tert-butyl N-{[trans-4-{[(2-{[(3-bromo-2-methylphenyl)methyl]amino}-5-nitropyrimidin-4-yl)amino]methyl} cyclohexyl]methyl}carbamate

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Chemical Name:tert-butyl N-{[trans-4-{[(2-{[(3-bromo-2-methylphenyl)methyl]amino}-5-nitropyrimidin-4-yl)amino]methyl} cyclohexyl]methyl}carbamate
CAS No.:1236133-21-3
Molecular Formula:C₂₅H₃₅BrN₆O₄
Molecular Weight:563.495
Hs Code.:

Synonyms:tert-butyl N-{[trans-4-{[(2-{[(3-bromo-2-methylphenyl)methyl]amino}-5-nitropyrimidin-4-yl)amino]methyl} cyclohexyl]methyl}carbamate

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Chemical Property of tert-butyl N-{[trans-4-{[(2-{[(3-bromo-2-methylphenyl)methyl]amino}-5-nitropyrimidin-4-yl)amino]methyl} cyclohexyl]methyl}carbamate

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Technology Process of tert-butyl N-{[trans-4-{[(2-{[(3-bromo-2-methylphenyl)methyl]amino}-5-nitropyrimidin-4-yl)amino]methyl} cyclohexyl]methyl}carbamate

There total 4 articles about tert-butyl N-{[trans-4-{[(2-{[(3-bromo-2-methylphenyl)methyl]amino}-5-nitropyrimidin-4-yl)amino]methyl} cyclohexyl]methyl}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: 89.0%

: 1412438-57-3
2-(3-bromo-2-methyl-benzylamino)-4-thiocyanato-5-nitro pyrimidine

: 166168-16-7
trans-((4-aminomethyl)cyclohexylmethyl)carbamic acid tert-butyl ester

: 1236133-21-3
tert-butyl N-{[trans-4-{[(2-{[(3-bromo-2-methylphenyl)methyl]amino}-5-nitropyrimidin-4-yl)amino]methyl} cyclohexyl]methyl}carbamate

Guidance literature:: In N,N-dimethyl-formamide; at 20 ℃;

Reference yield:

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

: 1236133-21-3
tert-butyl N-{[trans-4-{[(2-{[(3-bromo-2-methylphenyl)methyl]amino}-5-nitropyrimidin-4-yl)amino]methyl} cyclohexyl]methyl}carbamate

Guidance literature:: Multi-step reaction with 4 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: triethylamine / ethanol / 20 °C

4.1: N,N-dimethyl-formamide / 20 °C

With dimethylsulfide borane complex; ammonium chloride; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; N-ethyl-N,N-diisopropylamine; In ethanol; N,N-dimethyl-formamide;

Reference yield:

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

: 1236133-21-3
tert-butyl N-{[trans-4-{[(2-{[(3-bromo-2-methylphenyl)methyl]amino}-5-nitropyrimidin-4-yl)amino]methyl} cyclohexyl]methyl}carbamate

Guidance literature:: Multi-step reaction with 3 steps

1.1: dimethylsulfide borane complex / Reflux

1.2: 0.17 h / 20 °C

1.3: 1 h / 20 °C

2.1: triethylamine / ethanol / 20 °C

3.1: N,N-dimethyl-formamide / 20 °C

With dimethylsulfide borane complex; triethylamine; In ethanol; N,N-dimethyl-formamide;