HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
3-Bromoaniline → N-(3-bromophenyl)-7H-purin-6-amine
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 3-Bromoaniline | HCID 11562 | — |
| Edukt | 6-Chloropurine | HCID 5359277 | — |
| Katalysator | Hydrochloric Acid | HCID 313 | — |
| Lösungsmittel | Isopropanol | HCID 3776 | — |
| Produkt | N-(3-bromophenyl)-7H-purin-6-amine | HCID 9814520 | 102,8% |
Reaktionsbedingungen
| Temperatur | 80 °C |
|---|
Reaktionsschritte
A mixture of 6-chloropurine (1.0 g, 6.47 mmol), 3-bromoaniline (0.78 mL, 7.12 mmol), and conc HCl (4 drops) in isopropanol (10 mL) is stirred at 80° C. for 5 h. Upon cooling, it precipitates. The solid is filtered and washed with isopropanol and air dried to yield N6-(3-bromophenyl)adenine (1.93 g, 91%) as a light yellow solid. 1H NMR (DMSO) δ 11.38 (1H, s), 8.78 (1H, s), 8.75 (1H, s), 7.90 (1H, d, J=8.0 Hz), 7.38-7.34 (2H, m).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US06455534B2 |
| Quelldatensatz | uspto-grants-2002_09 |
| ORD ID | ord-7de2fa3d3c2544a5b286fbdcf2116439 |
| Quellennotiz | uspto-grants-2002_09 |