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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 9895생성일: 2026년 10월 23일

3-Chloroaniline → 2-chloro-N-(3-chlorophenyl)-9H-purin-6-amine

https://huagongshe.com/ko/reaction/9895

반응식

참여 물질

역할이름HCID투입량
반응물3-ChloroanilineHCID 7932—
반응물2,6-DichloropurineHCID 5324412—
용매IsopropanolHCID 3776—
용매1-PentanolHCID 6276—
생성물2-chloro-N-(3-chlorophenyl)-9H-purin-6-amineHCID 21988232—

반응 조건

온도100 °C

반응 단계

1.4 ml (13 mmol) of 3-chloro-aniline are added to a suspension of 650 mg (3.44 mmol) of 2,6-dichloro-purine in 5 ml of 1-pentanol. The reaction mixture is stirred at 100° C. (oil bath temperature) for 3 hours. After cooling to room temperature, the mixture is diluted with isopropanol and stirred at 10° C. for 90 minutes. The precipitate is filtered off and rinsed with isopropanol and diethyl ether. The crystals are partitioned between 50 ml of 2 N (two normal) sodium hydroxide solution, 100 ml of water and 700 ml of ethyl acetate. The aqueous phase is subsequently extracted twice with ethyl acetate. The combined organic extracts are washed twice with water and once with saturated sodium chloride solution and dried over sodium sulfate. After filtration, the filtrate is concentrated under reduced pressure. The crude product is stirred with diethyl ether and the crystals are dried at 50° C. under an HV. 2-Chloro-6-(3-chloro-phenyl-amino)-purine is obtained; Rf=0.47 (ethyl acetate:hexane=3:1); APCI-MS: (M+H)+=280; HPLC: tret(grad 20/1)=10.26 minutes.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07091346B1
출처 데이터셋uspto-grants-2006_08
ORD IDord-cf753584cff448f29f411f9c50bea731
출처 메모uspto-grants-2006_08