4-(4-(4-fluorophenyl)-2-(methylsulfinyl)-1H-imidazol-5-yl)-N-(tetrahydro-2H-pyran-4-yl)pyridin-2-amine

Base Information

• Chemical Name: 4-(4-(4-fluorophenyl)-2-(methylsulfinyl)-1H-imidazol-5-yl)-N-(tetrahydro-2H-pyran-4-yl)pyridin-2-amine
• CAS No.: 1289617-08-8
• Molecular Formula: C₂₀H₂₁FN₄O₂S
• Molecular Weight: 400.477

Synonyms:4-(4-(4-fluorophenyl)-2-(methylsulfinyl)-1H-imidazol-5-yl)-N-(tetrahydro-2H-pyran-4-yl)pyridin-2-amine

Chemical Property of 4-(4-(4-fluorophenyl)-2-(methylsulfinyl)-1H-imidazol-5-yl)-N-(tetrahydro-2H-pyran-4-yl)pyridin-2-amine

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Technology Process of 4-(4-(4-fluorophenyl)-2-(methylsulfinyl)-1H-imidazol-5-yl)-N-(tetrahydro-2H-pyran-4-yl)pyridin-2-amine

There total 4 articles about 4-(4-(4-fluorophenyl)-2-(methylsulfinyl)-1H-imidazol-5-yl)-N-(tetrahydro-2H-pyran-4-yl)pyridin-2-amine 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: 85.7%

{4-[4-(4-fluorophenyl)-2-(methylsulfanyl)-1H-imidazol-5-yl]-2-pyridyl}(tetrahydro-2H-pyran-4-yl)amine (1015445-59-6) → 4-(4-(4-fluorophenyl)-2-(methylsulfinyl)-1H-imidazol-5-yl)-N-(tetrahydro-2H-pyran-4-yl)pyridin-2-amine (1289617-08-8)

Guidance literature:

With potassium peroxomonosulfate; In tetrahydrofuran; water; at 0 ℃; for 2h;

DOI:10.1021/jm101623p

Reference yield:

4-aminotetrahydropyran (38041-19-9) → 4-(4-(4-fluorophenyl)-2-(methylsulfinyl)-1H-imidazol-5-yl)-N-(tetrahydro-2H-pyran-4-yl)pyridin-2-amine (1289617-08-8)

Guidance literature:

Multi-step reaction with 2 steps

1: 24 h / 160 °C / Autoclave

2: potassium peroxomonosulfate / tetrahydrofuran; water / 2 h / 0 °C

With potassium peroxomonosulfate; In tetrahydrofuran; water;

DOI:10.1021/jm101623p

Reference yield:

2-fluoro-4-[5-(4-fluorophenyl)-2-methylsulfanyl-3H-imidazol-4-yl]pyridine (549505-59-1) → 4-(4-(4-fluorophenyl)-2-(methylsulfinyl)-1H-imidazol-5-yl)-N-(tetrahydro-2H-pyran-4-yl)pyridin-2-amine (1289617-08-8)

Guidance literature:

Multi-step reaction with 2 steps

1: 24 h / 160 °C / Autoclave

2: potassium peroxomonosulfate / tetrahydrofuran; water / 2 h / 0 °C

With potassium peroxomonosulfate; In tetrahydrofuran; water;

DOI:10.1021/jm101623p

upstream raw materials:

4-aminotetrahydropyran

{4-[4-(4-fluorophenyl)-2-(methylsulfanyl)-1H-imidazol-5-yl]-2-pyridyl}(tetrahydro-2H-pyran-4-yl)amine

2-fluoro-4-[5-(4-fluorophenyl)-2-methylsulfanyl-3H-imidazol-4-yl]pyridine

4-(4-fluorophenyl)-5-(2-fluoropyridin-4-yl)-1,3-dihydro-2H-imidazole-2-thione

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