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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1638293Generated: October 30, 2026

Maleic Anhydride → HCID 67867837, compound

https://huagongshe.com/reaction/1638293

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMaleic AnhydrideHCID 7923—
ReactantHpr 611HCID 3082453—
SolventPyridineHCID 1049—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67867837HCID 6786783750.5%

Reaction Steps

A solution of 5-chloro-3-(4-hydroxypiperidinocarbonylmetyl)benzothiazolin-2-one (3.2 g) in dry pyridine (2.5 ml) and dry tetrahydrofuran (50 ml) was cooled, to which a solution of maleic anhydride (1.0 g) in dry tetrahydrofuran (5 ml) was gradually dropwise added under stirring. The mixture was refluxed for two hours and then left overnight. The solvent was evaporated off under vacuum from the reaction mixture, and the residue was dissolved in 5% aqueous sodium bicarbonate (20 ml). The solution was cooled and adjusted to pH 2 with 1% hydrochloric acid. The precipitated crystals were collected by filtration, washed with water and then subjected to chromatography on silica gel eluting with ethanol/benzene (1:1). The solvent was evaporated off under vacuum from the eluate at below 50° C. The residue was recrystallized from isopropyl alcohol to yield the title compound as colorless crystals (2.1 g). m.p. 197°-198° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04879301
Source datasetuspto-grants-1989_11
ORD IDord-ddc001b8c45d46b593853b708261050a
Source noteuspto-grants-1989_11