3-[1-(4-methanesulfonyl-phenyl)-4-methyl-1H-imidazol-2-yl]-pyridine 1-oxide

Base Information

Chemical Name:3-[1-(4-methanesulfonyl-phenyl)-4-methyl-1H-imidazol-2-yl]-pyridine 1-oxide
CAS No.:298205-05-7
Molecular Formula:C₁₆H₁₅N₃O₃S
Molecular Weight:329.379
Hs Code.:

3-[1-(4-methanesulfonyl-phenyl)-4-methyl-1<i>H</i>-imidazol-2-yl]-pyridine 1-oxide

Synonyms:3-[1-(4-methanesulfonyl-phenyl)-4-methyl-1H-imidazol-2-yl]-pyridine 1-oxide

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Chemical Property of 3-[1-(4-methanesulfonyl-phenyl)-4-methyl-1H-imidazol-2-yl]-pyridine 1-oxide

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Technology Process of 3-[1-(4-methanesulfonyl-phenyl)-4-methyl-1H-imidazol-2-yl]-pyridine 1-oxide

There total 5 articles about 3-[1-(4-methanesulfonyl-phenyl)-4-methyl-1H-imidazol-2-yl]-pyridine 1-oxide 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:

: 298205-04-6
3-[4-methyl-1-[4-(methylthio)phenyl]-1H-imidazol-2-yl]pyridine

: 298205-05-7
3-[1-(4-methanesulfonyl-phenyl)-4-methyl-1H-imidazol-2-yl]-pyridine 1-oxide

Guidance literature:: With 3-chloro-benzenecarboperoxoic acid; In dichloromethane; at 0 - 5 ℃; for 1.5h;
DOI:10.1021/jm0000719

Reference yield:

: 298204-73-6
N-[4-(methylthio)phenyl]-3-pyridinecarboxamide

: 298205-05-7
3-[1-(4-methanesulfonyl-phenyl)-4-methyl-1H-imidazol-2-yl]-pyridine 1-oxide

Guidance literature:: Multi-step reaction with 3 steps

1.1: sodium bis(trimethylsilyl) amide / tetrahydrofuran / 0.25 h

1.2: 24 percent / tetrahydrofuran / 20 °C

2.1: 78 percent / pyridinium p-toluenesulfonate / tetrahydrofuran / 4 h / Heating

3.1: 213 mg / m-chloroperoxybenzoic acid / CH₂Cl₂ / 1.5 h / 0 - 5 °C

With sodium hexamethyldisilazane; pyridinium p-toluenesulfonate; 3-chloro-benzenecarboperoxoic acid; In tetrahydrofuran; dichloromethane; 1.1: deprotonation / 1.2: Alkylation / 2.1: Cyclization / 3.1: Oxidation;
DOI:10.1021/jm0000719

Reference yield:

: 298205-03-5
N-(2-methoxy-2-propenyl)-N-[4-(methylthio)phenyl]-3-pyridinecarboximidamide

: 298205-05-7
3-[1-(4-methanesulfonyl-phenyl)-4-methyl-1H-imidazol-2-yl]-pyridine 1-oxide

Guidance literature:: Multi-step reaction with 2 steps

1: 78 percent / pyridinium p-toluenesulfonate / tetrahydrofuran / 4 h / Heating

2: 213 mg / m-chloroperoxybenzoic acid / CH₂Cl₂ / 1.5 h / 0 - 5 °C

With pyridinium p-toluenesulfonate; 3-chloro-benzenecarboperoxoic acid; In tetrahydrofuran; dichloromethane; 1: Cyclization / 2: Oxidation;
DOI:10.1021/jm0000719