HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1403181Generated: October 26, 2026
Methanol → 5-Fluoro-2-(methylsulfonyl)pyrimidin-4-amine
https://huagongshe.com/reaction/1403181
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanol | HCID 887 | — |
| Reactant | 5-Fluoro-2-(methylthio)pyrimidin-4-amine | HCID 20593351 | — |
| Reactant | Sodium Bisulfite | HCID 23665763 | — |
| Reactant | Potassium hydroxy sulfite | HCID 23707502 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-Fluoro-2-(methylsulfonyl)pyrimidin-4-amine | HCID 58318934 | 63% |
Reaction Steps
To a solution of 5-fluoro-2-methylsulfanylpyrimidin-4-ylamine (5.02 g, 31.6 mmol) in methyl alcohol (MeOH; 105 mL) was added dropwise a solution of OXONE™ (Registered trademark of E.I. du Pont de Nemours & Co, Inc.; 42.7 g, 69.4 mmol) in H2O (210 mL) over a 20 minute (min) period at −45° C., and the resulting mixture was slowly warmed to 10° C. over a period of 14 h. The mixture was treated with sodium bisulfite (10 g) and the majority of the MeOH was removed on the rotary evaporator. The aqueous residue was extracted with EtOAc (2×250 mL), and the organic extracts were combined, washed with brine (100 mL), dried over Na2SO4, filtered, and concentrated to give 5-fluoro-2-methanesulfonylpyrimidin-4-ylamine (3.79 g, 63%) as a white solid: mp 157-159° C.; 1H NMR (300 MHz, DMSO-d6) δ 8.35 (d, J=3.6 Hz, 1H), 8.11 (s, 2H), 3.27 (s, 3H); CIMS m/z 191 ([M]+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08912207B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-e2468e004a5b4b2a94afdb7b64a0ccfd |
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| Source note | uspto-grants-2014_12 |
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