HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Bicarbonate Ion → 6-{[(Naphthalen-1-yl-methyl)-amino]-methyl}-2,4-pteridinediamine
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Bicarbonate Ion | HCID 769 | — |
| Edukt | 1-Naphthalenemethanamine | HCID 8355 | — |
| Edukt | 6-(Bromomethyl)-2-imino-2,3-dihydropteridin-4-amine--hydrogen bromide (1/1) | HCID 12503242 | — |
| Lösungsmittel | Dimethylacetamide | HCID 31374 | — |
| Produkt | 6-{[(Naphthalen-1-yl-methyl)-amino]-methyl}-2,4-pteridinediamine | HCID 18455749 | 15% |
Reaktionsbedingungen
| Temperatur | 50 °C |
|---|
Reaktionsschritte
To a solution of 6-bromomethyl-2,4-pteridinediamine hydrobromide (51 mg, 0.2 mmol) in anhydrous N,N dimethylacetamide was added 1-aminomethyl-naphthalene (31.67 ul, 0.22 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. 9 mg product was obtained. Yield: 15%; 1H NMR(500 MHz, DMSO-d6): δ 4.6479(s, 2H ), 4.7893(s, 2H), 7.575–7.6244(m, 3H), 7.74232–7.7570(d, J=6.91 Hz, 1H), 7.9935–8.0276(dd, J1=8.06 Hz, J2 =8.995 Hz, 2H), 8.1670–8.1831(d, J=8.04 Hz, 1H), 8.8430(s, 1H); ESI-MS: m/z 332 (M++1)
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07208493B2 |
| Quelldatensatz | uspto-grants-2007_04 |
| ORD ID | ord-d75a0c5d00004cd6bb08de995d0f6bfe |
| Quellennotiz | uspto-grants-2007_04 |