4-((E)-2-(4-chlorophenyl)ethenyl)-1-(2-cyclopropyl-3-methylimidazo[1,2-a]pyridin-6-yl)pyridin-2(1H)-one

Base Information

Chemical Name:4-((E)-2-(4-chlorophenyl)ethenyl)-1-(2-cyclopropyl-3-methylimidazo[1,2-a]pyridin-6-yl)pyridin-2(1H)-one
CAS No.:1447913-64-5
Molecular Formula:C₂₄H₂₀ClN₃O
Molecular Weight:401.895
Hs Code.:

Synonyms:4-((E)-2-(4-chlorophenyl)ethenyl)-1-(2-cyclopropyl-3-methylimidazo[1,2-a]pyridin-6-yl)pyridin-2(1H)-one

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Chemical Property of 4-((E)-2-(4-chlorophenyl)ethenyl)-1-(2-cyclopropyl-3-methylimidazo[1,2-a]pyridin-6-yl)pyridin-2(1H)-one

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Technology Process of 4-((E)-2-(4-chlorophenyl)ethenyl)-1-(2-cyclopropyl-3-methylimidazo[1,2-a]pyridin-6-yl)pyridin-2(1H)-one

There total 8 articles about 4-((E)-2-(4-chlorophenyl)ethenyl)-1-(2-cyclopropyl-3-methylimidazo[1,2-a]pyridin-6-yl)pyridin-2(1H)-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:

: 1447913-20-3
4-bromo-1-(2-cyclopropyl-3-methylimidazo[1,2-a]pyridin-6-yl)pyridin-2(1H)-one

: 154230-29-2
(E)-4-chlorostyrylboronic acid

: 1447913-64-5
4-((E)-2-(4-chlorophenyl)ethenyl)-1-(2-cyclopropyl-3-methylimidazo[1,2-a]pyridin-6-yl)pyridin-2(1H)-one

Guidance literature:: With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; potassium carbonate; In tetrahydrofuran; water; at 70 ℃; Inert atmosphere;

Reference yield:

: 1447911-19-4
1-(2-cyclopropyl-3-methylimidazo[1,2-a]pyridin-6-yl)-4-hydroxypyridin-2(1H)-one

: 1447913-64-5
4-((E)-2-(4-chlorophenyl)ethenyl)-1-(2-cyclopropyl-3-methylimidazo[1,2-a]pyridin-6-yl)pyridin-2(1H)-one

Guidance literature:: Multi-step reaction with 2 steps

1: phosphorus(V) oxybromide / N,N-dimethyl-formamide / 20 - 110 °C

2: potassium carbonate; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride / tetrahydrofuran; water / 70 °C / Inert atmosphere

With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; potassium carbonate; phosphorus(V) oxybromide; In tetrahydrofuran; water; N,N-dimethyl-formamide;

Reference yield:

: 1447910-77-1
2-cyclopropyl-6-iodo-3-methylimidazo[1,2-a]pyridine

: 1447913-64-5
4-((E)-2-(4-chlorophenyl)ethenyl)-1-(2-cyclopropyl-3-methylimidazo[1,2-a]pyridin-6-yl)pyridin-2(1H)-one

Guidance literature:: Multi-step reaction with 4 steps

1: potassium carbonate; copper(l) iodide; N,N`-dimethylethylenediamine / dimethyl sulfoxide / 1 h / 110 °C / Microwave irradiation

2: hydrogen; palladium 10% on activated carbon / methanol / 4 h / 20 °C

3: phosphorus(V) oxybromide / N,N-dimethyl-formamide / 20 - 110 °C

4: potassium carbonate; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride / tetrahydrofuran; water / 70 °C / Inert atmosphere

With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; copper(l) iodide; palladium 10% on activated carbon; hydrogen; potassium carbonate; N,N`-dimethylethylenediamine; phosphorus(V) oxybromide; In tetrahydrofuran; methanol; water; dimethyl sulfoxide; N,N-dimethyl-formamide;