4-(1-(5-bromopyrimidin-2-yl)piperidin-4-yloxy)-1-(4-(methylsulfonyl)phenyl)pyridin-2(1H)-one

Base Information

Chemical Name:4-(1-(5-bromopyrimidin-2-yl)piperidin-4-yloxy)-1-(4-(methylsulfonyl)phenyl)pyridin-2(1H)-one
CAS No.:1104444-75-8
Molecular Formula:C₂₁H₂₁BrN₄O₄S
Molecular Weight:505.392
Hs Code.:

Synonyms:4-(1-(5-bromopyrimidin-2-yl)piperidin-4-yloxy)-1-(4-(methylsulfonyl)phenyl)pyridin-2(1H)-one

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Chemical Property of 4-(1-(5-bromopyrimidin-2-yl)piperidin-4-yloxy)-1-(4-(methylsulfonyl)phenyl)pyridin-2(1H)-one

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Technology Process of 4-(1-(5-bromopyrimidin-2-yl)piperidin-4-yloxy)-1-(4-(methylsulfonyl)phenyl)pyridin-2(1H)-one

There total 9 articles about 4-(1-(5-bromopyrimidin-2-yl)piperidin-4-yloxy)-1-(4-(methylsulfonyl)phenyl)pyridin-2(1H)-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: 92.0%

: 1104442-13-8
1-(4-(methylsulfonyl)phenyl)-4-(piperidin-4-yloxy)pyridin-2(1H)-one hydrochloride

: 32779-36-5
5-Bromo-2-chloropyrimidine

: 1104444-75-8
4-(1-(5-bromopyrimidin-2-yl)piperidin-4-yloxy)-1-(4-(methylsulfonyl)phenyl)pyridin-2(1H)-one

Guidance literature:: With hydrogenchloride; potassium carbonate; In N,N-dimethyl-formamide; at 80 ℃; for 18h; Inert atmosphere;
DOI:10.1021/jm501175v

Reference yield:

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

: 1104444-75-8
4-(1-(5-bromopyrimidin-2-yl)piperidin-4-yloxy)-1-(4-(methylsulfonyl)phenyl)pyridin-2(1H)-one

Guidance literature:: Multi-step reaction with 2 steps

1: hydrogenchloride / methanol; dichloromethane / 0.83 h / 20 °C / Inert atmosphere

2: potassium carbonate; hydrogenchloride / N,N-dimethyl-formamide / 18 h / 80 °C / Inert atmosphere

With hydrogenchloride; potassium carbonate; In methanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jm501175v

Reference yield:

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

: 1104444-75-8
4-(1-(5-bromopyrimidin-2-yl)piperidin-4-yloxy)-1-(4-(methylsulfonyl)phenyl)pyridin-2(1H)-one

Guidance literature:: Multi-step reaction with 5 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

4: hydrogenchloride / methanol; dichloromethane / 0.83 h / 20 °C / Inert atmosphere

5: potassium carbonate; hydrogenchloride / N,N-dimethyl-formamide / 18 h / 80 °C / Inert atmosphere

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