HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
(2-Amino-5-chloro-phenyl)-(2-methyl-pyridin-3-yl)-methanone → 3-(4-[4-Chloro-2-(2-methyl-pyridine-3-carbonyl)-phenylsulfamoyl]-phenyl)-propionic acid methyl ester
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | (2-Amino-5-chloro-phenyl)-(2-methyl-pyridin-3-yl)-methanone | HCID 22327321 | — |
| Edukt | Methyl 3-[4-(chlorosulfonyl)phenyl]propanoate | HCID 23158517 | — |
| Produkt | 3-(4-[4-Chloro-2-(2-methyl-pyridine-3-carbonyl)-phenylsulfamoyl]-phenyl)-propionic acid methyl ester | HCID 10027807 | — |
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)-(2-methyl-pyridin-3-yl)-methanone and 3-(4-Chlorosulfonyl-phenyl)-propionic acid methyl ester and purified by HPLC. 1H-NMR (CDCl3) δ 10.75 (br s, 1H, NH), 8.64 (dm, 1H, J=4.8 Hz), 7.79 (dd, 1H, J=9.2 Hz, J=1.1 Hz), 7.75 (d, 2H, J=7.3 Hz), 7.49 (dm, 1H,J=9.2 Hz), 7.1-7.3 (m, 5H), 3.65 (s, 3H), 2.97(t, 2H, J=7.6 Hz), 2.61 (t, 2H, J=7.6 Hz), 2.35 (s, 3H). MS: m/z 473 (M+1).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07420055B2 |
| Quelldatensatz | uspto-grants-2008_09 |
| ORD ID | ord-391c4fec674349d6bc9dbb6fd0e54d75 |
| Quellennotiz | uspto-grants-2008_09 |