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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 470140Erstellt: 23. Oktober 2026

2-Methyl-5-Nitroaniline → N-(5-Amino-2-methyl-phenyl)-4-oxo-1H-quinoline-3-carboxamide

https://huagongshe.com/de/reaction/470140

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Methyl-5-NitroanilineHCID 7444—
EduktStannous chloride dihydrateHCID 61436—
EduktDiisopropylethylamineHCID 81531—
EduktSodium BicarbonateHCID 516892—
EduktMethanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 2733084—
EduktHCID 178524710HCID 178524710—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktN-(5-Amino-2-methyl-phenyl)-4-oxo-1H-quinoline-3-carboxamideHCID 575672938%

Reaktionsbedingungen

Temperatur150 °C

Reaktionsschritte

To a solution of 4-hydroxy-quinoline-3-carboxylic acid (A-1) (50 mg, 0.26 mmol), HBTU (99 mg, 0.26 mmol) and DIEA (138 μL, 0.79 mmol) in THF (2.6 mL) was added 2-methyl-5-nitro-phenylamine (40 mg, 0.26 mmol). The mixture was heated at 150° C. in the microwave for 20 min and the resulting solution was concentrated. The residue was dissolved in EtOH (2 mL) and SnCl2.2H2O (293 mg, 1.3 mmol) was added. The reaction was stirred at room temperature overnight. The reaction mixture was basified with sat. NaHCO3 solution to pH 7-8 and extracted with ethyl acetate. The combined organic layers were washed with brine, dried over Na2SO4, filtered and concentrated. The residue was dissolved in DMSO and purified by HPLC (10-99% CH3CN/H2O) to yield the product, N-(5-amino-2-methyl-phenyl)-4-oxo-1H-quinoline-3-carboxamide (94) (6 mg, 8%). HPLC ret. time 2.06 min, 10-99% CH3CN, 5 min run; ESI-MS 294.2 m/z (MH+).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08629162B2
Quelldatensatzuspto-grants-2014_01
ORD IDord-32ae22329eda4ac7af27218644e6e6a9
Quellennotizuspto-grants-2014_01