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N-Ethyl-4-hydroxy-1-methyl-2-oxo-N-phenyl-1,2-dihydroquinoline-3-carboxamide

Base Information Edit
  • Chemical Name:N-Ethyl-4-hydroxy-1-methyl-2-oxo-N-phenyl-1,2-dihydroquinoline-3-carboxamide
  • CAS No.:84088-99-3
  • Molecular Formula:C19H18N2O3
  • Molecular Weight:322.364
  • Hs Code.:
  • Mol file:84088-99-3.mol
N-Ethyl-4-hydroxy-1-methyl-2-oxo-N-phenyl-1,2-dihydroquinoline-3-carboxamide

Synonyms:deschloro laquinimod;N-ethyl-N-phenyl-1,2-dihydro-4-hydroxy-1-methyl-2-oxoquinoline-3-carboxamide;N-ETHYL-4-HYDROXY-1-METHYL-2-OXO-N-PHENYL-1,2-DIHYDROQUINOLINE-3-CARBOXAMIDE;

Suppliers and Price of N-Ethyl-4-hydroxy-1-methyl-2-oxo-N-phenyl-1,2-dihydroquinoline-3-carboxamide
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
Total 2 raw suppliers
Chemical Property of N-Ethyl-4-hydroxy-1-methyl-2-oxo-N-phenyl-1,2-dihydroquinoline-3-carboxamide Edit
Chemical Property:
  • PSA:62.54000 
  • LogP:2.91080 
Purity/Quality:

99% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
Technology Process of N-Ethyl-4-hydroxy-1-methyl-2-oxo-N-phenyl-1,2-dihydroquinoline-3-carboxamide

There total 4 articles about N-Ethyl-4-hydroxy-1-methyl-2-oxo-N-phenyl-1,2-dihydroquinoline-3-carboxamide 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:
Guidance literature:
With thionyl chloride; N-ethyl-N,N-diisopropylamine; In dichloromethane; at 0 - 5 ℃; for 3h;
Guidance literature:
Multi-step reaction with 3 steps
1.1: sodium methylate / N,N-dimethyl-formamide / 25 - 85 °C / Inert atmosphere
1.2: 0.5 h / 80 - 85 °C / Inert atmosphere
1.3: 25 - 30 °C / pH 1
2.1: hydrogenchloride; acetic acid / 2 h / 80 - 85 °C
3.1: thionyl chloride; N-ethyl-N,N-diisopropylamine / dichloromethane / 3 h / 0 - 5 °C
With hydrogenchloride; thionyl chloride; sodium methylate; acetic acid; N-ethyl-N,N-diisopropylamine; In dichloromethane; N,N-dimethyl-formamide;
Guidance literature:
Multi-step reaction with 4 steps
1.1: potassium carbonate / N,N-dimethyl-formamide / 1 h / 0 - 30 °C
2.1: sodium methylate / N,N-dimethyl-formamide / 25 - 85 °C / Inert atmosphere
2.2: 0.5 h / 80 - 85 °C / Inert atmosphere
2.3: 25 - 30 °C / pH 1
3.1: hydrogenchloride; acetic acid / 2 h / 80 - 85 °C
4.1: thionyl chloride; N-ethyl-N,N-diisopropylamine / dichloromethane / 3 h / 0 - 5 °C
With hydrogenchloride; thionyl chloride; sodium methylate; potassium carbonate; acetic acid; N-ethyl-N,N-diisopropylamine; In dichloromethane; N,N-dimethyl-formamide;
Refernces Edit
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