Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 240473Generated: October 31, 2026

Sodium hydride → HCID 68749054, compound

https://huagongshe.com/reaction/240473

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant4-Nitro-1H-indoleHCID 145766—
ReactantHCID 67041431HCID 67041431—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68749054HCID 6874905416%

Reaction Steps

The title compound was also prepared according to the following method. Specifically, sodium hydride (144 mg, 6 mmol) was added to a solution of 4-nitroindole (973 mg, 6 mmol) in THF and the resulting mixture was stirred for 4 h. 1-(t-butyloxycarbonyl)-4-chloromethyl-7-azaindole (Int-11, 1.5 g, 5.5 mmol) was then added. After the reaction was complete (by TLC), the mixture was quenched with saturated aqueous ammonium chloride. The organic layer was separated and the aqueous layer was extracted with ethyl acetate. The combined organic layers were washed with brine, dried over anhydrous sodium sulfate, filtered, concentrated under reduced pressure, and purified by flash column chromatography to provide 4-[(4-nitro-1H-indol-1-yl)methyl]-1H-pyrrolo[2,3-b]pyridine (254 mg, 16%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08648086B2
Source datasetuspto-grants-2014_02
ORD IDord-879beefdebae4d33a279950311c57c7a
Source noteuspto-grants-2014_02