HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 72684Generated: October 30, 2026
Potassium Carbonate → HCID 24962321, compound
https://huagongshe.com/reaction/72684
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 58089378 | HCID 58089378 | — |
| Reactant | HCID 60140024 | HCID 60140024 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 24962321 | HCID 24962321 | — |
Reaction Steps
A suspension of 3-[4-chloro-6-(4-fluorophenyl)-2-(trifluoromethyl)pyrimidin-5-yl]benzenesulfonamide (0.15 g, 0.35 mmol), 4-hydroxy-N,3-dimethoxybenzamide (0.102 g, 0.52 mmol) and potassium carbonate (0.52 mmol) in acetonitrile (3 ml) were heated to reflux (65° C.) for 2 hours. Subsequently the reaction mixture was poured onto ice-cold water, extracted with dichloromethane (50 ml) and washed with brine. Evaporation of the organic layer furnished a crude material, which was purified by column chromatography; elution with 2% MeOH in dichloromethane furnished the required compound. 1H-NMR (DMSO-d6) δ: 3.73 (s, 3H), 3.79 (s, 3H), 7.16-7.20 (m, 2H), 7.37 (d, 1H), 7.41-7.45 (m, 5H), 7.53 (s, 1H), 7.62-7.63 (d, 2H), 7.85 (d, 1H), 7.89 (s, 1H). 11.9 (s, 1H); MS m/z: 593 (M++1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08828999B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-453eb2f7bf99405d819849786b15e304 |
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| Source note | uspto-grants-2014_09 |
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