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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 353890Generated: October 31, 2026

Benzoyl chloride → HCID 23512658, compound

https://huagongshe.com/reaction/353890

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantTriethylamineHCID 8471—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 22344442HCID 22344442—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 23512658HCID 2351265862.3%

Reaction Steps

A solution containing 1-(3-amino-2,2-dimethylpropyl)-2-(2-methoxyethyl)-1H-imidazo[4,5-c]quinolin-4-amine (1.0 g, 3.05 mmol) and triethylamine (470 μL, 3.36 mmol) in 1-methyl-2-pyrrolidinone (30 mL) was cooled to 0C. Benzoyl chloride (345 μL, 3.05 mmol) was slowly added dropwise. The reaction mixture was allowed to slowly warm to ambient temperature overnight. The reaction mixture was combined with 1% aqueous sodium bicarbonate solution (150 mL) and then stirred overnight. A fine white precipitate was isolated by filtration and washed with hexanes. The material was dissolved in dichloromethane, methanol and toluene. The solution was concentrated under vacuum. The material was purified by column chromatography (60 g silica gel eluting with 7.5% methanol in dichloromethane) and then dried in a vacuum oven at 50° C. for 2 days to provide 0.82 g of N-{3-[4-amino-2-(2-methoxyethyl)-1H-imidazo[4,5-c]quinolin-1-yl]-2,2-dimethylpropyl}benzamide as an off white powder, m.p. 103-125° C. Analysis: Calculated for C25H29N5O2.0.30 H2O: % C, 68.72; % H, 6.83; % N, 16.03. Found: % C, 68.50; % H, 6.55; % N, 16.02.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06756382B2
Source datasetuspto-grants-2004_06
ORD IDord-4d1f47a870524a74a0d4f21c1651c166
Source noteuspto-grants-2004_06