4-({[(±)-1-(tert-butoxycarbonyl)-5-benzyl-4-oxo-4,5-dihydro-1H-imidazol-2-yl]amino}methyl)benzoic acid

Base Information

Chemical Name:4-({[(±)-1-(tert-butoxycarbonyl)-5-benzyl-4-oxo-4,5-dihydro-1H-imidazol-2-yl]amino}methyl)benzoic acid
CAS No.:1448350-31-9
Molecular Formula:C₂₃H₂₅N₃O₅
Molecular Weight:423.469
Hs Code.:

Synonyms:4-({[(±)-1-(tert-butoxycarbonyl)-5-benzyl-4-oxo-4,5-dihydro-1H-imidazol-2-yl]amino}methyl)benzoic acid

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Chemical Property of 4-({[(±)-1-(tert-butoxycarbonyl)-5-benzyl-4-oxo-4,5-dihydro-1H-imidazol-2-yl]amino}methyl)benzoic acid

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Technology Process of 4-({[(±)-1-(tert-butoxycarbonyl)-5-benzyl-4-oxo-4,5-dihydro-1H-imidazol-2-yl]amino}methyl)benzoic acid

There total 3 articles about 4-({[(±)-1-(tert-butoxycarbonyl)-5-benzyl-4-oxo-4,5-dihydro-1H-imidazol-2-yl]amino}methyl)benzoic acid 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: 33.0%

: 10541-83-0,937737-33-2
N-methyl-p-aminobenzoic acid

: 1448350-28-4
(±)-1-(tert-butoxycarbonyl)-5-benzyl-2-(methylsulfanyl)-4,5-dihydro-1H-imidazol-4-one

: 1448350-31-9
4-({[(±)-1-(tert-butoxycarbonyl)-5-benzyl-4-oxo-4,5-dihydro-1H-imidazol-2-yl]amino}methyl)benzoic acid

Guidance literature:: In ethanol; for 18h; Inert atmosphere; Reflux;
DOI:10.1021/jm400634n

Reference yield:

: 13734-34-4
N-tert-butoxycarbonyl-L-phenylalanine

: 1448350-31-9
4-({[(±)-1-(tert-butoxycarbonyl)-5-benzyl-4-oxo-4,5-dihydro-1H-imidazol-2-yl]amino}methyl)benzoic acid

Guidance literature:: Multi-step reaction with 3 steps

1: pyridine / acetonitrile / 18 h / 20 °C

2: potassium carbonate / acetonitrile / 2.5 h / 20 °C / Inert atmosphere

3: ethanol / 18 h / Inert atmosphere; Reflux

With pyridine; potassium carbonate; In ethanol; acetonitrile;
DOI:10.1021/jm400634n

Reference yield:

: 1356003-49-0
tert-butyl (S)-5-benzyl-4-oxo-2-thioxoimidazolidine-1-carboxylate

: 1448350-31-9
4-({[(±)-1-(tert-butoxycarbonyl)-5-benzyl-4-oxo-4,5-dihydro-1H-imidazol-2-yl]amino}methyl)benzoic acid

Guidance literature:: Multi-step reaction with 2 steps

1: potassium carbonate / acetonitrile / 2.5 h / 20 °C / Inert atmosphere

2: ethanol / 18 h / Inert atmosphere; Reflux

With potassium carbonate; In ethanol; acetonitrile;
DOI:10.1021/jm400634n