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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 561209Generated: October 30, 2026

Triethylamine → 3-[4-(2-Bromo-5-fluorophenoxy)piperidin-1-yl]isoxazole-5-carbonitrile

https://huagongshe.com/reaction/561209

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTrifluoroacetic anhydrideHCID 9845—
Reactant3-[4-(2-Bromo-5-fluorophenoxy)piperidin-1-yl]isoxazole-5-carboxamideHCID 53388529—
SolventDichloromethaneHCID 6344—
Product3-[4-(2-Bromo-5-fluorophenoxy)piperidin-1-yl]isoxazole-5-carbonitrileHCID 53388530—

Reaction Steps

To a suspension of 3-[4-(2-bromo-5-fluorophenoxy)piperidin-1-yl]isoxazole-5-carboxamide (1.6 g, 4.2 mmol) and Et3N (1.5 mL, 10.8 mmol) in CH2Cl2 (20 mL) was added TFAA (0.8 mL, 5.7 mmol) at ice-water bath temperature. A homogeneous solution resulted. After addition, the cooling bath was removed and the mixture was stirred at room temperature for 2 h. The mixture was quenched with water (10-15 mL), followed by saturated aqueous NaHCO3 (15-20 mL) and extracted with CH2Cl2 (2×30 mL). The combined CH2Cl2 extracts were washed with diluted brine (40 mL), dried (Na2SO4) and concentrated. Chromatography over silica gel and elution with hexanes:EtOAc (4:1) gave the title compound as a colorless gum.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08063224B2
Source datasetuspto-grants-2011_11
ORD IDord-11528afec91e475b8df732a2970c3f15
Source noteuspto-grants-2011_11