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Institute of Organic Chemistry & Biochemistry, Collection of Czechoslovak Chemical Communications, 5(60), p. 875-882, 1995

DOI: 10.1135/cccc19950875

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Synthesis of Acyclic Nucleotide Analogues Derived from 2-(Aminomethyl)adenine and 2-(Aminomethyl)hypoxanthine

Journal article published in 1995 by Michal Hocek ORCID, Milena Masojídková, Antonín Holý
This paper is available in a repository.
This paper is available in a repository.

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Abstract

Synthesis of a series of 2-(aminomethyl)-9-(2-phosphonomethoxyalkyl)adenines VI and hypoxanthines VII is reported. The protected 2-(aminomethyl)adenine I was selectively alkylated with [bis(2-propoxy)phosphonylmethoxy]alkyl chlorides or tosylates II and the obtained 9-[bis(2-propoxy)phosphonylmethoxy]alkyl-2-(benzyloxycarbonyla minomethyl)adenines IV were oxodeaminated to give the corresponding hypoxanthine derivatives V . The intermediates IV and V were completely deprotected by treatment with iodotrimethylsilane under formation of the title compounds VI and VII .