1345044-53-2

Upstream product

• 1234616-02-4 1-chloro-4-iodo-2,7-diazanaphthalene 
• 28557-00-8 phenylzinc chloride 
• 959558-50-0 4-iodine-2,7-naphthyridine-1(2H)-one 
• 67988-50-5 2,7-naphthyridinyl-1(2H)-one 
• 140-29-4 phenylacetonitrile 
• 10177-29-4 4-chloronicotinic acid 
• 1345044-48-5 4-phenyl-3,4-dihydro-2H-[2,7]naphthyridin-1-one 
• 1345044-46-3 C₁₅H₁₂N₂O₂ 
• 1345044-42-9 4-[α-cyano(phenyl)methyl]nicotinic acid 

Downstream Products

• 1345044-60-1 1-(morpholin-4-yl)-4-phenyl-[2,7]naphthyridine 
• 1345044-61-2 1-azido-4-phenyl-[2,7]naphthyridine 
• 1345044-59-8 1-cyclohexylamino-4-phenyl-[2,7]naphthyridine 
• 1345044-58-7 1-allylamino-4-phenyl-[2,7]naphthyridine 
• 1345044-55-4 1-benzylamino-4-phenyl-[2,7]naphthyridine 
• 1345044-63-4 1-(N,O-dimethylhydroxylamino)-4-phenyl-[2,7]naphthyridine 

Relevant academic research and scientific papers

Preparation of Polyfunctional Naphthyridines by Cobalt-Catalyzed Cross-Couplings of Halogenated Naphthyridines with Magnesium and Zinc Organometallics

CoCl2 (5%) catalyzes cross-couplings of various halogenated naphthyridines with alkyl- and arylmagnesium halides. Also, arylzinc halides undergo smooth cross-couplings with various naphthyridines in the presence of CoCl2·2LiCl (5%) a

A novel approach for the synthesis of lophocladines A, B and C1 analogues

A novel approach for the syntheses of lophocladines A and B has been developed. These compounds were prepared in 4-6 steps with moderate to excellent overall yields. The key step involved the nucleophilic substitution of 4-chloronicotinic acid with the ca