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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 557604Generated: October 29, 2026

Methanesulfonyl chloride → HCID 17962880, compound

https://huagongshe.com/reaction/557604

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 numberUS08058441B2
Source datasetuspto-grants-2011_11
ORD IDord-d732457a7f624025ba12af0a7ff8b0d8
Source noteuspto-grants-2011_11