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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 15872생성일: 2026년 10월 24일

Diisopropylethylamine → N-(3-{2-[4-(2-methyl-5-quinazolinyl)-1-piperazinyl]ethyl}phenyl)methanesulfonamide

https://huagongshe.com/ko/reaction/15872

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물HCID 57444358HCID 57444358—
반응물2-{3-[(Methylsulfonyl)amino]phenyl}ethyl methanesulfonateHCID 57444359—
용매DimethylformamideHCID 6228—
생성물N-(3-{2-[4-(2-methyl-5-quinazolinyl)-1-piperazinyl]ethyl}phenyl)methanesulfonamideHCID 5744435737.6%

반응 조건

온도100 °C

반응 단계

A mixture of 2-methyl-5-(1-piperazinyl)quinazoline (50 mg), 2-{3-[(methylsulfonyl)amino]phenyl}ethyl methanesulfonate (65 mg), diisopropylethylamine (192 μL) and DMF (0.5 mL) was heated to 100° C. in a sealed tube and stirred for 24 hours. The mixture was cooled to room temperature and partitioned between aqueous ammonium chloride solution and ethyl acetate. The organic layer was washed (water, brine), dried (sodium sulfate) and concentrated in vacuo. The residue was purified by column chromatography [SiO2; DCM-MeOH: (100:0)→(95:5)] to give the title compound as a beige foam (35 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07732600B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-54de705710c246bd894c0bfe20ad94e2
출처 메모uspto-grants-2010_06