N-hydroxy-4-(4-(4-(3-hydroxypropoxy)phenyl)-2-oxopyridin-1(2H)-yl)-2-methyl-2-(methylsulfonyl)butanamide

Base Information

Chemical Name:N-hydroxy-4-(4-(4-(3-hydroxypropoxy)phenyl)-2-oxopyridin-1(2H)-yl)-2-methyl-2-(methylsulfonyl)butanamide
CAS No.:1312473-72-5
Molecular Formula:C₂₀H₂₆N₂O₇S
Molecular Weight:438.502
Hs Code.:

Synonyms:N-hydroxy-4-(4-(4-(3-hydroxypropoxy)phenyl)-2-oxopyridin-1(2H)-yl)-2-methyl-2-(methylsulfonyl)butanamide

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Chemical Property of N-hydroxy-4-(4-(4-(3-hydroxypropoxy)phenyl)-2-oxopyridin-1(2H)-yl)-2-methyl-2-(methylsulfonyl)butanamide

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Technology Process of N-hydroxy-4-(4-(4-(3-hydroxypropoxy)phenyl)-2-oxopyridin-1(2H)-yl)-2-methyl-2-(methylsulfonyl)butanamide

There total 8 articles about N-hydroxy-4-(4-(4-(3-hydroxypropoxy)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: 20.1%

: 1312479-02-9
4-(4-(4-(3-hydroxypropoxy)phenyl)-2-oxopyridin-1(2H)-yl)-2-methyl-2-(methylsulfonyl)-N-(tetrahydro-2H-pyran-2-yloxy)butanamide

: 1312473-72-5
N-hydroxy-4-(4-(4-(3-hydroxypropoxy)phenyl)-2-oxopyridin-1(2H)-yl)-2-methyl-2-(methylsulfonyl)butanamide

Guidance literature:: With hydrogenchloride; In 1,4-dioxane; methanol; for 1h;

Reference yield:

: 22282-70-8
2-fluoro-4-iodopyridine

: 1312473-72-5
N-hydroxy-4-(4-(4-(3-hydroxypropoxy)phenyl)-2-oxopyridin-1(2H)-yl)-2-methyl-2-(methylsulfonyl)butanamide

Guidance literature:: Multi-step reaction with 6 steps

1: acetic acid / water / Reflux

2: caesium carbonate / tetrahydrofuran / 20 - 50 °C

3: water; lithium hydroxide monohydrate / tetrahydrofuran; methanol / 3 h / 20 - 25 °C

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

5: potassium carbonate / tris-(dibenzylideneacetone)dipalladium⁽⁰⁾ / 1,2-dimethoxyethane; methanol / 16 h / 80 °C / Inert atmosphere

6: hydrogenchloride / 1,4-dioxane; methanol / 1 h

With hydrogenchloride; lithium hydroxide monohydrate; water; potassium carbonate; benzotriazol-1-ol; caesium carbonate; acetic acid; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; In tetrahydrofuran; 1,4-dioxane; methanol; 1,2-dimethoxyethane; dichloromethane; water;

Reference yield:

: 858839-90-4
4-iodo-1,2-dihydropyridin-2-one

: 1312473-72-5
N-hydroxy-4-(4-(4-(3-hydroxypropoxy)phenyl)-2-oxopyridin-1(2H)-yl)-2-methyl-2-(methylsulfonyl)butanamide

Guidance literature:: Multi-step reaction with 5 steps

1: caesium carbonate / tetrahydrofuran / 20 - 50 °C

2: water; lithium hydroxide monohydrate / tetrahydrofuran; methanol / 3 h / 20 - 25 °C

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

4: potassium carbonate / tris-(dibenzylideneacetone)dipalladium⁽⁰⁾ / 1,2-dimethoxyethane; methanol / 16 h / 80 °C / Inert atmosphere

5: hydrogenchloride / 1,4-dioxane; methanol / 1 h

With hydrogenchloride; lithium hydroxide monohydrate; water; potassium carbonate; benzotriazol-1-ol; caesium carbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; In tetrahydrofuran; 1,4-dioxane; methanol; 1,2-dimethoxyethane; dichloromethane;