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

Base Information

Chemical Name:2-oxo-2-phenylethyl 2-(2-(4-fluorobenzylthio)-4-oxo-4,5,6,7-tetrahydro-1H-cyclopenta[d]pyrimidin-1-yl)acetate
CAS No.:1417526-26-1
Molecular Formula:C₂₄H₂₁FN₂O₄S
Molecular Weight:452.506
Hs Code.:

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

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Chemical Property of 2-oxo-2-phenylethyl 2-(2-(4-fluorobenzylthio)-4-oxo-4,5,6,7-tetrahydro-1H-cyclopenta[d]pyrimidin-1-yl)acetate

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Technology Process of 2-oxo-2-phenylethyl 2-(2-(4-fluorobenzylthio)-4-oxo-4,5,6,7-tetrahydro-1H-cyclopenta[d]pyrimidin-1-yl)acetate

There total 5 articles about 2-oxo-2-phenylethyl 2-(2-(4-fluorobenzylthio)-4-oxo-4,5,6,7-tetrahydro-1H-cyclopenta[d]pyrimidin-1-yl)acetate 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:

: 70-11-1
α-bromoacetophenone

: 356058-42-9
{2-[(4-fluorobenzyl)sulfanyl]-4-oxo-4,5,6,7-tetrahydro-1H-cyclopenta[d]pyrimidin-1-yl}acetic acid

: 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

Guidance literature:: With potassium carbonate; In acetone; at 20 ℃; for 6h;

Reference yield:

: 459-46-1
4-Fluorobenzyl bromide

: 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

Guidance literature:: Multi-step reaction with 4 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

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

Reference yield:

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

: 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

Guidance literature:: Multi-step reaction with 4 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

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