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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2037031Generated: October 31, 2026

Cesium carbonate → 5-(4-(1H-pyrazol-1-yl)phenylamino)-7-(cyclopropylamino)-2-methylpyrazolo[1,5-a]pyrimidine-3-carbaldehyde

https://huagongshe.com/reaction/2037031

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactant4-(1H-Pyrazol-1-yl)anilineHCID 594274—
ReactantBinap, (A+-)-HCID 634876—
ReactantTert-butyl 5-chloro-3-formyl-2-methylpyrazolo[1,5-a]pyrimidin-7-yl(cyclopropyl)carbamateHCID 86654658—
Catalystpalladium(II) acetateHCID 167845—
SolventDiethyl EtherHCID 3283—
Solvent1,4-DioxaneHCID 31275—
Product5-(4-(1H-pyrazol-1-yl)phenylamino)-7-(cyclopropylamino)-2-methylpyrazolo[1,5-a]pyrimidine-3-carbaldehydeHCID 5831403423%

Reaction Steps

To 4-(1H-pyrazol-1-yl)aniline (54 mg, 0.34 mmol), Cs2CO3 (130 mg, 0.4 mmol) were added to tert-butyl 5-chloro-3-formyl-2-methylpyrazolo[1,5-a]pyrimidin-7-yl(cyclopropyl)carbamate (100 mg, 0.29 mmol) dissolved in 1,4-dioxane (1.1 mL). Racemic BINAP (11 mg, 0.017 mmol) and palladium(II) acetate (8 mg, 0.011 mmol) were then added. The mixture was sealed and irradiated at 110° C. for 60 min in the microwave. Et2O (3 mL) was added and the solution was filtered. The filtrate was concentrated in vacuo. The crude residue was dissolved in dichloromethane (1.5 mL) and trifluoroacetic acid (1.5 mL). After stirring at room temperature for 1 hour, the solution was concentrated under a stream of air. The crude material was purified by silica gel chromatography (15% acetone/dichloromethane) to yield the product, 5-(4-(1H-pyrazol-1-yl)phenylamino)-7-(cyclopropylamino)-2-methylpyrazolo[1,5-a]pyrimidine-3-carbaldehyde (24 mg, 23% yield). LCMS (M+1=374)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08575177B2
Source datasetuspto-grants-2013_11
ORD IDord-eed4c1aebf52456a835c4946b5d16a04
Source noteuspto-grants-2013_11