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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 44749Generated: October 24, 2026

Trimethyl orthovalerate → 4-[(2-butyl-1H-imidazo[4,5-c]quinolin-1-yl)methyl]tetrahydro-2H-pyran-4-ol

https://huagongshe.com/en/reaction/44749

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethyl orthovalerateHCID 83755—
ReactantPyridinium chlorideHCID 10176127—
Reactant4-[(3-Aminoquinolin-4-ylamino)methyl]tetrahydropyran-4-olHCID 57457824—
SolventTolueneHCID 1140—
Product4-[(2-butyl-1H-imidazo[4,5-c]quinolin-1-yl)methyl]tetrahydro-2H-pyran-4-olHCID 57515444—

Reaction Steps

Trimethylorthovalerate (1.8 mL, 10.4 mmol) and pyridine hydrochloride (92 mg, 0.8 mmol) were added to a suspension of 4-[(3-aminoquinolin-4-ylamino)methyl]tetrahydropyran-4-ol (8.0 mmol) in toluene (40 mL). The reaction mixture was heated at reflux for 2.5 hours and then cooled to ambient temperature. A precipitate was isolated by filtration and dried to provide 4-[(2-butyl-1H-imidazo[4,5-c]quinolin-1-yl)methyl]tetrahydro-2H-pyran-4-ol as a white solid, mp 180-181° C. MS (ESI) m/z 340 (M+H)+; Anal. calcd for C20H25N3O2: C, 70.77; H, 7.42; N, 12.38. Found: C, 70.58; H, 7.53; N, 12.40.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08541438B2
Source datasetuspto-grants-2013_09
ORD IDord-03cbea450e964af3a7ec7dbb0fcdfc4f
Source noteuspto-grants-2013_09