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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 20994Erstellt: 24. Oktober 2026

Triethylamine → 3-Amino-6-[1-(tert-butoxycarbonyl)indol-2-yl]phthalimide

https://huagongshe.com/de/reaction/20994

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktTri-o-tolylphosphineHCID 80271—
Edukt1-(tert-Butoxycarbonyl)indole-2-boronic Acid (contains varying amounts of Anhydride)HCID 2773302—
Edukt4-amino-7-bromo-2,3-dihydro-1H-isoindole-1,3-dioneHCID 68489089—
Katalysatorpalladium(II) acetateHCID 167845—
LösungsmittelWaterHCID 962—
LösungsmittelAcetonitrileHCID 6342—
Produkt3-Amino-6-[1-(tert-butoxycarbonyl)indol-2-yl]phthalimideHCID 6849281267,7%

Reaktionsschritte

3-Amino-6-bromophthalimide (100 mg, 0.415 mmol) was dissolved in acetonitrile (7 mL), and the solution was added with 1-(tert-butoxycarbonyl)indole-2-boronic acid (217 mg, 0.830 mmol), palladium acetate (7.5 mg, 0.033 mmol), tri(o-tolyl)phosphine (20 mg, 0.066 mmol) and triethylamine (0.578 mL, 4.15 mmol), followed by stirring under reflux for 7.5 hours under argon atmosphere. The reaction mixture was added with water and extracted with ethyl acetate. The organic layer was washed with saturated brine and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure and the residue was purified by preparative thin-layer chromatography (chloroform/methanol=20/1, chloroform/acetonitrile=15/1) to obtain 3-amino-6-[1-(tert-butoxycarbonyl)indol-2-yl]phthalimide (106 mg, yield 67%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07745641B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-9c1c603f370e42a6815d8cd8dc0247c2
Quellennotizuspto-grants-2010_06