4-(3-(8-((3,4-dimethoxyphenyl)amino)imidazo[1,2-a]pyrazin-6-yl)benzamido)benzoic acid

Base Information

Chemical Name:4-(3-(8-((3,4-dimethoxyphenyl)amino)imidazo[1,2-a]pyrazin-6-yl)benzamido)benzoic acid
CAS No.:1181326-55-5
Molecular Formula:C₂₈H₂₃N₅O₅
Molecular Weight:509.521
Hs Code.:

Synonyms:4-(3-(8-((3,4-dimethoxyphenyl)amino)imidazo[1,2-a]pyrazin-6-yl)benzamido)benzoic acid

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Chemical Property of 4-(3-(8-((3,4-dimethoxyphenyl)amino)imidazo[1,2-a]pyrazin-6-yl)benzamido)benzoic acid

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Technology Process of 4-(3-(8-((3,4-dimethoxyphenyl)amino)imidazo[1,2-a]pyrazin-6-yl)benzamido)benzoic acid

There total 7 articles about 4-(3-(8-((3,4-dimethoxyphenyl)amino)imidazo[1,2-a]pyrazin-6-yl)benzamido)benzoic 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: 31.0%

: 1181326-92-0
benzyl 4-(3-(8-((3,4-dimethoxyphenyl)amino)imidazo[1,2-a]-pyrazin-6-yl)benzamido)benzoate

: 1181326-55-5
4-(3-(8-((3,4-dimethoxyphenyl)amino)imidazo[1,2-a]pyrazin-6-yl)benzamido)benzoic acid

Guidance literature:: With hydrogen; palladium on activated charcoal; In ethanol; ethyl acetate; at 60 ℃; for 1.16667h; Inert atmosphere;

Reference yield:

: 14786-27-7
benzyl 4-nitrobenzoate

: 1181326-55-5
4-(3-(8-((3,4-dimethoxyphenyl)amino)imidazo[1,2-a]pyrazin-6-yl)benzamido)benzoic acid

Guidance literature:: Multi-step reaction with 4 steps

1: iron; sulfuric acid / ethanol; water / 2.5 h / 60 °C

2: N-ethyl-N,N-diisopropylamine / dichloromethane / 13 h / 20 °C

3: tetrakis(triphenylphosphine) palladium⁽⁰⁾ / 1,4-dioxane / 2.5 h / Inert atmosphere; Reflux

4: palladium 10% on activated carbon; hydrogen / ethanol; ethyl acetate / 0.5 h / 60 °C

With tetrakis(triphenylphosphine) palladium⁽⁰⁾; sulfuric acid; palladium 10% on activated carbon; hydrogen; iron; N-ethyl-N,N-diisopropylamine; In 1,4-dioxane; ethanol; dichloromethane; water; ethyl acetate; 3: |Suzuki-Miyaura Coupling;
DOI:10.1021/jm500228a

Reference yield:

: 19008-43-6
benzyl 4-aminobenzoate

: 1181326-55-5
4-(3-(8-((3,4-dimethoxyphenyl)amino)imidazo[1,2-a]pyrazin-6-yl)benzamido)benzoic acid

Guidance literature:: Multi-step reaction with 3 steps

1: N-ethyl-N,N-diisopropylamine / dichloromethane / 13 h / 20 °C

2: tetrakis(triphenylphosphine) palladium⁽⁰⁾ / 1,4-dioxane / 2.5 h / Inert atmosphere; Reflux

3: palladium 10% on activated carbon; hydrogen / ethanol; ethyl acetate / 0.5 h / 60 °C

With tetrakis(triphenylphosphine) palladium⁽⁰⁾; palladium 10% on activated carbon; hydrogen; N-ethyl-N,N-diisopropylamine; In 1,4-dioxane; ethanol; dichloromethane; ethyl acetate; 2: |Suzuki-Miyaura Coupling;
DOI:10.1021/jm500228a