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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2202235Generated: October 31, 2026

2-(6-Methoxypyridin-2-yl)ethan-1-amine → HCID 178470231, compound

https://huagongshe.com/reaction/2202235

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(6-Methoxypyridin-2-yl)ethan-1-amineHCID 21243519—
Reactanthydrogen chloride CPMEHCID 66926893—
ReactantEthyl glyoxylate tolueneHCID 86599969—
SolventEthanolHCID 702—
ProductHCID 178470231HCID 17847023182%

Reaction Steps

A solution of 2-(6-methoxypyridin-2-yl)ethanamine (14.43 g, 94.81 mmol), 4N hydrogen chloride/CPME (26.1 mL, 104.29 mmol) and 47% ethyl glyoxylate/toluene solution (polymer form) (30.0 mL, 142.22 mmol) in EtOH (175 mL) was heated under reflux for 8 hr. To the reaction mixture were added 4N hydrogen chloride/CPME (26.1 mL, 104.29 mmol) and 47% ethyl glyoxylate/toluene solution (polymer form) (30.0 mL, 142.22 mmol), and the mixture was heated again under reflux for 16 hr. The reaction mixture was concentrated under reduced pressure to half volume, and to the residue was added diethyl ether (ca. 150 mL). The precipitate was collected by filtration, and washed with EtOH/diethyl ether to give crude ethyl 2-hydroxy-5,6,7,8-tetrahydro-1,6-naphthyridine-5-carboxylate hydrochloride (20.01 g, 77 mmol, 82%) as an off-white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365520B2
Source datasetuspto-grants-2016_06
ORD IDord-8147c7eedd4e41ee8e937e2a4ff624a3
Source noteuspto-grants-2016_06