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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 704849Generated: October 29, 2026

Ethyl orthoformate → 4-chloro-1-isobutyl-1H-imidazo[4,5-c]quinoline

https://huagongshe.com/reaction/704849

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl orthoformateHCID 31214—
Reactant2-Chloro-N~4~-(2-methylpropyl)quinoline-3,4-diamineHCID 11747039—
SolventEthanolHCID 702—
Product4-chloro-1-isobutyl-1H-imidazo[4,5-c]quinolineHCID 38396192%

Reaction Steps

A suspension of 2-chloro-N4 -(2-methylpropyl)-3,4-quinolinediamine (35 g) and triethylorthoformate (52.3 g, 2.5 eq) was heated at 145° C. for 10 h, during which time ethanol was removed by distillation. The resulting mixture was cooled to room temperature and the solid was removed by filtration. The solid was dissolved in hydrochloric acid (100 mL, 4N). The resulting solution was added to a solution of sodium hydroxide. The precipitate was filtered and washed with water to afford the product 4-chloro-1-(2-methylpropyl)-1H-imidazo[4,5-c]quinoline in 92% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04988815
Source datasetuspto-grants-1991_01
ORD IDord-7bae1df222914b5c9c0fc21d3185bffd
Source noteuspto-grants-1991_01