Using a Johnson‐Claisen Rearrangement Strategy to Construct Azaindoles – A Streamlined and Concise Route for the Commercial Process of Fevipiprant-Reference-Cited by-同舟云学术

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Using a Johnson‐Claisen Rearrangement Strategy to Construct Azaindoles – A Streamlined and Concise Route for the Commercial Process of Fevipiprant

Published:2021-08-18 Issue:31 Volume:2021 Page:4490-4494
ISSN:1434-193X
Container-title:European Journal of Organic Chemistry
language:en
Short-container-title:Eur. J. Org. Chem.

Author:

Mathes Christian¹,Riss Bernard¹,Rüegger Ueli¹,Hueber Lukas¹,Dedic Darija¹,Fei Zhongbo²,Reijer Carolien¹,Königsberger Kurt¹,Napp Matthias¹,Schlama Thierry¹,Dempsey Glen³,Lustenberger Philipp¹^ORCID

Affiliation:

1. Chemical and Analytical Development Novartis Pharma AG CH-4056 Basel Switzerland

2. Chemical and Analytical Development Suzhou Novartis Pharma Technology Company Ltd. Changshu, Jiangsu 215537 China

3. Novartis Technical Operations/Small Molecules Novartis Ringaskiddy Limited Ringaskiddy, County Cork Ireland

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ejoc.202100686

Reference34 articles.

2. Discovery of Fevipiprant (NVP-QAW039), a Potent and Selective DP2 Receptor Antagonist for Treatment of Asthma

4. Synthesis and reactivity of 7-azaindole (1H-pyrrolo[2,3-b]pyridine)

Cited by 1 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. Streamlined Synthesis of Fevipiprant;Synfacts;2021-10-19

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