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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 21194Erstellt: 24. Oktober 2026

Water → 4-Methyl-7-[1-(tert-butoxycarbonyl)-5-formylindol-2-yl]isoindolinone

https://huagongshe.com/de/reaction/21194

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktPotassium CarbonateHCID 11430—
EduktTrimethylboroxineHCID 574072—
Edukt4-Trifluoromethanesulfonyloxy-7-[1-(tert-butoxycarbonyl)-5-formylindol-2-yl]isoindolinoneHCID 86628287—
Lösungsmittel1,2-DimethoxyethaneHCID 8071—
Produkt4-Methyl-7-[1-(tert-butoxycarbonyl)-5-formylindol-2-yl]isoindolinoneHCID 8662828886%

Reaktionsschritte

In a similar manner to Step 1 of Example 152, 4-trifluoromethanesulfonyloxy-7-[1-(tert-butoxycarbonyl)-5-formylindol-2-yl]isoindolinone (176 mg, 0.336 mmol) was dissolved in dimethoxyethane (8.8 mL), and the solution was treated with trimethylboroxine (0.140 mL, 1.01 mmol), [bis(diphenylphosphino)ferrocene]dichloropalladium (32.9 mg, 0.0403 mmol), potassium carbonate (231 mg, 1.68 mmol) and water (0.121 mL), followed by purification by preparative thin-layer chromatography (chloroform/acetonitrile=4/1) to obtain 4-methyl-7-[1-(tert-butoxycarbonyl)-5-formylindol-2-yl]isoindolinone (112 mg, yield 86%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07745641B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-e0bc7869ef5b4cfd9259b65a4d68cf53
Quellennotizuspto-grants-2010_06