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HRID 859010作成日:2026年10月25日

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

https://huagongshe.com/reaction/859010

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物2-Amino-4-hydroxybenzothiazoleHCID 24057—
反応物4-Chloro-6-(4-(trifluoromethyl)phenyl)pyrimidineHCID 16747837—
溶媒DimethylformamideHCID 6228—
生成物4-[6-(4-Trifluoromethyl-phenyl)-pyrimidin-4-yloxy]-benzothiazol-2-ylamineHCID 10091650—

反応条件

温度80 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07148221B2
出典データセットuspto-grants-2006_12
ORD IDord-a6691a36fcf84a59b4f38c6553275b75
出典メモuspto-grants-2006_12