2-Phenylimidazo[1,2-a]pyridine-6-carbonitrile

Base Information

• Chemical Name: 2-Phenylimidazo[1,2-a]pyridine-6-carbonitrile
• CAS No.: 214958-29-9
• Molecular Formula: C14H9N3
• Molecular Weight: 219.246
• Hs Code.: 2933998090
• DSSTox Substance ID: DTXSID801254820
• Mol file: 214958-29-9.mol

Synonyms:2-phenylimidazo[1,2-a]pyridine-6-carbonitrile;214958-29-9;SCHEMBL14046613;DTXSID801254820;MFCD03787072;AKOS015992670;CS-0333611;3W-0042;AQ-776/42801535;imidazo[1,2-a]pyridine-6-carbonitrile,2-phenyl-

Chemical Property of 2-Phenylimidazo[1,2-a]pyridine-6-carbonitrile

Chemical Property:

• PSA: 41.09000
• LogP: 2.87298
• XLogP3: 3.1
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 1
• Exact Mass: 219.079647300
• Heavy Atom Count: 17
• Complexity: 313

Purity/Quality:

99% ^*data from raw suppliers

2-Phenylimidazo[1,2-a]pyridine-6-carbonitrile ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C(C=C1)C2=CN3C=C(C=CC3=N2)C#N

Technology Process of 2-Phenylimidazo[1,2-a]pyridine-6-carbonitrile

There total 1 articles about 2-Phenylimidazo[1,2-a]pyridine-6-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: 56.0%

6-aminonicotinonitrile (4214-73-7) + ethylbenzene (100-41-4,27536-89-6) → 2-phenylimidazo[1,2-a]pyridine-6-carbonitrile (214958-29-9)

Guidance literature:

ethylbenzene; With N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile); In water; ethyl acetate; at 65 ℃; for 1.5h;

6-aminonicotinonitrile; With sodium carbonate; In water; at 80 ℃;

DOI:10.3390/molecules24050893

Reference yield: 88.0%

p-aminoethylbenzoate (94-09-7) + 2-phenylimidazo[1,2-a]pyridine-6-carbonitrile (214958-29-9) → (E)-ethyl-4-((6-cyano-2-phenylimidazo[1,2-a]pyridin-3-yl)diazenyl)benzoate

Guidance literature:

With tert.-butylnitrite; In ethanol; at 20 ℃; for 8h; Green chemistry;

DOI:10.1039/c6ra03070j

Reference yield: 85.0%

1,1,3-triphenylprop-2-yn-1-ol (1522-13-0) + 2-phenylimidazo[1,2-a]pyridine-6-carbonitrile (214958-29-9) → 2-phenyl-3-(1,3,3-triphenylpropa-1,2-dien-1-yl)imidazo[1,2-a]pyridine-6-carbonitrile

Guidance literature:

With zinc trifluoromethanesulfonate; In toluene; at 110 ℃; for 16h;

DOI:10.1021/acs.joc.6b01916

upstream raw materials:

6-aminonicotinonitrile

ethylbenzene

Downstream raw materials:

2-Phenyl-imidazo[1,2-a]pyridine-6-carbaldehyde

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