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Makki, M.S.T., Abdel-Rahman, R.M. and AbuAli, O.A. (2015) Synthesis of New Fluorinated 1,2,4-Triazino [3,4-b] [1,3,4]thiadiazolones as Antiviral Probes-Part II-Reactivities of Fluorinated 3-Aminophenyl-1,2,4-triazinothiadiazolon. International Journal of Organic Chemistry, 5, 153-165.
https://doi.org/10.4236/ijoc.2015.53017

has been cited by the following article:

• TITLE: Synthetic Approach for Novel Fluorine Substituted α-Aminophosphonic Acids Containing 1,2,4-Triazin-5-One Moiety as Antioxidant Agents

  AUTHORS: Mohammed S. T. Makki, Reda M. Abdel-Rahman, Abdulrahman S. Alharbi

  KEYWORDS: Synthetic, Fluorine α-Amino Acids, 1, 2, 4-Triazin-5-One Moiety, Antioxidants Activity

  JOURNAL NAME: International Journal of Organic Chemistry, Vol.8 No.1, January 16, 2018

  ABSTRACT: Novel fluorine substituted α-amino phosphonic acids containing 1,2,4-triazin- 5-one (6a-f) have been obtained from fluoroacylation of 6-(2′-amino-5′-nitrophenyl)-3-thioxo-1,2,4-triazin-5(4H)-one (1) followed by ammonilysis to give the corresponding 3-amino-derivative 3. Condensation of compound 3 with nitro/halogenated aromatic aldehydes yielded the Schiff bases 4. The simple addition of diethyl phosphonate to compound 4 produced the α-amino phosphonates 5. Acidic hydrolysis of compound 5 produced the fluorine substituted α-amino acids derivatives 6. Structures of the new compounds have been established with the help of elemental analysis and spectral measurements. Also, the products evaluated as antioxidants, where the fluorinated α-amino phosphonic acids 6 are more active than the other synthesized systems.