Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 378290생성일: 2026년 10월 24일
4,6-Dichloro-n-methylpyrimidin-2-amine → N-(6-chloro-2-methylamino-pyrimidin-4-yl)-4-fluoro-benzenesulfonamide
https://huagongshe.com/ko/reaction/378290
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | 4,6-Dichloro-n-methylpyrimidin-2-amine | HCID 259880 | — |
| 반응물 | 4-Fluoro-benzenesulfonamide potassium salt | HCID 131721324 | — |
| 용매 | N-methyl-2-pyrrolidone | HCID 13387 | — |
| 생성물 | N-(6-chloro-2-methylamino-pyrimidin-4-yl)-4-fluoro-benzenesulfonamide | HCID 19353544 | 56% |
반응 단계
0.46 g (0.0026 mol) of (4,6-dichloro-pyrimidin-2-yl)-methylamine and 1.1 g (0.0051 mol) of 4-fluoro-benzenesulfonamide potassium salt were stirred in 10 ml of 1-methyl-2-pyrrolidone in 150° C. for 8 hours. Then, the solvent was distilled off in a high vacuum, the residue was partitioned in ethyl acetate/water and extracted. The aqueous phase was saturated with sodium chloride, evaporated briefly in a vacuum and made acid with 4N HCl, with a precipitate separating. The mixture was suctioned filtered, the extract and the solid were combined and chromatographed over silica gel with cyclohexane/ethyl acetate 2:1 as the eluent. The product was recrystallized from ethyl acetate/n-hexane. There was obtained 0.46 g (56%) of N-(6-chloro-2-methylamino-pyrimidin-4-yl)-4-fluoro-benzenesulfonamide as white crystals; m.p. 121-123C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06030976 |
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| 출처 데이터셋 | uspto-grants-2000_02 |
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| ORD ID | ord-ba76fd18be1544219176b04f09dfd7fd |
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| 출처 메모 | uspto-grants-2000_02 |
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