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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1627159Generated: October 26, 2026

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

https://huagongshe.com/reaction/1627159

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantSodium HydroxideHCID 14798—
Reactant5-fluoro-3-iodo-1H-pyrrolo[2,3-b]pyridine-4-carbaldehydeHCID 86654207—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product5-fluoro-3-iodo-1-tosyl-1H-pyrrolo[2,3-b]pyridine-4-carbaldehydeHCID 5829349255%

Reaction Steps

To a solution of 5-fluoro-3-iodo-1H-pyrrolo[2,3-b]pyridine-4-carbaldehyde in DMF (12 mL) was added NaOH (0.716 g, 17.91 mmol). The deep red solution was stirred for 30 min after which 4-methylbenzene-1-sulfonyl chloride (3.13 g, 16.42 mmol) was added. The reaction mixture was stirred for 2 h, subsequently diluted with EtOAc, and washed with water and brine. The extracts were dried over MgSO4 and concentrated. Purification by silica column chromatography (DCM, 100%) afforded the title compound as light yellow solid (3.65 g, 55%). 1H NMR (400 MHz, DMSO-d6) δ 2.36 (s, 3 H) 7.45 (m, J=8.08 Hz, 2 H) 8.02 (m, J=8.34 Hz, 2 H) 8.42 (s, 1 H) 8.59 (d, J=2.53 Hz, 1 H) 11.13 (s, 1 H). [M+H] calc'd for C15H10FIN2O3S, 445; found, 445.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785429B2
Source datasetuspto-grants-2014_07
ORD IDord-5a026da4d0574933a27f2e379f2ad739
Source noteuspto-grants-2014_07