78649-11-3

Upstream product

• 2107-70-2 3,4-methoxycinnamic acid 
• 51842-87-6 3-(3,4-dimethoxy-phenyl)-propionyl chloride 
• 59282-10-9 methyl N-<3-(3,4-dimethoxyphenyl)propanoyl>anthranilate 
• 134-20-3 2-carbomethoxyaniline 

Downstream Products

• 1353723-59-7 C₂₅H₂₂ClN₃O₃ 
• 1353723-58-6 C₂₆H₂₅N₃O₃ 
• 1353723-56-4 2-[2-(3,4-dimethoxy-phenyl)ethyl]-3-[(E)-1-(4-pyridyl)methylideneamino]quinazolin-4(3H)-one 
• 78649-14-6 2-<2-(3,4-dimethoxyphenyl)ethyl>quinazolin-4(3H)-one 

Relevant academic research and scientific papers

Modification of the Pictet-Spengler reaction in the synthesis of fused 2,3-benzodiazocines

A new strategy for the synthesis of the eight-membered heterocyclic skeleton of tetrahydro-quinazolino[3,2-c][2,3]benzodiazocin-15-ones, based on the Pictet-Spengler reaction of 3-amino-2-[2-(3,4-dimethoxyphenyl)ethyl] quinazolin-4(3H)-one with carbonyl c

Intramolecular Reactions of N-Nitrenes: Oxidation of 3-Amino-2-(arylalkyl)quinazolin-4(3H)-ones

Oxidation of the title compounds yields N-nitrenes which react intramolecularly with methoxy-substituted aryl rings.The particular substitution pattern in the aryl rings which is required for effective trapping of the nitrenes is in accord with an electro

Intramolecular Reactions of N-Nitrenes: Oxidation of 3-Amino-2-(arylalkyl)quinazolones

Oxidation of the title compounds yields N-nitrenes which react intramolecularly with electron-rich aryl groups via 7-membered transition states; substituent effects are in accord with an electrophilic aromatic substitution rather than concerted addition.