291276-26-1

Upstream product

• 394-35-4 methyl 2-fluorobenzoate 
• 49579-12-6 3-(2-chloro-phenyl)-6-fluoro-2-methyl-3H-quinazolin-4-one 
• 443-26-5 2-fluoro-benzoic acid ethyl ester 
• 95-51-2 o-chloroaniline 
• 49579-56-8 2-acetamido-5-fluorobenzoic acid 

Relevant academic research and scientific papers

Methaqualone derivatives are potent noncompetitive AMPA receptor antagonists

Quinazolin-4-one derivatives of methaqualone substituted at C-2 define new class of noncompetitive antagonists at AMPA receptors. (C) 2000 Elsevier Science Ltd. All rights reserved.

Quinazolin-4-one α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptor antagonists: Structure-activity relationship of the C-2 side chain tether

A series of 6-fluoro-3-(2-chlorophenyl)quinazolin-4-ones has been prepared, which contains a 2-fluorophenyl ring attached to C-2 by a variety of two-atom tethers. These compounds were used to probe the structure-activity relationship (SAR) for AMPA recept

Methods of preparing substituted 3-phenyl and 3-pyridyl-4(3H)-quinazolinones and atropisomers thereof

This invention is directed to methods for the preparation of quinazolin-4-one derivatives of the formula*(formula 02)*and the pharmaceutically acceptable salts and atropisomers of the formula*(formula 03)*and the pharmaceutically acceptable salts thereof,