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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2411542Generated: November 1, 2026

(R)-3-methylisothiazolidine 1,1-dioxide → (R)-[2-methanesulfonyl-4-(3-methyl-1,1-dioxo-1lambda6-isothiazolidin-2-yl)phenyl][4-(3,5,6-trimethylpyridin-2-yl)piperazin-1-yl]methanone

https://huagongshe.com/reaction/2411542

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(R)-3-methylisothiazolidine 1,1-dioxideHCID 16664802—
Reactant(4-Bromo-2-methanesulfonylphenyl)[4-(3,5,6-trimethylpyridin-2-yl)piperazin-1-yl]methanoneHCID 58484785—
Product(R)-[2-methanesulfonyl-4-(3-methyl-1,1-dioxo-1lambda6-isothiazolidin-2-yl)phenyl][4-(3,5,6-trimethylpyridin-2-yl)piperazin-1-yl]methanoneHCID 7125236748.5%

Reaction Steps

Using (4-bromo-2-methanesulfonylphenyl)[4-(3,5,6-trimethylpyridin-2-yl)piperazin-1-yl]methanone (370 mg) described in Preparation Example 122 and (R)-3-methylisothiazolidine 1,1-dioxide (107 mg) described in Preparation Example 2 and by the reaction and treatment in the same manner as in Example 4, the title compound (200 mg) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08816079B2
Source datasetuspto-grants-2014_08
ORD IDord-7d55bb89ac764674af4915aa3fac170a
Source noteuspto-grants-2014_08