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Mendeleev Communications, 2024, Volume 34, Issue 1, Pages 129–130
DOI: https://doi.org/10.1016/j.mencom.2024.01.039
(Mi mendc64)
 

Communications

New synthesis of 6,8-diamino-substituted pyrano[3,4-c]pyridines from related pyrano[3,4-c]pyridin-6-one

E. G. Paronikyan, A. G. Ayvazyan, S. S. Mamyan, Sh. Sh. Dashyan

Scientific Technological Center of Organic and Pharmaceutical Chemistry, National Academy of Sciences of the Republic of Armenia, Yerevan, Armenia
Abstract: The tosylation of 3,3-dimethyl-8-(morpholin-4-yl)-6-oxo-3,4,6,7-tetrahydro-1H-pyrano[3,4-c]pyridine-5-carbonitrile with TsCl occurs at the oxo group of the NH-lactam moiety. The subsequent nucleophilic displacement of O-tosylate by various amines affords the title compounds in good yields.
Keywords: pyrano[3,4-c]pyridines, p-toluenesulfonyl chloride, alkylation, regioselectivity, O-tosylate, amines.
Document Type: Article
Language: English
Supplementary materials:
Supplementary_data_1.pdf (2.1 Mb)


Citation: E. G. Paronikyan, A. G. Ayvazyan, S. S. Mamyan, Sh. Sh. Dashyan, “New synthesis of 6,8-diamino-substituted pyrano[3,4-c]pyridines from related pyrano[3,4-c]pyridin-6-one”, Mendeleev Commun., 34:1 (2024), 129–130
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