3-(((1r,4r)-4-aminocyclohexyl)(ethyl)amino)-5-chloro-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-chloro-N-((4,6-dimethyl-2-oxo-1,2-dihydropyridin-3-yl)methyl)-2-methylbenzamide
CAS No.:1403596-82-6
Molecular Formula:C₂₄H₃₃ClN₄O₂
Molecular Weight:445.005
Hs Code.:

Synonyms:3-(((1r,4r)-4-aminocyclohexyl)(ethyl)amino)-5-chloro-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-chloro-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-chloro-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-chloro-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: 98.0%

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

: 1403596-82-6
3-(((1r,4r)-4-aminocyclohexyl)(ethyl)amino)-5-chloro-N-((4,6-dimethyl-2-oxo-1,2-dihydropyridin-3-yl)methyl)-2-methylbenzamide

Guidance literature:: With trifluoroacetic acid; In dichloromethane; at 20 ℃; for 2h;

Reference yield:

: 1403597-77-2
methyl 3-(((trans)-4-((tert-butoxycarbonyl)amino)cyclohexyl)amino)-5-chloro-2-methylbenzoate

: 1403596-82-6
3-(((1r,4r)-4-aminocyclohexyl)(ethyl)amino)-5-chloro-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 / 1,2-dichloro-ethane / 0.33 h / 20 °C

1.2: 0 - 20 °C

2.1: sodium hydroxide; water / ethanol / 2 h / 70 °C

2.2: 0 °C / pH 6

3.1: benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate / dimethyl sulfoxide / 20 °C

4.1: trifluoroacetic acid / dichloromethane / 2 h / 20 °C

With benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; water; acetic acid; trifluoroacetic acid; sodium hydroxide; In ethanol; dichloromethane; dimethyl sulfoxide; 1,2-dichloro-ethane;

Reference yield:

: 1403596-80-4
methyl 3-(((trans)-4-((tert-butoxycarbonyl) amino)cyclohexyl)(ethyl)amino)-5-chloro-2-methylbenzoate

: 1403596-82-6
3-(((1r,4r)-4-aminocyclohexyl)(ethyl)amino)-5-chloro-N-((4,6-dimethyl-2-oxo-1,2-dihydropyridin-3-yl)methyl)-2-methylbenzamide

Guidance literature:: Multi-step reaction with 3 steps

1.1: sodium hydroxide; water / ethanol / 2 h / 70 °C

1.2: 0 °C / pH 6

2.1: benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate / dimethyl sulfoxide / 20 °C

3.1: trifluoroacetic acid / dichloromethane / 2 h / 20 °C

With benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; water; trifluoroacetic acid; sodium hydroxide; In ethanol; dichloromethane; dimethyl sulfoxide;