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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1818102Generated: November 1, 2026

2,4-Dimethoxybenzeneboronic acid → 2-butyl-7-(2,4-dimethoxyphenyl)-1-isobutyl-1H-imidazo[4,5-c]quinolin-4-amine

https://huagongshe.com/reaction/1818102

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-Dimethoxybenzeneboronic acidHCID 2734341—
Reactant7-bromo-2-butyl-1-isobutyl-1H-imidazo[4,5-c]quinolineHCID 21984359—
Reactant2-butyl-7-(2,4-dimethoxyphenyl)-1-isobutyl-1H-imidazo[4,5-c]quinolineHCID 21984377—
Product2-butyl-7-(2,4-dimethoxyphenyl)-1-isobutyl-1H-imidazo[4,5-c]quinolin-4-amineHCID 21984169—

Reaction Steps

7-Bromo-2-butyl-1-isobutyl-1H-imidazo[4,5-c]quinoline and 2,4-dimethoxybenzeneboronic acid were coupled according to the general procedure described in Part J of Example 1. The resulting 2-butyl-7-(2,4-dimethoxyphenyl)-1-isobutyl-1H-imidazo[4,5-c]quinoline was oxidized and then aminated according to the general procedures described in Parts H and I of Example 1 and purified by chromatography on silica gel (8% methanol in CH2Cl2 to 10% methanol in CH2Cl2 gradient) followed by recrystallization from 1/1 ethyl acetate/hexane to afford 2-butyl-7-(2,4-dimethoxyphenyl)-1-isobutyl-1H-imidazo[4,5-c]quinolin-4-amine as a pale orange solid, m.p. 187-189° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07598382B2
Source datasetuspto-grants-2009_10
ORD IDord-3a1f123083cf4718a3dd5159dfc4c29b
Source noteuspto-grants-2009_10