An update on the compound challenge: 1569-17-1

This literature about this compound(1569-17-1)Application In Synthesis of 4-Methyl-1,8-naphthyridinehas given us a lot of inspiration, and I hope that the research on this compound(4-Methyl-1,8-naphthyridine) can be further advanced. Maybe we can get more compounds in a similar way.

Most of the natural products isolated at present are heterocyclic compounds, so heterocyclic compounds occupy an important position in the research of organic chemistry. A compound: 1569-17-1, is researched, SMILESS is CC1=C2C=CC=NC2=NC=C1, Molecular C9H8N2Journal, Chemical & Pharmaceutical Bulletin called Syntheses of nitrogen-containing compounds. XVII. Improvement of one-step synthesis of naphthyridine derivatives and their methylation with demethyl sulfoxide in the presence of base, Author is Hamada, Yoshiki; Takeuchi, Isao; Hirota, Minoru, the main research direction is naphthyridine methylation MD calculation.Application In Synthesis of 4-Methyl-1,8-naphthyridine.

1,8-Naphthyridines were synthesized in a high yield by the reaction of 2-aminopyridines with glycerol, in the presence of Na m-nitrobenzenesulfonate, in H2SO4. Methylation of naphthyridines with Me2SO in the presence of NaH or KOBu-tert afforded their mono-Me or di-Me compounds This methylation with methylsulfinyl carbanion was examined from the Hueckel MO method; the calculation agreed with the exptl. results.

This literature about this compound(1569-17-1)Application In Synthesis of 4-Methyl-1,8-naphthyridinehas given us a lot of inspiration, and I hope that the research on this compound(4-Methyl-1,8-naphthyridine) can be further advanced. Maybe we can get more compounds in a similar way.

Reference:
1,8-Naphthyridine – Wikipedia,
1,8-Naphthyridine | C8H6N2 – PubChem