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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 751603Generated: October 29, 2026

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

https://huagongshe.com/reaction/751603

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 59753627HCID 59753627—
CatalystIronHCID 23925—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 5-chloro-1H-pyrrolo[3,2-b]pyridine-2-carboxylateHCID 45480460—

Reaction Steps

To a solution of 3-(2-chloro-5-nitropyridin-6-yl)-2-oxopropionic acid ethyl ester (Preparation 4, 1.53 g, 5.6 mmol) in THF (65 mL) and ethanol (30 mL) was added saturated aqueous ammonium chloride solution (30 mL) and the suspension was vigorously stirred at rt. Iron powder (1.95 g, 34.8 mmol) was added portionwise and the mixture was heated under reflux for 2 h then allowed to cool prior to filtration through a celite plug, and washed through with warm THF. The mixture was concentrated under reduced pressure to give an aqueous suspension, which was filtered through a sinter, washing with water. The wet solid was washed with methanol and dried. The residue was adsorbed onto silica gel and purified via flash chromatography eluting with ethyl acetate/hexane (1:19) to give the title compound as a white solid. δH (CD3OD): 1.42 (3H, t, 7.03 Hz), 4.42 (2H, q, 7.32 Hz), 7.15 (1H, s), 7.30 (1H, d, 8.79 Hz), 7.89 (1H, d, 8.35 Hz); m/z (ES+)=225.03 [M+H]+; RT=3.32 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07405210B2
Source datasetuspto-grants-2008_07
ORD IDord-74aa059e114a48f88ba011a67bbfc9e6
Source noteuspto-grants-2008_07