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

Gulrukh Salieva; Malokhat Uktamova; Kohei Torikai; Tursunali Kholikov

doi:10.3390/M1965

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

Gulrukh Salieva
, Malokhat Uktamova
, Kohei Torikai
, Tursunali Kholikov

無機・分析化学

研究成果: ジャーナルへの寄稿 › 学術誌 › 査読

2 被引用数 (Scopus)

抄録

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.

本文言語	フランス語
論文番号	M1965
ジャーナル	MolBank
巻	2025
号	1
DOI	https://doi.org/10.3390/M1965
出版ステータス	出版済み - 3月 2025

!!!All Science Journal Classification (ASJC) codes

生化学
物理化学および理論化学
有機化学

文献へのアクセス

10.3390/M1965

他のファイルとリンク

引用スタイル

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title = "2-(Heptylthio)pyrimidine-4,6-diamine",

abstract = "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.",

keywords = "4,6-diamino-2-mercaptopyrimidine, S-alkylation, alkylation",

author = "Gulrukh Salieva and Malokhat Uktamova and Kohei Torikai and Tursunali Kholikov",

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doi = "10.3390/M1965",

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T1 - 2-(Heptylthio)pyrimidine-4,6-diamine

AU - Salieva, Gulrukh

AU - Uktamova, Malokhat

AU - Torikai, Kohei

AU - Kholikov, Tursunali

PY - 2025/3

Y1 - 2025/3

N2 - 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.

AB - 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.

KW - 4,6-diamino-2-mercaptopyrimidine

KW - S-alkylation

KW - alkylation

UR - https://www.scopus.com/pages/publications/105001247287

UR - https://www.scopus.com/pages/publications/105001247287#tab=citedBy

U2 - 10.3390/M1965

DO - 10.3390/M1965

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AN - SCOPUS:105001247287

SN - 1422-8599

VL - 2025

JO - MolBank

JF - MolBank

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