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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 441024Generated: October 25, 2026

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

https://huagongshe.com/reaction/441024

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-(4-[2-(N-Methyl-N-(2-benzoxazolyl)amino)ethoxy]benzylidene)-2,4-thiazolidinedioneHCID 54450184—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
Solvent1,4-DioxaneHCID 31275—
Product5-(4-[2-(N-Methyl-N-(2-benzoxazolyl)amino)ethoxy] benzyl)-2,4-thiazolidinedione hemihydrateHCID 88043875—

Reaction Steps

5-(4-[2-(N-Methyl-N-(2-benzoxazolyl)amino)ethoxy]benzylidene) -2,4-thiazolidinedione (1.5 g) in dry 1,4-dioxan (80 ml) was reduced under hydrogen in the presence of 10% palladium on charcoal (2 g) at ambient temperature and atmospheric pressure 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 147°-9° C.) was obtained after crystallisation from methanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05521201
Source datasetuspto-grants-1996_05
ORD IDord-27de2a73d12d453b83a312fa8793542c
Source noteuspto-grants-1996_05