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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 748348Generated: October 30, 2026

Triethylamine → HCID 59750361, compound

https://huagongshe.com/reaction/748348

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl AcetateHCID 8857—
Reactant1-(4-Fluorophenyl)piperazineHCID 75260—
Reactant6-(4-oxo-4H-1,3-benzothiazin-2-yl)-2-pyridylmethanesulfonateHCID 86596462—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 59750361HCID 5975036151.1%

Reaction Conditions

Temperature70 °C

Reaction Steps

6-(4-Oxo-4H-1,3-benzothiazin-2-yl)-2-pyridylmethanesulfonate (0.30 g, 0.86 mmol), triethylamine (0.20 ml, 1.42 mmol) and 1-(4-fluorophenyl)piperazine (0.17 g, 0.95 mmol) were dissolved in DMF (30 ml), and the mixture was stirred at 70° C. for 18 hrs. The reaction mixture was combined with ethyl acetate and water. The organic layer was washed with saturated brine and dried over anhydrous magnesium sulfate. The solvent was evaporated, and the residue was recrystallized from n-hexane-ethyl acetate to give the titled compound (0.19 g, 50%) as pale yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07399759B2
Source datasetuspto-grants-2008_07
ORD IDord-9c0c4d9d87714e2b8d933b149ddfd238
Source noteuspto-grants-2008_07