2-[2-(4-{[4-chloro-3-(trifluoromethyl)phenyl]oxy}phenyl)ethyl]-1-methyl-5-(5-pyrimidinylmethyl)-4(1H)-pyrimidinone

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Chemical Name:2-[2-(4-{[4-chloro-3-(trifluoromethyl)phenyl]oxy}phenyl)ethyl]-1-methyl-5-(5-pyrimidinylmethyl)-4(1H)-pyrimidinone
CAS No.:1380426-78-7
Molecular Formula:C₂₅H₂₀ClF₃N₄O₂
Molecular Weight:500.908
Hs Code.:

Synonyms:2-[2-(4-{[4-chloro-3-(trifluoromethyl)phenyl]oxy}phenyl)ethyl]-1-methyl-5-(5-pyrimidinylmethyl)-4(1H)-pyrimidinone

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Chemical Property of 2-[2-(4-{[4-chloro-3-(trifluoromethyl)phenyl]oxy}phenyl)ethyl]-1-methyl-5-(5-pyrimidinylmethyl)-4(1H)-pyrimidinone

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Technology Process of 2-[2-(4-{[4-chloro-3-(trifluoromethyl)phenyl]oxy}phenyl)ethyl]-1-methyl-5-(5-pyrimidinylmethyl)-4(1H)-pyrimidinone

There total 8 articles about 2-[2-(4-{[4-chloro-3-(trifluoromethyl)phenyl]oxy}phenyl)ethyl]-1-methyl-5-(5-pyrimidinylmethyl)-4(1H)-pyrimidinone 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: 7.8%

: 1380426-75-4
2-[2-(4-{[4-chloro-3-(trifluoromethyl)phenyl]oxy}phenyl)ethyl]-5-(5-pyrimidinylmethyl)-4(1H)-pyrimidinone

: 74-88-4
methyl iodide

: 1380426-78-7
2-[2-(4-{[4-chloro-3-(trifluoromethyl)phenyl]oxy}phenyl)ethyl]-1-methyl-5-(5-pyrimidinylmethyl)-4(1H)-pyrimidinone

Guidance literature:: 2-[2-(4-{[4-chloro-3-(trifluoromethyl)phenyl]oxy}phenyl)ethyl]-5-(5-pyrimidinylmethyl)-4(1H)-pyrimidinone; With N-ethyl-N,N-diisopropylamine; In 1,2-dichloro-ethane; at 20 ℃; for 0.5h;

methyl iodide; In 1,2-dichloro-ethane; at 20 ℃;

Reference yield:

: 866621-24-1,224776-14-1
(E)-methyl 3-(5-pyrimidinyl)acrylate

: 1380426-78-7
2-[2-(4-{[4-chloro-3-(trifluoromethyl)phenyl]oxy}phenyl)ethyl]-1-methyl-5-(5-pyrimidinylmethyl)-4(1H)-pyrimidinone

Guidance literature:: Multi-step reaction with 4 steps

1.1: hydrogen / palladium on activated charcoal / methanol / 50 °C

2.1: potassium tert-butylate / tetrahydrofuran / 4 h / Cooling with ice; Inert atmosphere

2.2: pH 5

3.1: potassium carbonate / 1-methyl-pyrrolidin-2-one / 2 h / 120 °C / Microwave irradiation

4.1: N-ethyl-N,N-diisopropylamine / 1,2-dichloro-ethane / 0.5 h / 20 °C

4.2: 20 °C

With potassium tert-butylate; hydrogen; potassium carbonate; N-ethyl-N,N-diisopropylamine; palladium on activated charcoal; In tetrahydrofuran; 1-methyl-pyrrolidin-2-one; methanol; 1,2-dichloro-ethane;

Reference yield:

: 6294-93-5
4-chloro-3-trifluoromethylphenol

: 1380426-78-7
2-[2-(4-{[4-chloro-3-(trifluoromethyl)phenyl]oxy}phenyl)ethyl]-1-methyl-5-(5-pyrimidinylmethyl)-4(1H)-pyrimidinone

Guidance literature:: Multi-step reaction with 6 steps

1.1: potassium carbonate / N,N-dimethyl-formamide / 0.33 h / 120 °C / Microwave irradiation

2.1: sodium hydroxide / dichloromethane; water / 4 h / 0 - 20 °C

3.1: hydrogen / palladium on activated charcoal / tetrahydrofuran / 25 °C

4.1: methanol; acetyl chloride / toluene / 2.08 h / 0 - 20 °C

4.2: 0 - 20 °C

5.1: potassium carbonate / 1-methyl-pyrrolidin-2-one / 2 h / 120 °C / Microwave irradiation

6.1: N-ethyl-N,N-diisopropylamine / 1,2-dichloro-ethane / 0.5 h / 20 °C

6.2: 20 °C

With methanol; hydrogen; potassium carbonate; N-ethyl-N,N-diisopropylamine; acetyl chloride; sodium hydroxide; palladium on activated charcoal; In tetrahydrofuran; 1-methyl-pyrrolidin-2-one; dichloromethane; water; 1,2-dichloro-ethane; N,N-dimethyl-formamide; toluene; 2.1: Wittig Reaction;