2-phenyl-1-(pyridin-4-ylmethyl)-4-(3,4,5-trimethoxybenzylidene)-1H-imidazol-5(4H)-one

Base Information

Chemical Name:2-phenyl-1-(pyridin-4-ylmethyl)-4-(3,4,5-trimethoxybenzylidene)-1H-imidazol-5(4H)-one
CAS No.:1373956-89-8
Molecular Formula:C₂₅H₂₃N₃O₄
Molecular Weight:429.475
Hs Code.:

Synonyms:2-phenyl-1-(pyridin-4-ylmethyl)-4-(3,4,5-trimethoxybenzylidene)-1H-imidazol-5(4H)-one

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Chemical Property of 2-phenyl-1-(pyridin-4-ylmethyl)-4-(3,4,5-trimethoxybenzylidene)-1H-imidazol-5(4H)-one

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Technology Process of 2-phenyl-1-(pyridin-4-ylmethyl)-4-(3,4,5-trimethoxybenzylidene)-1H-imidazol-5(4H)-one

There total 3 articles about 2-phenyl-1-(pyridin-4-ylmethyl)-4-(3,4,5-trimethoxybenzylidene)-1H-imidazol-5(4H)-one which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 61.0%

: 3731-53-1
4-(aminomethyl)pyridine

: 62616-09-5
2-Phenyl-4-(3',4',5'-trimethoxybenzylidene)oxazolone

: 1373956-89-8
2-phenyl-1-(pyridin-4-ylmethyl)-4-(3,4,5-trimethoxybenzylidene)-1H-imidazol-5(4H)-one

Guidance literature:: With potassium acetate; acetic acid; Heating;
DOI:10.1016/j.bmc.2012.02.037

Reference yield:

: 495-69-2,140480-84-8,21251-67-2,91787-63-2,66407-11-2
Hippuric Acid

: 86-81-7
3,4,5-trimethoxy-benzaldehyde

: 1373956-89-8
2-phenyl-1-(pyridin-4-ylmethyl)-4-(3,4,5-trimethoxybenzylidene)-1H-imidazol-5(4H)-one

Guidance literature:: Multi-step reaction with 2 steps

1: potassium acetate; acetic anhydride / Heating

2: potassium acetate; acetic acid / Heating

With potassium acetate; acetic anhydride; acetic acid;
DOI:10.1016/j.bmc.2012.02.037

Reference yield:

: 98-88-4
benzoyl chloride

: 1373956-89-8
2-phenyl-1-(pyridin-4-ylmethyl)-4-(3,4,5-trimethoxybenzylidene)-1H-imidazol-5(4H)-one

Guidance literature:: Multi-step reaction with 3 steps

1.1: sodium hydroxide

1.2: Cooling with ice

2.1: potassium acetate; acetic anhydride / Heating

3.1: potassium acetate; acetic acid / Heating

With potassium acetate; acetic anhydride; acetic acid; sodium hydroxide;
DOI:10.1016/j.bmc.2012.02.037