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HRID 458619作成日:2026年10月26日

Potassium Iodide → 8-Chloro-7-(2-iodobenzyl)-1,3-dimethyl-3,7-dihydropurine-2,6-dione

https://huagongshe.com/reaction/458619

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium IodideHCID 4875—
反応物8-ChlorotheophyllineHCID 10661—
反応物Potassium CarbonateHCID 11430—
反応物1-(Chloromethyl)-2-iodobenzeneHCID 101064—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
溶媒Ethyl AcetateHCID 8857—
生成物8-Chloro-7-(2-iodobenzyl)-1,3-dimethyl-3,7-dihydropurine-2,6-dioneHCID 22508626—

反応手順

8-Chlorotheophylline (8.5 g, 39.6 mmol) was dissolved in 400 ml of DMF and 2-iodobenzyl chloride (10.0 g, 39.6 mmol), potassium carbonate (5.47 g, 39.6 mmol), and potassium iodide (10 mg, 0.06 mmol) were added. The mixture was stirred at room temperature for 7 days. Water (2500 ml) and EtOAc (800 ml) were added and the layers were separated. The aqueous layer was extracted with 2×500 ml of EtOAc, and the combined organic layer was washed with 500 ml of water, 500 ml of brine, dried over sodium sulphate, and filtered. The solvent was evaporated and the crude product was crystallized from diethyl ether and petrol, to give compound (5A) as white crystals. The mother liquor was evaporated and resuspended in diethyl ether and petrol, to give a second crop of compound (5A).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07192952B2
出典データセットuspto-grants-2007_03
ORD IDord-7334a02c700b42bdb9c1f534b68ac804
出典メモuspto-grants-2007_03