[CuI(PPh3)3]-Mediated Arylation of 1,2,3-Triazoles

DOI: 10.14469/hpc/14893 Metadata

Created: 2024-12-23 09:22

Last modified: 2025-05-08 14:27

Author: Silvia Diez-Gonzalez

License: Creative Commons: Public Domain Dedication 1.0

Funding: (none given)

Co-author: Jialei Qian
Co-author: Matthew Foulkes
Co-author: Raul Alberto Pacheco Muino
Co-author: Vera Kleene

Description

The arylation of 1,4-disubstituted triazoles with [CuI(PPh3)3] is reported. The reactions were carried out in relatively concentrated solutions of hot DMF in the presence of air and moisture. These conditions were suitable for a range of substrates, specifically triazoles containing a pyridyl group, which are particularly interesting in a diverse applications such as ancillary ligands or bioactive compounds, for instance

Members

DOIDescription
10.14469/hpc/15055 2j: 1-octyl-4-phenyl-1H-1,2,3-triazole
10.14469/hpc/14922 2a: 1-benzyl-5-(4-methoxyphenyl)-4-phenyl-1H-1,2,3-triazole
10.14469/hpc/14934 2b: 1-benzyl-4-phenyl-5-(p-tolyl)-1H-1,2,3-triazole
10.14469/hpc/14940 2k: 2-(1-benzyl-5-(4-methoxyphenyl)-1H-1,2,3-triazol-4-yl)pyridine
10.14469/hpc/14935 2c: 1-benzyl-4,5-diphenyl-1H-1,2,3-triazole
10.14469/hpc/14936 2d: 1-benzyl-5-(naphthalen-1-yl)-4-phenyl-1H-1,2,3-triazole
10.14469/hpc/14937 2e: 1-benzyl-5-(4-chlorophenyl)-4-phenyl-1H-1,2,3-triazole
10.14469/hpc/14946 2r: 3-(1-benzyl-5-(4-chlorophenyl)-1H-1,2,3-triazol-4-yl)pyridine
10.14469/hpc/14938 2g: 6-(4-phenyl-5-(p-tolyl)-1H-1,2,3-triazol-1-yl)hexanenitrile
10.14469/hpc/14939 2h: 6-(5-(4-methoxyphenyl)-4-phenyl-1H-1,2,3-triazol-1-yl)hexanenitrile
10.14469/hpc/14945 2q: 3-(1-benzyl-5-(naphthalen-1-yl)-1H-1,2,3-triazol-4-yl)pyridine
10.14469/hpc/14944 2p: 3-(1-benzyl-5-(p-tolyl)-1H-1,2,3-triazol-4-yl)pyridine
10.14469/hpc/14943 2n: 2-(1-benzyl-5-(4-chlorophenyl)-1H-1,2,3-triazol-4-yl)pyridine
10.14469/hpc/14942 2m: 2-(1-benzyl-5-(naphthalen-1-yl)-1H-1,2,3-triazol-4-yl)pyridine
10.14469/hpc/14941 2l: 2-(1-benzyl-5-(p-tolyl)-1H-1,2,3-triazol-4-yl)pyridine

Associated DOIs

Current dataset ...DOIDescription
References 10.1002/cctc.202500111 Published article

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