Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1837573Generated: October 30, 2026

Butyl isocyanate → HCID 10408458, compound

https://huagongshe.com/reaction/1837573

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButyl isocyanateHCID 8110—
ReactantTriethylamineHCID 8471—
ReactantPotassium CarbonateHCID 11430—
Reactant1-(3-aminopropyl)-2-butyl-1H-imidazo[4,5-c]quinolin-4-amineHCID 22344413—
SolventWaterHCID 962—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 10408458HCID 1040845840%

Reaction Steps

Triethylamine (765 mg, 7.56 mmol) was added to a solution of 1-(3-aminopropyl)-2-butyl-1H-imidazo[4,5-c]quinolin-4-amine (1.5 g, 5.04 mmol) in 1-methyl-2-pyrrolidinone (100 mL). Butyl isocyanate (549 mg, 5.55 mmol) was added dropwise with stirring. The reaction mixture was allowed to stir overnight and then it was poured into water (500 mL). The pH was adjusted to 10 using solid potassium carbonate. The resulting precipitate was isolated by filtration, washed with water and then purified by column chromatography (silica gel eluting with 5% methanol in dichloromethane and then with 10% methanol in dichloromethane. The purified material was recrystallized from acetonitrile to provide 800 mg of N-[3-(4-amino-2-butyl-1H-imidazo[4,5-c]quinolin-1-yl)propyl]-N′-butylurea as a white solid, m.p. 185.5-186.40C. Analysis: Calculated for C22H32N6O: %C, 66.64; %H, 8.13; %N, 21.29; Found: %C, 66.38; %H, 8.19; %N, 21.10.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06784188B2
Source datasetuspto-grants-2004_08
ORD IDord-4d9200e3234b48388968ebde580b5541
Source noteuspto-grants-2004_08