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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 632741Generated: October 25, 2026

Water → 4-Bromo-1,6-dihydro-6-methyl-1-((4-methylphenyl)sulfonyl)-7H-pyrrolo(2,3-c)pyridin-7-one

https://huagongshe.com/reaction/632741

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactant4-bromo-1-tosyl-1H-pyrrolo[2,3-c]pyridin-7(6H)-oneHCID 89657580—
SolventDimethylformamideHCID 6228—
Product4-Bromo-1,6-dihydro-6-methyl-1-((4-methylphenyl)sulfonyl)-7H-pyrrolo(2,3-c)pyridin-7-oneHCID 8965630496.6%

Reaction Steps

Sodium hydride (0.875 g, 36.5 mmol, 1.46 g of a 60% in oil dispersion) was added to a stirring solution of 4-bromo-1-tosyl-1H-pyrrolo[2,3-c]pyridin-7(6H)-one (11.2 g, 30.4 mmol) in dimethylformamide (217 mL) under nitrogen. After 30 minutes, iodomethane (2.27 mL, 36.5 mmol) was added and the solution was stirred at room temperature for 3 h. Upon addition of water (250 mL) a precipitate formed. The precipitate was collected by vacuum filtration, rinsed with water (50 mL) and dried in a vacuum oven at 55° C. overnight to provide 11.2 g of 4-bromo-6-methyl-1-tosyl-1H-pyrrolo[2,3-c]pyridin-7(6H)-one (96%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09321765B2
Source datasetuspto-grants-2016_04
ORD IDord-0e7a7c5b7f2b4e74a2f216b2c291a745
Source noteuspto-grants-2016_04