benzyloxy-5-[2-{[1-(2-benzyloxy-ethyl)-4-hydroxy-piperidin-4-ylmethyl]-amino}-(1R)-(tert-butyl-dimethyl-silanyloxy)-ethyl]-1H-quinolin-2-one

Base Information

Chemical Name:benzyloxy-5-[2-{[1-(2-benzyloxy-ethyl)-4-hydroxy-piperidin-4-ylmethyl]-amino}-(1R)-(tert-butyl-dimethyl-silanyloxy)-ethyl]-1H-quinolin-2-one
CAS No.:948894-78-8
Molecular Formula:C₃₉H₅₃N₃O₅Si
Molecular Weight:671.952
Hs Code.:

Synonyms:benzyloxy-5-[2-{[1-(2-benzyloxy-ethyl)-4-hydroxy-piperidin-4-ylmethyl]-amino}-(1R)-(tert-butyl-dimethyl-silanyloxy)-ethyl]-1H-quinolin-2-one

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Chemical Property of benzyloxy-5-[2-{[1-(2-benzyloxy-ethyl)-4-hydroxy-piperidin-4-ylmethyl]-amino}-(1R)-(tert-butyl-dimethyl-silanyloxy)-ethyl]-1H-quinolin-2-one

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Technology Process of benzyloxy-5-[2-{[1-(2-benzyloxy-ethyl)-4-hydroxy-piperidin-4-ylmethyl]-amino}-(1R)-(tert-butyl-dimethyl-silanyloxy)-ethyl]-1H-quinolin-2-one

There total 7 articles about benzyloxy-5-[2-{[1-(2-benzyloxy-ethyl)-4-hydroxy-piperidin-4-ylmethyl]-amino}-(1R)-(tert-butyl-dimethyl-silanyloxy)-ethyl]-1H-quinolin-2-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:

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

: 948894-77-7
4-aminomethyl-1-(2-benzyloxy-ethyl)-piperidin-4-ol

: 948894-78-8
benzyloxy-5-[2-{[1-(2-benzyloxy-ethyl)-4-hydroxy-piperidin-4-ylmethyl]-amino}-(1R)-(tert-butyl-dimethyl-silanyloxy)-ethyl]-1H-quinolin-2-one

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In 1-methyl-pyrrolidin-2-one; at 100 ℃; for 1.5h; Microwave irradiation;

Reference yield:

: 41979-39-9
4-piperidone hydrochloride

: 948894-78-8
benzyloxy-5-[2-{[1-(2-benzyloxy-ethyl)-4-hydroxy-piperidin-4-ylmethyl]-amino}-(1R)-(tert-butyl-dimethyl-silanyloxy)-ethyl]-1H-quinolin-2-one

Guidance literature:: Multi-step reaction with 3 steps

1.1: potassium carbonate / potassium iodide / acetonitrile / 24 h / Heating / reflux

2.1: zinc(II) iodide / 4 h / 0 - 60 °C

2.2: 2 h / 0 °C

2.3: 20 °C

3.1: N-ethyl-N,N-diisopropylamine / 1-methyl-pyrrolidin-2-one / 1.5 h / 100 °C / Microwave irradiation

With potassium carbonate; N-ethyl-N,N-diisopropylamine; zinc(II) iodide; potassium iodide; In 1-methyl-pyrrolidin-2-one; acetonitrile;

Reference yield:

: 1462-37-9
bromoethyl-2-benzyl ether

: 948894-78-8
benzyloxy-5-[2-{[1-(2-benzyloxy-ethyl)-4-hydroxy-piperidin-4-ylmethyl]-amino}-(1R)-(tert-butyl-dimethyl-silanyloxy)-ethyl]-1H-quinolin-2-one

Guidance literature:: Multi-step reaction with 3 steps

1.1: potassium carbonate / potassium iodide / acetonitrile / 24 h / Heating / reflux

2.1: zinc(II) iodide / 4 h / 0 - 60 °C

2.2: 2 h / 0 °C

2.3: 20 °C

3.1: N-ethyl-N,N-diisopropylamine / 1-methyl-pyrrolidin-2-one / 1.5 h / 100 °C / Microwave irradiation

With potassium carbonate; N-ethyl-N,N-diisopropylamine; zinc(II) iodide; potassium iodide; In 1-methyl-pyrrolidin-2-one; acetonitrile;