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ChemicalBook CAS DataBase List 6-Hydroxy-3-methylindazole
201286-99-9

6-Hydroxy-3-methylindazole synthesis

6synthesis methods
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Yield:201286-99-9 81%

Reaction Conditions:

Stage #1: 6-methoxy-3-methyl-1H-indazolewith boron tribromide in dichloromethane at 20;Cooling with ice;
Stage #2: with water;sodium hydrogencarbonate in dichloromethane;Cooling with ice;

Steps:

14

To an ice cold solution of 6-methoxy-3-methyl-1 H-indazole (620 mg, 3.82 mmol) in CH2CI2 (25 mL) was added a solution of BBr3 in CH2CI2 (1 M, 17 ml_). The ice bath was removed and the reaction was allowed to warm to room temperature and stirred overnight. The solution was carefully quenched by slowly pouring into iced saturated aqueous NaHCO3. The phases were separated and the aqueous phase was extracted with EtOAc (3x). The combined organic extracts were concentrated and the crude material was purified Biotage (4OS column, 45-60% acetone/heptane) to provide 3-methyl-1 H-indazol-6-ol (458 mg, 81 %).

References:

WO2009/144554,2009,A1 Location in patent:Page/Page column 50

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