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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 21090Erstellt: 25. Oktober 2026

Triethylamine → 1h-Isoindol-1-one,7-amino-2,3-dihydro-4-phenyl-

https://huagongshe.com/reaction/21090

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktPhenylboronic AcidHCID 66827—
EduktTri-o-tolylphosphineHCID 80271—
Edukt7-Amino-4-bromo-2,3-dihydroisoindol-1-oneHCID 19701932—
Katalysatorpalladium(II) acetateHCID 167845—
LösungsmittelAcetonitrileHCID 6342—
Produkt1h-Isoindol-1-one,7-amino-2,3-dihydro-4-phenyl-HCID 6849063189%

Reaktionsschritte

In a similar manner to Step 2 of Example 1, 7-amino-4-bromoisoindolinone (250 mg, 1.10 mmol) was dissolved in acetonitrile (15 mL), and the solution was treated with phenylboronic acid (402 mg, 3.30 mmol), palladium acetate (20 mg, 0.088 mmol), tri(o-tolyl)phosphine (53.6 mg, 0.176 mmol) and triethylamine (1.53 mL, 11.0 mmol), followed by purification by preparative thin-layer chromatography (chloroform/methanol=15/1, chloroform/acetonitrile=6/1) to obtain 7-amino-4-phenylisoindolinone (219 mg, yield 89%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07745641B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-9c1111f45233410abb4e3e361e2834b7
Quellennotizuspto-grants-2010_06