(2R)-2-methyl-2-(methylsulfonyl)-4-{2-oxo-4-(2-phenylethyl)pyridin-1(2H)-yl}-N-(tetrahydro-2H-pyran-2-yloxy)butanamide

Base Information

Chemical Name:(2R)-2-methyl-2-(methylsulfonyl)-4-{2-oxo-4-(2-phenylethyl)pyridin-1(2H)-yl}-N-(tetrahydro-2H-pyran-2-yloxy)butanamide
CAS No.:1312478-66-2
Molecular Formula:C₂₄H₃₂N₂O₆S
Molecular Weight:476.594
Hs Code.:

Synonyms:(2R)-2-methyl-2-(methylsulfonyl)-4-{2-oxo-4-(2-phenylethyl)pyridin-1(2H)-yl}-N-(tetrahydro-2H-pyran-2-yloxy)butanamide

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Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of (2R)-2-methyl-2-(methylsulfonyl)-4-{2-oxo-4-(2-phenylethyl)pyridin-1(2H)-yl}-N-(tetrahydro-2H-pyran-2-yloxy)butanamide

Chemical Property:

Purity/Quality:: 98% ^*data from raw suppliers

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Technology Process of (2R)-2-methyl-2-(methylsulfonyl)-4-{2-oxo-4-(2-phenylethyl)pyridin-1(2H)-yl}-N-(tetrahydro-2H-pyran-2-yloxy)butanamide

There total 10 articles about (2R)-2-methyl-2-(methylsulfonyl)-4-{2-oxo-4-(2-phenylethyl)pyridin-1(2H)-yl}-N-(tetrahydro-2H-pyran-2-yloxy)butanamide 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: 100.0%

: 1312478-65-1
(2R)-2-methyl-2-(methylsulfonyl)-4-{2-oxo-4-[(E)-2-phenylvinyl]pyridin-1(2H)-yl}-N-(tetrahydro-2H-pyran-2-yloxy)butanamide

: 1312478-66-2
(2R)-2-methyl-2-(methylsulfonyl)-4-{2-oxo-4-(2-phenylethyl)pyridin-1(2H)-yl}-N-(tetrahydro-2H-pyran-2-yloxy)butanamide

Guidance literature:: With cyclohexa-1,4-diene; palladium 10% on activated carbon; In ethanol; at 20 ℃;
DOI:10.1021/jm2014875

Reference yield:

: 1312478-59-3
(2R)-4-(4-iodo-2-oxopyridin-1(2H)-yl)-2-methyl-2-(methylsulfonyl)butanoic acid

: 1312478-66-2
(2R)-2-methyl-2-(methylsulfonyl)-4-{2-oxo-4-(2-phenylethyl)pyridin-1(2H)-yl}-N-(tetrahydro-2H-pyran-2-yloxy)butanamide

Guidance literature:: Multi-step reaction with 3 steps

1: triethylamine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / dichloromethane / 20 - 25 °C

2: potassium carbonate / Pd EnCat_.(TM). / 1,4-dioxane; water / 80 °C

3: cyclohexa-1,4-diene / ethanol / 72 h / 20 - 25 °C / Inert atmosphere

With cyclohexa-1,4-diene; potassium carbonate; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; Pd EnCat; In 1,4-dioxane; ethanol; dichloromethane; water;

Reference yield:

: 1312478-57-1
(2R)-4-(4-iodo-2-oxopyridin-1(2H)-yl)-2-methyl-2-(methylsulfonyl)-N-(tetrahydro-2H-pyran-2-yloxy)butanamide

: 1312478-66-2
(2R)-2-methyl-2-(methylsulfonyl)-4-{2-oxo-4-(2-phenylethyl)pyridin-1(2H)-yl}-N-(tetrahydro-2H-pyran-2-yloxy)butanamide

Guidance literature:: Multi-step reaction with 2 steps

1: potassium carbonate / Pd EnCat_.(TM). / 1,4-dioxane; water / 80 °C

2: cyclohexa-1,4-diene / ethanol / 72 h / 20 - 25 °C / Inert atmosphere

With cyclohexa-1,4-diene; potassium carbonate; Pd EnCat; In 1,4-dioxane; ethanol; water;