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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1270101Generated: October 25, 2026

Pyridine → 8-bromo-4-(2-fluorobenzenesulfonyl)-2,2-dimethyl-3,4-dihydro-2H-benzo[1,4]oxazine

https://huagongshe.com/reaction/1270101

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant2-Fluorobenzenesulphonyl chlorideHCID 137761—
Reactant8-bromo-2,2-dimethyl-3,4-dihydro-2H-benzo[1,4]oxazine hydrochlorideHCID 18449099—
SolventHydrochloric AcidHCID 313—
SolventDichloromethaneHCID 6344—
Product8-bromo-4-(2-fluorobenzenesulfonyl)-2,2-dimethyl-3,4-dihydro-2H-benzo[1,4]oxazineHCID 2255728271,214.898%

Reaction Steps

8-Bromo-2,2-dimethyl-3,4-dihydro-2H-benzo[1,4]oxazine hydrochloride (518 mg, 2.14 mmol) was dissolved in 5 ml methylene chloride, to which pyridine (253.85 g, 3.21 mmol) was then added. The reaction mix was stirred at room temperature, and 2-fluorobenzenesulfonyl chloride (416.37 mg, 2.14 mmol) was added drop-wise to the reaction mix, after which stirring at room temperature was continued for 2 hours. The reaction mix was then heated to reflux for 1 hour, and cooled to room temperature. The reaction mix was diluted with 5 ml of methylene chloride and 10% aqueous HCl was added. The organic layer was separated, washed with water, then saturated NaHCO3, and dried (Na2SO4). Solvent was removed under reduced pressure, and the residue was purified via flash chromatography (EtOAc in hexane, 5% to 20%) to afford 610 g (71.3%) of 8-bromo-4-(2-fluoro-benzenesulfonyl)-2,2-dimethyl-3,4-dihydro-2H-benzo[1,4]oxazine as an oil which solidified upon standing. MP: 108.0–110.1° C. MS: (M+H) 401.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07202241B2
Source datasetuspto-grants-2007_04
ORD IDord-d936c3d72ff44970bc78b4df1aba9344
Source noteuspto-grants-2007_04