2-(Heptylthio)pyrimidine-4,6-diamine
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.
Authors
- Tursunali Kholikov
- Malokhat Uktamova
- Kohei Torikai (ORCID: https://orcid.org/0000-0002-9928-4300)
- Gulrukh Salieva (ORCID: https://orcid.org/0009-0008-2006-9060)
Institutions
- Kyushu University (JP)
- National University of Uzbekistan (UZ)
Publication Details
- Journal
- Molbank
- Published
- 2025-02-06
- DOI
- https://doi.org/10.3390/m1965
- Citations
- 2
- Primary Topic
- Synthesis and Characterization of Heterocyclic Compounds
- Type
- article
- Field-Weighted Citation Impact
- 1.87
Funders
- Japan International Cooperation Agency
- Japan Science and Technology Agency
- Science and Technology Research Partnership for Sustainable Development