2-[2-(4-chloro-phenyl)-5-methyl-pyrimidin-4-yl]-5-[hydroxy-(tetrahydro-pyran-4-yl)methyl]-3-methoxy-cyclopent-2-enone

Base Information

Chemical Name:2-[2-(4-chloro-phenyl)-5-methyl-pyrimidin-4-yl]-5-[hydroxy-(tetrahydro-pyran-4-yl)methyl]-3-methoxy-cyclopent-2-enone
CAS No.:1262512-40-2
Molecular Formula:C₂₃H₂₅ClN₂O₄
Molecular Weight:428.915
Hs Code.:

Synonyms:2-[2-(4-chloro-phenyl)-5-methyl-pyrimidin-4-yl]-5-[hydroxy-(tetrahydro-pyran-4-yl)methyl]-3-methoxy-cyclopent-2-enone

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Chemical Property of 2-[2-(4-chloro-phenyl)-5-methyl-pyrimidin-4-yl]-5-[hydroxy-(tetrahydro-pyran-4-yl)methyl]-3-methoxy-cyclopent-2-enone

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Technology Process of 2-[2-(4-chloro-phenyl)-5-methyl-pyrimidin-4-yl]-5-[hydroxy-(tetrahydro-pyran-4-yl)methyl]-3-methoxy-cyclopent-2-enone

There total 5 articles about 2-[2-(4-chloro-phenyl)-5-methyl-pyrimidin-4-yl]-5-[hydroxy-(tetrahydro-pyran-4-yl)methyl]-3-methoxy-cyclopent-2-enone 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: 53.0%

: 50675-18-8
3,4,5,6-tetrahydro-2H-pyran-4-carbaldehyde

: 1262512-38-8
2-[2-(4-chloro-phenyl)-5-methyl-pyrimidin-4-yl]-3-methoxy-cyclopent-2-enone

: 1262512-40-2
2-[2-(4-chloro-phenyl)-5-methyl-pyrimidin-4-yl]-5-[hydroxy-(tetrahydro-pyran-4-yl)methyl]-3-methoxy-cyclopent-2-enone

Guidance literature:: 2-[2-(4-chloro-phenyl)-5-methyl-pyrimidin-4-yl]-3-methoxy-cyclopent-2-enone; With lithium diisopropyl amide; In tetrahydrofuran; hexane; ethylbenzene; at -78 ℃; for 0.75h; Inert atmosphere;

3,4,5,6-tetrahydro-2H-pyran-4-carbaldehyde; In tetrahydrofuran; hexane; ethylbenzene; at -78 - 20 ℃;

With water; ammonium chloride; In tetrahydrofuran; hexane; ethylbenzene; ethyl acetate;

Reference yield:

: 115297-57-9
4-chlorobenzene-1-carboximidamide hydrogeniodide

: 1262512-40-2
2-[2-(4-chloro-phenyl)-5-methyl-pyrimidin-4-yl]-5-[hydroxy-(tetrahydro-pyran-4-yl)methyl]-3-methoxy-cyclopent-2-enone

Guidance literature:: Multi-step reaction with 5 steps

1.1: ethanol; sodium / 1 h / 20 °C / Inert atmosphere

1.2: 20 °C

1.3: pH 1

2.1: trichlorophosphate / 2 h / Reflux

3.1: potassium phosphate / palladium diacetate; XPhos / 1,4-dioxane / 0.5 h / 150 °C / microwave irradiation

4.1: potassium carbonate / acetone / 0.08 h / 20 °C

4.2: 3 h / Reflux

5.1: lithium diisopropyl amide / tetrahydrofuran; hexane; ethylbenzene / 0.75 h / -78 °C / Inert atmosphere

5.2: -78 - 20 °C

With potassium phosphate; ethanol; sodium; potassium carbonate; lithium diisopropyl amide; trichlorophosphate; palladium diacetate; XPhos; In tetrahydrofuran; 1,4-dioxane; hexane; ethylbenzene; acetone;

Reference yield:

: 180606-47-7
2-(4-chloro-phenyl)-5-methyl-3H-pyrimidin-4-one

: 1262512-40-2
2-[2-(4-chloro-phenyl)-5-methyl-pyrimidin-4-yl]-5-[hydroxy-(tetrahydro-pyran-4-yl)methyl]-3-methoxy-cyclopent-2-enone

Guidance literature:: Multi-step reaction with 4 steps

1.1: trichlorophosphate / 2 h / Reflux

2.1: potassium phosphate / palladium diacetate; XPhos / 1,4-dioxane / 0.5 h / 150 °C / microwave irradiation

3.1: potassium carbonate / acetone / 0.08 h / 20 °C

3.2: 3 h / Reflux

4.1: lithium diisopropyl amide / tetrahydrofuran; hexane; ethylbenzene / 0.75 h / -78 °C / Inert atmosphere

4.2: -78 - 20 °C

With potassium phosphate; potassium carbonate; lithium diisopropyl amide; trichlorophosphate; palladium diacetate; XPhos; In tetrahydrofuran; 1,4-dioxane; hexane; ethylbenzene; acetone;