4-(4-(benzyloxycarbonylamino)piperidin-1-yl)phenethyl 4-methylbenzenesulfonate

Base Information

Chemical Name:4-(4-(benzyloxycarbonylamino)piperidin-1-yl)phenethyl 4-methylbenzenesulfonate
CAS No.:1315251-47-8
Molecular Formula:C₂₈H₃₂N₂O₅S
Molecular Weight:508.638
Hs Code.:

Synonyms:4-(4-(benzyloxycarbonylamino)piperidin-1-yl)phenethyl 4-methylbenzenesulfonate

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Chemical Property of 4-(4-(benzyloxycarbonylamino)piperidin-1-yl)phenethyl 4-methylbenzenesulfonate

Chemical Property:

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Technology Process of 4-(4-(benzyloxycarbonylamino)piperidin-1-yl)phenethyl 4-methylbenzenesulfonate

There total 7 articles about 4-(4-(benzyloxycarbonylamino)piperidin-1-yl)phenethyl 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: 68.0%

: 1315251-45-6
benzyl 1-(4-(2-hydroxyethyl)phenyl)piperidin-4-ylcarbamate

: 98-59-9
p-toluenesulfonyl chloride

: 1315251-47-8
4-(4-(benzyloxycarbonylamino)piperidin-1-yl)phenethyl 4-methylbenzenesulfonate

Guidance literature:: With pyridine; for 4h; Cooling with ice;

Reference yield:

: 1315251-41-2
ethyl 4-(4-(benzyloxycarbonylamino)piperidin-1-yl)benzoate

: 1315251-47-8
4-(4-(benzyloxycarbonylamino)piperidin-1-yl)phenethyl 4-methylbenzenesulfonate

Guidance literature:: Multi-step reaction with 4 steps

1.1: diisobutylaluminium hydride / dichloromethane; hexane / 1 h / -78 °C

1.2: 21 h / 60 °C

2.1: n-butyllithium / hexane; tetrahydrofuran / 0.5 h / 0 °C

2.2: 17 h / 20 °C

3.1: hydrogenchloride / ethyl acetate; water / 1 h

3.2: 1 h / 0 °C

4.1: pyridine / 4 h / Cooling with ice

With pyridine; hydrogenchloride; n-butyllithium; diisobutylaluminium hydride; In tetrahydrofuran; hexane; dichloromethane; water; ethyl acetate;

Reference yield:

: 1315251-43-4
benzyl 1-(4-formylphenyl)piperidin-4-ylcarbamate

: 1315251-47-8
4-(4-(benzyloxycarbonylamino)piperidin-1-yl)phenethyl 4-methylbenzenesulfonate

Guidance literature:: Multi-step reaction with 3 steps

1.1: n-butyllithium / hexane; tetrahydrofuran / 0.5 h / 0 °C

1.2: 17 h / 20 °C

2.1: hydrogenchloride / ethyl acetate; water / 1 h

2.2: 1 h / 0 °C

3.1: pyridine / 4 h / Cooling with ice

With pyridine; hydrogenchloride; n-butyllithium; In tetrahydrofuran; hexane; water; ethyl acetate;