<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Dotsenko VV</submitter><funding>National Natural Science Foundation of China</funding><funding>Russian Science Foundation</funding><pagination>11874</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12733256</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>26(24)</volume><pubmed_abstract>This work aimed to synthesize new derivatives of 2-hydrazinylpyridine-3-carbonitrile and to investigate their biological activity as safeners for the 2,4-D herbicide. The new 2-hydrazinylnicotinonitriles were obtained in high yields (up to quantitative) under mild conditions (25 °C, dioxane) by treating 4,6-diaryl-2-bromo-3-cyanopyridines with hydrazine hydrate. The latter were synthesized by brominating 2-(3-oxo-1,3-diarylpropyl)malononitriles, the Michael adducts, which are readily available from 1,3-diarylpropenones (chalcones) and malononitrile. An unusual side product of the bromination/carbocyclization was isolated and characterized; it consisted of co-crystals of 3-benzoyl-4-hydroxy-4-phenyl-2,6-di-(p-tolyl)cyclohexane-1,1-dicarbonitrile and 3-benzoyl-5-bromo-4-hydroxy-4-phenyl-2,6-</pubmed_abstract><journal>International journal of molecular sciences</journal><pubmed_title>Synthesis, Reactions, and Agrochemical Studies of New 4,6-Diaryl-2-hydrazinylnicotinonitriles.</pubmed_title><pmcid>PMC12733256</pmcid><funding_grant_id>24-43-00003</funding_grant_id><funding_grant_id>22361132526</funding_grant_id><pubmed_authors>Daus ES</pubmed_authors><pubmed_authors>Achmiz RG</pubmed_authors><pubmed_authors>Kindop VK</pubmed_authors><pubmed_authors>Dotsenko VV</pubmed_authors><pubmed_authors>Feng YQ</pubmed_authors><pubmed_authors>Temerdashev AZ</pubmed_authors><pubmed_authors>Zhu QF</pubmed_authors><pubmed_authors>Yudaev IV</pubmed_authors><pubmed_authors>Dakhno PG</pubmed_authors><pubmed_authors>Daus YV</pubmed_authors><pubmed_authors>Levchenko AG</pubmed_authors><pubmed_authors>Aksenov AV</pubmed_authors><pubmed_authors>Aksenov NA</pubmed_authors><pubmed_authors>Aksenova IV</pubmed_authors></additional><is_claimable>false</is_claimable><name>Synthesis, Reactions, and Agrochemical Studies of New 4,6-Diaryl-2-hydrazinylnicotinonitriles.</name><description>This work aimed to synthesize new derivatives of 2-hydrazinylpyridine-3-carbonitrile and to investigate their biological activity as safeners for the 2,4-D herbicide. The new 2-hydrazinylnicotinonitriles were obtained in high yields (up to quantitative) under mild conditions (25 °C, dioxane) by treating 4,6-diaryl-2-bromo-3-cyanopyridines with hydrazine hydrate. The latter were synthesized by brominating 2-(3-oxo-1,3-diarylpropyl)malononitriles, the Michael adducts, which are readily available from 1,3-diarylpropenones (chalcones) and malononitrile. An unusual side product of the bromination/carbocyclization was isolated and characterized; it consisted of co-crystals of 3-benzoyl-4-hydroxy-4-phenyl-2,6-di-(p-tolyl)cyclohexane-1,1-dicarbonitrile and 3-benzoyl-5-bromo-4-hydroxy-4-phenyl-2,6-</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Dec</publication><modification>2026-05-27T08:02:59.606Z</modification><creation>2026-05-27T03:12:25.183Z</creation></dates><accession>S-EPMC12733256</accession><cross_references><pubmed>41465303</pubmed><doi>10.3390/ijms262411874</doi></cross_references></HashMap>