5-(2-Furyl)pyridine-2-carbonitrile

Base Information

• Chemical Name: 5-(2-Furyl)pyridine-2-carbonitrile
• CAS No.: 619334-50-8
• Molecular Formula: C₁₀H₆N₂O
• Molecular Weight: 170.17
• DSSTox Substance ID: DTXSID60454585
• Wikidata: Q82276192
• Mol file: 619334-50-8.mol

Synonyms:5-(2-furyl)pyridine-2-carbonitrile;619334-50-8;5-(furan-2-yl)pyridine-2-carbonitrile;5-(furan-2-yl)picolinonitrile;SCHEMBL5493920;DTXSID60454585;AKOS006308140

Chemical Property of 5-(2-Furyl)pyridine-2-carbonitrile

Chemical Property:

• PSA: 49.82000
• LogP: 2.21328
• XLogP3: 1.6
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 1
• Exact Mass: 170.048012819
• Heavy Atom Count: 13
• Complexity: 220

Purity/Quality:

5-(2-FURYL)PYRIDINE-2-CARBONITRILE 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=COC(=C1)C2=CN=C(C=C2)C#N

Technology Process of 5-(2-Furyl)pyridine-2-carbonitrile

There total 2 articles about 5-(2-Furyl)pyridine-2-carbonitrile 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: 83.0%

2-(tributylstannyl)furan (118486-94-5) + 2-Cyano-5-bromopyridine (97483-77-7) → 5-(furan-2-yl)pyridine-2-carbonitrile (619334-50-8)

Guidance literature:

With tetrakis(triphenylphosphine) palladium⁽⁰⁾; In 1,4-dioxane; at 100 - 110 ℃; for 24h;

DOI:10.1021/jm0302602

Reference yield:

2,5-dibromopyridine (624-28-2) → 5-(furan-2-yl)pyridine-2-carbonitrile (619334-50-8)

Guidance literature:

Multi-step reaction with 2 steps

1: 74 percent / dimethylformamide / 12 h / 110 - 120 °C

2: 83 percent / tetrakis(triphenylphosphine)palladium / dioxane / 24 h / 100 - 110 °C

With tetrakis(triphenylphosphine) palladium⁽⁰⁾; In 1,4-dioxane; N,N-dimethyl-formamide; 2: Stille coupling;

DOI:10.1021/jm0302602

Reference yield:

5-(furan-2-yl)pyridine-2-carbonitrile (619334-50-8) → 5-[5-(4-cyano-phenyl)-furan-2-yl]-pyridine-2-carbonitrile (619334-52-0)

Guidance literature:

Multi-step reaction with 2 steps

1: 93 percent / N-bromosuccinimide / dimethylformamide / 20 °C

2: 64 percent / aq. NaHCO₃; tetrakis(triphenylphosphine) palladium / toluene; methanol / 24 h / 80 °C

With N-Bromosuccinimide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; sodium hydrogencarbonate; In methanol; N,N-dimethyl-formamide; toluene; 2: Suzuki coupling;

DOI:10.1021/jm0302602

upstream raw materials:

2-(tributylstannyl)furan

2-Cyano-5-bromopyridine

2,5-dibromopyridine

Downstream raw materials:

5-[5-(4-cyano-phenyl)-furan-2-yl]-pyridine-2-carbonitrile

N-hydroxy-5-{5-[4-(N-hydroxycarbamimidoyl)-phenyl]-furan-2-yl}-pyridine-2-carboxamidine

N-acetoxy-5-{5-[4-(N-acetoxycarbamimidoyl)-phenyl]-furan-2-yl}-pyridine-2-carboxamidine