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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 846671Generated: October 31, 2026

Potassium Iodide → 7-hexyloxy-2-methyl-2-phenylthiazolo[3,2-a]indol-3(2H)-one

https://huagongshe.com/reaction/846671

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
Reactant1-BromohexaneHCID 8101—
Reactant7-hydroxy-2-methyl-2-phenylthiazolo[3,2-a]indol-3(2H)-oneHCID 15724969—
Product7-hexyloxy-2-methyl-2-phenylthiazolo[3,2-a]indol-3(2H)-oneHCID 1572497093%

Reaction Steps

To a solution of 7-hydroxy-2-methyl-2-phenylthiazolo[3,2-a]indol-3(2H)-one (2.86 g), n-hexyl bromide (1.76 g) and a small amount of potassium iodide, and the mixture was heated and refluxed for 33 hours. The reaction mixture was allowed to cool. Then insoluble matter was filtered. The solvent was evaporated off under reduced pressure. Water was added to the residue, and the mixture was extracted with ethyl acetate. The organic layer was washed with water and a saturated aqueous sodium chloride solution, and was dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (diluting solvent: n-hexane/ethyl acetate=9:1) to give 3.4 g (yield: 93%) of 7-hexyloxy-2-methyl-2-phenylthiazolo[3,2-a]indol-3-(2H)-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05137909
Source datasetuspto-grants-1992_08
ORD IDord-33607370258d4c6eaa76f09e5f211e59
Source noteuspto-grants-1992_08