Asosiy kontentga oʻtish
Maqola

Diversification of a Thieno[2,3-<i>d</i>]pyrimidin-4-one Scaffold via Regioselective Alkylation Reactions

Sergey G. DzhavakhishviliDepartment of Heterocyclic Compounds, SSI “Institute for Single Crystals” of National Academy Science of Ukraine, Lenin Avenue 60, Kharkiv 61001, Ukraine, and, Fachbereich Chemie der Universitat Konstanz, Fach M-720, Universitatsstrausse 10, 78457 Konstanz, GermanyNikolay Yu. GorobetsDepartment of Heterocyclic Compounds, SSI “Institute for Single Crystals” of National Academy Science of Ukraine, Lenin Avenue 60, Kharkiv 61001, Ukraine, and, Fachbereich Chemie der Universitat Konstanz, Fach M-720, Universitatsstrausse 10, 78457 Konstanz, GermanySvitlana ShishkinaState Scientific Institution “Institute for Single Crystals” of National Academy of Sciences of UkraineОлег В. ШишкинDepartment of Heterocyclic Compounds, SSI “Institute for Single Crystals” of National Academy Science of Ukraine, Lenin Avenue 60, Kharkiv 61001, Ukraine, and, Fachbereich Chemie der Universitat Konstanz, Fach M-720, Universitatsstrausse 10, 78457 Konstanz, GermanySergey M. DesenkoState Scientific Institution “Institute for Single Crystals” of National Academy of Sciences of UkraineUlrich GrothState Scientific Institution “Institute for Single Crystals” of National Academy of Sciences of Ukraine
2009en

Ochiq kirish: yoʻq

ABI

Annotatsiya

The 2-aryl-2,3,5,6,7,8-hexahydro[1]benzothieno[2,3-d]pyrimidin-4(1H)-ones and 2-aryl-5,6,7,8-tetrahydro[1]benzothieno[2,3-d]pyrimidin-4(3H)-ones have been diversified by alkylation reactions, applying benzylchlorides and N-substituted 2-chloroacetamides as alkylating agents. Under the found uniform conditions the substitution direction does not depend on the structure of the alkylating agent and gives monoalkylated products in high yields with simple workup. The alkylation of the 2,3-dihydropyrimidin-4(1H)-one derivatives proceeds onto the N1-position; however, in the case of pyrimidin-4(3H)-ones the O-alkylated products are formed selectively. An alternative strategy for the synthesis of the N1-benzyl-2,3-dihydropyrimidin-4(1H)-one derivatives is also developed. It applies the redaction of N2-substituted Gewald's amides with aromatic aldehydes and allows simple introduction of various substituents in the final molecule.

Hali tarjima qilinmagan

Identifikatorlar

Iqtiboslar va manbalar

2 ta iqtibos0 ta foydalanilgan manba