N-{[8-(4-bromo-2-fluorophenyl)-6-hydroxy-5-quinoxalinyl]carbonyl}glycine

Base Information

Chemical Name:N-{[8-(4-bromo-2-fluorophenyl)-6-hydroxy-5-quinoxalinyl]carbonyl}glycine
CAS No.:1160684-46-7
Molecular Formula:C₁₇H₁₁BrFN₃O₄
Molecular Weight:420.194
Hs Code.:

Synonyms:N-{[8-(4-bromo-2-fluorophenyl)-6-hydroxy-5-quinoxalinyl]carbonyl}glycine

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Chemical Property of N-{[8-(4-bromo-2-fluorophenyl)-6-hydroxy-5-quinoxalinyl]carbonyl}glycine

Chemical Property:

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Technology Process of N-{[8-(4-bromo-2-fluorophenyl)-6-hydroxy-5-quinoxalinyl]carbonyl}glycine

There total 8 articles about N-{[8-(4-bromo-2-fluorophenyl)-6-hydroxy-5-quinoxalinyl]carbonyl}glycine 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: 14.09%

: 216393-64-5
(4-bromo-2-fluorophenyl)boronic acid

: 1160683-93-1
ethyl N-[(8-bromo-6-hydroxy-5-quinoxalinyl)carbonyl]glycinate

: 1160684-46-7
N-{[8-(4-bromo-2-fluorophenyl)-6-hydroxy-5-quinoxalinyl]carbonyl}glycine

Guidance literature:: (4-bromo-2-fluorophenyl)boronic acid; ethyl N-[(8-bromo-6-hydroxy-5-quinoxalinyl)carbonyl]glycinate; With potassium carbonate; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In 1,4-dioxane; water; at 120 ℃; for 1h; Microwave irradiation;

With water; sodium hydroxide; In 1,4-dioxane; methanol; at 20 ℃; for 0.5h;

With hydrogenchloride; In 1,4-dioxane; methanol; water;

Reference yield:

: 773134-11-5
4-bromo-2,6-difluorobenzoic acid methyl ester

: 1160684-46-7
N-{[8-(4-bromo-2-fluorophenyl)-6-hydroxy-5-quinoxalinyl]carbonyl}glycine

Guidance literature:: Multi-step reaction with 7 steps

1.1: sulfuric acid; nitric acid / 0 - 20 °C

2.1: ammonium hydroxide / methanol; water / 20 °C

3.1: sodium methylate / methanol / 0 - 20 °C

4.1: hydrogen / palladium on activated charcoal / methanol / 2 h

4.2: 2 h / Reflux

5.1: boron tribromide / dichloromethane / 20 °C

6.1: benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; triethylamine / N,N-dimethyl-formamide / 2 h / 20 °C

7.1: potassium carbonate / tetrakis(triphenylphosphine) palladium⁽⁰⁾ / 1,4-dioxane; water / 1 h / 120 °C / Microwave irradiation

7.2: 0.5 h / 20 °C

With ammonium hydroxide; sulfuric acid; benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; hydrogen; nitric acid; sodium methylate; boron tribromide; potassium carbonate; triethylamine; tetrakis(triphenylphosphine) palladium⁽⁰⁾; palladium on activated charcoal; In 1,4-dioxane; methanol; dichloromethane; water; N,N-dimethyl-formamide;

Reference yield:

: 1160684-07-0
8-bromo-6-hydroxy-5-quinoxalinecarboxylic acid

: 1160684-46-7
N-{[8-(4-bromo-2-fluorophenyl)-6-hydroxy-5-quinoxalinyl]carbonyl}glycine

Guidance literature:: Multi-step reaction with 2 steps

1.1: benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; triethylamine / N,N-dimethyl-formamide / 2 h / 20 °C

2.1: potassium carbonate / tetrakis(triphenylphosphine) palladium⁽⁰⁾ / 1,4-dioxane; water / 1 h / 120 °C / Microwave irradiation

2.2: 0.5 h / 20 °C

With benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; potassium carbonate; triethylamine; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In 1,4-dioxane; water; N,N-dimethyl-formamide;