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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 335867생성일: 2026년 10월 25일

Potassium Iodide → HCID 67438988, 화합물

https://huagongshe.com/reaction/335867

반응식

참여 물질

역할이름HCID투입량
반응물Potassium IodideHCID 4875—
반응물DimethylformamideHCID 6228—
반응물Cesium carbonateHCID 10796—
반응물Oxetane, 3-(bromomethyl)-3-methyl-HCID 144860—
반응물(S)-2-amino-1'-bromo-7'-(pyridin-3-yl)-5H-spiro[oxazole-4,9'-xanthen]-2'-olHCID 58466223—
용매WaterHCID 962—
용매Ethyl AcetateHCID 8857—
생성물HCID 67438988HCID 67438988—

반응 단계

To a slurry of (S)-2-amino-1′-bromo-7′-(pyridin-3-yl)-5H-spiro[oxazole-4,9′-xanthen]-2′-ol (710 mg, 1.674 mmol), cesium carbonate (1091 mg, 3.35 mmol) and potassium iodide (306 mg, 1.841 mmol) in DMF (6694 μL, 1.674 mmol) at 0° C. was added 3-(bromomethyl)-3-methyloxetane (304 mg, 1.841 mmol). The reaction was removed from the ice bath and allowed to warm to rt. Reaction was allowed to stir at rt overnight before being diluted with water (250 mL) and poured into a separatory funnel containing ethyl acetate (100 mL). The layers were separated and the aqueous layer was extracted with ethyl acetate (2×100 mL). The combined organic layers were washed with brine, dried over sodium sulfate, filtered and concentrated in vacuo to provide a red oil that was purified by silica gel chromatography (Redi-Sep pre-packed silica gel column (40 g), 0-100% CH2Cl2 to 10:1 methanol in methylenechloride with 0.1% ammonium hydroxide) to provide (S)-1′-bromo-2′-((3-methyloxetan-3-yl)methoxy)-7′-(pyridin-3-yl)-5H-spiro[oxazole-4,9′-xanthen]-2-amine as an off white solid. MS m/z=508.0 [M+H].

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08883782B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-44db42f9fb184262906a595d542d549a
출처 메모uspto-grants-2014_11