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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 9896생성일: 2026년 10월 23일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물IodoethaneHCID 6340—
반응물Potassium CarbonateHCID 11430—
반응물2-chloro-N-(3-chlorophenyl)-9H-purin-6-amineHCID 21988232—
용매DimethylformamideHCID 6228—
생성물2-Chloro-n-(3-chlorophenyl)-9-ethyl-9h-purin-6-amineHCID 11001320—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07091346B1
출처 데이터셋uspto-grants-2006_08
ORD IDord-d405be57821f4dbb93ac2b274583a947
출처 메모uspto-grants-2006_08