2-(4-Imidazol-1-ylanilino)-1,4-dihydroimidazol-5-one

Base Information

Chemical Name:2-(4-Imidazol-1-ylanilino)-1,4-dihydroimidazol-5-one
CAS No.:116027-14-6
Molecular Formula:C₁₂H₁₁N₅O
Molecular Weight:241.252
Hs Code.:
ChEMBL ID:CHEMBL68833
DSSTox Substance ID:DTXSID001161962

Synonyms:CHEMBL68833;116027-14-6;DTXSID001161962;BDBM50227202;3,5-Dihydro-2-[[4-(1H-imidazol-1-yl)phenyl]amino]-4H-imidazol-4-one

Suppliers and Price of 2-(4-Imidazol-1-ylanilino)-1,4-dihydroimidazol-5-one

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 2-(4-Imidazol-1-ylanilino)-1,4-dihydroimidazol-5-one

Chemical Property:

XLogP3:0.3
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:241.09635999
Heavy Atom Count:18
Complexity:348

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1C(=O)NC(=N1)NC2=CC=C(C=C2)N3C=CN=C3

Technology Process of 2-(4-Imidazol-1-ylanilino)-1,4-dihydroimidazol-5-one

There total 2 articles about 2-(4-Imidazol-1-ylanilino)-1,4-dihydroimidazol-5-one 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: 90.0%

: 2221-00-3
4-(N-imidazolyl)aniline

: 54855-80-0
2-methylsulfanyl-3,5-dihydro-imidazol-4-one hydroiodide

: 116027-14-6
2-<<4-(N-imidazolyl)phenyl>amino>-2-imidazolin-4-one

Guidance literature:: With potassium hydroxide; In ethanol; for 4h; Heating;
DOI:10.1021/jm00119a014

Reference yield:

: 540-37-4
p-aminoiodobenzene

: 116027-14-6
2-<<4-(N-imidazolyl)phenyl>amino>-2-imidazolin-4-one

Guidance literature:: Multi-step reaction with 2 steps

1: 37 percent / potassium carbonate, copper(I) iodide / dimethylformamide / 100 °C

2: 90 percent / potassium hydroxide / ethanol / 4 h / Heating

With potassium hydroxide; copper(l) iodide; potassium carbonate; In ethanol; N,N-dimethyl-formamide;
DOI:10.1021/jm00119a014