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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1818100Generated: November 3, 2026

Trimethyl orthovalerate → 7-bromo-2-butyl-1-isobutyl-1H-imidazo[4,5-c]quinoline

https://huagongshe.com/reaction/1818100

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethyl orthovalerateHCID 83755—
Reactant7-bromo-N4-isobutylquinoline-3,4-diamineHCID 68818159—
CatalystPyridinium chlorideHCID 10176127—
SolventTolueneHCID 1140—
Product7-bromo-2-butyl-1-isobutyl-1H-imidazo[4,5-c]quinolineHCID 2198435943.9%

Reaction Steps

7-Bromo-N4-isobutylquinoline-3,4-diamine (39.4 g of crude material), trimethyl orthovalerate (32 g, 0.20 mol), and pyridine hydrochloride (0.31 g, 2.7 mmol) were combined with anhydrous toluene (500 mL) and heated to reflux for 30 min. The reaction was cooled to room temperature, concentrated, and the residue was purified by chromatography on silica gel (75% ethyl acetate in hexane to 100% ethyl acetate gradient) to afford 21.2 g of 7-bromo-2-butyl-1-isobutyl-1H-imidazo[4,5-c]quinoline as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07598382B2
Source datasetuspto-grants-2009_10
ORD IDord-2ce973852df043cb9ceeab06a2d77bfa
Source noteuspto-grants-2009_10