methyl 2-(6-chloro-4-(3-(3,4-dichlorophenyl)propylcarbamoyl)-1-methyl-2-oxo-1,2-dihydroquinolin-3-yloxy)acetate

Base Information

Chemical Name:methyl 2-(6-chloro-4-(3-(3,4-dichlorophenyl)propylcarbamoyl)-1-methyl-2-oxo-1,2-dihydroquinolin-3-yloxy)acetate
CAS No.:1429187-96-1
Molecular Formula:C₂₃H₂₁Cl₃N₂O₅
Molecular Weight:511.789
Hs Code.:

Synonyms:methyl 2-(6-chloro-4-(3-(3,4-dichlorophenyl)propylcarbamoyl)-1-methyl-2-oxo-1,2-dihydroquinolin-3-yloxy)acetate

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Chemical Property of methyl 2-(6-chloro-4-(3-(3,4-dichlorophenyl)propylcarbamoyl)-1-methyl-2-oxo-1,2-dihydroquinolin-3-yloxy)acetate

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Technology Process of methyl 2-(6-chloro-4-(3-(3,4-dichlorophenyl)propylcarbamoyl)-1-methyl-2-oxo-1,2-dihydroquinolin-3-yloxy)acetate

There total 9 articles about methyl 2-(6-chloro-4-(3-(3,4-dichlorophenyl)propylcarbamoyl)-1-methyl-2-oxo-1,2-dihydroquinolin-3-yloxy)acetate 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: 76.0%

: 1429185-45-4
6-chloro-N-(3-(3,4-dichlorophenyl)propyl)-3-hydroxy-1-methyl-2-oxo-1,2-dihydroquinoline-4-carboxamide

: 96-32-2
bromoacetic acid methyl ester

: 1429187-96-1
methyl 2-(6-chloro-4-(3-(3,4-dichlorophenyl)propylcarbamoyl)-1-methyl-2-oxo-1,2-dihydroquinolin-3-yloxy)acetate

Guidance literature:: With caesium carbonate; In N,N-dimethyl-formamide; at 20 ℃; for 2h;

Reference yield:

: ethyl 6-chloro-3-methoxy-1-methyl-2-oxo-1,2-dihydroquinoline-4-carboxylate

: 1429187-96-1
methyl 2-(6-chloro-4-(3-(3,4-dichlorophenyl)propylcarbamoyl)-1-methyl-2-oxo-1,2-dihydroquinolin-3-yloxy)acetate

Guidance literature:: Multi-step reaction with 4 steps

1.1: sodium hydroxide / methanol; water / 72 h / 20 °C

2.1: oxalyl dichloride / dichloromethane; N,N-dimethyl-formamide / 4 h / 20 °C

2.2: 14 h

3.1: boron tribromide / dichloromethane / 1 h / 0 °C / Inert atmosphere

4.1: caesium carbonate / N,N-dimethyl-formamide / 2 h / 20 °C

With oxalyl dichloride; boron tribromide; caesium carbonate; sodium hydroxide; In methanol; dichloromethane; water; N,N-dimethyl-formamide;

Reference yield:

: 1429187-95-0
6-chloro-N-(3-(3,4-dichlorophenyl)propyl)-3-methoxy-1-methyl-2-oxo-1,2-dihydroquinoline-4-carboxamide

: 1429187-96-1
methyl 2-(6-chloro-4-(3-(3,4-dichlorophenyl)propylcarbamoyl)-1-methyl-2-oxo-1,2-dihydroquinolin-3-yloxy)acetate

Guidance literature:: Multi-step reaction with 2 steps

1: boron tribromide / dichloromethane / 1 h / 0 °C / Inert atmosphere

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

With boron tribromide; caesium carbonate; In dichloromethane; N,N-dimethyl-formamide;