HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
3-Chloropropanesulphonyl chloride → [4-(3,5-Dicyclopropylpyridin-2-yl)piperazin-1-yl][6-(1,1-dioxo-1lambda6-isothiazolidin-2-yl)-4-methylpyridin-3-yl]methanone
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 3-Chloropropanesulphonyl chloride | HCID 15410 | — |
| Edukt | 4-Methoxybenzylamine | HCID 75452 | — |
| Edukt | [4-(3,5-Dicyclopropylpyridin-2-yl)piperazin-1-yl](6-fluoro-4-methylpyridin-3-yl)methanone | HCID 58484583 | — |
| Edukt | HCID 71252763 | HCID 71252763 | — |
| Produkt | [4-(3,5-Dicyclopropylpyridin-2-yl)piperazin-1-yl][6-(1,1-dioxo-1lambda6-isothiazolidin-2-yl)-4-methylpyridin-3-yl]methanone | HCID 71251880 | — |
Reaktionsschritte
Using [4-(3,5-dicyclopropylpyridin-2-yl)piperazin-1-yl](6-fluoro-4-methylpyridin-3-yl)methanone (410 mg) described in Preparation Example 178, 4-methoxybenzylamine (2 mL) and 3-chloropropane-1-sulfonyl chloride (0.24 mL) and by the reaction and treatment in the same manner as in Example 229, the title compound (295 mg) was obtained via (6-amino-4-methylpyridin-3-yl)[4-(3,5-dicyclopropylpyridin-2-yl)piperazin-1-yl]methanone.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US08816079B2 |
| Quelldatensatz | uspto-grants-2014_08 |
| ORD ID | ord-4ae20a01665a478ea228ead441bd2273 |
| Quellennotiz | uspto-grants-2014_08 |