37029-32-6

Upstream product

• 104-94-9 4-methoxy-aniline 
• 37641-48-8 3-(2-methylphenyl)-4-oxo-2-thioxo-1,2,3,4-tetrahydroquinazoline 
• 96-34-4 methyl chloroacetate 
• 17425-17-1 N-(2-methylphenyl)-methyl dithiocarbamic acid 
• 118-92-3 anthranilic acid 
• 95-53-4 o-toluidine 
• 53662-44-5 o-tolyl-dithiocarbamic acid ; compound with triethylamine 
• 28831-24-5 methyl <3,4-dihydro-3-(o-methylphenyl)-4-oxo-2-quinazolinyl>thioacetate 

Downstream Products

• 1382310-41-9 2-((4-acetyl-5-methyl-5-phenyl-4,5-dihydro-1,3,4-oxadiazol-2-yl)methylthio)-3-o-tolylquinazolin-4(3H)-one 
• 56671-11-5 (4-oxo-3-o-tolyl-3,4-dihydro-quinazolin-2-ylsulfanyl)-acetic acid (4-chloro-benzylidene)-hydrazide 

Relevant academic research and scientific papers

Synthesis and characterization of new (E)-N'-(substituted benzylidene)-2-(3-(2-methyl)-4-oxo-3,4-dihydroquinazolin-2-ylthio) acetohydrazides

A small library of new azomethine derivatives of 3-aryl-2-thioxo-2,3- dihydroquinazolin-4(1H)-ones was synthesized. The key intermediates 2-thioxo-quinazolinones (3a-e), obtained in 2 steps from the corresponding anilines, were treated with methyl chloroa

Synthesis and antimicrobial evaluation of some new 1,3,4-oxadiazoles

A series of 2-((4-acetyl-5-(aryl)-5-methyl-4,5-dihydro-1,3,4-oxadiazol-2- yl) methylthio)-3-o-tolylquinazolin-4(3H)-one 5 was synthesized by the cyclization of imines 4 using acetic anhydride. The Schiffs base 4 are obtained by the reaction of appropriate