HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 361482Erstellt: 26. Oktober 2026
Dimethyl Sulfoxide → 3-Methyl-7-(methylpivaloyl)xanthine
https://huagongshe.com/reaction/361482
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Dimethyl Sulfoxide | HCID 679 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | 3-Methylxanthine | HCID 70639 | — |
| Edukt | 4-Chloro-2,2-dimethylbutanoate | HCID 21753047 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 3-Methyl-7-(methylpivaloyl)xanthine | HCID 21584233 | 90,2% |
Reaktionsschritte
This example illustrates a synthesis of 1-(11,10-Oxidoundecanyl)-3-methyl-7-methylpivalylxanthine (inventive compound no. 1412). A mixture of 3-methylxanthine (Aldrich, 1.00 g, 6.0 mmol), sodium hydride (145 mg, 6.0 mmol) and dimethyl sulfoxide (20 mL) was stirred until homogeneous (0.5 hours). Chloromethylpivalate (865 mL, 904 mg, 6.0 mmol) was added and the reaction stirred for 18 hours. The reaction mixture was poured into water (70 mL) and then extracted with 25% ethano/dichloromethane (4×60 mL). The combined organic extracts were dried over sodium sulfate and evaporated under vacuum to a volume of 40 mL. This solution was cooled in icewater, whereupon a thick white precipitate formed. The solid was filtered off under suction and dried under vacuum to yield 1.43 g (90% yield) 3-methyl-7-(methylpivaloyl)xanthine (inventive compound no. 1404).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05866576 |
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| Quelldatensatz | uspto-grants-1999_02 |
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| ORD ID | ord-2177ddf5787b4adfb9a33a5cc43679ce |
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| Quellennotiz | uspto-grants-1999_02 |
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