(2S,4R)-1-[1-(2-phenyl-tetrahydro-pyran-4-yl)-piperidin-4-yl]-1,3-dihydro-benzoimidazol-2-one

Base Information

Chemical Name:(2S,4R)-1-[1-(2-phenyl-tetrahydro-pyran-4-yl)-piperidin-4-yl]-1,3-dihydro-benzoimidazol-2-one
CAS No.:1190840-60-8
Molecular Formula:C₂₃H₂₇N₃O₂
Molecular Weight:377.486
Hs Code.:

Synonyms:(2S,4R)-1-[1-(2-phenyl-tetrahydro-pyran-4-yl)-piperidin-4-yl]-1,3-dihydro-benzoimidazol-2-one

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Chemical Property of (2S,4R)-1-[1-(2-phenyl-tetrahydro-pyran-4-yl)-piperidin-4-yl]-1,3-dihydro-benzoimidazol-2-one

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Technology Process of (2S,4R)-1-[1-(2-phenyl-tetrahydro-pyran-4-yl)-piperidin-4-yl]-1,3-dihydro-benzoimidazol-2-one

There total 4 articles about (2S,4R)-1-[1-(2-phenyl-tetrahydro-pyran-4-yl)-piperidin-4-yl]-1,3-dihydro-benzoimidazol-2-one 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: 35.0%

: 20662-53-7
4-(2-keto-1-benzimidazolinyl)piperidine

: 82110-28-9
(S)-2-phenyl-tetrahydropyran-4-one

: 1190840-60-8
(2S,4R)-1-[1-(2-phenyl-tetrahydro-pyran-4-yl)-piperidin-4-yl]-1,3-dihydro-benzoimidazol-2-one

Guidance literature:: 4-(2-keto-1-benzimidazolinyl)piperidine; (S)-2-phenyl-tetrahydropyran-4-one; With sodium tris(acetoxy)borohydride; acetic acid; In tetrahydrofuran; at 20 ℃;

With di-tert-butyl dicarbonate; sodium hydroxide; In tetrahydrofuran; water; for 0.25h;

Reference yield:

: 82065-19-8,82065-23-4,82110-16-5,82110-20-1,132149-01-0
2-phenyltetrahydro-2H-pyran-4-ol

: 1190840-60-8
(2S,4R)-1-[1-(2-phenyl-tetrahydro-pyran-4-yl)-piperidin-4-yl]-1,3-dihydro-benzoimidazol-2-one

Guidance literature:: Multi-step reaction with 3 steps

1.1: oxalyl dichloride; dimethyl sulfoxide / dichloromethane / 0.5 h / -78 °C

1.2: 3 h / -78 °C

2.1: Chiralcel OD-H / isopropyl alcohol / 40 °C / Resolution of racemate

3.1: sodium tris(acetoxy)borohydride; acetic acid / tetrahydrofuran / 20 °C

3.2: 0.25 h

With oxalyl dichloride; Chiralcel OD-H; sodium tris(acetoxy)borohydride; acetic acid; dimethyl sulfoxide; In tetrahydrofuran; dichloromethane; isopropyl alcohol;

Reference yield:

: 100-52-7
benzaldehyde

: 1190840-60-8
(2S,4R)-1-[1-(2-phenyl-tetrahydro-pyran-4-yl)-piperidin-4-yl]-1,3-dihydro-benzoimidazol-2-one

Guidance literature:: Multi-step reaction with 4 steps

1.1: sulfuric acid / water / 16 h / 5 - 20 °C

2.1: oxalyl dichloride; dimethyl sulfoxide / dichloromethane / 0.5 h / -78 °C

2.2: 3 h / -78 °C

3.1: Chiralcel OD-H / isopropyl alcohol / 40 °C / Resolution of racemate

4.1: sodium tris(acetoxy)borohydride; acetic acid / tetrahydrofuran / 20 °C

4.2: 0.25 h

With oxalyl dichloride; Chiralcel OD-H; sulfuric acid; sodium tris(acetoxy)borohydride; acetic acid; dimethyl sulfoxide; In tetrahydrofuran; dichloromethane; water; isopropyl alcohol;