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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1825744Generated: November 2, 2026

Sodium Iodide → HCID 54023975, compound

https://huagongshe.com/reaction/1825744

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantDimethylformamideHCID 6228—
ReactantSodium hydrideHCID 24758—
Reactant2-(Chloromethoxy)ethyl benzoateHCID 2724500—
Reactant1H-Pyrrolo[2,3-b]pyridine-3-carbaldehydeHCID 5372812—
SolventWaterHCID 962—
ProductHCID 54023975HCID 5402397599%

Reaction Steps

A solution of 7-azaindole-3-carboxaldehyde (2 g, 13.7 mmol) in dry N,N-dimethylformamide (30 ml) was added dropwise, under nitrogen atmosphere, to a stirring suspension of 60% sodium hydride (oil dispersion) (0.6 g, 15 mmol) in dry N,N-dimethylformamide (10 ml) keeping the temperature between 5–10° C. (ice-water bath). After addition was completed, stirring was continued at the same temperature for 30 min. Then a solution of benzoyloxyethyl chloromethyl ether (3.8 g, 15 mmol) in dry N,N-dimethylformamide (40 ml) was added dropwise. After addition was complete, a catalytic amount of sodium iodide was added, and the temperature was allowed to rise to room temperature. The reaction mixture was allowed to stand at room temperature under nitrogen for 6 days, with intermittent stirring. Then water (100 ml) was added, and the mixture extracted with dichloromethane (3×100 ml). The organic phase was washed with water (100 ml), dried over anhydrous magnesium sulfate, filtered and the solvent removed under reduced pressure to give an oil (4.4 g, 99%), which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07049312B1
Source datasetuspto-grants-2006_05
ORD IDord-11ef4ea945284c92873d0393a5085c2f
Source noteuspto-grants-2006_05