N-(tert-butoxycarbonyl)-N'-(3,4-dichlorophenyl)-N''-(1-isopropyl-4-oxo-4,5-dihydro-1H-imidazol-2-yl)guanidine

Base Information

Chemical Name:N-(tert-butoxycarbonyl)-N'-(3,4-dichlorophenyl)-N''-(1-isopropyl-4-oxo-4,5-dihydro-1H-imidazol-2-yl)guanidine
CAS No.:1310682-48-4
Molecular Formula:C₁₈H₂₃Cl₂N₅O₃
Molecular Weight:428.318
Hs Code.:

Synonyms:N-(tert-butoxycarbonyl)-N'-(3,4-dichlorophenyl)-N''-(1-isopropyl-4-oxo-4,5-dihydro-1H-imidazol-2-yl)guanidine

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Chemical Property of N-(tert-butoxycarbonyl)-N'-(3,4-dichlorophenyl)-N''-(1-isopropyl-4-oxo-4,5-dihydro-1H-imidazol-2-yl)guanidine

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Technology Process of N-(tert-butoxycarbonyl)-N'-(3,4-dichlorophenyl)-N''-(1-isopropyl-4-oxo-4,5-dihydro-1H-imidazol-2-yl)guanidine

There total 6 articles about N-(tert-butoxycarbonyl)-N'-(3,4-dichlorophenyl)-N''-(1-isopropyl-4-oxo-4,5-dihydro-1H-imidazol-2-yl)guanidine 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: 50.0%

: 24424-99-5
di-tert-butyl dicarbonate

: 1310682-45-1
N-(3,4-dichlorophenyl)-N'-(1-isopropyl-4-oxo-4,5-dihydro-1H-imidazol-2-yl)guanidine

: 1310682-48-4
N-(tert-butoxycarbonyl)-N'-(3,4-dichlorophenyl)-N''-(1-isopropyl-4-oxo-4,5-dihydro-1H-imidazol-2-yl)guanidine

Guidance literature:: With dmap; triethylamine; In N,N-dimethyl-formamide; at 25 ℃; for 12h; Inert atmosphere;
DOI:10.1021/jm200111g

Reference yield: 50.0%

: 1310682-48-4
N-(t-butoxycarbonyl)-N'-(3,4-dichlorophenyl)-N''-(1-isopropyl-4-oxo-4,5-dihydro-1H-imidazol-2-yl)guanidine

Guidance literature:

Reference yield:

: 3183-21-9
2-(2-propylamino)acetic acid

: 1310682-48-4
N-(tert-butoxycarbonyl)-N'-(3,4-dichlorophenyl)-N''-(1-isopropyl-4-oxo-4,5-dihydro-1H-imidazol-2-yl)guanidine

Guidance literature:: Multi-step reaction with 5 steps

1: 140 °C / Inert atmosphere

2: N,N-dimethyl-formamide / Inert atmosphere

3: water / Alkaline conditions; Cooling with ice; Inert atmosphere

4: ethanol / Inert atmosphere; Heating

5: dmap; triethylamine / N,N-dimethyl-formamide / 12 h / 25 °C / Inert atmosphere

With dmap; triethylamine; In ethanol; water; N,N-dimethyl-formamide;
DOI:10.1021/jm200111g