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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 531431Generated: October 31, 2026

4-Toluenesulfonyl chloride → 5-bromo-3-iodo-1-tosyl-1H-pyrrolo[2,3-b]pyridine

https://huagongshe.com/reaction/531431

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantEthyl AcetateHCID 8857—
ReactantSodium hydrideHCID 24758—
Reactant5-Bromo-3-iodo-1H-pyrrolo(2,3-b)pyridineHCID 24229212—
SolventDimethylformamideHCID 6228—
SolventHexaneHCID 8058—
Product5-bromo-3-iodo-1-tosyl-1H-pyrrolo[2,3-b]pyridineHCID 4975906696.3%

Reaction Steps

5-Bromo-3-iodo-1H-pyrrolo[2,3-b]pyridine (7 g, 21.6 mmol) dissolved in dry DMF (50 ml) was added drop wise to a stirred slurry of sodium hydride (1.73 g, 43.2 mmol) in dry DMF (20 ml) at 0° C. and stirred for 30 min. Tosyl chloride (6.15 g, 32.4 mmol) dissolved in dry DMF (14 ml) and added slowly to the above reaction mixture and the reaction temperature was brought to RT and stirred for 30 min. The reaction was monitored by TLC (15% Ethyl acetate in hexane). The reaction mixture was quenched with ice water (500 ml) at 0° C. and filtered the solid precipitated and dried under vacuum to afford 9.92 g (96.3% yield) of 5-bromo-3-iodo-1-tosyl-1H-pyrrolo[2,3-b]pyridine MS: m/z=476.8 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09353107B2
Source datasetuspto-grants-2016_05
ORD IDord-27a01fb27ce247cd953422da19621bc7
Source noteuspto-grants-2016_05