1,1-dimethylethyl [4-(4-{[1-methyl-3-({[(1-methylethyl)oxy]carbonyl}amino)-3-oxopropyl]amino}phenyl)-1H-imidazol-1-yl]acetate

Base Information

Chemical Name:1,1-dimethylethyl [4-(4-{[1-methyl-3-({[(1-methylethyl)oxy]carbonyl}amino)-3-oxopropyl]amino}phenyl)-1H-imidazol-1-yl]acetate
CAS No.:1301198-61-7
Molecular Formula:C₂₃H₃₂N₄O₅
Molecular Weight:444.531
Hs Code.:

Synonyms:1,1-dimethylethyl [4-(4-{[1-methyl-3-({[(1-methylethyl)oxy]carbonyl}amino)-3-oxopropyl]amino}phenyl)-1H-imidazol-1-yl]acetate

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Chemical Property of 1,1-dimethylethyl [4-(4-{[1-methyl-3-({[(1-methylethyl)oxy]carbonyl}amino)-3-oxopropyl]amino}phenyl)-1H-imidazol-1-yl]acetate

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Technology Process of 1,1-dimethylethyl [4-(4-{[1-methyl-3-({[(1-methylethyl)oxy]carbonyl}amino)-3-oxopropyl]amino}phenyl)-1H-imidazol-1-yl]acetate

There total 5 articles about 1,1-dimethylethyl [4-(4-{[1-methyl-3-({[(1-methylethyl)oxy]carbonyl}amino)-3-oxopropyl]amino}phenyl)-1H-imidazol-1-yl]acetate 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%

: 1300031-97-3
1-methylethyl (2E)-2-butenoylcarbamate

: 1301198-62-8
1,1-dimethylethyl [4-(4-aminophenyl)-1H-imidazol-1-yl]acetate

: 1301198-61-7
1,1-dimethylethyl [4-(4-{[1-methyl-3-({[(1-methylethyl)oxy]carbonyl}amino)-3-oxopropyl]amino}phenyl)-1H-imidazol-1-yl]acetate

Guidance literature:: With 1,8-diazabicyclo[5.4.0]undec-7-ene; In acetonitrile; at 50 ℃; for 48h;

Reference yield:

: 38980-93-7
4-(4-nitrophenyl)-1H-imidazole

: 1301198-61-7
1,1-dimethylethyl [4-(4-{[1-methyl-3-({[(1-methylethyl)oxy]carbonyl}amino)-3-oxopropyl]amino}phenyl)-1H-imidazol-1-yl]acetate

Guidance literature:: Multi-step reaction with 3 steps

1: potassium carbonate / N,N-dimethyl-formamide / 16 h / 50 °C

2: ammonium formate / palladium 10% on activated carbon / ethanol / 6 h / Reflux

3: 1,8-diazabicyclo[5.4.0]undec-7-ene / acetonitrile / 48 h / 50 °C

With ammonium formate; potassium carbonate; 1,8-diazabicyclo[5.4.0]undec-7-ene; palladium 10% on activated carbon; In ethanol; N,N-dimethyl-formamide; acetonitrile;

Reference yield:

: 99-81-0
4-Nitrophenacyl bromide

: 1301198-61-7
1,1-dimethylethyl [4-(4-{[1-methyl-3-({[(1-methylethyl)oxy]carbonyl}amino)-3-oxopropyl]amino}phenyl)-1H-imidazol-1-yl]acetate

Guidance literature:: Multi-step reaction with 4 steps

1: 72 h / 150 °C

2: potassium carbonate / N,N-dimethyl-formamide / 16 h / 50 °C

3: ammonium formate / palladium 10% on activated carbon / ethanol / 6 h / Reflux

4: 1,8-diazabicyclo[5.4.0]undec-7-ene / acetonitrile / 48 h / 50 °C

With ammonium formate; potassium carbonate; 1,8-diazabicyclo[5.4.0]undec-7-ene; palladium 10% on activated carbon; In ethanol; N,N-dimethyl-formamide; acetonitrile;