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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 412640Generated: October 29, 2026

Sodium Iodide → HCID 178523836, compound

https://huagongshe.com/reaction/412640

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantPotassium CarbonateHCID 11430—
Reactant(2S)-1-(1,3-benzoxazol-2-yl)-N2-[(3S)-pyrrolidin-3-yl]-2-piperidinecarboxamideHCID 57068119—
ReactantHCID 178478450HCID 178478450—
SolventAcetonitrileHCID 6342—
ProductAmmoniaHCID 222—
ProductHCID 178523836HCID 17852383610.9%

Reaction Steps

3-(Chloromethyl)-1H-1,2,4-triazole (70.8 mg) [see Bazhenov D. N. et al Zh. Org. Khim, (1994), 30(5), 791-792 and references cited therein] was added to a solution of (2S)-1-(1,3-benzoxazol-2-yl)-N2-[(3S)pyrrolidin-3-yl]-2-piperidinecarboxamide (91.8 mg) [see Example 4], potassium carbonate (91 mg) and sodium iodide (10 mg) in acetonitrile (10 ml) at 0° C. The reaction mixture was stirred at room temperature for 18 hours, after which time the solvent was removed under reduced pressure and the residue partitioned between ethyl acetate and water. The organic layer was separated, dried over magnesium sulphate and the solvent removed under reduced pressure. The crude product was purified by column chromatography on silica gel eluting with a solvent system of 93:7:1, by volume, dichloromethane:methanol:0.88 aqueous ammonia solution to afford (2S)-1-(1,3-benzoxazol-2-yl)-N2-[(3S)-1-(1H-1,2,4-triazol-3-ylmethyl)pyrrolidin-3-yl]-2-piperidinecarboxamide (12.6 mg) as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06562964B1
Source datasetuspto-grants-2003_05
ORD IDord-fbd69d8c6dbb4fcd993c55af994ea6e4
Source noteuspto-grants-2003_05