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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | methyl (2S,3R)-3-(4-methoxyphenyl)oxirane-2-carboxylate | HCID 719742 | — |
| Reactant | (+)-N-methyl-2-{2-[2-(4-phenylpiperazin-1-yl)ethyloxy]phenyl}thiazolidine-3-carbothioamide | HCID 13767979 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-methyl-2-{2-[2-(4-phenylpiperazin-1-yl)ethyloxy]phenyl}thiazolidine-3-carboxamide | HCID 13767927 | 75.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04689327 |
|---|
| Source dataset | uspto-grants-1987_08 |
|---|
| ORD ID | ord-f3e68c165c3c48f0b4660070a759059b |
|---|
| Source note | uspto-grants-1987_08 |
|---|