N-((7-(4-(4-(2,3-dichlorophenyl)piperazin-1-yl)butoxy)-2-oxo-1,2,3,4-tetrahydroquinolin-4-yl)methyl)-2-(2,5-dioxo-2,5-dihydro-1H-pyrrol-1-yl)acetamide

Base Information

Chemical Name:N-((7-(4-(4-(2,3-dichlorophenyl)piperazin-1-yl)butoxy)-2-oxo-1,2,3,4-tetrahydroquinolin-4-yl)methyl)-2-(2,5-dioxo-2,5-dihydro-1H-pyrrol-1-yl)acetamide
CAS No.:1567360-68-2
Molecular Formula:C₃₀H₃₃Cl₂N₅O₅
Molecular Weight:614.529
Hs Code.:

Synonyms:N-((7-(4-(4-(2,3-dichlorophenyl)piperazin-1-yl)butoxy)-2-oxo-1,2,3,4-tetrahydroquinolin-4-yl)methyl)-2-(2,5-dioxo-2,5-dihydro-1H-pyrrol-1-yl)acetamide

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Chemical Property of N-((7-(4-(4-(2,3-dichlorophenyl)piperazin-1-yl)butoxy)-2-oxo-1,2,3,4-tetrahydroquinolin-4-yl)methyl)-2-(2,5-dioxo-2,5-dihydro-1H-pyrrol-1-yl)acetamide

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Technology Process of N-((7-(4-(4-(2,3-dichlorophenyl)piperazin-1-yl)butoxy)-2-oxo-1,2,3,4-tetrahydroquinolin-4-yl)methyl)-2-(2,5-dioxo-2,5-dihydro-1H-pyrrol-1-yl)acetamide

There total 12 articles about N-((7-(4-(4-(2,3-dichlorophenyl)piperazin-1-yl)butoxy)-2-oxo-1,2,3,4-tetrahydroquinolin-4-yl)methyl)-2-(2,5-dioxo-2,5-dihydro-1H-pyrrol-1-yl)acetamide 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:

: 55750-61-3
(2,5-dioxo-2,5-dihydropyrrol-1-yl)acetic acid 2,5-dioxopyrrolidin-1-yl ester

: 1567360-54-6
4-(aminomethyl)-7-(4-(4-(2,3-dichlorophenyl)piperazin-1-yl)butoxy)-3,4-dihydroquinolin-2(1H)-one

: 1567360-68-2
N-((7-(4-(4-(2,3-dichlorophenyl)piperazin-1-yl)butoxy)-2-oxo-1,2,3,4-tetrahydroquinolin-4-yl)methyl)-2-(2,5-dioxo-2,5-dihydro-1H-pyrrol-1-yl)acetamide

Guidance literature:: With tributyl-amine; In N,N-dimethyl-formamide; at 20 ℃; for 1.5h;

Reference yield:

: 1567360-56-8
7-methoxy-2-oxo-1,2,3,4-tetrahydroquinoline-4-carbonitrile

: 1567360-68-2
N-((7-(4-(4-(2,3-dichlorophenyl)piperazin-1-yl)butoxy)-2-oxo-1,2,3,4-tetrahydroquinolin-4-yl)methyl)-2-(2,5-dioxo-2,5-dihydro-1H-pyrrol-1-yl)acetamide

Guidance literature:: Multi-step reaction with 7 steps

1: triethylamine; hydrogen / methanol / 4 h / 20 °C

2: boron tribromide / dichloromethane / -14 - 20 °C

3: triethylamine / methanol / 2 h / 20 °C

4: potassium carbonate / N,N-dimethyl-formamide / 20 °C

5: potassium carbonate / N,N-dimethyl-formamide / 20 °C

6: trifluoroacetic acid / dichloromethane / 2.5 h / 20 °C

7: tributyl-amine / N,N-dimethyl-formamide / 1.5 h / 20 °C

With tributyl-amine; hydrogen; boron tribromide; potassium carbonate; triethylamine; trifluoroacetic acid; In methanol; dichloromethane; N,N-dimethyl-formamide;

Reference yield:

: 1567360-58-0
tert-butyl ((7-hydroxy-2-oxo-1,2,3,4-tetrahydroquinolin-4-yl)methyl)carbamate

: 1567360-68-2
N-((7-(4-(4-(2,3-dichlorophenyl)piperazin-1-yl)butoxy)-2-oxo-1,2,3,4-tetrahydroquinolin-4-yl)methyl)-2-(2,5-dioxo-2,5-dihydro-1H-pyrrol-1-yl)acetamide

Guidance literature:: Multi-step reaction with 4 steps

1: potassium carbonate / N,N-dimethyl-formamide / 20 °C

2: potassium carbonate / N,N-dimethyl-formamide / 20 °C

3: trifluoroacetic acid / dichloromethane / 2.5 h / 20 °C

4: tributyl-amine / N,N-dimethyl-formamide / 1.5 h / 20 °C

With tributyl-amine; potassium carbonate; trifluoroacetic acid; In dichloromethane; N,N-dimethyl-formamide;