HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1461737Generated: November 1, 2026
Hydrochloric Acid → 1-{3-[4-(4-Fluorobenzoyl)piperidino]propyl}-4-(2-pyridylmethyl) piperazine 2,6-dione hydrochloride
https://huagongshe.com/reaction/1461737
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | [1-(3-Chloropropyl)piperidin-4-yl](4-fluorophenyl)methanone | HCID 12404419 | — |
| Reactant | 4-(2-Pyridylmethyl)-2,6-piperazinedione | HCID 14882692 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-{3-[4-(4-Fluorobenzoyl)piperidino]propyl}-4-(2-pyridylmethyl) piperazine 2,6-dione hydrochloride | HCID 14882694 | — |
Reaction Steps
A solution of 1.86 g of 4-(2-pyridylmethyl)piperazine 2,6-dione in 30 ml of dimethylformamide is added at 20° C. to a suspension of 0.36 g of sodium hydride. The mixture is brought to 60° C. for 30 minutes and 2.7 g of 1-(3-chloropropyl)-4-(4-fluorobenzoyl)piperidine, dissolved in 30 ml of dimethylformamide, are then added, again at 20° C. The mixture is kept stirring at 20° C. for approximately 15 hours and the reaction is completed by bringing to 70° C. for 2 hours. After concentration, the residue is taken up in water and the product is extracted with benzene. The oil obtained is purified by chromatography under pressure on 280 g of b 230-400 mesh silica, eluting with a mixture of dichloromethane and methanol (93.5:6.5 V/V). The base obtained is converted to the hydrochloride in ethanol. The precipitate obtained is then filtered off.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05077288 |
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| Source dataset | uspto-grants-1991_12 |
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| ORD ID | ord-f9fc9fc4a1d34e958e3ec71fbbd0d3cc |
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| Source note | uspto-grants-1991_12 |
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