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Benzamide, N-[3-(7-amino-1,2-dihydro-1-methyl-2-oxo-1,6-naphthyridin-3-yl)-4-meth ylphenyl]-3-(trifluoromethyl)-

Base Information Edit
  • Chemical Name:Benzamide, N-[3-(7-amino-1,2-dihydro-1-methyl-2-oxo-1,6-naphthyridin-3-yl)-4-meth ylphenyl]-3-(trifluoromethyl)-
  • CAS No.:850450-22-5
  • Molecular Formula:C24H19F3N4O2
  • Molecular Weight:452.436
  • Hs Code.:
  • Mol file:850450-22-5.mol
Benzamide,
N-[3-(7-amino-1,2-dihydro-1-methyl-2-oxo-1,6-naphthyridin-3-yl)-4-meth
ylphenyl]-3-(trifluoromethyl)-

Synonyms:

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Chemical Property of Benzamide, N-[3-(7-amino-1,2-dihydro-1-methyl-2-oxo-1,6-naphthyridin-3-yl)-4-meth ylphenyl]-3-(trifluoromethyl)- Edit
Chemical Property:
Purity/Quality:
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MSDS Files:
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Technology Process of Benzamide, N-[3-(7-amino-1,2-dihydro-1-methyl-2-oxo-1,6-naphthyridin-3-yl)-4-meth ylphenyl]-3-(trifluoromethyl)-

There total 16 articles about Benzamide, N-[3-(7-amino-1,2-dihydro-1-methyl-2-oxo-1,6-naphthyridin-3-yl)-4-meth ylphenyl]-3-(trifluoromethyl)- 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:
Multi-step reaction with 7 steps
1: potassium hydroxide; water / methanol / 14 h / Heating / reflux
2: hydrogenchloride / 1,4-dioxane / 14 h / Heating / reflux
3: hydrogen / palladium 10% on activated carbon / ethanol / 16 h / 20 °C
4: sodium carbonate / N,N-dimethyl-formamide / 16 h / 100 °C
5: N-ethyl-N,N-diisopropylamine / dichloromethane / 4 h / 20 °C
6: potassium tert-butylate; 1,3-bis[2,6-diisopropylphenyl]imidazolium chloride / tris-(dibenzylideneacetone)dipalladium(0) / 1,4-dioxane / 14 h / 100 °C
7: hydrogen / palladium 10% on activated carbon / ethanol / 16 h / 20 °C / 2585.81 Torr
With hydrogenchloride; potassium hydroxide; potassium tert-butylate; water; hydrogen; sodium carbonate; N-ethyl-N,N-diisopropylamine; 1,3-bis[2,6-diisopropylphenyl]imidazolium chloride; tris-(dibenzylideneacetone)dipalladium(0); palladium 10% on activated carbon; In 1,4-dioxane; methanol; ethanol; dichloromethane; N,N-dimethyl-formamide;
Guidance literature:
Multi-step reaction with 6 steps
1: lithium aluminium tetrahydride / tetrahydrofuran / 3 h / 78 °C
2: manganese(IV) oxide / dichloromethane / 2 h / 20 °C
3: sodium carbonate / N,N-dimethyl-formamide / 16 h / 100 °C
4: N-ethyl-N,N-diisopropylamine / dichloromethane / 4 h / 20 °C
5: potassium tert-butylate; 1,3-bis[2,6-diisopropylphenyl]imidazolium chloride / tris-(dibenzylideneacetone)dipalladium(0) / 1,4-dioxane / 14 h / 100 °C
6: hydrogen / palladium 10% on activated carbon / ethanol / 16 h / 20 °C / 2585.81 Torr
With manganese(IV) oxide; lithium aluminium tetrahydride; potassium tert-butylate; hydrogen; sodium carbonate; N-ethyl-N,N-diisopropylamine; 1,3-bis[2,6-diisopropylphenyl]imidazolium chloride; tris-(dibenzylideneacetone)dipalladium(0); palladium 10% on activated carbon; In tetrahydrofuran; 1,4-dioxane; ethanol; dichloromethane; N,N-dimethyl-formamide;
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