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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1586417생성일: 2026년 10월 27일

Isobutyl iodide → 2-amino-6-(2,6-dichlorophenyl)-8-isobutyl-8H-pyrido[2,3-d]pyrimidin-7-one

https://huagongshe.com/reaction/1586417

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참여 물질

역할이름HCID투입량
반응물Isobutyl iodideHCID 10556—
반응물Sodium hydrideHCID 24758—
반응물2-Amino-6-(2,6-dichlorophenyl)-pyrido[2,3-d]pyrimidin-7-olHCID 10494915—
용매DimethylformamideHCID 6228—
생성물2-amino-6-(2,6-dichlorophenyl)-8-isobutyl-8H-pyrido[2,3-d]pyrimidin-7-oneHCID 532862851%

반응 조건

온도60 °C

반응 단계

To a suspension of NaH (60% in mineral oil, 36 mg) in 8 mL of dimethylformamide was added 2-amino-6-(2,6-dichlorophenyl)-pyrido[2,3-d]pyrimidin-7(8H)-one (205 mg, 0.67 mmol). The mixture was heated at 60° C. for 20 minutes resulting in a clear solution. 1-Iodo-2-methylpropane (110 μL, 0.94 mmol) was added, and the solution was stirred at 50° C. for 30 minutes. An additional amount of 1-iodo-2-methylpropane (40 μL, 0.34 mmol) was added, and the solution was stirred at 50° C. for 40 minutes, then cooled to room temperature and poured onto 40 mL of ice water. The resulting precipitate was removed by filtration and washed with water. The gummy residue was dissolved in ethyl acetate and washed with water. The organic layer was dried over magnesium sulfate, filtered, and concentrated in vacuo. The resulting solid was purified by flash chromatography, eluting with 1:1 hexane:ethyl acetate to provide 123 mg (51%) of 2-amino-6-(2,6-dichlorophenyl)-8-isobutyl-8H-pyrido[2,3-d]pyrimidin-7-one; mp 193-195° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05945422
출처 데이터셋uspto-grants-1999_08
ORD IDord-5256673fe4434e498da1306f15061f88
출처 메모uspto-grants-1999_08