HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
4-Iodoanisole → N-[3-(1-{[1-(4-Methoxyphenyl)-1H-indol-5-YL]methyl}-4-piperidinyl)phenyl]-2-methylpropanamide
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 4-Iodoanisole | HCID 69676 | — |
| Edukt | N-(4-methylphenyl)indole | HCID 9794286 | — |
| Edukt | N-{3-[1-(1H-indol-5-ylmethyl)-4-piperidinyl]phenyl)-2-methylpropanamide | HCID 22049334 | — |
| Produkt | N-[3-(1-{[1-(4-Methoxyphenyl)-1H-indol-5-YL]methyl}-4-piperidinyl)phenyl]-2-methylpropanamide | HCID 22049409 | 56,1% |
Reaktionsschritte
According to the procedure used for the synthesis of 1-(4-methylphenyl)1H-indole, N-{3-[1-(1H-indol-5-ylmethyl)-4-piperidinyl]phenyl}-2-methylpropanamide (37.5 mg, 0.100 mmol) and 1-iodo-4-methoxybenzene (46.8 mg, 0.200 mmol) gave the desired product (27 mg, 56%). 1H NMR (400 MHz, CDCl3) δ 7.70–6.58 (m, 14H), 3.88 (s, 3H), 3.67 (s, 2H), 3.14–3.01 (m, 2H), 2.57–2.41 (m, 2H), 2.25–2.01 (m, 2H), 1.93–1.69 (m, 4H), 1.24 (d, 6H, J=7.2 Hz); ESMS m/e: 482.2 (M+H)+.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07067534B1 |
| Quelldatensatz | uspto-grants-2006_06 |
| ORD ID | ord-a6fd79f82bb248b28b9a25fc8204e6b9 |
| Quellennotiz | uspto-grants-2006_06 |