313405-40-2

Upstream product

• 18543-22-1 2-benzoylaminobenzamide 
• 118-92-3 anthranilic acid 
• 98-88-4 benzoyl chloride 
• 1022-46-4 2-phenyl-4H-3,1-benzoxazin-4-one 
• 1022-45-3 2-phenyl-4(3H)-quinazolinone 
• 105-39-5 chloroacetic acid ethyl ester 

Downstream Products

• 1257629-14-3 C₂₀H₁₆N₄O₃ 
• 1257629-16-5 4-(1,3,4-oxadiazol-2-ylmethoxy)-2-phenylquinazoline 
• 1257629-19-8 5-{[(2-phenylquinazolin-4-yl)oxy]methyl}-2,4-dihydro-3H-1,2,4-triazol-3-thione 

Relevant academic research and scientific papers

Synthesis and Antimicrobial Activity of Methyl 2-(2-(2-Arylquinazolin-4-yl)oxy) Acetylamino Alkanoates

A series of methyl 2-(2-(2-arylquinazolin-4-yl)oxy) acetylamino alkanoate have been developed via N,N′-dicyclohexylcarbodiimide coupling of (2-arylquinazolin-4-yloxy) acetic acids with amino acid ester hydrochlorides. The O-substituted carboxylic acids we

Synthesis, antimicrobial evaluation, and docking studies of novel 4-substituted quinazoline derivatives as DNA-gyrase inhibitors

Quinazoline derivatives are reported to have anti-inflammatory, analgesic, antibacterial, and anticancer activities. The incorporation of "OCH 2CONH2" (oxymethylcarbamide) at 4th position of the quinazoline ring was found

Synthesis of new quinazoline derivatives of expected potential bioresponses

The reactivity of the novel compound ethyl (2-phenylquinazolin-4-oxy)-acetate (1), towards carbon electrophiles and nitrogen nucleophiles is described. Reaction of (2-phenylquinazolin-4-oxy)acetic hydrazine (5) with carbon electrophiles is also investigated. Futhermore, the behaviour of 4-chloro-2-phenylquinazoline (6) towards a variety of nitrogen and carbon nucleophiles is studied.