HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
1H-Indole-5-sulfonamide → 7-Bromo-1-ethyl-1H-indole-5-sulfonamide
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 1H-Indole-5-sulfonamide | HCID 21683100 | — |
| Edukt | 7-Bromo-1-ethylindoline-5-sulfonamide | HCID 86718885 | — |
| Produkt | 7-Bromo-1-ethyl-1H-indole-5-sulfonamide | HCID 71062283 | 32,3% |
Reaktionsschritte
Following a procedure analogous to that for the synthesis of Intermediate 54, 7-bromo-1-ethylindoline-5-sulfonamide (Intermediate 76, 140 mg, 0.46 mmol) was converted to the title compound (45 mg, 31%). 1H NMR (DMSO-d6) δ 8.04 (d, J=1.8 Hz, 1H), 7.77 (d, J=1.5 Hz, 1H), 7.63 (d, J=3.1 Hz, 1H), 7.26 (s, 2H), 6.72 (d, J=3.3 Hz, 1H), 4.60 (q, J=7.1 Hz, 2H), 1.38 (t, J=7.2 Hz, 3H); MS(ESI+) m/z 305.2 (M+H)+.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US09346795B2 |
| Quelldatensatz | uspto-grants-2016_05 |
| ORD ID | ord-9dfc17c0778a430e938297f9845a9c41 |
| Quellennotiz | uspto-grants-2016_05 |