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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-(6-Methoxypyridin-2-yl)ethan-1-amine | HCID 21243519 | — |
| Reactant | hydrogen chloride CPME | HCID 66926893 | — |
| Reactant | Ethyl glyoxylate toluene | HCID 86599969 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178470231 | HCID 178470231 | 82% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09365520B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-8147c7eedd4e41ee8e937e2a4ff624a3 |
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| Source note | uspto-grants-2016_06 |
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