2-(3-amino-6-phenyl-4-(trifluoromethyl)-1H-pyrazolo[3,4-b]pyridin-1-yl)-N-(furan-2-ylmethyl)acetamide

Base Information

• Chemical Name: 2-(3-amino-6-phenyl-4-(trifluoromethyl)-1H-pyrazolo[3,4-b]pyridin-1-yl)-N-(furan-2-ylmethyl)acetamide
• CAS No.: 1469293-90-0
• Molecular Formula: C₂₀H₁₆F₃N₅O₂
• Molecular Weight: 415.375

Synonyms:2-(3-amino-6-phenyl-4-(trifluoromethyl)-1H-pyrazolo[3,4-b]pyridin-1-yl)-N-(furan-2-ylmethyl)acetamide

Chemical Property of 2-(3-amino-6-phenyl-4-(trifluoromethyl)-1H-pyrazolo[3,4-b]pyridin-1-yl)-N-(furan-2-ylmethyl)acetamide

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Technology Process of 2-(3-amino-6-phenyl-4-(trifluoromethyl)-1H-pyrazolo[3,4-b]pyridin-1-yl)-N-(furan-2-ylmethyl)acetamide

There total 4 articles about 2-(3-amino-6-phenyl-4-(trifluoromethyl)-1H-pyrazolo[3,4-b]pyridin-1-yl)-N-(furan-2-ylmethyl)acetamide 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: 85.0%

furan-2-ylmethanamine (617-89-0) + ethyl 2-(3-amino-6-phenyl-4-(trifluoromethyl)-1H-pyrazolo[3,4-b]pyridin-1-yl)acetate (1469293-82-0) → 2-(3-amino-6-phenyl-4-(trifluoromethyl)-1H-pyrazolo[3,4-b]pyridin-1-yl)-N-(furan-2-ylmethyl)acetamide (1469293-90-0)

Guidance literature:

at 80 - 90 ℃;

DOI:10.1016/j.bmcl.2013.08.089

Reference yield:

2-oxo-6-phenyl-4-(trifluoromethyl)-1,2-dihydropyridine-3-carbonitrile (3335-44-2) → 2-(3-amino-6-phenyl-4-(trifluoromethyl)-1H-pyrazolo[3,4-b]pyridin-1-yl)-N-(furan-2-ylmethyl)acetamide (1469293-90-0)

Guidance literature:

Multi-step reaction with 4 steps

1: sodium iodide; potassium carbonate / acetone / 6 h / Reflux

2: hydrazine hydrate / 6 h / 100 °C

3: sodium iodide; potassium carbonate / acetone / 24 h / Reflux

4: 80 - 90 °C

With potassium carbonate; hydrazine hydrate; sodium iodide; In acetone;

DOI:10.1016/j.bmcl.2013.08.089

Reference yield:

2-O-acetamido-3-cyano-4-trifluoromethyl-6-phenylpyridine → 2-(3-amino-6-phenyl-4-(trifluoromethyl)-1H-pyrazolo[3,4-b]pyridin-1-yl)-N-(furan-2-ylmethyl)acetamide (1469293-90-0)

Guidance literature:

Multi-step reaction with 3 steps

1: hydrazine hydrate / 6 h / 100 °C

2: sodium iodide; potassium carbonate / acetone / 24 h / Reflux

3: 80 - 90 °C

With potassium carbonate; hydrazine hydrate; sodium iodide; In acetone;

DOI:10.1016/j.bmcl.2013.08.089

upstream raw materials:

2-oxo-6-phenyl-4-(trifluoromethyl)-1,2-dihydropyridine-3-carbonitrile

furan-2-ylmethanamine

ethyl 2-(3-amino-6-phenyl-4-(trifluoromethyl)-1H-pyrazolo[3,4-b]pyridin-1-yl)acetate

6-phenyl-4-(trifluoromethyl)-1H-pyrazolo[3,4-b]pyridin-3-amine

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