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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 964944Generated: October 30, 2026

Water → HCID 19074438, compound

https://huagongshe.com/reaction/964944

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant3-Hydroxy-1lambda~6~,2-benzothiazine-1,1(4H)-dioneHCID 117972—
ReactantHCID 16767631HCID 16767631—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
ProductHCID 19074438HCID 1907443853.6%

Reaction Steps

In toluene (7 mL) were suspended 2H-1,2-benzothiazin-3(4H)-one 1,1-dioxide (250 mg, 1.3 mmol.), 1-chloro-3-morpholino-1-phenylpropane (340 mg, 1.4 mmol.), potassium carbonate (250 mg, 1.8 mmol.) and a catalytic amount of cupper powder. The suspension was heated for 12 hours under refluxing. The reaction liquid was cooled, and the insolubles were filtered off. The solvent was distilled off to leave a residue. To the residue were added water and ethyl acetate, and the organic layer was taken out. The organic solution was washed with water and an aqueous saturated sodium chloride solution, and dried over anhydrous sodium sulfate. The solvent was distilled off, and the resulting residue was treated by silica gel column chromatogrpahy (ethyl acetate) to give the free base of the desired compound (180 mg) as an oil. The free base was treated in the conventional manner to convert into the desired fumarate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05773437
Source datasetuspto-grants-1998_06
ORD IDord-0d30936c5c4b4103b4ece3eb66b324f1
Source noteuspto-grants-1998_06