HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 525183Generated: October 30, 2026
Cesium carbonate → HCID 68261003, compound
https://huagongshe.com/reaction/525183
Participants
| Role | Name | HCID | Charge |
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| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzofuran | HCID 2795190 | — |
| Reactant | HCID 71087482 | HCID 71087482 | — |
| Catalyst | HCID 178418807 | HCID 178418807 | — |
| Product | HCID 68261003 | HCID 68261003 | 68.1% |
Reaction Steps
To a microwave vial were added 4-(4-bromo-2,3-difluorophenyl)-5-{[(3S)-1-(cyclopropylcarbonyl)-3-pyrrolidinyl]methyl}-2,4-dihydro-3H-1,2,4-triazol-3-one (50 mg, 0.117 mmol), 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1-benzofuran (42.8 mg, 0.176 mmol), cesium carbonate (114 mg, 0.351 mmol), and dichloro[1,1′-bis(diphenylphosphino)ferrocene]palladium(II)-dichloromethane adduct (6.0 mg, 0.00735 mmol). The mixture was purged with nitrogen, followed by the addition of 1,4-dioxane (1 mL) and water (0.5 mL). The resulting suspension was heated overnight at 100° C., at which point analysis by LCMS indicated desired product formation and consumption of starting material. The mixture was filtered through a syringe filter and purified by reverse phase HPLC (10-90% acetonitrile/water+0.1% TFA). The desired fractions were collected and added to a reparatory funnel containing ethyl acetate. The aqueous phase was adjusted to pH˜6 with 1N aq HCl. The aqueous phase was extracted with ethyl acetate (3×), and the combined organics were washed with brine, dried over Na2SO4 and concentrated in vacuo to afford the title product as a white solid (37 mg, 68%). MS(ES)+ m/e 465.1 M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09340529B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-ee06d58594384aa28378b89640364d47 |
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| Source note | uspto-grants-2016_05 |
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