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HRID 9193Erstellt: 24. Oktober 2026
1,2-Dibromo-1,1,2,2-tetrachloroethane → 7-Bromo-2-methoxypyrazolo[1,5-a]pyridine
https://huagongshe.com/de/reaction/9193
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 1,2-Dibromo-1,1,2,2-tetrachloroethane | HCID 69426 | — |
| Edukt | 2-Methoxypyrazolo[1,5-a]pyridine | HCID 12284427 | — |
| Edukt | Butyllithium | HCID 178418339 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Lösungsmittel | Hexane | HCID 8058 | — |
| Produkt | 7-Bromo-2-methoxypyrazolo[1,5-a]pyridine | HCID 21984658 | 64,8% |
Reaktionsschritte
A solution of 2-methoxypyrazolo[1,5-a]pyridine (7.15 g) [CAS No.59942-88-0] in tetrahydrofuran (140 mL) was cooled to −78° C. under a nitrogen stream, and then a solution of n-butyllithium in hexane (1.6 M; 46 mL) was added dropwise and the mixture was stirred for 30 minutes. A solution of 1,2-dibromo-1,1,2,2-tetrachloroethane (18.9 g) in tetrahydrofuran (30 mL) was added dropwise at −78° C., and stirring was continued for 1 hour. After increasing the temperature of the reaction mixture to room temperature and adding water, extraction was performed with ethyl acetate and the extract was washed with brine. After drying the obtained organic layer over anhydrous magnesium sulfate and filtering it, the solvent was concentrated under reduced pressure, the residue was purified by silica gel column chromatography, and the title compound (7.1 g) was obtained from the n-hexane:ethyl acetate (50:1) fraction as a yellow oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07091215B2 |
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| Quelldatensatz | uspto-grants-2006_08 |
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| ORD ID | ord-0fcd62becadc4836ba07d9659cf62752 |
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| Quellennotiz | uspto-grants-2006_08 |
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