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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1515736Generated: November 4, 2026

Triacetoxyperiodinane → 1-(1-benzenesulfonyl-1H-pyrrolo[2,3-b]pyridin-2-yl)-2-(tetrahydro-pyran-2-yl)-ethanone

https://huagongshe.com/reaction/1515736

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriacetoxyperiodinaneHCID 159087—
Reactant1-(1-benzenesulfonyl-1H-pyrrolo[2,3-b]pyridin-2-yl)-2-(tetrahydro-pyran-2-yl)-ethanolHCID 67229695—
SolventDichloromethaneHCID 6344—
Product1-(1-benzenesulfonyl-1H-pyrrolo[2,3-b]pyridin-2-yl)-2-(tetrahydro-pyran-2-yl)-ethanoneHCID 6722922184%

Reaction Conditions

Temperature25 °C

Reaction Steps

To a solution of 1-(1-benzenesulfonyl-1H-pyrrolo[2,3-b]pyridin-2-yl)-2-(tetrahydro-pyran-2-yl)-ethanol (2.5 g, 6.5 mmol) in dichloromethane (100 mL) at 25° C. was added Dess-Martin periodinane (9.6 g, 23 mmol). The reaction mixture was stirred at 25° C. for 1 h and then quenched with a saturated aqueous sodium bicarbonate solution (100 mL). The mixture was extracted with dichloromethane (50 mL), washed with a saturated aqueous sodium bicarbonate solution (3×100 mL), brine, dried over anhydrous sodium sulfate and then concentrated in vacuo to afford 1-(1-benzenesulfonyl-1H-pyrrolo[2,3-b]pyridin-2-yl)-2-(tetrahydro-pyran-2-yl)-ethanone (2.1 g, 84%) as a light yellow solid: LC/MS m/e calcd for C20H20N2O4S [M+H]+ 385.46, observed 385.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08222416B2
Source datasetuspto-grants-2012_07
ORD IDord-9fe605cfcc894735bd6379610d5724d6
Source noteuspto-grants-2012_07