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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1362928Generated: October 30, 2026

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

https://huagongshe.com/reaction/1362928

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 6, 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 was 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. 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 numberUS07884112B2
Source datasetuspto-grants-2011_02
ORD IDord-d718cd4ceb7647aa822432dd70de2d4d
Source noteuspto-grants-2011_02