T3P-Mediated N–N Cyclization for the Synthesis of 1,2,4-Triazolo[1,5-a]pyridines-Reference-Cited by-同舟云学术

T3P-Mediated N–N Cyclization for the Synthesis of 1,2,4-Triazolo[1,5-a]pyridines

Published:2019-10-28 Issue:11 Volume:23 Page:2510-2515
ISSN:1083-6160
Container-title:Organic Process Research & Development
language:en
Short-container-title:Org. Process Res. Dev.

Author:

Ayothiraman Rajaram¹,Bandaru Durgarao¹,Paranthaman Ranjitha¹,Fenster Michaël²^ORCID,Eastgate Martin D.²^ORCID,Vaidyanathan Rajappa¹^ORCID

Affiliation:

1. Chemical Development and API Supply, Biocon Bristol-Myers Squibb Research and Development Center, Biocon Park, Jigani Link Road, Bommasandra IV, Bengaluru 560099, India

2. Chemical and Synthetic Development, Bristol-Myers Squibb, 1 Squibb Drive, New Brunswick, New Jersey 08903, United States

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.oprd.9b00396

Reference8 articles.

1. 2-Amino-[1,2,4]triazolo[1,5-a]pyridines as JAK2 inhibitors

2. Design, synthesis, and evaluation of novel VEGFR2 kinase inhibitors: Discovery of [1,2,4]triazolo[1,5-a]pyridine derivatives with slow dissociation kinetics

3. Dimethylformamide dimethyl acetal as a building block in heterocyclic synthesis

4. Heterocycles. CXVIII. Pyridazines. LXVI. Novel method of annelation of the 1,2,4-triazole ring of the N2-C3 bond to azines

5. New Method for the General Synthesis of [1,2,4]Triazolo[1,5-a]pyridines

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5. Base-Promoted Tandem S_NAr/Boulton–Katritzky Rearrangement: Access to [1,2,4]Triazolo[1,5-a]pyridines;Organic Letters;2022-04-20