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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1837571Generated: October 30, 2026

4-Toluenesulfonyl chloride → HCID 10024938, compound

https://huagongshe.com/reaction/1837571

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantAmmonium HydroxideHCID 14923—
ReactantHCID 22479020HCID 22479020—
SolventDichloromethaneHCID 6344—
ProductHCID 10024938HCID 10024938—

Reaction Steps

Concentrated ammonium hydroxide (35 mL) was added with stirring to a solution of N-[3-(2-butyl-5-oxido-1H-imidazo[4,5-c]quinolin-1-yl)propyl]-N′-phenylurea (2.25 g, 5.39 mmol) in dichloromethane (100 mL). Tosyl chloride (1.13 g,5.93 mmol) was added in small portions over a period of 30 minutes. After 1 hour the layers were separated. The aqueous layer was extracted with dichloromethane (2×25 mL). The organics were combined and extracted with water (3×50 mL). The aqueous layers were combined and filtered to provide 1.64 g of an off white solid. This material was recrystallized sequentially from 1,2-dichloroethane, isopropyl alcohol and methanol to provide 960 mg of N-[3-(4-amino-2-butyl-1H-imidazo[4,5-c]quinolin-1-yl)propyl]-N′-phenylurea as light tan needles, m.p. 191-192° C. Analysis: Calculated for C24H28N6O: %C, 69.21; %H, 6.78; %N, 20.18; Found: %C; 68.94; %H, 6.77; %N, 19.90.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06784188B2
Source datasetuspto-grants-2004_08
ORD IDord-a4a1ed9efdf94b3993ffb2d4234d352a
Source noteuspto-grants-2004_08