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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 594013Generated: October 27, 2026

Acetic Acid → 4-Chloro-1H-pyrrolo[2,3-B]pyridin-2(3H)-one

https://huagongshe.com/reaction/594013

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantMethanolHCID 887—
ReactantEthyl AcetateHCID 8857—
Reactant3,3-Dibromo-4-chloro-1H-pyrrolo[2,3-b]pyridin-2(3H)-oneHCID 22390981—
CatalystZincHCID 23994—
SolventSodium chloride; waterHCID 57417360—
Product4-Chloro-1H-pyrrolo[2,3-B]pyridin-2(3H)-oneHCID 11194563—

Reaction Steps

The title compound was prepared according to the procedure described in WO2001046196A1. A mixture of 3,3-dibromo-4-chloro-1H-pyrrolo[2,3-b]pyridin-2(3H)-one (4.07 g, 12.5 mmol), zinc dust (8.15 g, 125 mmol), AcOH (54.2 ml, 12.5 mmol), and MeOH (54.2 ml, 12.5 mmol) was stirred at rt. After 3 h, the reaction mixture was passed through a pad of celite with an aid of EtOAc. The filtrate was then diluted with brine. The whole was extracted with EtOAc. The organic layer was further washed with brine, dried over MgSO4, filtered, concentrated. The product was purified by column chromatography on silica gel using 70:30 DCM:(90:10:1 DCM:MeOH:NH4OH). Fractions containing the product were concentrated. White cotton-like solid, 4-chloro-1H-pyrrolo[2,3-b]pyridin-2(3H)-one was obtained. MS Calcd for C7H5ClN2O: [M]+=168. Found: [M+H]+=169.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242961B2
Source datasetuspto-grants-2016_01
ORD IDord-38c9864941ea4259925e34cf6e5e9c6e
Source noteuspto-grants-2016_01