Zolimidine

Base Information

• Chemical Name: Zolimidine
• CAS No.: 1222-57-7
• Molecular Formula: C14H12 N2 O2 S
• Molecular Weight: 272.327
• Hs Code.: 2933990090
• European Community (EC) Number: 214-947-4
• UNII: YCF001N8QB
• DSSTox Substance ID: DTXSID9057630
• Nikkaji Number: J7.463B
• Wikipedia: Zolimidine
• Wikidata: Q8073565
• NCI Thesaurus Code: C66705
• Metabolomics Workbench ID: 154386
• ChEMBL ID: CHEMBL2105534
• Mol file: 1222-57-7.mol

Synonyms:Solimidine;Solmidin;zolimidine

Chemical Property of Zolimidine

Chemical Property:

• Melting Point: 242-244°
• Refractive Index: 1.6000 (estimate)
• Boiling Point: °Cat760mmHg
• Flash Point: °C
• PSA: 59.82000
• Density: 1.31 g/cm³
• LogP: 3.48560
• XLogP3: 2.7
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 2
• Exact Mass: 272.06194880
• Heavy Atom Count: 19
• Complexity: 410

Purity/Quality:

97% ^*data from raw suppliers

2-[4-(METHYLSULFONYL)PHENYL]-IMIDAZO[1,2-A]PYRIDINE 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CS(=O)(=O)C1=CC=C(C=C1)C2=CN3C=CC=CC3=N2
• Therapeutic Function: Antiulcer

Technology Process of Zolimidine

There total 21 articles about Zolimidine 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: 94.0%

2-aminopyridine (504-29-0) + 4-(methanesulfonyl)acetophenone (10297-73-1) → zolimidine (1222-57-7)

Guidance literature:

With tetrabutylammonium tetrafluoroborate; hydrogen iodide; In ethanol; at 50 ℃; for 24h; Electrochemical reaction; Schlenk technique; Green chemistry;

DOI:10.1039/c8gc03622e

Reference yield: 91.0%

2-aminopyridine (504-29-0) + 2-bromo-1-(4-methanesulfonylphenyl)ethanone (50413-24-6) → zolimidine (1222-57-7)

Guidance literature:

In water; at 20 ℃; for 18h; Green chemistry;

DOI:10.14233/ajchem.2017.20533

Reference yield: 85.0%

2-(4-methylsulfanylphenyl)imidazo[1,2-a]pyridine (2076-70-2) → zolimidine (1222-57-7)

Guidance literature:

With diethylene glycol dibutyl ether; oxygen; at 110 ℃; for 20h; Green chemistry;

DOI:10.1039/c9gc03713f

upstream raw materials:

2-(4-methylsulfanylphenyl)imidazo[1,2-a]pyridine

2-aminopyridine

4-ethynylthioanisole

4-(methanesulfonyl)acetophenone

Downstream raw materials:

4-((2-(4-(methylsulfonyl)phenyl)imidazo[1,2-a]pyridin-3-yl)methyl)morpholine

2-(4-(methylsulfonyl)phenyl)imidazo[1,2-a]pyridine-3-carbaldehyde

2-(4-(methylsulfonyl)phenyl)-3-(naphthalen-1-ylthio)imidazo[1,2-a]pyridine

2-(4-(methylsulfonyl)phenyl)-3-(phenylthio)imidazo[1,2-a]pyridine

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