1-[1-(2-chlorobenzyl)-1H-benzimidazol-4-yl]-3-hydroxypyridin-4(1H)-one

Base Information

Chemical Name:1-[1-(2-chlorobenzyl)-1H-benzimidazol-4-yl]-3-hydroxypyridin-4(1H)-one
CAS No.:1333331-69-3
Molecular Formula:C₁₉H₁₄ClN₃O₂
Molecular Weight:351.792
Hs Code.:

Synonyms:1-[1-(2-chlorobenzyl)-1H-benzimidazol-4-yl]-3-hydroxypyridin-4(1H)-one

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Chemical Property of 1-[1-(2-chlorobenzyl)-1H-benzimidazol-4-yl]-3-hydroxypyridin-4(1H)-one

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Technology Process of 1-[1-(2-chlorobenzyl)-1H-benzimidazol-4-yl]-3-hydroxypyridin-4(1H)-one

There total 4 articles about 1-[1-(2-chlorobenzyl)-1H-benzimidazol-4-yl]-3-hydroxypyridin-4(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: 58.0%

: 1333332-16-3
3-(benzyloxy)-1-[1-(2-chlorobenzyl)-1H-benzimidazol-4-yl]pyridin-4(1H)-one

: 1333331-69-3
1-[1-(2-chlorobenzyl)-1H-benzimidazol-4-yl]-3-hydroxypyridin-4(1H)-one

Guidance literature:: With boron trifluoride diethyl etherate; ethanethiol; In dichloromethane; at 18 - 25 ℃; for 4h;

Reference yield:

: 10597-52-1
4-nitro-benzimidazole

: 1333331-69-3
1-[1-(2-chlorobenzyl)-1H-benzimidazol-4-yl]-3-hydroxypyridin-4(1H)-one

Guidance literature:: Multi-step reaction with 3 steps

1.1: hydrogen / palladium 10% on activated carbon / acetic acid / 3 h / 2482.38 Torr

2.1: ethanol; water / Reflux

2.2: 18 - 80 °C

3.1: ethanethiol; boron trifluoride diethyl etherate / dichloromethane / 4 h / 18 - 25 °C

With boron trifluoride diethyl etherate; hydrogen; ethanethiol; palladium 10% on activated carbon; In ethanol; dichloromethane; water; acetic acid;

Reference yield:

: 501-30-4,123712-78-7
5-hydroxy-2-(hydroxymethyl)-4H-pyran-4-one

: 1333331-69-3
1-[1-(2-chlorobenzyl)-1H-benzimidazol-4-yl]-3-hydroxypyridin-4(1H)-one

Guidance literature:: Multi-step reaction with 4 steps

1.1: sodium hydroxide / water; methanol / 4.5 h / Reflux

2.1: Jones reagent / acetone / 0 - 25 °C

3.1: ethanol; water / Reflux

3.2: 18 - 80 °C

4.1: ethanethiol; boron trifluoride diethyl etherate / dichloromethane / 4 h / 18 - 25 °C

With Jones reagent; boron trifluoride diethyl etherate; ethanethiol; sodium hydroxide; In methanol; ethanol; dichloromethane; water; acetone;