One-Pot Synthesis of 6-Aminopyrido[2,3-d ]pyrimidin-7-ones-Reference-Cited by-同舟云学术

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One-Pot Synthesis of 6-Aminopyrido[2,3-d ]pyrimidin-7-ones

Published:2018-11-25 Issue:46 Volume:2018 Page:6519-6523
ISSN:1434-193X
Container-title:European Journal of Organic Chemistry
language:en
Short-container-title:Eur. J. Org. Chem.

Author:

Zinchenko Anna M.¹,Muzychka Lyubov V.¹,Kucher Olexandr V.¹,Sadkova Iryna V.²,Mykhailiuk Pavel K.²³^ORCID,Smolii Oleg B.¹

Affiliation:

1. Institute of Bioorganic Chemistry and Petrochemistry of the National Academy of Sciences of Ukraine; Murmanska 1 02094 Kyiv Ukraine

2. Enamine Ltd.; Chervonotkatska 78 01103 Kyiv Ukraine

3. Chemistry Department; Taras Shevchenko National University of Kyiv; Volodymyrska 64 01601 Kyiv Ukraine

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ejoc.201801204/fullpdf

Reference60 articles.

1. Recent advances in the chemistry and biology of pyridopyrimidines

2. Discovery of the Irreversible Covalent FGFR Inhibitor 8-(3-(4-Acryloylpiperazin-1-yl)propyl)-6-(2,6-dichloro-3,5-dimethoxyphenyl)-2-(methylamino)pyrido[2,3-d]pyrimidin-7(8H)-one (PRN1371) for the Treatment of Solid Tumors

3. Synthesis and antitumor activity of 2,4-diamino-6-(2,5-dimethoxybenzyl)-5-methylpyrido[2,3-d]pyrimidine

Cited by 6 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Design, Synthesis, and Bioevaluation of Pyrido[2,3-d]pyrimidin-7-ones as Potent SOS1 Inhibitors;ACS Medicinal Chemistry Letters;2023-01-12

2. о-Aminopyrimidine Aldehydes and Ketones: Synthesis and use as Precursors to Fused Pyrimidines;Chemistry of Heterocyclic Compounds;2022-11

3. Bicyclic 6-6 Systems: Three Heteroatoms 1:2;Comprehensive Heterocyclic Chemistry IV;2022

4. Expanding the Diversity at the C-4 Position of Pyrido[2,3-d]pyrimidin-7(8H)-ones to Achieve Biological Activity against ZAP-70;Pharmaceuticals;2021-12-15

5. Six-Membered Ring Systems: Diazines and Benzo Derivatives;Progress in Heterocyclic Chemistry;2020

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