HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 493425Generated: October 27, 2026
Triphenylphosphine → 6-(1-Isopropyl-piperidin-4-yloxy)-quinoline-2-carboxylic acid ethyl ester
https://huagongshe.com/reaction/493425
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 1-Isopropylpiperidin-4-ol | HCID 79681 | — |
| Reactant | Ethyl 6-hydroxyquinoline-2-carboxylate | HCID 57681568 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 6-(1-Isopropyl-piperidin-4-yloxy)-quinoline-2-carboxylic acid ethyl ester | HCID 57681570 | — |
Reaction Steps
A mixture of 1 g (0.0046 mol) of 6-hydroxy-quinoline-2-carboxylic acid ethyl ester, 2.4 g (0.0092 mol) of triphenylphospine (Fluka), 2.4 g (0.0092 mol) of 1-isopropyl-piperidin-4-ol and 1.6 ml (0.0092 mol) of di-tert.-butyl azadicarboxylate 40% in toluene in 100 ml THF was stirred for a prolonged period of time at 35° C. The mixture was filtered through a pad of silica and washed with 30 ml THF. The mixture was evaporated to dryness and purified on silica eluting with a gradient of DCM/MeOH 98/2. The product fractions were evaporated and the residue was triturated with diethyl ether to yield after drying under vacuum 1.3 mg (83%) of the title compound as white solid. MS (m/e): 343.3 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07534891B2 |
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| Source dataset | uspto-grants-2009_05 |
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| ORD ID | ord-6c18ae715d054cf2a288f8d498a16e65 |
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| Source note | uspto-grants-2009_05 |
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