Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 499477Generated: October 29, 2026

Ethanesulfonyl chloride → HCID 59750102, compound

https://huagongshe.com/reaction/499477

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanesulfonyl chlorideHCID 11667—
ReactantSodium BicarbonateHCID 516892—
Reactant2-[6-(Aminomethyl)-2-pyridyl]-4h-1,3-benzothiazine-4-one trifluoroacetic acid saltHCID 68458297—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductHCID 59750102HCID 5975010221.5%

Reaction Steps

2-[6-(Aminomethyl)-2-pyridyl]-4H-1,3-benzothiazine-4-one trifluoroacetic acid salt (500 mg, 1.3 mmol) and ethanesulfonyl chloride (270 mg, 2.1 mmol) were dissolved in ethyl acetate (10 ml) and water (5 ml), and sodium hydrogen carbonate (270 mg, 3.2 mmol) was added thereto. The mixture was stirred at room temperature for 3 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 subjected to a silica gel column chromatography. The fractions eluted with ethyl acetate-hexane (2:1, v/v) were collected, concentrated and recrystallized from hexane-tetrahydrofuran to give the titled compound (101 mg, 21%) as pale yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07767665B2
Source datasetuspto-grants-2010_08
ORD IDord-edf8ed2614b34ccab0e8b43fff8de5f0
Source noteuspto-grants-2010_08