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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1515682Generated: November 3, 2026

Benzenesulfonyl chloride → 1-benzenesulfonyl-5-methoxymethyl-1H-pyrrolo[2,3-b]pyridine

https://huagongshe.com/reaction/1515682

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantSodium HydroxideHCID 14798—
Reactant5-methoxymethyl-1H-pyrrolo[2,3-b]pyridineHCID 67229000—
CatalystTetrabutylammonium BromideHCID 74236—
SolventDichloromethaneHCID 6344—
Product1-benzenesulfonyl-5-methoxymethyl-1H-pyrrolo[2,3-b]pyridineHCID 6722969347.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of tetrabutylammonium bromide (104 mg, 0.32 mmol) and 5-methoxymethyl-1H-pyrrolo[2,3-b]pyridine (1.74 g, 10.76 mmol) in dichloromethane (100 mL) was added sodium hydroxide powder (1.3 g, 32.4 mmol) at 0° C. The mixture was stirred at 0° C. for 5 min and then treated with benzene sulfonyl chloride (1.7 mL, 14.0 mmol). The mixture was stirred at 0° C. for another 15 min before it was warmed to 25° C. and stirred for 12 h. The resulting mixture was filtered and then concentrated in vacuo. Purification by flash silica gel chromatography (silica gel from QingDao, 200-300 mesh, glass column from Shanghai SD company, 25% ethyl acetate/hexanes) afforded 1-benzenesulfonyl-5-methoxymethyl-1H-pyrrolo[2,3-b]pyridine (1.54 g, 47.5%) as a white solid: LC/MS m/e calcd for C15H14N2O3S [M+H]+ 303.35, observed 302.9.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08222416B2
Source datasetuspto-grants-2012_07
ORD IDord-3b32470ce88e4ef09bd0a6dc32046745
Source noteuspto-grants-2012_07