N-{4-chloro-3-[3-methyl-6-(4-trifluoromethyl-piperidin-1-yl)-1H-benzimidazol-2-ylamino]-benzyl}-2,2-dimethyl-propionamide

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Chemical Name:N-{4-chloro-3-[3-methyl-6-(4-trifluoromethyl-piperidin-1-yl)-1H-benzimidazol-2-ylamino]-benzyl}-2,2-dimethyl-propionamide
CAS No.:1380919-26-5
Molecular Formula:C₂₆H₃₁ClF₃N₅O
Molecular Weight:522.013
Hs Code.:

Synonyms:N-{4-chloro-3-[3-methyl-6-(4-trifluoromethyl-piperidin-1-yl)-1H-benzimidazol-2-ylamino]-benzyl}-2,2-dimethyl-propionamide

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Chemical Property of N-{4-chloro-3-[3-methyl-6-(4-trifluoromethyl-piperidin-1-yl)-1H-benzimidazol-2-ylamino]-benzyl}-2,2-dimethyl-propionamide

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Technology Process of N-{4-chloro-3-[3-methyl-6-(4-trifluoromethyl-piperidin-1-yl)-1H-benzimidazol-2-ylamino]-benzyl}-2,2-dimethyl-propionamide

There total 10 articles about N-{4-chloro-3-[3-methyl-6-(4-trifluoromethyl-piperidin-1-yl)-1H-benzimidazol-2-ylamino]-benzyl}-2,2-dimethyl-propionamide 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: 20.0%

: 1380921-23-2
N-(4-chloro-3-{3-[2-methylamino-5-(4-trifluoromethyl-piperidin-1-yl)-phenyl]-thioureido}-benzyl)-2,2-dimethyl-propionamide

: 1380919-26-5
N-{4-chloro-3-[3-methyl-6-(4-trifluoromethyl-piperidin-1-yl)-1H-benzimidazol-2-ylamino]-benzyl}-2,2-dimethyl-propionamide

Guidance literature:: With diisopropyl-carbodiimide; In acetonitrile; at 60 - 80 ℃; for 168h;

Reference yield:

: 3282-30-2
pivaloyl chloride

: 1380919-26-5
N-{4-chloro-3-[3-methyl-6-(4-trifluoromethyl-piperidin-1-yl)-1H-benzimidazol-2-ylamino]-benzyl}-2,2-dimethyl-propionamide

Guidance literature:: Multi-step reaction with 5 steps

1: triethylamine / tetrahydrofuran / 1.5 h / 20 °C

2: hydrogen / Raney-Nickel / tetrahydrofuran / 48 h / 20 °C

3: dichloromethane / 1.5 h / 20 °C

4: tetrahydrofuran / 4 h / 20 °C

5: diisopropyl-carbodiimide / acetonitrile / 168 h / 60 - 80 °C

With hydrogen; triethylamine; diisopropyl-carbodiimide; Raney-Nickel; In tetrahydrofuran; dichloromethane; acetonitrile;

Reference yield:

: 657-36-3
4-Trifluormethyl-piperidin

: 1380919-26-5
N-{4-chloro-3-[3-methyl-6-(4-trifluoromethyl-piperidin-1-yl)-1H-benzimidazol-2-ylamino]-benzyl}-2,2-dimethyl-propionamide

Guidance literature:: Multi-step reaction with 4 steps

1: sodium t-butanolate / palladium diacetate; tri-tert-butyl phosphine / toluene / 100 °C / Inert atmosphere

2: hydrogen / palladium 10% on activated carbon / methanol / 18 h / 20 °C

3: tetrahydrofuran / 4 h / 20 °C

4: diisopropyl-carbodiimide / acetonitrile / 168 h / 60 - 80 °C

With hydrogen; sodium t-butanolate; diisopropyl-carbodiimide; tri-tert-butyl phosphine; palladium 10% on activated carbon; palladium diacetate; In tetrahydrofuran; methanol; toluene; acetonitrile;