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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 341832Generated: October 30, 2026

4,5-dihydro-2-(2-phenylethyl)-6H-imidazo[4,5,1-ij]-quinolin-6-one → 5,6-dihydro-2-(2-phenylethyl)-4H-imidazo[4,5,1-ij]quinolin-6-ol

https://huagongshe.com/reaction/341832

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4,5-dihydro-2-(2-phenylethyl)-6H-imidazo[4,5,1-ij]-quinolin-6-oneHCID 15838462—
SolventTetrahydrofuranHCID 8028—
Product5,6-dihydro-2-(2-phenylethyl)-4H-imidazo[4,5,1-ij]quinolin-6-olHCID 986045379.4%

Reaction Steps

(-)-Diisopinocanphenylchloroborane (87.2 g) was dissolved in dry tetrahydrofuran (170 mL) under an argon atmosphere. Fifty grams of 4,5-dihydro-2-(2-phenylethyl)-6H-imidazo[4,5,1-ij]quinolin-6-one obtained in Example 1 was dissolved in 340 mL of dry tetrahydrofuran and the solution was added slowly at -20° C. to -25° C. After stirring for 3 hrs at the same temperature, the solvent was removed under reduced pressure. The residue was dissolved in ethyl acetate (700 mL) and, following the addition of diethanolamine (52.2 mL), the mixture was stirred at room temperature for 2 hrs. The precipitate was separated by filtration and washed with ethyl acetate; thereafter, the filtrate was concentrated. The residue was purified by silica gel column chromatography to yield 40 g of the titled compound with an optical purity of 71.8% ee. The compound was recrystallized from a solvent system consisting of a mixture of ethanol (100 mL) and hexane (400 mL) to yield the titled compound with an optical purity of 99.6% ee or more as colorless crystals (19.9 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05856334
Source datasetuspto-grants-1999_01
ORD IDord-82b01b7ced3244fcb6867a8f69d6167a
Source noteuspto-grants-1999_01