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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 751613Generated: October 28, 2026

Ammonium Chloride → Ethyl 5-chloro-1H-pyrrolo[2,3-c]pyridine-2-carboxylate

https://huagongshe.com/reaction/751613

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantEthyl 3-(2-chloro-5-nitropyridin-4-yl)-2-oxopropanoateHCID 53472030—
CatalystIronHCID 23925—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 5-chloro-1H-pyrrolo[2,3-c]pyridine-2-carboxylateHCID 44630703—

Reaction Steps

3-(2-Chloro-5-nitropyridin-4-yl)-2-oxopropionic acid ethyl ester (Preparation 16, 3.0 g, 11.0 mmol) was dissolved in ethanol (100 mL) and THF (50 mL). Iron powder (3.7 g, 66.0 mmol) and saturated ammonium chloride solution (50 mL) were added and the mixture heated under reflux for 2 h. The mixture was cooled, filtered through celite and washed several times with ethyl acetate. The organic layers were combined, washed with brine (100 mL), dried (MgSO4) and concentrated in vacuo to give the title compound as a brown solid. δH (CD3OD): 1.42 (3H, t), 4.44 (2H, q), 7.15 (1H, s), 7.70 (1H, s), 8.59 (1H, s); m/z (ES+)=225 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07405210B2
Source datasetuspto-grants-2008_07
ORD IDord-1fbe2dbaf43e4ae8b16725f1ecec4fb7
Source noteuspto-grants-2008_07