N-(5-((3,5-difluorophenyl)thio)-1H-pyrazolo[3,4-b]pyrazin-3-yl)-4-(4-methylpiperazin-1-yl)-2-((tetrahydro-2H-pyran-4-yl)amino)benzamide

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Chemical Name:N-(5-((3,5-difluorophenyl)thio)-1H-pyrazolo[3,4-b]pyrazin-3-yl)-4-(4-methylpiperazin-1-yl)-2-((tetrahydro-2H-pyran-4-yl)amino)benzamide
CAS No.:1392151-64-2
Molecular Formula:C₂₈H₃₀F₂N₈O₂S
Molecular Weight:580.661
Hs Code.:

Synonyms:N-(5-((3,5-difluorophenyl)thio)-1H-pyrazolo[3,4-b]pyrazin-3-yl)-4-(4-methylpiperazin-1-yl)-2-((tetrahydro-2H-pyran-4-yl)amino)benzamide

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Chemical Property of N-(5-((3,5-difluorophenyl)thio)-1H-pyrazolo[3,4-b]pyrazin-3-yl)-4-(4-methylpiperazin-1-yl)-2-((tetrahydro-2H-pyran-4-yl)amino)benzamide

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Technology Process of N-(5-((3,5-difluorophenyl)thio)-1H-pyrazolo[3,4-b]pyrazin-3-yl)-4-(4-methylpiperazin-1-yl)-2-((tetrahydro-2H-pyran-4-yl)amino)benzamide

There total 15 articles about N-(5-((3,5-difluorophenyl)thio)-1H-pyrazolo[3,4-b]pyrazin-3-yl)-4-(4-methylpiperazin-1-yl)-2-((tetrahydro-2H-pyran-4-yl)amino)benzamide 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: 57.0%

: 1392151-65-3
N-(5-(3,5-difluorophenylthio)-1-(4-(4-methylpiperazine-1-yl)-2-(2,2,2-trifluoro-N-(tetrahydro-2H-pyran-4-yl)acetamido) benzoyl)-1H-pyrazolo[3,4-b]pyrazine-3-yl)-4-(4-methylpiperazine-1-yl)-2-(2,2,2-trifluoro-N-(tetrahydro-2H-pyran-4-yl)acetamido)benzamide

: 1392151-64-2
N-(5-((3,5-difluorophenyl)thio)-1H-pyrazolo[3,4-b]pyrazin-3-yl)-4-(4-methylpiperazin-1-yl)-2-((tetrahydro-2H-pyran-4-yl)amino)benzamide

Guidance literature:: With triethylamine; In methanol; at 20 - 65 ℃;

Reference yield:

: 1034975-61-5
4-(4-methylpiperazin-1-yl)-2-(2,2,2-trifluoro-N-(tetrahydro-2H-pyran-4-yl)acetamido)benzoic acid

: 1392151-64-2
N-(5-((3,5-difluorophenyl)thio)-1H-pyrazolo[3,4-b]pyrazin-3-yl)-4-(4-methylpiperazin-1-yl)-2-((tetrahydro-2H-pyran-4-yl)amino)benzamide

Guidance literature:: Multi-step reaction with 3 steps

1: oxalyl dichloride / N,N-dimethyl-formamide / dichloromethane / 2 h / 20 °C

2: N-ethyl-N,N-diisopropylamine / pyridine / 0 - 25 °C

3: triethylamine / methanol / 20 - 65 °C

With oxalyl dichloride; triethylamine; N-ethyl-N,N-diisopropylamine; N,N-dimethyl-formamide; In pyridine; methanol; dichloromethane;

Reference yield:

: 766515-33-7
3-cyano-2-hydroxy-5-iodopyridine

: 1392151-64-2
N-(5-((3,5-difluorophenyl)thio)-1H-pyrazolo[3,4-b]pyrazin-3-yl)-4-(4-methylpiperazin-1-yl)-2-((tetrahydro-2H-pyran-4-yl)amino)benzamide

Guidance literature:: Multi-step reaction with 5 steps

1: trichlorophosphate / sulfuric acid / 0 - 110 °C

2: hydrazine / isopropyl alcohol / 20 - 85 °C

3: potassium carbonate; copper(l) iodide / isopropyl alcohol / 2 h / 80 °C

4: N-ethyl-N,N-diisopropylamine / pyridine / 0 - 25 °C

5: triethylamine / methanol / 20 - 65 °C

With copper(l) iodide; potassium carbonate; triethylamine; N-ethyl-N,N-diisopropylamine; hydrazine; trichlorophosphate; sulfuric acid; In pyridine; methanol; isopropyl alcohol;