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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2419952Erstellt: 24. Oktober 2026

2-Methylpyridine-3-carbonitrile → 1-Amino-3(2-ethyl-pyridyl)-4-methyl-2,5-naphthyridine

https://huagongshe.com/de/reaction/2419952

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Methylpyridine-3-carbonitrileHCID 4738308—
Edukt2-(Phenylmethyl)-3-pyridinecarbonitrileHCID 12428725—
Edukt3-Cyano-2-phenethylpyridineHCID 12428728—
Edukt2-EthylnicotinonitrileHCID 15454017—
Edukt3-Cyano-2-phenylpropylpyridineHCID 23467632—
Produkt1-Amino-3(2-ethyl-pyridyl)-4-methyl-2,5-naphthyridineHCID 23467682—

Reaktionsschritte

In a similar manner by substituting the 3-cyano-2-methylpyridine with equivalent quantities of 3-cyano-2-ethylpyridine, 3-cyano-2-benzylpyridine, 3-cyano-2-phenethylpyridine and 3-cyano-2-phenylpropylpyridine and by substantially following the procedure of this example there is produced 1-amino-3(2-ethyl-3-pyridyl)-4-methyl-2,5-naphthyridine; 1-amino-3-(2-benzyl-3-pyridyl)-4-phenyl-2,5-naphthyridine; 1-amino-3-(2-phenethyl-3-pyridyl)-4-benzyl-2,5-naphthyridine; 1-amino-3-(2-phenylpropyl-3-pyridyl)-4-phenethyl-2,5-naphthyridine, respectively. Similarly, in those instances wherein it is desired to produce those compounds bearing substituents on the pyridyl, phenyl and benzyl moieties of the foregoing then, as expected, the appropriately substituted starting reactants are then similarly reacted.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04107166
Quelldatensatzuspto-grants-1978_08
ORD IDord-6e47948c31d74bc5b3b06ab6c5ea1136
Quellennotizuspto-grants-1978_08