ethyl 5-(4-(2-ethoxy-2-oxoethyl)-2-methoxyphenoxy)-4-nitro-1H-indole-2-carboxylate

Base Information

Chemical Name:ethyl 5-(4-(2-ethoxy-2-oxoethyl)-2-methoxyphenoxy)-4-nitro-1H-indole-2-carboxylate
CAS No.:1080522-09-3
Molecular Formula:C₂₂H₂₂N₂O₈
Molecular Weight:442.425
Hs Code.:

Synonyms:ethyl 5-(4-(2-ethoxy-2-oxoethyl)-2-methoxyphenoxy)-4-nitro-1H-indole-2-carboxylate

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Chemical Property of ethyl 5-(4-(2-ethoxy-2-oxoethyl)-2-methoxyphenoxy)-4-nitro-1H-indole-2-carboxylate

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Technology Process of ethyl 5-(4-(2-ethoxy-2-oxoethyl)-2-methoxyphenoxy)-4-nitro-1H-indole-2-carboxylate

There total 4 articles about ethyl 5-(4-(2-ethoxy-2-oxoethyl)-2-methoxyphenoxy)-4-nitro-1H-indole-2-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:

Reference yield: 33.0%

: 617-35-6
2-oxo-propionic acid ethyl ester

: 1080522-07-1
C₂₂H₂₇N₃O₈

: 1080522-09-3
ethyl 5-(4-(2-ethoxy-2-oxoethyl)-2-methoxyphenoxy)-4-nitro-1H-indole-2-carboxylate

Guidance literature:: With Eaton’s reagent; In dichloromethane; at 45 ℃;
DOI:10.1016/j.bmcl.2014.04.092

Reference yield:

: 1080522-04-8
ethyl 2-(4-(4-iodo-2-nitrophenoxy)-3-methoxyphenyl)acetate

: 1080522-09-3
ethyl 5-(4-(2-ethoxy-2-oxoethyl)-2-methoxyphenoxy)-4-nitro-1H-indole-2-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: caesium carbonate / copper(l) iodide / N,N-dimethyl-formamide / 1.17 h / 20 - 90 °C

2: Eaton's reagent / dichloromethane / 5.17 h / 20 - 45 °C

With Eaton's reagent; caesium carbonate; copper(l) iodide; In dichloromethane; N,N-dimethyl-formamide;

Reference yield:

: 364-75-0
1-fluoro-4-iodo-2-nitro-benzene

: 1080522-09-3
ethyl 5-(4-(2-ethoxy-2-oxoethyl)-2-methoxyphenoxy)-4-nitro-1H-indole-2-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1: caesium carbonate / dimethyl sulfoxide / 2 h / 20 - 100 °C

2: caesium carbonate / copper(l) iodide / N,N-dimethyl-formamide / 1.17 h / 20 - 90 °C

3: Eaton's reagent / dichloromethane / 5.17 h / 20 - 45 °C

With Eaton's reagent; caesium carbonate; copper(l) iodide; In dichloromethane; dimethyl sulfoxide; N,N-dimethyl-formamide;