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HRID 1836196생성일: 2026년 10월 25일

Sodium hydride → 6-Amino-2-methoxy-4-(4-acetoxybutyl)pyrimidine

https://huagongshe.com/reaction/1836196

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물1-Butanol, 4-bromo-, 1-acetateHCID 78491—
반응물Lithium BromideHCID 82050—
반응물6-Amino-2-methoxy-3,4-dihydropyrimidin-4-oneHCID 135404214—
용매DimethylformamideHCID 6228—
생성물6-Amino-2-methoxy-4-(4-acetoxybutyl)pyrimidineHCID 2349908816%

반응 단계

Sodium hydride (60% dispersion in mineral oil, 8.2 g, 205 mmol) was added to a mixture of 6-amino-2-methoxy-4-pyrimidone (24.0 g, 170 mmol) in DMF at 0° C. After 0.5 hours, lithium bromide (19.2 g, 221 mmol) was added to the mixture and stirred for 0.5 hours at room temperature. The temperature was slowly increased to 70° C., and a solution of 4-bromobutyl acetate (50 g, 256 mmol) in DMF was added dropwise to the reaction mixture. The mixture was stirred at 70° C. for 3 hours. After cooling to room temperature, the solvent was removed in vacuo. The residue was purified by chromatography on silica gel using CHCl3/MeOH (1-5%) as eluent to give first 6.5 g (15%) of 6-amino-2-methoxy-4-(4-acetoxybutyl)pyrimidine as a white solid followed by 23.4 g (yield 54%) of 6-amino-2-methoxy-3-(4-acetoxybutyl)-4-pyrimidone as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06777420B2
출처 데이터셋uspto-grants-2004_08
ORD IDord-f59ba468b9db4e56939ac0bf61cb8952
출처 메모uspto-grants-2004_08