methyl 1,5-diphenyl-4,5-dihydro-1H-imidazol-2-ylcarbamate

Base Information

Chemical Name:methyl 1,5-diphenyl-4,5-dihydro-1H-imidazol-2-ylcarbamate
CAS No.:143538-94-7
Molecular Formula:C17H17N3O2
Molecular Weight:295.341
Hs Code.:
DSSTox Substance ID:DTXSID801147879
Nikkaji Number:J478.602E
Mol file:143538-94-7.mol

Synonyms:DTXSID801147879;methyl 1,5-diphenyl-4,5-dihydro-1H-imidazol-2-ylcarbamate;143538-94-7;N-(1,5-diphenyl-4,5-dihydro-1H-imidazol-2-yl)-carbamic acid methyl ester;Carbamic acid, (4,5-dihydro-1,5-diphenyl-1H-imidazol-2-yl)-, methyl ester

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

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Chemical Property of methyl 1,5-diphenyl-4,5-dihydro-1H-imidazol-2-ylcarbamate

Chemical Property:

XLogP3:2.5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:4
Exact Mass:295.132076794
Heavy Atom Count:22
Complexity:412

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:COC(=O)NC1=NCC(N1C2=CC=CC=C2)C3=CC=CC=C3

Technology Process of methyl 1,5-diphenyl-4,5-dihydro-1H-imidazol-2-ylcarbamate

There total 4 articles about methyl 1,5-diphenyl-4,5-dihydro-1H-imidazol-2-ylcarbamate 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: 75.0%

: 143538-88-9
C₁₉H₂₂N₄O₄

: 143538-94-7
(1,5-Diphenyl-4,5-dihydro-1H-imidazol-2-yl)-carbamic acid methyl ester

Guidance literature:: With toluene-4-sulfonic acid; In ethanol; Heating;
DOI:10.1055/s-1992-26194

Reference yield:

: 4553-59-7
2-anilino-2-phenylacetonitrile

: 143538-94-7
(1,5-Diphenyl-4,5-dihydro-1H-imidazol-2-yl)-carbamic acid methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: H₂, methanolic NH₃ / Raney nickel / 1875.1 Torr / Ambient temperature

2: 76 percent / ethanol / 0.25 h / Heating

3: 75 percent / p-toluenesulfonic acid (p-TsOH) / ethanol / Heating

With ammonia; hydrogen; toluene-4-sulfonic acid; nickel; In ethanol;
DOI:10.1055/s-1992-26194

Reference yield:

: 538-51-2
benzylidene phenylamine

: 143538-94-7
(1,5-Diphenyl-4,5-dihydro-1H-imidazol-2-yl)-carbamic acid methyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 95 percent / glacial acetic acid / H₂O / 0.5 h / 0 °C

2: H₂, methanolic NH₃ / Raney nickel / 1875.1 Torr / Ambient temperature

3: 76 percent / ethanol / 0.25 h / Heating

4: 75 percent / p-toluenesulfonic acid (p-TsOH) / ethanol / Heating

With ammonia; hydrogen; toluene-4-sulfonic acid; acetic acid; nickel; In ethanol; water;
DOI:10.1055/s-1992-26194