2-[(6-methoxy-1H-benzimidazol-2-yl)sulfanyl]-N-(2-methylphenyl)acetamide

Base Information

Chemical Name:2-[(6-methoxy-1H-benzimidazol-2-yl)sulfanyl]-N-(2-methylphenyl)acetamide
CAS No.:356587-79-6
Molecular Formula:C₁₇H₁₇N₃O₂S
Molecular Weight:327.407
Hs Code.:
Mol file:356587-79-6.mol

Synonyms:2-((5-methoxy-1H-benzo[d]imidazol-2-yl)thio)-N-(o-tolyl)acetamide

Suppliers and Price of 2-[(6-methoxy-1H-benzimidazol-2-yl)sulfanyl]-N-(2-methylphenyl)acetamide

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
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price

American Custom Chemicals Corporation
2-[(6-METHOXY-1H-BENZIMIDAZOL-2-YL)SULFANYL]-N-(2-METHYLPHENYL)ACETAMIDE 95.00%
5MG
$ 502.91

Total 1 raw suppliers

Chemical Property of 2-[(6-methoxy-1H-benzimidazol-2-yl)sulfanyl]-N-(2-methylphenyl)acetamide

Chemical Property:

Purity/Quality:: 2-[(6-METHOXY-1H-BENZIMIDAZOL-2-YL)SULFANYL]-N-(2-METHYLPHENYL)ACETAMIDE 95.00% ^*data from reagent suppliers

Safty Information:

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Technology Process of 2-[(6-methoxy-1H-benzimidazol-2-yl)sulfanyl]-N-(2-methylphenyl)acetamide

There total 5 articles about 2-[(6-methoxy-1H-benzimidazol-2-yl)sulfanyl]-N-(2-methylphenyl)acetamide 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: 68.0%

: 37052-78-1
5-methoxy-1,3-dihydro-2H-benzo[d]imidazole-2-thione

: 37394-93-7
2-chloro-N-(2-methylphenyl)acetamide

: 356587-79-6
2-((5-methoxy-1H-benzo[d]imidazol-2-yl)thio)-N-(o-tolyl)acetamide

Guidance literature:: 5-methoxy-1,3-dihydro-2H-benzo[d]imidazole-2-thione; With potassium carbonate; In acetone; at 20 ℃; for 0.25h;

2-chloro-N-(2-methylphenyl)acetamide; In acetone; at 20 ℃;
DOI:10.1021/acs.jmedchem.7b00587

Reference yield: 53.0%

: 37052-78-1
2-Mercapto-5-methoxybenzimidazole

: 37394-93-7
2-chloro-N-(2-methylphenyl)acetamide

: 356587-79-6
2-((5-methoxy-1H-benzo[d]imidazol-2-yl)thio)-N-(o-tolyl)acetamide

Guidance literature:: With potassium carbonate; In acetone; at 20 ℃; for 4h;
DOI:10.1007/s00044-013-0732-z

Reference yield:

: 95-53-4
o-toluidine

: 356587-79-6
2-((5-methoxy-1H-benzo[d]imidazol-2-yl)thio)-N-(o-tolyl)acetamide

Guidance literature:: Multi-step reaction with 2 steps

1.1: triethylamine / N,N-dimethyl-formamide / 0.17 h / 20 °C

1.2: 0 - 20 °C

2.1: potassium carbonate / acetone / 4 h / 20 °C

With potassium carbonate; triethylamine; In N,N-dimethyl-formamide; acetone;
DOI:10.1007/s00044-013-0732-z