4-chloro-3-[5-chloro-1-methyl-6-(3-(trifluoromethyl)piperidin-1-yl)-1H-benzo[d]imidazol-2-ylamino]benzylamine

Base Information

Chemical Name:4-chloro-3-[5-chloro-1-methyl-6-(3-(trifluoromethyl)piperidin-1-yl)-1H-benzo[d]imidazol-2-ylamino]benzylamine
CAS No.:1380920-96-6
Molecular Formula:C₂₁H₂₂Cl₂F₃N₅
Molecular Weight:472.34
Hs Code.:

Synonyms:4-chloro-3-[5-chloro-1-methyl-6-(3-(trifluoromethyl)piperidin-1-yl)-1H-benzo[d]imidazol-2-ylamino]benzylamine

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Chemical Property of 4-chloro-3-[5-chloro-1-methyl-6-(3-(trifluoromethyl)piperidin-1-yl)-1H-benzo[d]imidazol-2-ylamino]benzylamine

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Technology Process of 4-chloro-3-[5-chloro-1-methyl-6-(3-(trifluoromethyl)piperidin-1-yl)-1H-benzo[d]imidazol-2-ylamino]benzylamine

There total 9 articles about 4-chloro-3-[5-chloro-1-methyl-6-(3-(trifluoromethyl)piperidin-1-yl)-1H-benzo[d]imidazol-2-ylamino]benzylamine 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: 99.0%

: 1380920-95-5
tert-butyl N-{4-chloro-3-[5-chloro-1-methyl-6-(3-(trifluoromethyl) piperidin-1-yl)]-1H-benzo[d]imidazol-2-ylaminolbenzyl}-carbamate

: 1380920-96-6
4-chloro-3-[5-chloro-1-methyl-6-(3-(trifluoromethyl)piperidin-1-yl)-1H-benzo[d]imidazol-2-ylamino]benzylamine

Guidance literature:: tert-butyl N-{4-chloro-3-[5-chloro-1-methyl-6-(3-(trifluoromethyl) piperidin-1-yl)]-1H-benzo[d]imidazol-2-ylaminolbenzyl}-carbamate; With hydrogenchloride; In 1,4-dioxane; at 20 ℃; for 2h;

With potassium carbonate; In 1,4-dioxane; water; at 20 ℃; for 1h;

Reference yield:

: 2339-78-8
1,2-dichloro-4-fluoro-5-nitrobenzene

: 1380920-96-6
4-chloro-3-[5-chloro-1-methyl-6-(3-(trifluoromethyl)piperidin-1-yl)-1H-benzo[d]imidazol-2-ylamino]benzylamine

Guidance literature:: Multi-step reaction with 5 steps

1.1: N,N-dimethyl-formamide; toluene

2.1: potassium carbonate / N,N-dimethyl-formamide / 70 - 80 °C

2.2: 26 h / 20 - 100 °C

3.1: hydrogen / platinum on activated charcoal / tetrahydrofuran; methanol / 4 h / 35 °C / 2400.24 Torr

4.1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / acetonitrile / 20 °C

5.1: hydrogenchloride / 1,4-dioxane / 2 h / 20 °C

5.2: 1 h / 20 °C

With hydrogenchloride; hydrogen; potassium carbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; platinum on activated charcoal; In tetrahydrofuran; 1,4-dioxane; methanol; N,N-dimethyl-formamide; toluene; acetonitrile;

Reference yield:

: 107342-18-7
4,5-dichloro-N-methyl-2-nitrobenzenamine

: 1380920-96-6
4-chloro-3-[5-chloro-1-methyl-6-(3-(trifluoromethyl)piperidin-1-yl)-1H-benzo[d]imidazol-2-ylamino]benzylamine

Guidance literature:: Multi-step reaction with 4 steps

1.1: potassium carbonate / N,N-dimethyl-formamide / 70 - 80 °C

1.2: 26 h / 20 - 100 °C

2.1: hydrogen / platinum on activated charcoal / tetrahydrofuran; methanol / 4 h / 35 °C / 2400.24 Torr

3.1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / acetonitrile / 20 °C

4.1: hydrogenchloride / 1,4-dioxane / 2 h / 20 °C

4.2: 1 h / 20 °C

With hydrogenchloride; hydrogen; potassium carbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; platinum on activated charcoal; In tetrahydrofuran; 1,4-dioxane; methanol; N,N-dimethyl-formamide; acetonitrile;