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ethyl 1-{[3-chlorophenyl]amino}-5,6,7,8-tetrahydro-5,8-methanoisoquinoline-4-carboxylate

Base Information Edit
  • Chemical Name:ethyl 1-{[3-chlorophenyl]amino}-5,6,7,8-tetrahydro-5,8-methanoisoquinoline-4-carboxylate
  • CAS No.:1357185-93-3
  • Molecular Formula:C19H19ClN2O2
  • Molecular Weight:342.825
  • Hs Code.:
  • Mol file:1357185-93-3.mol
ethyl 1-{[3-chlorophenyl]amino}-5,6,7,8-tetrahydro-5,8-methanoisoquinoline-4-carboxylate

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Chemical Property of ethyl 1-{[3-chlorophenyl]amino}-5,6,7,8-tetrahydro-5,8-methanoisoquinoline-4-carboxylate Edit
Chemical Property:
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Technology Process of ethyl 1-{[3-chlorophenyl]amino}-5,6,7,8-tetrahydro-5,8-methanoisoquinoline-4-carboxylate

There total 6 articles about ethyl 1-{[3-chlorophenyl]amino}-5,6,7,8-tetrahydro-5,8-methanoisoquinoline-4-carboxylate 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 3 steps
1: chloro-trimethyl-silane; sodium iodide / acetonitrile / 19 h / 20 - 50 °C
2: trichlorophosphate / 1 h / 100 °C
3: 7 h / 180 °C
With chloro-trimethyl-silane; sodium iodide; trichlorophosphate; In acetonitrile;
Guidance literature:
Multi-step reaction with 5 steps
1: N-Bromosuccinimide / chloroform / 36 h / 20 °C
2: 1,1'-bis-(diphenylphosphino)ferrocene; palladium diacetate; triethylamine / N,N-dimethyl-formamide / 15 h / 100 °C
3: chloro-trimethyl-silane; sodium iodide / acetonitrile / 19 h / 20 - 50 °C
4: trichlorophosphate / 1 h / 100 °C
5: 7 h / 180 °C
With 1,1'-bis-(diphenylphosphino)ferrocene; N-Bromosuccinimide; chloro-trimethyl-silane; palladium diacetate; triethylamine; sodium iodide; trichlorophosphate; In chloroform; N,N-dimethyl-formamide; acetonitrile;
Guidance literature:
Multi-step reaction with 7 steps
1: 3-chloro-benzenecarboperoxoic acid / chloroform / 2 h / 20 °C / Cooling with ice
2: sodium methylate / methanol / 15 h / Reflux
3: N-Bromosuccinimide / chloroform / 36 h / 20 °C
4: 1,1'-bis-(diphenylphosphino)ferrocene; palladium diacetate; triethylamine / N,N-dimethyl-formamide / 15 h / 100 °C
5: chloro-trimethyl-silane; sodium iodide / acetonitrile / 19 h / 20 - 50 °C
6: trichlorophosphate / 1 h / 100 °C
7: 7 h / 180 °C
With 1,1'-bis-(diphenylphosphino)ferrocene; N-Bromosuccinimide; chloro-trimethyl-silane; sodium methylate; palladium diacetate; triethylamine; 3-chloro-benzenecarboperoxoic acid; sodium iodide; trichlorophosphate; In methanol; chloroform; N,N-dimethyl-formamide; acetonitrile;
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