2-(3-(4-(ethylsulfonyl)phenoxy)-5-((2S,3R)-3-hydroxybutan-2-yloxy)phenyl)pyrimidin-4(3H)-one

Base Information

Chemical Name:2-(3-(4-(ethylsulfonyl)phenoxy)-5-((2S,3R)-3-hydroxybutan-2-yloxy)phenyl)pyrimidin-4(3H)-one
CAS No.:1352570-44-5
Molecular Formula:C₂₂H₂₄N₂O₆S
Molecular Weight:444.508
Hs Code.:

Synonyms:2-(3-(4-(ethylsulfonyl)phenoxy)-5-((2S,3R)-3-hydroxybutan-2-yloxy)phenyl)pyrimidin-4(3H)-one

Suppliers and Price of 2-(3-(4-(ethylsulfonyl)phenoxy)-5-((2S,3R)-3-hydroxybutan-2-yloxy)phenyl)pyrimidin-4(3H)-one

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of 2-(3-(4-(ethylsulfonyl)phenoxy)-5-((2S,3R)-3-hydroxybutan-2-yloxy)phenyl)pyrimidin-4(3H)-one

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 2-(3-(4-(ethylsulfonyl)phenoxy)-5-((2S,3R)-3-hydroxybutan-2-yloxy)phenyl)pyrimidin-4(3H)-one

There total 7 articles about 2-(3-(4-(ethylsulfonyl)phenoxy)-5-((2S,3R)-3-hydroxybutan-2-yloxy)phenyl)pyrimidin-4(3H)-one 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:

: 1352571-49-3
C₃₆H₄₆N₂O₇SSi

: 1352570-44-5
2-(3-(4-(ethylsulfonyl)phenoxy)-5-((2S,3R)-3-hydroxybutan-2-yloxy)phenyl)pyrimidin-4(3H)-one

Guidance literature:: With hydrogenchloride; water; In 1,4-dioxane; methanol; at 20 ℃; for 3h;

Reference yield:

: 136-36-7
benzoate d'hydroxy-3 phenyle

: 1352570-44-5
2-(3-(4-(ethylsulfonyl)phenoxy)-5-((2S,3R)-3-hydroxybutan-2-yloxy)phenyl)pyrimidin-4(3H)-one

Guidance literature:: Multi-step reaction with 7 steps

1: potassium carbonate / N,N-dimethyl-formamide / 90 °C

2: water; lithium hydrochloride monohydrate / tetrahydrofuran / 20 °C

3: 1H-imidazole / dichloromethane / 20 °C

4: 4,4'-di-tert-butyl-2,2'-bipyridine; (1,5-cyclooctadiene)(methoxy)iridium(I) dimer / tert-butyl methyl ether / 16 h / 100 °C / Inert atmosphere; Microwave irradiation; Sealed tube

5: water; sodium carbonate / (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride / acetonitrile / 0.5 h / 140 °C / Inert atmosphere; Microwave irradiation

6: N,N-dimethyl-formamide / 120 °C / Sealed tube

7: hydrogenchloride; water / 1,4-dioxane; methanol / 3 h / 20 °C

With 1H-imidazole; hydrogenchloride; lithium hydrochloride monohydrate; water; sodium carbonate; potassium carbonate; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; (1,5-cyclooctadiene)(methoxy)iridium(I) dimer; 4,4'-di-tert-butyl-2,2'-bipyridine; In tetrahydrofuran; 1,4-dioxane; methanol; dichloromethane; tert-butyl methyl ether; N,N-dimethyl-formamide; acetonitrile; 5: Suzuki Coupling;

Reference yield:

: 1352571-35-7
3-((2S,3R)-3-hydroxybutan-2-yloxy)phenol

: 1352570-44-5
2-(3-(4-(ethylsulfonyl)phenoxy)-5-((2S,3R)-3-hydroxybutan-2-yloxy)phenyl)pyrimidin-4(3H)-one

Guidance literature:: Multi-step reaction with 5 steps

1: 1H-imidazole / dichloromethane / 20 °C

2: 4,4'-di-tert-butyl-2,2'-bipyridine; (1,5-cyclooctadiene)(methoxy)iridium(I) dimer / tert-butyl methyl ether / 16 h / 100 °C / Inert atmosphere; Microwave irradiation; Sealed tube

3: water; sodium carbonate / (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride / acetonitrile / 0.5 h / 140 °C / Inert atmosphere; Microwave irradiation

4: N,N-dimethyl-formamide / 120 °C / Sealed tube

5: hydrogenchloride; water / 1,4-dioxane; methanol / 3 h / 20 °C

With 1H-imidazole; hydrogenchloride; water; sodium carbonate; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; (1,5-cyclooctadiene)(methoxy)iridium(I) dimer; 4,4'-di-tert-butyl-2,2'-bipyridine; In 1,4-dioxane; methanol; dichloromethane; tert-butyl methyl ether; N,N-dimethyl-formamide; acetonitrile; 3: Suzuki Coupling;