《Naphthyridine chemistry. XI. Synthesis and reactivity of 2,7-naphthyridine》 was published in Journal of Heterocyclic Chemistry in 1970. These research results belong to Paudler, William W.; Cornrich, Sandra J.. Name: 2,7-Naphthyridin-1-amine The article mentions the following:
1,3,6,8-Tetra-chloronaphthyridine was selectively reduced to give 70% 2,7 – naphthyridine (I), m. 96-7°, by treatment with H and Pd-C in KOAc buffered solution I underwent Eisch bromination to give 4-bromo-2,7-naphthyridine and 4,5-dibromonaphthyridine. Chichibabin amination of I gave 1-amino-2,7-naphthyridine. After reading the article, we found that the author used 2,7-Naphthyridin-1-amine(cas: 27225-00-9Name: 2,7-Naphthyridin-1-amine)
2,7-Naphthyridin-1-amine(cas: 27225-00-9) belongs to naphthyridines. Functionalized naphthyridines and their benzo/heterofused analogs are present in numerous marine products and reported to possess wide-ranging activities such as antiproliferative , antiaggressive, and HIV-1 integrase inhibition in addition to their use as anti-HCV agents .Name: 2,7-Naphthyridin-1-amine
Referemce:
1,8-Naphthyridine – Wikipedia,
1,8-Naphthyridine | C8H6N2 – PubChem