HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 475449Generated: October 29, 2026
Potassium Carbonate → HCID 66991490, compound
https://huagongshe.com/reaction/475449
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Phenylboronic Acid | HCID 66827 | — |
| Reactant | HCID 86659070 | HCID 86659070 | — |
| Product | HCID 66991490 | HCID 66991490 | — |
Reaction Steps
A flask charged with trifluoromethanesulfonic acid 6-[5-((S)-2-methyl-1-methylcarbamoyl-propylcarbamoyl)-furan-2-yl]-pyridin-3-yl ester (50 mg, 0.11 mmol), phenylboronic acid (27 mg, 0.22 mmol), palladiumtetrakistriphenylphosphine (13 mg, 0.01 mmol), and potassium carbonate (61 mg, 0.44 mmol) is flushed with argon. Toluene (2 mL), ethanol (0.5 mL), and water (1 mL) are added and the reaction is stirred at 100° C. for 2 hours. The reaction is cooled to room temperature, ethyl acetate (10 mL), is added and the mixture washed with water (10 mL), brine (10 mL), and dried over MgSO4. The solution is filtered and evaporated in vacuo to give an oil that is purified by preparative HPLC. 5-(5-Phenyl-pyridin-2-yl)-furan-2-carboxylic acid ((S)-2-methyl-1-methylcarbamoyl-propyl)-amide is obtained as a white solid, 16 mg, 38%, LC/MS ESI m/z (M+H)+=377.43.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08637550B2 |
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| Source dataset | uspto-grants-2014_01 |
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| ORD ID | ord-2fe2342826df4f37a55d8ee076244c54 |
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| Source note | uspto-grants-2014_01 |
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