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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 338700Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/338700

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAnilineHCID 6115—
Edukt4-MethylmorpholineHCID 7972—
Edukt4-Bromopyridine-2-carboxylic acidHCID 735150—
EduktMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
LösungsmittelDimethylformamideHCID 6228—
Produkt4-Bromo-pyridine-2-carboxylic acid phenylamideHCID 8669582671,2%

Reaktionsschritte

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%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08889870B2
Quelldatensatzuspto-grants-2014_11
ORD IDord-5ff8ad58779c434bace6846b494b7950
Quellennotizuspto-grants-2014_11