HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 84275Generated: October 26, 2026
Cesium carbonate → ethyl 4-(4-iodo-3-methyl-2-oxopyridin-1(2H)-yl)-2-methyl-2-(methylsulfonyl)butanoate
https://huagongshe.com/reaction/84275
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 4-iodo-3-methylpyridin-2(1H)-one | HCID 67262043 | — |
| Reactant | Ethyl 4-bromo-2-methyl-2-(methylsulfonyl)butanoate | HCID 86670634 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | ethyl 4-(4-iodo-3-methyl-2-oxopyridin-1(2H)-yl)-2-methyl-2-(methylsulfonyl)butanoate | HCID 67249750 | — |
Reaction Steps
To a solution of ethyl 4-bromo-2-methyl-2-(methylsulfonyl)butanoate (2.08 g, 7.25 mmol) and 4-iodo-3-methylpyridin-2(1H)-one (1.42 g, 6.04 mmol) in tetrahydrofuran (60.4 mL) was added cesium carbonate (4.06 g, 12.1) at ambient temperature. The resulting mixture was stirred at 50° C. overnight. The mixture was allowed to cool to ambient temperature and filtered through a celite pad. The pad was washed with ethyl acetate and the filtrate was concentrated to a crude residue. The material was purified via filtration through a silica gel pad, eluting with heptanes/ethyl acetate. The desired fractions were isolated, the solvent removed via rotary evaporation affording ethyl 4-(4-iodo-3-methyl-2-oxopyridin-1(2H)-yl)-2-methyl-2-(methylsulfonyl)butanoate as an oil. 1.97 g
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08846933B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-ae3625238b924fd3be119d12e7021e06 |
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| Source note | uspto-grants-2014_09 |
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