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Synthesis of New Pyrimido[4,5-e][1,2,4]triazolo[3,4-b][1,3,4]thiadiazine Derivatives via S/N Smiles Rearrangement
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Several new pyrimido[4,5-e][1,2,4]triazolo[3,4-b][1,3,4]thiadiazine derivatives (href="#jhet2572-eo-0011" rel="references:#jhet2572-eo-0011 #jhet2572-eo-0012 #jhet2572-eo-0013 #jhet2572-eo-0014 #jhet2572-eo-0015 #jhet2572-eo-0016 #jhet2572-eo-0017">) were synthesized through the pan class="TH_term4">condensation reactionpan> of http://www.wiley.com/namespaces/wiley" xmlns:cr="urn://wiley-online-library/content/render" xmlns:mml="http://www.w3.org/1998/Math/MathML" id="jhet2572-eo-0001">pan class="TH_term3">5-bromo-4,6-dichloropyrimidinepan> (href="#jhet2572-eo-0001" rel="references:#jhet2572-eo-0001">) and http://www.wiley.com/namespaces/wiley" xmlns:cr="urn://wiley-online-library/content/render" xmlns:mml="http://www.w3.org/1998/Math/MathML" id="jhet2572-eo-0002">pan class="TH_term3">4-amino-5-methyl-4H-1,2,4-triazole-3-thiolpan> (href="#jhet2572-eo-0002" rel="references:#jhet2572-eo-0002">). The single crystal X-ray data of one of the derivatives confirmed the occurrence of the S/N type pan class="TH_term4">Smiles rearrangementpan> during the course of the reaction.

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