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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1591962Generated: October 30, 2026

HCID 10171560, compound → HCID 10171430, compound

https://huagongshe.com/reaction/1591962

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 10171560HCID 10171560—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 10171430HCID 10171430—

Reaction Steps

To a solution of the title C compound in Example 5, 5-(3-nitrobenzyl)-1,1-dioxo-1,2,5-thiadiazolidin-3-one (30 mg, 0.11 mmol) in EtOH (5 mL) is added palladium on carbon (10 mg) and the mixture is stirred under 1 atm of hydrogen for 1 h. The catalyst is removed by filtration through a plug of Celite which is washed with MeCN/water (1:1), (20 mL). The solvents are evaporated to afford 5-(3-Aminobenzyl)-1,1-dioxo-1,2,5-thiadiazolidin-3-one as a brown solid: [M−1]−=240.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07291635B2
Source datasetuspto-grants-2007_11
ORD IDord-69f3f3c1e8a84171857021c18c2e4a16
Source noteuspto-grants-2007_11