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2(1H)-Isoquinolinepropanoic acid, 3,4-dihydro-6-[3-(methylamino)-2-nitrophenoxy]-1-oxo-, ethyl ester

Base Information
  • Chemical Name:2(1H)-Isoquinolinepropanoic acid, 3,4-dihydro-6-[3-(methylamino)-2-nitrophenoxy]-1-oxo-, ethyl ester
  • CAS No.:866082-81-7
  • Molecular Formula:C21H23N3O6
  • Molecular Weight:413.43
  • Hs Code.:
2(1H)-Isoquinolinepropanoic acid,
3,4-dihydro-6-[3-(methylamino)-2-nitrophenoxy]-1-oxo-, ethyl ester

Synonyms:

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Chemical Property of 2(1H)-Isoquinolinepropanoic acid, 3,4-dihydro-6-[3-(methylamino)-2-nitrophenoxy]-1-oxo-, ethyl ester
Chemical Property:
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Technology Process of 2(1H)-Isoquinolinepropanoic acid, 3,4-dihydro-6-[3-(methylamino)-2-nitrophenoxy]-1-oxo-, ethyl ester

There total 6 articles about 2(1H)-Isoquinolinepropanoic acid, 3,4-dihydro-6-[3-(methylamino)-2-nitrophenoxy]-1-oxo-, ethyl ester 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 N-ethyl-N,N-diisopropylamine; In DMF (N,N-dimethyl-formamide); at 25 ℃; for 18h;
Guidance literature:
Multi-step reaction with 2 steps
1: caesium carbonate / N,N-dimethyl-formamide / 80 °C
2: tetrahydrofuran; N,N-dimethyl-formamide / 23 °C
With caesium carbonate; In tetrahydrofuran; N,N-dimethyl-formamide;
DOI:10.1016/j.bmcl.2008.11.074
Guidance literature:
Multi-step reaction with 3 steps
1: 10% palladium on activated carbon; hydrogen / ethanol / 760.05 Torr
2: caesium carbonate / N,N-dimethyl-formamide / 80 °C
3: tetrahydrofuran; N,N-dimethyl-formamide / 23 °C
With 10% palladium on activated carbon; hydrogen; caesium carbonate; In tetrahydrofuran; ethanol; N,N-dimethyl-formamide;
DOI:10.1016/j.bmcl.2008.11.074
upstream raw materials:

C20H19FN2O6

methylamine

C21H23NO4

C14H17NO4

Downstream raw materials:

C21H25N3O4

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