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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1941668Generated: November 2, 2026

1-[6-(Benzyloxy)pyridin-3-YL]ethanone → 5-(4-{2-[1-(2-Benzyloxy-5-pyridyl)ethylideneaminooxy]ethoxy}benzyl)thiazolidine-2,4-dione

https://huagongshe.com/reaction/1941668

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-[6-(Benzyloxy)pyridin-3-YL]ethanoneHCID 21833927—
Reactant5-(4-[2-Aminooxyethoxy)benzyl]thiazolidine-2,4-dione hydrochlorideHCID 21833965—
Product5-(4-{2-[1-(2-Benzyloxy-5-pyridyl)ethylideneaminooxy]ethoxy}benzyl)thiazolidine-2,4-dioneHCID 7384798078%

Reaction Steps

Following a procedure similar to that described in Example 40(f), 130 mg of 5-acetyl-2-benzyloxypyridine were reacted with 182 mg of 5-[4-(2-aminooxyethoxy)-benzyl]thiazolidine-2,4-dione hydrochloride [prepared as described in Example 40(e)]. The reaction mixture was concentrated by evaporation under reduced pressure, and the resulting residue was extracted with ethyl acetate. The extract was washed with water and the solvent was removed by distillation under reduced pressure, to give 219 mg of the title compound, melting at 160°-161° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05703096
Source datasetuspto-grants-1997_12
ORD IDord-a84920e3e8b7402bb26a28b013afc6c3
Source noteuspto-grants-1997_12