4.6 Article

A fully automated, multistep flow synthesis of 5-amino-4-cyano-1,2,3-triazoles

Journal

ORGANIC & BIOMOLECULAR CHEMISTRY
Volume 9, Issue 6, Pages 1938-1947

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c0ob00815j

Keywords

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Funding

  1. Paul Mellon Fellowship
  2. EPSRC
  3. Royal Society
  4. BP [1702]
  5. EPSRC [EP/F069685/1, EP/G028125/1] Funding Source: UKRI
  6. Engineering and Physical Sciences Research Council [EP/F069685/1, EP/G028125/1] Funding Source: researchfish

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Having demonstrated in the preceding publication the flow synthesis of aryl azides, we describe here a general protocol for the in-line purification of these versatile intermediates. As part of this investigation, we evaluated the use of ReactIR 45m as a tool for real-time detection of hazardous azide contaminants. This azide synthesis and purification process was then incorporated into a multistep flow sequence to generate a small collection of 5-amino-4-cyano-1,2,3-triazoles directly from aniline starting materials in a fully automated fashion.

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