5-chloro-3-{ethyl[(1r,4r)-4-(dimethylamino)cyclohexyl]amino}-N-[(5-fluoro-4,6-dimethyl-2-oxo-1,2-dihydropyridin-3-yl)methyl]-2-methylbenzamide

Base Information

Chemical Name:5-chloro-3-{ethyl[(1r,4r)-4-(dimethylamino)cyclohexyl]amino}-N-[(5-fluoro-4,6-dimethyl-2-oxo-1,2-dihydropyridin-3-yl)methyl]-2-methylbenzamide
CAS No.:1403591-20-7
Molecular Formula:C₂₆H₃₆ClFN₄O₂
Molecular Weight:491.049
Hs Code.:

Synonyms:5-chloro-3-{ethyl[(1r,4r)-4-(dimethylamino)cyclohexyl]amino}-N-[(5-fluoro-4,6-dimethyl-2-oxo-1,2-dihydropyridin-3-yl)methyl]-2-methylbenzamide

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Chemical Property of 5-chloro-3-{ethyl[(1r,4r)-4-(dimethylamino)cyclohexyl]amino}-N-[(5-fluoro-4,6-dimethyl-2-oxo-1,2-dihydropyridin-3-yl)methyl]-2-methylbenzamide

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Technology Process of 5-chloro-3-{ethyl[(1r,4r)-4-(dimethylamino)cyclohexyl]amino}-N-[(5-fluoro-4,6-dimethyl-2-oxo-1,2-dihydropyridin-3-yl)methyl]-2-methylbenzamide

There total 5 articles about 5-chloro-3-{ethyl[(1r,4r)-4-(dimethylamino)cyclohexyl]amino}-N-[(5-fluoro-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: 52.0%

: 1354822-90-4
3-(aminomethyl)-5-fluoro-4,6-dimethyl-2(1H)-pyridinone

: 1403596-47-3
5-chloro-3-(((trans)-4-(dimethylamino)cyclohexyl)(ethyl)amino)-2-methylbenzoic acid

: 1403591-20-7
5-chloro-3-{ethyl[(1r,4r)-4-(dimethylamino)cyclohexyl]amino}-N-[(5-fluoro-4,6-dimethyl-2-oxo-1,2-dihydropyridin-3-yl)methyl]-2-methylbenzamide

Guidance literature:: 5-chloro-3-(((trans)-4-(dimethylamino)cyclohexyl)(ethyl)amino)-2-methylbenzoic acid; With N-ethyl-N,N-diisopropylamine; HATU; In N,N-dimethyl-formamide; at 0 ℃; for 0.166667h; Inert atmosphere;

3-(aminomethyl)-5-fluoro-4,6-dimethyl-2(1H)-pyridinone; In N,N-dimethyl-formamide; at 0 - 20 ℃; for 18h;

Reference yield:

: 759-02-4
3-fluoro-2,4-pentanedione

: 1403591-20-7
5-chloro-3-{ethyl[(1r,4r)-4-(dimethylamino)cyclohexyl]amino}-N-[(5-fluoro-4,6-dimethyl-2-oxo-1,2-dihydropyridin-3-yl)methyl]-2-methylbenzamide

Guidance literature:: Multi-step reaction with 3 steps

1.1: piperidine / ethanol / 99 h / 20 - 75 °C

2.1: hydrogenchloride; hydrogen / palladium(II) hydroxide / methanol / 23 °C

3.1: N-ethyl-N,N-diisopropylamine; HATU / N,N-dimethyl-formamide / 0.17 h / 0 °C / Inert atmosphere

3.2: 18 h / 0 - 20 °C

With piperidine; hydrogenchloride; hydrogen; N-ethyl-N,N-diisopropylamine; HATU; palladium(II) hydroxide; In methanol; ethanol; N,N-dimethyl-formamide;

Reference yield:

: 769-28-8
3-Cyano-4,6-dimethyl-2(1H)-pyridon

: 1403591-20-7
5-chloro-3-{ethyl[(1r,4r)-4-(dimethylamino)cyclohexyl]amino}-N-[(5-fluoro-4,6-dimethyl-2-oxo-1,2-dihydropyridin-3-yl)methyl]-2-methylbenzamide

Guidance literature:: Multi-step reaction with 3 steps

1.1: Selectfluor / acetonitrile

2.1: hydrogenchloride; hydrogen / palladium(II) hydroxide / methanol / 23 °C

3.1: N-ethyl-N,N-diisopropylamine; HATU / N,N-dimethyl-formamide / 0.17 h / 0 °C / Inert atmosphere

3.2: 18 h / 0 - 20 °C

With hydrogenchloride; hydrogen; Selectfluor; N-ethyl-N,N-diisopropylamine; HATU; palladium(II) hydroxide; In methanol; N,N-dimethyl-formamide; acetonitrile;