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New N-nitrosoamines. 2. Transformations of tetrahydro-1,3-oxazines into nitrates of N-nitrosoamino alcohols
Authors:Korepin  A G  Galkin  P V  Perepelkina  E K  Glushakova  N M  Lodygina  V P  Eremenko  I L  Nefedov  S E  Eremenko  L T
Institution:(1) Institute of Problems of Chemical Physics, Russian Academy of Sciences, 142432 Chernogolovka, Moscow Region, Russian Federation;(2) N. S. Kurnakov Institute of General and Inorganic Chemistry, Russian Academy of Sciences, 31 Leninsky prosp., 119991 Moscow, Russian Federation
Abstract:The reactions of HNO3 with tetrahydro-1,3-oxazines 1a—c produced by aminomethylation of diketopiperazine, isatin, and succinimide, respectively, afforded nitrates of amino alcohols RCH2NH2(CH2)3ONO2]+NO3 (4a—c) whose subsequent N-nitrosation (NaNO2, AcOH) gave nitrates of N-nitrosoamino alcohols RCH2N(NO)(CH2)3ONO2 (5a—c). The structures of compound 5b,c were established by X-ray diffraction analysis.
Keywords:heterocyclic agr-carbonyl-containing NH-acids" target="_blank">gif" alt="agr" align="BASELINE" BORDER="0">-carbonyl-containing NH-acids  amides  tetrahydro-1  3-oxazines  destructive nitration  N-nitrosation  nitrates of amino alcohols and N-nitrosoamino alcohols  X-ray diffraction analysis
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