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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 540889Generated: October 29, 2026

Chloride → HCID 68972752, compound

https://huagongshe.com/reaction/540889

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorideHCID 312—
ReactantTriphenylphosphineHCID 11776—
Reactant4-BenzyloxyanilineHCID 22860—
ReactantDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
Reactant3-BenzyloxyanilineHCID 92892—
ReactantTert-butyl 4-hydroxypiperidine-1-carboxylateHCID 643502—
ReactantHCID 86611427HCID 86611427—
ReactantHCID 136347851HCID 136347851—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68972752HCID 68972752—

Reaction Steps

A modification on the methods described in Parts A-H of Example 2 were used to prepare 2-(2-methoxyethyl)-1-propyl-1H-imidazo[4,5-c]quinolin-7-ol, with 3-benzyloxyaniline and 3-methoxypropanol chloride used in lieu of 4-benzyloxyaniline and ethoxyacetyl, chloride, respectively. A solution of diisopropyl azodicarboxylate (6.28 mL, 31.9 mmol) in tetrahydrofuran (25.5 mL) was added dropwise to a mixture of 2-(2-methoxyethyl)-1-propyl-1H-imidazo[4,5-c]quinolin-7-ol (7.28 g, 25.5 mmol), triphenylphosphine (8.36 g, 31.9 mmol), and t-butyl 4-hydroxypiperidine-1-carboxylate (6.42 g, 31.9 mmol) in tetrahydrofuran (191 mL) at 5° C. The mixture was allowed to warm to room temperature. After 2 days, the solvent was removed under reduced pressure and the residue was purified by flash chromatography (silica gel, gradient elution with 1.5-4% methanol in dichloromethane) to yield 9.77 g of tert-butyl 4-{[2-(2-methoxyethyl)-1-propyl-1H-imidazo[4,5-c]quinolin-7-yl]oxy}piperidine-1-carboxylate as a gray amorphous solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871782B2
Source datasetuspto-grants-2014_10
ORD IDord-de8f15eaebd042308eadff162a5d80e9
Source noteuspto-grants-2014_10