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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | N,N,N',N'-Tetramethylethylenediamine | HCID 8037 | — |
| 반응물 | Hexane | HCID 8058 | — |
| 반응물 | 1-Chloro-2-iodoethane | HCID 136438 | — |
| 반응물 | HCID 86667343 | HCID 86667343 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 1-(2-(2-chloro-8-iodo-6-morpholino-9H-purin-9-yl)ethyl)cyclopropanol | HCID 86667345 | 71.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08883799B2 |
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| 출처 데이터셋 | uspto-grants-2014_11 |
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| ORD ID | ord-87381f2609c54f44a742010e8c1e2bdf |
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| 출처 메모 | uspto-grants-2014_11 |
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