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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2180303Generated: October 31, 2026

Methanesulfonyl chloride → HCID 10338633, compound

https://huagongshe.com/reaction/2180303

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 numberUS06888000B2
Source datasetuspto-grants-2005_05
ORD IDord-c89cc2d7c3114a90b45804e287a49c61
Source noteuspto-grants-2005_05