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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 547293Generated: October 25, 2026

1,1,1-Triethoxybutane → 1-{2-[2-(methylsulfonyl)ethoxy]ethyl}-2-propyl-1H-imidazo[4,5-c]quinoline

https://huagongshe.com/reaction/547293

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1,1-TriethoxybutaneHCID 371779—
ReactantPyridinium chlorideHCID 10176127—
ReactantN4-{2-[2-(methylsulfonyl)ethoxy]ethyl}quinoline-3,4-diamineHCID 86064731—
SolventAcetonitrileHCID 6342—
Product1-{2-[2-(methylsulfonyl)ethoxy]ethyl}-2-propyl-1H-imidazo[4,5-c]quinolineHCID 6720397785.3%

Reaction Steps

Triethyl orthobutyrate (2.2 mL, 14 mmol) was added to a stirred solution of N4-{2-[2-(methylsulfonyl)ethoxy]ethyl}quinoline-3,4-diamine (3.6 g, 12 mmol) in acetonitrile (60 mL). Pyridine hydrochloride (0.3 g) was added and the reaction mixture was heated to reflux with the volatiles being collected in a Dean Stark trap. After 40 minutes analysis by TLC indicated that the starting material was consumed. The reaction mixture was concentrated under reduced pressure to provide 3.7 g of 1-{2-[2-(methylsulfonyl)ethoxy]ethyl}-2-propyl-1H-imidazo[4,5-c]quinoline as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07939526B2
Source datasetuspto-grants-2011_05
ORD IDord-a8602f05cb754a1689b7a06ba4ceaf0b
Source noteuspto-grants-2011_05