HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1586508Generated: November 2, 2026
2-Ethoxybenzylamine → HCID 15923150, compound
https://huagongshe.com/reaction/1586508
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Ethoxybenzylamine | HCID 123465 | — |
| Reactant | 1,6-Naphthyridine-2-carboxylic acid | HCID 735908 | — |
| Reactant | Ethyl acetate hexane | HCID 21226206 | — |
| Reactant | HCID 178526939 | HCID 178526939 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 15923150 | HCID 15923150 | 96.4% |
Reaction Steps
To a stirring mixture of 2-[1,6]naphthyridinecarboxylic acid (50 mg, 0.287 mmol) in anhydrous DMF (6.3 mL) at room temperature was added sequentially 1 hydroxybenzotriazole hydrate (42.7 mg, 0.316 mmol), 2-ethoxybenzyl amine (64.9 μL, 0.431 mmol) and 1-(3-dimethylaminopropyl)-3-ethylcarboiimide hydrochloride (61.8 mg, 0.316 mmol). The resulting mixture was allowed to stir at room temperature overnight and it was found to be clear. The solvent was removed under vacuum and the resulting residue was redissolved in CH2Cl2 (50 mL). The organic layer was washed with aq. NaHCO3, dried over anhydrous Na2SO4, and concentrated to give the crude mixture. Flash column chromatography of the crude (50% hexane/ethyl acetate to 100% ethyl acetate) afforded the desired product as a white solid (85.0 mg, 96%): m.p. 79-80° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05945431 |
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| Source dataset | uspto-grants-1999_08 |
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| ORD ID | ord-e9bb01efd4144479ba60bd634c94f7f0 |
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| Source note | uspto-grants-1999_08 |
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