6-Iodo-2-phenylimidazo[1,2-a]pyridine

Base Information

• Chemical Name: 6-Iodo-2-phenylimidazo[1,2-a]pyridine
• CAS No.: 61982-63-6
• Molecular Formula: C13H9IN2
• Molecular Weight: 320.132
• DSSTox Substance ID: DTXSID50358604
• Nikkaji Number: J3.139.200D
• Wikidata: Q82139284
• Mol file: 61982-63-6.mol

Synonyms:6-iodo-2-phenylimidazo[1,2-a]pyridine;61982-63-6;6-Iodo-2-phenylH-imidazo[1,2-a]pyridine;Bionet2_001199;Oprea1_523586;SCHEMBL6491308;DTXSID50358604;HMS1367G11;STK208467;AKOS005086280;CS-0367316;2R-0664;AG-690/33029044

Chemical Property of 6-Iodo-2-phenylimidazo[1,2-a]pyridine

Chemical Property:

• PSA: 17.30000
• LogP: 3.60590
• XLogP3: 4.1
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 1
• Exact Mass: 319.98105
• Heavy Atom Count: 16
• Complexity: 240

Purity/Quality:

99% ^*data from raw suppliers

6-Iodo-2-phenylH-imidazo[1,2-a]pyridine AldrichCPR ^*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)I

Technology Process of 6-Iodo-2-phenylimidazo[1,2-a]pyridine

There total 7 articles about 6-Iodo-2-phenylimidazo[1,2-a]pyridine 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%

2-amino-5-iodopyridine (20511-12-0) + α-bromoacetophenone (70-11-1) → 2-phenyl-6-iodoimidazo[1,2-a]pyridine (61982-63-6)

Guidance literature:

2-amino-5-iodopyridine; α-bromoacetophenone; In ethanol; for 2h; Reflux;

With sodium hydrogencarbonate; In ethanol; for 5h; Reflux;

DOI:10.1002/anie.201006823

Reference yield: 78.0%

2-aminopyridine (504-29-0) + acetophenone (98-86-2) → 2-phenyl-6-iodoimidazo[1,2-a]pyridine (61982-63-6)

Guidance literature:

With CYANAMID; iodine; In ethanol; at 78 ℃; Temperature; Solvent;

DOI:10.1039/c5ob01313e

Reference yield: 70.0%

2-amino-5-iodopyridine (20511-12-0) + nitromethane (75-52-5) + benzaldehyde (100-52-7) → 2-phenyl-6-iodoimidazo[1,2-a]pyridine (61982-63-6)

Guidance literature:

With iron(III) chloride; In N,N-dimethyl-formamide; at 110 ℃; for 5h;

DOI:10.1016/j.tetlet.2014.07.094

upstream raw materials:

2-amino-5-iodopyridine

α-bromoacetophenone

phenylacetylene

acetophenone

Downstream raw materials:

2-phenyl-6-(trifluoromethyl)imidazo[1,2-a]pyridine