1-(4-chlorobenzyl)-N-(2-cyanoethyl)-2-(3,4-dichlorophenyl)-1H-benzimidazole-5-carboxamide

Base Information

Chemical Name:1-(4-chlorobenzyl)-N-(2-cyanoethyl)-2-(3,4-dichlorophenyl)-1H-benzimidazole-5-carboxamide
CAS No.:1393711-26-6
Molecular Formula:C₂₄H₁₇Cl₃N₄O
Molecular Weight:483.784
Hs Code.:

Synonyms:1-(4-chlorobenzyl)-N-(2-cyanoethyl)-2-(3,4-dichlorophenyl)-1H-benzimidazole-5-carboxamide

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 1-(4-chlorobenzyl)-N-(2-cyanoethyl)-2-(3,4-dichlorophenyl)-1H-benzimidazole-5-carboxamide

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Technology Process of 1-(4-chlorobenzyl)-N-(2-cyanoethyl)-2-(3,4-dichlorophenyl)-1H-benzimidazole-5-carboxamide

There total 4 articles about 1-(4-chlorobenzyl)-N-(2-cyanoethyl)-2-(3,4-dichlorophenyl)-1H-benzimidazole-5-carboxamide 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: 65.0%

: 1119-28-4
β-aminopropionitrile fumarate

: C₂₁H₁₂Cl₄N₂O

: 1393711-26-6
1-(4-chlorobenzyl)-N-(2-cyanoethyl)-2-(3,4-dichlorophenyl)-1H-benzimidazole-5-carboxamide

Guidance literature:: With triethylamine; In chloroform; at 20 ℃;
DOI:10.1111/j.1747-0285.2012.01393.x

Reference yield:

: sodium; (3,4-dichloro-phenyl)-hydroxy-methanesulfonate

: 1393711-26-6
1-(4-chlorobenzyl)-N-(2-cyanoethyl)-2-(3,4-dichlorophenyl)-1H-benzimidazole-5-carboxamide

Guidance literature:: Multi-step reaction with 4 steps

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

2: sodium hydroxide / ethanol; water / 1 h / Reflux

3: thionyl chloride / benzene / 2 h / 80 °C

4: triethylamine / chloroform / 20 °C

With thionyl chloride; triethylamine; sodium hydroxide; In ethanol; chloroform; water; N,N-dimethyl-formamide; benzene;
DOI:10.1111/j.1747-0285.2012.01393.x

Reference yield:

: 6287-38-3
3,4-dichlorobenzaldehyde

: 1393711-26-6
1-(4-chlorobenzyl)-N-(2-cyanoethyl)-2-(3,4-dichlorophenyl)-1H-benzimidazole-5-carboxamide

Guidance literature:: Multi-step reaction with 5 steps

1: sodium hydrogensulfite / ethanol; water / Cooling

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

3: sodium hydroxide / ethanol; water / 1 h / Reflux

4: thionyl chloride / benzene / 2 h / 80 °C

5: triethylamine / chloroform / 20 °C

With thionyl chloride; sodium hydrogensulfite; triethylamine; sodium hydroxide; In ethanol; chloroform; water; N,N-dimethyl-formamide; benzene;
DOI:10.1111/j.1747-0285.2012.01393.x