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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2382324Generated: November 3, 2026

Methanesulfonyl chloride → HCID 17962880, compound

https://huagongshe.com/reaction/2382324

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 17962902HCID 17962902—
SolventPyridineHCID 1049—
ProductHCID 17962880HCID 17962880—

Reaction Steps

Sulfonylation of 1-acetyl-6-(2-hydroxybenzoyl)amino-4-phenyl-1,2,3,4-tetrahydro-2,2,4-trimethylquinoline (12 mg) with methylsulfonyl chloride (6.5 μl) was performed in pyridine (1 ml). TLC analysis after stirring for 16 h showed conversion to a higher-running product. The mixture was concentrated, the residue was dissolved in dichloromethane and washed with water. The organic layer was dried (Na2SO4) and concentrated in vacuo. The crude product was purified by silica gel column chromatography. Eluent: heptane/ethyl acetate=8/2 (v/v).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08258293B2
Source datasetuspto-grants-2012_09
ORD IDord-233160ceb3664bed9735db9756111afa
Source noteuspto-grants-2012_09