Corpus ID: 73640130

Synthesis andmolluscicide activity of some new pyrazole heterocycles

@inproceedings{AbdelMegid2008SynthesisAA,
  title={Synthesis andmolluscicide activity of some new pyrazole heterocycles},
  author={Mohamed H. Abdel-Megid and M. A. A. Awas and Magdy H. Seada and Kamelia M. El-Mahdy},
  year={2008}
}
  • Mohamed H. Abdel-Megid, M. A. A. Awas, +1 author Kamelia M. El-Mahdy
  • Published 2008
  • Chemistry
  • Some newpyrazolopyrimidines, pyrazoloimidazolopyrimidines, pyraz- olopyrimidopyrimidines, pyrazolyltetrazole, pyrazolyloxadiazole, and N,N-di-heterocyclylamidine have been synthesis starting from 5-amino-4-cyano-1- phenylpyrazole (1). Some of the newly synthesized pyrazole heterocycles have been tested as Mollucicidal agents. 

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    M.Abdel Megid; Pharmazie

    • D.S.Dhanoa, S.Meegalla, +7 authors PCT.Tnt.Appl.Wo
    • A.Kreutzberger, K.Bargwitz; Arch.Pharm.,
    • 1980

    2922 CH aliph ), 3062  (CH arom

    3044 (CH arom ), 3164 (NH) 1.34(t, 3H, OCH 2 CH 3 ), 3.34(s, 1H, C-H), 3,88 (s,3H

    •  Cn
    • 1731 (C=O), 2214(CN), 2885 (CH aliph )

    33(s, 1H, C-3-H pyrimidine ) (15) 1600 -1596 (C=N, C=C), 2206 (CN), 2923 CH aliph

    57(s, 1H,C-3-H pyrazole ), 8.64(s, 1H, C-6-H pyrimidine )

    • 1678 C= O benzamido ),3053 õ (CH arom ), 3371,3129 õ (2N-H) 7.38-8.16(m, 10H, H arom )

    73(s, 1H, C-6-H pyrimidine )

    •  Co
    • 2922 (CH aliph ), 3012 (CH arom )

    86(s,1H, exocyclic NH)

    IR (/ cm -1 )

    • Comp

    NH) 2.49(s, 1H, CO-CH 3 ), 3.30 (s, 3H, CH 3 of oxaiazole ), 7.46-8.19 (m, 5H, H arom ), 8.57(s,1H, C-3-H pyrazole ),8.77(s, 1H, NH)