173199-87-6

Usage

Chemical class

Pyrazinone

Structure

Pyrazinone ring with substituents (chlorine atom, methyl group, and phenylmethyl group)

药理活性

Diverse pharmacological activities and potential therapeutic applications

Interest

Medicinal chemistry and potential drug development

Further studies required

Yes

Upstream product

• 594-27-4 tetramethylstannane 
• 138610-71-6 1-benzyl-3,5-dichloro-6-phenyl-2(1H)-pyrazinone 

Downstream Products

• 173199-91-2 1-benzyl-3-bromomethyl-5-chloro-6-phenyl-2(1H)-pyrazinone 
• 853687-88-4 1-benzyl-3-methyl-6-phenyl-2(1H)-pyrazinone 
• 853687-93-1 1-benzyl-5-bromo-3-methyl-6-phenyl-2(1H)-pyrazinone 

Relevant academic research and scientific papers

Stereoselective transformation of pyrazinones into substituted analogues of cis-5-amino-6-oxo-2-piperidinemethanol and cis-5-amino-2-piperidinemethanol

Various analogues of cis-5-amino-6-oxo-2-piperidinemethanol and cis-5-amino-2-piperidinemethanol have been prepared via Diels-Alder reaction of substituted pyrazinones with ethene followed by acid methanolysis of the bridged lactam adducts. Further reduct

Intramolecular Diels-Alder Reactions of 2(1H)-Pyrazinones: Synthesis of New Furo/Pyrano-pyridinones and -pyridines

2(1H)-Pyrazinones 2-5 with in 3-position either a 3- or 4-alkynyloxy side chain and 2(1H)-pyrazinones 9-10 carrying the corresponding 2- or 3-alkynyloxy(m)ethyl substituent are shown to undergo intramolecular Diels-Alder reaction.The formation of either f