HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2272910Erstellt: 25. Oktober 2026
Sodium Sulfite → 2-(5-ethylthio-1-methyl-3-trifluoromethyl-1H-pyrazol-4-yl)-6-trifluoromethylthiazolo[5,4-b]pyridine
https://huagongshe.com/reaction/2272910
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Sodium Sulfite | HCID 24437 | — |
| Edukt | Sodium Bicarbonate | HCID 516892 | — |
| Edukt | HCID 57579702 | HCID 57579702 | — |
| Edukt | HCID 178507667 | HCID 178507667 | — |
| Katalysator | Cupric Chloride | HCID 24014 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Lösungsmittel | Dimethylacetamide | HCID 31374 | — |
| Produkt | 2-(5-ethylthio-1-methyl-3-trifluoromethyl-1H-pyrazol-4-yl)-6-trifluoromethylthiazolo[5,4-b]pyridine | HCID 117974278 | 44,9% |
Reaktionsschritte
A mixture of 0.24 g of 3-amino-5-(trifluoromethyl)pyridine-2-thiol, 0.27 g of 5-ethylthio-1-methyl-3-trifluoromethyl-1H-pyrazole-4-carboaldehyde, 0.19 g of sodium sulfite, 0.33 g of copper(II) chloride (anhydrous) and 2 ml of N,N-dimethylacetamide was stirred at 150° C. for 8 hours. Ethyl acetate and a saturated aqueous sodium bicarbonate solution were poured into the cooled reaction mixture, and the mixture was filtered. The aqueous layer of the filtrate was extracted with ethyl acetate and then combined with the organic layer of the filtrate, and the mixture was washed with water and dried over anhydrous magnesium sulfate. The mixture was concentrated under reduced pressure, then the resulting residue was applied to a silica gel column chromatography to obtain 0.21 g of 2-(5-ethylthio-1-methyl-3-trifluoromethyl-1H-pyrazol-4-yl)-6-trifluoromethylthiazolo[5,4-b]pyridine (Compound of Present Invention (27)).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09120792B2 |
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| Quelldatensatz | uspto-grants-2015_09 |
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| ORD ID | ord-340dc02121174dc59712c588c68771a3 |
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| Quellennotiz | uspto-grants-2015_09 |
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