4-(4-carbamoyl-2'-cyclohexylamino-3-phenyl-[2,4']bipyridinyl-6-yl)-piperazine-1-carboxylic acid tert-butyl ester

Base Information

Chemical Name:4-(4-carbamoyl-2'-cyclohexylamino-3-phenyl-[2,4']bipyridinyl-6-yl)-piperazine-1-carboxylic acid tert-butyl ester
CAS No.:1201675-41-3
Molecular Formula:C₃₂H₄₀N₆O₃
Molecular Weight:556.708
Hs Code.:

Synonyms:4-(4-carbamoyl-2'-cyclohexylamino-3-phenyl-[2,4']bipyridinyl-6-yl)-piperazine-1-carboxylic acid tert-butyl ester

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Chemical Property of 4-(4-carbamoyl-2'-cyclohexylamino-3-phenyl-[2,4']bipyridinyl-6-yl)-piperazine-1-carboxylic acid tert-butyl ester

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Technology Process of 4-(4-carbamoyl-2'-cyclohexylamino-3-phenyl-[2,4']bipyridinyl-6-yl)-piperazine-1-carboxylic acid tert-butyl ester

There total 8 articles about 4-(4-carbamoyl-2'-cyclohexylamino-3-phenyl-[2,4']bipyridinyl-6-yl)-piperazine-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: 75.0%

: 1201675-40-2
4-(4-carbamoyl-2'-fluoro-3-phenyl-[2,4']bipyridinyl-6-yl)-piperazine-1-carboxylic acid tert-butyl ester

: 108-91-8,157973-60-9
cyclohexylamine

: 1201675-41-3
4-(4-carbamoyl-2'-cyclohexylamino-3-phenyl-[2,4']bipyridinyl-6-yl)-piperazine-1-carboxylic acid tert-butyl ester

Guidance literature:: With copper (II)-fluoride; at 150 ℃; for 12h;

Reference yield:

: 1201674-86-3
4-(6-bromo-4-methoxycarbonylpyridin-2-yl)piperazine-1-carboxylic acid tert-butyl ester

: 1201675-41-3
4-(4-carbamoyl-2'-cyclohexylamino-3-phenyl-[2,4']bipyridinyl-6-yl)-piperazine-1-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 6 steps

1.1: sodium carbonate / dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂ / 1,2-dimethoxyethane / 4 h / 80 °C

2.1: bromine; potassium acetate / dichloromethane / 0 °C

3.1: sodium carbonate / dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂ / 1,2-dimethoxyethane / 0.75 h / 130 °C / Microwave irradiation

4.1: water; lithium hydroxide / tetrahydrofuran / 20 °C

4.2: pH 6

5.1: ammonium chloride; N-ethyl-N,N-diisopropylamine; HATU / N,N-dimethyl-formamide

6.1: copper (II)-fluoride / 12 h / 150 °C

With copper (II)-fluoride; water; bromine; potassium acetate; sodium carbonate; ammonium chloride; N-ethyl-N,N-diisopropylamine; HATU; lithium hydroxide; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; In tetrahydrofuran; 1,2-dimethoxyethane; dichloromethane; N,N-dimethyl-formamide;

Reference yield:

: 1201675-37-7
3-bromo-6-(4-tert-butoxycarbonyl-piperazin-1-yl)-2'-fluoro-[2,4']bipyridinyl-4-carboxylic acid methyl ester

: 1201675-41-3
4-(4-carbamoyl-2'-cyclohexylamino-3-phenyl-[2,4']bipyridinyl-6-yl)-piperazine-1-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 4 steps

1.1: sodium carbonate / dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂ / 1,2-dimethoxyethane / 0.75 h / 130 °C / Microwave irradiation

2.1: water; lithium hydroxide / tetrahydrofuran / 20 °C

2.2: pH 6

3.1: ammonium chloride; N-ethyl-N,N-diisopropylamine; HATU / N,N-dimethyl-formamide

4.1: copper (II)-fluoride / 12 h / 150 °C

With copper (II)-fluoride; water; sodium carbonate; ammonium chloride; N-ethyl-N,N-diisopropylamine; HATU; lithium hydroxide; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; In tetrahydrofuran; 1,2-dimethoxyethane; N,N-dimethyl-formamide;