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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 748646Generated: October 30, 2026

Ethyl Acetate → 6-Chloro-1H-pyrrolo[2,3-b]pyridine

https://huagongshe.com/reaction/748646

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium HydroxideHCID 14798—
Reactant(6-Chloro-1H-pyrrolo[2,3-b]pyridin-1-yl)(phenyl)methanoneHCID 15013892—
SolventMethanolHCID 887—
Product6-Chloro-1H-pyrrolo[2,3-b]pyridineHCID 11344118—

Reaction Steps

A solution of (Intermediate C3) (3.12 mmol) in MeOH (90 mL) was treated with 1 M NaOH (30 mL) at rt for 18 h. The solution was freed of MeOH under reduced pressure and ethyl acetate was added to the aqueous layer. The aqueous layer was extracted with ethyl acetate and the combined organic layers were washed with sat. NaHCO3, and dried over Na2SO4. The mixture was filtered and the solvent was evaporated to give a solid 6-chloro-1H-pyrrolo[2,3-b]pyridine (Intermediate C4).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07399868B2
Source datasetuspto-grants-2008_07
ORD IDord-12104a8f793c40f4a9680a0d47d24369
Source noteuspto-grants-2008_07