Реакция #833

ord-6ca5406ed1914cc08b2221358d36ecf3

Уравнение реакции

N#Cc1cnn2c(NC3COC3)cc(Cl)nc12
N#Cc1cnn2c(NC3COC3)c
CC(=O)Nc1cc(N)ccc1C1CC1
CC(=O)Nc1cc(N)ccc1C1
CC(=O)Nc1cc(Nc2cc(NC3COC3)n3ncc(C#N)c3n2)ccc1C1CC1
CC(=O)Nc1cc(Nc2cc(NC

Растворители

Условия реакции

Температура
90°CELSIUS

Методика

Ref: _Angew. Chem. Int. Ed._ **2006** , _45_ , 6523-6527 1\. To a microwave tube was added N-(5-amino-2-cyclopropylphenyl)acetamide (0.038 g, 0.20 mmol), 5-chloro-7-(oxetan-3-ylamino)pyrazolo[1,5-a]pyrimidine-3-carbonitrile (0.060 g, 0.24 mmol), Cs2CO3 (0.196 g, 0.60 mmol), Pd2dba3 (0.018 g, 0.02 mmol), and di-tert-butyl(2',4',6'-triisopropylbiphenyl-2-yl)phosphine (0.017 g, 0.04 mmol). The mixture was dissolved in DMF (0.5 mL) and sealed. The tube was de- gassed and inflated with N2. 2\. The reaction was heated at 90°C in oil-bath overnight. LCMS showed SM and byproducts and small amount of product mass. did not workup

Источник

750 AstraZeneca ELN dataset