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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1764396Erstellt: 24. Oktober 2026

2-Methylpyridine-3-carbonitrile → 1-Amino-3-methyl-4-phenyl-2,5-naphthyridine

https://huagongshe.com/reaction/1764396

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Methylpyridine-3-carbonitrileHCID 4738308—
Edukt2-(Phenylmethyl)-3-pyridinecarbonitrileHCID 12428725—
Edukt3-Cyano-2-phenethylpyridineHCID 12428728—
Edukt2-EthylnicotinonitrileHCID 15454017—
Produkt1-Amino-3-methyl-4-phenyl-2,5-naphthyridineHCID 23467600—
Produkt1-Amino-3,4-dimethyl-2,5-naphthyridineHCID 23467654—
Produkt1-Amino-3-methyl-4-benzyl-2,5-naphthyridineHCID 23467667—

Reaktionsschritte

Similarly, by substituting the 3-cyano-2-methylpyridine reactant with equivalent quantities of 3-cyano-2-ethylpyridine, 3-cyano-2-benzylpyridine, 3-cyano-2-phenethylpyridine and by substantially following the foregoing reaction procedure there is produced 1-amino-3,4-dimethyl-2,5-naphthyridine, 1-amino-3-methyl-4-phenyl-2,5-naphthyridine, 1-amino-3-methyl-4-benzyl-2,5-naphthyridine, respectively. Similarly, in each of those reactions wherein the 3-cyano-2-methylpyridine has been substituted with another 3-cyano-2-substituted pyridine the acetonitrile reactant may also be substituted with the aforementioned nitriles and by substantially following the procedure described in the example, there is produced the appropriate 1-amino-3- and 4-substituted, 2,5-naphthyridines.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04115395
Quelldatensatzuspto-grants-1978_09
ORD IDord-0d7f2d739b214f2f994299e30d253e8e
Quellennotizuspto-grants-1978_09