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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1372719Erstellt: 27. Oktober 2026

Isoquinoline-1-carboxylic acid → Ethyl (3-bromo-4-((1-isoquinolinylcarbonyl)amino)phenyl)acetate

https://huagongshe.com/reaction/1372719

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIsoquinoline-1-carboxylic acidHCID 68092—
Edukt1-HydroxybenzotriazoleHCID 75771—
Edukt1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
EduktEthyl 2-(4-amino-3-bromophenyl)acetateHCID 19702145—
Katalysator4-(Dimethylamino)pyridineHCID 14284—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylformamideHCID 6228—
ProduktEthyl (3-bromo-4-((1-isoquinolinylcarbonyl)amino)phenyl)acetateHCID 5877861869%

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

In DMF (15 ml) were dissolved 1-isoquinolinecarboxylic acid (1.00 g, 5.77 mmol), ethyl 4-amino-3-bromophenylacetate (1.49 g, 5.77 mmol), HOBt (0.39 g, 2.89 mmol), and DMAP (0.14 g, 1.15 mmol). To the resulting solution was added EDC HCl (1.33 g, 6.93 mmol). After stirring at 60° C. for 5 hours, the reaction mixture was cooled to room temperature. Water was added, followed by extraction with ethyl acetate. The extract was washed with saturated brine, dried over anhydrous sodium sulfate, and distilled under reduced pressure to remove the solvent. The residue was purified by chromatography on a silica gel column, whereby from n-hexane:ethyl acetate (4:1, v/v) eluate fractions, ethyl (3-bromo-4-((1-isoquinolinylcarbonyl)amino)phenyl)acetate (1.64 g, 69%) was obtained as a yellow solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07157487B2
Quelldatensatzuspto-grants-2007_01
ORD IDord-4f6477460f244b1295b64770b1c2e833
Quellennotizuspto-grants-2007_01