HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1435247Generated: October 31, 2026
Hexane → (4-Amino-2-(ethylsulfinyl)pyrimidin-5-yl)(2,3-difluoro-6-methoxyphenyl)methanone
https://huagongshe.com/reaction/1435247
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hexane | HCID 8058 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | (4-Amino-2-(ethylthio)pyrimidin-5-yl)(2,3-difluoro-6-methoxyphenyl)methanone | HCID 11723824 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (4-Amino-2-(ethylsulfinyl)pyrimidin-5-yl)(2,3-difluoro-6-methoxyphenyl)methanone | HCID 21070554 | — |
Reaction Steps
A stirred solution of (4-amino-2-ethylsulfanyl-pyrimidin-5-yl)-(2,3-difluoro-6-methoxy-phenyl)-methanone (7.4 g, 23 mmol, Example 102) in dichloromethane (150 mL) at 0° C. was treated portionwise with 74% meta-chloroperoxybenzoic acid (6 g, 26 mmol) over about 30 minutes. The cold reaction mixture was quenched with 25 ml of 10% aqueous sodium thiosulfate solution and the layers separated. The organic layer was washed once with 10% aqueous sodium thiosulfate solution, twice with saturated aqueous sodium carbonate solution, once with brine, dried (Na2SO4) and evaporated. Trituration of the residue with hexane provided a quantitative yield of (4-amino-2-ethanesulfinyl-pyrimidin-5-yl)-(2,3-difluoro-6-methoxy-phenyl)-methanone as a colorless solid, mp 165 dec. Mass Spectrum (LR-ES) (M+H)+: 342.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07615634B2 |
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| Source dataset | uspto-grants-2009_11 |
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| ORD ID | ord-bd791886cc894ce1981b7c10332cdff4 |
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| Source note | uspto-grants-2009_11 |
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