Facile, regioselective syntheses of N-alkylated 2,3-diaminopyridines and imidazo[4,5-b]pyridines

DOI: 10.1021/jo00109a029

Source and publish data:

Journal of Organic Chemistry p. 960 - 965 (1995)

Update date:2022-07-31

Topics:

Authors:

Khanna Khanna

Weier Weier

Lentz Lentz

Swenton Swenton

Lankin Lankin

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Article abstract of DOI:10.1021/jo00109a029

Useful strategies are reported for the differentiation and selective synthetic manipulations of amino groups at the 2- and 3-positions of pyridines. It has been found that 2,3-diaminopyridine reacts with aldehydes under reductive amination conditions to g

Full text of DOI:10.1021/jo00109a029

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Product name:Formamide, N-(3-amino-2-pyridinyl)- (9CI)

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