2,5-Dimethylbenzyl 2-{(4,6-diaminopyrimidin-2-yl)thio}acetate

2,5-Dimethylbenzyl 2-{(4,6-diaminopyrimidin-2-yl)thio}acetate was prepared by an alkylation reaction between the sodium salt of 4,6-diamino-2-mercaptopyrimidine and chloroacetic acid. The structure was unambiguously elucidated based on high-resolution mass spectrometry (HRMS) as well as spectroscopies such as infrared (IR) and nuclear magnetic resonance (NMR).

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Publication Details

Journal
Molbank
Published
2025-11-19
DOI
https://doi.org/10.3390/m2091
Primary Topic
Synthesis and biological activity
Type
article
Field-Weighted Citation Impact
0.00

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article

2,5-Dimethylbenzyl 2-{(4,6-diaminopyrimidin-2-yl)thio}acetate

Tursunali Kholikov, Sardorbek Otajonov, Malokhat Uktamova, Kohei Torikai et al.
Molbank
Synthesis and biological activity
article

2,5-Dimethylbenzyl 2-{(4,6-diaminopyrimidin-2-yl)thio}acetate

Tursunali Kholikov, Sardorbek Otajonov, Malokhat Uktamova, Kohei Torikai, Gulrukh Salieva
article en

Abstract

2,5-Dimethylbenzyl 2-{(4,6-diaminopyrimidin-2-yl)thio}acetate was prepared by an alkylation reaction between the sodium salt of 4,6-diamino-2-mercaptopyrimidine and chloroacetic acid. The structure was unambiguously elucidated based on high-resolution mass spectrometry (HRMS) as well as spectroscopies such as infrared (IR) and nuclear magnetic resonance (NMR).

MolbankVol. 2025(4)
Kyushu University (JP), Tashkent Pharmaceutical Institute (UZ), Tashkent Pediatric Medical Institute (UZ), National University of Uzbekistan (UZ)
Japan International Cooperation Agency, Japan Science and Technology Agency, Science and Technology Research Partnership for Sustainable Development
Openalex Percentile: Top 73%
Synthesis and biological activity
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