تفاعل #169224

معادلة التفاعل

4-[6-[4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-1-(tetrahydro-pyran-2-yl)-3-vinyl-1H-pyrazolo[3,4-b]pyridine-4-carbonyl]-piperazine-1-carboxylic acid tert-butyl ester

(4-iodo-phenyl)-piperidin-1-yl-methanone

tri(o-tolyl)phosphine

triethylamine

→

title compound

المردود 75.4%

4-[6-(4-Hydroxy-phenyl)-3-{(E)-2-[4-(piperidine-1-carbonyl)-phenyl]-vinyl}-1-(tetrahydro-pyran-2-yl)-1H-pyrazolo[3,4-b]pyridine-4-carbonyl]-piperazine-1-carboxylic acid tert-butyl ester

المردود 75.4%

المذيبات

DMF

ظروف التفاعل

المعالجة

1. 1
   أخرىThe resulting solution was degassed
2. 2
   workup.ADDITIONwas then added
3. 3
   تركيزThe reaction mixture was concentrated under vacuum
4. 4
   ترشيحThe precipitate was filtered
5. 5
   غسيلwashed with water
6. 6
   أخرىdried under vacuum
7. 7
   أخرىThe crude residue was purified on a silica gel column chromatography

الإجراء التجريبي

To a solution of 4-[6-[4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-1-(tetrahydro-pyran-2-yl)-3-vinyl-1H-pyrazolo[3,4-b]pyridine-4-carbonyl]-piperazine-1-carboxylic acid tert-butyl ester (0.3 g, 0.46 mmol) in DMF (2.1 mL) were added (4-iodo-phenyl)-piperidin-1-yl-methanone (0.175 g, 0.56 mmol), tri(o-tolyl)phosphine (28 mg, 0.09 mmol) and triethylamine (2.1 mL). The resulting solution was degassed using argon, palladium acetate (5 mg, 0.02 mmol) was then added and the reaction mixture was heated at 125° C. overnight. The reaction mixture was concentrated under vacuum and the residue taken up in water and then acidified to pH=1. The precipitate was filtered, washed with water and then dried under vacuum. The crude residue was purified on a silica gel column chromatography using a gradient of methanol (0-3%) in dichloromethane to yield the title compound as a light brown solid (0.25 g, 65%).

المصدر