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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Isoquinoline, 1-chloro- | HCID 140539 | — |
| Edukt | m-Bromobenzohydrazide | HCID 520941 | — |
| Lösungsmittel | P-Xylene | HCID 7809 | — |
| Produkt | N-(3-Bromobenzoyl)-N-(1-isoquinolyl)hydrazine | HCID 66709633 | 90,6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09034486B2 |
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| Quelldatensatz | uspto-grants-2015_05 |
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| ORD ID | ord-a111e756426347d48c5a10da0b2ef81a |
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| Quellennotiz | uspto-grants-2015_05 |
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