HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 454655Generated: October 30, 2026
Potassium Carbonate → HCID 66990822, compound
https://huagongshe.com/reaction/454655
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | HCID 66990269 | HCID 66990269 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 66990822 | HCID 66990822 | — |
Reaction Steps
Potassium carbonate (1.0 g) and 1-methylpiperazine (0.83 mL) were added to an acetone (7.5 mL) solution of tert-butyl 2-(2-(benzyloxy)-5-(2-bromoethoxy)benzamido)-4-phenylbenzoate (1.5 g), followed by heating to reflux for 2 hours. The reaction mixture was cooled to room temperature, and potassium carbonate (0.34 g) and 1-methylpiperazine (0.28 mL) were added thereto, followed by heating to reflux for 2 hours. After cooling the reaction mixture to room temperature, the solvent was evaporated under reduced pressure, and water and chloroform were added to the residue. The organic layer was separated, and the solvent was removed under reduced pressure. The obtained residue was purified by silica gel column chromatography [eluent: 100-95% chloroform/methanol] to obtain tert-butyl 2-(2-(benzyloxy)-5-(2-(4-methylpiperazin-1-yl)ethoxy)benzamido)-4-phenylbenzoate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08492582B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-31b59f62ddd64f128e756b12f736797e |
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| Source note | uspto-grants-2013_07 |
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