HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 525201Generated: October 30, 2026
Potassium Carbonate → HCID 67376741, compound
https://huagongshe.com/reaction/525201
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1H-Indazole-5-boronic acid pinacol ester | HCID 17750469 | — |
| Reactant | 4-(4-bromo-2-fluorophenyl)-5-{[(3S)-1-(cyclopropylcarbonyl)-3-pyrrolidinyl]methyl}-2,4-dihydro-3H-1,2,4-triazol-3-one | HCID 67375886 | — |
| Catalyst | HCID 178418807 | HCID 178418807 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 67376741 | HCID 67376741 | 32% |
Reaction Steps
A solution of 4-(4-bromo-2-fluorophenyl)-5-{[(3S)-1-(cyclopropylcarbonyl)-3-pyrrolidinyl]methyl}-2,4-dihydro-3H-1,2,4-triazol-3-one (0.244 mmol) in dioxane (1.5 mL) was treated with 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indazole (0.269 mmol), dichloro[1,1′-bis(diphenylphosphino)ferrocene]palladium(II)-dichloromethane adduct (10 mg), and 2M aq potassium carbonate (0.733 mmol). The reaction mixture was purged with nitrogen, sealed, and stirred at 100° C. overnight. The reaction mixture was cooled to room temperature and was diluted with water (50 mL). The aqueous layer was acidified to pH˜4 using 1N aq HCl and was extracted with dichloromethane. The organic layer was dried over magnesium sulfate, filtered, and concentrated in vacuo. The crude residue was purified by reverse phase HPLC (10-50% acetonitrile/water+0.1% NH4OH) to afford the title compound as a beige solid (32%). MS(ES)+ m/e 447.2 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09340529B2 |
|---|
| Source dataset | uspto-grants-2016_05 |
|---|
| ORD ID | ord-cebaea1116744ceaade35cbf3ef13165 |
|---|
| Source note | uspto-grants-2016_05 |
|---|