HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1513656Generated: October 26, 2026
Tetrahydrofuran → 7-Methoxy-4-((5-phenyl-[1,2,3]triazolo[1,5-a]pyridin-3-yl)methoxy)quinoline
https://huagongshe.com/reaction/1513656
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Lithium aluminum hydride | HCID 28112 | — |
| Reactant | Methyl 5-phenyl-[1,2,3]triazolo[1,5-a]pyridine-3-carboxylate | HCID 67502437 | — |
| Reactant | (5-Phenyl-[1,2,3]triazolo[1,5-a]pyridin-3-yl)methanol | HCID 67502444 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 7-Methoxy-4-((5-phenyl-[1,2,3]triazolo[1,5-a]pyridin-3-yl)methoxy)quinoline | HCID 57691340 | — |
Reaction Steps
(5-Phenyl-[1,2,3]triazolo[1,5-a]pyridin-3-yl)methanol. To a cooled (ice bath) suspension of lithium tetrahydroaluminate (0.0929 g, 2.45 mmol) in 2 mL THF (anhy) was added slowly a solution of methyl 5-phenyl-[1,2,3]triazolo[1,5-a]pyridine-3-carboxylate (0.310 g, 1.22 mmol) in 20 mL THF (internal temp remained <20 C). The mixture was allowed to stir in the ice bath 10 minutes. The mixture was diluted with EtOAc, washed with water, sat. NaHCO3, the organic layer dried over Na2SO4, and filtered. The aqueous layer still had uv activity so a solution of Rochelle's salt and EA were added and the mixture stirred 30 min. The organic layer was washed with sat NaHCO3, dried over Na2SO4, filtered, combined with main portion and evaporated. The title compound was isolated as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08217177B2 |
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| Source dataset | uspto-grants-2012_07 |
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| ORD ID | ord-46ab08c6755f4cbab140edc46ebe3ec7 |
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| Source note | uspto-grants-2012_07 |
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