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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1819662Generated: November 3, 2026

Isopropyl iodide → HCID 67316166, compound

https://huagongshe.com/reaction/1819662

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropyl iodideHCID 6362—
ReactantPotassium CarbonateHCID 11430—
Reactanttert-Butyl bromoacetateHCID 79177—
Reactant4-(5-Fluoro-2-methyl-1H-indol-3-yl)-2H-benzo[e][1,2,3]thiadiazine 1,1-dioxideHCID 136388612—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
SolventDichloromethaneHCID 6344—
ProductHCID 67316166HCID 67316166—

Reaction Conditions

Temperature80 °C

Reaction Steps

2-Iodopropane (7 μL, 67 μmol) and K2CO3 (10 mg, 72 mmol) were added to a solution of 4-(5-fluoro-2-methyl-1H-indol-3-yl)-2H-benzo[e][1,2,3]thiadiazine 1,1-dioxide (20 mg, 61 Amok) in CH3CN (1 mL), and stirred overnight at 80° C. An additional amount of K2CO3 (10 mg, 72 μmol) and tert-butyl bromoacetate (14 mL, 92 μmol) was added, and the reaction mixture stirred an additional 2 h at 80° C. The reaction mixture was diluted with H2O and CH2Cl2, and filtered through an Extrelut column. The Extrelut column was washed with CH2Cl2, and the filtrate was concentrated to afford the sub-title compound, which was carried onto the next step without further purification or characterization.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07601749B2
Source datasetuspto-grants-2009_10
ORD IDord-844da3a6e328487cb3127b669d3a3427
Source noteuspto-grants-2009_10