tert-butyl 3-(4-((4-(2-(3-(2-methoxy-2-oxoethyl)pyridin-2-yl)ethyl)-5-(trifluoromethyl)pyrimidin-2-yl)amino)phenyl)piperidine-1-carboxylate

Base Information

Chemical Name:tert-butyl 3-(4-((4-(2-(3-(2-methoxy-2-oxoethyl)pyridin-2-yl)ethyl)-5-(trifluoromethyl)pyrimidin-2-yl)amino)phenyl)piperidine-1-carboxylate
CAS No.:1393901-84-2
Molecular Formula:C₃₁H₃₆F₃N₅O₄
Molecular Weight:599.653
Hs Code.:

Synonyms:tert-butyl 3-(4-((4-(2-(3-(2-methoxy-2-oxoethyl)pyridin-2-yl)ethyl)-5-(trifluoromethyl)pyrimidin-2-yl)amino)phenyl)piperidine-1-carboxylate

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Chemical Property of tert-butyl 3-(4-((4-(2-(3-(2-methoxy-2-oxoethyl)pyridin-2-yl)ethyl)-5-(trifluoromethyl)pyrimidin-2-yl)amino)phenyl)piperidine-1-carboxylate

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Technology Process of tert-butyl 3-(4-((4-(2-(3-(2-methoxy-2-oxoethyl)pyridin-2-yl)ethyl)-5-(trifluoromethyl)pyrimidin-2-yl)amino)phenyl)piperidine-1-carboxylate

There total 13 articles about tert-butyl 3-(4-((4-(2-(3-(2-methoxy-2-oxoethyl)pyridin-2-yl)ethyl)-5-(trifluoromethyl)pyrimidin-2-yl)amino)phenyl)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: 49.0%

: 1393901-83-1
tert-butyl 3-(4-((4-((3-(2-methoxy-2-oxoethyl)pyridin-2-yl)ethynyl)-5-(trifluoromethyl)pyrimidin-2-yl)amino)phenyl)piperidine-1-carboxylate

: 1393901-84-2
tert-butyl 3-(4-((4-(2-(3-(2-methoxy-2-oxoethyl)pyridin-2-yl)ethyl)-5-(trifluoromethyl)pyrimidin-2-yl)amino)phenyl)piperidine-1-carboxylate

Guidance literature:: With hydrogen; triethylamine; palladium on activated charcoal; In N,N-dimethyl-formamide; at 20 ℃; for 35h;

Reference yield:

: 1692-25-7
3-pyridylboronic acid

: 1393901-84-2
tert-butyl 3-(4-((4-(2-(3-(2-methoxy-2-oxoethyl)pyridin-2-yl)ethyl)-5-(trifluoromethyl)pyrimidin-2-yl)amino)phenyl)piperidine-1-carboxylate

Guidance literature:: Multi-step reaction with 5 steps

1.1: caesium carbonate / triphenylphosphine; palladium diacetate / N,N-dimethyl-formamide / 18 h / 80 °C

2.1: hydrogenchloride; hydrogen / water; methanol / 48 h / 2068.65 Torr / Inert atmosphere

2.2: 20 h / 20 °C

3.1: zinc(II) chloride / diethyl ether; 1,2-dichloro-ethane; tert-butyl alcohol / 0.5 h / 0 °C

3.2: 60 h / 0 - 20 °C

4.1: triethylamine / triphenylphosphine; copper(l) iodide; bis-triphenylphosphine-palladium(II) chloride / N,N-dimethyl-formamide; tetrahydrofuran / 0.67 h / 120 °C / Inert atmosphere; microwave irradiation

5.1: triethylamine; hydrogen / palladium on activated charcoal / N,N-dimethyl-formamide / 35 h / 20 °C

With hydrogenchloride; hydrogen; caesium carbonate; triethylamine; zinc(II) chloride; bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; palladium on activated charcoal; palladium diacetate; triphenylphosphine; In tetrahydrofuran; methanol; diethyl ether; water; 1,2-dichloro-ethane; N,N-dimethyl-formamide; tert-butyl alcohol;

Reference yield:

: 636-98-6
p-nitrobenzene iodide

: 1393901-84-2
tert-butyl 3-(4-((4-(2-(3-(2-methoxy-2-oxoethyl)pyridin-2-yl)ethyl)-5-(trifluoromethyl)pyrimidin-2-yl)amino)phenyl)piperidine-1-carboxylate

Guidance literature:: Multi-step reaction with 5 steps

1.1: caesium carbonate / triphenylphosphine; palladium diacetate / N,N-dimethyl-formamide / 18 h / 80 °C

2.1: hydrogenchloride; hydrogen / water; methanol / 48 h / 2068.65 Torr / Inert atmosphere

2.2: 20 h / 20 °C

3.1: zinc(II) chloride / diethyl ether; 1,2-dichloro-ethane; tert-butyl alcohol / 0.5 h / 0 °C

3.2: 60 h / 0 - 20 °C

4.1: triethylamine / triphenylphosphine; copper(l) iodide; bis-triphenylphosphine-palladium(II) chloride / N,N-dimethyl-formamide; tetrahydrofuran / 0.67 h / 120 °C / Inert atmosphere; microwave irradiation

5.1: triethylamine; hydrogen / palladium on activated charcoal / N,N-dimethyl-formamide / 35 h / 20 °C

With hydrogenchloride; hydrogen; caesium carbonate; triethylamine; zinc(II) chloride; bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; palladium on activated charcoal; palladium diacetate; triphenylphosphine; In tetrahydrofuran; methanol; diethyl ether; water; 1,2-dichloro-ethane; N,N-dimethyl-formamide; tert-butyl alcohol;