Technology Process of 2-(3-(2-(2-((4-(piperidin-4-yl)phenyl)amino)-5-(trifluoromethyl)pyrimidin-4-yl)ethyl)pyrazin-2-yl)acetamide
There total 11 articles about 2-(3-(2-(2-((4-(piperidin-4-yl)phenyl)amino)-5-(trifluoromethyl)pyrimidin-4-yl)ethyl)pyrazin-2-yl)acetamide 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:
- Guidance literature:
-
tert-butyl 4-(4-((4-(2-(3-(2-amino-2-oxoethyl)pyrazin-2-yl)ethyl)-5-(trifluoromethyl)pyrimidin-2-yl)amino)phenyl)piperidine-1-carboxylate;
With
trifluoroacetic acid;
In
dichloromethane;
at 20 ℃;
for 17h;
With
sodium hydroxide;
In
water;
- Guidance literature:
-
Multi-step reaction with 6 steps
1.1: triethylamine / triphenylphosphine; copper(l) iodide; bis-triphenylphosphine-palladium(II) chloride / N,N-dimethyl-formamide / 18 h / 90 °C / Inert atmosphere; sealed tube
2.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 0.03 h / 0 °C
3.1: triethylamine / triphenylphosphine; copper(l) iodide; bis-triphenylphosphine-palladium(II) chloride / N,N-dimethyl-formamide / 0.25 h / 120 °C / Inert atmosphere; microwave irradiation
4.1: triethylamine; hydrogen / N,N-dimethyl-formamide / 17 h
5.1: water; lithium hydroxide monohydrate / tetrahydrofuran; methanol / 17 h / 20 °C
5.2: 2 h
6.1: trifluoroacetic acid / dichloromethane / 17 h / 20 °C
With
lithium hydroxide monohydrate; tetrabutyl ammonium fluoride; water; hydrogen; triethylamine; trifluoroacetic acid;
bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; triphenylphosphine;
In
tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl-formamide;
- Guidance literature:
-
Multi-step reaction with 5 steps
1.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 0.03 h / 0 °C
2.1: triethylamine / triphenylphosphine; copper(l) iodide; bis-triphenylphosphine-palladium(II) chloride / N,N-dimethyl-formamide / 0.25 h / 120 °C / Inert atmosphere; microwave irradiation
3.1: triethylamine; hydrogen / N,N-dimethyl-formamide / 17 h
4.1: water; lithium hydroxide monohydrate / tetrahydrofuran; methanol / 17 h / 20 °C
4.2: 2 h
5.1: trifluoroacetic acid / dichloromethane / 17 h / 20 °C
With
lithium hydroxide monohydrate; tetrabutyl ammonium fluoride; water; hydrogen; triethylamine; trifluoroacetic acid;
bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; triphenylphosphine;
In
tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl-formamide;