Synthesis and Azido-Tetrazole Tautomerism of New Methylsulfanyl Thieno[3,2-d]pyrimidine Derivatives
- Authors: Sirakanyan S.N.1, Hakobyan E.K.1, Hovakimyan A.A.1
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Affiliations:
- Mnjoyan Institute of Fine Organic Chemistry, Scientific Technological Center of Organic and Pharmaceutical Chemistry
- Issue: Vol 55, No 12 (2019)
- Pages: 1840-1846
- Section: Article
- URL: https://journal-vniispk.ru/1070-4280/article/view/221446
- DOI: https://doi.org/10.1134/S1070428019120054
- ID: 221446
Cite item
Abstract
New 7-amino, 7-azido, and 7-alkylsulfanyl derivatives have been synthesized from 7-chloro-9-(methylsulfanyl)-4-(propan-2-yl)-2,3-dihydro-1H-cyclopenta[4′,5′]pyrido[3′,2′:4,5]thieno[3,2-d]pyrimidine. 7-Azido-9-(methylsulfanyl)-4-(propan-2-yl)-2,3-dihydro-1H-cyclopenta[4′,5′]pyrido[3′,2′:4,5]thieno[3,2-d]-pyrimidine has been found to exist in solution as a mixture of azido and tetrazole tautomers, whereas only its tetrazole form is present in the crystalline state.
About the authors
S. N. Sirakanyan
Mnjoyan Institute of Fine Organic Chemistry, Scientific Technological Center of Organic and Pharmaceutical Chemistry
Author for correspondence.
Email: shnnr@mail.ru
Armenia, Yerevan, 0014
E. K. Hakobyan
Mnjoyan Institute of Fine Organic Chemistry, Scientific Technological Center of Organic and Pharmaceutical Chemistry
Email: shnnr@mail.ru
Armenia, Yerevan, 0014
A. A. Hovakimyan
Mnjoyan Institute of Fine Organic Chemistry, Scientific Technological Center of Organic and Pharmaceutical Chemistry
Email: shnnr@mail.ru
Armenia, Yerevan, 0014
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