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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 651651Generated: November 1, 2026

Phosphorus tribromide → 1-benzenesulfonyl-2-bromomethyl-5-chloro-1H-pyrrolo[3,2-b]pyridine

https://huagongshe.com/reaction/651651

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus tribromideHCID 24614—
Reactant(1-benzenesulfonyl-5-chloro-1H-pyrrolo[3,2-b]pyridin-2-yl)-methanolHCID 18176284—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
SolventEthyl ether methylene chlorideHCID 21881112—
Product1-benzenesulfonyl-2-bromomethyl-5-chloro-1H-pyrrolo[3,2-b]pyridineHCID 18176356—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of (1-benzenesulfonyl-5-chloro-1H-pyrrolo[3,2-b]pyridin-2-yl)-methanol (0.16 g, 0.50 mmol) in 4 mL Et2O/CH2Cl2 (1:1) at 0° C. is added phosphorous tribromide (0.023 mL, 0.25 mmol) dropwise. The reaction vessel is kept in the dark and stirred at 0° C. for 1 hour, then at room temperature for 2 hours. The mixture is diluted with water and EtOAc and the layers are separated. The aqueous layer is extracted with EtOAc. The combined organic layers are washed with water, saturated NaHCO3 solution and saturated NaCl solution, then dried over MgSO4, filtered and concentrated. The crude product (0.16 g, 0.41 mmol) is used in the subsequent step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06281227B1
Source datasetuspto-grants-2001_08
ORD IDord-c64473eb2c1f46a78d680ef6b9c0e3b0
Source noteuspto-grants-2001_08