62576-13-0

Upstream product

• 49656-78-2 2-methylamino-1-phenyl-1-propanone hydrochloride 
• 215675-50-6 1,5-dimethyl-4-phenylimidazole 3-oxide 
• 166593-11-9 1,3-dihydro-1,5-dimethyl-4-phenyl-2H-imidazole-2-thione 
• 158585-81-0 4-bromo-1,5-dimethyl-1H-imidazole 
• 98-80-6 phenylboronic acid 

Relevant academic research and scientific papers

Reactions of 2-unsubstituted 1H-imidazole 3-oxides with 2,2-bis(trifluoromethyl)ethene-1,1-dicarbonitrile: A stepwise 1,3-dipolar cycloaddition

The reaction of 1,4,5-trisubstituted 1H-imidazole-3-oxides 1 with 2,2-bis(trifluoromethyl)ethene-1,1-dicarbonitrile (7, BTF) yielded the corresponding 1,3-dihydro-2H-imidazol-2-ones 10 and 2-(1,3-dihydro-2H-imidazol- 2-vlidene)malononitriles 11, respectiv

Novel imidazoles and hydantoins moderately strained by incorporation with 2-azabicyclo[2.2.1]heptene skeleton

The reactions of 3-acyl-2-azabicyclo[2.2.1]hept-5-enes with phenyl isocyanate, phenyl isothiocyanate, and ethoxycarbonyl isothiocyanate followed by cyclization reactions under basic conditions respectively provided a hydantoin, a thiohydantoin, and a 1,3-

Carboxylate protection for the synthesis of 4,5-disubstituted 1-methylimidazoles

Using the carboxylate function as a readily removed blocking group for the 2-position, a regioselective synthesis of diverse 4,5-disubstituted 1-methylimidazoles has been developed starting from 1-methyltribromoimidazole, 5.