2-(2-Methoxy-4-methylsulfanyl-phenyl)-6-nitro-1H-imidazo[4,5-b]pyridine

Base Information

Chemical Name:2-(2-Methoxy-4-methylsulfanyl-phenyl)-6-nitro-1H-imidazo[4,5-b]pyridine
CAS No.:127356-22-3
Molecular Formula:C₁₄H₁₂N₄O₃S
Molecular Weight:316.34
Hs Code.:

Synonyms:2-(2-Methoxy-4-methylsulfanyl-phenyl)-6-nitro-1H-imidazo[4,5-b]pyridine

Suppliers and Price of 2-(2-Methoxy-4-methylsulfanyl-phenyl)-6-nitro-1H-imidazo[4,5-b]pyridine

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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 2-(2-Methoxy-4-methylsulfanyl-phenyl)-6-nitro-1H-imidazo[4,5-b]pyridine

Chemical Property:

Purity/Quality:

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MSDS Files:: SDS file from LookChem

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Technology Process of 2-(2-Methoxy-4-methylsulfanyl-phenyl)-6-nitro-1H-imidazo[4,5-b]pyridine

There total 1 articles about 2-(2-Methoxy-4-methylsulfanyl-phenyl)-6-nitro-1H-imidazo[4,5-b]pyridine 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: 70.0%

: 72856-73-6
2-methoxy-4-(methylsulfanyl)benzoic acid

: 3537-14-2
5-nitro-pyridine-2,3-diamine

: 127356-22-3
2-(2-Methoxy-4-methylsulfanyl-phenyl)-6-nitro-1H-imidazo[4,5-b]pyridine

Guidance literature:: With trichlorophosphate; 1.) RT, 0.5 h, 2.) reflux, 6 h;
DOI:10.1021/jm00170a030

Reference yield:

: 127356-22-3
2-(2-Methoxy-4-methylsulfanyl-phenyl)-6-nitro-1H-imidazo[4,5-b]pyridine

: 127356-23-4
2-(4-Methanesulfinyl-2-methoxy-phenyl)-6-nitro-1H-imidazo[4,5-b]pyridine

Guidance literature:: With 3-chloro-benzenecarboperoxoic acid; In chloroform; at -15 ℃; for 1.5h; Yield given;
DOI:10.1021/jm00170a030

Reference yield:

: 127356-22-3
2-(2-Methoxy-4-methylsulfanyl-phenyl)-6-nitro-1H-imidazo[4,5-b]pyridine

: 127356-05-2
2-(4-Methanesulfinyl-2-methoxy-phenyl)-1H-imidazo[4,5-b]pyridin-6-ylamine

Guidance literature:: Multi-step reaction with 2 steps

1: m-chloroperbenzoic acid / CHCl₃ / 1.5 h / -15 °C

2: 43 percent / H₂ / 10percent Pd/C / ethanol / 760 Torr

With hydrogen; 3-chloro-benzenecarboperoxoic acid; palladium on activated charcoal; In ethanol; chloroform;
DOI:10.1021/jm00170a030