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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1789352Generated: October 30, 2026

Acetic Acid → 2-{2-[2-(4-Phenylpiperazin-1-yl)ethyloxy]phenyl}thiazolidine-3-carboxamide

https://huagongshe.com/reaction/1789352

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantPotassium CarbonateHCID 11430—
ReactantNaNCOHCID 11051568—
Reactant2-{2-[2-(4-Phenylpiperazin-1-yl)ethyloxy]phenyl}thiazolidineHCID 13768099—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product2-{2-[2-(4-Phenylpiperazin-1-yl)ethyloxy]phenyl}thiazolidine-3-carboxamideHCID 1376803682.2%

Reaction Steps

A solution of 1.07 g of sodium isocyanate in 20 ml of water is added to a solution of 3.03 g of 2-{2-[2-(4-phenylpiperazin-1-yl)ethyloxy]phenyl}thiazolidine in 40 ml of ethanol, and 2.46 g of acetic acid are added thereto. The mixture is stirred at room temperature for 2 hours. 200 ml of water are added to the mixture, and the aqueous mixture is made alkaline with potassium carbonate. The aqueous mixture is extracted with ethyl acetate and chloroform, successively. The extracts are combined, washed with water, dried and then concentrated under reduced pressure to remove solvent. The residue is recrystallized from ethyl acetate. 2.78 g of 2-{2-[2-(4-phenylpiperazin-1-yl)ethyloxy]phenyl}thiazolidine-3-carboxamide are obtained. Yield: 82.2%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04689327
Source datasetuspto-grants-1987_08
ORD IDord-99a875cbc0914ffc94f639c96f95744e
Source noteuspto-grants-1987_08