2026

Hexane → 1,5-Naphthyridine

https://huagongshe.com/reaction/372829

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 described in J. Org. Chem., 1963, 1757 and was isolated as colourless 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
PatentnummerUS04092418
Quelldatensatzuspto-grants-1978_05
ORD IDord-df3d0aeec4c8496095d7f9e632740537
Quellennotizuspto-grants-1978_05