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ЖУРНАЛЫ // Mendeleev Communications // Архив

Mendeleev Commun., 2023, том 33, выпуск 3, страницы 323–324 (Mi mendc385)

Эта публикация цитируется в 2 статьях

Communications

Spirocyclic azetidines for drug discovery: Novel Boc-protected 7'H-spiro[azetidine-3,5'-furo[3,4-d ]pyrimidines]

A. Lukina, L. Vinogradovaa, K. Komarovaa, M. Krasavinbc

a M.V. Lomonosov Institute of Fine Chemical Technologies, MIREA - Russian Technological University, Moscow, Russian Federation
b Immanuel Kant Baltic Federal University, Kaliningrad, Russian Federation
c Institute of Chemistry, St. Petersburg State University, St. Petersburg, Russian Federation


Аннотация: A novel spirocyclic scaffold of 7'H-spiro[azetidine-3,5'-furo[3,4-d]pyrimidine] chemotype was synthesized in N-Boc-protected form. However, the scaffold was revealed to be unstable to storage when deprotected. The solution was found in the brief removal of the Boc protecting group and rapid acylation of the liberated NH-azetidine with a carboxylic acid imidazolide.

Ключевые слова: azetidines, spirocycles, pyrimidines, instability in deprotected form, privileged scaffold, 5-nitrofuroyl.

Язык публикации: английский

DOI: 10.1016/j.mencom.2023.04.008



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