2-((2-((3-(aminomethyl)phenyl)amino)-5-chloropyrimidin-4-yl)amino)-N-methylbenzamide

Base Information

Chemical Name:2-((2-((3-(aminomethyl)phenyl)amino)-5-chloropyrimidin-4-yl)amino)-N-methylbenzamide
CAS No.:1346447-89-9
Molecular Formula:C₁₉H₁₉ClN₆O
Molecular Weight:382.852
Hs Code.:

Synonyms:2-((2-((3-(aminomethyl)phenyl)amino)-5-chloropyrimidin-4-yl)amino)-N-methylbenzamide

Suppliers and Price of 2-((2-((3-(aminomethyl)phenyl)amino)-5-chloropyrimidin-4-yl)amino)-N-methylbenzamide

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of 2-((2-((3-(aminomethyl)phenyl)amino)-5-chloropyrimidin-4-yl)amino)-N-methylbenzamide

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 2-((2-((3-(aminomethyl)phenyl)amino)-5-chloropyrimidin-4-yl)amino)-N-methylbenzamide

There total 7 articles about 2-((2-((3-(aminomethyl)phenyl)amino)-5-chloropyrimidin-4-yl)amino)-N-methylbenzamide 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: 63.0%

: 1346447-88-8
tert-butyl 3-((5-chloro-4-((2-(methylcarbamoyl)phenyl)amino)pyrimidin-2-yl)amino)benzylcarbamate

: 1346447-89-9
2-((2-((3-(aminomethyl)phenyl)amino)-5-chloropyrimidin-4-yl)amino)-N-methylbenzamide

Guidance literature:: With trifluoroacetic acid; at 20 ℃; for 2h;

Reference yield:

: 7409-18-9
3-nitrobenzylamine

: 1346447-89-9
2-((2-((3-(aminomethyl)phenyl)amino)-5-chloropyrimidin-4-yl)amino)-N-methylbenzamide

Guidance literature:: Multi-step reaction with 4 steps

1: sodium hydroxide / water; tetrahydrofuran / 1 h / 0 - 20 °C

2: hydrogen / palladium 10% on activated carbon / ethanol / 0.5 h / 20 °C

3: potassium carbonate / tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; XPhos / iso-butanol / 6 h / 80 °C

4: trifluoroacetic acid / 2 h / 20 °C

With hydrogen; potassium carbonate; trifluoroacetic acid; sodium hydroxide; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; palladium 10% on activated carbon; XPhos; In tetrahydrofuran; ethanol; water; iso-butanol;

Reference yield:

: 118-48-9
isatoic anhydride

: 1346447-89-9
2-((2-((3-(aminomethyl)phenyl)amino)-5-chloropyrimidin-4-yl)amino)-N-methylbenzamide

Guidance literature:: Multi-step reaction with 4 steps

1: 1,4-dioxane / 0.33 h

2: potassium carbonate / N,N-dimethyl-formamide / 1 h / 80 °C

3: potassium carbonate / tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; XPhos / iso-butanol / 6 h / 80 °C

4: trifluoroacetic acid / 2 h / 20 °C

With potassium carbonate; trifluoroacetic acid; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; XPhos; In 1,4-dioxane; N,N-dimethyl-formamide; iso-butanol;