HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1643952Generated: November 1, 2026
Potassium Carbonate → 1-[2-Oxo-1-phenyl-2-(4-pyridin-4-ylpiperazin-1-yl)ethyl]-1,3-dihydrobenzimidazol-2-one
https://huagongshe.com/reaction/1643952
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-(4-Pyridyl)piperazine | HCID 70517 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | (2-Oxo-2,3-dihydrobenzimidazol-1-yl)phenylacetic acid | HCID 66754578 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-[2-Oxo-1-phenyl-2-(4-pyridin-4-ylpiperazin-1-yl)ethyl]-1,3-dihydrobenzimidazol-2-one | HCID 24901169 | — |
Reaction Steps
179 mg (0.94 mmol) of EDCl were added to a solution of 193 mg (0.72 mmol) of (2-oxo-2,3-dihydrobenzimidazol-1-yl)phenylacetic acid (VIIId), 106 mg (0.79 mmol) of HOBt, 117 mg (0.72 mmol) of 1-pyridin-4-ylpiperazine and 0.49 ml (2.87 mmol) of ethyldiisopropylamine in dichloromethane (8 ml) while stirring in an ice-water bath. The reaction solution was slowly warmed and stirred at room temperature for 16 h. Half-saturated aqueous potassium carbonate solution was added, and the organic phase was separated off. The aqueous phase was extracted with ethyl acetate (4×50 ml) and the combined organic phases were washed with sat. NaHCO3 solution, dried over magnesium sulfate and concentrated under reduced pressure. The reaction product was used without further purification for the next reaction step. Yield: 292 mg (98%) of yellow solid
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08119676B2 |
|---|
| Source dataset | uspto-grants-2012_02 |
|---|
| ORD ID | ord-7a107e1d5fab4b2fad6d6a6daa41f6da |
|---|
| Source note | uspto-grants-2012_02 |
|---|