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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1789349Generated: October 31, 2026

methyl (2S,3R)-3-(4-methoxyphenyl)oxirane-2-carboxylate → N-methyl-2-{2-[2-(4-phenylpiperazin-1-yl)ethyloxy]phenyl}thiazolidine-3-carboxamide

https://huagongshe.com/reaction/1789349

Reaction equation

Participants

RoleNameHCIDCharge
Reactantmethyl (2S,3R)-3-(4-methoxyphenyl)oxirane-2-carboxylateHCID 719742—
Reactant(+)-N-methyl-2-{2-[2-(4-phenylpiperazin-1-yl)ethyloxy]phenyl}thiazolidine-3-carbothioamideHCID 13767979—
SolventEthanolHCID 702—
ProductN-methyl-2-{2-[2-(4-phenylpiperazin-1-yl)ethyloxy]phenyl}thiazolidine-3-carboxamideHCID 1376792775.7%

Reaction Steps

480 mg of (+)-N-methyl-2-{2-[2-(4-phenylpiperazin-1-yl)ethyloxy]phenyl}thiazolidine-3-carbothioamide and 339 mg of methyl trans-3-(4-methoxyphenyl)glycidate are dissolved in 40 ml of ethanol, and the solution is refluxed for 11 hours under heating. 339 mg of methyl trans-3-(4-methoxyphenyl)glycidate are added to the mixture, and the mixture is further refluxed for 3 hours. The mixture is concentrated under reduced pressure to remove solvent. The residue is purified by silica gel chromatography (solvent, chloroform:ethanol=40:1), and the resultant product is recrystallized from a mixture of ethyl acetate and n-hexane. 350 mg of (+)-N-methyl-2-{2-[2-(4-phenylpiperazin-1-yl)ethyloxy]phenyl}thiazolidine-3-carboxamide are obtained. Yield: 75.7%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04689327
Source datasetuspto-grants-1987_08
ORD IDord-f3e68c165c3c48f0b4660070a759059b
Source noteuspto-grants-1987_08