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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1381557Erstellt: 27. Oktober 2026

6-Chloroindoline-2,3-dione → 5-Amino-6-chloroindole-3-acetonitrile

https://huagongshe.com/reaction/1381557

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt6-Chloroindoline-2,3-dioneHCID 241331—
Edukt6-chloro-5-nitro-1H-indoleHCID 18932857—
Edukt6-Chloro-5-nitroindole-3-acetonitrileHCID 21276200—
Edukt6-Chloro-5-nitroisatinHCID 23354431—
EduktHCID 178418361HCID 178418361—
KatalysatorPalladiumHCID 23938—
LösungsmittelEthanolHCID 702—
Produkt5-Amino-6-chloroindole-3-acetonitrileHCID 21276186—

Reaktionsschritte

This intermediate was prepared by the sequence 6-chloroisatin, 6-chloro-5-nitroisatin, 6-chloro-5-nitroindole, 6-chloro-5-nitrogramine and 6-chloro-5-nitroindole-3-acetonitrile which was hydrogenated with 10% Pd/C until 3 equiv. of hydrogen were taken up. The catalyst was removed by filtration and the residue concentrated in vacuo to give a dark brown solid. Trituration with cold EtOH gave desired pure product.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04803218
Quelldatensatzuspto-grants-1989_02
ORD IDord-0a418df9f188460d8a5d72c1cd6bec41
Quellennotizuspto-grants-1989_02