2-phenyl-3-(4-(4-(trifluoromethyl)phenyl)piperidin-1-yl)quinoxaline-6-carboxylic acid

Base Information

Chemical Name:2-phenyl-3-(4-(4-(trifluoromethyl)phenyl)piperidin-1-yl)quinoxaline-6-carboxylic acid
CAS No.:1268862-36-7
Molecular Formula:C₂₇H₂₂F₃N₃O₂
Molecular Weight:477.486
Hs Code.:

Synonyms:2-phenyl-3-(4-(4-(trifluoromethyl)phenyl)piperidin-1-yl)quinoxaline-6-carboxylic acid

Suppliers and Price of 2-phenyl-3-(4-(4-(trifluoromethyl)phenyl)piperidin-1-yl)quinoxaline-6-carboxylic acid

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

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Chemical Property of 2-phenyl-3-(4-(4-(trifluoromethyl)phenyl)piperidin-1-yl)quinoxaline-6-carboxylic acid

Chemical Property:

Purity/Quality:: 98% ^*data from raw suppliers

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Technology Process of 2-phenyl-3-(4-(4-(trifluoromethyl)phenyl)piperidin-1-yl)quinoxaline-6-carboxylic acid

There total 10 articles about 2-phenyl-3-(4-(4-(trifluoromethyl)phenyl)piperidin-1-yl)quinoxaline-6-carboxylic acid 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: 51.0%

: 1268865-26-4
methyl 2-phenyl-3-(4-(4-(trifluoromethyl)phenyl)piperidin-1-yl)quinoxaline-6-carboxylate

: 1268862-36-7
2-phenyl-3-(4-(4-(trifluoromethyl)phenyl)piperidin-1-yl)quinoxaline-6-carboxylic acid

Guidance literature:: With sodium hydroxide; In methanol; at 50 ℃; for 2h;

Reference yield:

: 402-43-7
p-trifluoromethylphenyl bromide

: 1268862-36-7
2-phenyl-3-(4-(4-(trifluoromethyl)phenyl)piperidin-1-yl)quinoxaline-6-carboxylic acid

Guidance literature:: Multi-step reaction with 6 steps

1.1: sodium t-butanolate / 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾ / toluene / 100 °C

2.1: trifluoroacetic acid / dichloromethane / 2 h / 30 °C

2.2: pH 7 - 8

3.1: potassium phosphate / tricyclohexylphosphine; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾ / 1,4-dioxane / 100 °C / Inert atmosphere; Sealed tube

4.1: hydrogen; trifluoroacetic acid / 5% Pd(II)/C(eggshell) / methanol / 30 °C

4.2: pH 8 - 9

5.1: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 100 °C

6.1: sodium hydroxide / methanol / 2 h / 50 °C

With potassium phosphate; hydrogen; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; sodium hydroxide; sodium t-butanolate; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; 5% Pd(II)/C(eggshell); 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; tricyclohexylphosphine; In 1,4-dioxane; methanol; dichloromethane; N,N-dimethyl-formamide; toluene;

Reference yield:

: 30459-17-7
1-[4-(trifluoromethyl)phenyl]piperazine

: 1268862-36-7
2-phenyl-3-(4-(4-(trifluoromethyl)phenyl)piperidin-1-yl)quinoxaline-6-carboxylic acid

Guidance literature:: Multi-step reaction with 4 steps

1.1: potassium phosphate / tricyclohexylphosphine; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾ / 1,4-dioxane / 100 °C / Inert atmosphere; Sealed tube

2.1: hydrogen; trifluoroacetic acid / 5% Pd(II)/C(eggshell) / methanol / 30 °C

2.2: pH 8 - 9

3.1: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 100 °C

4.1: sodium hydroxide / methanol / 2 h / 50 °C

With potassium phosphate; hydrogen; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; sodium hydroxide; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; 5% Pd(II)/C(eggshell); tricyclohexylphosphine; In 1,4-dioxane; methanol; N,N-dimethyl-formamide;