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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 334125생성일: 2026년 10월 25일

N,N,N',N'-Tetramethylethylenediamine → 1-(2-(2-chloro-8-iodo-6-morpholino-9H-purin-9-yl)ethyl)cyclopropanol

https://huagongshe.com/reaction/334125

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참여 물질

역할이름HCID투입량
반응물N,N,N',N'-TetramethylethylenediamineHCID 8037—
반응물HexaneHCID 8058—
반응물1-Chloro-2-iodoethaneHCID 136438—
반응물HCID 86667343HCID 86667343—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물1-(2-(2-chloro-8-iodo-6-morpholino-9H-purin-9-yl)ethyl)cyclopropanolHCID 8666734571.9%

반응 조건

온도0 °C

반응 단계

A solution of 1-(2-(2-chloro-6-morpholino-9H-purin-9-yl)ethyl)cyclopropanol (220 mg, 0.68 mmol) and N,N,N′,N′-tetramethylethylene-diamine (0.15 mL, 1.0 mmol) in THF (4.9 mL) was cooled to −42° C. and treated with a solution of 2.5M n-butyllithium in hexane (1.5 mL, 3.7 mmol) dropwise over 5 minutes. After 30 minutes at −42° C., 1-chloro-2-iodoethane (0.31 mL, 3.3 mmol) was added and the reaction mixture was slowly warmed to 0° C. over 1 hr. The mixture was quenched with a saturated solution of NH4Cl, and diluted with ethyl acetate. The aqueous layer was extracted into ethyl acetate (3×), and the combined organics were dried over sodium sulfate, filtered, and absorbed onto celite for purification by flash chromatography to afford 1-(2-(2-chloro-8-iodo-6-morpholino-9H-purin-9-yl)ethyl)cyclopropanol as a colorless oil (220 mg, 71%). LC/MS (ESI+): m/z 450 (M+H)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08883799B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-87381f2609c54f44a742010e8c1e2bdf
출처 메모uspto-grants-2014_11