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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1682443Generated: November 4, 2026

Potassium Iodide → Ethyl 2-[4-(5-chlorobenzothiazol-2-yl) methyl-3,4-dihydro-3-oxo-2H-1,4-benzoxazin-2-yl]acetate

https://huagongshe.com/reaction/1682443

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPotassium CarbonateHCID 11430—
ReactantAmmonium ChlorideHCID 25517—
ReactantEthyl (3-oxo-3,4-dihydro-2h-1,4-benzoxazine-2-yl)acetateHCID 15292312—
Reactant2-(Bromomethyl)-5-chloro-1,3-benzothiazoleHCID 15292313—
SolventDimethyl SulfoxideHCID 679—
ProductEthyl 2-[4-(5-chlorobenzothiazol-2-yl) methyl-3,4-dihydro-3-oxo-2H-1,4-benzoxazin-2-yl]acetateHCID 15292314—

Reaction Steps

Ethyl 2-(3,4-dihydro-3-oxo-2H-1,4-benzoxazin-2-yl]acetate (150 mg), 2-bromomethyl-5-chlorobenzothiazole (186 mg) and potassium iodide (13 mg) were dissolved in dimethyl sulfoxide (2 ml). Potassium carbonate (133 mg) was added and the mixture was stirred at room temperature for 15 hours. A saturated aqueous solution of ammonium chloride was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine and dried over anhydrous sodium sulfate, and the solvent was distilled away.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05635505
Source datasetuspto-grants-1997_06
ORD IDord-3bee6e69b6374e498dbfb46ae3ead3c6
Source noteuspto-grants-1997_06