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HRID 38246作成日:2026年10月25日

Triethylamine → N-(3-methoxy-4-(pyrimidin-2-yloxy)phenyl)picolinamide

https://huagongshe.com/reaction/38246

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Picolinoyl Chloride HydrochlorideHCID 135033—
反応物3-Methoxy-4-(pyrimidin-2-yloxy)anilineHCID 62110961—
溶媒DichloromethaneHCID 6344—
生成物N-(3-methoxy-4-(pyrimidin-2-yloxy)phenyl)picolinamideHCID 4264523819.1%

反応手順

According to Scheme 3 Step 3: Picolinoyl chloride hydrochloride (1.33 mmol, 256 mg) and Et3N (2.67 mmol, 0.37 mL) were added sequentially to a solution of 3-methoxy-4-(pyrimidin-2-yloxy)aniline (0.89 mmol, 193 mg) in DCM (3 mL) at 0° C. The reaction mixture was stirred at room temperature for 2 hours. The organic phase was washed with a saturated solution of NaHCO3. The aqueous phase was extracted with AcOEt. The organic phase was washed with brine, was dried over MgSO4, was filtered and was concentrated under reduced pressure. The crude product was purified by flash chromatography over C18 column using water/ACN (70:30) as eluent to afford N-(3-methoxy-4-(pyrimidin-2-yloxy)phenyl)picolinamide (0.17 mmol, 55 mg, 19%) as a white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08524726B2
出典データセットuspto-grants-2013_09
ORD IDord-a7f5fcf130d348a486c01d6789d738a7
出典メモuspto-grants-2013_09