22126-97-2

Upstream product

• 1020001-28-8 tert-butyl (4-oxo-3-phenyl-3,4-dihydroquinazolin-2-yl)methylcarbamate 
• 22312-77-2 2-chloromethyl-3-phenyl-3H-quinazolin-4-one 
• 62-53-3 aniline 
• 80096-25-9 2-Azidomethyl-3,4-dihydro-3-phenyl-4-chinazolinon 
• 131532-69-9 4-(3-phenyl-4(3H)-quinazolinon-2-yl)-3-thiosemicarbazone 
• 14422-49-2 2-chloroacetamidobenzoic acid 

Downstream Products

• 76462-04-9 5-oxo-4-phenyl-1-thioxo-1,2,4,5-tetrahydroimidazolo<4,3-a>quinazoline 
• 1020000-31-0 C₂₈H₂₈ClN₅O₂ 
• 1020000-34-3 C₃₀H₃₃N₅O₂ 
• 1020000-35-4 C₃₀H₃₃N₅O₂ 
• 1020000-39-8 C₂₉H₃₁N₅O₃ 
• 1020000-40-1 C₃₀H₃₃N₅O₃ 
• 1020000-49-0 C₂₉H₃₁N₅O₂ 
• 1020000-50-3 C₂₉H₃₀FN₅O₂ 
• 1020000-52-5 C₂₉H₃₀ClN₅O₂ 
• 1020000-53-6 C₂₉H₃₀ClN₅O₂ 
• 1020000-54-7 C₂₉H₃₀ClN₅O₂ 
• 1020000-55-8 C₂₉H₂₉Cl₂N₅O₂ 
• 1020000-56-9 C₃₁H₃₅N₅O₂ 
• 1020000-57-0 C₃₁H₃₅N₅O₂ 

Relevant academic research and scientific papers

Novel quinazolinone derivatives as 5-HT7 receptor ligands

5-HT7 receptor antagonists generated antidepressant-like effects in animal model and the involvement of the 5-HT7 receptor in other pathophysiological mechanisms such as thermoregulation, learning and memory, and sleep has been highl

METHOD OF PREPARING 3-PHENYL-2-[9H-PURIN-6-YLAMINO)-METHYL]-3H-QUINAZOLIN-4-ONE AND SUBSTITUTED AND RELATED COMPOUNDS

A method of synthesizing compounds of structural formulae (II), (IIa), and (III), in high yield and high stereospecific selectivity is disclosed. (IIa, R5≠H, S-enantiomer)

Electroreduction of Some Potential Antimicrobial Thiosemicarbazide Derivatives of Quinazolin-4(3H)-one

Polarographic data for a series of 3-phenyl-2-substituted thiocarbamoylhydrazonomethylquinazolin-4(3H)-ones (with antimicrobial activity), in 50percent ethanolic aqueous buffers covering a wide range of pH are reported and discussed.A mechanism interpreting the electrode process, in both acidic and alkaline media, is proposed and confirmed via the identification of CPE products, Hammett's ?-E1/2 relation and pKa determination.

Quinazolinones, 2. Syntheses and Some Reactions of 2-Azido-methyl-3-aryl-4-quinazolinones

Starting with the chloromethyl compounds 7 the new 2-azidomethyl-3-aryl-4-quinazolinones 8a-h were prepared, some of which have been reduced so far to the corresponding amines 9a, b, e, g by H2S in good yield.As a first example for the capability of the a