Reduction of 2-amino-3-and-5-nitropyridine derivatives with hydrazine hydrate
NN Smolyar, YM Yutilov
Index: Smolyar; Yutilov Russian Journal of Organic Chemistry, 2009 , vol. 45, # 1 p. 115 - 118
Full Text: HTML
Citation Number: 3
Abstract
Abstract The reactions of 2-amino-3-nitropyridine and 2-amino-5-nitropyridine with hydrazine hydrate resulted in elimination of the amino group and reduction of the nitro group with formation of 3-aminopyridine. A probable reaction mechanism involves addition of hydrazine hydrate at the NC 2 bond, followed by elimination of ammonia and reduction of the nitro group to amino. 2-Amino-4-methyl-3-nitropyridine and 2-amino-5-methyl-3- ...
Related Articles:
[Timperley, Christopher M.; Banks, R. Eric; Young, Ian M.; Haszeldine, Robert N. Journal of Fluorine Chemistry, 2011 , vol. 132, # 8 p. 541 - 547]
Synthesis of 3-aminopyridine-2-carboxaldehyde thiosemicarbazone (3-AP)
[Niu, Chuansheng; Li, Jun; Doyle, Terrence W.; Chen, Shu-Hui Tetrahedron, 1998 , vol. 54, # 23 p. 6311 - 6318]
[Alsabeh, Pamela G.; Lundgren, Rylan J.; McDonald, Robert; Johansson Seechurn, Carin C. C.; Colacot, Thomas J.; Stradiotto, Mark Chemistry - A European Journal, 2013 , vol. 19, # 6 p. 2131 - 2141]
Site-selective azaindole arylation at the azine and azole rings via N-oxide activation
[Organic Letters, , vol. 11, # 6 p. 1357 - 1360]
[Wachi, Kazuyuki; Terada, Atsusuke Chemical and Pharmaceutical Bulletin, 1980 , vol. 28, # 10 p. 3020 - 3028]