Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 499523Generated: November 1, 2026

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

https://huagongshe.com/reaction/499523

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropyl mercaptanHCID 7848—
ReactantEthyl AcetateHCID 8857—
ReactantSodium hydrideHCID 24758—
Reactant6-(4-oxo-4H-1,3-benzothiazin-2-yl)-2-pyridyl methanesulfonateHCID 22939272—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product2-[6-[(n-Propylthio)methyl]-2-pyridyl]-4H-1,3-benzothiazine-4-oneHCID 5975044620%

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-pyridyl methanesulfonate (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 numberUS07767665B2
Source datasetuspto-grants-2010_08
ORD IDord-f8b491ac082f4fe191c955cae97ca7d6
Source noteuspto-grants-2010_08