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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2108883Erstellt: 26. Oktober 2026

Triethylamine → 5-Bromo-N-(7-(trifluoromethyl)quinolin-4-yl)pentanamide

https://huagongshe.com/reaction/2108883

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukt5-Bromovaleryl chlorideHCID 521173—
Edukt4-Amino-7-(trifluoromethyl)quinolineHCID 2735960—
LösungsmittelWaterHCID 962—
LösungsmittelChloroformHCID 6212—
Produkt5-Bromo-N-(7-(trifluoromethyl)quinolin-4-yl)pentanamideHCID 5762942390%

Reaktionsbedingungen

Temperatur20 °C

Reaktionsschritte

4-Amino-7-trifluoromethylquinoline (120 mg, 0.56 mmol), triethylamine (170 mg, 1.7 mmol) and CHCl3 (4 mL) were charged in a 10 ml round-bottomed flask equipped with a magnetic stirrer. 5-Bromovaleryl chloride (140 mg, 0.7 mmol in CHCl3 (2 mL) were added and the reaction mixture was stirred for 15 h at 20° C. The reaction mixture was poured in 10 mL of H2O and extracted with CH2Cl2 (100 mL). The organic layer was washed with brine (2×10 mL), dried over MgSO4, filtered and evaporated at 30° C. to dryness. The crude compound was purified by column chromatography (SiO2; CH2Cl2:MeOH=99.5:0.5 to 98:2) to give after evaporation 5-bromo-N-(7-(trifluoromethyl)quinolin-4-yl)pentanamide 32 (190 mg, 90% yield) as a beige solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07514432B2
Quelldatensatzuspto-grants-2009_04
ORD IDord-f75ee1d4f13044f584c5438a19a7d8f4
Quellennotizuspto-grants-2009_04