7-(3,5-dimethyl-4-isoxazolyl)-8-(methyloxy)-2-(4-morpholinyl)-1-[(1R)-1-phenylethyl]-1H-imidazo[4,5-c]quinoline

Base Information

Chemical Name:7-(3,5-dimethyl-4-isoxazolyl)-8-(methyloxy)-2-(4-morpholinyl)-1-[(1R)-1-phenylethyl]-1H-imidazo[4,5-c]quinoline
CAS No.:1403491-63-3
Molecular Formula:C₂₈H₂₉N₅O₃
Molecular Weight:483.57
Hs Code.:

Synonyms:7-(3,5-dimethyl-4-isoxazolyl)-8-(methyloxy)-2-(4-morpholinyl)-1-[(1R)-1-phenylethyl]-1H-imidazo[4,5-c]quinoline

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Chemical Property of 7-(3,5-dimethyl-4-isoxazolyl)-8-(methyloxy)-2-(4-morpholinyl)-1-[(1R)-1-phenylethyl]-1H-imidazo[4,5-c]quinoline

Chemical Property:

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Technology Process of 7-(3,5-dimethyl-4-isoxazolyl)-8-(methyloxy)-2-(4-morpholinyl)-1-[(1R)-1-phenylethyl]-1H-imidazo[4,5-c]quinoline

There total 13 articles about 7-(3,5-dimethyl-4-isoxazolyl)-8-(methyloxy)-2-(4-morpholinyl)-1-[(1R)-1-phenylethyl]-1H-imidazo[4,5-c]quinoline 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: 0.75%

: 110-91-8,99108-56-2
morpholine

: 1403491-35-9
2-chloro-7-(3,5-dimethyl-4-isoxazolyl)-8-(methyloxy)-1-[(1R)-1-phenylethyl]-1H-imidazo[4,5-c]quinoline

: 1403491-63-3
7-(3,5-dimethyl-4-isoxazolyl)-8-(methyloxy)-2-(4-morpholinyl)-1-[(1R)-1-phenylethyl]-1H-imidazo[4,5-c]quinoline

Guidance literature:: In 1-methyl-pyrrolidin-2-one; at 150 ℃; for 1h; Microwave irradiation;

Reference yield:

: 110-91-8,99108-56-2
morpholine

: 1300735-73-2
7-(3,5-dimethyl-4-isoxazolyl)-8-(methyloxy)-1-[(1R)-1-phenylethyl]-1,3-dihydro-2H-imidazo[4,5-c]quinolin-2-one

: 1403491-63-3
7-(3,5-dimethyl-4-isoxazolyl)-8-(methyloxy)-2-(4-morpholinyl)-1-[(1R)-1-phenylethyl]-1H-imidazo[4,5-c]quinoline

Guidance literature:: 7-(3,5-dimethyl-4-isoxazolyl)-8-(methyloxy)-1-[(1R)-1-phenylethyl]-1,3-dihydro-2H-imidazo[4,5-c]quinolin-2-one; With trichlorophosphate; at 100 ℃; for 72h;

morpholine; In 1-methyl-pyrrolidin-2-one; at 150 ℃; for 1h;

Reference yield:

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

: 1403491-63-3
7-(3,5-dimethyl-4-isoxazolyl)-8-(methyloxy)-2-(4-morpholinyl)-1-[(1R)-1-phenylethyl]-1H-imidazo[4,5-c]quinoline

Guidance literature:: Multi-step reaction with 9 steps

1.1: caesium carbonate / 1,2-dimethoxyethane; water / 0.17 h / Inert atmosphere

1.2: 4 h / 90 °C / Inert atmosphere

2.1: hydrogen / 5%-palladium/activated carbon / ethyl acetate; ethanol; water / 24 h

3.1: 1 h / 130 °C

4.1: diphenylether / 0.33 h / Reflux

5.1: sodium hydroxide; water / ethanol; water / Reflux

5.2: 40 °C / pH 4

6.1: trichlorophosphate / 4 h / 20 °C / Heating

6.2: 0.5 h / Cooling with ice

7.1: N-ethyl-N,N-diisopropylamine / 1-methyl-pyrrolidin-2-one / 18 h / 120 °C

8.1: potassium hydroxide / methanol / 0.33 h / Cooling with ice

8.2: 3 h

9.1: trichlorophosphate / 72 h / 100 °C

9.2: 1 h / 150 °C

With water; hydrogen; caesium carbonate; N-ethyl-N,N-diisopropylamine; potassium hydroxide; sodium hydroxide; trichlorophosphate; 5%-palladium/activated carbon; In 1-methyl-pyrrolidin-2-one; methanol; 1,2-dimethoxyethane; diphenylether; ethanol; water; ethyl acetate;