N-[(6-hydroxy-2-{3-[(1-methylethyl)oxy]phenyl}-5-quinoxalinyl)carbonyl]glycine

Base Information

Chemical Name:N-[(6-hydroxy-2-{3-[(1-methylethyl)oxy]phenyl}-5-quinoxalinyl)carbonyl]glycine
CAS No.:1160684-40-1
Molecular Formula:C₂₀H₁₉N₃O₅
Molecular Weight:381.388
Hs Code.:

Synonyms:N-[(6-hydroxy-2-{3-[(1-methylethyl)oxy]phenyl}-5-quinoxalinyl)carbonyl]glycine

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Chemical Property of N-[(6-hydroxy-2-{3-[(1-methylethyl)oxy]phenyl}-5-quinoxalinyl)carbonyl]glycine

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Technology Process of N-[(6-hydroxy-2-{3-[(1-methylethyl)oxy]phenyl}-5-quinoxalinyl)carbonyl]glycine

There total 10 articles about N-[(6-hydroxy-2-{3-[(1-methylethyl)oxy]phenyl}-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: 39.4%

: 1160684-41-2
Ethyl N-[(6-hydroxy-2-{3-[(1-methylethyl)oxy]phenyl}-5-quinoxalinyl)carbonyl]glycinate

: 1160684-40-1
N-[(6-hydroxy-2-{3-[(1-methylethyl)oxy]phenyl}-5-quinoxalinyl)carbonyl]glycine

Guidance literature:: Ethyl N-[(6-hydroxy-2-{3-[(1-methylethyl)oxy]phenyl}-5-quinoxalinyl)carbonyl]glycinate; With water; sodium hydroxide; In tetrahydrofuran; at 20 ℃; for 0.166667h;

With hydrogenchloride; In water; pH=3;

Reference yield:

: 13671-00-6
methyl 2,6-difluorobenzoate

: 1160684-40-1
N-[(6-hydroxy-2-{3-[(1-methylethyl)oxy]phenyl}-5-quinoxalinyl)carbonyl]glycine

Guidance literature:: Multi-step reaction with 10 steps

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

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

3.1: sodium hydride / mineral oil / 1 h / 0 - 20 °C

4.1: hydrogen / palladium 10% on activated carbon / ethyl acetate / 2585.81 Torr

5.1: toluene; acetonitrile / 0.25 h / 20 °C

6.1: trichlorophosphate / Reflux

7.1: boron tribromide / dichloromethane / 20 °C

8.1: triethylamine; HATU / N,N-dimethyl-formamide

9.1: potassium carbonate / tetrakis(triphenylphosphine) palladium⁽⁰⁾ / 1,4-dioxane; water / 0.5 h / 120 °C / Inert atmosphere; Microwave irradiation

10.1: water; sodium hydroxide / tetrahydrofuran / 0.17 h / 20 °C

10.2: pH 3

With ammonium hydroxide; sulfuric acid; water; hydrogen; nitric acid; boron tribromide; sodium hydride; potassium carbonate; triethylamine; HATU; sodium hydroxide; trichlorophosphate; tetrakis(triphenylphosphine) palladium⁽⁰⁾; palladium 10% on activated carbon; In tetrahydrofuran; 1,4-dioxane; ethanol; dichloromethane; water; ethyl acetate; N,N-dimethyl-formamide; toluene; acetonitrile; mineral oil;

Reference yield:

: 1160682-17-6
methyl 2,3-diamino-6-methoxybenzoate

: 1160684-40-1
N-[(6-hydroxy-2-{3-[(1-methylethyl)oxy]phenyl}-5-quinoxalinyl)carbonyl]glycine

Guidance literature:: Multi-step reaction with 6 steps

1.1: toluene; acetonitrile / 0.25 h / 20 °C

2.1: trichlorophosphate / Reflux

3.1: boron tribromide / dichloromethane / 20 °C

4.1: triethylamine; HATU / N,N-dimethyl-formamide

5.1: potassium carbonate / tetrakis(triphenylphosphine) palladium⁽⁰⁾ / 1,4-dioxane; water / 0.5 h / 120 °C / Inert atmosphere; Microwave irradiation

6.1: water; sodium hydroxide / tetrahydrofuran / 0.17 h / 20 °C

6.2: pH 3

With water; boron tribromide; potassium carbonate; triethylamine; HATU; sodium hydroxide; trichlorophosphate; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In tetrahydrofuran; 1,4-dioxane; dichloromethane; water; N,N-dimethyl-formamide; toluene; acetonitrile;