Some scientific research about 484-47-9

As far as I know, this compound(484-47-9)Formula: C21H16N2 can be applied in many ways, which is helpful for the development of experiments. Therefore many people are doing relevant researches.

Most of the natural products isolated at present are heterocyclic compounds, so heterocyclic compounds occupy an important position in the research of organic chemistry. A compound: 484-47-9, is researched, SMILESS is C1(C2=CC=CC=C2)=NC(C3=CC=CC=C3)=C(C4=CC=CC=C4)N1, Molecular C21H16N2Journal, RSC Advances called Novel synthesis of divergent aryl imidazoles from ketones involving copper-catalyzed α-amination and oxidative C-C bond cleavage, Author is Huang, Jiangkun; Luo, Lan; Xing, Naiguo; Gu, Linghui; Li, Chen; Han, Qiao; Zheng, Shilong; He, Ling, the main research direction is aryl imidazole preparation; ketone amination oxidative bond cleavage copper catalyst; aldehyde ketone amination oxidative bond cleavage copper catalyst.Formula: C21H16N2.

A one-pot synthesis, initiated by a copper salt with inorganic (NH4)2CO3 as the nitrogen source, forms divergent aryl imidazole derivatives I [R = H, Et, thiophen-2-yl, naphthalen-1-yl, 2H-1,3-benzodioxol-5-yl, etc.; R1 = Me, Et, n-Pr, Ph; Ar = 4-bromophenyl, thiophen-2-yl, 2,3-dihydro-1,4-benzodioxin-6-yl, etc.] and II [Ar1 = 1H-indol-3-yl, 2-phenyl-1H-indol-3-yl, 5-bromo-1H-indol-3-yl, etc.; Ar2 = Ph, 4-methylphenyl; R2 = Me, 4-methylphenyl; R3 = Me, Et] from ketones ArC(O)CH2R/Ar1C(O)CH2Ar2/R2C(O)(R3) via α-amination and oxidative C-C bond cleavage reactions. The approach provides a simple and rapid synthesis of imidazole derivatives I and II and has certain versatility.

As far as I know, this compound(484-47-9)Formula: C21H16N2 can be applied in many ways, which is helpful for the development of experiments. Therefore many people are doing relevant researches.

Reference:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts