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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 737Generated: October 28, 2026

N-(5-amino-2-cyclopropylphenyl)acetamide → N-[5-[[3-cyano-7-(oxetan-3-ylamino)pyrazolo[1,5-a]pyrimidin-5-yl]amino]-2-cyclopropylphenyl]acetamide

https://huagongshe.com/reaction/737

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(5-amino-2-cyclopropylphenyl)acetamideHCID 89098640—
ReactantHCID 178418222HCID 178418222—
ReagentCesium carbonateHCID 10796—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
CatalystDi-tert-butyl(2',4',6'-tris(propan-2-yl)-(1,1'-biphenyl)-2-yl)phosphaneHCID 11618717—
SolventDimethylformamideHCID 6228—
ProductN-[5-[[3-cyano-7-(oxetan-3-ylamino)pyrazolo[1,5-a]pyrimidin-5-yl]amino]-2-cyclopropylphenyl]acetamideHCID 721642890%

Reaction Conditions

Temperature90 °C

Reaction Steps

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

Provenance & Evidence

Source dataset750 AstraZeneca ELN dataset
ORD IDord-6ca5406ed1914cc08b2221358d36ecf3
Source note750 AstraZeneca ELN dataset