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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1828232Generated: October 30, 2026

3-Chlorobenzenesulphonyl chloride → HCID 10412212, compound

https://huagongshe.com/reaction/1828232

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Chlorobenzenesulphonyl chlorideHCID 17909—
ReactantHCID 22065940HCID 22065940—
CatalystSilver(I) trifluoromethanesulfonateHCID 76223—
SolventNitrobenzeneHCID 7416—
ProductHCID 10412212HCID 1041221227%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 1-[(1-benzylpyrrolidin-2-yl)methyl]-1H-pyrrolo[2,3-b]pyridine (2.0 g, 6.86 mmol), 3-chlorophenylsulfonyl chloride (1.63 g, 7.55 mmol) and silver trifluoromethanesulfonate (AgOTf) (2.32 g, 8.92 mmol) in nitrobenzene is heated at 100° C. under a nitrogen atmosphere for 36 h, cooled to room temperature, quenched with 10% aqueous sodium carbonate, and extracted with CH2Cl2. The extracts are combined, washed sequentially with water and brine and concentrated in vacuo. The resultant residue is purified by flash column chromatography (0–5% methanol in CH2Cl2 as eluent) to afford the title compound as a semi-solid, 865 mg (27% yield), identified by HNMR and mass spectral analyses.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07057039B2
Source datasetuspto-grants-2006_06
ORD IDord-dfaf401ac2984cd99c28986710cd5cc4
Source noteuspto-grants-2006_06