Studied the nitration of 3-amino pyridine. It is shown that the nitration of 3-aminopyridine, they form nitroaminy not capable of entering into Bamberger rearrangement. 3 Alkilaminoproizvodnye, however, are capable of such a rearrangement may nitrated to 2,4,6-trinitroproizvodnyh.
3-аминопиридин, нитрование, перегруппировка Бамбергера, электрофильное замещение, 3-aminopyridine, nitration, Bamberger rearrangement, electrophilic substitution
1. I.F. Falyahov ,R.Z. Gil'manov , G.P. Sharnin,F.G. Hayrutdinov , T.N.Sobachkina., V.G.Nikitin ,Z.G. Ahtyamova. Himiya nitroproizodnyh piridina. Soobsch. 3. Zakonomernosti nitrovaniya aminoproizvodnyh piridina. Vestnik KGTU.№10, 2010.
2. R.Z. Gil'manov, I.F.Falyahov, V.G Nikitin, B.S.Fedorov, Yu.V.Filippov, F.G. Hayrutdinov. Sintez biologicheski aktivnyh veschestv i lekarstvennyh substanciy na osnove proizvodnyh piridinovogo ryada Vestnik KGTU.№10, 2011.
3. Plazek, E. Weber line syntheses des 3,5 dinitropyridins / E. Plazek // Rec. trav. Chem. - 1953. - V.72. - S. 569.
4. Tayrins, A. Tautomerism of 2-nitraminopyridins / A., Tayrins, S. J.Vison // Can. J. Chem. - 1953. - V. 31. -. 1048.
5. Orlova, E.Yu. Himiya i tehnologiya brizantnyh vzryvchatyh veschestv / E.Yu. Orlova. - M.: 1973. - 319 s.
