2-Propyl-3-[2'-(5-thioxo-4,5-dihydro-[1,2,4]oxadiazol-3-yl)-biphenyl-4-ylmethyl]-3H-benzoimidazole-4-carboxylic acid methyl ester

Base Information

• Chemical Name: 2-Propyl-3-[2'-(5-thioxo-4,5-dihydro-[1,2,4]oxadiazol-3-yl)-biphenyl-4-ylmethyl]-3H-benzoimidazole-4-carboxylic acid methyl ester
• CAS No.: 147403-63-2
• Molecular Formula: C₂₇H₂₄N₄O₃S
• Molecular Weight: 484.579

Synonyms:2-Propyl-3-[2'-(5-thioxo-4,5-dihydro-[1,2,4]oxadiazol-3-yl)-biphenyl-4-ylmethyl]-3H-benzoimidazole-4-carboxylic acid methyl ester

Chemical Property of 2-Propyl-3-[2'-(5-thioxo-4,5-dihydro-[1,2,4]oxadiazol-3-yl)-biphenyl-4-ylmethyl]-3H-benzoimidazole-4-carboxylic acid methyl ester

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Technology Process of 2-Propyl-3-[2'-(5-thioxo-4,5-dihydro-[1,2,4]oxadiazol-3-yl)-biphenyl-4-ylmethyl]-3H-benzoimidazole-4-carboxylic acid methyl ester

There total 2 articles about 2-Propyl-3-[2'-(5-thioxo-4,5-dihydro-[1,2,4]oxadiazol-3-yl)-biphenyl-4-ylmethyl]-3H-benzoimidazole-4-carboxylic acid methyl ester 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: 29.0%

carbon disulfide (75-15-0,12122-00-8) + C28H28N4O4 (147404-84-0) → 2-Propyl-3-[2'-(5-thioxo-4,5-dihydro-[1,2,4]oxadiazol-3-yl)-biphenyl-4-ylmethyl]-3H-benzoimidazole-4-carboxylic acid methyl ester (147403-63-2)

Guidance literature:

With sodium hydride; In N,N-dimethyl-formamide; at 0 ℃; for 0.833333h;

DOI:10.1021/jm960547h

Reference yield:

3-[2'-(N-Hydroxycarbamimidoyl)-biphenyl-4-ylmethyl]-2-propyl-3H-benzoimidazole-4-carboxylic acid methyl ester (147404-00-0) → 2-Propyl-3-[2'-(5-thioxo-4,5-dihydro-[1,2,4]oxadiazol-3-yl)-biphenyl-4-ylmethyl]-3H-benzoimidazole-4-carboxylic acid methyl ester (147403-63-2)

Guidance literature:

Multi-step reaction with 2 steps

1: 86 percent / Et₃N / CH₂Cl₂ / 2 h / Ambient temperature

2: 29 percent / NaH / dimethylformamide / 0.83 h / 0 °C

With sodium hydride; triethylamine; In dichloromethane; N,N-dimethyl-formamide;

DOI:10.1021/jm960547h

Reference yield: 76.0%

2-Propyl-3-[2'-(5-thioxo-4,5-dihydro-[1,2,4]oxadiazol-3-yl)-biphenyl-4-ylmethyl]-3H-benzoimidazole-4-carboxylic acid methyl ester (147403-63-2) → 2-Propyl-3-[2'-(5-thioxo-4,5-dihydro-[1,2,4]oxadiazol-3-yl)-biphenyl-4-ylmethyl]-3H-benzoimidazole-4-carboxylic acid

Guidance literature:

With lithium hydroxide; In tetrahydrofuran; Ambient temperature;

DOI:10.1021/jm960547h

upstream raw materials:

carbon disulfide

C₂₈H₂₈N₄O₄

3-[2'-(N-Hydroxycarbamimidoyl)-biphenyl-4-ylmethyl]-2-propyl-3H-benzoimidazole-4-carboxylic acid methyl ester

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