N-[6-(2-dimethylaminoethyl)-11-methyl-6H-indolo[2,3-b]quinol-9-yl]-N-(2-dimethylaminoethyl)-p-toluenesulfonamide

Base Information

Chemical Name:N-[6-(2-dimethylaminoethyl)-11-methyl-6H-indolo[2,3-b]quinol-9-yl]-N-(2-dimethylaminoethyl)-p-toluenesulfonamide
CAS No.:1402935-97-0
Molecular Formula:C₃₁H₃₇N₅O₂S
Molecular Weight:543.733
Hs Code.:

Synonyms:N-[6-(2-dimethylaminoethyl)-11-methyl-6H-indolo[2,3-b]quinol-9-yl]-N-(2-dimethylaminoethyl)-p-toluenesulfonamide

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Chemical Property of N-[6-(2-dimethylaminoethyl)-11-methyl-6H-indolo[2,3-b]quinol-9-yl]-N-(2-dimethylaminoethyl)-p-toluenesulfonamide

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Technology Process of N-[6-(2-dimethylaminoethyl)-11-methyl-6H-indolo[2,3-b]quinol-9-yl]-N-(2-dimethylaminoethyl)-p-toluenesulfonamide

There total 4 articles about N-[6-(2-dimethylaminoethyl)-11-methyl-6H-indolo[2,3-b]quinol-9-yl]-N-(2-dimethylaminoethyl)-p-toluenesulfonamide 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: 52.0%

: 1402935-95-8
N-[6-(2-dimethylaminoethyl)-11-methyl-6H-indolo[2,3-b]quinol-9-yl]-p-toluenesulfonamide

: 4584-46-7
(2-chloroethyl)dimethylamine hydrochloride

: 1402935-97-0
N-[6-(2-dimethylaminoethyl)-11-methyl-6H-indolo[2,3-b]quinol-9-yl]-N-(2-dimethylaminoethyl)-p-toluenesulfonamide

Guidance literature:: With tetrabutylammomium bromide; potassium carbonate; In N,N-dimethyl-formamide; at 50 ℃; for 16h;
DOI:10.1016/j.bmcl.2012.08.032

Reference yield:

: 11-methyl-9-nitro-6H-indolo[2,3-b]quinoline

: 1402935-97-0
N-[6-(2-dimethylaminoethyl)-11-methyl-6H-indolo[2,3-b]quinol-9-yl]-N-(2-dimethylaminoethyl)-p-toluenesulfonamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: tetrabutylammomium bromide; sodium hydroxide / water; toluene / 5 h / Reflux

2.1: tin(ll) chloride; hydrogenchloride / water; ethanol / 1 h / Reflux

2.2: 0.5 h / 20 °C

3.1: pyridine / 3 h / 20 °C

3.2: 0.5 h / 20 °C

4.1: tetrabutylammomium bromide; potassium carbonate / N,N-dimethyl-formamide / 16 h / 50 °C

With pyridine; hydrogenchloride; tetrabutylammomium bromide; potassium carbonate; tin(ll) chloride; sodium hydroxide; In ethanol; water; N,N-dimethyl-formamide; toluene;
DOI:10.1016/j.bmcl.2012.08.032

Reference yield:

: 1402935-89-0
6-(2-dimethylaminoethyl)-11-methyl-6H-indolo[2,3-b]quinolin-9-yl-amine

: 1402935-97-0
N-[6-(2-dimethylaminoethyl)-11-methyl-6H-indolo[2,3-b]quinol-9-yl]-N-(2-dimethylaminoethyl)-p-toluenesulfonamide

Guidance literature:: Multi-step reaction with 2 steps

1.1: pyridine / 3 h / 20 °C

1.2: 0.5 h / 20 °C

2.1: tetrabutylammomium bromide; potassium carbonate / N,N-dimethyl-formamide / 16 h / 50 °C

With pyridine; tetrabutylammomium bromide; potassium carbonate; In N,N-dimethyl-formamide;
DOI:10.1016/j.bmcl.2012.08.032