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

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Chemical Name:8-(benzyloxy)-5-{(1R)-1-{[tert-butyl(dimethyl)silyl]oxy}-2-[({4-methyl-1-[2-(2-phenylethoxy)ethyl]piperidin-4-yl}methyl)amino]ethyl}quinolin-2(1H)-one
CAS No.:948894-28-8
Molecular Formula:C₄₁H₅₇N₃O₄Si
Molecular Weight:684.007
Hs Code.:

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

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

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

There total 10 articles about 8-(benzyloxy)-5-{(1R)-1-{[tert-butyl(dimethyl)silyl]oxy}-2-[({4-methyl-1-[2-(2-phenylethoxy)ethyl]piperidin-4-yl}methyl)amino]ethyl}quinolin-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:

: 74121-91-8
(2-Hydroxyethyl)phenylethyl ether

: 948894-28-8
8-(benzyloxy)-5-{(1R)-1-{[tert-butyl(dimethyl)silyl]oxy}-2-[({4-methyl-1-[2-(2-phenylethoxy)ethyl]piperidin-4-yl}methyl)amino]ethyl}quinolin-2(1H)-one

Guidance literature:: Multi-step reaction with 4 steps

1.1: pyridine; dmap / 14 h / 20 °C

2.1: triethylamine / 1-methyl-pyrrolidin-2-one / 3 h / 85 °C

3.1: lithium aluminium tetrahydride / tetrahydrofuran / -78 - 20 °C

3.2: 0 °C

4.1: sodium hydrogencarbonate / sodium iodide / dimethyl sulfoxide / 8 h / 100 °C

With pyridine; dmap; lithium aluminium tetrahydride; sodium hydrogencarbonate; triethylamine; sodium iodide; In tetrahydrofuran; 1-methyl-pyrrolidin-2-one; dimethyl sulfoxide;

Reference yield:

: 81228-03-7
2-phenethyloxyacetic acid

: 948894-28-8
8-(benzyloxy)-5-{(1R)-1-{[tert-butyl(dimethyl)silyl]oxy}-2-[({4-methyl-1-[2-(2-phenylethoxy)ethyl]piperidin-4-yl}methyl)amino]ethyl}quinolin-2(1H)-one

Guidance literature:: Multi-step reaction with 5 steps

1.1: borane-THF / tetrahydrofuran / 1.5 h / 0 - 20 °C

2.1: pyridine; dmap / 14 h / 20 °C

3.1: triethylamine / 1-methyl-pyrrolidin-2-one / 3 h / 85 °C

4.1: lithium aluminium tetrahydride / tetrahydrofuran / -78 - 20 °C

4.2: 0 °C

5.1: sodium hydrogencarbonate / sodium iodide / dimethyl sulfoxide / 8 h / 100 °C

With pyridine; dmap; lithium aluminium tetrahydride; borane-THF; sodium hydrogencarbonate; triethylamine; sodium iodide; In tetrahydrofuran; 1-methyl-pyrrolidin-2-one; dimethyl sulfoxide;

Reference yield:

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

: 948894-28-8
8-(benzyloxy)-5-{(1R)-1-{[tert-butyl(dimethyl)silyl]oxy}-2-[({4-methyl-1-[2-(2-phenylethoxy)ethyl]piperidin-4-yl}methyl)amino]ethyl}quinolin-2(1H)-one

Guidance literature:: Multi-step reaction with 2 steps

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

2: sodium hydrogencarbonate / sodium iodide / dimethyl sulfoxide / 8 h / 100 °C

With 2,6-dimethylpyridine; sodium hydrogencarbonate; sodium iodide; In dimethyl sulfoxide; N,N-dimethyl-formamide;