ethyl 2-{[(4-{[4-chloro-3-(trifluoromethyl)phenyl]oxy}phenyl)methyl]thio}-4-oxo-1,4-dihydro-5-pyrimidinecarboxylate

Base Information

Chemical Name:ethyl 2-{[(4-{[4-chloro-3-(trifluoromethyl)phenyl]oxy}phenyl)methyl]thio}-4-oxo-1,4-dihydro-5-pyrimidinecarboxylate
CAS No.:1380429-72-0
Molecular Formula:C₂₁H₁₆ClF₃N₂O₄S
Molecular Weight:484.883
Hs Code.:

Synonyms:ethyl 2-{[(4-{[4-chloro-3-(trifluoromethyl)phenyl]oxy}phenyl)methyl]thio}-4-oxo-1,4-dihydro-5-pyrimidinecarboxylate

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Chemical Property of ethyl 2-{[(4-{[4-chloro-3-(trifluoromethyl)phenyl]oxy}phenyl)methyl]thio}-4-oxo-1,4-dihydro-5-pyrimidinecarboxylate

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Technology Process of ethyl 2-{[(4-{[4-chloro-3-(trifluoromethyl)phenyl]oxy}phenyl)methyl]thio}-4-oxo-1,4-dihydro-5-pyrimidinecarboxylate

There total 5 articles about ethyl 2-{[(4-{[4-chloro-3-(trifluoromethyl)phenyl]oxy}phenyl)methyl]thio}-4-oxo-1,4-dihydro-5-pyrimidinecarboxylate 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: 100.0%

: 38026-46-9
ethyl 4-oxo-2-thioxo-1,2,3,4-tetrahydropyrimidine-5-carboxilate

: 1369255-78-6
1-chloro-4-(4-(chloromethyl)phenoxy)-2-(trifluoromethyl)benzene

: 1380429-72-0
ethyl 2-{[(4-{[4-chloro-3-(trifluoromethyl)phenyl]oxy}phenyl)methyl]thio}-4-oxo-1,4-dihydro-5-pyrimidinecarboxylate

Guidance literature:: With potassium carbonate; In N,N-dimethyl-formamide; at 80 ℃; for 0.5h; Microwave irradiation;

Reference yield:

: 459-57-4
4-fluorobenzaldehyde

: 1380429-72-0
ethyl 2-{[(4-{[4-chloro-3-(trifluoromethyl)phenyl]oxy}phenyl)methyl]thio}-4-oxo-1,4-dihydro-5-pyrimidinecarboxylate

Guidance literature:: Multi-step reaction with 4 steps

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

2: methanol; sodium tetrahydroborate / 20 °C

3: thionyl chloride / dichloromethane / 1.5 h / 20 °C

4: potassium carbonate / N,N-dimethyl-formamide / 0.5 h / 80 °C / Microwave irradiation

With methanol; sodium tetrahydroborate; thionyl chloride; potassium carbonate; In dichloromethane; N,N-dimethyl-formamide;

Reference yield:

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

: 1380429-72-0
ethyl 2-{[(4-{[4-chloro-3-(trifluoromethyl)phenyl]oxy}phenyl)methyl]thio}-4-oxo-1,4-dihydro-5-pyrimidinecarboxylate

Guidance literature:: Multi-step reaction with 4 steps

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

2: methanol; sodium tetrahydroborate / 20 °C

3: thionyl chloride / dichloromethane / 1.5 h / 20 °C

4: potassium carbonate / N,N-dimethyl-formamide / 0.5 h / 80 °C / Microwave irradiation

With methanol; sodium tetrahydroborate; thionyl chloride; potassium carbonate; In dichloromethane; N,N-dimethyl-formamide;