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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 583901Generated: October 30, 2026

Methanesulfonyl chloride → HCID 10338633, compound

https://huagongshe.com/reaction/583901

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 22180889HCID 22180889—
SolventPyridineHCID 1049—
ProductHCID 10338633HCID 1033863328.7%

Reaction Steps

Methanesulfonyl chloride (1.27 g, 11.1 mmol) was slowly added to a solution of 1-(2-aminoethyl)-2-butyl-1H-imidazo[4,5-c]quinolin-4-amine (3.0 g, 10.6 mmol) in pyridine (60 mL). The reaction was maintained at ambient temperature overnight and then it was concentrated to dryness. The residue was combined with warm dichloroethane and water and then filtered to provide an off white solid. The dichloroethane layer was concentrated to provide an off white solid. The two solids were combined and then recrystallized from N,N-dimethylformamide to provide 1.1 g of N-[2-(4-amino-2-butyl-1H-imidazo[4,5-c]quinolin-1-yl)ethyl]methanesulfonamide as a white solid, m.p. 210.0-211.0° C. Analysis: Calculated for C17H23N5O2S: % C, 56.49; % H, 6.41; % N, 19.37; Found: % C, 56.45; % H, 6.49; % N, 19.50.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06924293B2
Source datasetuspto-grants-2005_08
ORD IDord-22c5639ab4a54a88b88031fdd818e71e
Source noteuspto-grants-2005_08