3-(2'-Cyano-biphenyl-4-ylmethyl)-2-propyl-3H-benzoimidazole-4-carboxylic acid methyl ester

Base Information

Chemical Name:3-(2'-Cyano-biphenyl-4-ylmethyl)-2-propyl-3H-benzoimidazole-4-carboxylic acid methyl ester
CAS No.:136285-43-3
Molecular Formula:C₂₆H₂₃N₃O₂
Molecular Weight:409.488
Hs Code.:

Synonyms:3-(2'-Cyano-biphenyl-4-ylmethyl)-2-propyl-3H-benzoimidazole-4-carboxylic acid methyl ester

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Chemical Property of 3-(2'-Cyano-biphenyl-4-ylmethyl)-2-propyl-3H-benzoimidazole-4-carboxylic acid methyl ester

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Technology Process of 3-(2'-Cyano-biphenyl-4-ylmethyl)-2-propyl-3H-benzoimidazole-4-carboxylic acid methyl ester

There total 8 articles about 3-(2'-Cyano-biphenyl-4-ylmethyl)-2-propyl-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: 73.0%

: 141-75-3
butyryl chloride

: 136304-78-4
methyl 3-amino-2-[[(2'-cyanobiphenyl-4-yl)methyl]amino]benzoate

: 136285-43-3
3-(2'-Cyano-biphenyl-4-ylmethyl)-2-propyl-3H-benzoimidazole-4-carboxylic acid methyl ester

Guidance literature:: With triethylamine; In dichloromethane; for 2h; Ambient temperature;
DOI:10.1021/jm00067a016

Reference yield:

: 21606-04-2
methyl 2-carboxy-3-nitrobenzoate

: 136285-43-3
3-(2'-Cyano-biphenyl-4-ylmethyl)-2-propyl-3H-benzoimidazole-4-carboxylic acid methyl ester

Guidance literature:: Multi-step reaction with 7 steps

1: SOCl₂, DMF / toluene / 0.5 h / Heating

2: NaN₃ / acetone; H₂O / 1 h

3: 1.5 h / Heating

4: 85 percent / K₂CO₃ / acetonitrile / 4 h / Heating

5: 77 percent / 30percent ethanolic HCl / ethyl acetate / 1 h / Ambient temperature

6: 1.) FeCl₃*6H₂O, activated carbon, 2.) hydrazine monohydrate / 1.) MeOH, THF, reflux, 30 min, 2.) MeOH, THF, reflux, 14 h

7: 73 percent / Et₃N / CH₂Cl₂ / 2 h / Ambient temperature

With hydrogenchloride; thionyl chloride; sodium azide; potassium carbonate; pyrographite; hydrazine hydrate; triethylamine; N,N-dimethyl-formamide; In dichloromethane; water; ethyl acetate; acetone; toluene; acetonitrile;
DOI:10.1021/jm00067a016

Reference yield:

: 73833-13-3
acid chloride of 1-methylhydrogen-3-nitrophthalate

: 136285-43-3
3-(2'-Cyano-biphenyl-4-ylmethyl)-2-propyl-3H-benzoimidazole-4-carboxylic acid methyl ester

Guidance literature:: Multi-step reaction with 6 steps

1: NaN₃ / acetone; H₂O / 1 h

2: 1.5 h / Heating

3: 85 percent / K₂CO₃ / acetonitrile / 4 h / Heating

4: 77 percent / 30percent ethanolic HCl / ethyl acetate / 1 h / Ambient temperature

5: 1.) FeCl₃*6H₂O, activated carbon, 2.) hydrazine monohydrate / 1.) MeOH, THF, reflux, 30 min, 2.) MeOH, THF, reflux, 14 h

6: 73 percent / Et₃N / CH₂Cl₂ / 2 h / Ambient temperature

With hydrogenchloride; sodium azide; potassium carbonate; pyrographite; hydrazine hydrate; triethylamine; In dichloromethane; water; ethyl acetate; acetone; acetonitrile;
DOI:10.1021/jm00067a016