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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 919922생성일: 2026년 10월 25일

Hydrochloric Acid → 1-Benzyl-5-hydroxy-2-oxo-3-pyrimidin-5-yl-1,2-dihydro-[1,7]naphthyridine-6-carboxylic acid methyl ester

https://huagongshe.com/reaction/919922

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Ethyl AcetateHCID 8857—
반응물5-(Tributylstannyl)pyrimidineHCID 2763249—
반응물1-Benzyl-3-bromo-5-hydroxy-2-oxo-1,2-dihydro-[1,7]naphthyridine-6-carboxylic acid methyl esterHCID 68297477—
촉매HCID 178418476HCID 178418476—
용매DimethylformamideHCID 6228—
용매Sodium chloride; waterHCID 57417360—
생성물1-Benzyl-5-hydroxy-2-oxo-3-pyrimidin-5-yl-1,2-dihydro-[1,7]naphthyridine-6-carboxylic acid methyl esterHCID 6829761671.1%

반응 조건

온도120 °C

반응 단계

A mixture of 1-benzyl-3-bromo-5-hydroxy-2-oxo-1,2-dihydro-[1,7]naphthyridine-6-carboxylic acid methyl ester (80 mg, 0.21 mmol), 5-tributylstannanyl-pyrimidine (0.1 mL, 0.31 mmol), and PdCl2(PPh3)2 (29 mg, 0.041 mmol) in DMF (5 mL) was heated at 120° C. under nitrogen atmosphere for 2 h. After the mixture was cooled to r.t., brine and EtOAc were added. 1 M HCl was added until pH was about 4. The aqueous layer was extracted with additional EtOAc, and the organic layers were combined, washed with water, and dried over MgSO4. After evaporating the solvent, the crude product was purified by silica gel chromatography (90% EtOAc/hexanes+1% AcOH) to give 58 mg of the title compound. MS: (+) m/z 389.27 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09271970B2
출처 데이터셋uspto-grants-2016_03
ORD IDord-88af359115a24ad09e136f6d49f98e68
출처 메모uspto-grants-2016_03