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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 746571Generated: October 29, 2026

Benzoyl chloride → HCID 23512661, compound

https://huagongshe.com/reaction/746571

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantTriethylamineHCID 8471—
Reactant1-(8-Aminooctyl)-2-butyl-1H-imidazo[4,5-c]quinolin-4-amineHCID 22344448—
SolventDichloromethaneHCID 6344—
ProductHCID 23512661HCID 2351266146.8%

Reaction Steps

A solution of 1-(8-aminooctyl)-2-butyl-1H-imidazo[4,5-c]quinolin-4-amine (1.2 g, 3.26 mmol) and triethylamine (500 μL, 3.59 mmol) in dichloromethane (30 mL) was cooled to 0° C. Benzoyl chloride (380 μL, 3.26 mmol) was slowly added dropwise. The reaction mixture was allowed to slowly warm to ambient temperature. After several hours the reaction mixture was washed with distilled water (1×50 mL) and brine (2×50 mL), dried over sodium sulfate and then concentrated under reduced pressure to provide 1.5 g of crude orange gooey material. This material was purified by column chromatography (65 g of silica gel, eluting with 7.5% methanol in dichloromethane). The purified material was dissolved in a small amount of dichloromethane and the solution was diluted with hexane to precipitate a white powder. This material was isolated by filtration, washed with hexanes and then dried in a vacuum oven at 60° C. overnight to provide 0.72 g of N-[8-(4-amino-2-butyl-1H-imidazo[4,5-c]quinolin-1-yl)octyl]benzamide as a white powder, m.p. 149.5-151.3° C. Analysis: Calculated for C29H37N5O: % C, 73.85; % H, 7.91; % N, 14.85;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07393859B2
Source datasetuspto-grants-2008_07
ORD IDord-a4224cb40b1f4bdd9202e3dbca7b363e
Source noteuspto-grants-2008_07