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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1404642Generated: November 1, 2026

Dimethyl Sulfoxide → Azemiglitazone

https://huagongshe.com/reaction/1404642

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantPhosphorus oxide (P4O10)HCID 14812—
Reactant5-{4-[2-Hydroxy-2-(3-methoxyphenyl)ethoxy]benzyl}-1,3-thiazolidine-2,4-dioneHCID 46911040—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductAzemiglitazoneHCID 2523026654%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirring solution of 5-{4-[2-hydroxy-2-(3-methoxyphenyl)ethoxy]benzyl}-1,3-thiazolidine-2,4-dione (0.62 g, 1.7 mmol) in DCM (15 mL) was added DMSO (0.5 mL) and the solution was cooled to 0° C. Added phosphorus pentoxide (0.52 g, 1.8 mmol) followed by triethylamine (1.2 mL, 8.3 mmol). The reaction was allowed to slowly warm to RT. After 2 hours water was added and the phases were separated. The pH of the aqueous phase was adjusted to ca. 7 with 2M NaOH. The aqueous phase was extracted with EtOAc. The combined extracts were washed with brine, dried (Na2SO4), filtered and evaporated in vacuo. The resulting white solid was chromatographed on a small silica gel column eluting with 10% EtOAc/DCM. Fractions containing product were combined and evaporated in vacuo to give 0.33 g (54%) of the title compound as a white solid. MS (ESI+) for C19H17NO5S m/z 372.0 (M+H)+. MS (ESI−) for C19H17NO5S m/z 370.1 (M−H)−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08912335B2
Source datasetuspto-grants-2014_12
ORD IDord-6986faae720342058b80e43425787285
Source noteuspto-grants-2014_12