2015
DOI: 10.3906/kim-1408-78
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Microwave-assisted synthesis of novel 8-chloro-[1,2,4]triazolo[4,3-$a$]pyridine derivatives

Abstract: A series of novel 1,2,4-triazolo[4,3-a ]pyridine derivatives were synthesized from 2,3-dichloropyridine and hydrazine hydrate as starting materials by multistep reactions under microwave assistance, and their structures were characterized by 1 H NMR, MS, and elemental analysis. This method provides several advantages such as high yields, facile work-up, and environmental friendliness.

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Cited by 26 publications
(14 citation statements)
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“…Microwave technology was applied to the synthetic reaction to shorten the reaction time and increase the yields of urea derivatives 4 . The key intermediate 2‐{[2‐(diethylamino)‐6‐methylpyrimidin‐4‐yl]oxy}acetohydrazide 3 and the substituted isocyanatobenzenes were synthesized according to our previous work . The reaction mechanism is a nucleophile substitution reaction.…”
Section: Resultssupporting
confidence: 88%
“…Microwave technology was applied to the synthetic reaction to shorten the reaction time and increase the yields of urea derivatives 4 . The key intermediate 2‐{[2‐(diethylamino)‐6‐methylpyrimidin‐4‐yl]oxy}acetohydrazide 3 and the substituted isocyanatobenzenes were synthesized according to our previous work . The reaction mechanism is a nucleophile substitution reaction.…”
Section: Resultssupporting
confidence: 88%
“…For example, penthiopyrad is one of new succinate dehydrogenase inhibitors which can inhibit Colletotrichum, invented by Mitsui Chemicals Co. Ltd. On the other hand, pyridine derivatives also displayed diversity activities. [9][10][11][12][13] Chlorantraniliprole, discovered by DuPont, is a novel class of insecticide which target insect ryanodine receptors (RyR) and commercialized in 2008.…”
Section: Introductionmentioning
confidence: 99%
“…In line with our continued efforts in the synthesis of novel lead compounds for pesticide , the commercial carboxamide fungicide penflufen was selected as a lead compound. The scaffold of the lead compound is maintained at the 1‐methyl‐3‐methyl‐1 H ‐pyrazole‐4‐carboxamide section.…”
Section: Introductionmentioning
confidence: 99%