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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1162361Generated: October 30, 2026

Potassium Iodide → HCID 178482548, compound

https://huagongshe.com/reaction/1162361

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
Reactanttert-Butyl 4-(2-bromoethyl)piperidine-1-carboxylateHCID 10541625—
ReactantN-methyl-2-ThiazolamineHCID 11959081—
SolventDimethylformamideHCID 6228—
ProductHCID 178482548HCID 17848254822%

Reaction Steps

To a solution of tert-butyl 4-(2-bromoethyl)-1-piperidinecarboxylate (D. Brundish et al., J. Med. Chem., 42, 4584 (1999); 5.0 g) and 2-methylaminothiazole (O. Kemal et al., J. Chem. Soc. Perkin I, 5, 1569 (1981); 3.9 g) in DMF (50 ml) was added potassium iodide (5.7 g), and mixed at 80° C. for 12 hours. The reaction mixture was concentrated under reduced pressure, and the residue was dissolved in chloroform and a saturated aqueous potassium hydrogen carbonate solution. The organic layer was collected by separation, dried over anhydrous sodium sulfate, and then concentrated under reduced pressure. The residue was purified with silica gel column to obtain the title compound as a brown oil (1.25 g, 22%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07820673B2
Source datasetuspto-grants-2010_10
ORD IDord-21653e90c22f4829967f96fc069a661e
Source noteuspto-grants-2010_10