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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2411606Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/2411606

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-Chloropropanesulphonyl chlorideHCID 15410—
Edukt4-MethoxybenzylamineHCID 75452—
Edukt[4-(3,5-Dicyclopropylpyridin-2-yl)piperazin-1-yl](6-fluoro-4-methylpyridin-3-yl)methanoneHCID 58484583—
EduktHCID 71252763HCID 71252763—
Produkt[4-(3,5-Dicyclopropylpyridin-2-yl)piperazin-1-yl][6-(1,1-dioxo-1lambda6-isothiazolidin-2-yl)-4-methylpyridin-3-yl]methanoneHCID 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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08816079B2
Quelldatensatzuspto-grants-2014_08
ORD IDord-4ae20a01665a478ea228ead441bd2273
Quellennotizuspto-grants-2014_08