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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2264903Generated: October 25, 2026

Sodium ethoxide → ethyl 3-amino-1H-pyrrolo[3,2-c]pyridine-2-carboxylate

https://huagongshe.com/reaction/2264903

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ethoxideHCID 2723922—
ReactantEthyl-4-(3-cyanopyridine)glycinateHCID 67212023—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Productethyl 3-amino-1H-pyrrolo[3,2-c]pyridine-2-carboxylateHCID 2321818555%

Reaction Steps

To a solution of ethyl-4-(3-cyanopyridine)glycinate (2.47 g, 12.1 mmol) under nitrogen in EtOH (60 mL) was added sodium ethoxide (0.90 g, 13.3 mmol) and the mixture was heated at reflux for 1 hour. The mixture was allowed to cool to ambient temperature then quenched by the addition of water (3 mL) and saturated ammonium chloride solution (5 mL). The solvent was concentrated in vacuo, to provide a residue that was diluted with water (30 mL), and extracted with EtOAc (2×40 mL). The combined organic layers were dried (Na2SO4), filtered and evaporated to give the title compound as a brown solid (1.35 g, 55%). LCMS (method B): RT=0.61 min, M+H+=206.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07855216B2
Source datasetuspto-grants-2010_12
ORD IDord-45af08c7d9864d7e8e1a48054187e9c9
Source noteuspto-grants-2010_12