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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1055043Generated: October 29, 2026

Water → 1H-​Pyrrolo[2,​3-​b]​pyridine, 3-​bromo-​5-​fluoro-​1-​[(4-​methylphenyl)​sulfonyl]​-

https://huagongshe.com/reaction/1055043

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantSodium hydrideHCID 24758—
Reactant3-Bromo-5-fluoro-1H-pyrrolo[2,3-b]pyridineHCID 53412568—
SolventDimethylformamideHCID 6228—
Product1H-​Pyrrolo[2,​3-​b]​pyridine, 3-​bromo-​5-​fluoro-​1-​[(4-​methylphenyl)​sulfonyl]​-HCID 7125133096%

Reaction Conditions

Temperature0 °C

Reaction Steps

3-bromo-5-fluoro-1H-pyrrolo[2,3-b]pyridine (5.0 g, 23.3 mmol) was dissolved in DMF (37.5 mL) and cooled to 0° C. Sodium hydride (1.5 g, 37.2 mmol) was added and the reaction mixture was stirred for 10 minutes and then treated with tosyl chloride (6.6 g, 34.9 mmol). The mixture was stirred for 30 minutes at 0° C. and then at room temperature for another 90 minutes. The reaction mixture was poured into water (100 mL) and the resulting solid was collected, washed with water and hexanes three times and dried in vacuo to afford 8.26 g of 3-bromo-5-fluoro-1-(p-tolylsulfonyl)pyrrolo[2,3-b]pyridine, 22a: 1H NMR (300 MHz, DMSO-d6) δ 8.48 (s, 1H), 8.31 (s, 1H), 8.01 (d, J=8.3 Hz, 2H), 7.92 (dd, J=8.4, 2.7 Hz, 1H), 7.44 (d, J=8.5 Hz, 2H), 2.35 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09394302B2
Source datasetuspto-grants-2016_07
ORD IDord-9b76740955354210a9331abef05e4599
Source noteuspto-grants-2016_07