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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 341839Generated: October 29, 2026

Water → 5,6-dihydro-6-methoxy-2-(2-phenylethyl)-4H-imidazo[4,5,1-ij]quinoline

https://huagongshe.com/reaction/341839

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactant5,6-dihydro-2-(2-phenylethyl)-4H-imidazo[4,5,1-ij]quinolin-6-olHCID 9860453—
SolventTetrahydrofuranHCID 8028—
Product5,6-dihydro-6-methoxy-2-(2-phenylethyl)-4H-imidazo[4,5,1-ij]quinolineHCID 1583846849%

Reaction Steps

A portion (115 mg) of 60% sodium hydride was added to anhydrous tetrahydrofuran (15 mL) under an argon atmosphere; 0.2 g of 5,6-dihydro-2-(2-phenylethyl)-4H-imidazo[4,5,1-ij]quinolin-6-ol obtained in Example 4 was dissolved in anhydrous tetrahydrofuran (4 mL) and the solution was added dropwise to the first mentioned solution at room temperature. After stirring for 35 min at room temperature, methyl iodide (1.02 g) was added dropwise and the mixture was stirred for 4 hrs. Water was added to the reaction solution and the mixture was stirred; thereafter, the reaction solution was extracted with dichloromethane, washed with saturated brine and dried over anhydrous sodium sulfate. The solvent was removed under reduced pressure and the residue was purified by silica gel column chromatography (eluent: hexane/ethyl acetate) to yield the titled compound as a yellow oil (103 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05856334
Source datasetuspto-grants-1999_01
ORD IDord-1cf4f09a45d64ca1861103abf45f5aa5
Source noteuspto-grants-1999_01