Amphenidone

Base Information

• Chemical Name: Amphenidone
• CAS No.: 134-37-2
• Molecular Formula: C11H10 N2 O
• Molecular Weight: 186.213
• Hs Code.: 2933399090
• UNII: M61FM2VCSV
• DSSTox Substance ID: DTXSID50158449
• Nikkaji Number: J5.593J
• Wikidata: Q27283535
• NCI Thesaurus Code: C76934
• Metabolomics Workbench ID: 155705
• ChEMBL ID: CHEMBL2104057
• Mol file: 134-37-2.mol

Synonyms:AMPHENIDONE;134-37-2;Dornwal;Amphenidone [INN];Aminophenylpyridone;1-(m-Aminophenyl)-2(1H)-pyridone;Amfenidona;Amphenidonum;1-(3-Aminophenyl)-2-pyridone;Amfenidona [INN-Spanish];Amphenidonum [INN-Latin];1-m-Aminophenyl-2-pyridone;UNII-M61FM2VCSV;M61FM2VCSV;amfenidone;BRN 1526918;1-(3-Aminophenyl)-2-(1H)-pyridinone;1-(m-Aminofenylo)-2-pirydonu [Polish];1-(m-Aminofenylo)-2-pirydonu;2(1H)-Pyridone, 1-(m-aminophenyl)-;1-(3-AMINOPHENYL)-2(1H)-PYRIDINONE;5-21-07-00122 (Beilstein Handbook Reference);1-(3-aminophenyl)pyridin-2-one;AMPHENIDONE [MI];SCHEMBL586236;CHEMBL2104057;DTXSID50158449;CHEBI:134830;AKOS006273137;2(1H)-Pyridinone, 1-(3-aminophenyl)-;LS-133822;1-(3-aminophenyl)-1,2-dihydropyridin-2-one;Q27283535

Chemical Property of Amphenidone

Chemical Property:

• Vapor Pressure: 2.02E-07mmHg at 25°C
• Melting Point: 182.5-184.5°
• Refractive Index: 1.5300 (estimate)
• Boiling Point: 424.7°Cat760mmHg
• Flash Point: 210.7°C
• PSA: 48.02000
• Density: 1.266g/cm³
• LogP: 2.00090
• XLogP3: 1.3
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 1
• Exact Mass: 186.079312947
• Heavy Atom Count: 14
• Complexity: 283

Purity/Quality:

99% ^*data from raw suppliers

1-(3-AMINOPHENYL)-1,2-DIHYDROPYRIDIN-2-ONE 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC(=O)N(C=C1)C2=CC=CC(=C2)N

Technology Process of Amphenidone

There total 3 articles about Amphenidone 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: 87.0%

2-Pyridone (142-08-5,1199357-22-6) + m-Bromoaniline (591-19-5) → 1-(3-aminophenyl)-1H-pyridin-2-one (134-37-2)

Guidance literature:

With potassium carbonate; copper(l) iodide; 4,7-dimethoxy-1,10-phenanthroline; In dimethyl sulfoxide; at 110 ℃; for 24h;

DOI:10.1021/ol062904g

Reference yield: 82.0%

2-Pyridone (142-08-5,1199357-22-6) + 3-Iodoaniline (626-01-7) → 1-(3-aminophenyl)-1H-pyridin-2-one (134-37-2)

Guidance literature:

With N,N'-(1R,2R)-cyclohexane-1,2-diyl-bis-[1-(pyridine-2-yl)methanimine]; 3 A molecular sieve; caesium carbonate; copper(I) oxide; In acetonitrile; at 82 ℃; for 48h;

DOI:10.1002/chem.200400582

Reference yield:

→ 1-(3-aminophenyl)-1H-pyridin-2-one (134-37-2)

Guidance literature:

entspr. Pyridon (I-Taf.I), Zn/H+;

upstream raw materials:

2-Pyridone

3-Iodoaniline

m-Bromoaniline