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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 408018Generated: October 31, 2026

HCID 86688121, compound → HCID 66800463, compound

https://huagongshe.com/reaction/408018

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86688121HCID 86688121—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 66800463HCID 66800463104.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

(S)-Benzyl 4-(3-(6-(methylsulfonyl)pyridin-3-ylamino)-2-oxopyrrolidin-1-yl)piperidine-1-carboxylate (0.23 g, 0.49 mmol) was dissolved in MeOH (5 mL) and cooled to 0° C. The material was purged with N2 by three vacuum pump/N2 balloon cycles. Palladium on carbon (10 wt. % dry basis, wet, Degussa type, 0.053 g, 0.49 mmol) was added and the system was purged with 1 atm H2 by three vacuum pump/H2 balloon cycles. The reaction continued to stir under H2 until the starting material was consumed. The mixture was filtered through GF/F paper and concentrated to give (S)-3-(6-(methylsulfonyl)pyridin-3-ylamino)-1-(piperidin-4-yl)pyrrolidin-2-one (0.17 g, 0.51 mmol, 100% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08754226B2
Source datasetuspto-grants-2014_06
ORD IDord-19d702d5fb4d40228e0c5e08b4c0b599
Source noteuspto-grants-2014_06