HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
(2-Amino-5-chloro-phenyl)-(6-methyl-pyridin-3-yl)methanone → 3-{4-[4-Chloro-2-(6-methyl-pyridine-3-carbonyl)-phenylsulfamoyl]-phenyl}-propionic acid methyl ester
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | (2-Amino-5-chloro-phenyl)-(6-methyl-pyridin-3-yl)methanone | HCID 22327305 | — |
| Edukt | Methyl 3-[4-(chlorosulfonyl)phenyl]propanoate | HCID 23158517 | — |
| Produkt | 3-{4-[4-Chloro-2-(6-methyl-pyridine-3-carbonyl)-phenylsulfamoyl]-phenyl}-propionic acid methyl ester | HCID 10322607 | — |
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 3-(4-Chlorosulfonyl-phenyl)-propionic acid methyl ester and purified by HPLC. 1H NMR (CDCl3) δ 9.66 (br s, 1H, NH), 8.34 (d, 1H, J=2.2 Hz), 7.75 (d, 1H, J=8.8 Hz), 7.72 (d, 1H, J=8.0 Hz, J=2.2 Hz), 7.56 (d, 2H, J=8.4 Hz), 7.51 (dd, 1H, J =8.8 Hz, J=2.2 Hz), 7.32 (d 1H, J=2.2 Hz), 7.26 (d, 1H, J=7 Hz), 7.09 (d, 2H, J=8.4 Hz), 3.65 (s, 3H), 2.97(t, 2H, J=7.6 Hz), 2.66 (s, 3H), 2.51 (t, 2H, J=7.6 Hz). 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-ae256ad3b0b9401da6875972c652d264 |
| Quellennotiz | uspto-grants-2008_09 |