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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1820905Generated: October 26, 2026

Dichloromethane → 1-Benzenesulfonyl-5-(3,4-dimethoxy-phenyl)-3-iodo-1H-pyrrolo[2,3-b]pyridine

https://huagongshe.com/reaction/1820905

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantBenzenesulfonyl chlorideHCID 7369—
Reactant5-(3,4-Dimethoxy-phenyl)-3-iodo-1H-pyrrolo[2,3-b]pyridineHCID 59812169—
CatalystTetrabutylammonium BromideHCID 74236—
SolventWaterHCID 962—
SolventSodium HydroxideHCID 14798—
Product1-Benzenesulfonyl-5-(3,4-dimethoxy-phenyl)-3-iodo-1H-pyrrolo[2,3-b]pyridineHCID 59811902—

Reaction Steps

Into a Round bottom flask was added 5-(3,4-Dimethoxy-phenyl)-3-iodo-1H-pyrrolo[2,3-b]pyridine, 133, (0.403 g, 0.00106 mol) and Tetra-N-butylammonium bromide (0.0342 g, 0.000106 mol), in 5.000 M of Sodium hydroxide in Water (2.73 mL). Benzenesulfonyl chloride (0.225 g, 0.00127 mol) in Methylene chloride (0.747 mL, 0.0116 mol) was added dropwise. After 2 h, 30 mL of Methylene chloride and 30 mL of water were added. The organic layer was separated and washed with 1M sodium bicarbonate (aq.) (30 ml×2) followed by water (30 ml) and brine (30 mL). The organic layer was collected and dried over anhydrous sodium sulfate, then concentrated under reduced pressure. The residue was purified by chromatography (Silica gel, ethyl acetate/hexanes) to give 295 mg of the desired product as a white solid. MS(ESI) [M+H+]+=521.04

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07605168B2
Source datasetuspto-grants-2009_10
ORD IDord-52bd2d1f0d5143619a19d974581fbd5d
Source noteuspto-grants-2009_10