HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 622125Erstellt: 27. Oktober 2026
4-Methoxystyrene → Trans-6-[2-(4-methoxyphenyl)ethenyl]-2-(3-piperidinopropyl)phthalazin-1(2H)-one hydrobromide
https://huagongshe.com/reaction/622125
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 4-Methoxystyrene | HCID 12507 | — |
| Edukt | 2-Chloroethyldiisopropylammonium chloride | HCID 77942 | — |
| Edukt | N-(3-chloropropyl)piperidine hydrochloride | HCID 79624 | — |
| Edukt | Tri-o-tolylphosphine | HCID 80271 | — |
| Edukt | 6-Bromo-2-(3-piperidinopropyl)phthalazin-1(2H)-one | HCID 21293347 | — |
| Katalysator | palladium(II) acetate | HCID 167845 | — |
| Lösungsmittel | Dimethyl Sulfoxide | HCID 679 | — |
| Lösungsmittel | Isopropanol | HCID 3776 | — |
| Lösungsmittel | Acetonitrile | HCID 6342 | — |
| Produkt | Trans-6-[2-(4-methoxyphenyl)ethenyl]-2-(3-piperidinopropyl)phthalazin-1(2H)-one hydrobromide | HCID 21293325 | — |
Reaktionsschritte
6-Bromo-2-(3-piperidinopropyl)phthalazin-1(2H)-one (7.2 gm, 0.018 mole) (prepared as in Example I, except that 1-(3-chloropropyl)piperidine hydrochloride was substituted for the 2-(diisopropylamino)ethyl chloride hydrochloride) was stirred into 10 ml DMSO plus 10 ml acetonitrile. To the resulting mixture was added 2.8 gm 4-methoxystyrene (0.021 mole), 0.1 gm tri(o-tolyl)phosphine, and 0.02 gm palladium acetate. The reaction mixture was stirred at reflux (95°-100° C.) for 24 hours. Allowed to cool to about 60° C. and diluted with 40 ml of isopropanol. Stirred for an hour, filtered, washed to colorless washings with isopropanol and dried. The product weighed 8.6 gm. After recrystallization from 50 ml methoxyethanol the product weighed 6.4 gm and melted at 248°-250° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04769369 |
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| Quelldatensatz | uspto-grants-1988_09 |
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| ORD ID | ord-92b25b7f9dfd4d2bb4eea1a7d0574cb1 |
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| Quellennotiz | uspto-grants-1988_09 |
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