trans-{4-[(1RS)-1-hydroxy-2-(7-methoxy-2-oxo-2H-quinolin-1-yl)ethyl]cyclohexyl}carbamic acid benzyl ester

Base Information

Chemical Name:trans-{4-[(1RS)-1-hydroxy-2-(7-methoxy-2-oxo-2H-quinolin-1-yl)ethyl]cyclohexyl}carbamic acid benzyl ester
CAS No.:1198355-07-5
Molecular Formula:C₂₆H₃₀N₂O₅
Molecular Weight:450.535
Hs Code.:

Synonyms:trans-{4-[(1RS)-1-hydroxy-2-(7-methoxy-2-oxo-2H-quinolin-1-yl)ethyl]cyclohexyl}carbamic acid benzyl ester

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Chemical Property of trans-{4-[(1RS)-1-hydroxy-2-(7-methoxy-2-oxo-2H-quinolin-1-yl)ethyl]cyclohexyl}carbamic acid benzyl ester

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Technology Process of trans-{4-[(1RS)-1-hydroxy-2-(7-methoxy-2-oxo-2H-quinolin-1-yl)ethyl]cyclohexyl}carbamic acid benzyl ester

There total 5 articles about trans-{4-[(1RS)-1-hydroxy-2-(7-methoxy-2-oxo-2H-quinolin-1-yl)ethyl]cyclohexyl}carbamic acid benzyl ester 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: 98.0%

: 1198355-06-4
rac-1-[trans-2-(4-aminocyclohexyl)-2-hydroxyethyl]-7-methoxy-1H-quinolin-2-one

: 501-53-1,94274-21-2
benzyl chloroformate

: 1198355-07-5
trans-{4-[(1RS)-1-hydroxy-2-(7-methoxy-2-oxo-2H-quinolin-1-yl)ethyl]cyclohexyl}carbamic acid benzyl ester

Guidance literature:: With sodium hydrogencarbonate; In water; acetone; at 0 - 20 ℃;

Reference yield:

: 1198355-04-2
rac-{trans-4-[2-(7-methoxy-2-oxo-2H-quinolin-1-yl)acetyl]cyclohexyl}carbamic acid tert-butyl ester

: 1198355-07-5
trans-{4-[(1RS)-1-hydroxy-2-(7-methoxy-2-oxo-2H-quinolin-1-yl)ethyl]cyclohexyl}carbamic acid benzyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: sodium tetrahydroborate / tetrahydrofuran; methanol / 1 h

2: trifluoroacetic acid / dichloromethane / 0.33 h / 20 °C

3: sodium hydrogencarbonate / water; acetone / 0 - 20 °C

With sodium tetrahydroborate; sodium hydrogencarbonate; trifluoroacetic acid; In tetrahydrofuran; methanol; dichloromethane; water; acetone;

Reference yield:

: 1198355-05-3
rac-{trans-4-[hydroxy-(7-methoxy-2-oxo-2H-quinolin-1-yl)methyl]cyclohexyl}carbamic acid tert-butyl ester

: 1198355-07-5
trans-{4-[(1RS)-1-hydroxy-2-(7-methoxy-2-oxo-2H-quinolin-1-yl)ethyl]cyclohexyl}carbamic acid benzyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: trifluoroacetic acid / dichloromethane / 0.33 h / 20 °C

2: sodium hydrogencarbonate / water; acetone / 0 - 20 °C

With sodium hydrogencarbonate; trifluoroacetic acid; In dichloromethane; water; acetone;