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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 574035Erstellt: 24. Oktober 2026

Isoquinoline, 1-chloro- → N-(3-Bromobenzoyl)-N-(1-isoquinolyl)hydrazine

https://huagongshe.com/de/reaction/574035

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIsoquinoline, 1-chloro-HCID 140539—
Eduktm-BromobenzohydrazideHCID 520941—
LösungsmittelP-XyleneHCID 7809—
ProduktN-(3-Bromobenzoyl)-N-(1-isoquinolyl)hydrazineHCID 6670963390,6%

Reaktionsbedingungen

Temperatur150 °C

Reaktionsschritte

To a 200-mL three-neck flask were added 3.3 g (20 mmol) of 1-chloroisoquinoline, 4.3 g (20 mmol) of 3-bromobenzoylhydrazine, and 80 mL of para-xylene. This mixture was refluxed at 150° C. for 14 hours under a nitrogen stream. After a predetermined time elapsed, this mixture was cooled to room temperature, and the precipitated solid was collected by suction filtration. The obtained solid was washed with toluene, a saturated aqueous solution of sodium hydrogen carbonate, and water. This solid was dried, so that the substance which was the object of the synthesis was obtained as 6.2 g of a pale yellow powder in 90% yield.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09034486B2
Quelldatensatzuspto-grants-2015_05
ORD IDord-a111e756426347d48c5a10da0b2ef81a
Quellennotizuspto-grants-2015_05