2-bromo-5-chloro-N-((4,6-dimethyl-2-oxo-1,2-dihydropyridin-3-yI)methyl)-3-(ethyl(tetrahydro-2H-pyran-4-yl)amino)benzamide

Base Information

Chemical Name:2-bromo-5-chloro-N-((4,6-dimethyl-2-oxo-1,2-dihydropyridin-3-yI)methyl)-3-(ethyl(tetrahydro-2H-pyran-4-yl)amino)benzamide
CAS No.:1403591-14-9
Molecular Formula:C₂₂H₂₇BrClN₃O₃
Molecular Weight:496.832
Hs Code.:

Synonyms:2-bromo-5-chloro-N-((4,6-dimethyl-2-oxo-1,2-dihydropyridin-3-yI)methyl)-3-(ethyl(tetrahydro-2H-pyran-4-yl)amino)benzamide

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Chemical Property of 2-bromo-5-chloro-N-((4,6-dimethyl-2-oxo-1,2-dihydropyridin-3-yI)methyl)-3-(ethyl(tetrahydro-2H-pyran-4-yl)amino)benzamide

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Technology Process of 2-bromo-5-chloro-N-((4,6-dimethyl-2-oxo-1,2-dihydropyridin-3-yI)methyl)-3-(ethyl(tetrahydro-2H-pyran-4-yl)amino)benzamide

There total 6 articles about 2-bromo-5-chloro-N-((4,6-dimethyl-2-oxo-1,2-dihydropyridin-3-yI)methyl)-3-(ethyl(tetrahydro-2H-pyran-4-yl)amino)benzamide 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:

: 771579-27-2
3-(aminomethyl)-4,6-dimethyl-1,2-dihydropyridin-2-one

: 1403596-36-0
2-bromo-5-chloro-3-[ethyl(oxan-4-yl)amino]benzoic acid

: 1403591-14-9
2-bromo-5-chloro-N-((4,6-dimethyl-2-oxo-1,2-dihydropyridin-3-yI)methyl)-3-(ethyl(tetrahydro-2H-pyran-4-yl)amino)benzamide

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In N,N-dimethyl-formamide; at 20 ℃; for 1h; Inert atmosphere;

Reference yield:

: 27007-53-0
methyl-2-bromo-5-chlorobenzoate

: 1403591-14-9
2-bromo-5-chloro-N-((4,6-dimethyl-2-oxo-1,2-dihydropyridin-3-yI)methyl)-3-(ethyl(tetrahydro-2H-pyran-4-yl)amino)benzamide

Guidance literature:: Multi-step reaction with 6 steps

1.1: nitric acid; sulfuric acid / 2 h / 0 °C

2.1: ammonium chloride / water; methanol / 20 - 70 °C

2.2: 3 h / 70 °C

3.1: acetic acid / 1,2-dichloro-ethane / 20 °C / Inert atmosphere

3.2: 41 h / 20 °C

4.1: acetic acid / 1,2-dichloro-ethane / 0.08 h / 20 °C / Inert atmosphere

5.1: sodium hydroxide / tetrahydrofuran / 20 h / 50 °C

5.2: pH 2 - 3

6.1: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 1 h / 20 °C / Inert atmosphere

With sulfuric acid; nitric acid; ammonium chloride; acetic acid; N-ethyl-N,N-diisopropylamine; sodium hydroxide; In tetrahydrofuran; methanol; water; 1,2-dichloro-ethane; N,N-dimethyl-formamide;

Reference yield:

: 1403596-31-5
methyl 2-bromo-5-chloro-3-nitrobenzoate

: 1403591-14-9
2-bromo-5-chloro-N-((4,6-dimethyl-2-oxo-1,2-dihydropyridin-3-yI)methyl)-3-(ethyl(tetrahydro-2H-pyran-4-yl)amino)benzamide

Guidance literature:: Multi-step reaction with 5 steps

1.1: ammonium chloride / water; methanol / 20 - 70 °C

1.2: 3 h / 70 °C

2.1: acetic acid / 1,2-dichloro-ethane / 20 °C / Inert atmosphere

2.2: 41 h / 20 °C

3.1: acetic acid / 1,2-dichloro-ethane / 0.08 h / 20 °C / Inert atmosphere

4.1: sodium hydroxide / tetrahydrofuran / 20 h / 50 °C

4.2: pH 2 - 3

5.1: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 1 h / 20 °C / Inert atmosphere

With ammonium chloride; acetic acid; N-ethyl-N,N-diisopropylamine; sodium hydroxide; In tetrahydrofuran; methanol; water; 1,2-dichloro-ethane; N,N-dimethyl-formamide;