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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 550556Generated: October 29, 2026

Sodium Iodide → HCID 15603142, compound

https://huagongshe.com/reaction/550556

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantDichloromethaneHCID 6344—
ReactantPotassium CarbonateHCID 11430—
ReactantSodium BicarbonateHCID 516892—
Reactant(1S,5R)-1-[4-(trifluoromethyl)phenyl]-3-azabicyclo[3.1.0]hexaneHCID 59337591—
ReactantHCID 86761315HCID 86761315—
SolventDimethylformamideHCID 6228—
ProductHCID 15603142HCID 15603142—

Reaction Conditions

Temperature60 °C

Reaction Steps

(1S,5R)-1-[4-(trifluoromethyl)phenyl]-3-azabicyclo[3.1.0]hexane (70 mg) and 4-{5-[(cyclopropylmethyl)thio]-4-methyl-4H-1,2,4-triazol-3-yl}butyl methanesulfonate (70 mg) were dissolved in dimethylformamide (0.6 ml). Sodium Iodide (12 mg) and potassium carbonate (35 mg) were added. Reaction was heated at 60° C. for 20 h. Dichloromethane and NaHCO3 saturated solution were added. Solvent was removed, under reduced pressure, from organic phase. Crude was purified by silica column to give the free base of the title compound (5.5 mg). To a solution of this compound in DCM (0.5 mL), HCl 1N in diethylether (0.012 mL) was added and the solvent removed under reduced pressure to give the title compound as a slightly hygroscopic solid. (6.7 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07947683B2
Source datasetuspto-grants-2011_05
ORD IDord-1e6181f3d51b4c7c88d52611e61a10df
Source noteuspto-grants-2011_05