HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2386279Generated: November 2, 2026
Potassium hydroxy sulfite → HCID 86651597, compound
https://huagongshe.com/reaction/2386279
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium hydroxy sulfite | HCID 23707502 | — |
| Reactant | HCID 86651596 | HCID 86651596 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 86651597 | HCID 86651597 | 65.4% |
Reaction Steps
To a solution of 2-chloro-6a-methyl-5-(tetrahydro-2H-thiopyran-4-yl)-6a,7,9,10-tetrahydro-[1,4]oxazino[3,4-h]pteridin-6(5H)-one (9.4 mg, 0.026 mmol) in MeOH (1 ml) at 0° C. was added dropwise a solution of oxone (40.7 mg, 0.066 mmol) in water (1 ml), and the reaction mixture was stirred at room temperature for 16 h, followed by solvent removal in vacuo. The residue was partitioned between EtOAc and water. The phases were separated and the aqueous phase was extracted with EtOAc. The combined organic phases were dried and concentrated in vacuo to give 2-chloro-5-(1,1-dioxidotetrahydro-2H-thiopyran-4-yl)-6a-methyl-6a,7,9,10-tetrahydro[1,4]oxazino[3,4-h]pteridin-6(5H)-one (6.5 mg, 0.017 mmol, 63% yield) as a white solid. This was used in the next step without further purification. MS [M+H] found 387.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08268819B2 |
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| Source dataset | uspto-grants-2012_09 |
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| ORD ID | ord-589639eae2784a51bb8a040ddf2d8917 |
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| Source note | uspto-grants-2012_09 |
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