5-{(1R)-1-{[tert-butyl(dimethyl)silyl]oxy}-2-[({4-hydroxy-1-[2-(2-phenylethoxy)ethyl]piperidin-4-yl}methyl)amino]ethyl}-8-hydroxyquinolin-2(1H)-one

Base Information

Chemical Name:5-{(1R)-1-{[tert-butyl(dimethyl)silyl]oxy}-2-[({4-hydroxy-1-[2-(2-phenylethoxy)ethyl]piperidin-4-yl}methyl)amino]ethyl}-8-hydroxyquinolin-2(1H)-one
CAS No.:948893-93-4
Molecular Formula:C₃₃H₄₉N₃O₅Si
Molecular Weight:595.855
Hs Code.:

Synonyms:5-{(1R)-1-{[tert-butyl(dimethyl)silyl]oxy}-2-[({4-hydroxy-1-[2-(2-phenylethoxy)ethyl]piperidin-4-yl}methyl)amino]ethyl}-8-hydroxyquinolin-2(1H)-one

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Chemical Property of 5-{(1R)-1-{[tert-butyl(dimethyl)silyl]oxy}-2-[({4-hydroxy-1-[2-(2-phenylethoxy)ethyl]piperidin-4-yl}methyl)amino]ethyl}-8-hydroxyquinolin-2(1H)-one

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Technology Process of 5-{(1R)-1-{[tert-butyl(dimethyl)silyl]oxy}-2-[({4-hydroxy-1-[2-(2-phenylethoxy)ethyl]piperidin-4-yl}methyl)amino]ethyl}-8-hydroxyquinolin-2(1H)-one

There total 12 articles about 5-{(1R)-1-{[tert-butyl(dimethyl)silyl]oxy}-2-[({4-hydroxy-1-[2-(2-phenylethoxy)ethyl]piperidin-4-yl}methyl)amino]ethyl}-8-hydroxyquinolin-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:

: 743461-21-4
5-((1R)-2-amino-1-{[tert-butyl(dimethyl)silyl]oxy}ethyl)-8-hydroxyquinolin-2(1H)-one

: 948893-92-3
6-[2-(2-phenylethoxy)ethyl]-1-oxa-6-azaspiro[2.5]octane

: 948893-93-4
5-{(1R)-1-{[tert-butyl(dimethyl)silyl]oxy}-2-[({4-hydroxy-1-[2-(2-phenylethoxy)ethyl]piperidin-4-yl}methyl)amino]ethyl}-8-hydroxyquinolin-2(1H)-one

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In methanol; for 72h; Heating / reflux;

Reference yield:

: 530084-79-8
8-(benzyloxy)-5-[(1R)-2-bromo-1-hydroxyethyl]quinolin-2(1H)-one

: 948893-93-4
5-{(1R)-1-{[tert-butyl(dimethyl)silyl]oxy}-2-[({4-hydroxy-1-[2-(2-phenylethoxy)ethyl]piperidin-4-yl}methyl)amino]ethyl}-8-hydroxyquinolin-2(1H)-one

Guidance literature:: Multi-step reaction with 4 steps

1: 2,6-dimethylpyridine / N,N-dimethyl-formamide / 0 - 20 °C

2: sodium azide; sodium iodide / dimethyl sulfoxide / 3 h / 65 °C

3: hydrogen / palladium 10% on activated carbon / ethanol / 4 h / 3750.38 Torr

4: N-ethyl-N,N-diisopropylamine / methanol / 72 h / Heating / reflux

With 2,6-dimethylpyridine; sodium azide; hydrogen; N-ethyl-N,N-diisopropylamine; sodium iodide; palladium 10% on activated carbon; In methanol; ethanol; dimethyl sulfoxide; N,N-dimethyl-formamide;

Reference yield:

: 530084-74-3
(R)-8-(benzyloxy)-5-(2-bromo-1-((tert-butyldimethylsilyl)oxy)ethyl)quinolin-2(1H)-one

: 948893-93-4
5-{(1R)-1-{[tert-butyl(dimethyl)silyl]oxy}-2-[({4-hydroxy-1-[2-(2-phenylethoxy)ethyl]piperidin-4-yl}methyl)amino]ethyl}-8-hydroxyquinolin-2(1H)-one

Guidance literature:: Multi-step reaction with 3 steps

1: sodium azide; sodium iodide / dimethyl sulfoxide / 3 h / 65 °C

2: hydrogen / palladium 10% on activated carbon / ethanol / 4 h / 3750.38 Torr

3: N-ethyl-N,N-diisopropylamine / methanol / 72 h / Heating / reflux

With sodium azide; hydrogen; N-ethyl-N,N-diisopropylamine; sodium iodide; palladium 10% on activated carbon; In methanol; ethanol; dimethyl sulfoxide;