3-fluoro-5-[3-{3-[5-(2-hydroxy-2-methylpropoxy)pyrimidin-2-yl]benzyl}-4-oxopyridazin-1(4H)-yl]benzonitrile

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Chemical Name:3-fluoro-5-[3-{3-[5-(2-hydroxy-2-methylpropoxy)pyrimidin-2-yl]benzyl}-4-oxopyridazin-1(4H)-yl]benzonitrile
CAS No.:1314380-63-6
Molecular Formula:C₂₆H₂₂FN₅O₃
Molecular Weight:471.491
Hs Code.:

Synonyms:3-fluoro-5-[3-{3-[5-(2-hydroxy-2-methylpropoxy)pyrimidin-2-yl]benzyl}-4-oxopyridazin-1(4H)-yl]benzonitrile

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Chemical Property of 3-fluoro-5-[3-{3-[5-(2-hydroxy-2-methylpropoxy)pyrimidin-2-yl]benzyl}-4-oxopyridazin-1(4H)-yl]benzonitrile

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Technology Process of 3-fluoro-5-[3-{3-[5-(2-hydroxy-2-methylpropoxy)pyrimidin-2-yl]benzyl}-4-oxopyridazin-1(4H)-yl]benzonitrile

There total 5 articles about 3-fluoro-5-[3-{3-[5-(2-hydroxy-2-methylpropoxy)pyrimidin-2-yl]benzyl}-4-oxopyridazin-1(4H)-yl]benzonitrile 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:

: 1314389-31-5
3-[3-(chloromethyl)-4-oxopyridazin-1(4H)-yl]-5-fluorobenzonitrile

: 1314391-62-2
2-methyl-1-({2-[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]pyrimidin-5-yl}oxy)propan-2-ol

: 1314380-63-6
3-fluoro-5-[3-{3-[5-(2-hydroxy-2-methylpropoxy)pyrimidin-2-yl]benzyl}-4-oxopyridazin-1(4H)-yl]benzonitrile

Guidance literature:: With potassium phosphate; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; In 1,2-dimethoxyethane; water; at 100 ℃; for 1h; Inert atmosphere;

Reference yield:

: 210992-28-2
3-amino-5-fluoro-benzonitrile

: 1314380-63-6
3-fluoro-5-[3-{3-[5-(2-hydroxy-2-methylpropoxy)pyrimidin-2-yl]benzyl}-4-oxopyridazin-1(4H)-yl]benzonitrile

Guidance literature:: Multi-step reaction with 5 steps

1.1: hydrogenchloride; sodium nitrite / water / 1.25 h / 0 - 4 °C

1.2: 1 h / 0 °C

2.1: 5 h / 75 °C

2.2: 20 h / 100 °C

3.1: 4-methyl-morpholine; isobutyl chloroformate / tetrahydrofuran / 1 h / 0 °C / Inert atmosphere

3.2: 1 h / 20 °C

4.1: thionyl chloride / acetonitrile / 2.5 h / 20 °C

5.1: potassium phosphate / dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂ / 1,2-dimethoxyethane; water / 1 h / 100 °C / Inert atmosphere

With 4-methyl-morpholine; hydrogenchloride; potassium phosphate; thionyl chloride; sodium nitrite; isobutyl chloroformate; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; In tetrahydrofuran; 1,2-dimethoxyethane; water; acetonitrile;

Reference yield:

: 1314389-38-2
3-fluoro-5-[3-(hydroxymethyl)-4-oxopyridazin-1(4H)-yl]benzonitrile

: 1314380-63-6
3-fluoro-5-[3-{3-[5-(2-hydroxy-2-methylpropoxy)pyrimidin-2-yl]benzyl}-4-oxopyridazin-1(4H)-yl]benzonitrile

Guidance literature:: Multi-step reaction with 2 steps

1: thionyl chloride / acetonitrile / 2.5 h / 20 °C

2: potassium phosphate / dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂ / 1,2-dimethoxyethane; water / 1 h / 100 °C / Inert atmosphere

With potassium phosphate; thionyl chloride; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; In 1,2-dimethoxyethane; water; acetonitrile;