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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 356121Generated: October 30, 2026

Potassium Carbonate → HCID 18941131, compound

https://huagongshe.com/reaction/356121

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantFumaric AcidHCID 444972—
ReactantHCID 18941009HCID 18941009—
SolventFormic AcidHCID 284—
SolventFormaldehydeHCID 712—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
SolventAcetonitrileHCID 6342—
ProductHCID 18941131HCID 18941131—

Reaction Conditions

Temperature90 °C

Reaction Steps

In 0.13 ml of formic acid and 0.3 ml of a 35% aqueous formaldehyde solution, 94 mg of 2-(3-piperidylmethyl)-8H-indeno[1,2-d]thiazole was dissolved, followed by heating at 90° C. for 14 hours. The reaction mixture was diluted with water and chloroform, followed by the addition of potassium carbonate to adjust the pH of the aqueous layer to about 8. An organic layer was separated, and the resulting aqueous layer was extracted twice with chloroform. The organic layers were combined and washed with a saturated aqueous solution of sodium chloride. After drying over anhydrous sodium sulfate, the solvent was evaporated under reduced pressure. The resulting residue was purified by silica gel column chromatography (eluent: chloroform-methanol), whereby 99 mg of a brawn oily substance was obtained. The substance was dissolved in 1 ml of acetonitrile, and 40 mg of fumaric acid was added thereto. The resulting mixture was stirred at room temperature for 30 minutes and the crystals formed were collected by filtration, whereby 90 mg of 2-[(1-methyl-3-piperidyl)methyl]-8H-indeno[1,2-d]thiazole fumarate was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05834499
Source datasetuspto-grants-1998_11
ORD IDord-400f04e3f9be41a78f86566f8074e487
Source noteuspto-grants-1998_11