HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 425246Generated: October 30, 2026
Potassium hydroxy sulfite → HCID 58298341, compound
https://huagongshe.com/reaction/425246
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium hydroxy sulfite | HCID 23707502 | — |
| Reactant | HCID 58298339 | HCID 58298339 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 58298341 | HCID 58298341 | 2,180.4% |
Reaction Steps
To a solution of Oxone (9.12 g) in water (50 mL) was added a solution of 8-(4-bromo-2,6-dimethyl-phenyl)-2-methyl-4-methylsulfanyl-pyrrolo[1,2-a]pyrimidine-6-carboxylic acid amide (3.00 g) in ethanol (50 mL) in an ice-cooling bath. The reaction mixture was stirred under ice-cooling for 30 minutes, poured into water and extracted with ethyl acetate. The organic layer was washed with a saturated aqueous sodium hydrogencarbonate and brine, dried over anhydrous sodium sulfate and filtered. The filtrate was concentrated under reduced pressure and the residue was purified by a silica gel column chromatography (silica gel: Wako Gel (C200), eluent: ethyl acetate) to give 8-(4-bromo-2,6-dimethyl-phenyl)-4-methanesulfinyl-2-methyl-pyrrolo[1,2-a]pyrimidine-6-carboxylic acid amide (1:68 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08106194B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-fe1c4efe6cbe4cd59425184c915dfcc3 |
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| Source note | uspto-grants-2012_01 |
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