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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 217607Generated: October 26, 2026

Water → 1-Propanesulfonamide, N-[3-[(5-bromo-1H-pyrrolo[2,3-b]pyridin-3-yl)carbonyl]-2,4-difluorophenyl]-

https://huagongshe.com/reaction/217607

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantAluminum(III) ChlorideHCID 6451240—
Reactant5-bromo-1H-pyrrolo[2,3-b]pyridineHCID 10307932—
Reactant2,6-Difluoro-3-(propane-1-sulfonylamino)-benzoyl chlorideHCID 58086861—
SolventDichloromethaneHCID 6344—
Product1-Propanesulfonamide, N-[3-[(5-bromo-1H-pyrrolo[2,3-b]pyridin-3-yl)carbonyl]-2,4-difluorophenyl]-HCID 11984556—

Reaction Steps

To aluminum trichloride (8.89 g, 66.7 mmol) was added methylene chloride (150 mL) under an atmosphere of nitrogen below 5° C. Into this, 5-bromo-1H-pyrrolo[2,3-b]pyridine (55, 1.64 g, 8.34 mmol) in methylene chloride (20 mL) was added. The reaction was stirred for 60.0 minutes and 2,6-difluoro-3-(propane-1-sulfonylamino)-benzoyl chloride (54, 3.50 g, 11.8 mmol) in methylene chloride (20 mL) was added. The reaction was stirred for 6 hours and warmed to room temperature overnight. The reaction mixture was poured into water and extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate, filtrated and concentrated. The desired compound was isolated by silica gel column chromatography (methylene chloride/methanol 5%) to give a white solid (56, 1.2 g, 31.4%). MS (ESI) [M+H+]+=460.0, 462.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08198273B2
Source datasetuspto-grants-2012_06
ORD IDord-53145a70d33541a3918f8bb911555e46
Source noteuspto-grants-2012_06