HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 470328Generated: October 30, 2026
Potassium Carbonate → pyridinylpiperazine ethyl-1H-isoindole-1,3(2H)-dione
https://huagongshe.com/reaction/470328
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 53486023 | HCID 53486023 | — |
| Reactant | 5,6-Dihydrobenzo[h]quinazolin-2-ol | HCID 178517548 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | pyridinylpiperazine ethyl-1H-isoindole-1,3(2H)-dione | HCID 67058601 | — |
Reaction Steps
To a solution of bromoethyl phthalimide 1 (5 mmol) and 2-pyridyl piperazine 2 (5 mmol) in acetonitrile (10 mL) was added potassium carbonate (0.690 g, 5 mmol) and resulting reaction mixture was stirred under reflux. After completion of the reaction, solvent was removed on rotavap and residue was dissolved in chloroform (20 mL). Then washed with water (5 mL) and saturated sodium bicarbonate solution (5 mL), dried over anhydrous sodium sulfate. Filtered and evaporation of solvent gave pyridinylpiperazine ethyl-1H-isoindole-1,3(2H)-dione. Then dissolved in methanol (10 mL), hydrazine hydrate (0.48 mL, 15 mmol) was added and stirred under reflux to give a precipitate. Filtered, washed with methanol (5 mL) and evaporation of solvent gave 2-(4-pyridin-2-ylpiperazin-1-yl)ethanamine 3 which was used as such in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08629147B2 |
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| Source dataset | uspto-grants-2014_01 |
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| ORD ID | ord-3b10dbd18b7e4cf482b7de47818bc2bc |
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| Source note | uspto-grants-2014_01 |
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