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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 560742생성일: 2026년 10월 26일

4-Fluorobenzyl bromide → ethyl 2-(1-(4-fluorobenzyl)-5-oxo-1H-1,2,4-triazol-4(5H)-yl)-4-methylthiazole-5-carboxylate

https://huagongshe.com/reaction/560742

반응식

참여 물질

역할이름HCID투입량
반응물4-Fluorobenzyl bromideHCID 68021—
반응물1-(Bromomethyl)-4-(trifluoromethyl)benzeneHCID 123062—
반응물ethyl 4-methyl-2-(5-oxo-1H-1,2,4-triazol-4(5H)-yl)thiazole-5-carboxylateHCID 57920013—
생성물ethyl 2-(1-(4-fluorobenzyl)-5-oxo-1H-1,2,4-triazol-4(5H)-yl)-4-methylthiazole-5-carboxylateHCID 5791996484%

반응 단계

Following the procedure as described in Example 19, making variation as required to replace 4-(trifluoromethyl)benzyl bromide with 1-(bromomethyl)-4-fluorobenzene to react with ethyl 4-methyl-2-(5-oxo-1H-1,2,4-triazol-4(5H)-yl)thiazole-5-carboxylate, the title compound was obtained as a white solid in 84% yield: 1H NMR (300 MHz, CDCl3) δ 8.27 (s, 1H), 7.47-7.30 (m, 2H), 7.11-6.97 (m, 2H), 4.98 (s, 2H), 4.32 (q, J=7.1 Hz, 2H), 2.65 (s, 3H), 1.34 (t, J=7.1 Hz, 3H); MS (ES+) m/z 363.1 (M+

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08063084B2
출처 데이터셋uspto-grants-2011_11
ORD IDord-06ca0f19290142baa989cf5414ee2296
출처 메모uspto-grants-2011_11