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HRID 1984701作成日:2026年10月27日

3,5-Dimethylaniline → N-(3,5-Dimethylphenyl)-2-(2-fluoropyridin-4-ylmethylthio)pyridine-3-carboxamide

https://huagongshe.com/reaction/1984701

反応式

関与物質

役割名称HCID仕込み量
反応物3,5-DimethylanilineHCID 7949—
反応物DiisopropylethylamineHCID 81531—
反応物Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
反応物2-(2-Fluoropyridin-4-ylmethylthio)pyridine-3-carboxylic acidHCID 23094028—
溶媒DimethylformamideHCID 6228—
溶媒Ethyl AcetateHCID 8857—
生成物N-(3,5-Dimethylphenyl)-2-(2-fluoropyridin-4-ylmethylthio)pyridine-3-carboxamideHCID 1006754344%

反応手順

O-(7-Azabenzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium hexafluorophosphate (3.0 g, 7.9 mmol) was added to a solution of 2-(2-fluoropyridin-4-ylmethylthio)pyridine-3-carboxylic acid (Reference compound No. 2-1, 1.5 g, 5.7 mmol), 3,5-xylidine (0.90 g, 7.4 mmol) and N,N-diisopropylethylamine (2.0 mL, 11 mmol) in N,N-dimethylformamide (20 mL) at room temperature, and the mixture was stirred for 12 hours. Ethyl acetate (30 mL) was added to the reaction mixture, the whole was washed with brine (50 mL), and then the organic layer was dried over anhydrous magnesium sulfate. The organic layer was evaporated under reduced pressure, and the resulting residue was purified by silica gel column chromatography to give 0.91 g of the title reference compound as a colorless solid. (Yield 44%)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07544703B2
出典データセットuspto-grants-2009_06
ORD IDord-ea30108da48641dab223eac646c5af13
出典メモuspto-grants-2009_06