N-[2-(4-cyano-benzyl)-1-methyl-1H-benzoimidazol-5-yl]benzenesulfonamide

Base Information

Chemical Name:N-[2-(4-cyano-benzyl)-1-methyl-1H-benzoimidazol-5-yl]benzenesulfonamide
CAS No.:236417-29-1
Molecular Formula:C₂₂H₁₈N₄O₂S
Molecular Weight:402.477
Hs Code.:

Synonyms:N-[2-(4-cyano-benzyl)-1-methyl-1H-benzoimidazol-5-yl]benzenesulfonamide

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of N-[2-(4-cyano-benzyl)-1-methyl-1H-benzoimidazol-5-yl]benzenesulfonamide

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Technology Process of N-[2-(4-cyano-benzyl)-1-methyl-1H-benzoimidazol-5-yl]benzenesulfonamide

There total 5 articles about N-[2-(4-cyano-benzyl)-1-methyl-1H-benzoimidazol-5-yl]benzenesulfonamide 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: 91.0%

: 98-09-9
benzenesulfonyl chloride

: 236417-28-0
4-(5-amino-1-methyl-1H-benzoimidazol-2-ylmethyl)benzonitrile

: 236417-29-1
N-[2-(4-cyano-benzyl)-1-methyl-1H-benzoimidazol-5-yl]benzenesulfonamide

Guidance literature:: With pyridine; at 20 ℃; for 1h;
DOI:10.1021/jm0109513

Reference yield:

: 5462-71-5
4-cyanophenylacetic acid

: 236417-29-1
N-[2-(4-cyano-benzyl)-1-methyl-1H-benzoimidazol-5-yl]benzenesulfonamide

Guidance literature:: Multi-step reaction with 4 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: 91 percent / pyridine / 1 h / 20 °C

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

Reference yield:

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

: 236417-29-1
N-[2-(4-cyano-benzyl)-1-methyl-1H-benzoimidazol-5-yl]benzenesulfonamide

Guidance literature:: Multi-step reaction with 4 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: 91 percent / pyridine / 1 h / 20 °C

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