N-(1-(4-(2-cyanopropan-2-yl)phenyl)-3-methyl-2-oxo-2,3-dihydro-1H-imidazo[4,5-c]quinolin-8-yl)acetamide

Base Information

• Chemical Name: N-(1-(4-(2-cyanopropan-2-yl)phenyl)-3-methyl-2-oxo-2,3-dihydro-1H-imidazo[4,5-c]quinolin-8-yl)acetamide
• CAS No.: 1610680-67-5
• Molecular Formula: C₂₃H₂₁N₅O₂
• Molecular Weight: 399.452
• Mol file: 1610680-67-5.mol

Synonyms:

Chemical Property of N-(1-(4-(2-cyanopropan-2-yl)phenyl)-3-methyl-2-oxo-2,3-dihydro-1H-imidazo[4,5-c]quinolin-8-yl)acetamide

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of N-(1-(4-(2-cyanopropan-2-yl)phenyl)-3-methyl-2-oxo-2,3-dihydro-1H-imidazo[4,5-c]quinolin-8-yl)acetamide

There total 10 articles about N-(1-(4-(2-cyanopropan-2-yl)phenyl)-3-methyl-2-oxo-2,3-dihydro-1H-imidazo[4,5-c]quinolin-8-yl)acetamide 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: 8.0%

2-(4-(8-amino-3-methyl-2-oxo-2,3-dihydro-1H-imidazo[4,5-c]quinolin-1-yl)phenyl)-2-methylpropanenitrile (1610680-66-4) + acetyl chloride (75-36-5) → N-(1-(4-(2-cyanopropan-2-yl)phenyl)-3-methyl-2-oxo-2,3-dihydro-1H-imidazo[4,5-c]quinolin-8-yl)acetamide (1610680-67-5)

Guidance literature:

With potassium carbonate; In dichloromethane; at 20 ℃; for 24h;

DOI:10.1021/jm500361r

Reference yield:

6-iodo-3-nitroquinolin-4-ol (1203578-70-4,1345447-23-5) → N-(1-(4-(2-cyanopropan-2-yl)phenyl)-3-methyl-2-oxo-2,3-dihydro-1H-imidazo[4,5-c]quinolin-8-yl)acetamide (1610680-67-5)

Guidance literature:

Multi-step reaction with 7 steps

1: trichlorophosphate / 2 h / 20 - 120 °C

2: acetic acid / 3 h / 20 °C / Inert atmosphere

3: iron; ammonium chloride / ethanol; water / 2 h / Reflux; Heating

4: triethylamine / dichloromethane / 2 h / 0 - 20 °C

5: sodium hydroxide; tetrabutylammomium bromide / dichloromethane / 24 h / 20 °C / Sealed tube

6: copper(II) oxide; ammonia; potassium phosphate; tetrabutylammomium bromide / water / 3 h / 20 - 110 °C / Sealed tube

7: potassium carbonate / dichloromethane / 24 h / 20 °C

With potassium phosphate; tetrabutylammomium bromide; ammonia; iron; potassium carbonate; ammonium chloride; acetic acid; triethylamine; copper(II) oxide; sodium hydroxide; trichlorophosphate; In ethanol; dichloromethane; water;

DOI:10.1021/jm500361r

Reference yield:

5-iodo-2-((2-nitrovinyl)amino)benzoic acid (1345447-21-3) → N-(1-(4-(2-cyanopropan-2-yl)phenyl)-3-methyl-2-oxo-2,3-dihydro-1H-imidazo[4,5-c]quinolin-8-yl)acetamide (1610680-67-5)

Guidance literature:

Multi-step reaction with 8 steps

1: potassium acetate; acetic anhydride / 1.5 h / 120 °C

2: trichlorophosphate / 2 h / 20 - 120 °C

3: acetic acid / 3 h / 20 °C / Inert atmosphere

4: iron; ammonium chloride / ethanol; water / 2 h / Reflux; Heating

5: triethylamine / dichloromethane / 2 h / 0 - 20 °C

6: sodium hydroxide; tetrabutylammomium bromide / dichloromethane / 24 h / 20 °C / Sealed tube

7: copper(II) oxide; ammonia; potassium phosphate; tetrabutylammomium bromide / water / 3 h / 20 - 110 °C / Sealed tube

8: potassium carbonate / dichloromethane / 24 h / 20 °C

With potassium phosphate; tetrabutylammomium bromide; ammonia; potassium acetate; acetic anhydride; iron; potassium carbonate; ammonium chloride; acetic acid; triethylamine; copper(II) oxide; sodium hydroxide; trichlorophosphate; In ethanol; dichloromethane; water;

DOI:10.1021/jm500361r

upstream raw materials:

2-(4-(8-amino-3-methyl-2-oxo-2,3-dihydro-1H-imidazo[4,5-c]quinolin-1-yl)phenyl)-2-methylpropanenitrile

acetyl chloride

6-iodo-3-nitroquinolin-4-ol

5-iodo-2-((2-nitrovinyl)amino)benzoic acid