HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1433816Generated: November 1, 2026
HCID 23087388, compound → HCID 23087488, compound
https://huagongshe.com/reaction/1433816
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 23087388 | HCID 23087388 | — |
| Reactant | HCID 57933849 | HCID 57933849 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Acetic Anhydride | HCID 7918 | — |
| Product | HCID 23087488 | HCID 23087488 | — |
Reaction Steps
Synthesized from 4-(4-cyano-2-fluorophenoxy)piperidine-1-carboxylic acid tert-butyl ester (2.8 g) according to an analogous synthetic method to Example 215 described below, the total amount of 3-fluoro-4-(piperidin-4-yloxy)benzonitrile crude product was dissolved in acetic anhydride (30 ml) and pyridine (30 ml), and the solution was stirred overnight at room temperature. The solvent was evaporated in vacuo, the solution was extracted with ethyl acetate, then sequentially washed with a saturated aqueous solution of sodium bicarbonate, water and brine, dried over anhydrous magnesium sulfate, and then the solvent was evaporated in vacuo. The residue was purified by NH silica gel column chromatography (hexane-ethyl acetate system) to provide the title compound (2.2 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07612114B2 |
|---|
| Source dataset | uspto-grants-2009_11 |
|---|
| ORD ID | ord-cc3f8d8fbd414fa281c8363849547104 |
|---|
| Source note | uspto-grants-2009_11 |
|---|