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An Efficient and Facile Synthesis of 1,2,4-Aryl Triazoles and 4-Thiazolidinones Bearing 6-Fluorochroman Nucleus

机译:高效,简便地合成带有6-氟苯并吡喃核的1,2,4-芳基三唑和4-噻唑烷酮

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A new generation of chroman bearing heterocyclic five membered ring such as 1,2,4-triazoles and thiazolidinones was designed and synthesized. New chroman based nucleus 5-(6-fluorochroman-2-yl)-4-aryl-4H-1,2,4-triazole-3-thiol and 6-fluorochroman-N-(4-oxo-2-arylthiazolidinin-3-yl) chroman-2-carboxamides were synthesized. Aryl triazole compounds4a–4jwere synthesized from 6-fluorochroman-2-carbohydrazide2on reaction with base in methanol and CS2followed by reaction with substituted aniline. Thiazolidinone compounds5a–5jwere synthesized from 6-fluorochroman-2-carbohydrazide2on reaction with substituted aryl aldehyde and thioglycolic acid.
机译:设计并合成了新一代的含苯并二氢吡喃的五元环,如1,2,4-三唑和噻唑烷酮。新的基于苯并二氢吡喃的核(5-(6-氟代铬-2-基)-4-芳基-4H-1,2,4-三唑-3-硫醇和6-氟代-N-(4-氧代-2-芳基噻唑烷-3合成了-(yl)苯并二氢吡喃-2-甲酰胺。由6-氟苯并吡喃-2-碳酰肼2与甲醇中的碱和CS2反应,然后与取代的苯胺反应,合成了芳基三唑化合物4a-4。噻唑烷酮化合物5a-5由6-氟苯并吡喃-2-碳酰肼2与取代的芳基醛和巯基乙酸反应制得。

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