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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2417166Generated: October 30, 2026

Dansyl chloride → HCID 22180880, compound

https://huagongshe.com/reaction/2417166

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDansyl chlorideHCID 11801—
Reactant1-(4-aminobutyl)-1H-imidazo[4,5-c]quinolin-4-amineHCID 15453775—
SolventPyridineHCID 1049—
ProductHCID 22180880HCID 22180880—

Reaction Conditions

Temperature60 °C

Reaction Steps

A suspension of 1-(4-aminobutyl)-1H-imidazo[4,5-c]quinolin-4-amine (0.5 g, 2.0 mmol) in pyridine (250 mL) was warmed to 60° C. to dissolve the amine. The solution was allowed to cool to about 30° C. and then 5-dimethylamino-1-naphthaleneslfonyl chloride (0.5 g, 1.8 mmol) was slowly added. After 1 hour 0.3 g of 5-dimethylamino-1-naphthalenesulfonyl chloride was added. The reaction mixture was warmed to 60° C. and maintained at that temperature overnight. The reaction mixture was concentrated under vacuum. The residue was recrystallized from propyl acetate to provide N1-(4-(4-amino-1H-imidazo[4,5-c]quinolin-1-yl)butyl]-5-(dimethylamino)-1-naphthalenesulfonamide as a solid, m.p. 200-201° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06825350B2
Source datasetuspto-grants-2004_11
ORD IDord-da1d76e38d4f40ec94f21f0bfd59cdc4
Source noteuspto-grants-2004_11