Syntheses of substituted 2-(1-methyl-2-imidazolyl)quinolines was written by Khazan, Minoo;Hadizadeh, Farzin;Shafiee, Abbas. And the article was included in Journal of Heterocyclic Chemistry in 1997.Recommanded Product: 85692-37-1 This article mentions the following:
Reaction of methyllithium with 1-methyl-2-imidazolecarboxaldehyde afforded the corresponding alc. Oxidation of the alc. with manganese dioxide gave 2-acetyl-1-methylimidazole (I). I reacted with isatins to give quinoline-4-carboxylic acids, which were converted to amides, carbamates, and amines. In the experiment, the researchers used many compounds, for example, 1-(1-Methyl-1H-imidazol-2-yl)ethanone (cas: 85692-37-1Recommanded Product: 85692-37-1).
1-(1-Methyl-1H-imidazol-2-yl)ethanone (cas: 85692-37-1) belongs to imidazole derivatives. Among the different heterocyclic compounds, imidazole is better known due to its broad range of chemical and biological properties. Imidazole has become an important synthon in the development of new drugs. Imidazole has been usedin the lysis, wash and elution buffer for the purification of histidine tagged Sonic Hedgehog(shh-N) protein, in elution buffer in stepwise gradient for the purification of histidine tagged aldo keto reductases using nickel affinity chromatography, as a component of homogenization buffer for the purification of phagosomal compartments from dendritic cells.Recommanded Product: 85692-37-1
Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem