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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 748341Generated: October 30, 2026

Propyl mercaptan → 2-[6-[(n-Propylthio)methyl]-2-pyridyl]-4H-1,3-benzothiazine-4-one

https://huagongshe.com/reaction/748341

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropyl mercaptanHCID 7848—
ReactantEthyl AcetateHCID 8857—
ReactantSodium hydrideHCID 24758—
Reactant6-(4-oxo-4H-1,3-benzothiazin-2-yl)-2-pyridylmethanesulfonateHCID 86596462—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product2-[6-[(n-Propylthio)methyl]-2-pyridyl]-4H-1,3-benzothiazine-4-oneHCID 5975044620.3%

Reaction Steps

n-Propyl mercaptan (0.25 g, 3.30 mmol) and sodium hydride (60% in oil, 0.15 g, 3.60 mmol) were dissolved in DMF (30 ml), and 6-(4-oxo-4H-1,3-benzothiazin-2-yl)-2-pyridylmethanesulfonate (1.05 g, 3.00 mmol) was added thereto. The reaction mixture was stirred at room temperature for 18 hrs, 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 (0.20 g, 20%) as pale yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07399759B2
Source datasetuspto-grants-2008_07
ORD IDord-2b472e4295e7420dac61b7e219ebd8e6
Source noteuspto-grants-2008_07