(E)-3-chloro-N-(6-((4-(2-hydroxypropan-2-yl)piperidin-1-yl)methyl)-1-((1s,4s)-4-(isopropylcarbamoyl)cyclohexyl)-1H-benzo[d]imidazol-2(3H)-ylidene)benzamide

Base Information

Chemical Name:(E)-3-chloro-N-(6-((4-(2-hydroxypropan-2-yl)piperidin-1-yl)methyl)-1-((1s,4s)-4-(isopropylcarbamoyl)cyclohexyl)-1H-benzo[d]imidazol-2(3H)-ylidene)benzamide
CAS No.:1357920-50-3
Molecular Formula:C₃₃H₄₄ClN₅O₃
Molecular Weight:594.197
Hs Code.:

(E)-3-chloro-N-(6-((4-(2-hydroxypropan-2-yl)piperidin-1-yl)methyl)-1-((1s,4s)-4-(isopropylcarbamoyl)cyclohexyl)-1H-benzo[d]imidazol-2(3H)-ylidene)benzamide

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Chemical Property of (E)-3-chloro-N-(6-((4-(2-hydroxypropan-2-yl)piperidin-1-yl)methyl)-1-((1s,4s)-4-(isopropylcarbamoyl)cyclohexyl)-1H-benzo[d]imidazol-2(3H)-ylidene)benzamide

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Technology Process of (E)-3-chloro-N-(6-((4-(2-hydroxypropan-2-yl)piperidin-1-yl)methyl)-1-((1s,4s)-4-(isopropylcarbamoyl)cyclohexyl)-1H-benzo[d]imidazol-2(3H)-ylidene)benzamide

There total 5 articles about (E)-3-chloro-N-(6-((4-(2-hydroxypropan-2-yl)piperidin-1-yl)methyl)-1-((1s,4s)-4-(isopropylcarbamoyl)cyclohexyl)-1H-benzo[d]imidazol-2(3H)-ylidene)benzamide 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: 21.4%

: 1357920-41-2
(1s,4s)-4-(2-amino-6-((4-(2-hydroxypropan-2-yl)piperidin-1-yl)methyl)-1H-benzo[d]imidazol-1-yl)-N-isopropylcyclohexanecarboxamide

: 535-80-8
3-chlorobenzoate

: 1357920-50-3,1388225-87-3
(E)-3-chloro-N-(6-((4-(2-hydroxypropan-2-yl)piperidin-1-yl)methyl)-1-((1s,4s)-4-(isopropylcarbamoyl)cyclohexyl)-1H-benzo[d]imidazol-2(3H)-ylidene)benzamide

Guidance literature:: With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; In N,N-dimethyl-formamide; at 20 - 50 ℃;
DOI:10.1021/jm3005866

Reference yield:

: 22990-34-7
2-(piperidin-4-yl)propan-2-ol

: 1357920-50-3,1388225-87-3
(E)-3-chloro-N-(6-((4-(2-hydroxypropan-2-yl)piperidin-1-yl)methyl)-1-((1s,4s)-4-(isopropylcarbamoyl)cyclohexyl)-1H-benzo[d]imidazol-2(3H)-ylidene)benzamide

Guidance literature:: Multi-step reaction with 6 steps

1.1: sodium tris(acetoxy)borohydride; acetic acid / dichloromethane / 0.75 h / 5 °C

2.1: N-ethyl-N,N-diisopropylamine / acetonitrile / 24 h / 80 °C

3.1: 5%-palladium/activated carbon; ammonium formate / ethanol; water / 2.25 h / 5 °C / Inert atmosphere

4.1: 1,4-dioxane / 0.08 h / 100 °C

4.2: 1 h / 20 - 60 °C

5.1: hydrogenchloride / water / 24 h / 50 °C

6.1: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 20 - 50 °C

With hydrogenchloride; 5%-palladium/activated carbon; ammonium formate; sodium tris(acetoxy)borohydride; benzotriazol-1-ol; acetic acid; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; In 1,4-dioxane; ethanol; dichloromethane; water; N,N-dimethyl-formamide; acetonitrile;
DOI:10.1021/jm3005866

Reference yield:

: 1357923-87-5
2-(1-(3-fluoro-4-nitrobenzyl)piperidin-4-yl)propan-2-ol

: 1357920-50-3,1388225-87-3
(E)-3-chloro-N-(6-((4-(2-hydroxypropan-2-yl)piperidin-1-yl)methyl)-1-((1s,4s)-4-(isopropylcarbamoyl)cyclohexyl)-1H-benzo[d]imidazol-2(3H)-ylidene)benzamide

Guidance literature:: Multi-step reaction with 5 steps

1.1: N-ethyl-N,N-diisopropylamine / acetonitrile / 24 h / 80 °C

2.1: 5%-palladium/activated carbon; ammonium formate / ethanol; water / 2.25 h / 5 °C / Inert atmosphere

3.1: 1,4-dioxane / 0.08 h / 100 °C

3.2: 1 h / 20 - 60 °C

4.1: hydrogenchloride / water / 24 h / 50 °C

5.1: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 20 - 50 °C

With hydrogenchloride; 5%-palladium/activated carbon; ammonium formate; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; In 1,4-dioxane; ethanol; water; N,N-dimethyl-formamide; acetonitrile;
DOI:10.1021/jm3005866