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N1-methyl-N1-(2-morpholinoethyl)-N3-(4-(piperidin-1-yl)-2-(6-(trifluoromethyl)-1H-indole-2-carbonyl)phenyl)isophthalamide 2,2,2-trifluoroacetate

Base Information
  • Chemical Name:N1-methyl-N1-(2-morpholinoethyl)-N3-(4-(piperidin-1-yl)-2-(6-(trifluoromethyl)-1H-indole-2-carbonyl)phenyl)isophthalamide 2,2,2-trifluoroacetate
  • CAS No.:1354826-21-3
  • Molecular Formula:C2HF3O2*C36H38F3N5O4
  • Molecular Weight:775.748
  • Hs Code.:
N<sub>1</sub>-methyl-N<sub>1</sub>-(2-morpholinoethyl)-N<sub>3</sub>-(4-(piperidin-1-yl)-2-(6-(trifluoromethyl)-1H-indole-2-carbonyl)phenyl)isophthalamide 2,2,2-trifluoroacetate

Synonyms:N1-methyl-N1-(2-morpholinoethyl)-N3-(4-(piperidin-1-yl)-2-(6-(trifluoromethyl)-1H-indole-2-carbonyl)phenyl)isophthalamide 2,2,2-trifluoroacetate

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Chemical Property of N1-methyl-N1-(2-morpholinoethyl)-N3-(4-(piperidin-1-yl)-2-(6-(trifluoromethyl)-1H-indole-2-carbonyl)phenyl)isophthalamide 2,2,2-trifluoroacetate
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Technology Process of N1-methyl-N1-(2-morpholinoethyl)-N3-(4-(piperidin-1-yl)-2-(6-(trifluoromethyl)-1H-indole-2-carbonyl)phenyl)isophthalamide 2,2,2-trifluoroacetate

There total 17 articles about N1-methyl-N1-(2-morpholinoethyl)-N3-(4-(piperidin-1-yl)-2-(6-(trifluoromethyl)-1H-indole-2-carbonyl)phenyl)isophthalamide 2,2,2-trifluoroacetate 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:
N1-methyl-N1-(2-morpholinoethyl)-N3-(2-(1-(phenylsulfonyl)-6-(trifluoromethyl)-1H-indole-2-carbonyl)-4-(piperidin-1-yl)phenyl)isophthalamide; With tetrabutyl ammonium fluoride; In tetrahydrofuran; methanol; at 85 ℃;
trifluoroacetic acid; In water; acetonitrile;
Guidance literature:
Multi-step reaction with 5 steps
1.1: triethylamine / dichloromethane / 3 h / 0 - 20 °C
2.1: water; lithium hydroxide monohydrate / tetrahydrofuran / 1 h / 25 °C
2.2: pH 2 - 3
3.1: oxalyl dichloride / N,N-dimethyl-formamide / 2 h / 20 °C
4.1: pyridine / dichloromethane / 2 h / 20 °C
5.1: tetrabutyl ammonium fluoride / tetrahydrofuran; methanol / 85 °C
With pyridine; oxalyl dichloride; lithium hydroxide monohydrate; tetrabutyl ammonium fluoride; water; triethylamine; N,N-dimethyl-formamide; In tetrahydrofuran; methanol; dichloromethane;
Guidance literature:
Multi-step reaction with 5 steps
1.1: N-ethyl-N,N-diisopropylamine; n-butyllithium / tetrahydrofuran / 1 h / -80 - 0 °C / Inert atmosphere
1.2: 4.5 h / -80 - 20 °C
2.1: oxalyl dichloride; dimethyl sulfoxide / dichloromethane / 1 h / -80 °C / Inert atmosphere
2.2: 1 h / -80 - -20 °C
3.1: hydrogen / palladium on activated charcoal / methanol / 10 °C / Inert atmosphere
4.1: pyridine / dichloromethane / 2 h / 20 °C
5.1: tetrabutyl ammonium fluoride / tetrahydrofuran; methanol / 85 °C
With pyridine; n-butyllithium; oxalyl dichloride; tetrabutyl ammonium fluoride; hydrogen; dimethyl sulfoxide; N-ethyl-N,N-diisopropylamine; palladium on activated charcoal; In tetrahydrofuran; methanol; dichloromethane;
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