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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 388615Generated: October 31, 2026

Tetrahydrofuran → HCID 178455216, compound

https://huagongshe.com/reaction/388615

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantHCID 86633735HCID 86633735—
SolventPyridineHCID 1049—
ProductHCID 178455216HCID 17845521652.1%

Reaction Conditions

Temperature80 °C

Reaction Steps

1,1′-Carbonyldiimidazole (32.6 g, 201 mmol) was added to a solution of N4-[4-(tert-butyldimethylsilanyloxy)butyl]-2-chloroquinoline-3,4-diamine (50.96 g, 134.1 mmol), THF (250 mL), and pyridine (250 mL), and the reaction was heated at 80° C. overnight and allowed to cool. The volatiles were removed under reduced pressure. The residue was dissolved in ethyl acetate (600 mL), and the resulting solution was washed sequentially with brine (2×400 mL) and water (2×400 mL) and then concentrated under reduced pressure. The resulting solid was triturated with diethyl ether (1 L), collected by filtration, washed with diethyl ether (800 mL), and dried under vacuum for 30 minutes to provide 28.39 g of 1-[4-(tert-butyldimethylsilanyloxy)butyl]-4-chloro-1H-imidazo[4,5-c]quinolin-2-ol as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08377957B2
Source datasetuspto-grants-2013_02
ORD IDord-1e035d8b6e774ea1926dd07963d1f8d3
Source noteuspto-grants-2013_02