Ethyl 4-{[2-(1,1-di methylethyl)phenyl]amino}-7-(3,5-dimethyl-4-isoxazolyl)-6-(methoxy)-3-quinolinecarboxylate

Base Information

Chemical Name:Ethyl 4-{[2-(1,1-di methylethyl)phenyl]amino}-7-(3,5-dimethyl-4-isoxazolyl)-6-(methoxy)-3-quinolinecarboxylate
CAS No.:1300737-57-8
Molecular Formula:C₂₈H₃₁N₃O₄
Molecular Weight:473.572
Hs Code.:

Synonyms:Ethyl 4-{[2-(1,1-di methylethyl)phenyl]amino}-7-(3,5-dimethyl-4-isoxazolyl)-6-(methoxy)-3-quinolinecarboxylate

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Chemical Property of Ethyl 4-{[2-(1,1-di methylethyl)phenyl]amino}-7-(3,5-dimethyl-4-isoxazolyl)-6-(methoxy)-3-quinolinecarboxylate

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Technology Process of Ethyl 4-{[2-(1,1-di methylethyl)phenyl]amino}-7-(3,5-dimethyl-4-isoxazolyl)-6-(methoxy)-3-quinolinecarboxylate

There total 6 articles about Ethyl 4-{[2-(1,1-di methylethyl)phenyl]amino}-7-(3,5-dimethyl-4-isoxazolyl)-6-(methoxy)-3-quinolinecarboxylate 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: 27.7%

: 1300737-56-7
ethyl 4-chloro-7-(3,5-dimethyl-4-isoxazolyl)-6-(methoxy)-3-quinolinecarboxylate

: 6310-21-0
2-(1,1-dimethylethyl)-benzenamine

: 1300737-57-8
Ethyl 4-{[2-(1,1-di methylethyl)phenyl]amino}-7-(3,5-dimethyl-4-isoxazolyl)-6-(methoxy)-3-quinolinecarboxylate

Guidance literature:: ethyl 4-chloro-7-(3,5-dimethyl-4-isoxazolyl)-6-(methoxy)-3-quinolinecarboxylate; 2-(1,1-dimethylethyl)-benzenamine; In 1,4-dioxane; for 48h; Reflux;

With sodium hydroxide; In water;

Reference yield:

: 5399-03-1
2-iodo-1-methoxy-4-nitrobenzene

: 1300737-57-8
Ethyl 4-{[2-(1,1-di methylethyl)phenyl]amino}-7-(3,5-dimethyl-4-isoxazolyl)-6-(methoxy)-3-quinolinecarboxylate

Guidance literature:: Multi-step reaction with 6 steps

1: caesium carbonate / 1,2-dimethoxyethane; water / 4 h / 90 °C / Inert atmosphere

2: palladium on activated charcoal; hydrogen; sodium sulfite / ethanol; ethyl acetate / 24 h

3: 1 h / 130 °C

4: diphenylether / 0.75 h / 255 °C

5: trichlorophosphate / 120 °C

6: Heating

With diphenylether; palladium on activated charcoal; hydrogen; caesium carbonate; sodium sulfite; trichlorophosphate; In 1,2-dimethoxyethane; ethanol; water; ethyl acetate; 1: Suzuki coupling;
DOI:10.1016/j.bmcl.2012.01.125

Reference yield:

: 16114-47-9
3,5-dimethylisoxazole-4-boronic acid

: 1300737-57-8
Ethyl 4-{[2-(1,1-di methylethyl)phenyl]amino}-7-(3,5-dimethyl-4-isoxazolyl)-6-(methoxy)-3-quinolinecarboxylate

Guidance literature:: Multi-step reaction with 6 steps

1: caesium carbonate / 1,2-dimethoxyethane; water / 4 h / 90 °C / Inert atmosphere

2: palladium on activated charcoal; hydrogen; sodium sulfite / ethanol; ethyl acetate / 24 h

3: 1 h / 130 °C

4: diphenylether / 0.75 h / 255 °C

5: trichlorophosphate / 120 °C

6: Heating

With diphenylether; palladium on activated charcoal; hydrogen; caesium carbonate; sodium sulfite; trichlorophosphate; In 1,2-dimethoxyethane; ethanol; water; ethyl acetate; 1: Suzuki coupling;
DOI:10.1016/j.bmcl.2012.01.125