HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 11501Generated: October 28, 2026
Ethyl Acetate → HCID 178418796, compound
https://huagongshe.com/reaction/11501
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | HCID 178418721 | HCID 178418721 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178418796 | HCID 178418796 | — |
Reaction Steps
A solution of 3-{[4-(3-Iodo-propoxy)-phenylamino]-methylene}-1,3-dihydro-indol-2-one (66 mg, 0.157 mmol) in 1 mL THF is treated with 1-methylpiperazine (37.2 μL, 2.2 equiv.) and the resulting reaction mixture is heated at 50° C. for 4 h. The reaction mixture is cooled to room temperature and concentrated under reduced pressure. The residue is partitioned between EtOAc and H2O. The organic layer is collected and washed with saturated aqueous NaHCO3, brine, and dried over anhydrous Na2SO4. The yellow solid residue obtained upon evaporation is broken up in 1:9 EtOAc:hexane and collected by filtration to give the named compound as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07098236B2 |
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| Source dataset | uspto-grants-2006_08 |
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| ORD ID | ord-31d312c2e45f4f3c8790dd87c1ce3c70 |
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| Source note | uspto-grants-2006_08 |
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