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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1693260생성일: 2026년 10월 26일

Sodium Iodide → 1-(2-Amino-4,6-dichloropyrimidin-5-yl)-3-buten-1-ol

https://huagongshe.com/reaction/1693260

반응식

참여 물질

역할이름HCID투입량
반응물Sodium IodideHCID 5238—
반응물Allyl bromideHCID 7841—
반응물2-Amino-4,6-dichloropyrimidine-5-carboxaldehydeHCID 265546—
반응물IndiumHCID 5359967—
용매DimethylformamideHCID 6228—
생성물1-(2-Amino-4,6-dichloropyrimidin-5-yl)-3-buten-1-olHCID 5820118974%

반응 단계

Indium powder (45.81 g) was added to a mixture composed of 2-amino-4,6-dichloropyrimidine-5-carboaldehyde (63.83 g) and N,N-dimethylformamide (500 mL). Then, sodium iodide (99.66 g) was added at an internal temperature of 10° C. under cooling in an ice bath. Allyl bromide (67.5 mL) was added to the resulting mixture over 20 minutes. After confirming that the internal temperature once increased was decreased, the ice bath was removed and the mixture was stirred for two hours. The reaction mixture was concentrated to about 200 mL under reduced pressure. Then, ethyl acetate (1.5 L) and a saturated sodium bicarbonate solution (1 L) were added to the residue, followed by stirring. The mixture was filtered through Celite and the filtrate was separated. Then, the organic layer was sequentially washed with water and brine. The organic layer was dried over anhydrous sodium sulfate and filtered. Then, the filtrate was concentrated to about 150 mL under reduced pressure. Hexane was added to the resulting residue, followed by stirring. Then, the solid was collected by filtration to obtain the title compound (57.24 g, 74%) as a solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08158638B2
출처 데이터셋uspto-grants-2012_04
ORD IDord-862b2b09702c4f4287e4d8fc7bae9615
출처 메모uspto-grants-2012_04