4-chloro-6-((3-chloro-4-isopropoxyphenyl)amino)-1-(4-chlorobenzyl)-1,3,5-triazin-2(1H)-one

Base Information

• Chemical Name: 4-chloro-6-((3-chloro-4-isopropoxyphenyl)amino)-1-(4-chlorobenzyl)-1,3,5-triazin-2(1H)-one
• CAS No.: 1373947-37-5
• Molecular Formula: C₁₉H₁₇Cl₃N₄O₂
• Molecular Weight: 439.729
• Mol file: 1373947-37-5.mol

Synonyms:4-chloro-6-((3-chloro-4-isopropoxyphenyl)amino)-1-(4-chlorobenzyl)-1,3,5-triazin-2(1H)-one

Chemical Property of 4-chloro-6-((3-chloro-4-isopropoxyphenyl)amino)-1-(4-chlorobenzyl)-1,3,5-triazin-2(1H)-one

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 4-chloro-6-((3-chloro-4-isopropoxyphenyl)amino)-1-(4-chlorobenzyl)-1,3,5-triazin-2(1H)-one

There total 1 articles about 4-chloro-6-((3-chloro-4-isopropoxyphenyl)amino)-1-(4-chlorobenzyl)-1,3,5-triazin-2(1H)-one 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:

3-Chloro-4-isopropoxy-phenylamine (5211-04-1) → 4-chloro-6-((3-chloro-4-isopropoxyphenyl)amino)-1-(4-chlorobenzyl)-1,3,5-triazin-2(1H)-one (1373947-37-5)

Guidance literature:

Multi-step reaction with 2 steps

1: acetic acid / tert-butyl alcohol / 11 h / 115 °C

2: trichlorophosphate / 2 h / 50 °C

With acetic acid; trichlorophosphate; In tert-butyl alcohol;

DOI:10.1016/j.bmcl.2021.127833

Reference yield: 30.0%

ethyl (2E)-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)acrylate (1009307-13-4) + 4-chloro-6-((3-chloro-4-isopropoxyphenyl)amino)-1-(4-chlorobenzyl)-1,3,5-triazin-2(1H)-one (1373947-37-5) → ethyl (E)-3-(6-((3-chloro-4-isopropoxyphenyl)amino)-5-(4-chlorobenzyl)-4-oxo-4,5-dihydro-1,3,5-triazin-2-yl)acrylate (1360105-43-6)

Guidance literature:

With potassium carbonate; dichloro[1,1'-bis(di-t-butylphosphino)ferrocene]palladium(II); In tetrahydrofuran; water; for 7h; Reflux; Inert atmosphere;

Reference yield:

4-chloro-6-((3-chloro-4-isopropoxyphenyl)amino)-1-(4-chlorobenzyl)-1,3,5-triazin-2(1H)-one (1373947-37-5) → 3-(6-((3-chloro-4-isopropoxyphenyl)amino)-5-(4-chlorobenzyl)-4-oxo-4,5-dihydro-1,3,5-triazin-2-yl)propanoic acid (1239685-54-1)

Guidance literature:

Multi-step reaction with 3 steps

1: potassium carbonate / dichloro[1,1'-bis(di-t-butylphosphino)ferrocene]palladium(II) / tetrahydrofuran; water / 7 h / Reflux; Inert atmosphere

2: lithium hydroxide monohydrate; water / tetrahydrofuran; ethanol / 72 h / 20 °C

3: hydrogen / 10% Pt/activated carbon / methanol / 760.05 Torr

With lithium hydroxide monohydrate; water; hydrogen; potassium carbonate; dichloro[1,1'-bis(di-t-butylphosphino)ferrocene]palladium(II); 10% Pt/activated carbon; In tetrahydrofuran; methanol; ethanol; water;

upstream raw materials:

3-Chloro-4-isopropoxy-phenylamine

Downstream raw materials:

ethyl (E)-3-(6-((3-chloro-4-isopropoxyphenyl)amino)-5-(4-chlorobenzyl)-4-oxo-4,5-dihydro-1,3,5-triazin-2-yl)acrylate

3-(6-((3-chloro-4-isopropoxyphenyl)amino)-5-(4-chlorobenzyl)-4-oxo-4,5-dihydro-1,3,5-triazin-2-yl)propanoic acid

(E)-1-(4-chlorobenzyl)-6-(3-chloro-4-isopropoxyphenylamino)-4-hydroxycarbonylethenyl-1,3,5-triazine-2(1H)-one