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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 9898생성일: 2026년 10월 23일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물Isopropyl iodideHCID 6362—
반응물Cesium carbonateHCID 10796—
반응물2-chloro-N-(3-chlorophenyl)-9H-purin-6-amineHCID 21988232—
용매Ethyl AcetateHCID 8857—
용매1,4-DioxaneHCID 31275—
용매N,N-Dimethylformamide--water (1/1)HCID 21962138—
생성물2-Chloro-N-(3-chlorophenyl)-9-isopropyl-9H-purin-6-amineHCID 21988248—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07091346B1
출처 데이터셋uspto-grants-2006_08
ORD IDord-74fde67f2a9f47cb945db7fa6bea0160
출처 메모uspto-grants-2006_08