HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 915512Generated: October 28, 2026
Potassium Iodide → HCID 68414168, compound
https://huagongshe.com/reaction/915512
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-(Chloromethyl)-1,3-thiazole hydrochloride | HCID 2763289 | — |
| Reactant | HCID 10409873 | HCID 10409873 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 68414168 | HCID 68414168 | 48% |
Reaction Steps
Potassium carbonate (0.050 g, 0.357 mmol) followed by 4-(chloromethyl)thiazole hydrochloride (0.041 g, 0.238 mmol) were added to a solution of 2-(4-fluoro-phenyl)-5-isopropoxy-6-methanesulfonylamino-benzofuran-3-carboxylic acid methylamide (0.050 g, 0.119 mmol, which can be prepared according to one of the procedures described in Example 21 above), dissolved in acetonitrile (10 mL). The reaction was refluxed for 1 hour with no visible product formation observed by TLC, so potassium iodide (0.020 g, 0.120 mmol) was added to the reaction. The mixture was refluxed for an additional 2 hours, and then cooled to room temperature. The reaction mixture was concentrated, and the residue was dissolved in ethyl acetate and washed with water. The product was concentrated and purified by flash chromatography (silica gel, ethyl acetate/hexanes gradient) to provide 30 mg (48%) of the desired product as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07265152B2 |
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| Source dataset | uspto-grants-2007_09 |
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| ORD ID | ord-ab7eca47589f443aafb9a3d61aa0e44b |
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| Source note | uspto-grants-2007_09 |
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