| Literature DB >> 31181881 |
Siva Sankar Murthy Bandaru1, Shatrughn Bhilare2, Jesvita Cardozo2, Nicolas Chrysochos1, Carola Schulzke1, Yogesh S Sanghvi3, Krishna Chaitanya Gunturu4, Anant R Kapdi2,5.
Abstract
The thioetherification of heteroaryl chlorides is an essential synthetic methodology that provides access to bioactive drugs and agrochemicals. Due to their (actual or potential) industrial importance, the development of efficient and low-temperature protocols for accessing these compounds is a requirement for economic and ecologic reasons. A particular highly effective catalytic protocol using the Pd/PTABS system at only 50 °C was developed accordingly. The coupling between chloroheteroarenes and a variety of less reactive arylthiols and alkylthiols was carried out with a high efficiency. Heteroarenes of commercial relevance such as purines and pyrimidines were also found to be useful substrates for the reported transformation. The commercial drug Imuran (azathioprine) was synthesized as an example, and its preparation could be optimized. DFT studies were performed to understand the electronic effects of the tested ligands on the catalytic reaction.Entities:
Year: 2019 PMID: 31181881 DOI: 10.1021/acs.joc.9b00840
Source DB: PubMed Journal: J Org Chem ISSN: 0022-3263 Impact factor: 4.354