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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 10160생성일: 2026년 10월 23일

N-Iodosuccinimide → 6-Chloro-7-iodo-7-deazapurine

https://huagongshe.com/ko/reaction/10160

반응식

참여 물질

역할이름HCID투입량
반응물N-IodosuccinimideHCID 120273—
반응물7H-Pyrrolo(2,3-d)pyrimidine, 4-chloro-HCID 5356682—
용매DimethylformamideHCID 6228—
생성물6-Chloro-7-iodo-7-deazapurineHCID 1480928183%

반응 단계

6-Chloro-7-deazapurine 10.75 g (70 mmol) and N-iodosuccinimide (16.8 g, 75 mmol) were dissolved in 400 ml of dry DMF and left at ambient temperature in the darkness over night. The solvent was evaporated. The dark residue was distributed between 500 ml of ethyl acetate and 150 ml of 10% Na2SO3. Organic fraction was washed with 10% Na2SO3 (2×100 ml), brine (150 ml), dried over Na2SO4 and evaporated. The yellow residue was crystallized from ethanol to yield 16.2 g (83%) of the title compound as off white crystals. The mother liquid was evaporated, dissolved in toluene, and purified by flush chromatography on silica gel (7×4 cm). The column was washed with toluene until the eluent was colorless than the title compound was eluted with 5% ethyl acetate in toluene to give additional 3.5 g of the title product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07094768B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-080e4b8602244c829a89bdfa381e91f1
출처 메모uspto-grants-2006_08