HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 41273Erstellt: 23. Oktober 2026
1,4-Dioxane → tert-Butyl{3-[2,6-dimethoxy-4-(methoxymethyl)phenyl]-6-methoxy-2-methoxypyrazolo[5,1-b][1,3]thiazol-7-yl}carbamate
https://huagongshe.com/de/reaction/41273
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 1,4-Dioxane | HCID 31275 | — |
| Edukt | Tert-butyl{2-bromo-3-[2,6-dimethoxy-4-(methoxymethyl)phenyl]-6-methoxypyrazolo[5,1-b][1,3]thiazol-7-yl}carbamate | HCID 58223388 | — |
| Edukt | HCID 178477796 | HCID 178477796 | — |
| Katalysator | HCID 178418851 | HCID 178418851 | — |
| Lösungsmittel | Ethylacetate heptane | HCID 21899848 | — |
| Produkt | tert-Butyl{3-[2,6-dimethoxy-4-(methoxymethyl)phenyl]-6-methoxy-2-methoxypyrazolo[5,1-b][1,3]thiazol-7-yl}carbamate | HCID 131730840 | — |
Reaktionsschritte
To a dioxane (15 mL) solution of tert-butyl{2-bromo-3-[2,6-dimethoxy-4-(methoxymethyl)phenyl]-6-methoxypyrazolo[5,1-b][1,3]thiazol-7-yl}carbamate (323 mg, 0.612 mmol) were added 2M dimethyl zinc (0.612 mL, 1.22 mmol) and bis(tri-tert-butylphosphine)palladium(0) (15.6 mg, 0.031 mmol), and the mixture was heated at 60° C. for one hour. After the reaction was completed, the solvent was directly distilled off under reduced pressure. The residue was purified by silica gel column chromatography (a mixed solvent of n-heptane and ethyl acetate: n-heptane/ethyl acetate=1/1) to obtain the title compound (205 mg, 0.442 mmol).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08530504B2 |
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| Quelldatensatz | uspto-grants-2013_09 |
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| ORD ID | ord-191f418fb6ab49d39998070494b19864 |
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| Quellennotiz | uspto-grants-2013_09 |
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