71722-05-9

Upstream product

• 861032-74-8 4-chloro-2,6-diphenyl-5-propyl-pyrimidine 
• 591-51-5 phenyllithium 
• 71722-04-8 2-n-butyl-1,2-dihydro-2,4,6-triphenyl-1,3,5-triazine 
• 493-77-6 2,4,6-triphenyl-1,3,5-triazine 
• 858269-44-0 2,6-diphenyl-5-propyl-3H-pyrimidin-4-one 
• 24317-96-2 2-propyl-3-oxo-3-phenylpropionic acid ethyl ester 
• 98-85-1 1-Phenylethanol 
• 583-03-9 1-Phenyl-1-pentanol 
• 618-39-3 benzamidin 
• 100-51-6 benzyl alcohol 
• 1670-14-0 benzamidine monohydrochloride 

Relevant academic research and scientific papers

Copper-catalyzed three-component synthesis of pyrimidines from amidines and alcohols

An efficient copper-catalyzed one-pot three-component reaction of amidines, primary alcohols and secondary alcohols has been developed to synthesize multisubstituted pyrimidines. The significant merits of this method involve high atom efficiency, good fun

A sustainable multicomponent pyrimidine synthesis

Since alcohols are accessible from indigestible biomass (lignocellulose), the development of novel preferentially catalytic reactions in which alcohols are converted into important classes of fine chemicals is a central topic of sustainable synthesis. Multicomponent reactions are especially attractive in organic chemistry as they allow the synthesis of large libraries of diversely functionalized products in a short time when run in a combinatorial fashion. Herein, we report a novel, regioselective, iridium-catalyzed multicomponent synthesis of pyrimidines from amidines and up to three (different) alcohols. This reaction proceeds via a sequence of condensation and dehydrogenation steps which give rise to selective C-C and C-N bond formations. While the condensation steps deoxygenate the alcohol components, the dehydrogenations lead to aromatization. Two equiv of hydrogen and water are liberated in the course of the reactions. PN5P-Ir-pincer complexes, recently developed in our laboratory, catalyze this sustainable multicomponent process most efficiently. A total of 38 different pyrimidines were synthesized in isolated yields of up to 93%. Strong points of the new protocol are its regioselectivity and thus the immediate access to pyrimidines that are highly and unsymmetrically decorated with alkyl or aryl substituents. The combination of this novel protocol with established methods for converting alcohols to nitriles now allows to selectively assemble pyrimidines from four alcohol building blocks and 2 equiv of ammonia.