5-(1-((5-(4-fluorophenyl)pyridin-3-yl)methyl)piperidin-4-yl)-1H-benzo[d]imidazol-2(3H)-one

Base Information

Chemical Name:5-(1-((5-(4-fluorophenyl)pyridin-3-yl)methyl)piperidin-4-yl)-1H-benzo[d]imidazol-2(3H)-one
CAS No.:1581275-09-3
Molecular Formula:C₂₄H₂₃FN₄O
Molecular Weight:402.471
Hs Code.:

Synonyms:5-(1-((5-(4-fluorophenyl)pyridin-3-yl)methyl)piperidin-4-yl)-1H-benzo[d]imidazol-2(3H)-one

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Chemical Property of 5-(1-((5-(4-fluorophenyl)pyridin-3-yl)methyl)piperidin-4-yl)-1H-benzo[d]imidazol-2(3H)-one

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Technology Process of 5-(1-((5-(4-fluorophenyl)pyridin-3-yl)methyl)piperidin-4-yl)-1H-benzo[d]imidazol-2(3H)-one

There total 11 articles about 5-(1-((5-(4-fluorophenyl)pyridin-3-yl)methyl)piperidin-4-yl)-1H-benzo[d]imidazol-2(3H)-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: 62.0%

: 381684-96-4
5-(4-fluorophenyl)nicotinaldehyde

: 1581274-97-6
5-(piperidin-4-yl)-1H-benzo[d]imidazol-2(3H)-one trifluoroacetate

: 1581275-09-3
5-(1-((5-(4-fluorophenyl)pyridin-3-yl)methyl)piperidin-4-yl)-1H-benzo[d]imidazol-2(3H)-one

Guidance literature:: With sodium tris(acetoxy)borohydride; triethylamine; In dimethyl sulfoxide; at 20 ℃; for 6.5h;
DOI:10.3109/14756366.2013.776556

Reference yield: 62.0%

: 1581275-09-3
5-(1-((5-(4-fluorophenyl)pyridin-3-yl)methyl)piperidin-4-yl)-1H-benzo[d]imidazol-2(3H)-one

Guidance literature:: With sodium tris(acetoxy)borohydride; triethylamine; In dimethyl sulfoxide; at 0 - 20 ℃; for 6h;

Reference yield:

: 881-50-5
N-(4-bromo-2-nitrophenyl)acetamide

: 1581275-09-3
5-(1-((5-(4-fluorophenyl)pyridin-3-yl)methyl)piperidin-4-yl)-1H-benzo[d]imidazol-2(3H)-one

Guidance literature:: Multi-step reaction with 7 steps

1: potassium hydroxide / ethanol / 12 h / 80 °C

2: potassium carbonate; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride / N,N-dimethyl-formamide / 80 °C / Inert atmosphere

3: palladium on activated charcoal; hydrogen / tetrahydrofuran; ethanol / 3 h / 517.16 Torr

4: 1,1'-carbonyldiimidazole / tetrahydrofuran / 6 h / 60 °C

5: hydrogen / methanol / 12 h / 3102.97 Torr

6: methanol / dichloromethane / 6 h / 0 °C

7: sodium tris(acetoxy)borohydride; triethylamine / dimethyl sulfoxide / 6.5 h / 20 °C

With methanol; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; palladium on activated charcoal; hydrogen; sodium tris(acetoxy)borohydride; potassium carbonate; triethylamine; 1,1'-carbonyldiimidazole; potassium hydroxide; In tetrahydrofuran; methanol; ethanol; dichloromethane; dimethyl sulfoxide; N,N-dimethyl-formamide; 2: |Suzuki-Miyaura Coupling;
DOI:10.3109/14756366.2013.776556