tert-butyl 4-[2-cyano-4-[2-[(4-methoxycarbonylphenyl)amino]pyrimidin-4-yl]phenoxy]piperidine-1-carboxylate

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Chemical Name:tert-butyl 4-[2-cyano-4-[2-[(4-methoxycarbonylphenyl)amino]pyrimidin-4-yl]phenoxy]piperidine-1-carboxylate
CAS No.:1292317-82-8
Molecular Formula:C₂₉H₃₁N₅O₅
Molecular Weight:529.596
Hs Code.:

Synonyms:tert-butyl 4-[2-cyano-4-[2-[(4-methoxycarbonylphenyl)amino]pyrimidin-4-yl]phenoxy]piperidine-1-carboxylate

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Chemical Property of tert-butyl 4-[2-cyano-4-[2-[(4-methoxycarbonylphenyl)amino]pyrimidin-4-yl]phenoxy]piperidine-1-carboxylate

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Technology Process of tert-butyl 4-[2-cyano-4-[2-[(4-methoxycarbonylphenyl)amino]pyrimidin-4-yl]phenoxy]piperidine-1-carboxylate

There total 6 articles about tert-butyl 4-[2-cyano-4-[2-[(4-methoxycarbonylphenyl)amino]pyrimidin-4-yl]phenoxy]piperidine-1-carboxylate 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: 69.0%

: 1292317-58-8
tert-butyl 4-(4-(2-chloropyrimidin-4-yl)-2-cyanophenoxy)piperidine-1-carboxylate

: 619-45-4
4-methoxycarbonyl aniline

: 1292317-82-8
tert-butyl 4-[2-cyano-4-[2-[(4-methoxycarbonylphenyl)amino]pyrimidin-4-yl]phenoxy]piperidine-1-carboxylate

Guidance literature:: With caesium carbonate; palladium diacetate; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; In 1,4-dioxane; at 90 ℃; for 16h; Inert atmosphere;

Reference yield:

: 109384-19-2
t-butyl 4-hydroxy piperidine-1-carboxylate

: 1292317-82-8
tert-butyl 4-[2-cyano-4-[2-[(4-methoxycarbonylphenyl)amino]pyrimidin-4-yl]phenoxy]piperidine-1-carboxylate

Guidance literature:: Multi-step reaction with 4 steps

1: triphenylphosphine; diethylazodicarboxylate / tetrahydrofuran / 18 h / 20 °C

2: potassium acetate / dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂ / 1,4-dioxane / 20 h / 80 °C

3: potassium carbonate / tetrakis(triphenylphosphine) palladium⁽⁰⁾ / acetonitrile; water / 20 h / Reflux

4: caesium carbonate / palladium diacetate; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl / 1,4-dioxane / 16 h / 90 °C / Inert atmosphere

With potassium acetate; potassium carbonate; caesium carbonate; triphenylphosphine; diethylazodicarboxylate; tetrakis(triphenylphosphine) palladium⁽⁰⁾; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; palladium diacetate; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; In tetrahydrofuran; 1,4-dioxane; water; acetonitrile;

Reference yield:

: 40530-18-5
5-bromo-2-hydroxybenzonitrile

: 1292317-82-8
tert-butyl 4-[2-cyano-4-[2-[(4-methoxycarbonylphenyl)amino]pyrimidin-4-yl]phenoxy]piperidine-1-carboxylate

Guidance literature:: Multi-step reaction with 4 steps

1: triphenylphosphine; diethylazodicarboxylate / tetrahydrofuran / 18 h / 20 °C

2: potassium acetate / dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂ / 1,4-dioxane / 20 h / 80 °C

3: potassium carbonate / tetrakis(triphenylphosphine) palladium⁽⁰⁾ / acetonitrile; water / 20 h / Reflux

4: caesium carbonate / palladium diacetate; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl / 1,4-dioxane / 16 h / 90 °C / Inert atmosphere

With potassium acetate; potassium carbonate; caesium carbonate; triphenylphosphine; diethylazodicarboxylate; tetrakis(triphenylphosphine) palladium⁽⁰⁾; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; palladium diacetate; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; In tetrahydrofuran; 1,4-dioxane; water; acetonitrile;