4-(3-(3-(4-chloro-3-(trifluoromethyl)phenyl)thioureido)phenoxy)-N-ethylpicolinamide

Base Information

• Chemical Name: 4-(3-(3-(4-chloro-3-(trifluoromethyl)phenyl)thioureido)phenoxy)-N-ethylpicolinamide
• CAS No.: 1412891-56-5
• Molecular Formula: C₂₂H₁₈ClF₃N₄O₂S
• Molecular Weight: 494.925
• Mol file: 1412891-56-5.mol

Synonyms:4-(3-(3-(4-chloro-3-(trifluoromethyl)phenyl)thioureido)phenoxy)-N-ethylpicolinamide

Chemical Property of 4-(3-(3-(4-chloro-3-(trifluoromethyl)phenyl)thioureido)phenoxy)-N-ethylpicolinamide

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 4-(3-(3-(4-chloro-3-(trifluoromethyl)phenyl)thioureido)phenoxy)-N-ethylpicolinamide

There total 7 articles about 4-(3-(3-(4-chloro-3-(trifluoromethyl)phenyl)thioureido)phenoxy)-N-ethylpicolinamide 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: 69.7%

4-(3-aminophenoxy)-N-ethylpicolinamide (1153528-71-2) + 1-chloro-4-isothiocyanato-2-(trifluoromethyl)benzene (23163-86-2) → 4-(3-(3-(4-chloro-3-(trifluoromethyl)phenyl)thioureido)phenoxy)-N-ethylpicolinamide (1412891-56-5)

Guidance literature:

In dichloromethane; at 0 - 20 ℃; for 18h;

DOI:10.1016/j.bmcl.2012.09.031

Reference yield:

m-Hydroxyaniline (591-27-5) → 4-(3-(3-(4-chloro-3-(trifluoromethyl)phenyl)thioureido)phenoxy)-N-ethylpicolinamide (1412891-56-5)

Guidance literature:

Multi-step reaction with 2 steps

1: potassium tert-butylate; potassium carbonate / N,N-dimethyl-formamide / 1 h / 20 - 90 °C / Inert atmosphere

2: dichloromethane / 18 h / 0 - 20 °C

With potassium tert-butylate; potassium carbonate; In dichloromethane; N,N-dimethyl-formamide;

DOI:10.1016/j.bmcl.2012.09.031

Reference yield:

4-chloro-N-ethyl-2-pyridinecarboxamide (604813-07-2) → 4-(3-(3-(4-chloro-3-(trifluoromethyl)phenyl)thioureido)phenoxy)-N-ethylpicolinamide (1412891-56-5)

Guidance literature:

Multi-step reaction with 2 steps

1: potassium tert-butylate; potassium carbonate / N,N-dimethyl-formamide / 1 h / 20 - 90 °C / Inert atmosphere

2: dichloromethane / 18 h / 0 - 20 °C

With potassium tert-butylate; potassium carbonate; In dichloromethane; N,N-dimethyl-formamide;

DOI:10.1016/j.bmcl.2012.09.031

upstream raw materials:

m-Hydroxyaniline

4-chloro-N-ethyl-2-pyridinecarboxamide

2-Picolinic acid

4-(3-aminophenoxy)-N-ethylpicolinamide