HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 540918Generated: October 29, 2026
Triphenylphosphine → HCID 69507028, compound
https://huagongshe.com/reaction/540918
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Diisopropyl diazene-1,2-dicarboxylate | HCID 75555 | — |
| Reactant | Tert-butyl 4-hydroxypiperidine-1-carboxylate | HCID 643502 | — |
| Reactant | HCID 136347854 | HCID 136347854 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 69507028 | HCID 69507028 | 105.1% |
Reaction Steps
2-(Ethoxymethyl)-1-propyl-1H-imidazo[4,5-c]quinolin-7-ol (3.00 g, 10.5 mmol) and triphenylphosphine (3.43 g, 13.1 mmol) were slurried in THF (105 mL) and cooled with an ice/water bath. tert-Butyl 4-hydroxypiperidine-1-carboxylate (2.64 g, 13.1 mmol) was added followed by the dropwise addition of diisopropyl azodicarboxylate (2.58 mL, 13.1 mmol). The water bath was removed and the mixture was stirred for 72 hours under nitrogen. The solvent was removed under reduced pressure and the residue was purified by chromatography on a HORIZON HPFC system (silica gel, gradient elution with 1-15% CMA in chloroform) to afford 5.17 g of tert-butyl 4-{[2-(ethoxymethyl)-1-propyl-1H-imidazo[4,5-c]quinolin-7-yl]oxy}piperidine-1-carboxylate as an off-white crystalline solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08871782B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-edbcf0271a824362a8e2c009a07f5e50 |
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| Source note | uspto-grants-2014_10 |
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