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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1613676Generated: November 1, 2026

5-(4-[2-(N-Methyl-N-(2-pyrimidinyl)amino)ethoxy]benzylidene)-2,4-thiazolidinedione → 5-(4-[2-(N-Methyl-N-(2-pyrimidinyl)amino)ethoxy]benzyl)-2,4-thiazolidinedione

https://huagongshe.com/reaction/1613676

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-(4-[2-(N-Methyl-N-(2-pyrimidinyl)amino)ethoxy]benzylidene)-2,4-thiazolidinedioneHCID 54227469—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
Solvent1,4-DioxaneHCID 31275—
Product5-(4-[2-(N-Methyl-N-(2-pyrimidinyl)amino)ethoxy]benzyl)-2,4-thiazolidinedioneHCID 10361044—

Reaction Steps

5-(4-[2-(N-Methyl-N-(2-pyrimidinyl)amino) ethoxy]benzylidene)-2,4-thiazolidinedione (2.4 g) in dry 1,4-dioxan (150 ml) was reduced under hydrogen in the presence of 10% palladium on charcoal (3 g) until hydrogen uptake ceased. The solution was filtered through diatomaceous earth, the filter pad was washed exhaustively with dioxan and the combined filtrates were evaporated to dryness under vacuum. The title compound (mp 150°-51° C.) was obtained after crystallisation from methanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05194443
Source datasetuspto-grants-1993_03
ORD IDord-194407e67c1b4166bb09b592a738be45
Source noteuspto-grants-1993_03