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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 731606Generated: October 30, 2026

Triethylsilane → HCID 13285353, compound

https://huagongshe.com/reaction/731606

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylsilaneHCID 12052—
Reactant2-Chloro-1-(1H-pyrrolo[2,3-b]pyridin-3-yl)ethan-1-oneHCID 12778217—
SolventTrifluoroacetic acidHCID 6422—
SolventEthyl AcetateHCID 8857—
SolventSodium CarbonateHCID 10340—
ProductHCID 13285353HCID 13285353—

Reaction Steps

A stirred solution of 2-chloro-1-(1H-pyrrolo[2,3-b]pyridin-3-yl)ethanone (12.5 g) in TFA at room temperature is treated with triethylsilane (72 mL, 7 eq.), stirred for 16 h, diluted with EtOAc and saturated sodium carbonate to pH 8. The phases are separated and the organic phase is dried over MgSO4 and concentrated in vacuo. The resultant residue is purified by flash chromatography (silica gel, 10% EtOAc in ether as eluent) to give the title pyrrolo[2,3-b]pyridine compound, identified by NMR and mass spectral analyses.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07585876B2
Source datasetuspto-grants-2009_09
ORD IDord-1bffaa37e0494f60a8b432b4357e1136
Source noteuspto-grants-2009_09