5-ethyl-4-hydroxy-6-(4-(1-methylpiperidin-4-yl)phenyl)-2-oxo-1,2-dihydropyridine-3-carboxylic acid

Base Information

Chemical Name:5-ethyl-4-hydroxy-6-(4-(1-methylpiperidin-4-yl)phenyl)-2-oxo-1,2-dihydropyridine-3-carboxylic acid
CAS No.:1426669-04-6
Molecular Formula:C₂₀H₂₄N₂O₄
Molecular Weight:356.422
Hs Code.:

Synonyms:5-ethyl-4-hydroxy-6-(4-(1-methylpiperidin-4-yl)phenyl)-2-oxo-1,2-dihydropyridine-3-carboxylic acid

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Chemical Property of 5-ethyl-4-hydroxy-6-(4-(1-methylpiperidin-4-yl)phenyl)-2-oxo-1,2-dihydropyridine-3-carboxylic acid

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Technology Process of 5-ethyl-4-hydroxy-6-(4-(1-methylpiperidin-4-yl)phenyl)-2-oxo-1,2-dihydropyridine-3-carboxylic acid

There total 6 articles about 5-ethyl-4-hydroxy-6-(4-(1-methylpiperidin-4-yl)phenyl)-2-oxo-1,2-dihydropyridine-3-carboxylic 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:

: 1426670-25-8
methyl 5-ethyl-4-hydroxy-6-(4-(1-methylpiperidin-4-yl)phenyl)-2-oxo-1,2-dihydropyridine-3-carboxylate

: 1426669-04-6
5-ethyl-4-hydroxy-6-(4-(1-methylpiperidin-4-yl)phenyl)-2-oxo-1,2-dihydropyridine-3-carboxylic acid

Guidance literature:: methyl 5-ethyl-4-hydroxy-6-(4-(1-methylpiperidin-4-yl)phenyl)-2-oxo-1,2-dihydropyridine-3-carboxylate; With lithium iodide; In ethyl acetate; at 65 ℃; for 1h;

With hydrogenchloride; In water; for 0.166667h;

Reference yield:

: 1426670-19-0
methyl 6-(4-(1-(tert-butoxycarbonyl)-1,2,3,6-tetrahydropyridin-4-yl)phenyl)-1-(2,4-dimethoxybenzyl)-5-ethyl-4-(methoxymethoxy)-2-oxo-1,2-dihydropyridine-3-carboxylate

: 1426669-04-6
5-ethyl-4-hydroxy-6-(4-(1-methylpiperidin-4-yl)phenyl)-2-oxo-1,2-dihydropyridine-3-carboxylic acid

Guidance literature:: Multi-step reaction with 4 steps

1.1: palladium 10% on activated carbon; hydrogen / methanol; ethyl acetate / 760.05 Torr

2.1: trifluoroacetic acid / dichloromethane / 20 °C

3.1: sodium tris(acetoxy)borohydride; methanol / dichloromethane / 1 h / 20 °C

4.1: lithium iodide / ethyl acetate / 1 h / 65 °C

4.2: 0.17 h

With methanol; palladium 10% on activated carbon; hydrogen; sodium tris(acetoxy)borohydride; trifluoroacetic acid; lithium iodide; In methanol; dichloromethane; ethyl acetate;

Reference yield:

: 1426670-17-8
methyl 6-(4-chlorophenyl)-1-(2,4-dimethoxybenzyl)-5-ethyl-4-(methoxymethoxy)-2-oxo-1,2-dihydropyridine-3-carboxylate

: 1426669-04-6
5-ethyl-4-hydroxy-6-(4-(1-methylpiperidin-4-yl)phenyl)-2-oxo-1,2-dihydropyridine-3-carboxylic acid

Guidance literature:: Multi-step reaction with 5 steps

1.1: potassium phosphate; dicyclohexyl-(2',6'-dimethoxybiphenyl-2-yl)-phosphane; palladium diacetate / water; toluene / 2 h / 100 °C / Inert atmosphere

2.1: palladium 10% on activated carbon; hydrogen / methanol; ethyl acetate / 760.05 Torr

3.1: trifluoroacetic acid / dichloromethane / 20 °C

4.1: sodium tris(acetoxy)borohydride; methanol / dichloromethane / 1 h / 20 °C

5.1: lithium iodide / ethyl acetate / 1 h / 65 °C

5.2: 0.17 h

With dicyclohexyl-(2',6'-dimethoxybiphenyl-2-yl)-phosphane; methanol; potassium phosphate; palladium 10% on activated carbon; hydrogen; palladium diacetate; sodium tris(acetoxy)borohydride; trifluoroacetic acid; lithium iodide; In methanol; dichloromethane; water; ethyl acetate; toluene;