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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2411400Generated: October 26, 2026

(6-Bromopyridin-3-yl)[4-(4-chlorobenzoyl)piperidin-1-yl]methanone → (S)-[4-(4-chlorobenzoyl)piperidin-1-yl][6-(3-isopropyl-1,1-dioxo-1lambda6-isothiazolidin-2-yl)pyridin-3-yl]methanone

https://huagongshe.com/reaction/2411400

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(6-Bromopyridin-3-yl)[4-(4-chlorobenzoyl)piperidin-1-yl]methanoneHCID 58484839—
Reactant(S)-3-isopropylisothiazolidine 1,1-dioxideHCID 86676751—
Product(S)-[4-(4-chlorobenzoyl)piperidin-1-yl][6-(3-isopropyl-1,1-dioxo-1lambda6-isothiazolidin-2-yl)pyridin-3-yl]methanoneHCID 7125259925.7%

Reaction Steps

Using (S)-3-isopropylisothiazolidine 1,1-dioxide (320 mg) described in Preparation Example 6 and (6-bromopyridin-3-yl)[4-(4-chlorobenzoyl)piperidin-1-yl]methanone (408 mg) described in Preparation Example 190 and by the reaction and treatment in the same manner as in Example 4, the title compound (126 mg) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08816079B2
Source datasetuspto-grants-2014_08
ORD IDord-3024547ced0a4d2881535ab885f3b7f2
Source noteuspto-grants-2014_08