({2-[(4-carbamimidoyl-phenylamino)-methyl]-1-methyl-1H-benzoimidazole-5-carbonyl}-phenyl-amino)-acetic acid ethyl ester

Base Information

Chemical Name:({2-[(4-carbamimidoyl-phenylamino)-methyl]-1-methyl-1H-benzoimidazole-5-carbonyl}-phenyl-amino)-acetic acid ethyl ester
CAS No.:749191-94-4
Molecular Formula:C₂₇H₂₈N₆O₃
Molecular Weight:484.558
Hs Code.:

({2-[(4-carbamimidoyl-phenylamino)-methyl]-1-methyl-1<i>H</i>-benzoimidazole-5-carbonyl}-phenyl-amino)-acetic acid ethyl ester

Synonyms:({2-[(4-carbamimidoyl-phenylamino)-methyl]-1-methyl-1H-benzoimidazole-5-carbonyl}-phenyl-amino)-acetic acid ethyl ester

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Chemical Property of ({2-[(4-carbamimidoyl-phenylamino)-methyl]-1-methyl-1H-benzoimidazole-5-carbonyl}-phenyl-amino)-acetic acid ethyl ester

Chemical Property:

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Technology Process of ({2-[(4-carbamimidoyl-phenylamino)-methyl]-1-methyl-1H-benzoimidazole-5-carbonyl}-phenyl-amino)-acetic acid ethyl ester

There total 5 articles about ({2-[(4-carbamimidoyl-phenylamino)-methyl]-1-methyl-1H-benzoimidazole-5-carbonyl}-phenyl-amino)-acetic acid ethyl 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:

: 211916-30-2
1-methyl-2-[N-(4-cyanophenyl)-aminomethyl]-benzimidazol-5-yl-carboxylic acid-N-phenyl-N-(ethoxycarbonylmethyl)-amide

: 749191-94-4
({2-[(4-carbamimidoyl-phenylamino)-methyl]-1-methyl-1H-benzoimidazole-5-carbonyl}-phenyl-amino)-acetic acid ethyl ester

Guidance literature:: 1-methyl-2-[N-(4-cyanophenyl)-aminomethyl]-benzimidazol-5-yl-carboxylic acid-N-phenyl-N-(ethoxycarbonylmethyl)-amide; With hydrogenchloride; In ethanol; at 0 ℃;

With ammonium carbonate; In ethanol; at 20 ℃; Further stages.;
DOI:10.1021/jm0109513

Reference yield:

: 82357-48-0
4-methylamino-3-nitro-benzoic acid chloride

: 749191-94-4
({2-[(4-carbamimidoyl-phenylamino)-methyl]-1-methyl-1H-benzoimidazole-5-carbonyl}-phenyl-amino)-acetic acid ethyl ester

Guidance literature:: Multi-step reaction with 5 steps

1.1: Et₃N / tetrahydrofuran / 20 °C

2.1: H₂ / 10percent Pd/C / methanol; CH₂Cl₂ / 20 °C

3.1: CDI / tetrahydrofuran / 50 °C

4.1: AcOH / Heating

5.1: HCl / ethanol / 0 °C

5.2: (NH₄)2CO₃ / ethanol / 20 °C

With hydrogenchloride; hydrogen; acetic acid; triethylamine; 1,1'-carbonyldiimidazole; 10percent Pd/C; In tetrahydrofuran; methanol; ethanol; dichloromethane; 5.1: Pinner reaction;
DOI:10.1021/jm0109513

Reference yield:

: 41263-74-5
4-(methylamino)-3-nitrobenzoic acid

: 749191-94-4
({2-[(4-carbamimidoyl-phenylamino)-methyl]-1-methyl-1H-benzoimidazole-5-carbonyl}-phenyl-amino)-acetic acid ethyl ester

Guidance literature:: Multi-step reaction with 6 steps

1.1: SOCl₂ / dimethylformamide / 0.5 h / Heating

2.1: Et₃N / tetrahydrofuran / 20 °C

3.1: H₂ / 10percent Pd/C / methanol; CH₂Cl₂ / 20 °C

4.1: CDI / tetrahydrofuran / 50 °C

5.1: AcOH / Heating

6.1: HCl / ethanol / 0 °C

6.2: (NH₄)2CO₃ / ethanol / 20 °C

With hydrogenchloride; thionyl chloride; hydrogen; acetic acid; triethylamine; 1,1'-carbonyldiimidazole; 10percent Pd/C; In tetrahydrofuran; methanol; ethanol; dichloromethane; N,N-dimethyl-formamide; 6.1: Pinner reaction;
DOI:10.1021/jm0109513