5-((4-methoxybenzyl)oxy)-1-methyl-4-oxo-1,4-dihydropyridin-2-carboxylic acid

Base Information

Chemical Name:5-((4-methoxybenzyl)oxy)-1-methyl-4-oxo-1,4-dihydropyridin-2-carboxylic acid
CAS No.:1401529-01-8
Molecular Formula:C₁₅H₁₅NO₅
Molecular Weight:289.288
Hs Code.:

Synonyms:5-((4-methoxybenzyl)oxy)-1-methyl-4-oxo-1,4-dihydropyridin-2-carboxylic acid

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Chemical Property of 5-((4-methoxybenzyl)oxy)-1-methyl-4-oxo-1,4-dihydropyridin-2-carboxylic acid

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Technology Process of 5-((4-methoxybenzyl)oxy)-1-methyl-4-oxo-1,4-dihydropyridin-2-carboxylic acid

There total 6 articles about 5-((4-methoxybenzyl)oxy)-1-methyl-4-oxo-1,4-dihydropyridin-2-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: 79.0%

: 108352-97-2
5-((4-methoxybenzyl)oxy)-4-oxo-4H-pyran-2-carboxylic acid

: 74-89-5
methylamine

: 1401529-01-8
5-((4-methoxybenzyl)oxy)-1-methyl-4-oxo-1,4-dihydropyridin-2-carboxylic acid

Guidance literature:: at 20 ℃; for 20h; Inert atmosphere;

Reference yield: 67.0%

: 132182-56-0
5-((4-methoxybenzyl)oxy)-1-methyl-4-oxo-1,4-dihydropyridine-2-carbaldehyde

: 1401529-01-8
5-((4-methoxybenzyl)oxy)-1-methyl-4-oxo-1,4-dihydropyridin-2-carboxylic acid

Guidance literature:: 5-((4-methoxybenzyl)oxy)-1-methyl-4-oxo-1,4-dihydropyridine-2-carbaldehyde; With sodium dihydrogen phosphate monohydrate; 2-methyl-but-2-ene; sodium chloride; In tetrahydrofuran; water; tert-butyl alcohol; at 20 ℃; for 1h;

With hydrogenchloride; In water; pH=12;

Reference yield:

: 824-94-2
p-methoxybenzyl chloride

: 1401529-01-8
5-((4-methoxybenzyl)oxy)-1-methyl-4-oxo-1,4-dihydropyridin-2-carboxylic acid

Guidance literature:: Multi-step reaction with 4 steps

1.1: potassium carbonate / N,N-dimethyl-formamide / 3 h / 80 °C

2.1: ethanol / 20 h / 20 °C

3.1: trimethylamine / dichloromethane; dimethyl sulfoxide / 2 h / 20 °C

4.1: 2-methyl-but-2-ene; sodium dihydrogen phosphate monohydrate; sodium chloride / water; tert-butyl alcohol; tetrahydrofuran / 1 h / 20 °C

4.2: pH 12

With sodium dihydrogen phosphate monohydrate; 2-methyl-but-2-ene; potassium carbonate; sodium chloride; trimethylamine; In tetrahydrofuran; ethanol; dichloromethane; water; dimethyl sulfoxide; N,N-dimethyl-formamide; tert-butyl alcohol;