HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1838349Generated: October 25, 2026
Dimethylformamide → 1-Benzenesulfonyl-2-(5-ethoxycarbonylpyridin-2-yl)-5-methanesulfonylindole
https://huagongshe.com/reaction/1838349
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Acetate | HCID 517044 | — |
| Reactant | 1-Benzenesulfonylamino-2-iodo-4-methanesulfonylbenzene | HCID 22504376 | — |
| Reactant | 5-Ethoxycarbonyl-2-trimethylsilylethynylpyridine | HCID 22504397 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1-Benzenesulfonyl-2-(5-ethoxycarbonylpyridin-2-yl)-5-methanesulfonylindole | HCID 22504409 | 31.5% |
Reaction Steps
A mixture of 5-ethoxycarbonyl-2-trimethylsilylethynylpyridine (3.80 g), 2-benzenesulfonylamino-3-iodo-5-methanesulfonylbenzene (3.50 g), potassium acetate (6.00 g), cuprous iodide (75 mg), dichlorobis(triphenylphosphine)palladium (0.27 g) and N,N-dimethylformamide (10 ml) was stirred under nitrogen atmosphere at 100° C. for 8 hours. To the reaction solution was then added water and ethyl acetate. The insolubles were filtered off. The filtrate was extracted with ethyl acetate and washed with a saturated aqueous NaCl solution, dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The resulting residue was subjected to silica gel column chromatography (methanol:dichloromethane=1:100) to obtain 1.22 g of the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06673797B1 |
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| Source dataset | uspto-grants-2004_01 |
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| ORD ID | ord-c7df2a42e2974b478d3bf9b281499f85 |
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| Source note | uspto-grants-2004_01 |
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