One-pot and one-step novel N-methylation of 2,6-diaminopyridine

Authors

  • Mehdi Nabati Chemistry Department, Faculty of Science, Azarbaijan Shahid Madani University, Tabriz, Iran
  • Mehrdad Mahkam Chemistry Department, Faculty of Science, Azarbaijan Shahid Madani University, Tabriz, Iran
Abstract:

2,6-diaminopyridine is extensively used as a pharmaceutical intermediate and a hair dye coupler as oxidation formulations. It is soluble in protic solvents. Primary and secondary amines are N-methylated by various methods such as direct alkylation of amines with Hofmann mechanism, but in many of these methods due to overalkylations, we earn a mixture of amino products. Consequently, they aren't selective in secondary amines preparation. Also, the selective synthesis of secondary amines is a problematic field in organic chemistry. 2,6-diaminopyridine can be selective N-methylated from reaction of this compound with sodium azide and orthoformic ester in low time with good yields.

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Journal title

volume 2  issue Issue 3, pp. 162-231

pages  162- 167

publication date 2014-05-01

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