methyl 2-(2-(2-(2-((4-(((tert-butoxycarbonyl)amino)methyl)phenyl)amino)-5-(trifluoromethyl)pyrimidin-4-yl)ethyl)phenyl)acetate

Base Information

Chemical Name:methyl 2-(2-(2-(2-((4-(((tert-butoxycarbonyl)amino)methyl)phenyl)amino)-5-(trifluoromethyl)pyrimidin-4-yl)ethyl)phenyl)acetate
CAS No.:1566584-41-5
Molecular Formula:C₂₈H₃₁F₃N₄O₄
Molecular Weight:544.574
Hs Code.:

Synonyms:methyl 2-(2-(2-(2-((4-(((tert-butoxycarbonyl)amino)methyl)phenyl)amino)-5-(trifluoromethyl)pyrimidin-4-yl)ethyl)phenyl)acetate

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Chemical Property of methyl 2-(2-(2-(2-((4-(((tert-butoxycarbonyl)amino)methyl)phenyl)amino)-5-(trifluoromethyl)pyrimidin-4-yl)ethyl)phenyl)acetate

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Technology Process of methyl 2-(2-(2-(2-((4-(((tert-butoxycarbonyl)amino)methyl)phenyl)amino)-5-(trifluoromethyl)pyrimidin-4-yl)ethyl)phenyl)acetate

There total 9 articles about methyl 2-(2-(2-(2-((4-(((tert-butoxycarbonyl)amino)methyl)phenyl)amino)-5-(trifluoromethyl)pyrimidin-4-yl)ethyl)phenyl)acetate 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: 74.0%

: 1566584-39-1
methyl 2-(2-((2-((4-(((tert-butoxycarbonyl)amino)methyl)phenyl)amino)-5-(trifluoromethyl)pyrimidin-4-yl)ethynyl)phenyl)acetate

: 1566584-41-5
methyl 2-(2-(2-(2-((4-(((tert-butoxycarbonyl)amino)methyl)phenyl)amino)-5-(trifluoromethyl)pyrimidin-4-yl)ethyl)phenyl)acetate

Guidance literature:: With palladium 10% on activated carbon; hydrogen; triethylamine; In N,N-dimethyl-formamide; at 20 ℃; for 16h;

Reference yield:

: 4403-71-8
(4-aminomethyl)aniline

: 1566584-41-5
methyl 2-(2-(2-(2-((4-(((tert-butoxycarbonyl)amino)methyl)phenyl)amino)-5-(trifluoromethyl)pyrimidin-4-yl)ethyl)phenyl)acetate

Guidance literature:: Multi-step reaction with 4 steps

1.1: triethylamine / dichloromethane / 20 °C

2.1: zinc(II) chloride / tert-butyl alcohol; 1,2-dichloro-ethane; diethyl ether / 0.33 h / 20 °C

2.2: 20 °C

3.1: copper(l) iodide; triethylamine; triphenylphosphine / N,N-dimethyl-formamide / 0.08 h

3.2: 0.33 h / 120 °C / Microwave irradiation

4.1: triethylamine; palladium 10% on activated carbon; hydrogen / N,N-dimethyl-formamide / 16 h / 20 °C

With copper(l) iodide; palladium 10% on activated carbon; hydrogen; triethylamine; triphenylphosphine; zinc(II) chloride; In diethyl ether; dichloromethane; 1,2-dichloro-ethane; N,N-dimethyl-formamide; tert-butyl alcohol;

Reference yield:

: 24424-99-5
di-tert-butyl dicarbonate

: 1566584-41-5
methyl 2-(2-(2-(2-((4-(((tert-butoxycarbonyl)amino)methyl)phenyl)amino)-5-(trifluoromethyl)pyrimidin-4-yl)ethyl)phenyl)acetate

Guidance literature:: Multi-step reaction with 4 steps

1.1: triethylamine / dichloromethane / 20 °C

2.1: zinc(II) chloride / tert-butyl alcohol; 1,2-dichloro-ethane; diethyl ether / 0.33 h / 20 °C

2.2: 20 °C

3.1: copper(l) iodide; triethylamine; triphenylphosphine / N,N-dimethyl-formamide / 0.08 h

3.2: 0.33 h / 120 °C / Microwave irradiation

4.1: triethylamine; palladium 10% on activated carbon; hydrogen / N,N-dimethyl-formamide / 16 h / 20 °C

With copper(l) iodide; palladium 10% on activated carbon; hydrogen; triethylamine; triphenylphosphine; zinc(II) chloride; In diethyl ether; dichloromethane; 1,2-dichloro-ethane; N,N-dimethyl-formamide; tert-butyl alcohol;