HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 459866Generated: October 30, 2026
Tetrahydrofuran → HCID 18444281, compound
https://huagongshe.com/reaction/459866
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | HCID 22930977 | HCID 22930977 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 18444281 | HCID 18444281 | 69.9% |
Reaction Steps
To a THF (2.5 ml) solution of 211 mg of 1-(4-aminophenyl)-4-[6-(3,4-dimethoxyphenyl)pyridine-2-carbonyl]piperazine were added 63.5 mg of methanesulfonyl chloride and 76.8 μl of triethylamine, followed by overnight stirring at room temperature. Further, 79 mg of methanesulfonyl chloride and 103 μl of triethylamine were added in twice thereto, and the whole was stirred at room temperature for 3 hours. Water was added to the reaction solution, followed by extraction with ethyl acetate. The organic layer was washed with brine and then dried over anhydrous magnesium sulfate, and thereafter, the solvent was evaporated. The residue was purified by silica gel column chromatography (chloroform-methanol) and then crystallization was carried out from ethyl acetate-diisopropyl ether to obtain 175 mg of 4′-{4-[6-(3,4-dimethoxyphenyl)pyridine-2-carbonyl]piperazin-1-yl}methanesulfonanilide as pale purple crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07196080B2 |
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| Source dataset | uspto-grants-2007_03 |
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| ORD ID | ord-d97e4a5ab38b46cb8b30841b7ba2e9a2 |
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| Source note | uspto-grants-2007_03 |
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