Мақола

2-(Heptylthio)pyrimidine-4,6-diamine

Gulrukh SalievaFaculty of Chemistry, National University of Uzbekistan Named After Mirzo Ulugbek, 4 University Str., Tashkent 100174, UzbekistanMalokhat UktamovaDepartment of Chemistry, Graduate School and Faculty of Science, Kyushu University, 744 Motooka, Nishi-ku, Fukuoka 819-0395, JapanKohei TorikaiDepartment of Chemistry, Graduate School and Faculty of Science, Kyushu University, 744 Motooka, Nishi-ku, Fukuoka 819-0395, JapanTursunali KholikovFaculty of Chemistry, National University of Uzbekistan Named After Mirzo Ulugbek, 4 University Str., Tashkent 100174, Uzbekistan

Molbankjournal2025en

ABI

Аннотация

Thiopyrimidines represent one of the most active classes of compounds, possessing a wide spectrum of biological activities. Herein, we report the synthesis of 2-(heptylthio)pyrimidine-4,6-diamine (HPDA) via S-alkylation. The structure of HPDA was elucidated using 1H and 13C nuclear magnetic resonance (NMR), heteronuclear multiple bond correlation (HMBC), high resolution mass (HRMS), and infrared (IR) spectroscopies.

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Мавзулар

Synthesis and Characterization of Heterocyclic Compounds Synthesis and biological activity Quinazolinone synthesis and applications

Идентификаторлар

DOI: 10.3390/m1965

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