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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1270103Generated: November 1, 2026

Hydrochloric Acid → 4-(2-fluoro-benzenesulfonyl)-2,2-dimethyl-8-piperazin-1-yl-3,4-dihydro-2H-benzo[1,4]oxazine

https://huagongshe.com/reaction/1270103

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant4-[4-(2-fluoro-benzenesulfonyl)-2,2-dimethyl-3,4-dihydro-2H-benzo[1,4]oxazin-8-yl]-piperazine-1-carboxylic acid tert-butyl esterHCID 58842135—
SolventEthanolHCID 702—
Product4-(2-fluoro-benzenesulfonyl)-2,2-dimethyl-8-piperazin-1-yl-3,4-dihydro-2H-benzo[1,4]oxazineHCID 1140707242.4%

Reaction Conditions

Temperature100 °C

Reaction Steps

4-[4-(2-Fluoro-benzenesulfonyl)-2,2-dimethyl-3,4-dihydro-2H-benzo[1,4]oxazin-8-yl]-piperazine-1-carboxylic acid tert-butyl ester (470 mg, 0.93 mmol) was dissolved in 3 ml ethanol. To this solution was added 1 ml of 10% ethanolic hydrochloric acid solution. The mixture was heated at 100° C. (steam bath) for 15 minutes, and then cooled to room temperature at which time a white crystalline solid formed. The solid was collected by filtration and dried at 70° C. under vacuum to provide 160 mg of 4-(2-fluoro-benzenesulfonyl)-2,2-dimethyl-8-piperazin-1-yl-3,4-dihydro-2H-benzo[1,4]oxazine as a hydrochloride salt. MP: 222.9–227.1° C. MS: (M+H) 479.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07202241B2
Source datasetuspto-grants-2007_04
ORD IDord-0173768f629d422193d357174da388b2
Source noteuspto-grants-2007_04