Sodium Hydroxide → 2-methylthiazolo[5,4-b]pyridine N-oxide
Reaktionsgleichung
[CH3:1][C:2]1[S:3][C:4]2[C:9]([N:10]=1)=[CH:8][CH:7]=[CH:6][N:5]=2.ClC1C=CC=C(C(OO)=[O:19])C=1.[OH-].[Na+]>C(Cl)Cl>[CH3:1][C:2]1[S:3][C:4]2[C:9]([N+:10]=1[O-:19])=[CH:8][CH:7]=[CH:6][N:5]=2Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
To a solution of the product of Step 2 (8.00 g) in 400 mL of CH2Cl2 was added m-chloroperbenzoic acid (26.0 g) and the mixture was stirred at room temperature overnight. NaOH 0.5M was added and the product was extracted in CH2Cl2 (6×), dried over Na2SO4, and purified by flash chromatography on silica with acetone: toluene 70:30 and acetone: toluene: methanol 40:40:20.
Aufarbeitung
- extractionthe product was extracted in CH2Cl2 (6×)
- dry with materialdried over Na2SO4
- custompurified by flash chromatography on silica with acetone: toluene 70:30 and acetone: toluene: methanol 40:40:20
Quellen und Nachweise
- ORD-Eintrag
- ord-f84899bed3a14723b2a584bddbc90dbb
- Quelldatensatz
- uspto-grants-1995_12
- Patentnummer
- US05472964
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