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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 9368Generated: October 26, 2026

Thiophene-3-boronic acid → 1-isobutyl-8-(thiophen-3-yl)-1H-imidazo[4,5-c]quinolin-4-amine

https://huagongshe.com/reaction/9368

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiophene-3-boronic acidHCID 581760—
Reactant8-bromo-1-isobutyl-1H-imidazo[4,5-c]quinolin-4-amineHCID 11174597—
Product1-isobutyl-8-(thiophen-3-yl)-1H-imidazo[4,5-c]quinolin-4-amineHCID 21984179—

Reaction Steps

8-Bromo-1-isobutyl-1H-imidazo[4,5-c]quinolin-4-amine and thiophene-3-boronic acid were coupled according to the general procedure described in Part J of Example 1. Recrystallization from isopropanol followed by chromatography on silica gel (7% methanol in CH2Cl2) afforded 1-isobutyl-8-(thiophen-3-yl)-1H-imidazo[4,5-c]quinolin-4-amine as a white solid, m.p. 235–236° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07091214B2
Source datasetuspto-grants-2006_08
ORD IDord-b5404f3d81c74fca9c293d91f37982f0
Source noteuspto-grants-2006_08