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
• Mol file: 1256382-45-2.mol

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

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

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

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%

ethyl 6-(4-methoxyphenyl)-4-oxo-4H-pyran-3-carboxylate (1256382-30-5) + n-Pentylamine (110-58-7) → ethyl 6-(4-methoxyphenyl)-4-oxo-1-pentyl-1,4-dihydropyridine-3-carboxylate (1256382-45-2)

Guidance literature:

With acetic acid; In ethanol; at 5 ℃; Reflux;

DOI:10.1021/jm100286k

Reference yield:

ethyl 2-[(dimethylamino)methylene]-3-oxobutanoate (134653-70-6,51145-57-4) → ethyl 6-(4-methoxyphenyl)-4-oxo-1-pentyl-1,4-dihydropyridine-3-carboxylate (1256382-45-2)

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:

ethyl acetoacetate (141-97-9) → ethyl 6-(4-methoxyphenyl)-4-oxo-1-pentyl-1,4-dihydropyridine-3-carboxylate (1256382-45-2)

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

upstream raw materials:

ethyl 6-(4-methoxyphenyl)-4-oxo-4H-pyran-3-carboxylate

n-Pentylamine

ethyl 2-[(dimethylamino)methylene]-3-oxobutanoate

ethyl acetoacetate

Downstream raw materials:

6-(4-methoxyphenyl)-4-oxo-1-pentyl-1,4-dihydropyridine-3-carboxylic acid

N₃-(1-adamantyl)-6-(4-methoxyphenyl)-1-pentyl-4-oxo-1,4-dihydropyridine-3-carboxamide