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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 859010생성일: 2026년 10월 24일

Potassium Carbonate → 4-[6-(4-Trifluoromethyl-phenyl)-pyrimidin-4-yloxy]-benzothiazol-2-ylamine

https://huagongshe.com/ko/reaction/859010

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물2-Amino-4-hydroxybenzothiazoleHCID 24057—
반응물4-Chloro-6-(4-(trifluoromethyl)phenyl)pyrimidineHCID 16747837—
용매DimethylformamideHCID 6228—
생성물4-[6-(4-Trifluoromethyl-phenyl)-pyrimidin-4-yloxy]-benzothiazol-2-ylamineHCID 10091650—

반응 조건

온도80 °C

반응 단계

To a solution of 4-chloro-6-(4-trifluoromethyl-phenyl)-pyrimidine, (Example 2(a), Method A), ((0.13 g, 0.5 mmol) and 2-amino-4-hydroxybenzothiazole (83 mg, 0.5 mmol, Astatech) in DMF (1 mL) was added potassium carbonate (0.14 g, 1 mmol) and the mixture was heated at 80° C. for 16 h with sirring. The reaction mixture was allowed to cool to room temperature and partitioned between EtOAc and brine. The layers were separated and the aq. layer was extracted with EtOAc. The combined organic extracts were dried over Na2SO4, filtered and concentrated under vacuum. Purification of the residue by silica gel chromatography (2:1 hexanes: EtOAc) provided the title compound as a white solid. MS (ESI, pos. ion) m/z: 389 (M+1). Mp: 232.0–233.5° C. Anal. Calcd for C18H11F3N4OS: C, 55.67; H, 2.85; N, 14.43; S, 8.26. Found: C, 55.52; H, 3.08; N, 14.23; S, 8.36.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07148221B2
출처 데이터셋uspto-grants-2006_12
ORD IDord-a6691a36fcf84a59b4f38c6553275b75
출처 메모uspto-grants-2006_12