HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Piperazine → N-(2-methoxyphenyl)-4-(piperazinyl)-3-nitrobenzenesulfonamide
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Piperazine | HCID 4837 | — |
| Edukt | 2-Methoxyaniline | HCID 7000 | — |
| Edukt | Benzenesulfonyl chloride, 4-chloro-3-nitro- | HCID 7323 | — |
| Edukt | 4-chloro-N-(2-methoxyphenyl)-3-nitrobenzenesulfonamide | HCID 2887683 | — |
| Lösungsmittel | Pyridine | HCID 1049 | — |
| Produkt | N-(2-methoxyphenyl)-4-(piperazinyl)-3-nitrobenzenesulfonamide | HCID 22272580 | — |
Reaktionsschritte
The compound was prepared from 4-chloro-3-nitrobenzenesulfonyl chloride (1 g, 3.9 mmol), 2-methoxyaniline (0.53 mL, 4.7 mmol) and pyridine (1.6 mL) in CH2CL2 (2 mL). 4-Chloro-N-(2-methoxyphenyl)-3-nitrobenzenesulfonamide (0.345 g) was reacted with piperazine (0.111 g) to afford N-(2-methoxyphenyl)-4-(piperazinyl)-3-nitrobenzenesulfonamide. This was then treated with Raney-Ni and hydrazine monohydrate. The final product was isolated as its HCl salt. 1H NMR (DMSO-d6) δ 7.18–7.20 (m, 1H), 7.08–7.10 (m, 2H), 6.93–6.96 (m, 1H), 6.91–6.93 (m, 2H); 6.84 (dt, 1H), 3.56 (s, 3H), 3.22–3.27 (m, 4H), 3.00–3.02 (m, 4H); MS (posESI) m/z=362.1 (M+H+).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07173035B2 |
| Quelldatensatz | uspto-grants-2007_02 |
| ORD ID | ord-b999818acafe4706a2da30e140fe503a |
| Quellennotiz | uspto-grants-2007_02 |