Literature DB >> 28720330

Generation of hazardous methyl azide and its application to synthesis of a key-intermediate of picarbutrazox, a new potent pesticide in flow.

Daisuke Ichinari1, Aiichiro Nagaki2, Jun-Ichi Yoshida3.   

Abstract

Generation and reactions of methyl azide (MeN3) were successfully performed by using a flow reactor system, demonstrating that the flow method serves as a safe method for handling hazardous explosive methyl azide. The reaction of NaN3 and Me2SO4 in a flow reactor gave a MeN3 solution, which was used for Huisgen reaction with benzoyl cyanide in a flow reactor after minimal washing. The resulting 1-methyl-5-benzoyltetrazole serves as a key intermediate of picarbutrazox (IX), a new potent pesticide.
Copyright © 2017. Published by Elsevier Ltd.

Entities:  

Keywords:  Flow synthesis; Methyl azide

Mesh:

Substances:

Year:  2017        PMID: 28720330     DOI: 10.1016/j.bmc.2017.07.005

Source DB:  PubMed          Journal:  Bioorg Med Chem        ISSN: 0968-0896            Impact factor:   3.641


  1 in total

1.  Synthesis, Cytotoxicity and Molecular Docking Studies of the 9-Substituted 5-Styryltetrazolo[1,5-c]quinazoline Derivatives.

Authors:  Malose J Mphahlele; Samantha Gildenhuys; Nishal Parbhoo
Journal:  Molecules       Date:  2017-10-26       Impact factor: 4.411

  1 in total

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