4-fluoro-5-[5-methoxy-4-oxo-3-(1-phenyl-1H-pyrazol-5-yl)pyridazin-1(4H)-yl]-1,3,3-trimethyl-1,3-dihydro-2H-indol-2-one

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Chemical Name:4-fluoro-5-[5-methoxy-4-oxo-3-(1-phenyl-1H-pyrazol-5-yl)pyridazin-1(4H)-yl]-1,3,3-trimethyl-1,3-dihydro-2H-indol-2-one
CAS No.:1357192-09-6
Molecular Formula:C₂₅H₂₂FN₅O₃
Molecular Weight:459.48
Hs Code.:

Synonyms:4-fluoro-5-[5-methoxy-4-oxo-3-(1-phenyl-1H-pyrazol-5-yl)pyridazin-1(4H)-yl]-1,3,3-trimethyl-1,3-dihydro-2H-indol-2-one

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Chemical Property of 4-fluoro-5-[5-methoxy-4-oxo-3-(1-phenyl-1H-pyrazol-5-yl)pyridazin-1(4H)-yl]-1,3,3-trimethyl-1,3-dihydro-2H-indol-2-one

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Technology Process of 4-fluoro-5-[5-methoxy-4-oxo-3-(1-phenyl-1H-pyrazol-5-yl)pyridazin-1(4H)-yl]-1,3,3-trimethyl-1,3-dihydro-2H-indol-2-one

There total 9 articles about 4-fluoro-5-[5-methoxy-4-oxo-3-(1-phenyl-1H-pyrazol-5-yl)pyridazin-1(4H)-yl]-1,3,3-trimethyl-1,3-dihydro-2H-indol-2-one 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:

: 5-{3-[3-(dimethylamino)prop-2-enoyl]-5-methoxy-4-oxopyridazin-1(4H)-yl}-4-fluoro-1,3,3-trimethyl-1,3-dihydro-2H-indol-2-one

: 100-63-0
phenylhydrazine

: 1357192-09-6
4-fluoro-5-[5-methoxy-4-oxo-3-(1-phenyl-1H-pyrazol-5-yl)pyridazin-1(4H)-yl]-1,3,3-trimethyl-1,3-dihydro-2H-indol-2-one

Guidance literature:: With trifluoroacetic acid; In ethanol; at 20 ℃;
DOI:10.1016/j.bmc.2015.10.002

Reference yield:

: 1357192-10-9
4-fluoro-3,3-dimethyl-5-nitro-1,3-dihydro-2H-indol-2-one

: 1357192-09-6
4-fluoro-5-[5-methoxy-4-oxo-3-(1-phenyl-1H-pyrazol-5-yl)pyridazin-1(4H)-yl]-1,3,3-trimethyl-1,3-dihydro-2H-indol-2-one

Guidance literature:: Multi-step reaction with 8 steps

1.1: hydrogen; 5%-palladium/activated carbon / methanol / 20 °C

2.1: hydrogenchloride; sodium nitrite / water / 0.25 h / 0 °C

2.2: 0 °C

3.1: acetonitrile / Reflux

4.1: sodium hydroxide / methanol / 2 h / 20 °C

5.1: 1,1'-carbonyldiimidazole / tetrahydrofuran / 2 h / 50 °C

5.2: 20 °C

6.1: tetrahydrofuran / 2 h / -78 °C

7.1: acetonitrile / 1 h / Reflux

8.1: trifluoroacetic acid / ethanol / 20 °C

With hydrogenchloride; 5%-palladium/activated carbon; hydrogen; 1,1'-carbonyldiimidazole; trifluoroacetic acid; sodium hydroxide; sodium nitrite; In tetrahydrofuran; methanol; ethanol; water; acetonitrile;
DOI:10.1016/j.bmc.2015.10.002

Reference yield:

: 1357192-11-0
5-amino-4-fluoro-3,3-dimethyl-1,3-dihydro-2H-indol-2-one

: 1357192-09-6
4-fluoro-5-[5-methoxy-4-oxo-3-(1-phenyl-1H-pyrazol-5-yl)pyridazin-1(4H)-yl]-1,3,3-trimethyl-1,3-dihydro-2H-indol-2-one

Guidance literature:: Multi-step reaction with 7 steps

1.1: hydrogenchloride; sodium nitrite / water / 0.25 h / 0 °C

1.2: 0 °C

2.1: acetonitrile / Reflux

3.1: sodium hydroxide / methanol / 2 h / 20 °C

4.1: 1,1'-carbonyldiimidazole / tetrahydrofuran / 2 h / 50 °C

4.2: 20 °C

5.1: tetrahydrofuran / 2 h / -78 °C

6.1: acetonitrile / 1 h / Reflux

7.1: trifluoroacetic acid / ethanol / 20 °C

With hydrogenchloride; 1,1'-carbonyldiimidazole; trifluoroacetic acid; sodium hydroxide; sodium nitrite; In tetrahydrofuran; methanol; ethanol; water; acetonitrile;
DOI:10.1016/j.bmc.2015.10.002