2-(5-((1-(methylsulfonyl)piperidin-4-yl)oxy)-2-(2-oxo-2-(4-(2-oxo-3,4-dihydroquinolin-1(2H)-yl)piperidin-1-yl)ethyl)phenoxy)ethyl 4-methylbenzenesulfonate

Base Information

Chemical Name:2-(5-((1-(methylsulfonyl)piperidin-4-yl)oxy)-2-(2-oxo-2-(4-(2-oxo-3,4-dihydroquinolin-1(2H)-yl)piperidin-1-yl)ethyl)phenoxy)ethyl 4-methylbenzenesulfonate
CAS No.:1369358-11-1
Molecular Formula:C₃₇H₄₅N₃O₉S₂
Molecular Weight:739.911
Hs Code.:

2-(5-((1-(methylsulfonyl)piperidin-4-yl)oxy)-2-(2-oxo-2-(4-(2-oxo-3,4-dihydroquinolin-1(2H)-yl)piperidin-1-yl)ethyl)phenoxy)ethyl 4-methylbenzenesulfonate

Synonyms:2-(5-((1-(methylsulfonyl)piperidin-4-yl)oxy)-2-(2-oxo-2-(4-(2-oxo-3,4-dihydroquinolin-1(2H)-yl)piperidin-1-yl)ethyl)phenoxy)ethyl 4-methylbenzenesulfonate

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Chemical Property of 2-(5-((1-(methylsulfonyl)piperidin-4-yl)oxy)-2-(2-oxo-2-(4-(2-oxo-3,4-dihydroquinolin-1(2H)-yl)piperidin-1-yl)ethyl)phenoxy)ethyl 4-methylbenzenesulfonate

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Technology Process of 2-(5-((1-(methylsulfonyl)piperidin-4-yl)oxy)-2-(2-oxo-2-(4-(2-oxo-3,4-dihydroquinolin-1(2H)-yl)piperidin-1-yl)ethyl)phenoxy)ethyl 4-methylbenzenesulfonate

There total 9 articles about 2-(5-((1-(methylsulfonyl)piperidin-4-yl)oxy)-2-(2-oxo-2-(4-(2-oxo-3,4-dihydroquinolin-1(2H)-yl)piperidin-1-yl)ethyl)phenoxy)ethyl 4-methylbenzenesulfonate 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: 70.0%

: 1369358-09-7
1-(1-(2-(2-hydroxy-4-(1-(methylsulfonyl)piperidin-4-yloxy)phenyl)acetyl)piperidin-4-yl)-3,4-dihydroquinolin-2(1H)-one

: 6315-52-2
1,2-bis-tosyloxyethane

: 1369358-11-1
2-(5-((1-(methylsulfonyl)piperidin-4-yl)oxy)-2-(2-oxo-2-(4-(2-oxo-3,4-dihydroquinolin-1(2H)-yl)piperidin-1-yl)ethyl)phenoxy)ethyl 4-methylbenzenesulfonate

Guidance literature:: With caesium carbonate; In N,N-dimethyl-formamide; at 20 ℃; for 16h; Inert atmosphere;
DOI:10.1016/j.bmc.2012.02.019

Reference yield:

: 1369358-04-2
2-(4-(1-(tert-butoxycarbonyl)piperidin-4-yloxy)-2-(methoxymethoxy)phenyl)acetic acid

: 1369358-11-1
2-(5-((1-(methylsulfonyl)piperidin-4-yl)oxy)-2-(2-oxo-2-(4-(2-oxo-3,4-dihydroquinolin-1(2H)-yl)piperidin-1-yl)ethyl)phenoxy)ethyl 4-methylbenzenesulfonate

Guidance literature:: Multi-step reaction with 4 steps

1: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 19 h / 20 °C / Inert atmosphere

2: hydrogenchloride / diethyl ether; dichloromethane / 12 h / 20 °C / Inert atmosphere

3: triethylamine / dichloromethane / 14 h / 20 °C

4: caesium carbonate / N,N-dimethyl-formamide / 16 h / 20 °C / Inert atmosphere

With hydrogenchloride; benzotriazol-1-ol; caesium carbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; N-ethyl-N,N-diisopropylamine; In diethyl ether; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/j.bmc.2012.02.019

Reference yield:

: 1369358-02-0
tert-butyl 4-(4-acetyl-3-(methoxymethoxy)phenoxy)piperidine-1-carboxylate

: 1369358-11-1
2-(5-((1-(methylsulfonyl)piperidin-4-yl)oxy)-2-(2-oxo-2-(4-(2-oxo-3,4-dihydroquinolin-1(2H)-yl)piperidin-1-yl)ethyl)phenoxy)ethyl 4-methylbenzenesulfonate

Guidance literature:: Multi-step reaction with 6 steps

1: sulfur / 5 h / 135 - 140 °C

2: sodium hydroxide / methanol; water / 24 h / Reflux

3: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 19 h / 20 °C / Inert atmosphere

4: hydrogenchloride / diethyl ether; dichloromethane / 12 h / 20 °C / Inert atmosphere

5: triethylamine / dichloromethane / 14 h / 20 °C

6: caesium carbonate / N,N-dimethyl-formamide / 16 h / 20 °C / Inert atmosphere

With hydrogenchloride; benzotriazol-1-ol; caesium carbonate; sulfur; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; N-ethyl-N,N-diisopropylamine; sodium hydroxide; In methanol; diethyl ether; dichloromethane; water; N,N-dimethyl-formamide; 1: Wilgerodt-Kindler reaction;
DOI:10.1016/j.bmc.2012.02.019