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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1433816Generated: November 1, 2026

HCID 23087388, compound → HCID 23087488, compound

https://huagongshe.com/reaction/1433816

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 23087388HCID 23087388—
ReactantHCID 57933849HCID 57933849—
SolventPyridineHCID 1049—
SolventAcetic AnhydrideHCID 7918—
ProductHCID 23087488HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07612114B2
Source datasetuspto-grants-2009_11
ORD IDord-cc3f8d8fbd414fa281c8363849547104
Source noteuspto-grants-2009_11