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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2411611Generated: November 3, 2026

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

https://huagongshe.com/reaction/2411611

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Chloropropanesulphonyl chlorideHCID 15410—
Reactant4-MethoxybenzylamineHCID 75452—
Reactant[4-(3-Cyclopropyl-5-methylpyridin-2-yl)piperazin-1-yl](6-fluoro-4-methylpyridin-3-yl)methanoneHCID 71252234—
Reactant(6-Amino-4-methylpyridin-3-yl)[4-(3-cyclopropyl-5-methylpyridin-2-yl)piperazin-1-yl]methanoneHCID 71252348—
Product[4-(3-Cyclopropyl-5-methylpyridin-2-yl)piperazin-1-yl][6-(1,1-dioxo-1lambda6-isothiazolidin-2-yl)-4-methylpyridin-3-yl]methanoneHCID 71252917—

Reaction Steps

Using [4-(3-cyclopropyl-5-methylpyridin-2-yl)piperazin-1-yl](6-fluoro-4-methylpyridin-3-yl)methanone (180 mg) described in Preparation Example 181, 4-methoxybenzylamine (2 mL) and 3-chloropropane-1-sulfonyl chloride (0.12 mL) and by the reaction and treatment in the same manner as in Example 229, the title compound (125 mg) was obtained via (6-amino-4-methylpyridin-3-yl)[4-(3-cyclopropyl-5-methylpyridin-2-yl)piperazin-1-yl]methanone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08816079B2
Source datasetuspto-grants-2014_08
ORD IDord-799cbaaf97ff4f8b942b5a78fd460425
Source noteuspto-grants-2014_08