ethyl 3-{3-[({5-cyano-4-[({4-[(tert-butoxycarbonylamino)methyl]cyclohexyl}methyl)amino]pyrimidin-2-yl}amino)methyl]-2-methylphenyl}benzoate

Base Information

Chemical Name:ethyl 3-{3-[({5-cyano-4-[({4-[(tert-butoxycarbonylamino)methyl]cyclohexyl}methyl)amino]pyrimidin-2-yl}amino)methyl]-2-methylphenyl}benzoate
CAS No.:1412438-68-6
Molecular Formula:C₃₅H₄₄N₆O₄
Molecular Weight:612.772
Hs Code.:

Synonyms:ethyl 3-{3-[({5-cyano-4-[({4-[(tert-butoxycarbonylamino)methyl]cyclohexyl}methyl)amino]pyrimidin-2-yl}amino)methyl]-2-methylphenyl}benzoate

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Chemical Property of ethyl 3-{3-[({5-cyano-4-[({4-[(tert-butoxycarbonylamino)methyl]cyclohexyl}methyl)amino]pyrimidin-2-yl}amino)methyl]-2-methylphenyl}benzoate

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Technology Process of ethyl 3-{3-[({5-cyano-4-[({4-[(tert-butoxycarbonylamino)methyl]cyclohexyl}methyl)amino]pyrimidin-2-yl}amino)methyl]-2-methylphenyl}benzoate

There total 4 articles about ethyl 3-{3-[({5-cyano-4-[({4-[(tert-butoxycarbonylamino)methyl]cyclohexyl}methyl)amino]pyrimidin-2-yl}amino)methyl]-2-methylphenyl}benzoate 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:

: 174959-91-2
tert-butyl ((4-(aminomethyl)cyclohexyl)methyl)carbamate

: 1412438-67-5
ethyl 3-[3-({[4-chloro-5-cyanopyrimidin-2-yl]amino}methyl)-2-methylphenyl]benzoate

: 1412438-68-6
ethyl 3-{3-[({5-cyano-4-[({4-[(tert-butoxycarbonylamino)methyl]cyclohexyl}methyl)amino]pyrimidin-2-yl}amino)methyl]-2-methylphenyl}benzoate

Guidance literature:: With triethylamine; In tetrahydrofuran; at 60 ℃; for 16h;

Reference yield:

: 76006-33-2
3-bromo-2-methylbenzoic acid

: 1412438-68-6
ethyl 3-{3-[({5-cyano-4-[({4-[(tert-butoxycarbonylamino)methyl]cyclohexyl}methyl)amino]pyrimidin-2-yl}amino)methyl]-2-methylphenyl}benzoate

Guidance literature:: Multi-step reaction with 5 steps

1.1: N-ethyl-N,N-diisopropylamine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol; ammonium chloride / N,N-dimethyl-formamide / 20 °C

2.1: dimethylsulfide borane complex / Reflux

2.2: 0.17 h / 20 °C

2.3: 1 h / 20 °C

3.1: caesium carbonate / dichloro[1,1'-bis(di-t-butylphosphino)ferrocene]palladium(II) / 1,4-dioxane / 100 °C / Inert atmosphere

4.1: diethylamine / N,N-dimethyl-formamide / 1 h / 20 °C

5.1: triethylamine / tetrahydrofuran / 16 h / 60 °C

With dimethylsulfide borane complex; ammonium chloride; benzotriazol-1-ol; caesium carbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; diethylamine; triethylamine; N-ethyl-N,N-diisopropylamine; dichloro[1,1'-bis(di-t-butylphosphino)ferrocene]palladium(II); In tetrahydrofuran; 1,4-dioxane; N,N-dimethyl-formamide;

Reference yield:

: 919363-09-0
3-bromo-2-methylbenzamide

: 1412438-68-6
ethyl 3-{3-[({5-cyano-4-[({4-[(tert-butoxycarbonylamino)methyl]cyclohexyl}methyl)amino]pyrimidin-2-yl}amino)methyl]-2-methylphenyl}benzoate

Guidance literature:: Multi-step reaction with 4 steps

1.1: dimethylsulfide borane complex / Reflux

1.2: 0.17 h / 20 °C

1.3: 1 h / 20 °C

2.1: caesium carbonate / dichloro[1,1'-bis(di-t-butylphosphino)ferrocene]palladium(II) / 1,4-dioxane / 100 °C / Inert atmosphere

3.1: diethylamine / N,N-dimethyl-formamide / 1 h / 20 °C

4.1: triethylamine / tetrahydrofuran / 16 h / 60 °C

With dimethylsulfide borane complex; caesium carbonate; diethylamine; triethylamine; dichloro[1,1'-bis(di-t-butylphosphino)ferrocene]palladium(II); In tetrahydrofuran; 1,4-dioxane; N,N-dimethyl-formamide;