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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1693373Generated: October 30, 2026

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

https://huagongshe.com/reaction/1693373

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantEthyl 3-(6-methoxy-3-nitropyridin-2-yl)-2-oxopropanoateHCID 59753655—
CatalystIronHCID 23925—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 5-methoxy-1H-pyrrolo[3,2-b]pyridine-2-carboxylateHCID 15275362—

Reaction Steps

To a suspension of 3-(6-methoxy-3-nitropyridin-2-yl)-2-oxopropionic acid ethyl ester (Preparation 34, 276 mg, 1.03 mmol) in THF (12 mL) and ethanol (5 mL) was added saturated aqueous ammonium chloride solution (5 mL) and iron powder (346 mg, 6.18 mmol) in one portion. The reaction mixture was heated under reflux for 1 h then filtered whilst still hot through a celite plug, washing with hot ethyl acetate. The filtrate was cooled and washed with brine (20 mL), dried (MgSO4), filtered and adsorbed onto silica gel in vacuo. Purification via flash column chromatography (SiO2, ethyl acetate/hexanes, 1:9) gave the title compound as a beige solid. δH (CDCl3): 1.40 (3H, t), 3.99 (3H, s), 4.41 (2H, q), 6.74 (1H, d), 7.20 (1H, m), 7.62 (1H, d), 9.27 (1H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08158622B2
Source datasetuspto-grants-2012_04
ORD IDord-f75b72cff74f48d8aefbf69c393c0884
Source noteuspto-grants-2012_04