HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 394036Generated: October 28, 2026
Potassium Iodide → HCID 16086063, compound
https://huagongshe.com/reaction/394036
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 16086059 | HCID 16086059 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 16086063 | HCID 16086063 | — |
Reaction Steps
To a solution of 19 mg of (2R)-1-((2S,4R)-4-hydroxy-1-{3,3,3-tris(4-fluorophenyl)propanoyl}pyrrolidin-2-yl)carbonyl-N-(4-piperidylmethyl)pyrrolidine-2-carboxamide in 1.5 ml of acetonitrile, 14 mg of methanesulfonic acid-cyclopentylmethyl, 13 mg of potassium carbonate and 5 mg of potassium iodide were added at room temperature, followed by 24 hours' stirring at 80° C. under heating. The reaction liquid was diluted with chloroform, washed successively with water and 1N aqueous sodium hydroxide solution, and drired over anhydrous sodium sulfate. Distilling the solvent off under reduced pressure, the resultant residue was purified by preparative thin-layer chromatography [Kieselgel™ 60F254, Art 5744 (Merck), chloroform/methanol/28% aqueous ammonia=100/10/1) to provide 16 mg of the title compound as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06809108B1 |
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| Source dataset | uspto-grants-2004_10 |
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| ORD ID | ord-8e05d17810704b4397bc9aa88fc4f1f3 |
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| Source note | uspto-grants-2004_10 |
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