ethyl 6-(4-methoxyphenyl)-4-oxo-1-pentyl-1,4-dihydropyridine-3-carboxylate

Base Information

Chemical Name:ethyl 6-(4-methoxyphenyl)-4-oxo-1-pentyl-1,4-dihydropyridine-3-carboxylate
CAS No.:1256382-45-2
Molecular Formula:C₂₀H₂₅NO₄
Molecular Weight:343.423
Hs Code.:

Synonyms:ethyl 6-(4-methoxyphenyl)-4-oxo-1-pentyl-1,4-dihydropyridine-3-carboxylate

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Chemical Property of ethyl 6-(4-methoxyphenyl)-4-oxo-1-pentyl-1,4-dihydropyridine-3-carboxylate

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Technology Process of ethyl 6-(4-methoxyphenyl)-4-oxo-1-pentyl-1,4-dihydropyridine-3-carboxylate

There total 4 articles about ethyl 6-(4-methoxyphenyl)-4-oxo-1-pentyl-1,4-dihydropyridine-3-carboxylate 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: 57.0%

: 1256382-30-5
ethyl 6-(4-methoxyphenyl)-4-oxo-4H-pyran-3-carboxylate

: 110-58-7
n-Pentylamine

: 1256382-45-2
ethyl 6-(4-methoxyphenyl)-4-oxo-1-pentyl-1,4-dihydropyridine-3-carboxylate

Guidance literature:: With acetic acid; In ethanol; at 5 ℃; Reflux;
DOI:10.1021/jm100286k

Reference yield:

: 134653-70-6,51145-57-4
ethyl 2-[(dimethylamino)methylene]-3-oxobutanoate

: 1256382-45-2
ethyl 6-(4-methoxyphenyl)-4-oxo-1-pentyl-1,4-dihydropyridine-3-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1.1: lithium hexamethyldisilazane / tetrahydrofuran / 0.25 h / -78 °C

1.2: 0.75 h / 20 °C

2.1: acetic acid / ethanol / 5 °C / Reflux

With acetic acid; lithium hexamethyldisilazane; In tetrahydrofuran; ethanol;
DOI:10.1021/jm100286k

Reference yield:

: 141-97-9
ethyl acetoacetate

: 1256382-45-2
ethyl 6-(4-methoxyphenyl)-4-oxo-1-pentyl-1,4-dihydropyridine-3-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1.1: triethylamine / dichloromethane / 2 h / 20 °C

2.1: lithium hexamethyldisilazane / tetrahydrofuran / 0.25 h / -78 °C

2.2: 0.75 h / 20 °C

3.1: acetic acid / ethanol / 5 °C / Reflux

With acetic acid; triethylamine; lithium hexamethyldisilazane; In tetrahydrofuran; ethanol; dichloromethane;
DOI:10.1021/jm100286k