HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
4-Methanesulfonylbenzene-1-sulfonyl chloride → N-[4-Chloro-2-(6-methyl-pyridine-3-carbonyl)-phenyl]-4-methanesulfonyl-benzenesulfonamide
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 4-Methanesulfonylbenzene-1-sulfonyl chloride | HCID 2735182 | — |
| Edukt | (2-Amino-5-chloro-phenyl)-(6-methyl-pyridin-3-yl)methanone | HCID 22327305 | — |
| Produkt | N-[4-Chloro-2-(6-methyl-pyridine-3-carbonyl)-phenyl]-4-methanesulfonyl-benzenesulfonamide | HCID 10367205 | — |
Reaktionsschritte
The title compound was prepared according to the general procedure for the synthesis of N-Aryl-benzenesulfonamides previously described using (2-Amino-5-chloro-phenyl )-(6-methyl-pyridin-3-yl )-methanone and 4-Methanesulfonyl-benzenesulfonyl chloride and purified by HPLC. 1H NMR (CDCl3) δ 9.77 (br s, 1H, NH), 8.44 (dm, 1H, J=2.2 Hz), 7.87 (d, 2H, J=8.8 Hz), 7.83 (d, 2H, J=8.8 Hz), 7.76 (d, 1H, J=8.8 Hz), 7.60 (dd, 1H, J=8.0 Hz, J=2.2 Hz), 7.55 (dd, 1H, J=8.8 Hz, J=2.2 Hz), 7.36 (d, 1H, J=2.2), 7.26 (d, 1H, J =8.0 Hz), 3.00 (s, 3H), 2.66 (s, 3H). MS: m/z 465 (M+1).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07420055B2 |
| Quelldatensatz | uspto-grants-2008_09 |
| ORD ID | ord-aaca2cfc13a44b3e9a31abe4a4bdd34a |
| Quellennotiz | uspto-grants-2008_09 |