HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1675135Generated: November 2, 2026
Triphenylphosphine → HCID 59149710, compound
https://huagongshe.com/reaction/1675135
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 2-(Oxan-2-yloxy)ethan-1-ol | HCID 4166833 | — |
| Reactant | Diisopropyl azodicarboxylate | HCID 5363146 | — |
| Reactant | HCID 67340083 | HCID 67340083 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 59149710 | HCID 59149710 | 53.4% |
Reaction Steps
DIAD (0.081 mL, 0.41 mmol) was added dropwise to 3-[1-[3-(trifluoromethyl)-[1,2,4]triazolo[4,3-b]pyridazin-6-yl]piperidin-4-yl]phenol (obtained as described in Example 670, preparation of starting materials) (125 mg, 0.34 mmol), triphenylphosphine (108 mg, 0.41 mmol) and 2-(tetrahydro-2H-pyran-2-yloxy)ethanol (60.4 mg, 0.41 mmol) in THF (3 mL) under nitrogen. The resulting mixture was stirred at ambient temperature for 4 hours, then added to an SCX column. The crude product was eluted from the column using 2M ammonia in methanol and the solvents were evaporated. The crude product was purified by flash silica chromatography, elution gradient 80 to 100% EtOAc in isohexane. Fractions containing product were evaporated then further purified by preparative HPLC (Waters XBridge Prep C18 OBD column, 5μ silica, 19 mm diameter, 100 mm length), using decreasingly polar mixtures of water (containing 1% ammonia) and MeCN as eluents. Fractions containing the desired compound were evaporated to dryness to afford 2-(3-(1-(3-(trifluoromethyl)-[1,2,4]triazolo[4,3-b]pyridazin-6-yl)piperidin-4-yl)phenoxy)ethanol (74 mg, 53%) as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08003649B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-35267e10a6384f4c88acb68597c98646 |
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| Source note | uspto-grants-2011_08 |
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