New Approaches to the Synthesis of 6-Amino-4-aryl-5-(4-arylthiazol-2-yl)-2-methoxynicotinonitriles

Abstract Reactions of (2E)-3-aryl-2-(4-arylthiazol-2-yl)acrylonitriles, malononitrile, and sodium methoxide or 2-[4-(4-bromophenyl)thiazol-2-yl]acetonitrile, 4-methoxybenzylidenemalononitrile, and potassium hydroxide in methanol proceed to give 6-amino-4-aryl-5-(4-arylthiazol-2-yl)-2-methoxynicotinonitriles in 38–47% yields.

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Publication Details

Journal
Russian Journal of General Chemistry
Published
2026-09-12
DOI
https://doi.org/10.1134/s1070363226601766
Primary Topic
Synthesis and Reactivity of Sulfur-Containing Compounds
Type
article
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article

New Approaches to the Synthesis of 6-Amino-4-aryl-5-(4-arylthiazol-2-yl)-2-methoxynicotinonitriles

D. V. Nikitenko, Andrei V. Churakov, N. A. Pakholka, С. Г. Кривоколыско
Russian Journal of General Chemistry
Synthesis and Reactivity of Sulfur-Containing Compounds
article

New Approaches to the Synthesis of 6-Amino-4-aryl-5-(4-arylthiazol-2-yl)-2-methoxynicotinonitriles

D. V. Nikitenko, Andrei V. Churakov, N. A. Pakholka, С. Г. Кривоколыско
article en

Abstract

Abstract Reactions of (2E)-3-aryl-2-(4-arylthiazol-2-yl)acrylonitriles, malononitrile, and sodium methoxide or 2-[4-(4-bromophenyl)thiazol-2-yl]acetonitrile, 4-methoxybenzylidenemalononitrile, and potassium hydroxide in methanol proceed to give 6-amino-4-aryl-5-(4-arylthiazol-2-yl)-2-methoxynicotinonitriles in 38–47% yields.

Russian Journal of General ChemistryVol. 96(10)
NS Kurnakova Institute of General and Inorganic Chemistry (RU), Institute of Physical and Organic Chemistry (BY), Luhansk State Medical University (UA)
Openalex Percentile: Top 20%
Synthesis and Reactivity of Sulfur-Containing Compounds
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