Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 930392Generated: October 29, 2026

Hydrochloric Acid → HCID 86732224, compound

https://huagongshe.com/reaction/930392

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1,4-DioxaneHCID 31275—
ReactantHCID 86732222HCID 86732222—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
ProductHCID 86732224HCID 86732224—

Reaction Steps

(R)-N-((2S,4S)-2-(2,3-difluorophenyl)-1,5,5,5-tetrafluoro-4-hydroxypentan-2-yl)-2-methylpropane-2-sulfinamide (2.48 g, 6.34 mmol) was dissolved in dichloromethane (12.0 mL) and MeOH (4.0 mL). To this solution was added hydrogen chloride, 4M in 1,4-dioxane (12.0 mL, 48.0 mmol). After stirred for 10 min, the mixture was concentrated, diluted with dichloromethane and washed with 1N NaOH followed by brine. The organic layer was dried over Na2SO4 and then filtered. The filtrate was concentrated and dried to afford (2S,4S)-4-amino-4-(2,3-difluorophenyl)-1,1,1,5-tetrafluoropentan-2-ol as colorless oil. This crude product was dissolved in THF (60 ml) and then treated with benzoyl isothiocyanate (0.938 mL, 6.97 mmol). After stirred for 1.5 h, triethylamine (1.058 mL, 7.60 mmol) and 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hcl (1.336 g, 6.97 mmol) were added, and the resulted reaction mixture was brought to 70° C. for 2 h. Reaction mixture was partitioned between EtOAc and water. The separated organic layer was washed with brine, dried over Na2SO4 and filtered. The filtrate was concentrated and purified by silica gel column (0-20% EtOAc/hexane) to afford N-((4S,6S)-4-(2,3-difluorophenyl)-4-(fluoromethyl)-6-(trifluoromethyl)-5,6-dihydro-4H-1,3-oxazin-2-yl)benzamide (2.22 g, 5.33 mmol, 84% yield) as white solid. MS m/z=417.1 [M+H]+. Calculated for C19H14F6N2O2: 416.3

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09296734B2
Source datasetuspto-grants-2016_03
ORD IDord-f1603099ea1c45079f45e0261ba2b8e3
Source noteuspto-grants-2016_03