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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1693353Generated: October 26, 2026

Ammonium Chloride → ethyl 1H-pyrrolo[2,3-c]pyridine-2-carboxylate

https://huagongshe.com/reaction/1693353

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantEthyl 3-(3-nitropyridin-4-yl)-2-oxopropanoateHCID 23269548—
CatalystIronHCID 23925—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
Productethyl 1H-pyrrolo[2,3-c]pyridine-2-carboxylateHCID 21819001—

Reaction Steps

To a solution of 3-(3-nitropyridin-4-yl)-2-oxopropionic acid ethyl ester (Preparation 13, 500 mg, 2.1 mmol) in ethanol (20 mL) and THF (10 mL) was added saturated ammonium chloride solution (10 mL) and iron powder (700 mg, 12.6 mmol). The reaction was heated under reflux for 1 h, then filtered through celite and washed through with hot ethyl acetate (3×30 mL). The combined organic fractions were washed with brine (20 mL), dried (MgSO4) and concentrated in vacuo to give the title compound as a brown solid. δH (CD3OD): 1.44 (3H, t), 4.43 (2H, q), 7.21 (1H, s), 7.69 (1H, d), 8.12 (1H, d), 8.80 (1H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08158622B2
Source datasetuspto-grants-2012_04
ORD IDord-9172b1f508d9421c88b8d20d627fea1f
Source noteuspto-grants-2012_04