2-(methyl((4-(5-(4-(2-methylpiperidin-1-yl)-3-(trifluoromethyl)phenyl)-1,2,4-oxadiazol-3-yl)pyridin-2-yl)methyl)amino)acetic acid

Base Information

Chemical Name:2-(methyl((4-(5-(4-(2-methylpiperidin-1-yl)-3-(trifluoromethyl)phenyl)-1,2,4-oxadiazol-3-yl)pyridin-2-yl)methyl)amino)acetic acid
CAS No.:1243558-46-4
Molecular Formula:C₂₄H₂₆F₃N₅O₃
Molecular Weight:489.497
Hs Code.:

Synonyms:2-(methyl((4-(5-(4-(2-methylpiperidin-1-yl)-3-(trifluoromethyl)phenyl)-1,2,4-oxadiazol-3-yl)pyridin-2-yl)methyl)amino)acetic acid

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Chemical Property of 2-(methyl((4-(5-(4-(2-methylpiperidin-1-yl)-3-(trifluoromethyl)phenyl)-1,2,4-oxadiazol-3-yl)pyridin-2-yl)methyl)amino)acetic acid

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Technology Process of 2-(methyl((4-(5-(4-(2-methylpiperidin-1-yl)-3-(trifluoromethyl)phenyl)-1,2,4-oxadiazol-3-yl)pyridin-2-yl)methyl)amino)acetic acid

There total 8 articles about 2-(methyl((4-(5-(4-(2-methylpiperidin-1-yl)-3-(trifluoromethyl)phenyl)-1,2,4-oxadiazol-3-yl)pyridin-2-yl)methyl)amino)acetic acid 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:

: 1243560-26-0
tert-butyl 2-(methyl((4-(5-(4-(2-methylpiperidin-1-yl)-3-(trifluoromethyl)phenyl)-1,2,4-oxadiazol-3-yl)pyridin-2-yl)methyl)amino)acetate

: 1243558-46-4
2-(methyl((4-(5-(4-(2-methylpiperidin-1-yl)-3-(trifluoromethyl)phenyl)-1,2,4-oxadiazol-3-yl)pyridin-2-yl)methyl)amino)acetic acid

Guidance literature:: With hydrogenchloride; In 1,4-dioxane; at 70 ℃; for 4h;

Reference yield:

: C₂₁H₂₃F₃N₄O₃

: 1243558-46-4
2-(methyl((4-(5-(4-(2-methylpiperidin-1-yl)-3-(trifluoromethyl)phenyl)-1,2,4-oxadiazol-3-yl)pyridin-2-yl)methyl)amino)acetic acid

Guidance literature:: Multi-step reaction with 4 steps

1: pyridine / acetonitrile / 0.5 h / 150 °C / Irradiation with microwave

2: methanesulfonyl chloride; N-ethyl-N,N-diisopropylamine / dichloromethane / 1 h / 20 °C

3: potassium carbonate / 1,4-dioxane / 96 h / 70 °C

4: hydrogenchloride / 1,4-dioxane / 4 h / 70 °C

With pyridine; hydrogenchloride; potassium carbonate; methanesulfonyl chloride; N-ethyl-N,N-diisopropylamine; In 1,4-dioxane; dichloromethane; acetonitrile;

Reference yield:

: 1140507-92-1
4-(2-methylpiperidin-1-yl)-3-(trifluoromethyl)benzonitrile

: 1243558-46-4
2-(methyl((4-(5-(4-(2-methylpiperidin-1-yl)-3-(trifluoromethyl)phenyl)-1,2,4-oxadiazol-3-yl)pyridin-2-yl)methyl)amino)acetic acid

Guidance literature:: Multi-step reaction with 6 steps

1.1: sodium hydroxide / methanol / 7 h / Heating; Reflux

1.2: 0 °C / pH 2

2.1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / acetonitrile / 18 h / 20 °C

3.1: pyridine / acetonitrile / 0.5 h / 150 °C / Irradiation with microwave

4.1: methanesulfonyl chloride; N-ethyl-N,N-diisopropylamine / dichloromethane / 1 h / 20 °C

5.1: potassium carbonate / 1,4-dioxane / 96 h / 70 °C

6.1: hydrogenchloride / 1,4-dioxane / 4 h / 70 °C

With pyridine; hydrogenchloride; potassium carbonate; methanesulfonyl chloride; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; sodium hydroxide; In 1,4-dioxane; methanol; dichloromethane; acetonitrile;