Реакция #766

ord-31892db8bbd04de79164da0921726b58

Уравнение реакции

CS(=O)(=O)Cc1cc(N)ccc1Cl
CS(=O)(=O)Cc1cc(N)cc
N#Cc1cnn2c(NC3CC3)cc(Cl)nc12
N#Cc1cnn2c(NC3CC3)cc
CS(=O)(=O)Cc1cc(Nc2cc(NC3CC3)n3ncc(C#N)c3n2)ccc1Cl
CS(=O)(=O)Cc1cc(Nc2c
Выход 35.0%

Растворители

Условия реакции

Температура
150°CELSIUS

Методика

In a 40mL vial (t=g) was 5-chloro-7-(cyclopropylamino)pyrazolo[1,5-a]pyrimidine-3-carbonitrile (88 mg, 0.38 mmol), [Reactants], and cesium carbonate (135 mg, 0.41 mmol) in DMA (0.5 mL) ([VOLUME]),Pd2(dba)3 (17.24 mg, 0.02 mmol) and (9,9-dimethyl-9H-xanthene-4,5-diyl)bis(diphenylphosphine) (21.79 mg, 0.04 mmol) were added. to give a brown suspension. The vial was filled with N2, 150C microwave for 30 min. LCMS showed completion. added DMF(3 mL), filtered through celite. concentrated. The residue was washed with EtOAc and water, MeoH to give about 55mg light brown solid

Источник

750 AstraZeneca ELN dataset