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HRID 9896作成日:2026年10月24日

Iodoethane → 2-Chloro-n-(3-chlorophenyl)-9-ethyl-9h-purin-6-amine

https://huagongshe.com/ja/reaction/9896

反応式

関与物質

役割名称HCID仕込み量
反応物IodoethaneHCID 6340—
反応物Potassium CarbonateHCID 11430—
反応物2-chloro-N-(3-chlorophenyl)-9H-purin-6-amineHCID 21988232—
溶媒DimethylformamideHCID 6228—
生成物2-Chloro-n-(3-chlorophenyl)-9-ethyl-9h-purin-6-amineHCID 11001320—

反応手順

676 mg (2.413 mmol) of 2-chloro-6-(3-chloro-phenyl-amino)-purine are dissolved in 10 ml of abs. DMF by means of gentle heating. 375 mg (2.713 mmol) of potassium carbonate, followed by 0.97 ml (12.01 mmol) of ethyl iodide are added at room temperature. The reaction mixture is stirred at room temperature for 2 hours. When the reaction is complete, the reaction mixture is poured onto ice/water (60 ml) and stirred for 10 minutes. The inhomogeneous mixture is extracted three times with ethyl acetate. The combined organic extracts are washed twice with water and once with saturated sodium chloride solution and dried over magnesium sulfate. After filtration, the filtrate is concentrated under reduced pressure at 35° C. and dried under an HV. The resulting crude product (crystalline oil) is purified by crystallization from diethyl ether/hexane. 2-Chloro-6-(3-chloro-phenyl-amino)-9-ethyl-9H-purine is obtained; Rf=0.55 (ethyl acetate:hexane=3:1); APCI-MS: (M+H)+=308; HPLC: tret(grad 20/1)=12.40 minutes; m.p. 127–128° 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-d405be57821f4dbb93ac2b274583a947
出典メモuspto-grants-2006_08