N-(4-methoxy-1H-benzo[d]imidazol-7-yl)-3-methyl-4-bromobenzenesulfonamide

Base Information

Chemical Name:N-(4-methoxy-1H-benzo[d]imidazol-7-yl)-3-methyl-4-bromobenzenesulfonamide
CAS No.:1314324-95-2
Molecular Formula:C₁₅H₁₄BrN₃O₃S
Molecular Weight:396.264
Hs Code.:

Synonyms:N-(4-methoxy-1H-benzo[d]imidazol-7-yl)-3-methyl-4-bromobenzenesulfonamide

Suppliers and Price of N-(4-methoxy-1H-benzo[d]imidazol-7-yl)-3-methyl-4-bromobenzenesulfonamide

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

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Chemical Property of N-(4-methoxy-1H-benzo[d]imidazol-7-yl)-3-methyl-4-bromobenzenesulfonamide

Chemical Property:

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Technology Process of N-(4-methoxy-1H-benzo[d]imidazol-7-yl)-3-methyl-4-bromobenzenesulfonamide

There total 6 articles about N-(4-methoxy-1H-benzo[d]imidazol-7-yl)-3-methyl-4-bromobenzenesulfonamide 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: 50.0%

: 1314324-71-4
4-methoxy-7-amino-1H-benzo[d]imidazole

: 72256-93-0
4-bromo-3-methylbenzenesulfonyl chloride

: 1314324-95-2
N-(4-methoxy-1H-benzo[d]imidazol-7-yl)-3-methyl-4-bromobenzenesulfonamide

Guidance literature:: With pyridine; In dichloromethane; at 20 ℃;
DOI:10.1080/10286020.2011.556091

Reference yield:

: 1314324-70-3
4-methoxy-7-nitro-1H-benzo[d]imidazole

: 1314324-95-2
N-(4-methoxy-1H-benzo[d]imidazol-7-yl)-3-methyl-4-bromobenzenesulfonamide

Guidance literature:: Multi-step reaction with 2 steps

1: palladium 10% on activated carbon; hydrogen / ethanol / 5 h / 20 °C / 760.05 Torr

2: pyridine / dichloromethane / 20 °C

With pyridine; palladium 10% on activated carbon; hydrogen; In ethanol; dichloromethane;
DOI:10.1080/10286020.2011.556091

Reference yield:

: 37466-89-0
3-methoxybenzene-1,2-diamine

: 1314324-95-2
N-(4-methoxy-1H-benzo[d]imidazol-7-yl)-3-methyl-4-bromobenzenesulfonamide

Guidance literature:: Multi-step reaction with 4 steps

1: Reflux

2: sodium nitrate; trifluoroacetic acid / 16 h / 70 °C

3: palladium 10% on activated carbon; hydrogen / ethanol / 5 h / 20 °C / 760.05 Torr

4: pyridine / dichloromethane / 20 °C

With pyridine; sodium nitrate; palladium 10% on activated carbon; hydrogen; trifluoroacetic acid; In ethanol; dichloromethane;
DOI:10.1080/10286020.2011.556091