(2R)-N-hydroxy-4-[4-{4-[(6-methoxypyridin-3-yl)methoxy]phenyl}-2-oxopyridin-1(2H)-yl]-2-methyl-2-(methylsulfonyl)butanamide

Base Information

Chemical Name:(2R)-N-hydroxy-4-[4-{4-[(6-methoxypyridin-3-yl)methoxy]phenyl}-2-oxopyridin-1(2H)-yl]-2-methyl-2-(methylsulfonyl)butanamide
CAS No.:1312474-00-2
Molecular Formula:C₂₄H₂₇N₃O₇S
Molecular Weight:501.56
Hs Code.:

Synonyms:(2R)-N-hydroxy-4-[4-{4-[(6-methoxypyridin-3-yl)methoxy]phenyl}-2-oxopyridin-1(2H)-yl]-2-methyl-2-(methylsulfonyl)butanamide

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Chemical Property of (2R)-N-hydroxy-4-[4-{4-[(6-methoxypyridin-3-yl)methoxy]phenyl}-2-oxopyridin-1(2H)-yl]-2-methyl-2-(methylsulfonyl)butanamide

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Technology Process of (2R)-N-hydroxy-4-[4-{4-[(6-methoxypyridin-3-yl)methoxy]phenyl}-2-oxopyridin-1(2H)-yl]-2-methyl-2-(methylsulfonyl)butanamide

There total 11 articles about (2R)-N-hydroxy-4-[4-{4-[(6-methoxypyridin-3-yl)methoxy]phenyl}-2-oxopyridin-1(2H)-yl]-2-methyl-2-(methylsulfonyl)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: 95.0%

: 1312479-60-9
(2R)-4-[4-{4-[(6-methoxypyridin-3-yl)methoxy]phenyl}-2-oxopyridin-1(2H)-yl]-2-methyl-2-(methylsulfonyl)-N-(tetrahydro-2H-pyran-2-yloxy)butanamide

: 1312474-00-2
(2R)-N-hydroxy-4-[4-{4-[(6-methoxypyridin-3-yl)methoxy]phenyl}-2-oxopyridin-1(2H)-yl]-2-methyl-2-(methylsulfonyl)butanamide

Guidance literature:: With hydrogenchloride; In water; isopropyl alcohol; for 1h;

Reference yield:

: 58584-63-7
(6-methoxypyridin-3-yl)methanol

: 1312474-00-2
(2R)-N-hydroxy-4-[4-{4-[(6-methoxypyridin-3-yl)methoxy]phenyl}-2-oxopyridin-1(2H)-yl]-2-methyl-2-(methylsulfonyl)butanamide

Guidance literature:: Multi-step reaction with 4 steps

1: triethylamine; triphenylphosphine; di-isopropyl azodicarboxylate / tetrahydrofuran / 48 h / 0 - 25 °C

2: potassium acetate / (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride / 1,4-dioxane / 18 h / Reflux

3: potassium carbonate / Pd EnCat_.(TM). / 1,4-dioxane; water / 2 h / 100 °C

4: hydrogenchloride / isopropyl alcohol; water / 1 h

With hydrogenchloride; di-isopropyl azodicarboxylate; potassium acetate; potassium carbonate; triethylamine; triphenylphosphine; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; In tetrahydrofuran; 1,4-dioxane; water; isopropyl alcohol;

Reference yield:

: 26218-80-4
6-methoxy-nicotinic acid methyl ester

: 1312474-00-2
(2R)-N-hydroxy-4-[4-{4-[(6-methoxypyridin-3-yl)methoxy]phenyl}-2-oxopyridin-1(2H)-yl]-2-methyl-2-(methylsulfonyl)butanamide

Guidance literature:: Multi-step reaction with 5 steps

1: ethanol; sodium tetrahydroborate / 72 h / 0 - 25 °C

2: triethylamine; triphenylphosphine; di-isopropyl azodicarboxylate / tetrahydrofuran / 48 h / 0 - 25 °C

3: potassium acetate / (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride / 1,4-dioxane / 18 h / Reflux

4: potassium carbonate / Pd EnCat_.(TM). / 1,4-dioxane; water / 2 h / 100 °C

5: hydrogenchloride / isopropyl alcohol; water / 1 h

With hydrogenchloride; sodium tetrahydroborate; ethanol; di-isopropyl azodicarboxylate; potassium acetate; potassium carbonate; triethylamine; triphenylphosphine; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; In tetrahydrofuran; 1,4-dioxane; water; isopropyl alcohol;