quinoline-8-sulfonic acid [2-(4-cyano-benzyl)-1-methyl-1H-benzoimidazol-5-yl]-N-(ethoxycarbonylmethyl)amide

Base Information

Chemical Name:quinoline-8-sulfonic acid [2-(4-cyano-benzyl)-1-methyl-1H-benzoimidazol-5-yl]-N-(ethoxycarbonylmethyl)amide
CAS No.:237750-99-1
Molecular Formula:C₂₉H₂₅N₅O₄S
Molecular Weight:539.615
Hs Code.:

Synonyms:quinoline-8-sulfonic acid [2-(4-cyano-benzyl)-1-methyl-1H-benzoimidazol-5-yl]-N-(ethoxycarbonylmethyl)amide

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Chemical Property of quinoline-8-sulfonic acid [2-(4-cyano-benzyl)-1-methyl-1H-benzoimidazol-5-yl]-N-(ethoxycarbonylmethyl)amide

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Technology Process of quinoline-8-sulfonic acid [2-(4-cyano-benzyl)-1-methyl-1H-benzoimidazol-5-yl]-N-(ethoxycarbonylmethyl)amide

There total 6 articles about quinoline-8-sulfonic acid [2-(4-cyano-benzyl)-1-methyl-1H-benzoimidazol-5-yl]-N-(ethoxycarbonylmethyl)amide 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: 43.0%

: 105-36-2
ethyl bromoacetate

: 237750-85-5
quinoline-8-sulfonic acid [2-(4-cyano-benzyl)-1-methyl-1H-benzoimidazol-5-yl]amide

: 237750-99-1
quinoline-8-sulfonic acid [2-(4-cyano-benzyl)-1-methyl-1H-benzoimidazol-5-yl]-N-(ethoxycarbonylmethyl)amide

Guidance literature:: With potassium carbonate; In dimethyl sulfoxide; at 20 ℃; for 5h;
DOI:10.1021/jm0109513

Reference yield:

: 5462-71-5
4-cyanophenylacetic acid

: 237750-99-1
quinoline-8-sulfonic acid [2-(4-cyano-benzyl)-1-methyl-1H-benzoimidazol-5-yl]-N-(ethoxycarbonylmethyl)amide

Guidance literature:: Multi-step reaction with 5 steps

1.1: CDI / tetrahydrofuran / 0.5 h / 50 °C

1.2: 79 percent / tetrahydrofuran / 2 h / 50 °C

2.1: 93 percent / glacial acetic acid / 1 h / Heating

3.1: 100 percent / H₂ / 10percent Pd/C / methanol; CH₂Cl₂

4.1: pyridine / 20 °C

5.1: 43 percent / K₂CO₃ / dimethylsulfoxide / 5 h / 20 °C

With pyridine; hydrogen; potassium carbonate; acetic acid; 1,1'-carbonyldiimidazole; 10percent Pd/C; In tetrahydrofuran; methanol; dichloromethane; dimethyl sulfoxide;
DOI:10.1021/jm0109513

Reference yield:

: 41939-61-1
N₁-methyl-4-nitrobenzene-1,2-diamine

: 237750-99-1
quinoline-8-sulfonic acid [2-(4-cyano-benzyl)-1-methyl-1H-benzoimidazol-5-yl]-N-(ethoxycarbonylmethyl)amide

Guidance literature:: Multi-step reaction with 5 steps

1.1: CDI / tetrahydrofuran / 0.5 h / 50 °C

1.2: 79 percent / tetrahydrofuran / 2 h / 50 °C

2.1: 93 percent / glacial acetic acid / 1 h / Heating

3.1: 100 percent / H₂ / 10percent Pd/C / methanol; CH₂Cl₂

4.1: pyridine / 20 °C

5.1: 43 percent / K₂CO₃ / dimethylsulfoxide / 5 h / 20 °C

With pyridine; hydrogen; potassium carbonate; acetic acid; 1,1'-carbonyldiimidazole; 10percent Pd/C; In tetrahydrofuran; methanol; dichloromethane; dimethyl sulfoxide;
DOI:10.1021/jm0109513