6-(1-methyl-1H-pyrazol-4-yl)-2-{3-[5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-pyrimidin-2-yl]benzyl}-2H-pyridazin-3-one

Base Information

Chemical Name:6-(1-methyl-1H-pyrazol-4-yl)-2-{3-[5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-pyrimidin-2-yl]benzyl}-2H-pyridazin-3-one
CAS No.:1100598-43-3
Molecular Formula:C₂₅H₂₇BN₆O₃
Molecular Weight:470.339
Hs Code.:

Synonyms:6-(1-methyl-1H-pyrazol-4-yl)-2-{3-[5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-pyrimidin-2-yl]benzyl}-2H-pyridazin-3-one

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Chemical Property of 6-(1-methyl-1H-pyrazol-4-yl)-2-{3-[5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-pyrimidin-2-yl]benzyl}-2H-pyridazin-3-one

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Technology Process of 6-(1-methyl-1H-pyrazol-4-yl)-2-{3-[5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-pyrimidin-2-yl]benzyl}-2H-pyridazin-3-one

There total 6 articles about 6-(1-methyl-1H-pyrazol-4-yl)-2-{3-[5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-pyrimidin-2-yl]benzyl}-2H-pyridazin-3-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:

: 1100598-42-2
2-[3-(5-bromo-pyrimidin-2-yl)benzyl]-6-(1-methyl-1H-pyrazol-4-yl)-2H-pyridazin-3-one

: 73183-34-3
bis(pinacol)diborane

: 1100598-43-3
6-(1-methyl-1H-pyrazol-4-yl)-2-{3-[5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-pyrimidin-2-yl]benzyl}-2H-pyridazin-3-one

Guidance literature:: With potassium acetate; bis-triphenylphosphine-palladium(II) chloride; In N,N-dimethyl-formamide; at 70 ℃; Inert atmosphere;

Reference yield:

: 87199-15-3
[3-(hydroxymethyl)phenyl]boronic acid

: 1100598-43-3
6-(1-methyl-1H-pyrazol-4-yl)-2-{3-[5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-pyrimidin-2-yl]benzyl}-2H-pyridazin-3-one

Guidance literature:: Multi-step reaction with 4 steps

1.1: potassium phosphate tribasic trihydrate / tetrakis(triphenylphosphine) palladium⁽⁰⁾ / 1,4-dioxane; water / 18 h / 90 °C / Inert atmosphere

2.1: thionyl chloride / dichloromethane / 3 h / 20 °C

3.1: caesium carbonate / N,N-dimethyl-formamide / 24 h / 20 °C

4.1: potassium acetate / N,N-dimethyl-formamide / 0.25 h / 70 °C / Inert atmosphere

4.2: 18 h / 70 °C / Inert atmosphere

With thionyl chloride; potassium phosphate tribasic trihydrate; potassium acetate; caesium carbonate; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In 1,4-dioxane; dichloromethane; water; N,N-dimethyl-formamide;

Reference yield:

: 943541-20-6
3-chloro-6-(1-methyl-1H-pyrazol-4-yl)pyridazine

: 1100598-43-3
6-(1-methyl-1H-pyrazol-4-yl)-2-{3-[5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-pyrimidin-2-yl]benzyl}-2H-pyridazin-3-one

Guidance literature:: Multi-step reaction with 3 steps

1.1: water; formic acid / 28 h / 80 °C

1.2: pH 7

2.1: caesium carbonate / N,N-dimethyl-formamide / 24 h / 20 °C

3.1: potassium acetate / N,N-dimethyl-formamide / 0.25 h / 70 °C / Inert atmosphere

3.2: 18 h / 70 °C / Inert atmosphere

With formic acid; water; potassium acetate; caesium carbonate; In N,N-dimethyl-formamide;