4-{4-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3-trifluoromethoxyphenylcarbamoyl]piperazin-1-yl}piperidine-1-carboxylic acid tert-butyl ester

Base Information

Chemical Name:4-{4-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3-trifluoromethoxyphenylcarbamoyl]piperazin-1-yl}piperidine-1-carboxylic acid tert-butyl ester
CAS No.:1477815-42-1
Molecular Formula:C₂₈H₄₂BF₃N₄O₆
Molecular Weight:598.471
Hs Code.:

4-{4-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3-trifluoromethoxyphenylcarbamoyl]piperazin-1-yl}piperidine-1-carboxylic acid tert-butyl ester

Synonyms:4-{4-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3-trifluoromethoxyphenylcarbamoyl]piperazin-1-yl}piperidine-1-carboxylic acid tert-butyl ester

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Chemical Property of 4-{4-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3-trifluoromethoxyphenylcarbamoyl]piperazin-1-yl}piperidine-1-carboxylic acid tert-butyl ester

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Technology Process of 4-{4-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3-trifluoromethoxyphenylcarbamoyl]piperazin-1-yl}piperidine-1-carboxylic acid tert-butyl ester

There total 4 articles about 4-{4-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3-trifluoromethoxyphenylcarbamoyl]piperazin-1-yl}piperidine-1-carboxylic acid tert-butyl ester 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: 30.0%

: 1477815-41-0
4-[4-(4-bromo-3-trifluoromethoxyphenylcarbamoyl)piperazin-1-yl]piperidine-1-carboxylic acid tert-butyl ester

: 73183-34-3
bis(pinacol)diborane

: 1477815-42-1
4-{4-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3-trifluoromethoxyphenylcarbamoyl]piperazin-1-yl}piperidine-1-carboxylic acid tert-butyl ester

Guidance literature:: With dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; potassium acetate; In 1,4-dioxane; at 100 ℃; Inert atmosphere;

Reference yield:

: 177276-41-4
4-(piperazin-1-yl)piperidine-1-carboxylic acid tert-butyl ester

: 1477815-42-1
4-{4-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3-trifluoromethoxyphenylcarbamoyl]piperazin-1-yl}piperidine-1-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 2 steps

1.1: dichloromethane / 20 °C / Inert atmosphere

1.2: 0.25 h / 20 °C / Inert atmosphere

2.1: dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; potassium acetate / 1,4-dioxane / 100 °C / Inert atmosphere

With dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; potassium acetate; In 1,4-dioxane; dichloromethane;

Reference yield:

: 79099-07-3
N-tert-butyloxycarbonylpiperidin-4-one

: 1477815-42-1
4-{4-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3-trifluoromethoxyphenylcarbamoyl]piperazin-1-yl}piperidine-1-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 4 steps

1.1: acetic acid / 1,2-dichloro-ethane / 1 h / 20 °C

1.2: 20 °C / Inert atmosphere

2.1: palladium on activated charcoal; hydrogen / isopropyl alcohol / 20 °C / 2585.81 Torr / Inert atmosphere

3.1: dichloromethane / 20 °C / Inert atmosphere

3.2: 0.25 h / 20 °C / Inert atmosphere

4.1: dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; potassium acetate / 1,4-dioxane / 100 °C / Inert atmosphere

With dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; palladium on activated charcoal; hydrogen; potassium acetate; acetic acid; In 1,4-dioxane; dichloromethane; 1,2-dichloro-ethane; isopropyl alcohol;