HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 491809Generated: October 29, 2026
Potassium Iodide → HCID 178500409, compound
https://huagongshe.com/reaction/491809
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Methyl 5-bromovalerate | HCID 79557 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 178478721 | HCID 178478721 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | HCID 178500409 | HCID 178500409 | — |
Reaction Steps
Trans-3-(4-aminocyclohexylcarbonylamino)-N-(5-chloropyridin-2-yl)benzofuran-2-carboxamide dihydrochloride (300 mg) obtained in Example 219 is suspended in N,N-dimethylacetamide (5 ml), and thereto are added methyl 5-bromovalerate (106 μl), N,N-diisopropylethylamine (537 μl), and potassium iodide (111 mg), and the mixture is stirred at 100° C. for 24 hours. Methyl 5-bromovalerate (106 μl), N,N-diisopropylethylamine (537 μl) and potassium iodide (111 mg) are further added thereto, and the mixture is stirred at 100° C. for 12 hours. The reaction solution is diluted with ethyl acetate, and washed successively with a saturated aqueous sodium hydrogen carbonate solution, water, a saturated brine, and dried over sodium sulfate. The solvent is evaporated under reduced pressure, and the resulting residue is purified by NH-silica gel column chromatography (eluent: n-hexane/ethyl acetate=1/1, then ethyl acetate) to give trans-3-[4-(4-methoxycarbonylbutylamino)cyclohexylcarbonylamino]-N-(5-chloropyridin-2-yl)-benzofuran-2-carboxamide (101 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07531537B2 |
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| Source dataset | uspto-grants-2009_05 |
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| ORD ID | ord-a30d33ea7bee41a79dd0e566e7c2b8a0 |
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| Source note | uspto-grants-2009_05 |
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