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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | HCID 57444358 | HCID 57444358 | — |
| 반응물 | 2-{3-[(Methylsulfonyl)amino]phenyl}ethyl methanesulfonate | HCID 57444359 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | N-(3-{2-[4-(2-methyl-5-quinazolinyl)-1-piperazinyl]ethyl}phenyl)methanesulfonamide | HCID 57444357 | 37.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07732600B2 |
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| 출처 데이터셋 | uspto-grants-2010_06 |
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| ORD ID | ord-54de705710c246bd894c0bfe20ad94e2 |
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| 출처 메모 | uspto-grants-2010_06 |
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