تفاعل #595379

معادلة التفاعل

Tert-butyl 3-bromo-1H-indazole-1-carboxylate

1-(4-methoxybenzyl)-5-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-1H-tetrazole

Sodium carbonate

→

3-(4-(1-(4-methoxybenzyl)-1H-tetrazol-5-yl)phenyl)-1H-indazole

المذيبات

1

1,1,1,3,3,3-hexafluoro-2-(4-(1-(2-(trifluoromethyl)phenylsulfonyl)-1H-indazol-3-yl)phenyl)propan-2-ol

1,4-dioxane

water

water

ظروف التفاعل

المعالجة

1. 1
   أخرىthe system was purged with nitrogen
2. 2
   درجة الحرارةthe reaction mixture was heated overnight
3. 3
   درجة الحرارةat reflux temperature under a nitrogen atmosphere
4. 4
   استخلاصextracted with ethyl acetate
5. 5
   غسيلThe combined organic phases were washed with brine
6. 6
   تجفيفdried over magnesium sulfate
7. 7
   ترشيحAfter filtration the solvent
8. 8
   أخرىwas removed under reduced pressure
9. 9
   أخرىThe residue was purified on SiO2 using 20 to 30% ethyl acetate in hexane as the eluent

الإجراء التجريبي

Tert-butyl 3-bromo-1H-indazole-1-carboxylate (5.0 g, 16.8 mmol) and a mixture of the regio-isomers of 1-(4-methoxybenzyl)-5-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-1H-tetrazole (Example 19, step ii) (7.92 g, 20.2 mmol) were dissolved in 100 ml of a 1 to 1 mixture of 1,4-dioxane and water under a nitrogen atmosphere. Sodium carbonate (5.35 g, 50.5 mmol) was added and the system was purged with nitrogen. Then Pd(PPh3)4 (486 mg, 0.42 mmol) was added and the reaction mixture was heated overnight at reflux temperature under a nitrogen atmosphere. After cooling to room temperature the mixture was diluted with water and extracted with ethyl acetate. The combined organic phases were washed with brine, dried over magnesium sulfate. After filtration the solvent was removed under reduced pressure. The residue was purified on SiO2 using 20 to 30% ethyl acetate in hexane as the eluent to give 3-(4-(1-(4-methoxybenzyl)-1H-tetrazol-5-yl)phenyl)-1H-indazole as a mixture of two regioisomers in a 2 to 1 ratio (2.8 g) as a white solid.

المصدر