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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1961625Generated: October 31, 2026

4-(4-Fluorobenzoyl)piperidine → HCID 178523664, compound

https://huagongshe.com/reaction/1961625

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(4-Fluorobenzoyl)piperidineHCID 2724440—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 178520748HCID 178520748—
SolventMethanolHCID 887—
ProductHCID 178523664HCID 17852366499%

Reaction Steps

4-(4-fluorobenzoyl)piperidine (trifluoro-acetic acid salt) (0.020 g, 0.062 mmol) was solved in 1,2-dichloromethane (0.300 mL) and Quinoline-4-carboxylic acid trans-[4-(2-oxo-ethyl)-cyclohexyl]-amide (0.020 g, 0.067 mmol) was added. Methanol (0.200 mL) was added to the mixture and it was stirred overnight. Sodium triacetoxyborohydride (0.024, 0.11 mmol) was added to the clear solution that was stirred 10 hours at room temperature. The mixture was concentrated to dryness and the residue was taken up on methanol and purified with preparative HPLC on reversed phase eluting with acetonitrile/water. The combined producted fractions were evaporated under reduced pressure to yield 0.03 g of a white solid (0.06 mmol, 99%). MS (m/e): 488.3 (M+H+)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08415350B2
Source datasetuspto-grants-2013_04
ORD IDord-d3c5d954372f4222869b2a2f9948f126
Source noteuspto-grants-2013_04