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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 660666Generated: October 29, 2026

5-{2-Benzyloxy-4-[(E)-2-((S)-2-methanesulfonyl-1,2,3,4-tetrahydroisoquinolin-3-yl)-vinyl]-phenyl}-1,1-dioxo-1,2,5-thiadiazolidin-3-one → 5-{2-Hydroxy-4-[2-((R)-2-methanesulfonyl-1,2,3,4-tetrahydroisoquinolin-3-yl)-ethyl]-phenyl}-1,1-dioxo-1,2,5-thiadiazolidin-3-one

https://huagongshe.com/reaction/660666

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-{2-Benzyloxy-4-[(E)-2-((S)-2-methanesulfonyl-1,2,3,4-tetrahydroisoquinolin-3-yl)-vinyl]-phenyl}-1,1-dioxo-1,2,5-thiadiazolidin-3-oneHCID 68996313—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product5-{2-Hydroxy-4-[2-((R)-2-methanesulfonyl-1,2,3,4-tetrahydroisoquinolin-3-yl)-ethyl]-phenyl}-1,1-dioxo-1,2,5-thiadiazolidin-3-oneHCID 57777422—

Reaction Steps

To a solution of 5-{2-benzyloxy-4-[(E)-2-((S)-2-methanesulfonyl-1,2,3,4-tetrahydroisoquinolin-3-yl)-vinyl]-phenyl}-1,1-dioxo-1,2,5-thiadiazolidin-3-one (0.090 g, 0.16 mmol) in EtOH (4 mL) is added a slurry of 10% Pd/C (0.1 g) in EtOH (6 mL). The reaction vessel is flushed twice with H2 and stirred at RT for 18 h under balloon pressure of H2. The mixture is filtered and purified by reverse phase chromatography using a gradient of 15 to 40% EtOH/water to afford the title compound as a white solid: LC retention time=1.0 min (Method A); (M+NH4)+=465.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08084448B2
Source datasetuspto-grants-2011_12
ORD IDord-307414afcf2f46b98007ff3d64ba7a53
Source noteuspto-grants-2011_12