methyl 3-(1,4'-bipiperidin-1'-ylmethyl)-6-(4-methyl-1-piperazinyl)-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylate

Base Information

Chemical Name:methyl 3-(1,4'-bipiperidin-1'-ylmethyl)-6-(4-methyl-1-piperazinyl)-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylate
CAS No.:1336966-92-7
Molecular Formula:C₃₄H₄₂F₃N₅O₂
Molecular Weight:609.735
Hs Code.:

Synonyms:methyl 3-(1,4'-bipiperidin-1'-ylmethyl)-6-(4-methyl-1-piperazinyl)-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylate

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Chemical Property of methyl 3-(1,4'-bipiperidin-1'-ylmethyl)-6-(4-methyl-1-piperazinyl)-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylate

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Technology Process of methyl 3-(1,4'-bipiperidin-1'-ylmethyl)-6-(4-methyl-1-piperazinyl)-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylate

There total 6 articles about methyl 3-(1,4'-bipiperidin-1'-ylmethyl)-6-(4-methyl-1-piperazinyl)-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylate 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: 86.0%

: 109-01-3
1-methyl-piperazine

: 1336903-80-0
methyl 3-(1,4'-bipiperidin-1'-ylmethyl)-6-bromo-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylate

: 1336966-92-7
methyl 3-(1,4'-bipiperidin-1'-ylmethyl)-6-(4-methyl-1-piperazinyl)-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylate

Guidance literature:: tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; In 1,4-dioxane; at 80 ℃; for 18h; Inert atmosphere;

Reference yield:

: 1533-03-5
3-(trifluoromethyl)propiophenone

: 1336966-92-7
methyl 3-(1,4'-bipiperidin-1'-ylmethyl)-6-(4-methyl-1-piperazinyl)-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylate

Guidance literature:: Multi-step reaction with 5 steps

1.1: potassium hydroxide / ethanol; water / 1 h / Reflux

1.2: pH 3

2.1: oxalyl dichloride / N,N-dimethyl-formamide / dichloromethane / 1 h / 0 °C

2.2: 0 - 20 °C

3.1: dibenzoyl peroxide; N-Bromosuccinimide / tetrachloromethane / 100 °C / Reflux

4.1: acetonitrile

5.1: 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾ / 1,4-dioxane / 18 h / 80 °C / Inert atmosphere

With N-Bromosuccinimide; oxalyl dichloride; potassium hydroxide; dibenzoyl peroxide; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; N,N-dimethyl-formamide; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; In 1,4-dioxane; tetrachloromethane; ethanol; dichloromethane; water; acetonitrile;

Reference yield:

: 87-48-9
5-Bromo-1H-indole-2,3-dione

: 1336966-92-7
methyl 3-(1,4'-bipiperidin-1'-ylmethyl)-6-(4-methyl-1-piperazinyl)-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylate

Guidance literature:: Multi-step reaction with 5 steps

1.1: potassium hydroxide / ethanol; water / 2.08 h / 100 °C

1.2: Cooling with ice

1.3: pH 1

2.1: oxalyl dichloride / N,N-dimethyl-formamide / dichloromethane / 1 h / 0 °C

2.2: 0 - 20 °C

3.1: dibenzoyl peroxide; N-Bromosuccinimide / tetrachloromethane / 100 °C / Reflux

4.1: acetonitrile

5.1: 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾ / 1,4-dioxane / 18 h / 80 °C / Inert atmosphere

With N-Bromosuccinimide; oxalyl dichloride; potassium hydroxide; dibenzoyl peroxide; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; N,N-dimethyl-formamide; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; In 1,4-dioxane; tetrachloromethane; ethanol; dichloromethane; water; acetonitrile;