HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 493427Generated: October 27, 2026
Triphenylphosphine → 6-(3-Piperidin-1-yl-propoxy)-quinoline-2-carboxylic acid ethyl ester
https://huagongshe.com/reaction/493427
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Piperidine-1-propanol | HCID 66032 | — |
| Reactant | Ethyl 6-hydroxyquinoline-2-carboxylate | HCID 57681568 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 6-(3-Piperidin-1-yl-propoxy)-quinoline-2-carboxylic acid ethyl ester | HCID 57681571 | — |
Reaction Steps
A mixture of 0.400 g (0.002 mol) of 6-hydroxy-quinoline-2-carboxylic acid ethyl ester, 0.966 g (0.004 mmol) of triphenylphospine (Fluka), 0.396 g (0.003 mmol) of 3-piperidin-1-yl-propan-1-ol and 0.68 ml (0.004 mmol) of di-tert.-butyl azadicarboxylate 40% in toluene in 40 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/NH4OH from 97/3/0.5 to 90/10/0.5. The product fractions were evaporated and the residue was triturated with diethyl ether to yield after drying under vacuum 0.600 g (93%) of the title compound as white solid. MS (m/e): 343.3 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07534891B2 |
|---|
| Source dataset | uspto-grants-2009_05 |
|---|
| ORD ID | ord-b00283c4652847368c5c1aa4a71f9cdd |
|---|
| Source note | uspto-grants-2009_05 |
|---|