tert-butyl 4-((6-(4-(methylsulfonyl)phenyl)pyridine-3-yloxy)methyl)piperidin-1-carboxylate

Base Information

Chemical Name:tert-butyl 4-((6-(4-(methylsulfonyl)phenyl)pyridine-3-yloxy)methyl)piperidin-1-carboxylate
CAS No.:1010113-01-5
Molecular Formula:C₂₃H₃₀N₂O₅S
Molecular Weight:446.568
Hs Code.:

Synonyms:tert-butyl 4-((6-(4-(methylsulfonyl)phenyl)pyridine-3-yloxy)methyl)piperidin-1-carboxylate

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

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Chemical Property of tert-butyl 4-((6-(4-(methylsulfonyl)phenyl)pyridine-3-yloxy)methyl)piperidin-1-carboxylate

Chemical Property:

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Technology Process of tert-butyl 4-((6-(4-(methylsulfonyl)phenyl)pyridine-3-yloxy)methyl)piperidin-1-carboxylate

There total 7 articles about tert-butyl 4-((6-(4-(methylsulfonyl)phenyl)pyridine-3-yloxy)methyl)piperidin-1-carboxylate 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: 88.0%

: 1010113-01-5
tert-butyl 4-((6-(4-(methylsulfonyl)phenyl)pyridine-3-yloxy)methyl)piperidin-1-carboxylate

Guidance literature:

Reference yield: 73.0%

: 1010115-38-4
tert-butyl 4-(((6-chloropyridin-3-yl)oxy)methyl)piperidine-1-carboxylate

: 149104-88-1
4-methanesulphonylphenylboronic acid

: 1010113-01-5
tert-butyl 4-((6-(4-(methylsulfonyl)phenyl)pyridine-3-yloxy)methyl)piperidin-1-carboxylate

Guidance literature:: With dichloro[1,1′-bis[bis(1,1-dimethylethyl)phosphino]ferrocene-P,P′]palladium; caesium carbonate; In 1,4-dioxane; water; for 2h; Reflux;

Reference yield:

: 24424-99-5
di-tert-butyl dicarbonate

: 1010113-01-5
tert-butyl 4-((6-(4-(methylsulfonyl)phenyl)pyridine-3-yloxy)methyl)piperidin-1-carboxylate

Guidance literature:: Multi-step reaction with 4 steps

1: dichloromethane / 3 h / 20 °C / Cooling with ice

2: triethylamine / dichloromethane / 15 h / 20 °C / Cooling with ice

3: caesium carbonate / acetonitrile / 3 h / Reflux

4: caesium carbonate; dichloro[1,1′-bis[bis(1,1-dimethylethyl)phosphino]ferrocene-P,P′]palladium / 1,4-dioxane / 2 h / Reflux

With dichloro[1,1′-bis[bis(1,1-dimethylethyl)phosphino]ferrocene-P,P′]palladium; caesium carbonate; triethylamine; In 1,4-dioxane; dichloromethane; acetonitrile; 4: |Suzuki Coupling;