70704-32-4

Upstream product

• 34897-85-3 o-azidobenzoyl chloride 
• 106-49-0 p-toluidine 
• 118-92-3 anthranilic acid 
• 31162-13-7 2-azidobenzoic acid 

Downstream Products

• 1087-99-6 3-(4-methylphenyl)quinazoline-2,4(1H,3H)-dione 
• 125701-60-2 2-(p-tolyl)amino-3-(p-tolyl)-4(3H)-quinazolinone 
• 118988-23-1 2-methylamino-3-(p-tolyl)-4(3H)-quinazolinone 
• 118988-24-2 2-(p-methoxyphenyl)amino-3-(p-tolyl)-4(3H)-quinazolinone 
• 125701-61-3 2-(m-tolyl)amino-3-(p-tolyl)-4(3H)-quinazolinone 
• 125701-59-9 2-(m-chlorophenyl)amino-3-(p-tolyl)-4(3H)-quinazolinone 
• 125701-62-4 2-(m-methoxyphenyl)amino-3-(p-tolyl)-4(3H)-quinazolinone 
• 125701-55-5 1,3-Di-m-tolyl-1-{4-[(Z)-p-tolylimino]-4H-benzo[d][1,3]oxazin-2-yl}-urea 
• 125701-52-2 1,3-Bis-(4-chloro-phenyl)-1-{4-[(Z)-p-tolylimino]-4H-benzo[d][1,3]oxazin-2-yl}-urea 
• 4543-89-9 2-phenylamino-3-(p-tolyl)-4(3H)-quinazolinone 
• 1182783-69-2 1-benzyl-2-p-tolyl-1H-indazol-3(2H)-one 

Relevant academic research and scientific papers

An efficient one-pot strategy for the synthesis of triazole-fused 1,4-benzodiazepinones from n-substituted 2-azidobenzamides

A catalyst-free, one-pot strategy for the synthesis of 1,2,3-triazole-fused 1,4-benzodiazepinone derivatives from N-substituted 2-azidobenzamides and propargyl bromide, in the presence of a base, is reported. The products are formed in good to excellent y

Microwave-assisted base-catalyzed cyclization and nucleophilic substitution of o-azidobenzanilides to synthesize 1,2-disubstituted indazol-3-ones

A series of 1,2-disubstituted indazol-3-ones were synthesized by microwave-assisted base-catalyzed cyclization and nucleophilic substitution of o-azidobenzanilides. Among five tested reaction conditions, the cyclization of o-azidobenzanilides catalyzed by