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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1030385Generated: November 2, 2026

Pyridine → HCID 86745686, compound

https://huagongshe.com/reaction/1030385

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantPotassium CarbonateHCID 11430—
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantHCID 19822186HCID 19822186—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
ProductHCID 86745686HCID 86745686—

Reaction Steps

A mixture of 0.5 g of t-butyl α-{5-[4-(6-t-butoxycarbonylmethoxy-2,5,7,8-tetramethyl-4-oxochroman-2-ylmethoxy)benzyl]-2,4-dioxothiazolidin-3-yl}acetate (prepared as described in Example 51), 0.2 g of hydroxylamine hydrochloride, 0.2 g of pyridine and 5 ml of methanol was allowed to stand at 25°-30° C. for 5 days. Ethyl acetate and an aqueous solution of potassium carbonate were added to the mixture, and the organic layer was separated. The organic layer was dried over anhydrous sodium sulfate. The solvent was distilled off and the residue was subjected to silica gel column chromatography (eluted with a 20:1 by volume mixture of benzene and ethyl acetate) to obtain the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05104888
Source datasetuspto-grants-1992_04
ORD IDord-bb48f719f4264d4b84fe1f449aba201c
Source noteuspto-grants-1992_04