HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
o-Xylyl bromide → 5-[1-(2-Methylbenzyl)piperidin-4-ylmethoxy]quinazoline-2,4-diamine
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | o-Xylyl bromide | HCID 6992 | — |
| Edukt | Benzylamine | HCID 7504 | — |
| Edukt | 5-(Piperidin-4-ylmethoxy)quinazoline-2,4-diamine | HCID 57576565 | — |
| Produkt | 5-[1-(2-Methylbenzyl)piperidin-4-ylmethoxy]quinazoline-2,4-diamine | HCID 25007432 | 89% |
Reaktionsschritte
The benzylamine was obtained by reacting 5-(piperidin-4-ylmethoxy)quinazoline-2,4-diamine (75 mg; 0.27 mmol) and 2-methylbenzyl bromide (65 mg; 0.35 mmol) via Method BB to yield 91 mg. (89% yield). 1HNMR (400 MHz, DMSO-d6) δ 7.34 (t, J=8.0 Hz, 1H), 7.21 (m, 3H), 7.14 (m, 3H), 6.76 (d, J=8.0 Hz, 1H), 6.52 (d, J=8.4, 11H), 5.94 (br s, 2H), 3.98 (d, J=6.4 Hz, 2H), 3.41 (s, 3H), 2.83 (br, d, J=11.6 Hz, 2H), 2.32 (s, 3H), 2.00 (t, J=10.4 Hz, 2H), 1.9 (m, 1H), 1.73 (d, J=12.8 Hz, 2H), 1.31 (m, 2H). MS m/z (ESI) 378 (M+H)+.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07985755B2 |
| Quelldatensatz | uspto-grants-2011_07 |
| ORD ID | ord-81168662ca804d8d8af55e487349895d |
| Quellennotiz | uspto-grants-2011_07 |