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HRID 10160作成日:2026年10月25日

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

https://huagongshe.com/reaction/10160

反応式

関与物質

役割名称HCID仕込み量
反応物N-IodosuccinimideHCID 120273—
反応物7H-Pyrrolo(2,3-d)pyrimidine, 4-chloro-HCID 5356682—
溶媒DimethylformamideHCID 6228—
生成物6-Chloro-7-iodo-7-deazapurineHCID 1480928183%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07094768B2
出典データセットuspto-grants-2006_08
ORD IDord-080e4b8602244c829a89bdfa381e91f1
出典メモuspto-grants-2006_08