2-(4-fluorophenyl)-N-[(5-methyl-1H-pyrazol-3-yl)methyl]-1H-pyrrolo[2,3-b]pyridin-5-amine

Base Information

• Chemical Name: 2-(4-fluorophenyl)-N-[(5-methyl-1H-pyrazol-3-yl)methyl]-1H-pyrrolo[2,3-b]pyridin-5-amine
• CAS No.: 1616385-66-0
• Molecular Formula: C₁₈H₁₆FN₅
• Molecular Weight: 321.357
• Mol file: 1616385-66-0.mol

Synonyms:2-(4-fluorophenyl)-N-[(5-methyl-1H-pyrazol-3-yl)methyl]-1H-pyrrolo[2,3-b]pyridin-5-amine

Chemical Property of 2-(4-fluorophenyl)-N-[(5-methyl-1H-pyrazol-3-yl)methyl]-1H-pyrrolo[2,3-b]pyridin-5-amine

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 2-(4-fluorophenyl)-N-[(5-methyl-1H-pyrazol-3-yl)methyl]-1H-pyrrolo[2,3-b]pyridin-5-amine

There total 9 articles about 2-(4-fluorophenyl)-N-[(5-methyl-1H-pyrazol-3-yl)methyl]-1H-pyrrolo[2,3-b]pyridin-5-amine 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: 43.0%

5-methyl-1H-pyrazole-3-carboxaldehyde (3273-44-7) + 2-(4-fluorophenyl)-1H-pyrrolo[2,3-b]pyridin-5-amine (1616387-98-4) → 2-(4-fluorophenyl)-N-[(5-methyl-1H-pyrazol-3-yl)methyl]-1H-pyrrolo[2,3-b]pyridin-5-amine (1616385-66-0)

Guidance literature:

With triethylsilane; trifluoroacetic acid; In acetonitrile; at 20 ℃;

Reference yield:

3-((4-fluorophenyl)ethynyl)pyridine-2,5-diamine (1616387-97-3) → 2-(4-fluorophenyl)-N-[(5-methyl-1H-pyrazol-3-yl)methyl]-1H-pyrrolo[2,3-b]pyridin-5-amine (1616385-66-0)

Guidance literature:

Multi-step reaction with 2 steps

1: potassium tert-butylate / 1-methyl-pyrrolidin-2-one / 2 h / 80 °C

2: triethylsilane; trifluoroacetic acid / acetonitrile / 20 °C

With triethylsilane; potassium tert-butylate; trifluoroacetic acid; In 1-methyl-pyrrolidin-2-one; acetonitrile;

Reference yield:

tert-butyl 5-[bis(tert-butoxycarbonyl)amino]pyrrolo[2,3-b]pyridine-1-carboxylate (1616388-24-9) → 2-(4-fluorophenyl)-N-[(5-methyl-1H-pyrazol-3-yl)methyl]-1H-pyrrolo[2,3-b]pyridin-5-amine (1616385-66-0)

Guidance literature:

Multi-step reaction with 4 steps

1: lithium diisopropyl amide / tetrahydrofuran / 2 h / 0 - 20 °C / Inert atmosphere

2: (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; potassium carbonate / 1,4-dioxane; water / 0.17 h / 80 °C / Microwave irradiation

3: hydrogenchloride / 1,4-dioxane; water; dichloromethane / 2 h / 20 °C

4: triethylsilane; trifluoroacetic acid / acetonitrile / 20 °C

With hydrogenchloride; triethylsilane; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; potassium carbonate; trifluoroacetic acid; lithium diisopropyl amide; In tetrahydrofuran; 1,4-dioxane; dichloromethane; water; acetonitrile;

upstream raw materials:

3-((4-fluorophenyl)ethynyl)pyridine-2,5-diamine

5-methyl-1H-pyrazole-3-carboxaldehyde

2-(4-fluorophenyl)-1H-pyrrolo[2,3-b]pyridin-5-amine

1H-pyrrolo[2,3-b]pyridin-5-amine