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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

반응식

참여 물질

역할이름HCID투입량
반응물Beta-AlanineHCID 239—
반응물Sodium MethoxideHCID 10942334—
반응물1-Benzyl-5-hydroxy-2-oxo-3-pyrimidin-5-yl-1,2-dihydro-[1,7]naphthyridine-6-carboxylic acid methyl esterHCID 68297616—
생성물3-[(1-Benzyl-5-hydroxy-2-oxo-3-pyrimidin-5-yl-1,2-dihydro-[1,7]naphthyridine-6-carbonyl)-amino]-propionic acidHCID 6829740665.9%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09271970B2
출처 데이터셋uspto-grants-2016_03
ORD IDord-ad475b3191c7484dac97da4d7ea1c480
출처 메모uspto-grants-2016_03