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Communications

Design and synthesis of spiro-linked azacycloalkane–dihydropyrano[4,3-d]pyrimidine compounds

M. E. Zhuravleva, K. Yu. Komarovaa, L. V. Khudiakovaa, M. V. Chudinova, A. Yu. Lukina, D. V. Dar’inb

a M. V. Lomonosov Institute of Fine Chemical Technologies, MIREA – Russian Technological University, 119454 Moscow, Russian Federation
b St. Petersburg State University, 198504 St. Petersburg, Russian Federation


Àííîòàöèÿ: New dihydropyrano[4,3-d]pyrimidines bearing 7-positioned spiro-linked azacycloalkane moieties were obtained by the Prins spirocyclization of commercially available N-protected azacycloalkanones followed by the regiospecific condensation with dimethylformamide dimethyl acetal and amidines. The new scaffold thus accessed appears to be a valuable building block for drug development.

Êëþ÷åâûå ñëîâà: spiro compounds, pyrimidine synthesis, pyrano[4,3-d]pyrimidine, regiospecificity, drug design.

Ïîñòóïèëà â ðåäàêöèþ: 07.11.2025
Ïðèíÿòà â ïå÷àòü: 12.01.2026

ßçûê ïóáëèêàöèè: àíãëèéñêèé

DOI: 10.71267/mencom.7965



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