Synthesis of Substituted Thienopyrimidinones Based on 2-Amino-4-(1,4-benzodioxan-2-yl) Thiophene-3-carboxylic Acid Ethyl Ester

Svetlana O. Vardanyan; Вартанян Светлана Ониковна; Alina S. Avagyan; Авакян Алина Суреновна; Amalya B. Sargsyan; Саргсян Амаля Багратовна; Seda A. Harutyunyan; Арутюнян Седа Арутюновна; Hrachik V. Gasparyan; Гаспарян Грачик Ваграмович; Asya A. Aghekyan; Агекян Aся Aгековна

doi:10.31857/S0514749225040109

Synthesis of Substituted Thienopyrimidinones Based on 2-Amino-4-(1,4-benzodioxan-2-yl) Thiophene-3-carboxylic Acid Ethyl Ester

作者: Vardanyan S.O.¹, Avagyan A.S.¹, Sargsyan A.B.¹, Harutyunyan S.A.¹, Gasparyan H.V.¹, Aghekyan A.A.¹
隶属关系:
1. Scientific Technological Center of Organic and Pharmaceutical Chemistry of the NAS of the Republic of Armenia
期: 卷 61, 编号 4 (2025)
页面: 447-452
栏目: ЭКСПЕРИМЕНТАЛЬНЫЕ СТАТЬИ
URL: https://consilium.orscience.ru/0514-7492/article/view/689667
DOI: https://doi.org/10.31857/S0514749225040109
EDN: https://elibrary.ru/SEAFNB
ID: 689667

如何引用文章

全文:

开放存取

##reader.subscriptionAccessGranted##
受限制的访问

订阅或者付费存取

详细
全文:
作者简介
参考
补充文件
统计

详细

The previously obtained N-arylamides of 2-amino-4-(1,4-benzodioxan-2-yl)thiophene-3-carboxylic acid ethyl ester were cyclized to 2-aryl-substituted 3-aminothienopyrimidin-4-ones by the action of hydrazine hydrate. By condensation of the starting amino ester with chloroacetic acid chloride was obtained chloramide, which was converted by the action of piperidine and morpholine into the corresponding aminomethylamides. The latters were also subjected to cyclization with hydrazine hydrate to 3-aminothienopyrimidin-4-one derivatives with aminomethyl substituents in the second position. The antihypoxic activity of the synthesized compounds was studied.

关键词

1,4-benzodioxane, chloramide, 2-amino-4-(1,4-benzodioxan-2-yl)thiophene-3-carboxylic acid ethyl ester, thienopyrimidin-4-one, cyclization

全文:

参考

The use of stems in the selection of International Nonprietary Names (INN) for pharmaceutical substances. Geneva, WHO, 2018.
Giri R.S., Thaker H. M., Giordano T., Williams J., Rogers D, Vasu K.K., Sudarsanam V. Bioorg. Med. Chem. 2010, 18, 2796. doi: 10.1016/j.bmc.2010.01.007
Tang J., Huber A.D, Pineda D. L., Boschert K.N., Wolf J.J., Kankanala J., Xie J., Sarafianos S.G., Wang Zh. Eur. J. Med. Chem. 2019, 164, 179. doi: 10.1016/j.ejmech.2018.12.047
Jin X., Merrett J., Tong Sh., Flower B., Xie J., Yu R., Tian Sh., Gao L., Zhao J., .Wang X, Jiang T., Proud Ch.G. Eur. J. Med. Chem. 2019, 162, 735–751. doi 10.1016/j. ejmech. 2018.10.070
Вартанян С.О., Агекян А.A., Авакян А.С., Арутюнян С.А., Гаспарян Г.В. ЖОрХ. 2019, 55, 690–693. [Vardanyan S.O., Aghekyan A.A., Avagyan A.S., Harutyunyan S.A., Gasparyan H.V. Russ. J. Org. Chem. 2019, 55, 598–601.] doi: 10.1134/S1070428019050038
Арутюнян С.А. Вестник МАНЭБ. 2005, 10, 169–173.