methyl 4-chloro-2-[(2,4-dichlorophenyl)amino]-1-(3-hydroxypropyl)-1H-benzimidazole-7-carboxylate

Base Information

Chemical Name:methyl 4-chloro-2-[(2,4-dichlorophenyl)amino]-1-(3-hydroxypropyl)-1H-benzimidazole-7-carboxylate
CAS No.:1173983-85-1
Molecular Formula:C₁₈H₁₆Cl₃N₃O₃
Molecular Weight:428.702
Hs Code.:

Synonyms:methyl 4-chloro-2-[(2,4-dichlorophenyl)amino]-1-(3-hydroxypropyl)-1H-benzimidazole-7-carboxylate

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Chemical Property of methyl 4-chloro-2-[(2,4-dichlorophenyl)amino]-1-(3-hydroxypropyl)-1H-benzimidazole-7-carboxylate

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Technology Process of methyl 4-chloro-2-[(2,4-dichlorophenyl)amino]-1-(3-hydroxypropyl)-1H-benzimidazole-7-carboxylate

There total 6 articles about methyl 4-chloro-2-[(2,4-dichlorophenyl)amino]-1-(3-hydroxypropyl)-1H-benzimidazole-7-carboxylate 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: 71.0%

: C₁₈H₁₈Cl₃N₃O₃S

: 1173983-85-1
methyl 4-chloro-2-[(2,4-dichlorophenyl)amino]-1-(3-hydroxypropyl)-1H-benzimidazole-7-carboxylate

Guidance literature:: With 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; In tetrahydrofuran; at 50 ℃; for 3h;
DOI:10.1016/j.bmc.2018.01.020

Reference yield:

: 3970-35-2
2-chloro-3-nitrobezoic acid

: 1173983-85-1
methyl 4-chloro-2-[(2,4-dichlorophenyl)amino]-1-(3-hydroxypropyl)-1H-benzimidazole-7-carboxylate

Guidance literature:: Multi-step reaction with 6 steps

1.1: tetrahydrofuran / 3 h / 0 - 20 °C

1.2: 14 h / 0 - 20 °C

2.1: triethylamine / methanol / 6 h / 50 °C

3.1: hydrogen; palladium 10% on activated carbon / tetrahydrofuran / 23 h / 20 °C

4.1: N-chloro-succinimide / acetonitrile / 17.5 h / 20 °C

5.1: tetrahydrofuran / 72 h / 20 °C

6.1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine / tetrahydrofuran / 3 h / 50 °C

With N-chloro-succinimide; palladium 10% on activated carbon; hydrogen; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; In tetrahydrofuran; methanol; acetonitrile;
DOI:10.1016/j.bmc.2018.01.020

Reference yield:

: 53553-14-3
2-chloro-3-nitrobenzoic acid methyl ester

: 1173983-85-1
methyl 4-chloro-2-[(2,4-dichlorophenyl)amino]-1-(3-hydroxypropyl)-1H-benzimidazole-7-carboxylate

Guidance literature:: Multi-step reaction with 5 steps

1: triethylamine / methanol / 6 h / 50 °C

2: hydrogen; palladium 10% on activated carbon / tetrahydrofuran / 23 h / 20 °C

3: N-chloro-succinimide / acetonitrile / 17.5 h / 20 °C

4: tetrahydrofuran / 72 h / 20 °C

5: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine / tetrahydrofuran / 3 h / 50 °C

With N-chloro-succinimide; palladium 10% on activated carbon; hydrogen; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; In tetrahydrofuran; methanol; acetonitrile;
DOI:10.1016/j.bmc.2018.01.020