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

Base Information

Chemical Name:2-(2-(4-fluorobenzylthio)-4-oxo-4,5,6,7-tetrahydro-1H-cyclopenta[d]pyrimidin-1-yl)acetonitrile
CAS No.:1417526-10-3
Molecular Formula:C₁₆H₁₄FN₃OS
Molecular Weight:315.371
Hs Code.:

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

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

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

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

: 1417526-08-9
2-(2-(4-fluorobenzylthio)-4-oxo-4,5,6,7-tetrahydro-1H-cyclopenta[d]pyrimidin-1-yl)acetamide

: 1417526-10-3
2-(2-(4-fluorobenzylthio)-4-oxo-4,5,6,7-tetrahydro-1H-cyclopenta[d]pyrimidin-1-yl)acetonitrile

Guidance literature:: With trifluoroacetic anhydride; In tetrahydrofuran; at -15 ℃; for 0.166667h; Inert atmosphere;

Reference yield:

: 459-46-1
4-Fluorobenzyl bromide

: 1417526-10-3
2-(2-(4-fluorobenzylthio)-4-oxo-4,5,6,7-tetrahydro-1H-cyclopenta[d]pyrimidin-1-yl)acetonitrile

Guidance literature:: Multi-step reaction with 5 steps

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

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

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

4.1: N,N-dimethyl-formamide; thionyl chloride / dichloromethane / 0.5 h / Cooling with ice

4.2: 0.17 h / Cooling with ice

5.1: trifluoroacetic anhydride / tetrahydrofuran / 0.17 h / -15 °C / Inert atmosphere

With thionyl chloride; lithium hydroxide monohydrate; water; potassium carbonate; N-ethyl-N,N-diisopropylamine; N,N-dimethyl-formamide; trifluoroacetic anhydride; potassium iodide; In tetrahydrofuran; dichloromethane; isopropyl alcohol; acetone;

Reference yield:

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

: 1417526-10-3
2-(2-(4-fluorobenzylthio)-4-oxo-4,5,6,7-tetrahydro-1H-cyclopenta[d]pyrimidin-1-yl)acetonitrile

Guidance literature:: Multi-step reaction with 5 steps

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

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

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

4.1: N,N-dimethyl-formamide; thionyl chloride / dichloromethane / 0.5 h / Cooling with ice

4.2: 0.17 h / Cooling with ice

5.1: trifluoroacetic anhydride / tetrahydrofuran / 0.17 h / -15 °C / Inert atmosphere

With thionyl chloride; lithium hydroxide monohydrate; water; potassium carbonate; N-ethyl-N,N-diisopropylamine; N,N-dimethyl-formamide; trifluoroacetic anhydride; potassium iodide; In tetrahydrofuran; dichloromethane; isopropyl alcohol; acetone;