N-methyl-2-(10-methylphenazin-5(10H)-yl)aniline

Base Information

Chemical Name:N-methyl-2-(10-methylphenazin-5(10H)-yl)aniline
CAS No.:1429049-15-9
Molecular Formula:C₂₀H₁₉N₃
Molecular Weight:301.391
Hs Code.:

Synonyms:N-methyl-2-(10-methylphenazin-5(10H)-yl)aniline

Suppliers and Price of N-methyl-2-(10-methylphenazin-5(10H)-yl)aniline

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 N-methyl-2-(10-methylphenazin-5(10H)-yl)aniline

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of N-methyl-2-(10-methylphenazin-5(10H)-yl)aniline

There total 15 articles about N-methyl-2-(10-methylphenazin-5(10H)-yl)aniline 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: 98.0%

: 1429049-10-4
N¹-(2-aminophenyl)-N²-(2-fluorophenyl)-N¹,N²-dimethylbenzene-1,2-diamine

: 1429049-15-9
N-methyl-2-(10-methylphenazin-5(10H)-yl)aniline

Guidance literature:: With lithium diisopropyl amide; In tetrahydrofuran; at 66 ℃; Inert atmosphere;
DOI:10.1021/jo302795w

Reference yield: 92.0%

: 1207629-92-2
N₁-(2-aminophenyl)-N₂-(2-chlorophenyl)-N₁,N₂-dimethylbenzene-1,2-diamine

: 1429049-15-9
N-methyl-2-(10-methylphenazin-5(10H)-yl)aniline

Guidance literature:: With lithium diisopropyl amide; In tetrahydrofuran; at 66 ℃; for 1h; Inert atmosphere;
DOI:10.1021/jo302795w

Reference yield:

: 88-74-4
2-nitro-aniline

: 1429049-15-9
N-methyl-2-(10-methylphenazin-5(10H)-yl)aniline

Guidance literature:: Multi-step reaction with 7 steps

1.1: bis(dibenzylideneacetone)-palladium⁽⁰⁾; caesium carbonate; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl / toluene / 24 h / 120 °C / Inert atmosphere; Sealed tube

2.1: potassium hydroxide / acetone / 1 h / Inert atmosphere; Reflux

3.1: copper(l) chloride; potassium borohydride / methanol / 2 h / 20 °C / Inert atmosphere

4.1: bis(dibenzylideneacetone)-palladium⁽⁰⁾; caesium carbonate; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl / toluene / 24 h / 130 °C / Inert atmosphere; Sealed tube

5.1: potassium hydride / N,N-dimethyl-formamide / 0.17 h / 20 °C / Inert atmosphere

5.2: 2 h / 80 °C / Inert atmosphere

6.1: copper(l) chloride; potassium borohydride / methanol / 2 h / 20 °C / Inert atmosphere

7.1: lithium diisopropyl amide / tetrahydrofuran / 66 °C / Inert atmosphere

With potassium borohydride; potassium hydride; caesium carbonate; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; copper(l) chloride; potassium hydroxide; bis(dibenzylideneacetone)-palladium⁽⁰⁾; lithium diisopropyl amide; In tetrahydrofuran; methanol; N,N-dimethyl-formamide; acetone; toluene; 1.1: |Buchwald-Hartwig Coupling / 4.1: |Buchwald-Hartwig Coupling;
DOI:10.1021/jo302795w