1-(2-{2-[2-(2-oxo-2,3-dihydro-1H-indol-5-ylamino)pyrimidin-4-yl]ethyl}-4-trifluoromethylphenyl)cyclobutanecarbonitrile

Base Information

Chemical Name:1-(2-{2-[2-(2-oxo-2,3-dihydro-1H-indol-5-ylamino)pyrimidin-4-yl]ethyl}-4-trifluoromethylphenyl)cyclobutanecarbonitrile
CAS No.:1360449-50-8
Molecular Formula:C₂₆H₂₂F₃N₅O
Molecular Weight:477.489
Hs Code.:

Synonyms:1-(2-{2-[2-(2-oxo-2,3-dihydro-1H-indol-5-ylamino)pyrimidin-4-yl]ethyl}-4-trifluoromethylphenyl)cyclobutanecarbonitrile

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Chemical Property of 1-(2-{2-[2-(2-oxo-2,3-dihydro-1H-indol-5-ylamino)pyrimidin-4-yl]ethyl}-4-trifluoromethylphenyl)cyclobutanecarbonitrile

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Technology Process of 1-(2-{2-[2-(2-oxo-2,3-dihydro-1H-indol-5-ylamino)pyrimidin-4-yl]ethyl}-4-trifluoromethylphenyl)cyclobutanecarbonitrile

There total 6 articles about 1-(2-{2-[2-(2-oxo-2,3-dihydro-1H-indol-5-ylamino)pyrimidin-4-yl]ethyl}-4-trifluoromethylphenyl)cyclobutanecarbonitrile 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:

: 20876-36-2
5-amino-1,3-dihydro-2H-indol-2-one

: 1360451-42-8
C₁₈H₁₅ClF₃N₃

: 1360449-50-8
1-(2-{2-[2-(2-oxo-2,3-dihydro-1H-indol-5-ylamino)pyrimidin-4-yl]ethyl}-4-trifluoromethylphenyl)cyclobutanecarbonitrile

Guidance literature:: In butan-1-ol; at 120 ℃; for 21h;

Reference yield:

: 1360451-37-1
C₁₂H₉BrF₃N

: 1360449-50-8
1-(2-{2-[2-(2-oxo-2,3-dihydro-1H-indol-5-ylamino)pyrimidin-4-yl]ethyl}-4-trifluoromethylphenyl)cyclobutanecarbonitrile

Guidance literature:: Multi-step reaction with 5 steps

1.1: copper(l) iodide; bis-triphenylphosphine-palladium(II) chloride; triphenylphosphine / N,N-dimethyl-formamide / 1 h

1.2: 18 h / 80 °C

2.1: potassium fluoride / methanol / 16 h / 20 °C / Inert atmosphere

3.1: copper(l) iodide; triethylamine / acetonitrile / 0.17 h

3.2: 0.5 h / 80 °C

4.1: palladium 10% on activated carbon; hydrogen / ethyl acetate / 30 °C / 15001.5 Torr

5.1: butan-1-ol / 21 h / 120 °C

With bis-triphenylphosphine-palladium(II) chloride; potassium fluoride; copper(l) iodide; palladium 10% on activated carbon; hydrogen; triethylamine; triphenylphosphine; In methanol; ethyl acetate; N,N-dimethyl-formamide; acetonitrile; butan-1-ol;

Reference yield:

: 1360451-39-3
1-(2-triethylsilanylethynyl-4-trifluoromethylphenyl)cyclobutanecarbonitrile

: 1360449-50-8
1-(2-{2-[2-(2-oxo-2,3-dihydro-1H-indol-5-ylamino)pyrimidin-4-yl]ethyl}-4-trifluoromethylphenyl)cyclobutanecarbonitrile

Guidance literature:: Multi-step reaction with 4 steps

1.1: potassium fluoride / methanol / 16 h / 20 °C / Inert atmosphere

2.1: copper(l) iodide; triethylamine / acetonitrile / 0.17 h

2.2: 0.5 h / 80 °C

3.1: palladium 10% on activated carbon; hydrogen / ethyl acetate / 30 °C / 15001.5 Torr

4.1: butan-1-ol / 21 h / 120 °C

With potassium fluoride; copper(l) iodide; palladium 10% on activated carbon; hydrogen; triethylamine; In methanol; ethyl acetate; acetonitrile; butan-1-ol;