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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1839068Generated: November 3, 2026

Triethylamine → N-[3-(4-amino-2-butyl-1H-imidazo[4,5-c]quinolin-1-yl)propyl]-5-(dimethylamino)naphthalene-1-sulfonamide

https://huagongshe.com/reaction/1839068

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPotassium CarbonateHCID 11430—
ReactantDansyl chlorideHCID 11801—
Reactant1-(3-aminopropyl)-2-butyl-1H-imidazo[4,5-c]quinolin-4-amineHCID 22344413—
SolventWaterHCID 962—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductN-[3-(4-amino-2-butyl-1H-imidazo[4,5-c]quinolin-1-yl)propyl]-5-(dimethylamino)naphthalene-1-sulfonamideHCID 1045967065.8%

Reaction Steps

Under a nitrogen atmosphere 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 (75 mL). A solution of 5-dimethylamino-1-naphthalenesulfonyl chloride (1.5 g, 5.55 mmol) in 1-methyl-2-pyrrolidinone was added. The reaction was monitored by HPLC. The reaction mixture was combined with water (500 mL) and the pH was adjusted to 10 with solid potassium carbonate. The resulting yellow precipitate was isolated by filtration, rinsed with water and then purified by column chromatography (silica gel eluting with 1-5% methanol in chloroform). The purified material was recrystallized from acetonitrile to provide 1.76 g of N-[3-(4-amino-2-butyl-1H-imidazo[4,5-c]quinolin-1-yl)propyl]-5-(dimethylamino)naphthalene-1-sulfonamide as a solid, m.p. 216.5-217.5° C. Analysis: Calculated for C29H34N6O2S: %C, 65.64; %H, 6.46; %N, 15.84; Found: %C, 65.52; %H, 6.44; %N, 15.90.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06677349B1
Source datasetuspto-grants-2004_01
ORD IDord-d3699ea368e845a385cee7f1ed348c09
Source noteuspto-grants-2004_01