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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 351976Generated: October 30, 2026

Sodium Iodide → 5-[4-[4-(4-Fluorophenyl)piperazin-1-yl]butyl]-2-methyl-2,3,4,5-tetrahydropyrrolo[2,3-e][1,2]thiazin-4-one 1,1-dioxide

https://huagongshe.com/reaction/351976

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantPotassium CarbonateHCID 11430—
Reactant1-(4-Fluorophenyl)piperazineHCID 75260—
Reactant5-(4-Chlorobutyl)-2-methyl-2,3,4,5-tetrahydropyrrolo[2,3-e][1,2]thiazin-4-one 1,1-dioxideHCID 22714965—
SolventAcetonitrileHCID 6342—
Product5-[4-[4-(4-Fluorophenyl)piperazin-1-yl]butyl]-2-methyl-2,3,4,5-tetrahydropyrrolo[2,3-e][1,2]thiazin-4-one 1,1-dioxideHCID 991079684%

Reaction Steps

A suspension of 233 mg (0.8 mmol) of Compound 17, 216 mg (1.2 mmol) of 1-(4-fluorophenyl)piperazine, 166 mg (1.2 mmol) of potassium carbonate and 240 mg (1.6 mmol) of sodium iodide in 20 ml of acetonitrile was refluxed for 23 hours. Post-treatment was conducted in a similar manner as in Example 18. The residue was purified by chromatography on a silica gel column (eluent: methanol/chloroform=1/49), whereby 291 mg of the title compound were obtained (yield: 84%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06743913B2
Source datasetuspto-grants-2004_06
ORD IDord-c6ab6adc4c4b4b4984ea26b36b799605
Source noteuspto-grants-2004_06