Iodine → 5-iodo-1-tosyl-1H-pyrazole
Reaktionsgleichung
[CH3:1][C:2]1[CH:7]=[CH:6][C:5]([S:8]([N:11]2[CH:15]=[CH:14][CH:13]=[N:12]2)(=[O:10])=[O:9])=[CH:4][CH:3]=1.C([Li])(C)(C)C.CCCCC.[I:26]I.[Cl-].[NH4+]>C1COCC1>[I:26][C:15]1[N:11]([S:8]([C:5]2[CH:6]=[CH:7][C:2]([CH3:1])=[CH:3][CH:4]=2)(=[O:10])=[O:9])[N:12]=[CH:13][CH:14]=1Komponenten
Edukt 5
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A solution of 1-[(4-methylphenyl)sulfonyl]-1H-pyrazole (2.0 g, 9.0 mmol) in THF (50 ml) was cooled to −78 C under a nitrogen atmosphere. To this was added tert butyl lithium (5.9 ml) in pentane (1.7M, 10 mmol). After 10 minutes iodine (2.53 g, 10 mmol) in THF (10 ml) was added and the reaction mixture was stirred for a further 30 minutes before allowing to warm to ambient temperature followed by stirring for 12 hours. A saturated solution of ammonium chloride was added and the mixture was partitioned between water and ethyl acetate. The organic layer was separated, dried over magnesium sulfate and evaporated under reduced pressure. The residue was purified by flash chromatography on silica eluting with a mixture of 20-100% dichloromethane in hexane to give the product as a solid (0.96 g, 30%).
Aufarbeitung
- stirringby stirring for 12 hours
- customthe mixture was partitioned between water and ethyl acetate
- customThe organic layer was separated
- dry with materialdried over magnesium sulfate
- customevaporated under reduced pressure
- customThe residue was purified by flash chromatography on silica eluting with a mixture of 20-100% dichloromethane in hexane
Quellen und Nachweise
- ORD-Eintrag
- ord-0045a542e99440d9bdd0be7f9c396df2
- Quelldatensatz
- uspto-grants-2009_03
- Patentnummer
- US07504408B2
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