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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 561208Generated: October 31, 2026

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

https://huagongshe.com/reaction/561208

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantSodium ThiosulfateHCID 24477—
ReactantSodium AcetateHCID 517045—
ReactantHCID 66696800HCID 66696800—
SolventWaterHCID 962—
SolventChlorobenzeneHCID 7964—
SolventEthyl AcetateHCID 8857—
Product3-[4-(2-Bromo-5-fluorophenoxy)piperidin-1-yl]isoxazole-5-carboxamideHCID 53388529—

Reaction Steps

To a stirred suspension of 3-[4-(2-bromo-5-fluorophenoxy)piperidin-1-yl]-4,5-dihydroisoxazole-5-carboxamide (2.3 g, 5.96 mmol) and sodium acetate (1.3 g, 15.85 mmol) in chlorobenzene (15 mL) was added iodine (2 g, 7.88 mmol). The mixture was heated at reflux temperature for 3 h. After cooling, a solution of Na2S2O3, water and EtOAc were added. The mixture was stirred for 5 min and filtered through celite to remove the insoluble material. The organic layer was then separated, washed with brine, dried (Na2SO4) and concentrated. The residue was triturated with Et2O to give the title compound as light brown powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08063224B2
Source datasetuspto-grants-2011_11
ORD IDord-091711a9d51d4572a203552b8c604b9d
Source noteuspto-grants-2011_11