HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 419424Generated: November 1, 2026
Water → 1-{1-[2,5-Bis(methyloxy)-4-nitrophenyl]-4-piperidinyl}-4-(2-fluoroethyl)piperazine
https://huagongshe.com/reaction/419424
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-Chloro-2,5-dimethoxy-4-nitrobenzene | HCID 81362 | — |
| Reactant | 1-(2-Fluoroethyl)-4-(4-piperidinyl)piperazine | HCID 59452795 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 1-{1-[2,5-Bis(methyloxy)-4-nitrophenyl]-4-piperidinyl}-4-(2-fluoroethyl)piperazine | HCID 59452919 | 75% |
Reaction Steps
4-Chloro-2,5-dimethoxynitrobenzene (1.0 g, 4.6 mmol) was dissolved in DMSO (10 mL). K2CO3 (0.953 g, 6.9 mmol) and 1-(2-fluoroethyl)-4-(4-piperidinyl)piperazine (0.989 g, 4.6 mmol) were added and the reaction mixture was heated to 80° C. and allowed to stir for 60 h. The mixture was then poured into H2O and extracted with EtOAc (2×). The combined organics were dried with MgSO4, filtered, and concentrated in vacuo. The resulting residue was adsorbed onto silica gel and flash chromatographed to give the title compound of step E (1.36 g, 75%). MS (M+H, ES+) 397.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08093239B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-ca07871b5ba04d9c8a437eaba32ff950 |
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| Source note | uspto-grants-2012_01 |
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