tert-butyl (1-(4-((4-(2-(2-amino-2-oxoethyl)phenethyl)-5-methylpyrimidin-2-yl)amino)phenyl)ethyl)carbamate

Base Information

Chemical Name:tert-butyl (1-(4-((4-(2-(2-amino-2-oxoethyl)phenethyl)-5-methylpyrimidin-2-yl)amino)phenyl)ethyl)carbamate
CAS No.:1566585-37-2
Molecular Formula:C₂₈H₃₅N₅O₃
Molecular Weight:489.618
Hs Code.:

Synonyms:tert-butyl (1-(4-((4-(2-(2-amino-2-oxoethyl)phenethyl)-5-methylpyrimidin-2-yl)amino)phenyl)ethyl)carbamate

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Chemical Property of tert-butyl (1-(4-((4-(2-(2-amino-2-oxoethyl)phenethyl)-5-methylpyrimidin-2-yl)amino)phenyl)ethyl)carbamate

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Technology Process of tert-butyl (1-(4-((4-(2-(2-amino-2-oxoethyl)phenethyl)-5-methylpyrimidin-2-yl)amino)phenyl)ethyl)carbamate

There total 9 articles about tert-butyl (1-(4-((4-(2-(2-amino-2-oxoethyl)phenethyl)-5-methylpyrimidin-2-yl)amino)phenyl)ethyl)carbamate 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: 29.0%

: 643086-68-4
[1-(4-amino-phenyl)-ethyl]carbamic acid tert-butyl ester

: 1566584-27-7
2-(2-(2-(2-chloro-5-methylpyrimidin-4-yl)ethyl)phenyl)acetamide

: 1566585-37-2
tert-butyl (1-(4-((4-(2-(2-amino-2-oxoethyl)phenethyl)-5-methylpyrimidin-2-yl)amino)phenyl)ethyl)carbamate

Guidance literature:: With palladium diacetate; caesium carbonate; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; In 1,4-dioxane; at 105 ℃; for 6h; Microwave irradiation;

Reference yield:

: 100-19-6
(4-nitrophenyl)ethanone

: 1566585-37-2
tert-butyl (1-(4-((4-(2-(2-amino-2-oxoethyl)phenethyl)-5-methylpyrimidin-2-yl)amino)phenyl)ethyl)carbamate

Guidance literature:: Multi-step reaction with 4 steps

1.1: ammonium acetate / methanol / 0.33 h / 20 °C

1.2: 48 h

2.1: triethylamine / dichloromethane / 21 h / 20 °C

3.1: palladium; hydrogen / ethyl acetate / 3 h

4.1: palladium diacetate; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; caesium carbonate / 1,4-dioxane / 6 h / 105 °C / Microwave irradiation

With ammonium acetate; hydrogen; palladium diacetate; caesium carbonate; palladium; triethylamine; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; In 1,4-dioxane; methanol; dichloromethane; ethyl acetate;

Reference yield:

: 42142-15-4
1-(4-nitro-phenyl)-ethylamine

: 1566585-37-2
tert-butyl (1-(4-((4-(2-(2-amino-2-oxoethyl)phenethyl)-5-methylpyrimidin-2-yl)amino)phenyl)ethyl)carbamate

Guidance literature:: Multi-step reaction with 3 steps

1: triethylamine / dichloromethane / 21 h / 20 °C

2: palladium; hydrogen / ethyl acetate / 3 h

3: palladium diacetate; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; caesium carbonate / 1,4-dioxane / 6 h / 105 °C / Microwave irradiation

With hydrogen; palladium diacetate; caesium carbonate; palladium; triethylamine; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; In 1,4-dioxane; dichloromethane; ethyl acetate;