HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 919986Generated: October 29, 2026
Gamma-Aminobutyric Acid → HCID 68297382, compound
https://huagongshe.com/reaction/919986
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Gamma-Aminobutyric Acid | HCID 119 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | HCID 68297518 | HCID 68297518 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | HCID 68297382 | HCID 68297382 | 36.1% |
Reaction Steps
A mixture of (S)-5-hydroxy-2-oxo-3-phenyl-1-(1-phenyl-ethyl)-1,2-dihydro-[1,7]naphthyridine-6-carboxylic acid methyl ester (40 mg, 0.1 mmol), 4-aminobutyric acid (825 mg, 8.0 mmol) and NaOMe solution (12 mL, 6.0 mmol, 0.5 M in MeOH) was refluxed for 16 h. After the mixture was cooled to r.t., the 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 aqueous layer was extracted with additional EtOAc, and the organic layers were combined, dried over MgSO4 and concentrated. The residue was purified by silica gel chromatography (5-60% 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 17 mg of the title compound. MS: (+) m/z 472.34 (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-5dd9b156295a4b389c3504c177302e7c |
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| Source note | uspto-grants-2016_03 |
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