(3S,4S)-3-(2-fluoro-4-(methylsulfonyl)phenoxy)-4-hydroxy-1-(piperidin-4-yl)pyrrolidin-2-one hydrochloride

Base Information

Chemical Name:(3S,4S)-3-(2-fluoro-4-(methylsulfonyl)phenoxy)-4-hydroxy-1-(piperidin-4-yl)pyrrolidin-2-one hydrochloride
CAS No.:1351168-23-4
Molecular Formula:C₁₆H₂₁FN₂O₅S*ClH
Molecular Weight:408.878
Hs Code.:

Synonyms:(3S,4S)-3-(2-fluoro-4-(methylsulfonyl)phenoxy)-4-hydroxy-1-(piperidin-4-yl)pyrrolidin-2-one hydrochloride

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Chemical Property of (3S,4S)-3-(2-fluoro-4-(methylsulfonyl)phenoxy)-4-hydroxy-1-(piperidin-4-yl)pyrrolidin-2-one hydrochloride

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Technology Process of (3S,4S)-3-(2-fluoro-4-(methylsulfonyl)phenoxy)-4-hydroxy-1-(piperidin-4-yl)pyrrolidin-2-one hydrochloride

There total 5 articles about (3S,4S)-3-(2-fluoro-4-(methylsulfonyl)phenoxy)-4-hydroxy-1-(piperidin-4-yl)pyrrolidin-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:

: 1351168-22-3
tert-butyl 4-((3S,4S)-3-(2-fluoro-4-(methylsulfonyl)phenoxy)-4-hydroxy-2-oxopyrrolidin-1-yl)piperidine-1-carboxylate

: 1351168-23-4
(3S,4S)-3-(2-fluoro-4-(methylsulfonyl)phenoxy)-4-hydroxy-1-(piperidin-4-yl)pyrrolidin-2-one hydrochloride

Guidance literature:: With hydrogenchloride; In 1,4-dioxane; dichloromethane; at 20 ℃; for 6h;

Reference yield:

: 1351168-19-8
tert-butyl 4-((3R,4S)-4-(benzyloxy)-3-(methylsulfonyloxy)-2-oxopyrrolidin-1-yl)piperidine-1-carboxylate

: 1351168-23-4
(3S,4S)-3-(2-fluoro-4-(methylsulfonyl)phenoxy)-4-hydroxy-1-(piperidin-4-yl)pyrrolidin-2-one hydrochloride

Guidance literature:: Multi-step reaction with 4 steps

1: potassium carbonate / dimethyl sulfoxide / 70 °C / Inert atmosphere

2: trans-1,2-cyclohexanediamine; copper(I) triflate benzene complex / dimethyl sulfoxide / 110 °C / Inert atmosphere

3: hydrogen / palladium 10% on activated carbon / ethanol

4: hydrogenchloride / dichloromethane; 1,4-dioxane / 6 h / 20 °C

With hydrogenchloride; hydrogen; potassium carbonate; copper(I) triflate benzene complex; palladium 10% on activated carbon; trans-1,2-cyclohexanediamine; In 1,4-dioxane; ethanol; dichloromethane; dimethyl sulfoxide;

Reference yield:

: 1351168-20-1
tert-butyl 4-((3S,4S)-4-(benzyloxy)-3-(4-bromo-2-fluorophenoxy)-2-oxopyrrolidin-1-yl)piperidine-1-carboxylate

: 1351168-23-4
(3S,4S)-3-(2-fluoro-4-(methylsulfonyl)phenoxy)-4-hydroxy-1-(piperidin-4-yl)pyrrolidin-2-one hydrochloride

Guidance literature:: Multi-step reaction with 3 steps

1: trans-1,2-cyclohexanediamine; copper(I) triflate benzene complex / dimethyl sulfoxide / 110 °C / Inert atmosphere

2: hydrogen / palladium 10% on activated carbon / ethanol

3: hydrogenchloride / dichloromethane; 1,4-dioxane / 6 h / 20 °C

With hydrogenchloride; hydrogen; copper(I) triflate benzene complex; palladium 10% on activated carbon; trans-1,2-cyclohexanediamine; In 1,4-dioxane; ethanol; dichloromethane; dimethyl sulfoxide;