Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 19495생성일: 2026년 10월 24일
4,6-Dichloropyrimidine → N-{3-[1-(6-chloro-pyrimidin-4-yl)-1H-imidazol-2-ylamino]-4-methyl-phenyl}-3-trifluoromethyl-benzamide
https://huagongshe.com/ko/reaction/19495
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | 4,6-Dichloropyrimidine | HCID 70943 | — |
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | N-[3-(1H-Imidazol-2-ylamino)-4-methyl-phenyl]-3-trifluoromethyl-benzamide | HCID 58973096 | — |
| 용매 | (+-)-2-Butanol | HCID 6568 | — |
| 생성물 | N-{3-[1-(6-chloro-pyrimidin-4-yl)-1H-imidazol-2-ylamino]-4-methyl-phenyl}-3-trifluoromethyl-benzamide | HCID 58973058 | — |
반응 단계
A mixture of N-[3-(1H-Imidazol-2-ylamino)-4-methyl-phenyl]-3-trifluoromethyl-benzamide (330 mg, 0.92 mmol), 4,6-dichloropyrimidine (409 mg, 2.75 mmol), N,N-diisopropylethyl amine (500 μL, 2.87 mmol) in 2-butanol (20 mL) is heated at 110° C. After 16 hours, the reaction mixture is concentrated. The solid is washed with saturated sodium carbonate, water, ethyl acetate, and dried to give the title compound. 1H NMR 600 MHz (DMSO-d6) δ 10.71 (s, 1H), 10.50 (s, 1H), 9.09 (s, 1H), 8.80 (s, 1H), 8.33 (s, 1H), 8.29 (d, J=7.8 Hz, 1H), 8.17 (s, 1H), 7.96 (d, J=8.4 Hz, 1H), 7.84 (s, 1H), 7.77 (t, J=8.4 Hz, 1H), 7.42 (d, J=7.2 Hz, 1H), 7.21 (d, J=8.4 Hz, 1H), 6.95 (s, 1H), 2.38 (s, 3H); MS m/z 473.3 (M+1).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07745437B2 |
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| 출처 데이터셋 | uspto-grants-2010_06 |
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| ORD ID | ord-ca0b4baae053415c9b2d4bcefe18a839 |
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| 출처 메모 | uspto-grants-2010_06 |
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