HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1477577Generated: October 30, 2026
Sodium Iodide → 3-(4-Chlorobenzyl)-6-[4-(4-fluorophenyl)piperazin-1-yl]-1,3,5-triazine-2,4(1H,3H)-dione
https://huagongshe.com/reaction/1477577
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | 1-Chloro-4-(chloromethyl)benzene | HCID 7723 | — |
| Reactant | Lithium hydride | HCID 62714 | — |
| Reactant | 6-[4-(4-Fluorphenyl)piperazin-1-yl]-1,3,5-triazine-2,4(1H,3H)-dione | HCID 117839334 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-(4-Chlorobenzyl)-6-[4-(4-fluorophenyl)piperazin-1-yl]-1,3,5-triazine-2,4(1H,3H)-dione | HCID 117839346 | 16.3% |
Reaction Steps
To an N,N-dimethylformamide solution of 6-[4-(4-fluorophenyl)piperazin-1-yl]-1,3,5-triazine-2,4(1H,3H)-dione (1.20 g, 4.12 mmol) synthesized in Reference Synthesis Example 18, lithium hydride (75 mg, 4.94 mmol), 4-chlorobenzyl chloride (0.70 g, 4.12 mmol), and sodium iodide (catalytic amount) were added at room temperature and the resultant solution was stirred at 50° C. for 8 hours. After completion of the reaction, the reaction solution was poured into water and the resultant mixture was washed with ethyl acetate. Diluted hydrochloric acid was added to the water phase to adjust pH to 3 and the obtained solid was collected by filtration. Extraction with a mixed solution of ethyl acetate and tetrahydrofuran from the filtrate was performed and the organic layer was concentrated under reduced pressure. The residue and the solid collected by filtration were combined to obtain the title compound (280 mg, yield 15%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09403798B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-65e621a028094e45bb7d8aa12bdbaf79 |
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| Source note | uspto-grants-2016_08 |
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