3-{difluoro-[3-(5-iodopyrimidin-2-yl)phenyl]methyl}-6-(1-methyl-1H-pyrazol-4-yl)-1,2,4-triazolo[4,3-b]-pyridazine

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Chemical Name:3-{difluoro-[3-(5-iodopyrimidin-2-yl)phenyl]methyl}-6-(1-methyl-1H-pyrazol-4-yl)-1,2,4-triazolo[4,3-b]-pyridazine
CAS No.:1201930-24-6
Molecular Formula:C₂₀H₁₃F₂IN₈
Molecular Weight:530.278
Hs Code.:

Synonyms:3-{difluoro-[3-(5-iodopyrimidin-2-yl)phenyl]methyl}-6-(1-methyl-1H-pyrazol-4-yl)-1,2,4-triazolo[4,3-b]-pyridazine

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Chemical Property of 3-{difluoro-[3-(5-iodopyrimidin-2-yl)phenyl]methyl}-6-(1-methyl-1H-pyrazol-4-yl)-1,2,4-triazolo[4,3-b]-pyridazine

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Technology Process of 3-{difluoro-[3-(5-iodopyrimidin-2-yl)phenyl]methyl}-6-(1-methyl-1H-pyrazol-4-yl)-1,2,4-triazolo[4,3-b]-pyridazine

There total 6 articles about 3-{difluoro-[3-(5-iodopyrimidin-2-yl)phenyl]methyl}-6-(1-methyl-1H-pyrazol-4-yl)-1,2,4-triazolo[4,3-b]-pyridazine 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:

: 1201929-66-9
3-{[3-(5-bromopyrimidin-2-yl)phenyl]difluoromethyl}-6-(1-methyl-1H-pyrazol-4-yl)-1,2,4-triazolo[4,3-b]pyridazine

: 1201930-24-6
3-{difluoro-[3-(5-iodopyrimidin-2-yl)phenyl]methyl}-6-(1-methyl-1H-pyrazol-4-yl)-1,2,4-triazolo[4,3-b]-pyridazine

Guidance literature:: With trans-N,N'-dimethyl-1,2-cyclohexyldiamine; copper(l) iodide; sodium iodide; In 1,4-dioxane; at 110 ℃; for 18h; Inert atmosphere;

Reference yield:

: 885068-75-7
2-(3-bromophenyl)-2,2-difluoroacetic acid ethyl ester

: 1201930-24-6
3-{difluoro-[3-(5-iodopyrimidin-2-yl)phenyl]methyl}-6-(1-methyl-1H-pyrazol-4-yl)-1,2,4-triazolo[4,3-b]-pyridazine

Guidance literature:: Multi-step reaction with 5 steps

1: hydrazine hydrate / methanol / 0.17 h / 45 °C

2: butan-1-ol / 114 h / 20 - 30 °C

3: potassium acetate / bis-triphenylphosphine-palladium(II) chloride / N,N-dimethyl-formamide / 18 h / 80 °C / Inert atmosphere

4: sodium carbonate / bis-triphenylphosphine-palladium(II) chloride / toluene; ethanol; water / 18 h / 80 °C / Inert atmosphere

5: sodium iodide; copper(l) iodide; trans-N,N'-dimethyl-1,2-cyclohexyldiamine / 1,4-dioxane / 18 h / 110 °C / Inert atmosphere

With trans-N,N'-dimethyl-1,2-cyclohexyldiamine; copper(l) iodide; hydrazine hydrate; potassium acetate; sodium carbonate; sodium iodide; bis-triphenylphosphine-palladium(II) chloride; In 1,4-dioxane; methanol; ethanol; water; N,N-dimethyl-formamide; toluene; butan-1-ol;

Reference yield:

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

: 1201930-24-6
3-{difluoro-[3-(5-iodopyrimidin-2-yl)phenyl]methyl}-6-(1-methyl-1H-pyrazol-4-yl)-1,2,4-triazolo[4,3-b]-pyridazine

Guidance literature:: Multi-step reaction with 4 steps

1: butan-1-ol / 114 h / 20 - 30 °C

2: potassium acetate / bis-triphenylphosphine-palladium(II) chloride / N,N-dimethyl-formamide / 18 h / 80 °C / Inert atmosphere

3: sodium carbonate / bis-triphenylphosphine-palladium(II) chloride / toluene; ethanol; water / 18 h / 80 °C / Inert atmosphere

4: sodium iodide; copper(l) iodide; trans-N,N'-dimethyl-1,2-cyclohexyldiamine / 1,4-dioxane / 18 h / 110 °C / Inert atmosphere

With trans-N,N'-dimethyl-1,2-cyclohexyldiamine; copper(l) iodide; potassium acetate; sodium carbonate; sodium iodide; bis-triphenylphosphine-palladium(II) chloride; In 1,4-dioxane; ethanol; water; N,N-dimethyl-formamide; toluene; butan-1-ol;