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

Base Information

Chemical Name:3-(4-fluorophenyl)-2-(4-(4-(trifluoromethyl)phenyl)piperidin-1-yl)quinoxaline-6-carboxylic acid
CAS No.:1268862-81-2
Molecular Formula:C₂₇H₂₁F₄N₃O₂
Molecular Weight:495.476
Hs Code.:

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

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

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

There total 6 articles about 3-(4-fluorophenyl)-2-(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%

: 1268865-74-2
methyl 3-(4-fluorophenyl)-2-(4-(4-(trifluoromethyl)phenyl)piperidin-1-yl)quinoxaline-6-carboxylate

: 1268862-81-2
3-(4-fluorophenyl)-2-(4-(4-(trifluoromethyl)phenyl)piperidin-1-yl)quinoxaline-6-carboxylic acid

Guidance literature:: methyl 3-(4-fluorophenyl)-2-(4-(4-(trifluoromethyl)phenyl)piperidin-1-yl)quinoxaline-6-carboxylate; With water; sodium hydroxide; In methanol; at 50 ℃; for 3h;

With hydrogenchloride; In water; pH=3;

Reference yield:

: 402-43-7
p-trifluoromethylphenyl bromide

: 1268862-81-2
3-(4-fluorophenyl)-2-(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 / Sealed tube

6.1: sodium hydroxide; water / methanol / 3 h / 50 °C

6.2: pH 3

With potassium phosphate; water; 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:

: 220000-88-4
4-(4-trifluoromethyl-phenyl)-pyridine

: 1268862-81-2
3-(4-fluorophenyl)-2-(4-(4-(trifluoromethyl)phenyl)piperidin-1-yl)quinoxaline-6-carboxylic acid

Guidance literature:: Multi-step reaction with 3 steps

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

1.2: pH 8 - 9

2.1: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 100 °C / Sealed tube

3.1: sodium hydroxide; water / methanol / 3 h / 50 °C

3.2: pH 3

With water; hydrogen; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; sodium hydroxide; 5% Pd(II)/C(eggshell); In methanol; N,N-dimethyl-formamide;