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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 361318Generated: October 26, 2026

Pyridine → Bia-2-024

https://huagongshe.com/reaction/361318

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantOxcarbazepineHCID 34312—
ReactantHydroxyamine hydrochlorideHCID 443297—
ProductBia-2-024HCID 85040065—

Reaction Steps

A suspension of 4.0 g (15.86 mmol) of 10,11-dihydro-10-oxo-5H-dibenz[b,f]azepine-5-carboxamide and 3.86 g (55.49 mmol) of hydroxylamine hydrochloride in 100 mL of absolute alcohol was treated with 3.76 g (47.57 mmol) of pyridine. The mixture was heated at reflux for 1 hour and then the ethanol was removed by evaporation under reduced pressure. The residue was partitioned between 150 mL of water and 150 mL of dichloromethane. The organic layer was separated and washed with 50 mL of 1M aqueous HCl, a saturated solution of NaHCO3 and brine, then dried by sodium sulphate. Filtration and evaporation of the solvent under reduced pressure gave an off-white solid which was triturated with hot ethanol to give the desired compound as a white powder of m.p. 230.4° to 231.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05866566
Source datasetuspto-grants-1999_02
ORD IDord-c416f4cbbac447c38f5cc84c273ef3c8
Source noteuspto-grants-1999_02