N-(4-chlorobenzyl)-4-[5,6-dichloro-1-(4-chlorobenzyl)-1H-benzimidazol-2-yl]benzamidine

Base Information

Chemical Name:N-(4-chlorobenzyl)-4-[5,6-dichloro-1-(4-chlorobenzyl)-1H-benzimidazol-2-yl]benzamidine
CAS No.:1393711-47-1
Molecular Formula:C₂₈H₂₀Cl₄N₄
Molecular Weight:554.306
Hs Code.:

Synonyms:N-(4-chlorobenzyl)-4-[5,6-dichloro-1-(4-chlorobenzyl)-1H-benzimidazol-2-yl]benzamidine

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Chemical Property of N-(4-chlorobenzyl)-4-[5,6-dichloro-1-(4-chlorobenzyl)-1H-benzimidazol-2-yl]benzamidine

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Technology Process of N-(4-chlorobenzyl)-4-[5,6-dichloro-1-(4-chlorobenzyl)-1H-benzimidazol-2-yl]benzamidine

There total 3 articles about N-(4-chlorobenzyl)-4-[5,6-dichloro-1-(4-chlorobenzyl)-1H-benzimidazol-2-yl]benzamidine 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: 56.0%

: 1393711-46-0
4-[5,6-dichloro-1-(4-chlorobenzyl)-1H-benzimidazol-2-yl]benzonitrile

: 104-86-9
4-chlorobenzylamine

: 1393711-47-1
N-(4-chlorobenzyl)-4-[5,6-dichloro-1-(4-chlorobenzyl)-1H-benzimidazol-2-yl]benzamidine

Guidance literature:: 4-[5,6-dichloro-1-(4-chlorobenzyl)-1H-benzimidazol-2-yl]benzonitrile; With hydrogenchloride; In ethanol; at 20 ℃; for 3.5h; Cooling;

4-chlorobenzylamine; In ethanol; at 25 - 30 ℃;
DOI:10.1111/j.1747-0285.2012.01393.x

Reference yield:

: 105-07-7
4-cyanobenzaldehyde

: 1393711-47-1
N-(4-chlorobenzyl)-4-[5,6-dichloro-1-(4-chlorobenzyl)-1H-benzimidazol-2-yl]benzamidine

Guidance literature:: Multi-step reaction with 3 steps

1.1: sodium hydrogensulfite / ethanol; water / Cooling

2.1: N,N-dimethyl-formamide / 4 h / 135 °C

3.1: hydrogenchloride / ethanol / 3.5 h / 20 °C / Cooling

3.2: 25 - 30 °C

With hydrogenchloride; sodium hydrogensulfite; In ethanol; water; N,N-dimethyl-formamide; 3.1: Pinner amidine synthesis / 3.2: Pinner amidine synthesis;
DOI:10.1111/j.1747-0285.2012.01393.x

Reference yield:

: 4-cyanobenzonitrile sodium metabisulfite adduct

: 1393711-47-1
N-(4-chlorobenzyl)-4-[5,6-dichloro-1-(4-chlorobenzyl)-1H-benzimidazol-2-yl]benzamidine

Guidance literature:: Multi-step reaction with 2 steps

1.1: N,N-dimethyl-formamide / 4 h / 135 °C

2.1: hydrogenchloride / ethanol / 3.5 h / 20 °C / Cooling

2.2: 25 - 30 °C

With hydrogenchloride; In ethanol; N,N-dimethyl-formamide; 2.1: Pinner amidine synthesis / 2.2: Pinner amidine synthesis;
DOI:10.1111/j.1747-0285.2012.01393.x