3-(((1R,4R)-4-aminocyclohexyl)(ethyl)amino)-5-bromo-N-((4,6-dimethyl-2-oxo-1,2-dihydropyridin-3-yl)methyl)-2-methylbenzamide

Base Information

Chemical Name:3-(((1R,4R)-4-aminocyclohexyl)(ethyl)amino)-5-bromo-N-((4,6-dimethyl-2-oxo-1,2-dihydropyridin-3-yl)methyl)-2-methylbenzamide
CAS No.:1403258-67-2
Molecular Formula:C₂₄H₃₃BrN₄O₂
Molecular Weight:489.456
Hs Code.:

Synonyms:3-(((1R,4R)-4-aminocyclohexyl)(ethyl)amino)-5-bromo-N-((4,6-dimethyl-2-oxo-1,2-dihydropyridin-3-yl)methyl)-2-methylbenzamide

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Chemical Property of 3-(((1R,4R)-4-aminocyclohexyl)(ethyl)amino)-5-bromo-N-((4,6-dimethyl-2-oxo-1,2-dihydropyridin-3-yl)methyl)-2-methylbenzamide

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Technology Process of 3-(((1R,4R)-4-aminocyclohexyl)(ethyl)amino)-5-bromo-N-((4,6-dimethyl-2-oxo-1,2-dihydropyridin-3-yl)methyl)-2-methylbenzamide

There total 6 articles about 3-(((1R,4R)-4-aminocyclohexyl)(ethyl)amino)-5-bromo-N-((4,6-dimethyl-2-oxo-1,2-dihydropyridin-3-yl)methyl)-2-methylbenzamide 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: 87.5%

: 1403258-28-5
tert-butyl ((1R,4R)-4-((5-bromo-3-(((4,6-dimethyl-2-oxo-1,2-dihydropyridin-3-yl)methyl)carbamoyl)-2-methylphenyl)(ethyl)amino)cyclohexyl)carbamate

: 1403258-67-2
3-(((1R,4R)-4-aminocyclohexyl)(ethyl)amino)-5-bromo-N-((4,6-dimethyl-2-oxo-1,2-dihydropyridin-3-yl)methyl)-2-methylbenzamide

Guidance literature:: With trifluoroacetic acid; In dichloromethane; at 20 ℃; for 1h;

Reference yield:

: 1403258-26-3
methyl 5-bromo-3-(((trans)-4-((tert-butoxycarbonyl)amino)cyclohexyl)-amino)-2-methylbenzoate

: 1403258-67-2
3-(((1R,4R)-4-aminocyclohexyl)(ethyl)amino)-5-bromo-N-((4,6-dimethyl-2-oxo-1,2-dihydropyridin-3-yl)methyl)-2-methylbenzamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: acetic acid / 1,1-dichloroethane / 0.33 h / 20 °C

1.2: 0 - 20 °C

2.1: sodium hydroxide; water / ethanol / 1 h / 60 °C

2.2: pH 6

2.3: pH 4

3.1: triethylamine / dimethyl sulfoxide / 0.25 h / 20 °C

3.2: 20 °C

4.1: trifluoroacetic acid / dichloromethane / 1 h / 20 °C

With water; acetic acid; triethylamine; trifluoroacetic acid; sodium hydroxide; In 1,1-dichloroethane; ethanol; dichloromethane; dimethyl sulfoxide;

Reference yield:

: 107650-20-4
5-bromo-2-methyl-3-nitro-benzoic acid

: 1403258-67-2
3-(((1R,4R)-4-aminocyclohexyl)(ethyl)amino)-5-bromo-N-((4,6-dimethyl-2-oxo-1,2-dihydropyridin-3-yl)methyl)-2-methylbenzamide

Guidance literature:: Multi-step reaction with 7 steps

1.1: sodium carbonate / N,N-dimethyl-formamide / 8 h / 60 °C

2.1: ammonium chloride; iron / ethanol; water / 7 h / 80 °C

3.1: acetic acid / methanol / 8 h / 20 °C

3.2: 0 °C

4.1: acetic acid / 1,1-dichloroethane / 0.33 h / 20 °C

4.2: 0 - 20 °C

5.1: sodium hydroxide; water / ethanol / 1 h / 60 °C

5.2: pH 6

5.3: pH 4

6.1: triethylamine / dimethyl sulfoxide / 0.25 h / 20 °C

6.2: 20 °C

7.1: trifluoroacetic acid / dichloromethane / 1 h / 20 °C

With water; iron; sodium carbonate; ammonium chloride; acetic acid; triethylamine; trifluoroacetic acid; sodium hydroxide; In methanol; 1,1-dichloroethane; ethanol; dichloromethane; water; dimethyl sulfoxide; N,N-dimethyl-formamide;