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(S)-1-((2'-(hydroxycarbamoyl)-[1,1'-biphenyl]-4-yl)methyl)-N-(1-(3-isopropyl phenyl)ethyl)-2,3-dimethyl-1H-indole-5-carboxamide

Base Information
  • Chemical Name:(S)-1-((2'-(hydroxycarbamoyl)-[1,1'-biphenyl]-4-yl)methyl)-N-(1-(3-isopropyl phenyl)ethyl)-2,3-dimethyl-1H-indole-5-carboxamide
  • CAS No.:1415255-72-9
  • Molecular Formula:C36H37N3O3
  • Molecular Weight:559.708
  • Hs Code.:
(S)-1-((2'-(hydroxycarbamoyl)-[1,1'-biphenyl]-4-yl)methyl)-N-(1-(3-isopropyl phenyl)ethyl)-2,3-dimethyl-1H-indole-5-carboxamide

Synonyms:(S)-1-((2'-(hydroxycarbamoyl)-[1,1'-biphenyl]-4-yl)methyl)-N-(1-(3-isopropyl phenyl)ethyl)-2,3-dimethyl-1H-indole-5-carboxamide

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Chemical Property of (S)-1-((2'-(hydroxycarbamoyl)-[1,1'-biphenyl]-4-yl)methyl)-N-(1-(3-isopropyl phenyl)ethyl)-2,3-dimethyl-1H-indole-5-carboxamide
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Technology Process of (S)-1-((2'-(hydroxycarbamoyl)-[1,1'-biphenyl]-4-yl)methyl)-N-(1-(3-isopropyl phenyl)ethyl)-2,3-dimethyl-1H-indole-5-carboxamide

There total 12 articles about (S)-1-((2'-(hydroxycarbamoyl)-[1,1'-biphenyl]-4-yl)methyl)-N-(1-(3-isopropyl phenyl)ethyl)-2,3-dimethyl-1H-indole-5-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:
Multi-step reaction with 2 steps
1.1: N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate / dichloromethane / 0.08 h
1.2: 0.5 h / 20 °C
2.1: trifluoroacetic acid / dichloromethane / 0.5 h / 20 °C
With N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; In dichloromethane;
DOI:10.1021/acsmedchemlett.5b00218
Guidance literature:
Multi-step reaction with 7 steps
1.1: pyridinium p-toluenesulfonate; magnesium sulfate / dichloromethane / 40 °C
2.1: dichloromethane; diethyl ether / 22 h / -50 - 20 °C
3.1: hydrogenchloride / water; methanol / 20 °C
4.1: N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate / dichloromethane / 0.08 h
4.2: 0.5 h / 20 °C
5.1: trifluoroacetic acid / dichloromethane / 0.5 h / 20 °C
6.1: N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate / dichloromethane / 0.08 h
6.2: 0.5 h / 20 °C
7.1: trifluoroacetic acid / dichloromethane / 0.5 h / 20 °C
With hydrogenchloride; pyridinium p-toluenesulfonate; magnesium sulfate; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; In methanol; diethyl ether; dichloromethane; water;
DOI:10.1021/acsmedchemlett.5b00218
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