84741-86-6Relevant articles and documents
Crystal structure, Hirshfeld surface analysis and DFT studies of N-(4-acetylphenyl)quinoline-3-carboxamide
Brito, Iván,Cisterna, Jonathan,Ferrer, Karoll,Gutiérrez, Margarita,Osorio, Edison,Polo-Cuadrado, Efraín
, (2021/08/05)
Crystalline organic compound, N-(4-acetylphenyl)quinoline-3-carboxamide (4) was readily prepared using our previously reported experimental procedure by the reaction of quinoline-3-carboxylic acid (1) with thionyl chloride to generate the acid chloride in
Heterocyclic compound and preparation and application thereof
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Paragraph 0222-0224, (2020/07/24)
The invention relates to bromodomain inhibitors, and provides a compound represented by a general formula I, a pharmaceutically acceptable salt, an enantiomer, a diastereoisomer, an atropisomer, a racemate, a polymorph, a solvate or an isotope-labeled compound (including deuterium substitution) thereof, a preparation method thereof, a pharmaceutical composition containing the same, and applicationthereof in pharmacy.
Ultrasound-assisted synthesis of novel chalcone, heterochalcone and bis-chalcone derivatives and the evaluation of their antioxidant properties and as acetylcholinesterase inhibitors
Polo, Efraín,Ibarra-Arellano,Prent-Pe?aloza, Luis,Morales-Bayuelo, Alejandro,Henao, José,Galdámez, Antonio,Gutiérrez, Margarita
, (2019/07/08)
The chalcone and bis-chalcone derivatives have been synthesized under sonication conditions via Claisen-Schmidt condensation with KOH in ethanol at room temperature (20–89%). The structures were established on the basis of NMR, IR, Single-crystal XRD, and