The preparation of ester heterocycles mostly uses heteroatoms as nucleophilic sites, which are achieved by intramolecular substitution or addition reactions. Compound: 5-Iodo-2-furaldehyde( cas:2689-65-8 ) is researched.Category: naphthyridine.Kovac, J.; Stetinova, J. published the article 《Furan derivatives. LXXX. Synthesis and properties of substituted furfurylideneoxindoles》 about this compound( cas:2689-65-8 ) in Chemicke Zvesti. Keywords: furfurylideneoxindole; oxindole furufurylidene; IR furfurylideneoxindole; UV furfurylideneoxindole; mass spectra furfurylideneoxindole. Let’s learn more about this compound (cas:2689-65-8).
Oxindoles I (R1 = R2 = H, R = H, NO2, Cl, Br, I, Me, MeS, CO2Me, p- and m-O2NC6H4, Me2N; R1 = H, R2 = NO2, R = H, Cl, Br, I, Me, MeS, Ac, 4-O2NC6H4; R1 = Ac, R2 = H, R = H, NO2, Cl, Br, I, Me, MeS, NMe2) were prepared by condensation of oxindole, 5-nitrooxindole, and 1-acetyloxindole, resp., with the resp. furancarboxyaldehydes, some I (R1 = Ac) were prepared by acetylation of I (R1 = H). UV, IR and mass spectra of I were interpreted.
This literature about this compound(2689-65-8)Category: naphthyridinehas given us a lot of inspiration, and I hope that the research on this compound(5-Iodo-2-furaldehyde) can be further advanced. Maybe we can get more compounds in a similar way.
Reference:
1,8-Naphthyridine – Wikipedia,
1,8-Naphthyridine | C8H6N2 – PubChem