تفاعل #974923

معادلة التفاعل

iodomethane

methyl 5-bromo-2-methyl-2H-indazole-4-carboxylate

diisopropylamine

butyllithium hexane

→

title compound

المردود 52.0%

methyl 5-bromo-2,3-dimethyl-2H-indazole-4-carboxylate

المردود 52.0%

المذيبات

ammonium chloride

tetrahydrofuran

tetrahydrofuran

ظروف التفاعل

المعالجة

1. 1
   workup.STIRRINGafter stirring for 30 min
2. 2
   workup.STIRRINGAfter stirring for 30 min
3. 3
   أخرىThe solvent was evaporated under reduced pressure
4. 4
   workup.ADDITIONThe residue was diluted with ethyl acetate
5. 5
   غسيلwashed with water and saturated brine
6. 6
   تجفيفdried over anhydrous sodium sulfate
7. 7
   أخرىThe solvent was evaporated under reduced pressure
8. 8
   أخرىthe residue was purified by silica gel column chromatography (ethyl acetate/hexane=20/80→50/50)

الإجراء التجريبي

To a solution of diisopropylamine (1.38 mL, 9.73 mmol) in tetrahydrofuran (25 mL) was added 1.6M butyllithium/hexane solution (5.62 mL, 8.99 mmol) at −78° C., and the mixture was stirred for 30 min. A solution of methyl 5-bromo-2-methyl-2H-indazole-4-carboxylate (2.00 g, 7.49 mmol) in tetrahydrofuran (50 mL) was added and, after stirring for 30 min, iodomethane (933 μL, 15.0 mmol) was added. After stirring for 30 min, the reaction solution was diluted with saturated aqueous ammonium chloride solution. The solvent was evaporated under reduced pressure. The residue was diluted with ethyl acetate, washed with water and saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (ethyl acetate/hexane=20/80→50/50) to give the title compound (1.10 g, yield 52%).

المصدر