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N-cyclopropyl-N-ethyl-6-oxo-5-benzyl-6,7,8,9,10,11-hexahydro-5H-cyclohepta[c]quinoline-2-carboxamide

Base Information
  • Chemical Name:N-cyclopropyl-N-ethyl-6-oxo-5-benzyl-6,7,8,9,10,11-hexahydro-5H-cyclohepta[c]quinoline-2-carboxamide
  • CAS No.:1616680-72-8
  • Molecular Formula:C27H30N2O2
  • Molecular Weight:414.547
  • Hs Code.:
N-cyclopropyl-N-ethyl-6-oxo-5-benzyl-6,7,8,9,10,11-hexahydro-5H-cyclohepta[c]quinoline-2-carboxamide

Synonyms:N-cyclopropyl-N-ethyl-6-oxo-5-benzyl-6,7,8,9,10,11-hexahydro-5H-cyclohepta[c]quinoline-2-carboxamide

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Chemical Property of N-cyclopropyl-N-ethyl-6-oxo-5-benzyl-6,7,8,9,10,11-hexahydro-5H-cyclohepta[c]quinoline-2-carboxamide
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Technology Process of N-cyclopropyl-N-ethyl-6-oxo-5-benzyl-6,7,8,9,10,11-hexahydro-5H-cyclohepta[c]quinoline-2-carboxamide

There total 10 articles about N-cyclopropyl-N-ethyl-6-oxo-5-benzyl-6,7,8,9,10,11-hexahydro-5H-cyclohepta[c]quinoline-2-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 4 steps
1.1: oxalyl dichloride; N,N-dimethyl-formamide / dichloromethane / 0.17 h / 20 °C
1.2: 2 h / 60 °C
2.1: palladium diacetate; caesium carbonate; tricyclohexylphosphine tetrafluoroborate / N,N-dimethyl acetamide / 4 h / 130 °C / Inert atmosphere
3.1: trifluoroacetic acid / 1.5 h / 80 °C
4.1: caesium carbonate; tetra-(n-butyl)ammonium iodide / N,N-dimethyl-formamide / 1 h / 90 °C
With oxalyl dichloride; palladium diacetate; tetra-(n-butyl)ammonium iodide; caesium carbonate; N,N-dimethyl-formamide; tricyclohexylphosphine tetrafluoroborate; trifluoroacetic acid; In dichloromethane; N,N-dimethyl acetamide; N,N-dimethyl-formamide; 2.1: |Heck Reaction;
DOI:10.1016/j.bmc.2014.05.022
Guidance literature:
Multi-step reaction with 5 steps
1.1: sodium dihydrogenphosphate; dihydrogen peroxide; sodium chlorite / water; acetonitrile / 20 °C
2.1: oxalyl dichloride; N,N-dimethyl-formamide / dichloromethane / 0.17 h / 20 °C
2.2: 2 h / 60 °C
3.1: palladium diacetate; caesium carbonate; tricyclohexylphosphine tetrafluoroborate / N,N-dimethyl acetamide / 4 h / 130 °C / Inert atmosphere
4.1: trifluoroacetic acid / 1.5 h / 80 °C
5.1: caesium carbonate; tetra-(n-butyl)ammonium iodide / N,N-dimethyl-formamide / 1 h / 90 °C
With sodium chlorite; sodium dihydrogenphosphate; oxalyl dichloride; dihydrogen peroxide; palladium diacetate; tetra-(n-butyl)ammonium iodide; caesium carbonate; N,N-dimethyl-formamide; tricyclohexylphosphine tetrafluoroborate; trifluoroacetic acid; In dichloromethane; N,N-dimethyl acetamide; water; N,N-dimethyl-formamide; acetonitrile; 3.1: |Heck Reaction;
DOI:10.1016/j.bmc.2014.05.022
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