2-(3-fluoro-4-((N-methylmethylsulfonamido) methyl)phenyl)-N-((2-(4-methylpiperidin-1-yl)-6-(trifluoromethyl)pyridin-3-yl)methyl)propanamide

Base Information

Chemical Name:2-(3-fluoro-4-((N-methylmethylsulfonamido) methyl)phenyl)-N-((2-(4-methylpiperidin-1-yl)-6-(trifluoromethyl)pyridin-3-yl)methyl)propanamide
CAS No.:1428790-03-7
Molecular Formula:C₂₅H₃₂F₄N₄O₃S
Molecular Weight:544.614
Hs Code.:

Synonyms:2-(3-fluoro-4-((N-methylmethylsulfonamido) methyl)phenyl)-N-((2-(4-methylpiperidin-1-yl)-6-(trifluoromethyl)pyridin-3-yl)methyl)propanamide

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Chemical Property of 2-(3-fluoro-4-((N-methylmethylsulfonamido) methyl)phenyl)-N-((2-(4-methylpiperidin-1-yl)-6-(trifluoromethyl)pyridin-3-yl)methyl)propanamide

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Technology Process of 2-(3-fluoro-4-((N-methylmethylsulfonamido) methyl)phenyl)-N-((2-(4-methylpiperidin-1-yl)-6-(trifluoromethyl)pyridin-3-yl)methyl)propanamide

There total 5 articles about 2-(3-fluoro-4-((N-methylmethylsulfonamido) methyl)phenyl)-N-((2-(4-methylpiperidin-1-yl)-6-(trifluoromethyl)pyridin-3-yl)methyl)propanamide 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:

: 935518-29-9
(2-(4-methylpiperidin-1-yl)-6-(trifluoromethyl)pyridin-3-yl)methanamine

: 1402586-75-7
2-(3-fluoro-4-((N-methylmethylsulfonamido )methyl)phenyl)propanoic acid

: 1428790-03-7
2-(3-fluoro-4-((N-methylmethylsulfonamido) methyl)phenyl)-N-((2-(4-methylpiperidin-1-yl)-6-(trifluoromethyl)pyridin-3-yl)methyl)propanamide

Guidance literature:: With benzotriazol-1-ol; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; triethylamine; In 1,4-dioxane; at 23 ℃;

Reference yield:

: 1402586-72-4
N-[(4-bromo-2-fluorophenyl)methyl]methanesulfonamide

: 1428790-03-7
2-(3-fluoro-4-((N-methylmethylsulfonamido) methyl)phenyl)-N-((2-(4-methylpiperidin-1-yl)-6-(trifluoromethyl)pyridin-3-yl)methyl)propanamide

Guidance literature:: Multi-step reaction with 4 steps

1: trifluoroacetic acid; manganese; bis(bipyridine)nickel(II) bromide / N,N-dimethyl-formamide / 36 h / 20 - 65 °C / Inert atmosphere

2: potassium carbonate / acetone / 15 h / Reflux

3: sodium hydroxide / tetrahydrofuran; water / 15 h / 20 °C

4: N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; benzotriazol-1-ol; triethylamine / 1,4-dioxane / 20 °C

With manganese; bis(bipyridine)nickel(II) bromide; potassium carbonate; benzotriazol-1-ol; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; triethylamine; trifluoroacetic acid; sodium hydroxide; In tetrahydrofuran; 1,4-dioxane; water; N,N-dimethyl-formamide; acetone;

Reference yield:

: 1402586-73-5
ethyl 2-(3-fluoro-4-(methylsulfonamidomethyl)phenyl)propanoate

: 1428790-03-7
2-(3-fluoro-4-((N-methylmethylsulfonamido) methyl)phenyl)-N-((2-(4-methylpiperidin-1-yl)-6-(trifluoromethyl)pyridin-3-yl)methyl)propanamide

Guidance literature:: Multi-step reaction with 3 steps

1: potassium carbonate / acetone / 15 h / Reflux

2: sodium hydroxide / tetrahydrofuran; water / 15 h / 20 °C

3: N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; benzotriazol-1-ol; triethylamine / 1,4-dioxane / 20 °C

With potassium carbonate; benzotriazol-1-ol; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; triethylamine; sodium hydroxide; In tetrahydrofuran; 1,4-dioxane; water; acetone;