HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Bicarbonate Ion → 6-(3,4-Dimethoxy-benzylamino)-2,4-pteridinediamine
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Bicarbonate Ion | HCID 769 | — |
| Edukt | Veratrylamine | HCID 79832 | — |
| Edukt | 6-(Bromomethyl)-2-imino-2,3-dihydropteridin-4-amine--hydrogen bromide (1/1) | HCID 12503242 | — |
| Lösungsmittel | Dimethylacetamide | HCID 31374 | — |
| Produkt | 6-(3,4-Dimethoxy-benzylamino)-2,4-pteridinediamine | HCID 18455733 | 35,2% |
Reaktionsbedingungen
| Temperatur | 50 °C |
|---|
Reaktionsschritte
To a solution of 6-bromomethyl-2,4-pteridinediamine hydrobromide (59 mg, 0.176 mmol) in anhydrous N,N dimethylacetamide was added 3,4-dimethoxy-benzylamine (51.15 ul, 0.3512 mmol). The reaction mixture was stirred at 50° C. overnight. The crude product was poured into saturated bicarbonate solution. The resulted precipitate was collected and purified by preparative HPLC. 20.3 mg product was obtained. Yield: 34%; 1H NMR (500 MHz, DMSO-d6): δ 3.67534(s, 3H), 3.70494(s, 3H), 4.05412 (b, 4H), 6.78852–6.80460 (d, J=8.04 Hz, 1H), 6.83624 (s, 1H), 6.83624–6.85393 (d, J=8.195 Hz, 1H); 8.96623(s, 1H), 9.00584(s, 2H), 9.5577(s, 2H); ESI-MS: 342 (M++1)
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07208493B2 |
| Quelldatensatz | uspto-grants-2007_04 |
| ORD ID | ord-1ccea85a2cd84eb489076c4a69a98a28 |
| Quellennotiz | uspto-grants-2007_04 |