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HRID 69084作成日:2026年10月24日

Sodium Iodide → HCID 86675785、化合物

https://huagongshe.com/ja/reaction/69084

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium IodideHCID 5238—
反応物DiisopropylethylamineHCID 81531—
反応物6-Bromo-2-chloro-3-(chloromethyl)quinolineHCID 17039790—
反応物HCID 178516143HCID 178516143—
溶媒WaterHCID 962—
溶媒Ceric ammonium nitrateHCID 180504—
生成物HCID 86675785HCID 86675785—

反応条件

温度70 °C

反応手順

6-Bromo-2-chloro-3-(chloromethyl)quinoline (0.60 g, 2.1 mmol), 6-(trifluoromethyl)-4-pyrimidinol (0.34 g, 2.1 mmol), DIEA (0.54 ml, 3.1 mmol) and sodium iodide (0.31 g, 2.1 mmol) were suspended in CAN (50 mL) and heated to 70° C. for 1 h. The reaction was cooled, diluted with water (100 mL) and extracted with EtOAc (200 mL). After drying with magnesium sulfate the organic was evaporated to dryness under reduced pressure. Purification using low pressure silica chromatography (0-10% methanol in DCM gradient) to give the desired 6-bromo-2-chloro-3-((6-(trifluoromethyl)pyrimidin-4-yloxy)methyl)quinoline. Step 2 and 3: The product from step 1 was taken through a procedure similar to that described in steps 3 and 4 of Example 9, to provide the titled compound, o-tolyl-3-((6-(trifluoromethyl)pyrimidin-4-yloxy)methyl)quinolin-2-amine. (ESI, pos. ion) m/z: 411 (M+1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08822485B2
出典データセットuspto-grants-2014_09
ORD IDord-2ba94ad31aea429aaca5434b4d9dc5cd
出典メモuspto-grants-2014_09