HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2381109Generated: November 4, 2026
4-(4-Fluorophenyl)piperidin-4-ol → HCID 44125832, compound
https://huagongshe.com/reaction/2381109
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-(4-Fluorophenyl)piperidin-4-ol | HCID 77497 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 6-Chloro-3-(trifluoromethyl)-(1,2,4)triazolo(4,3-b)pyridazine | HCID 613657 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 44125832 | HCID 44125832 | 74.3% |
Reaction Steps
6-Chloro-3-(trifluoromethyl)-[1,2,4]triazolo[4,3-b]pyridazine (obtained as described in Monatsh. Chem. 1972, 103, 1591) (251 mg, 1.13 mmol), 4-(4-fluorophenyl)piperidin-4-ol (215 mg, 1.13 mmol) and DIPEA (0.20 mL, 1.13 mmol) in DMF (3 mL) were stirred and heated at 80° C. for 1 hour. The resulting solution was cooled to ambient temperature, and quenched with water (10 mL). The precipitated solid was collected by filtration, washed sequentially with water, acetonitrile and ether and dried under vacuum to give 4-(4-fluorophenyl)-1-[3-(trifluoromethyl)[1,2,4]triazolo[4,3-b]pyridazin-6-yl]piperidin-4-ol (320 mg, 74%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08258140B2 |
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| Source dataset | uspto-grants-2012_09 |
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| ORD ID | ord-96ca5ab8194943d2b12139cad8da07f4 |
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| Source note | uspto-grants-2012_09 |
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