2-(4-fluorobenzylthio)-1-((5-phenyl-1H-imidazol-2-yl)methyl)-6,7-dihydro-1H-cyclopenta[d]pyrimidin-4(5H)-one

Base Information

Chemical Name:2-(4-fluorobenzylthio)-1-((5-phenyl-1H-imidazol-2-yl)methyl)-6,7-dihydro-1H-cyclopenta[d]pyrimidin-4(5H)-one
CAS No.:1417531-17-9
Molecular Formula:C₂₄H₂₁FN₄OS
Molecular Weight:432.521
Hs Code.:

Synonyms:2-(4-fluorobenzylthio)-1-((5-phenyl-1H-imidazol-2-yl)methyl)-6,7-dihydro-1H-cyclopenta[d]pyrimidin-4(5H)-one

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Chemical Property of 2-(4-fluorobenzylthio)-1-((5-phenyl-1H-imidazol-2-yl)methyl)-6,7-dihydro-1H-cyclopenta[d]pyrimidin-4(5H)-one

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Technology Process of 2-(4-fluorobenzylthio)-1-((5-phenyl-1H-imidazol-2-yl)methyl)-6,7-dihydro-1H-cyclopenta[d]pyrimidin-4(5H)-one

There total 6 articles about 2-(4-fluorobenzylthio)-1-((5-phenyl-1H-imidazol-2-yl)methyl)-6,7-dihydro-1H-cyclopenta[d]pyrimidin-4(5H)-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:

: 1417526-26-1
2-oxo-2-phenylethyl 2-(2-(4-fluorobenzylthio)-4-oxo-4,5,6,7-tetrahydro-1H-cyclopenta[d]pyrimidin-1-yl)acetate

: 1417531-17-9
2-(4-fluorobenzylthio)-1-((5-phenyl-1H-imidazol-2-yl)methyl)-6,7-dihydro-1H-cyclopenta[d]pyrimidin-4(5H)-one

Guidance literature:: With ammonium acetate; In toluene; for 1.5h; Dean-Stark; Inert atmosphere; Reflux;

Reference yield:

: 459-46-1
4-Fluorobenzyl bromide

: 1417531-17-9
2-(4-fluorobenzylthio)-1-((5-phenyl-1H-imidazol-2-yl)methyl)-6,7-dihydro-1H-cyclopenta[d]pyrimidin-4(5H)-one

Guidance literature:: Multi-step reaction with 5 steps

1: potassium carbonate; potassium iodide / acetone / 2 h / Reflux

2: N-ethyl-N,N-diisopropylamine / tetrahydrofuran / Inert atmosphere; Reflux

3: water; lithium hydroxide monohydrate / isopropyl alcohol / 2 h / 20 °C

4: potassium carbonate / acetone / 6 h / 20 °C

5: ammonium acetate / toluene / 1.5 h / Dean-Stark; Inert atmosphere; Reflux

With lithium hydroxide monohydrate; ammonium acetate; water; potassium carbonate; N-ethyl-N,N-diisopropylamine; potassium iodide; In tetrahydrofuran; isopropyl alcohol; acetone; toluene;

Reference yield:

: 35563-27-0
2-sulfanylidene-1,2,3,4,6,7-hexahydro-5H-cyclopenta[d]pyrimidin-4-one

: 1417531-17-9
2-(4-fluorobenzylthio)-1-((5-phenyl-1H-imidazol-2-yl)methyl)-6,7-dihydro-1H-cyclopenta[d]pyrimidin-4(5H)-one

Guidance literature:: Multi-step reaction with 5 steps

1: potassium carbonate; potassium iodide / acetone / 2 h / Reflux

2: N-ethyl-N,N-diisopropylamine / tetrahydrofuran / Inert atmosphere; Reflux

3: water; lithium hydroxide monohydrate / isopropyl alcohol / 2 h / 20 °C

4: potassium carbonate / acetone / 6 h / 20 °C

5: ammonium acetate / toluene / 1.5 h / Dean-Stark; Inert atmosphere; Reflux

With lithium hydroxide monohydrate; ammonium acetate; water; potassium carbonate; N-ethyl-N,N-diisopropylamine; potassium iodide; In tetrahydrofuran; isopropyl alcohol; acetone; toluene;