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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1042252Erstellt: 25. Oktober 2026

3-(Trifluoromethyl)aniline → 6-Methyl-5-nitro-N-(3-(trifluoromethyl)phenyl)isoquinolin-l-amine

https://huagongshe.com/reaction/1042252

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-(Trifluoromethyl)anilineHCID 7375—
Edukt1-Chloro-6-methyl-5-nitroisoquinolineHCID 22622221—
LösungsmittelIsopropanolHCID 3776—
Produkt6-Methyl-5-nitro-N-(3-(trifluoromethyl)phenyl)isoquinolin-l-amineHCID 6733947681,1%

Reaktionsbedingungen

Temperatur180 °C

Reaktionsschritte

1-Chloro-6-methyl-5-nitroisoquinoline (0.25 g, 1.1 mmol) and 3-(trifluoromethyl)benzenamine (0.17 mL, 1.3 mmol) were added to a microwave tube containing 3 mL of isopropanol. The tube was capped and heated at 180° C. for 1500 seconds. The volatiles were removed in vacuo. The residue was taken up in DCM and washed with saturated NaHCO3. The organic layer was dried with sodium sulfate and purified by column chromatography on silica gel using a gradient of 10 to 40% of ethyl acetate in hexanes to give the product as an orange solid (0.31 g, 79%). MS (M+H)+348.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08557830B2
Quelldatensatzuspto-grants-2013_10
ORD IDord-43e3276e1c7e41159343aece02cb4056
Quellennotizuspto-grants-2013_10