Багатокомпонентна конденсація у синтезі заміщених 2-алкілсульфаніл-4,6-діарилпіридин-3-карбонітрилів та їх похідних

• Datum: 2014
• 1. Verfasser: Dyachenko, I. V.
• Format: Artikel
• Sprache: Ukrainian
• Veröffentlicht: National University of Pharmacy 2014
• Schlagworte: багатокомпонентна конденсація; халкони; малононітрил; алкілгалогеніди; сірководень; N-метилморфолін; ціанотіоацетамід; реакція Міхаеля; 2-алкілсульфанілпіридини; тієно[2; 3-b]піридини; піридо[3’; 2’; 4; 5]тієно[3; 2-d]піримідин; УДК 547.825
• Online Zugang: https://ophcj.nuph.edu.ua/article/view/ophcj.14.809
• Назва журналу: Journal of Organic and Pharmaceutical Chemistry

The multi-component condensation of chalcones, malononitrile, alkylhalides, hydrogen sulphide and N-methyl-morpholine completes with forming 2-alkylsulphanil-4,6-diarylpyridine-3-carbonitriles, which are used in the synthesis of the substituted 1,4-bis(3-cyano-6’-methoxyphenyl-4’-phenylpyridin-2-ylthio)butane, 3-amino-4,6-diaryl-2-R-thieno[2,3-b]pyridine, pyrido[3’,2’:4,5]thieno[3,2-d]pyrimidine. During the reaction the interaction of malononitrile with hydrogen sulfide forms cyanothioacetamide, which is reactive with chalcone by Michael reaction. The corresponding adduct intramolecularly cyclizes into the substituted pyridine-2-thiolate N-methylmorpholinium. The latter can be alkylated in situ by alkyl halides into the aforementioned heterocyclic ring systems. The substituted 2-alkylsulphanil-pyridines with a labile hydrogen atom in the SCH2 fragment are capable to cyclize by Thorpe-Ziegler under alkaline conditions in direction to the intramolecular interaction with the cyano group of the pyridine ring vicinally located towards the methylensulphanil fragment. 3-Amino-6-(4-methoxyphenyl)-4-phenyl-2-cyanotieno[2,3-b]pyridine in refluxing in formamide easily forms 4-amino-7-(4-methoxyphenyl)-9-phenylpyrido[3’,2’:4,5]thieno[3,2-d]pyrimidine previously unknown. The composition and structure of the newly synthesized compounds have been confirmed by elemental analysis, infrared spectroscopy (IR), nuclear magnetic resonance of protons (1H NMR) and mass spectrometry.