1-((1-(3-chlorophenyl)-3-(trifluoromethyl)-1H-pyrazol-5-yl)methyl)-3-(6-(methylsulfonylmethyl)pyridin-3-yl)urea

Base Information

• Chemical Name: 1-((1-(3-chlorophenyl)-3-(trifluoromethyl)-1H-pyrazol-5-yl)methyl)-3-(6-(methylsulfonylmethyl)pyridin-3-yl)urea
• CAS No.: 1419605-07-4
• Molecular Formula: C₁₉H₁₇ClF₃N₅O₃S
• Molecular Weight: 487.89
• Mol file: 1419605-07-4.mol

Synonyms:1-((1-(3-chlorophenyl)-3-(trifluoromethyl)-1H-pyrazol-5-yl)methyl)-3-(6-(methylsulfonylmethyl)pyridin-3-yl)urea

Chemical Property of 1-((1-(3-chlorophenyl)-3-(trifluoromethyl)-1H-pyrazol-5-yl)methyl)-3-(6-(methylsulfonylmethyl)pyridin-3-yl)urea

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 1-((1-(3-chlorophenyl)-3-(trifluoromethyl)-1H-pyrazol-5-yl)methyl)-3-(6-(methylsulfonylmethyl)pyridin-3-yl)urea

There total 15 articles about 1-((1-(3-chlorophenyl)-3-(trifluoromethyl)-1H-pyrazol-5-yl)methyl)-3-(6-(methylsulfonylmethyl)pyridin-3-yl)urea 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: 40.0%

(1-(3-chlorophenyl)-3-(trifluoromethyl)-1H-pyrazol-5-yl)methanamine monohydrochloride (1419602-48-4) + phenyl 6-(methylsulfonylmethyl)pyridin-3-ylcarbamate (1419605-05-2) → 1-((1-(3-chlorophenyl)-3-(trifluoromethyl)-1H-pyrazol-5-yl)methyl)-3-(6-(methylsulfonylmethyl)pyridin-3-yl)urea (1419605-07-4)

Guidance literature:

With triethylamine; In dichloromethane; at 23 ℃; for 16h;

Reference yield:

(5-bromopyridin-2-yl)methanol (88139-91-7) → 1-((1-(3-chlorophenyl)-3-(trifluoromethyl)-1H-pyrazol-5-yl)methyl)-3-(6-(methylsulfonylmethyl)pyridin-3-yl)urea (1419605-07-4)

Guidance literature:

Multi-step reaction with 6 steps

1: N-Bromosuccinimide; triphenylphosphine / dichloromethane / 1 h / 0 - 23 °C

2: isopropyl alcohol / 4 h / 70 °C

3: tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; caesium carbonate / toluene / 5 h / Inert atmosphere; Reflux

4: hydrogenchloride; water / methanol / 0.5 h / 23 °C

5: pyridine / acetone / 1 h / 0 - 23 °C

6: triethylamine / dichloromethane / 16 h / 23 °C

With pyridine; hydrogenchloride; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; N-Bromosuccinimide; water; caesium carbonate; triethylamine; triphenylphosphine; In methanol; dichloromethane; isopropyl alcohol; acetone; toluene;

Reference yield:

5-bromo-2-(bromomethyl)pyridine (145218-19-5) → 1-((1-(3-chlorophenyl)-3-(trifluoromethyl)-1H-pyrazol-5-yl)methyl)-3-(6-(methylsulfonylmethyl)pyridin-3-yl)urea (1419605-07-4)

Guidance literature:

Multi-step reaction with 5 steps

1: isopropyl alcohol / 4 h / 70 °C

2: tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; caesium carbonate / toluene / 5 h / Inert atmosphere; Reflux

3: hydrogenchloride; water / methanol / 0.5 h / 23 °C

4: pyridine / acetone / 1 h / 0 - 23 °C

5: triethylamine / dichloromethane / 16 h / 23 °C

With pyridine; hydrogenchloride; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; water; caesium carbonate; triethylamine; In methanol; dichloromethane; isopropyl alcohol; acetone; toluene;

upstream raw materials:

(5-bromopyridin-2-yl)methanol

(1-(3-chlorophenyl)-3-(trifluoromethyl)-1H-pyrazol-5-yl)methanamine monohydrochloride

phenyl 6-(methylsulfonylmethyl)pyridin-3-ylcarbamate

2-Cyano-5-bromopyridine