2-(3-(methylsulfonamidomethyl)phenyl)-N-((2-(pyrrolidin-1-yl)-6-(trifluoromethyl)pyridin-3-yl)methyl)propanamide

Base Information

Chemical Name:2-(3-(methylsulfonamidomethyl)phenyl)-N-((2-(pyrrolidin-1-yl)-6-(trifluoromethyl)pyridin-3-yl)methyl)propanamide
CAS No.:1428789-43-8
Molecular Formula:C₂₂H₂₇F₃N₄O₃S
Molecular Weight:484.543
Hs Code.:

Synonyms:2-(3-(methylsulfonamidomethyl)phenyl)-N-((2-(pyrrolidin-1-yl)-6-(trifluoromethyl)pyridin-3-yl)methyl)propanamide

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Chemical Property of 2-(3-(methylsulfonamidomethyl)phenyl)-N-((2-(pyrrolidin-1-yl)-6-(trifluoromethyl)pyridin-3-yl)methyl)propanamide

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Technology Process of 2-(3-(methylsulfonamidomethyl)phenyl)-N-((2-(pyrrolidin-1-yl)-6-(trifluoromethyl)pyridin-3-yl)methyl)propanamide

There total 7 articles about 2-(3-(methylsulfonamidomethyl)phenyl)-N-((2-(pyrrolidin-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: 60.0%

: 1428790-16-2
2-(3-(aminomethyl)phenyl)-N-((2-(pyrrolidin-1-yl)-6-(trifluoromethyl)pyridin-3-yl)methyl)propanamide

: 124-63-0
methanesulfonyl chloride

: 1428789-43-8
2-(3-(methylsulfonamidomethyl)phenyl)-N-((2-(pyrrolidin-1-yl)-6-(trifluoromethyl)pyridin-3-yl)methyl)propanamide

Guidance literature:: With triethylamine; In dichloromethane; at 0 - 23 ℃; for 1.16667h;

Reference yield:

: 1878-71-3
2-(3-cyanophenyl)acetic acid

: 1428789-43-8
2-(3-(methylsulfonamidomethyl)phenyl)-N-((2-(pyrrolidin-1-yl)-6-(trifluoromethyl)pyridin-3-yl)methyl)propanamide

Guidance literature:: Multi-step reaction with 6 steps

1: sulfuric acid / 3 h / Reflux; Inert atmosphere

2: sodium hydride / tetrahydrofuran; mineral oil / 1 h / 0 - 20 °C

3: lithium hydroxide / tetrahydrofuran; water / 2 h / 0 - 20 °C

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

5: sodium tetrahydroborate; nickel(II) chloride hexahydrate / ethanol / 1.17 h / 0 - 20 °C

6: triethylamine / dichloromethane / 1.17 h / 0 - 20 °C

With sodium tetrahydroborate; nickel(II) chloride hexahydrate; sulfuric acid; sodium hydride; benzotriazol-1-ol; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; triethylamine; lithium hydroxide; In tetrahydrofuran; 1,4-dioxane; ethanol; dichloromethane; water; mineral oil;

Reference yield:

: 52798-00-2
(3-cyano-phenyl)-acetic acid methyl ester

: 1428789-43-8
2-(3-(methylsulfonamidomethyl)phenyl)-N-((2-(pyrrolidin-1-yl)-6-(trifluoromethyl)pyridin-3-yl)methyl)propanamide

Guidance literature:: Multi-step reaction with 5 steps

1: sodium hydride / tetrahydrofuran; mineral oil / 1 h / 0 - 20 °C

2: lithium hydroxide / tetrahydrofuran; water / 2 h / 0 - 20 °C

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

4: sodium tetrahydroborate; nickel(II) chloride hexahydrate / ethanol / 1.17 h / 0 - 20 °C

5: triethylamine / dichloromethane / 1.17 h / 0 - 20 °C

With sodium tetrahydroborate; nickel(II) chloride hexahydrate; sodium hydride; benzotriazol-1-ol; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; triethylamine; lithium hydroxide; In tetrahydrofuran; 1,4-dioxane; ethanol; dichloromethane; water; mineral oil;