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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1765671Generated: October 30, 2026

benzyl (3R)-1-[(2S)-2-((3S)-3-{[(6-chloro-2-naphthyl)sulfonyl]amino}-2-oxopyrrolidin-1-yl)propanoyl]piperidin-3-ylcarbamate → Benzyl(3R)-1-((2S)-2-{(3S)-3-[(2-naphthylsulfonyl)amino]-2-oxopyrrolidin-1-yl}propanoyl)piperidin-3-ylcarbamate

https://huagongshe.com/reaction/1765671

Reaction equation

Participants

RoleNameHCIDCharge
Reactantbenzyl (3R)-1-[(2S)-2-((3S)-3-{[(6-chloro-2-naphthyl)sulfonyl]amino}-2-oxopyrrolidin-1-yl)propanoyl]piperidin-3-ylcarbamateHCID 86593865—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductBenzyl(3R)-1-((2S)-2-{(3S)-3-[(2-naphthylsulfonyl)amino]-2-oxopyrrolidin-1-yl}propanoyl)piperidin-3-ylcarbamateHCID 865938643%

Reaction Steps

A mixture of benzyl (3R)-1 -[(2S)-2-((3S)-3-{[(6-chloro-2-naphthyl)sulfonyl]amino}-2-oxopyrrolidin-1-yl)propanoyl]piperidin-3-ylcarbamate (0.350 g), 10% palladium on carbon (0.035 g) and ethanol (1000 ml) was stirred under an atmosphere of hydrogen for 17 h. The reaction mixture was filtered through Harbolite™ and the filtrate was concentrated under reduced pressure to give an oil. The oil was partially purified using SPE (silica, eluting with methanol and then 10% aqueous ammonia in methanol) and then fully purified using mass directed preparative h.p.l.c. to give the title compounds (Example 403, 0.01 g; Example 404, 0.028 g), both as oils.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07226929B2
Source datasetuspto-grants-2007_06
ORD IDord-2b56c1fa60994d46b59b7c0c1d20fc31
Source noteuspto-grants-2007_06