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4-chloro-3-(4,6-dichloro-pyridin-3-yl)-N-[2-(2-dimethylamino-ethoxy)-phenyl]-N-methyl benzamide

Base Information
  • Chemical Name:4-chloro-3-(4,6-dichloro-pyridin-3-yl)-N-[2-(2-dimethylamino-ethoxy)-phenyl]-N-methyl benzamide
  • CAS No.:1070889-89-2
  • Molecular Formula:C23H22Cl3N3O2
  • Molecular Weight:478.806
  • Hs Code.:
4-chloro-3-(4,6-dichloro-pyridin-3-yl)-N-[2-(2-dimethylamino-ethoxy)-phenyl]-N-methyl benzamide

Synonyms:4-chloro-3-(4,6-dichloro-pyridin-3-yl)-N-[2-(2-dimethylamino-ethoxy)-phenyl]-N-methyl benzamide

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Chemical Property of 4-chloro-3-(4,6-dichloro-pyridin-3-yl)-N-[2-(2-dimethylamino-ethoxy)-phenyl]-N-methyl benzamide
Chemical Property:
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Technology Process of 4-chloro-3-(4,6-dichloro-pyridin-3-yl)-N-[2-(2-dimethylamino-ethoxy)-phenyl]-N-methyl benzamide

There total 6 articles about 4-chloro-3-(4,6-dichloro-pyridin-3-yl)-N-[2-(2-dimethylamino-ethoxy)-phenyl]-N-methyl 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:
Guidance literature:
With potassium fluoride; tris-(dibenzylideneacetone)dipalladium(0); tri tert-butylphosphoniumtetrafluoroborate; In 1,4-dioxane; at 110 ℃;
Guidance literature:
Multi-step reaction with 4 steps
1.1: oxalyl dichloride / N,N-dimethyl-formamide / dichloromethane / 1 h
2.1: sodium hydrogencarbonate / water; acetonitrile / 1.5 h
2.2: 16 h / 20 °C
3.1: potassium carbonate / N,N-dimethyl-formamide / 14 h / 80 °C
4.1: potassium fluoride / tris-(dibenzylideneacetone)dipalladium(0); tri tert-butylphosphoniumtetrafluoroborate / 1,4-dioxane / 110 °C
With potassium fluoride; oxalyl dichloride; sodium hydrogencarbonate; potassium carbonate; tris-(dibenzylideneacetone)dipalladium(0); N,N-dimethyl-formamide; tri tert-butylphosphoniumtetrafluoroborate; In 1,4-dioxane; dichloromethane; water; N,N-dimethyl-formamide; acetonitrile;
Guidance literature:
Multi-step reaction with 3 steps
1.1: sodium hydrogencarbonate / water; acetonitrile / 1.5 h
1.2: 16 h / 20 °C
2.1: potassium carbonate / N,N-dimethyl-formamide / 14 h / 80 °C
3.1: potassium fluoride / tris-(dibenzylideneacetone)dipalladium(0); tri tert-butylphosphoniumtetrafluoroborate / 1,4-dioxane / 110 °C
With potassium fluoride; sodium hydrogencarbonate; potassium carbonate; tris-(dibenzylideneacetone)dipalladium(0); tri tert-butylphosphoniumtetrafluoroborate; In 1,4-dioxane; water; N,N-dimethyl-formamide; acetonitrile;
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