HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2107320Generated: October 27, 2026
Water → 2-(2-Pyridylmethylthio)quinoxaline hydrochloride
https://huagongshe.com/reaction/2107320
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Picolyl chloride hydrochloride | HCID 23392 | — |
| Reactant | HCID 178418602 | HCID 178418602 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 2-(2-Pyridylmethylthio)quinoxaline hydrochloride | HCID 14052171 | 58.6% |
Reaction Steps
In 50 ml of acetone was dissolved 2.0 g of 2-mercaptoquinoxaline. To the solution were added 2.02 g of 2-picolyl chloride hydrochloride, 4.0 g of potassium carbonate and 5 ml of water. The resulting mixture was stirred at room temperature for 0.5 hr., and the solvent was removed under reduced pressure. The residue was extracted with chloroform after addition of chloroform and water. The organic layer was separated and dried over sodium sulfate. The sodium sulfate was removed by filtration, and the filtrate was placed under reduced pressure to remove the solvent. To the residue were added 20 ml of ethanol and 1.03 ml of conc. hydrchloric acid and then added ether. Thus precipitated crystals were washed with ethanol-ether (1:1) and dried under reduced pressure to give 2.09 g of 2-(2-pyridylmethylthio)quinoxaline hydrochloride as a yellow crystalline powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04933458 |
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| Source dataset | uspto-grants-1990_06 |
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| ORD ID | ord-f7c412f312af457ea217336fa833a0be |
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| Source note | uspto-grants-1990_06 |
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