HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Cyclopentylamine → 1-[3-Chloro-6-(2-cyclopentylamino-ethoxy)-5-[3-(4-fluoro-phenyl)-butoxy]-4-methoxy-2-methyl-phenyl]-ethanone
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Cyclopentylamine | HCID 2906 | — |
| Edukt | 1-{2-(2-Bromo-ethoxy)-5-chloro-3-[3-(4-fluoro-phenyl)-butoxy]-4-methoxy-6-methyl-phenyl}-ethanone | HCID 59583523 | — |
| Produkt | 1-[3-Chloro-6-(2-cyclopentylamino-ethoxy)-5-[3-(4-fluoro-phenyl)-butoxy]-4-methoxy-2-methyl-phenyl]-ethanone | HCID 25255007 | — |
Reaktionsschritte
Example 8a (100 mg, 0.21 mmol) was reacted with cyclopentylamine (6.0 eq.) as described under General Procedure G. The title compound was afforded as an oil (65 mg, 65%). 1H NMR (300 MHz, CDCl3) δ 7.17-7.13 (m, 2H), 6.99-6.93 (m, 2H), 4.07 (t, J=5.2 Hz, 2H), 3.92 (t, J=6.7 Hz, 2H), 3.81 (s, 3H), 3.06 (quintet, J=6.6 Hz, 1H), 3.01-2.93 (m, 1H), 2.81 (t, J=5.2 Hz, 2H), 2.46 (s, 3H), 2.16 (s, 3H), 2.03-1.96 (m, 2H), 1.84-1.76 (m, 2H), 1.68-1.49 (m, 4H), 1.33-1.23 (m, 2H), 1.27 (d, J=7.0 Hz, 3H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US08202513B2 |
| Quelldatensatz | uspto-grants-2012_06 |
| ORD ID | ord-2be7a5df49cd40f6b103aecedd6621e7 |
| Quellennotiz | uspto-grants-2012_06 |