A simple and efficient automatable one step synthesis of triazolopyridines from carboxylic acids
作者:Ying Wang、Kathy Sarris、Daryl R. Sauer、Stevan W. Djuric
DOI:10.1016/j.tetlet.2007.02.004
日期:2007.3
Triazolopyridines can be rapidly and efficiently synthesized from a variety of carboxylic acids with 2-hydrazinopyridines in one simple step. The use of commercially available PS-PPh3 resin combined with microwave heating delivered the product triazolopyridines in good yields and purities.
TBAI/TBHP-Catalyzed Synthesis of [1,2,4]Triazolo[4,3-a]pyridines and 3,5-Diaryl-1,2,4-oxadiazoles via Oxidative Cleavage of C=C Double Bond
作者:S. L. Matcha、S. Vidavalur
DOI:10.1134/s1070428021090141
日期:2021.9
Abstract A simple and efficient protocol has been described for the synthesis of [1,2,4]triazolo[4,3-a]pyridines and 3,5-disubstituted-1,2,4-oxadiazoles by reacting 2-hydrazinylpyridine and benzamidoximes, respectively, with styrenes via TBAI/TBHP-mediated oxidative cleavage of C=C bond under ligand- and metal-free conditions.
An iodobenzenediacetate (IBD)-mediated simple and green method was determined for the intramolecular oxidative cyclization of 3-aryl-2-pyridiylhydrazones of different aromatic aldehydes in an aqueous medium at room temperature. This efficient strategy provides a route to the synthesis of 3-aryl-1,2,4-triazolo[4,3-a]pyridines in water which eliminates the requirement to use costly and unsafe volatile
A metal-free iodine/TBHP-mediated oxidative C-N bond formation for the one-pot synthesis of N-fused 1,2,4-triazoles and related heterocycles via cyclization has been developed. This reaction which is amenable to scale-up affords the corresponding products with good to excellent yields and tolerates a wide range of functional groups. (C) 2018 Elsevier Ltd. All rights reserved.
ARYL AND HETEROARYL ETHER COMPOUNDS AS ROR GAMMA MODULATORS
申请人:GLENMARK PHARMACEUTICALS S.A.
公开号:US20170022195A1
公开(公告)日:2017-01-26
The present disclosure is directed to compounds of formula (I) and pharmaceutically acceptable salts thereof, wherein Ring A, Ring B, R, R
2
, R
3
, n, and p are as defined herein, which are active as modulators of retinoid-related orphan receptor gamma t (RORγt). These compounds prevent, inhibit, or suppress the action of RORγt and are therefore useful in the treatment of RORγt mediated diseases, disorders, syndromes or conditions such as, e.g., pain, inflammation, COPD, asthma, rheumatoid arthritis, colitis, multiple sclerosis, psoriasis, neurodegenerative diseases and cancer.