(3S,5S,6R)-3-amino-6-methyl-1-(2-methylpropyl)-5-phenylpiperidin-2-one hydrochloride

Base Information

Chemical Name:(3S,5S,6R)-3-amino-6-methyl-1-(2-methylpropyl)-5-phenylpiperidin-2-one hydrochloride
CAS No.:1375541-84-6
Molecular Formula:C₁₆H₂₄N₂O*ClH
Molecular Weight:296.84
Hs Code.:

Synonyms:(3S,5S,6R)-3-amino-6-methyl-1-(2-methylpropyl)-5-phenylpiperidin-2-one hydrochloride

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Chemical Property of (3S,5S,6R)-3-amino-6-methyl-1-(2-methylpropyl)-5-phenylpiperidin-2-one hydrochloride

Chemical Property:

Purity/Quality:

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Technology Process of (3S,5S,6R)-3-amino-6-methyl-1-(2-methylpropyl)-5-phenylpiperidin-2-one hydrochloride

There total 6 articles about (3S,5S,6R)-3-amino-6-methyl-1-(2-methylpropyl)-5-phenylpiperidin-2-one hydrochloride 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:

: 1375541-82-4
tert-butyl [(3S,5S,6R)-6-methyl-1-(2-methylpropyl)-2-oxo-5-phenylpiperidin-3-yl]carbamate

: 1375541-84-6
(3S,5S,6R)-3-amino-6-methyl-1-(2-methylpropyl)-5-phenylpiperidin-2-one hydrochloride

Guidance literature:: With hydrogenchloride; In ethyl acetate; at 0 - 23 ℃; for 2h;

Reference yield:

: 1375541-78-8
syn-tert-butyl ((5S,6R)-6-methyl-2-oxo-5-phenylpiperidin-3-yl)carbamate

: 1375541-84-6
(3S,5S,6R)-3-amino-6-methyl-1-(2-methylpropyl)-5-phenylpiperidin-2-one hydrochloride

Guidance literature:: Multi-step reaction with 3 steps

1.1: lithium hexamethyldisilazane / 1-methyl-pyrrolidin-2-one; tetrahydrofuran / 0.17 h / 0 °C

1.2: 20 h / 0 - 23 °C

2.1: hydrogen / palladium 10% on activated carbon / ethanol / 1 h / 23 °C

3.1: hydrogenchloride / ethyl acetate / 2 h / 0 - 23 °C

With hydrogenchloride; hydrogen; lithium hexamethyldisilazane; palladium 10% on activated carbon; In tetrahydrofuran; 1-methyl-pyrrolidin-2-one; ethanol; ethyl acetate;

Reference yield:

: 1375541-80-2
tert-butyl [(3S,5S,6R)-6-methyl-1-(2-methylprop-2-en-1-yl)-2-oxo-5-phenylpiperidin-3-yl]carbamate

: 1375541-84-6
(3S,5S,6R)-3-amino-6-methyl-1-(2-methylpropyl)-5-phenylpiperidin-2-one hydrochloride

Guidance literature:: Multi-step reaction with 2 steps

1: hydrogen / palladium 10% on activated carbon / ethanol / 1 h / 23 °C

2: hydrogenchloride / ethyl acetate / 2 h / 0 - 23 °C

With hydrogenchloride; hydrogen; palladium 10% on activated carbon; In ethanol; ethyl acetate;