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HRID 338700作成日:2026年10月25日

Aniline → 4-Bromo-pyridine-2-carboxylic acid phenylamide

https://huagongshe.com/reaction/338700

反応式

関与物質

役割名称HCID仕込み量
反応物AnilineHCID 6115—
反応物4-MethylmorpholineHCID 7972—
反応物4-Bromopyridine-2-carboxylic acidHCID 735150—
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—
溶媒DimethylformamideHCID 6228—
生成物4-Bromo-pyridine-2-carboxylic acid phenylamideHCID 8669582671.2%

反応手順

To a suspension of 4-bromo-pyridine-2-carboxylic acid (1.00 g, 5.00 mmol) in dimethylformamide (10 mL) was added 1-methylmorpholine (1.1 mL, 10 mmol) and O-(7-azabenzotriazol-1-yl)-N,N,N′,N′-tetramethyl-uronium hexafluorophosphate (HATU) (2.37 g, 6.23 mmol). The mixture became an orange solution after 10 minutes. Aniline (0.5 mL, 5.5 mmol) was added and the solution was stirred at room temperature for 66 hours. The dimethylformamide was evaporated in vacuo and the residue was partitioned between water and ethyl acetate. The separated water layer was extracted with ethyl acetate. The combined ethyl acetate extract was washed with water and saturated sodium bicarbonate. The organic layer was dried (MgSO4), filtered and evaporated to crude 2. Chromatography on silica gel (40 g) applied in dichloromethane and eluted with hexanes:ethyl acetate (1:1) gave the title compound (0.986 g, 71%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08889870B2
出典データセットuspto-grants-2014_11
ORD IDord-5ff8ad58779c434bace6846b494b7950
出典メモuspto-grants-2014_11