Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 217596Generated: October 28, 2026

Water → 1-Benzenesulfonyl-5-iodo-1H-pyrrolo[2,3-b]pyridine

https://huagongshe.com/reaction/217596

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantSodium HydroxideHCID 14798—
Reactant5-Iodo-1H-pyrrolo[2,3-b]pyridineHCID 24229214—
CatalystTetrabutylammonium BromideHCID 74236—
SolventTetrahydrofuranHCID 8028—
Product1-Benzenesulfonyl-5-iodo-1H-pyrrolo[2,3-b]pyridineHCID 5098946585.8%

Reaction Steps

5-Iodo-1H-pyrrolo[2,3-b]pyridine (24, 0.521 g, 2.13 mmol), tetra-N-butylammonium bromide (0.0689 g, 0.214 mmol), and 5.00 M sodium hydroxide in water (5.50 mL, 0.0275 mol) were combined in a round bottom flask. Benzenesulfonyl chloride (28, 0.327 mL, 2.56 mmol) in 5.0 mL of tetrahydrofuran was added dropwise at room temperature. The reaction was stirred at room temperature overnight and the two layers were separated. The aqueous layer was washed with ethyl acetate and the combined organic layers were washed with 1M aqueous sodium bicarbonate followed by water. The organic layer was washed with brine and dried over anhydrous sodium sulfate, then filtered and the filtrate concentrated. The crude material was purified by silica gel flash chromatography eluting with ethyl acetate and dichloromethane. The appropriate fractions were combined and the solvents removed under vacuum to provide the desired compound (29, 0.702 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08198273B2
Source datasetuspto-grants-2012_06
ORD IDord-e39f1fd2e13e4d8da6f1ea23de056630
Source noteuspto-grants-2012_06