HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1066Erstellt: 23. Oktober 2026
Pyrazole → 4-Methoxy-5-methyl-6-(5-cyclohexylcarbonyloxy-1-ethylpyrazol-4-yl)carbonylthiochroman-1,1-dioxide
https://huagongshe.com/de/reaction/1066
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Pyrazole | HCID 1048 | — |
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | Sodium Carbonate | HCID 10340 | — |
| Edukt | Cyclohexanecarbonyl chloride | HCID 75938 | — |
| Edukt | HCID 178418308 | HCID 178418308 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 4-Methoxy-5-methyl-6-(5-cyclohexylcarbonyloxy-1-ethylpyrazol-4-yl)carbonylthiochroman-1,1-dioxide | HCID 19693776 | 54% |
Reaktionsschritte
As a starting material, 4-methoxy-5-methyl-6-(1-ethyl-5-hydroxypyrazol-4-yl)carbonylthiochroman-1,1-dioxide corresponding to pyrazole derivative (I-H) was used. 0.4 Gram (1.1 mmol) thereof was dissolved in 4 ml of methylene chloride, and 0.22 g (2.2 mmol) of triethylamine as a base and 0.19 g (1.3 mmol) of cyclohexylcarbonyl chloride corresponding to compound B-A-Hal as a reaction reagent were added. The mixture was allowed to react at room temperature for 8 hours. A saturated sodium carbonate aqueous solution was added to the reaction mixture, and the resultant mixture was extracted with ethyl acetate. An organic layer was dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure, and the resultant oil was purified by flush column chromatography (Wako Gel C-300; hexane/ethyl acetate=1:1) to give 0.28 g (yield 54%) of 4-methoxy-5-methyl-6-(5-cyclohexylcarbonyloxy-1-ethylpyrazol-4-yl)carbonylthiochroman-1,1-dioxide.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05723408 |
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| Quelldatensatz | uspto-grants-1998_03 |
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| ORD ID | ord-3db0d270f6194dd0b5a468ba8e5ab869 |
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| Quellennotiz | uspto-grants-1998_03 |
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