Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 919923생성일: 2026년 10월 26일
Beta-Alanine → 3-[(1-Benzyl-5-hydroxy-2-oxo-3-pyrimidin-5-yl-1,2-dihydro-[1,7]naphthyridine-6-carbonyl)-amino]-propionic acid
https://huagongshe.com/reaction/919923
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Beta-Alanine | HCID 239 | — |
| 반응물 | Sodium Methoxide | HCID 10942334 | — |
| 반응물 | 1-Benzyl-5-hydroxy-2-oxo-3-pyrimidin-5-yl-1,2-dihydro-[1,7]naphthyridine-6-carboxylic acid methyl ester | HCID 68297616 | — |
| 생성물 | 3-[(1-Benzyl-5-hydroxy-2-oxo-3-pyrimidin-5-yl-1,2-dihydro-[1,7]naphthyridine-6-carbonyl)-amino]-propionic acid | HCID 68297406 | 65.9% |
반응 단계
A mixture of 1-benzyl-5-hydroxy-2-oxo-3-pyrimidin-5-yl-1,2-dihydro-[1,7]naphthyridine-6-carboxylic acid methyl ester (58 mg, 0.15 mmol), β-alanine (706 mg, 7.9 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 4. The organic layer was dried over MgSO4 and concentrated. The crude solid was dissolved in saturated NaHCO3 and washed several times with ether. The aqueous layer was acidified to pH about 4 with 6 M HCl, and the resulting precipitate was isolated by filtration to give 44 mg of the title compound. MS: (+) m/z 446.27 (M+1).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09271970B2 |
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| 출처 데이터셋 | uspto-grants-2016_03 |
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| ORD ID | ord-ad475b3191c7484dac97da4d7ea1c480 |
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| 출처 메모 | uspto-grants-2016_03 |
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