HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 583901Generated: October 30, 2026
Methanesulfonyl chloride → HCID 10338633, compound
https://huagongshe.com/reaction/583901
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | HCID 22180889 | HCID 22180889 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 10338633 | HCID 10338633 | 28.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06924293B2 |
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| Source dataset | uspto-grants-2005_08 |
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| ORD ID | ord-22c5639ab4a54a88b88031fdd818e71e |
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| Source note | uspto-grants-2005_08 |
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