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HRID 2055995作成日:2026年10月25日

Benzo(b)thiophen-4-ol → 4-(Benzo[b]thiophen-4-yloxy)-6-(4-trifluoromethyl-phenyl)-pyrimidine

https://huagongshe.com/reaction/2055995

反応式

関与物質

役割名称HCID仕込み量
反応物Benzo(b)thiophen-4-olHCID 19217—
反応物Sodium hydrideHCID 24758—
反応物4-Chloro-6-(4-(trifluoromethyl)phenyl)pyrimidineHCID 16747837—
溶媒DimethylformamideHCID 6228—
生成物4-(Benzo[b]thiophen-4-yloxy)-6-(4-trifluoromethyl-phenyl)-pyrimidineHCID 21865155—

反応手順

Sodium hydride (0.104 g, 2.6 mmol, 60% suspension in mineral oil, Aldrich) was added in small portions to a solution of benzo[b]thiophen-4-ol (0.3 g, 2 mmol, prepared according WO 01/68653) in DMF (4 mL) and the mixture was stirred at room temperature for 0.5 h. (4-Chloro-6-(4-trifluoromethyl-phenyl)-pyrimidine, (Example 2(a), Method A), (0.776 g, 3 mmol) was then added and the mixture was stirred at room temperature for 18 h. The solvent was evaporated under vacuum, the residue was dissolved in EtOAc (50 mL), washed with 1 N NaOH and water, dried over MgSO4, and filtered. The filtrate was evaporated under vacuum and the residue purified by silica gel chromatography (10% EtOAc in hexanes) to give the title compound. Mp: 122.3-122.4° C. MS (ESI, pos. ion) m/z: 373.1 (M+1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07332511B2
出典データセットuspto-grants-2008_02
ORD IDord-ce8a73d4d641424c8b4d333140c4da37
出典メモuspto-grants-2008_02