HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 356121Generated: October 30, 2026
Potassium Carbonate → HCID 18941131, compound
https://huagongshe.com/reaction/356121
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Fumaric Acid | HCID 444972 | — |
| Reactant | HCID 18941009 | HCID 18941009 | — |
| Solvent | Formic Acid | HCID 284 | — |
| Solvent | Formaldehyde | HCID 712 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 18941131 | HCID 18941131 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05834499 |
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| Source dataset | uspto-grants-1998_11 |
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| ORD ID | ord-400f04e3f9be41a78f86566f8074e487 |
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| Source note | uspto-grants-1998_11 |
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