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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2361104Generated: November 2, 2026

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

https://huagongshe.com/reaction/2361104

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 numberUS08686155B2
Source datasetuspto-grants-2014_04
ORD IDord-c78af1f07d164797b0fa6e32d73f592c
Source noteuspto-grants-2014_04