N-tert-butyl-4-[3-(1-methyl-6-oxo-1,6-dihydro-pyridin-3-yl)-propyl]-benzamide

Base Information

Chemical Name:N-tert-butyl-4-[3-(1-methyl-6-oxo-1,6-dihydro-pyridin-3-yl)-propyl]-benzamide
CAS No.:288093-37-8
Molecular Formula:C₂₀H₂₆N₂O₂
Molecular Weight:326.439
Hs Code.:

<i>N</i>-<i>tert</i>-butyl-4-[3-(1-methyl-6-oxo-1,6-dihydro-pyridin-3-yl)-propyl]-benzamide

Synonyms:N-tert-butyl-4-[3-(1-methyl-6-oxo-1,6-dihydro-pyridin-3-yl)-propyl]-benzamide

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Chemical Property of N-tert-butyl-4-[3-(1-methyl-6-oxo-1,6-dihydro-pyridin-3-yl)-propyl]-benzamide

Chemical Property:

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Technology Process of N-tert-butyl-4-[3-(1-methyl-6-oxo-1,6-dihydro-pyridin-3-yl)-propyl]-benzamide

There total 5 articles about N-tert-butyl-4-[3-(1-methyl-6-oxo-1,6-dihydro-pyridin-3-yl)-propyl]-benzamide 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:

: 1-methyl-5-(3-phenyl-1-propenyl)-2(1H)-pyridone

: 288093-37-8
N-tert-butyl-4-[3-(1-methyl-6-oxo-1,6-dihydro-pyridin-3-yl)-propyl]-benzamide

Guidance literature:: Multi-step reaction with 5 steps

1.1: 81 percent / H₂ / 5 percent Pd-C / ethanol / 6 h / 20 °C / 760 Torr

2.1: 85 percent / AlCl₃ / 1,2-dichloro-ethane / 2 h / 20 °C

3.1: NaOH; Br₂ / H₂O; dioxane / 1.5 h / 20 °C

3.2: 73 percent / aq. Na₂S₂O₅; conc. HCl / dioxane

4.1: SOCl₂ / 0.92 h / 0 - 50 °C

5.1: CH₂Cl₂ / 1 h

With sodium hydroxide; aluminium trichloride; thionyl chloride; hydrogen; bromine; palladium on activated charcoal; In 1,4-dioxane; ethanol; dichloromethane; water; 1,2-dichloro-ethane; 1.1: Catalytic hydrogenation / 2.1: Friedel-Crafts acetylation / 3.1: Oxidation / 3.2: Hydrolysis / 4.1: Substitution / 5.1: Substitution;
DOI:10.1002/(SICI)1521-4184(20005)333:5<145::AID-ARDP145>3.0.CO;2-Q

Reference yield:

: 288093-29-8
1-methyl-5-(3-phenylpropyl)-2(1H)-pyridone

: 288093-37-8
N-tert-butyl-4-[3-(1-methyl-6-oxo-1,6-dihydro-pyridin-3-yl)-propyl]-benzamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: 85 percent / AlCl₃ / 1,2-dichloro-ethane / 2 h / 20 °C

2.1: NaOH; Br₂ / H₂O; dioxane / 1.5 h / 20 °C

2.2: 73 percent / aq. Na₂S₂O₅; conc. HCl / dioxane

3.1: SOCl₂ / 0.92 h / 0 - 50 °C

4.1: CH₂Cl₂ / 1 h

With sodium hydroxide; aluminium trichloride; thionyl chloride; bromine; In 1,4-dioxane; dichloromethane; water; 1,2-dichloro-ethane; 1.1: Friedel-Crafts acetylation / 2.1: Oxidation / 2.2: Hydrolysis / 3.1: Substitution / 4.1: Substitution;
DOI:10.1002/(SICI)1521-4184(20005)333:5<145::AID-ARDP145>3.0.CO;2-Q

Reference yield:

: 288093-31-2
5-(3-(4-acetylphenyl)propyl)-1-methyl-2(1H)-pyridone

: 288093-37-8
N-tert-butyl-4-[3-(1-methyl-6-oxo-1,6-dihydro-pyridin-3-yl)-propyl]-benzamide

Guidance literature:: Multi-step reaction with 3 steps

1.1: NaOH; Br₂ / H₂O; dioxane / 1.5 h / 20 °C

1.2: 73 percent / aq. Na₂S₂O₅; conc. HCl / dioxane

2.1: SOCl₂ / 0.92 h / 0 - 50 °C

3.1: CH₂Cl₂ / 1 h

With sodium hydroxide; thionyl chloride; bromine; In 1,4-dioxane; dichloromethane; water; 1.1: Oxidation / 1.2: Hydrolysis / 2.1: Substitution / 3.1: Substitution;
DOI:10.1002/(SICI)1521-4184(20005)333:5<145::AID-ARDP145>3.0.CO;2-Q