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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2411495Generated: November 1, 2026

4-(4-Chlorobenzoyl)Piperidine → [4-(4-Chlorobenzoyl)piperidin-1-yl][6-(1,1-dioxo-1lambda6-isothiazolidin-2-yl)pyridin-3-yl]methanone

https://huagongshe.com/reaction/2411495

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(4-Chlorobenzoyl)PiperidineHCID 2777115—
ReactantEthyl 6-(1,1-dioxo-1lambda6-isothiazolidin-2-yl)nicotinateHCID 71251937—
Product[4-(4-Chlorobenzoyl)piperidin-1-yl][6-(1,1-dioxo-1lambda6-isothiazolidin-2-yl)pyridin-3-yl]methanoneHCID 712528726.2%

Reaction Steps

Using ethyl 6-(1,1-dioxo-1λ6-isothiazolidin-2-yl)nicotinate (363 mg) described in Preparation Example 25 and 4-(4-chlorobenzoyl)piperidine (300 mg) and by the reaction and treatment in the same manner as in Example 109, the title compound (37 mg) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08816079B2
Source datasetuspto-grants-2014_08
ORD IDord-825008482e8b464cb8150758582f6b62
Source noteuspto-grants-2014_08