Reaction of Nitrilimines with 2-Aminopicoline, 3-Amino-1,2,4-Triazole, 5-Aminotetrazole and 2-Aminopyrimidine
- 1 Department of Chemistry, Islamic University of Gaza, Gaza, Palestine
- 2 Department of Chemistry, Islamic University of Gaza, Gaza, Palestine
- 3 Department of Chemistry, Islamic University of Gaza, Gaza, Palestine
- 4 Manchester Institute of Biotechnology, School of Chemistry and EPS, The University of Manchester, Manchester, UK
- 5 Department of Chemistry, Islamic University of Gaza, Gaza, Palestine
- 6 Department of Chemistry, Islamic University of Gaza, Gaza, Palestine
Abstract
The reaction of picoline derivatives 3-6 with hydrazonoylhalide 1a produced imidazo[1,2-a]pyridines 7-10, while the reaction of the same picoline derivatives with hydrazonoylhalide 1b afforded imidazo[1,2-a]pyridine-2-ones 11-13. The reaction of 1b, c with 3-amino-1,2,4-triazole 14 produced the acyclic adducts 18 and 19, respectively. Reaction of 1b, 1c with 5-aminotetrazole 20 produced the acyclic products 23 and 24, respectively. Finally, the reaction of 1b with 4, 6-dimethyl-2-aminopyrimidine 27 afforded compound 29 rather than its isomeric structure 28. The structure of the products was confirmed by the different spectroscopic analytical methods including IR, MS, 1 HNMR and 13 CNMR.
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