HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 346427Erstellt: 26. Oktober 2026
3-Bromoaniline → N-(3-Bromophenyl)-6-nitroquinazolin-4-amine
https://huagongshe.com/reaction/346427
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 3-Bromoaniline | HCID 11562 | — |
| Edukt | 4-Chloro-6-nitroquinazoline | HCID 11356257 | — |
| Produkt | N-(3-Bromophenyl)-6-nitroquinazolin-4-amine | HCID 5328041 | — |
Reaktionsschritte
3-Bromoaniline is coupled with 4-chloro-6-nitroquinazoline, to produce 4-[(3-bromophenyl)amino]-6-nitroquinazoline, which is reduced thereafter to the corresponding 6-aminoquinazoline. The 4-[(3-bromophenyl)amino]-6-aminoquinazoline is then reacted with bistributyltin, using tetrakis(triphenylphosphine)palladium in triethylamine solution as the reaction catalyst. The stanylated quinazoline is then reacted with iodine-123, iodine-124 or iodine-131, in the presence of an oxidizing agent, to produce iodine-123 labeled, iodine-124 or iodine-131 labeled 4-[(3-bromophenyl)amino]-6-aminoquinazoline, as is described hereinbelow, which is further reacted with acryloyl chloride as described, to yield the final iodine-123 labeled, iodine-124 labeled or iodine-131 labeled product.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07172749B2 |
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| Quelldatensatz | uspto-grants-2007_02 |
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| ORD ID | ord-b75ccf5f34a9442d9046adfc5165c113 |
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| Quellennotiz | uspto-grants-2007_02 |
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