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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 411675Erstellt: 25. Oktober 2026

4-Bromo-3-phenyl-1H-pyrazol-5-amine → 3-[[(4-bromo-5-phenyl-1H-pyrazol-3-yl)amino]methylidene]-4-methyl-1H-indol-2-one

https://huagongshe.com/reaction/411675

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-Bromo-3-phenyl-1H-pyrazol-5-amineHCID 594319—
EduktHCID 178418806HCID 178418806—
EduktHCID 178423596HCID 178423596—
EduktHCID 178517101HCID 178517101—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt3-[[(4-bromo-5-phenyl-1H-pyrazol-3-yl)amino]methylidene]-4-methyl-1H-indol-2-oneHCID 178423595—

Reaktionsschritte

The named compound is prepared by substituting E & Z-3-[(hydroxy)-methylene]-4-methyl-1,3-dihydro-indol-2-one for E & Z-3-[(hydroxy)-methylene]-1,3-dihydro-indol-2-one and 4-bromo-5-phenyl-1H-pyrazol-3-ylamine for 3-aminopyrazole in the reaction of Example 1. Specifically, E & Z-3-[(hydroxy)-methylene]-4-methyl-1,3-dihydro-indol-2-one (0.1622 gms.) is reacted with 0.4530 gms. of 4-bromo-5-phenyl-1H-pyrazol-3-ylamine by refluxing in tetrahydrofuran (3.0 mL).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06559173B1
Quelldatensatzuspto-grants-2003_05
ORD IDord-60f37002e36a4a62a973846351568cc2
Quellennotizuspto-grants-2003_05