N-(2-acetyl-4-(pyrrolidin-1-yl)phenyl)-3-(ethylamino)benzamide

Base Information

• Chemical Name: N-(2-acetyl-4-(pyrrolidin-1-yl)phenyl)-3-(ethylamino)benzamide
• CAS No.: 1421447-00-8
• Molecular Formula: C₂₁H₂₅N₃O₂
• Molecular Weight: 351.448
• Mol file: 1421447-00-8.mol

Synonyms:N-(2-acetyl-4-(pyrrolidin-1-yl)phenyl)-3-(ethylamino)benzamide

Chemical Property of N-(2-acetyl-4-(pyrrolidin-1-yl)phenyl)-3-(ethylamino)benzamide

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of N-(2-acetyl-4-(pyrrolidin-1-yl)phenyl)-3-(ethylamino)benzamide

There total 4 articles about N-(2-acetyl-4-(pyrrolidin-1-yl)phenyl)-3-(ethylamino)benzamide 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: 30.7%

N-(2-acetyl-4-(pyrrolidin-1-yl)phenyl)-3-aminobenzamide (1421446-98-1) + ethyl iodide (75-03-6) → N-(2-acetyl-4-(pyrrolidin-1-yl)phenyl)-3-(ethylamino)benzamide (1421447-00-8)

Guidance literature:

With potassium carbonate; In N,N-dimethyl-formamide; for 6h; Reflux;

DOI:10.1016/j.bmcl.2012.11.105

Reference yield:

(2'-amino-5'-pyrrolidinyl)acetophenone (56915-84-5) → N-(2-acetyl-4-(pyrrolidin-1-yl)phenyl)-3-(ethylamino)benzamide (1421447-00-8)

Guidance literature:

Multi-step reaction with 3 steps

1: triethylamine / tetrahydrofuran / 2 h / 25 - 30 °C

2: hydrogen; palladium 10% on activated carbon / dichloromethane / 6 h / 20 °C

3: potassium carbonate / N,N-dimethyl-formamide / 6 h / Reflux

With palladium 10% on activated carbon; hydrogen; potassium carbonate; triethylamine; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide;

DOI:10.1016/j.bmcl.2012.11.105

Reference yield:

m-nitrobenzoic acid chloride (121-90-4) → N-(2-acetyl-4-(pyrrolidin-1-yl)phenyl)-3-(ethylamino)benzamide (1421447-00-8)

Guidance literature:

Multi-step reaction with 3 steps

1: triethylamine / tetrahydrofuran / 2 h / 25 - 30 °C

2: hydrogen; palladium 10% on activated carbon / dichloromethane / 6 h / 20 °C

3: potassium carbonate / N,N-dimethyl-formamide / 6 h / Reflux

With palladium 10% on activated carbon; hydrogen; potassium carbonate; triethylamine; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide;

DOI:10.1016/j.bmcl.2012.11.105

upstream raw materials:

N-(2-acetyl-4-(pyrrolidin-1-yl)phenyl)-3-aminobenzamide

ethyl iodide

(2'-amino-5'-pyrrolidinyl)acetophenone

m-nitrobenzoic acid chloride

Downstream raw materials:

C₂₁H₂₃N₃O