propane-1-sulfonic acid {3-[5-(1-acetyl-1H-indazol-5-yl)-1H-pyrrolo[2,3-b]pyridine-3-carbonyl]-2,4-difluoro-phenyl}-amide

Base Information

• Chemical Name: propane-1-sulfonic acid {3-[5-(1-acetyl-1H-indazol-5-yl)-1H-pyrrolo[2,3-b]pyridine-3-carbonyl]-2,4-difluoro-phenyl}-amide
• CAS No.: 1312939-69-7
• Molecular Formula: C₂₆H₂₁F₂N₅O₄S
• Molecular Weight: 537.547
• Mol file: 1312939-69-7.mol

Synonyms:propane-1-sulfonic acid {3-[5-(1-acetyl-1H-indazol-5-yl)-1H-pyrrolo[2,3-b]pyridine-3-carbonyl]-2,4-difluoro-phenyl}-amide

Chemical Property of propane-1-sulfonic acid {3-[5-(1-acetyl-1H-indazol-5-yl)-1H-pyrrolo[2,3-b]pyridine-3-carbonyl]-2,4-difluoro-phenyl}-amide

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of propane-1-sulfonic acid {3-[5-(1-acetyl-1H-indazol-5-yl)-1H-pyrrolo[2,3-b]pyridine-3-carbonyl]-2,4-difluoro-phenyl}-amide

There total 8 articles about propane-1-sulfonic acid {3-[5-(1-acetyl-1H-indazol-5-yl)-1H-pyrrolo[2,3-b]pyridine-3-carbonyl]-2,4-difluoro-phenyl}-amide 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:

N-[3-(5-bromo-1H-pyrrolo[2,3-b]pyridine-3-carbonyl)-2,4-difluoro-phenyl]propane-1-sulfonamide (918504-27-5) → propane-1-sulfonic acid {3-[5-(1-acetyl-1H-indazol-5-yl)-1H-pyrrolo[2,3-b]pyridine-3-carbonyl]-2,4-difluoro-phenyl}-amide (1312939-69-7)

Guidance literature:

Multi-step reaction with 3 steps

1: N-ethyl-N,N-diisopropylamine / dmap / toluene / 20 °C / Inert atmosphere

2: potassium carbonate / dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂ / dichloromethane; toluene; ethanol; water / 1.75 h / 110 - 145 °C / microwave irradiation

3: acetonitrile / 3 h / 20 °C

With potassium carbonate; N-ethyl-N,N-diisopropylamine; dmap; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; In ethanol; dichloromethane; water; toluene; acetonitrile;

Reference yield:

propane-1-sulfonic acid {2,4-difluoro-3-[5-(1H-indazol-5-yl)-1H-pyrrolo[2,3-b]pyridine-3-carbonyl]-phenyl}-amide (1312939-63-1) + acetic anhydride (108-24-7) → propane-1-sulfonic acid {3-[5-(1-acetyl-1H-indazol-5-yl)-1H-pyrrolo[2,3-b]pyridine-3-carbonyl]-2,4-difluoro-phenyl}-amide (1312939-69-7)

Guidance literature:

In acetonitrile; at 20 ℃; for 3h;

Reference yield:

5-bromo-1H-pyrrolo[2,3-b]pyridine (183208-35-7) → propane-1-sulfonic acid {3-[5-(1-acetyl-1H-indazol-5-yl)-1H-pyrrolo[2,3-b]pyridine-3-carbonyl]-2,4-difluoro-phenyl}-amide (1312939-69-7)

Guidance literature:

Multi-step reaction with 7 steps

1: potassium hydroxide / methanol / 20 °C / Inert atmosphere

2: Dess-Martin periodane / tetrahydrofuran / 2 h / 20 °C

3: trimethylsilyl iodide / acetonitrile / 20 °C / Inert atmosphere

4: pyridine / dichloromethane / 20 °C / Inert atmosphere

5: N-ethyl-N,N-diisopropylamine / dmap / toluene / 20 °C / Inert atmosphere

6: potassium carbonate / dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂ / dichloromethane; toluene; ethanol; water / 1.75 h / 110 - 145 °C / microwave irradiation

7: acetonitrile / 3 h / 20 °C

With pyridine; trimethylsilyl iodide; potassium carbonate; Dess-Martin periodane; N-ethyl-N,N-diisopropylamine; potassium hydroxide; dmap; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; In tetrahydrofuran; methanol; ethanol; dichloromethane; water; toluene; acetonitrile;

upstream raw materials:

propane-1-sulfonic acid {2,4-difluoro-3-[5-(1H-indazol-5-yl)-1H-pyrrolo[2,3-b]pyridine-3-carbonyl]-phenyl}-amide

acetic anhydride

5-bromo-1H-pyrrolo[2,3-b]pyridine

N-[3-(5-bromo-1H-pyrrolo[2,3-b]pyridine-3-carbonyl)-2,4-difluoro-phenyl]propane-1-sulfonamide