HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1477576Generated: October 29, 2026
Acetic Acid → 6-[4-(4-Fluorphenyl)piperazin-1-yl]-1,3,5-triazine-2,4(1H,3H)-dione
https://huagongshe.com/reaction/1477576
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | 2,4-Dichloro-6-[4-(4-fluorophenyl)piperazin-1-yl]-1,3,5-triazine | HCID 62857591 | — |
| Solvent | Water | HCID 962 | — |
| Product | 6-[4-(4-Fluorphenyl)piperazin-1-yl]-1,3,5-triazine-2,4(1H,3H)-dione | HCID 117839334 | 86% |
Reaction Steps
An acetic acid solution of 2,4-dichloro-6-[4-(4-fluorophenyl)piperazin-1-yl]-1,3,5-triazine (2.40 g, 7.31 mmol) synthesized in Reference Synthesis Example 1 and sodium acetate (1.80 g) was stirred at 80° C. for 8 hours. After completion of the reaction, the reaction solution was poured into water and the obtained solid was collected by filtration. Extraction with ethyl acetate was performed from the filtrate and the resultant ethyl acetate phase was concentrated under reduced pressure. The residue and the solid collected by filtration were combined and the combination was suspended into ethyl acetate, collected by filtration, washed with ethyl acetate, and dried under reduced pressure to obtain the title compound (1.82 g, yield 86%).
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-88a03e277fc74d18b707b7c77aa4a100 |
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| Source note | uspto-grants-2016_08 |
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