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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 499472Generated: October 30, 2026

Water → N-[[6-(4-Oxo-4H-1,3-benzothiazin-2-yl)-2-pyridyl]methyl]benzamide

https://huagongshe.com/reaction/499472

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzoyl chlorideHCID 7412—
ReactantEthyl AcetateHCID 8857—
Reactant2-[6-(Aminomethyl)-2-pyridyl]-4h-1,3-benzothiazine-4-one trifluoroacetic acid saltHCID 68458297—
SolventDimethylacetamideHCID 31374—
ProductN-[[6-(4-Oxo-4H-1,3-benzothiazin-2-yl)-2-pyridyl]methyl]benzamideHCID 5975033139%

Reaction Conditions

Temperature60 °C

Reaction Steps

2-[6-(Aminomethyl)-2-pyridyl]-4H-1,3-benzothiazine-4-one trifluoroacetic acid salt (330 mg, 0.86 mmol) was dissolved in N,N-dimethylacetamide (10 ml), and benzoyl chloride (264 mg, 1.87 mmol) was added thereto. The reaction mixture was stirred at 60° C. for 14 hrs and 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 hexane-ethyl acetate (1:3, v/v) were collected, concentrated and recrystallized from hexane-tetrahydrofuran to give the titled compound (125 mg, 39%) as white crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07767665B2
Source datasetuspto-grants-2010_08
ORD IDord-8ec9154cfe354a1d9b327b6dd1b17877
Source noteuspto-grants-2010_08