Issue 35, 2021

Ruthenium-catalyzed N-alkylation of amino-1,3,5-triazines using alcohols

Abstract

An efficient ruthenium-catalyzed N-alkylation of amino 1,3,5-triazines with alcohols was achieved via a BH/HA strategy. Following this simple, facile, and high atom economical protocol, a broad range of products was prepared in moderate to good yields and heterocyclic or benzylic alcohols containing various functionalities were tolerated. The application of the reaction is also further demonstrated by the synthesis of alkylated secondary amine-1,3,5-triazines from olefinated amino-1,3,5-triazines and alcohols via a one pot N-alkylation and reductive reactions.

Graphical abstract: Ruthenium-catalyzed N-alkylation of amino-1,3,5-triazines using alcohols

Supplementary files

Article information

Article type
Paper
Submitted
26 Jun 2021
Accepted
17 Jul 2021
First published
23 Jul 2021

New J. Chem., 2021,45, 15776-15779

Ruthenium-catalyzed N-alkylation of amino-1,3,5-triazines using alcohols

J. Zhao, P. Zhong, Z. Xie, W. Zhou, C. Zhang and D. Cui, New J. Chem., 2021, 45, 15776 DOI: 10.1039/D1NJ03116C

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