Nifurquinazol
Clinical data
Routes of
administration		?
ATC code
  • none
Legal status
Legal status
  • In general: uncontrolled
Identifiers
  • 2,2'-{[2-(5-nitrofuran-2-yl)quinazolin-4-yl]imino}diethanol
CAS Number
PubChem CID
ChemSpider
UNII
KEGG
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC16H16N4O5
Molar mass344.327 g·mol−1
3D model (JSmol)
  • O=[N+]([O-])c3oc(c1nc(N(CCO)CCO)c2c(n1)cccc2)cc3

Nifurquinazol (NF-1088) is an antibacterial agent of the nitrofuran class.[1] It was never marketed.[1]

Synthesis

Nifurquinazol synthesis:[2][3]

Treatment of the amide from 5-nitrofuroic acid with phosphorus oxychloride leads to the corresponding nitrile (2). This intermediate is then converted to the iminoether (3) with ethanolic hydrogen chloride. Condensation of anthranilic acid with the iminoether in the presence of sodium methoxide represents another method for preparing quinazolones. The reaction can be visualized as proceeding through the formation of the amidine from addition-elimination of anthranilic acid; cyclization then affords the observed product (4). The amide function is then converted to the iminochloride with phosphorus oxychloride. Displacement of the newly introduced halogen by means of diethanolamine affords nifurquinazol chlorine with diethanolamine leads to the formation of nifurquinazol (5), one of the antibacterial nitrofurans.

References

  1. 1 2 Dictionary of organic compounds. London: Chapman & Hall. 1996. ISBN 0-412-54090-8.
  2. ↑ Sherman WR, Von Esch A (1965). "Syntheses with 5-Nitro-2-furonitrile". Journal of Medicinal Chemistry. 8 (1): 25–28. doi:10.1021/jm00325a006.
  3. ↑ Burch HA (May 1966). "Nitrofuryl heterocycles. IV. 4-amino-2-(5-nitro-2-furyl)quinazoline derivatives". Journal of Medicinal Chemistry. 9 (3): 408–10. doi:10.1021/jm00321a034. PMID 5960915.
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