HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 919919Generated: October 31, 2026
D-Phenylalanine → HCID 68297757, compound
https://huagongshe.com/reaction/919919
Participants
| Role | Name | HCID | Charge |
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| Reactant | D-Phenylalanine | HCID 71567 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | 1-Benzyl-5-hydroxy-2-oxo-3-phenyl-1,2-dihydro-[1,7]naphthyridine-6-carboxylic acid methyl ester | HCID 68297358 | — |
| Solvent | 2-Methoxyethanol | HCID 8019 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | HCID 68297757 | HCID 68297757 | 43.3% |
Reaction Steps
A mixture of 1-benzyl-5-hydroxy-2-oxo-3-phenyl-1,2-dihydro-[1,7]naphthyridine-6-carboxylic acid methyl ester (60 mg, 0.16 mmol), D-phenylalanine (514 mg, 3.1 mmol), and NaOMe (126 mg, 2.3 mmol) in 2-methoxyethanol (10 mL) was refluxed for 2 h. After the mixture was cooled to r.t., solvent was evaporated in vacuo. The residue was partitioned between EtOAc and water. 1 M HCl was added with vigorous stirring until pH was about 3. The organic layer was dried over MgSO4 and concentrated. The residue was purified by silica gel chromatography (0-60% EtOAc/hexanes+1% AcOH). The product isolated was dissolved in saturated NaHCO3 and washed several times with ether. The aqueous layer was acidified to pH about 3 with 6 M HCl, and the resulting precipitate was isolated by filtration to give 36 mg of the title compound as a dull yellow solid. MS: (+) m/z 520.27 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09271970B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-7485cd7916354bb89a0f6aad1dff5dcb |
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| Source note | uspto-grants-2016_03 |
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