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HRID 9898作成日:2026年10月23日

Isopropyl iodide → 2-Chloro-N-(3-chlorophenyl)-9-isopropyl-9H-purin-6-amine

https://huagongshe.com/ja/reaction/9898

反応式

関与物質

役割名称HCID仕込み量
反応物Isopropyl iodideHCID 6362—
反応物Cesium carbonateHCID 10796—
反応物2-chloro-N-(3-chlorophenyl)-9H-purin-6-amineHCID 21988232—
溶媒Ethyl AcetateHCID 8857—
溶媒1,4-DioxaneHCID 31275—
溶媒N,N-Dimethylformamide--water (1/1)HCID 21962138—
生成物2-Chloro-N-(3-chlorophenyl)-9-isopropyl-9H-purin-6-amineHCID 21988248—

反応手順

500 mg (1.78 mmol) of 2-chloro-6-(3-chloro-phenyl-amino)-purine are dissolved in a mixture of 29.5 ml of DMF/water (85/15) and 5 ml of dioxane by means of gentle heating. 870 mg (2.67 mmol) of caesium carbonate, followed by 1.78 ml (17.8 mmol) of isopropyl iodide are added at room temperature. The reaction mixture is stirred at room temperature for 18 hours. To bring the reaction to completion, the reaction mixture is stirred at 45° C. for a further 24 hours. When the reaction has ended, the reaction mixture is diluted with ethyl acetate, washed with water (2 times) and saturated sodium chloride solution and dried over magnesium sulfate. After filtration, the filtrate is concentrated under reduced pressure at 35° C. and the residue is dried under an HV. The resulting crude product is purified by crystallization from diethyl ether/hexane. 2-Chloro-6-(3-chloro-phenyl-amino)-9-isopropyl-9H-purine is obtained; Rf=0.46 (ethyl acetate); m.p. 128–129° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07091346B1
出典データセットuspto-grants-2006_08
ORD IDord-74fde67f2a9f47cb945db7fa6bea0160
出典メモuspto-grants-2006_08