1-(2-(cyclopropyl(methoxy)methyl)-1-methyl-1H-benzimidazol-6-yl)-4-((4-fluorobenzyl)oxy)pyridin-2(1H)-one

Base Information

Chemical Name:1-(2-(cyclopropyl(methoxy)methyl)-1-methyl-1H-benzimidazol-6-yl)-4-((4-fluorobenzyl)oxy)pyridin-2(1H)-one
CAS No.:1447911-39-8
Molecular Formula:C₂₅H₂₄FN₃O₃
Molecular Weight:433.482
Hs Code.:

Synonyms:1-(2-(cyclopropyl(methoxy)methyl)-1-methyl-1H-benzimidazol-6-yl)-4-((4-fluorobenzyl)oxy)pyridin-2(1H)-one

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Chemical Property of 1-(2-(cyclopropyl(methoxy)methyl)-1-methyl-1H-benzimidazol-6-yl)-4-((4-fluorobenzyl)oxy)pyridin-2(1H)-one

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Technology Process of 1-(2-(cyclopropyl(methoxy)methyl)-1-methyl-1H-benzimidazol-6-yl)-4-((4-fluorobenzyl)oxy)pyridin-2(1H)-one

There total 7 articles about 1-(2-(cyclopropyl(methoxy)methyl)-1-methyl-1H-benzimidazol-6-yl)-4-((4-fluorobenzyl)oxy)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:

: 321-23-3
4-bromo-2-fluoronitrobenzene

: 1447911-39-8
1-(2-(cyclopropyl(methoxy)methyl)-1-methyl-1H-benzimidazol-6-yl)-4-((4-fluorobenzyl)oxy)pyridin-2(1H)-one

Guidance literature:: Multi-step reaction with 7 steps

1.1: ethanol; methanol / 1 h / 20 °C

2.1: iron; calcium chloride / ethanol; water / 3 h / 70 °C

2.2: 0 - 20 °C

3.1: sodium hydrogencarbonate / water; acetonitrile / 20 - 60 °C

4.1: tetrahydrofuran / 0.5 h / 0 °C / Inert atmosphere

5.1: potassium carbonate; copper(l) iodide; N,N`-dimethylethylenediamine / dimethyl sulfoxide / 1 h / 150 °C

6.1: sodium tetrahydroborate; methanol / tetrahydrofuran / 0.5 h / 20 °C

7.1: sodium hydride / N,N-dimethyl-formamide; mineral oil; tetrahydrofuran / 0.5 h / 20 °C

With methanol; sodium tetrahydroborate; copper(l) iodide; iron; sodium hydride; sodium hydrogencarbonate; potassium carbonate; calcium chloride; N,N`-dimethylethylenediamine; In tetrahydrofuran; methanol; ethanol; water; dimethyl sulfoxide; N,N-dimethyl-formamide; acetonitrile; mineral oil;

Reference yield:

: 1447911-40-1
1-(2-(cyclopropyl(hydroxy)methyl)-1-methyl-1H-benzimidazol-6-yl)-4-((4-fluorobenzyl)oxy)pyridin-2(1H)-one

: 74-88-4
methyl iodide

: 1447911-39-8
1-(2-(cyclopropyl(methoxy)methyl)-1-methyl-1H-benzimidazol-6-yl)-4-((4-fluorobenzyl)oxy)pyridin-2(1H)-one

Guidance literature:: With sodium hydride; In tetrahydrofuran; N,N-dimethyl-formamide; mineral oil; at 20 ℃; for 0.5h;

Reference yield:

: 1447911-37-6
(6-bromo-1-methyl-1H-benzimidazol-2-yl)(cyclopropyl)methanone

: 1447911-39-8
1-(2-(cyclopropyl(methoxy)methyl)-1-methyl-1H-benzimidazol-6-yl)-4-((4-fluorobenzyl)oxy)pyridin-2(1H)-one

Guidance literature:: Multi-step reaction with 3 steps

1: potassium carbonate; copper(l) iodide; N,N`-dimethylethylenediamine / dimethyl sulfoxide / 1 h / 150 °C

2: sodium tetrahydroborate; methanol / tetrahydrofuran / 0.5 h / 20 °C

3: sodium hydride / N,N-dimethyl-formamide; mineral oil; tetrahydrofuran / 0.5 h / 20 °C

With methanol; sodium tetrahydroborate; copper(l) iodide; sodium hydride; potassium carbonate; N,N`-dimethylethylenediamine; In tetrahydrofuran; dimethyl sulfoxide; N,N-dimethyl-formamide; mineral oil;