tert-butyl 4-(1-(4-(methylsulfonyl)phenyl)-2-oxo-1,2-dihydropyridin-4-yloxy)piperidine-1-carboxylate

Base Information

Chemical Name:tert-butyl 4-(1-(4-(methylsulfonyl)phenyl)-2-oxo-1,2-dihydropyridin-4-yloxy)piperidine-1-carboxylate
CAS No.:1104441-97-5
Molecular Formula:C₂₂H₂₈N₂O₆S
Molecular Weight:448.54
Hs Code.:

Synonyms:tert-butyl 4-(1-(4-(methylsulfonyl)phenyl)-2-oxo-1,2-dihydropyridin-4-yloxy)piperidine-1-carboxylate

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Chemical Property of tert-butyl 4-(1-(4-(methylsulfonyl)phenyl)-2-oxo-1,2-dihydropyridin-4-yloxy)piperidine-1-carboxylate

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Technology Process of tert-butyl 4-(1-(4-(methylsulfonyl)phenyl)-2-oxo-1,2-dihydropyridin-4-yloxy)piperidine-1-carboxylate

There total 5 articles about tert-butyl 4-(1-(4-(methylsulfonyl)phenyl)-2-oxo-1,2-dihydropyridin-4-yloxy)piperidine-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: 67.0%

: 1104442-05-8
4-hydroxy-1-(4-(methylsulfonyl)phenyl)pyridin-2(1H)-one

: 141699-59-4
1-(tert-butoxycarbonyl)piperidin-4-yl methanesulfonate

: 1104441-97-5
tert-butyl 4-(1-(4-(methylsulfonyl)phenyl)-2-oxo-1,2-dihydropyridin-4-yloxy)piperidine-1-carboxylate

Guidance literature:: With potassium carbonate; In N,N-dimethyl-formamide; at 90 ℃;

Reference yield:

: 53937-02-3
4-(benzyloxy)pyridin-2(1H)-one

: 1104441-97-5
tert-butyl 4-(1-(4-(methylsulfonyl)phenyl)-2-oxo-1,2-dihydropyridin-4-yloxy)piperidine-1-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1: copper(l) iodide; 8-quinolinol; potassium carbonate / dimethyl sulfoxide / 4 h / 145 °C / Inert atmosphere

2: palladium 10% on activated carbon; hydrogen / tetrahydrofuran; methanol / 1.5 h / 760.05 Torr / Inert atmosphere

3: potassium carbonate / N,N-dimethyl-formamide / 90 °C / Inert atmosphere

With copper(l) iodide; 8-quinolinol; palladium 10% on activated carbon; hydrogen; potassium carbonate; In tetrahydrofuran; methanol; dimethyl sulfoxide; N,N-dimethyl-formamide;
DOI:10.1021/jm501175v

Reference yield:

: 3466-32-8
4-bromoohenyl methyl sulfone

: 1104441-97-5
tert-butyl 4-(1-(4-(methylsulfonyl)phenyl)-2-oxo-1,2-dihydropyridin-4-yloxy)piperidine-1-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1: copper(l) iodide; 8-quinolinol; potassium carbonate / dimethyl sulfoxide / 4 h / 145 °C / Inert atmosphere

2: palladium 10% on activated carbon; hydrogen / tetrahydrofuran; methanol / 1.5 h / 760.05 Torr / Inert atmosphere

3: potassium carbonate / N,N-dimethyl-formamide / 90 °C / Inert atmosphere

With copper(l) iodide; 8-quinolinol; palladium 10% on activated carbon; hydrogen; potassium carbonate; In tetrahydrofuran; methanol; dimethyl sulfoxide; N,N-dimethyl-formamide;
DOI:10.1021/jm501175v