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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1818107Generated: November 4, 2026

Ethoxyacetyl chloride → 7-bromo-2-ethoxymethyl-1-isobutyl-1H-imidazo[4,5-c]quinoline

https://huagongshe.com/reaction/1818107

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthoxyacetyl chlorideHCID 84189—
Reactant7-bromo-N4-isobutylquinoline-3,4-diamineHCID 68818159—
SolventPyridineHCID 1049—
Product7-bromo-2-ethoxymethyl-1-isobutyl-1H-imidazo[4,5-c]quinolineHCID 2198438641.1%

Reaction Steps

A solution of 7-bromo-N4-isobutylquinoline-3,4-diamine (85 g, prepared according to Part F of Example 1) in anhydrous pyridine (413 mL) was immersed in an ice bath, and ethoxyacetyl chloride (36.9 g, 300 mmol) was added. The reaction was allowed to warm to room temperature and was then heated in an oil bath held at 85° C. for 3.5 h. The reaction mixture was concentrated under vacuum, and the residue was taken up in diethyl ether and washed with 2M Na2CO3 (2×) followed by H2O (1×). The organic layer was dried (MgSO4), filtered, and concentrated. Recrystallization of the resulting solid from boiling 15% ethyl acetate in hexanes afforded 43.0 g of 7-bromo-2-ethoxymethyl-1-isobutyl-1H-imidazo[4,5-c]quinoline as brown crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07598382B2
Source datasetuspto-grants-2009_10
ORD IDord-c6ca7fa8f9864465b67843bc4a223ee3
Source noteuspto-grants-2009_10