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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2411598Generated: November 3, 2026

3-Chloropropanesulphonyl chloride → [4-(5-Cyclopropyl-3-methylpyridin-2-yl)piperazin-1-yl][6-(1,1-dioxo-1lambda6-isothiazolidin-2-yl)-4-methylpyridin-3-yl]methanone dihydrochloride

https://huagongshe.com/reaction/2411598

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Chloropropanesulphonyl chlorideHCID 15410—
Reactant4-MethoxybenzylamineHCID 75452—
ReactantHCID 58484562HCID 58484562—
Reactant(6-Amino-4-methylpyridin-3-yl) [4-(5-cyclopropyl-3-methylpyridin-2-yl)piperazin-1-yl]methanoneHCID 71252201—
Reactant[4-(5-Cyclopropyl-3-methylpyridin-2-yl)piperazin-1-yl][6-(1,1-dioxo-1lambda6-isothiazolidin-2-yl)-4-methylpyridin-3-yl]methanoneHCID 71252334—
Product[4-(5-Cyclopropyl-3-methylpyridin-2-yl)piperazin-1-yl][6-(1,1-dioxo-1lambda6-isothiazolidin-2-yl)-4-methylpyridin-3-yl]methanone dihydrochlorideHCID 86676784—

Reaction Steps

Using [4-(5-cyclopropyl-3-methylpyridin-2-yl)piperazin-1-yl](6-fluoro-4-methylpyridin-3-yl)methanone (1.25 g) described in Preparation Example 140, 4-methoxybenzylamine (2 mL) and 3-chloropropane-1-sulfonyl chloride (0.55 ml) and by the reaction and treatment in the same manner as in Example 223, the title compound (950 mg) was obtained via (6-amino-4-methylpyridin-3-yl) [4-(5-cyclopropyl-3-methylpyridin-2-yl)piperazin-1-yl]methanone and [4-(5-cyclopropyl-3-methylpyridin-2-yl)piperazin-1-yl][6-(1,1-dioxo-1λ6-isothiazolidin-2-yl)-4-methylpyridin-3-yl]methanone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08816079B2
Source datasetuspto-grants-2014_08
ORD IDord-c3fff1a585fb48bda7c0cc068e39deb1
Source noteuspto-grants-2014_08