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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 624832Generated: October 30, 2026

5-Azido-7-(cyclopropylamino)pyrazolo[1,5-a]pyrimidine-3-carbaldehyde → 5-Amino-7-(cyclopropylamino)pyrazolo[1,5-a]pyrimidine-3-carbaldehyde

https://huagongshe.com/reaction/624832

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Azido-7-(cyclopropylamino)pyrazolo[1,5-a]pyrimidine-3-carbaldehydeHCID 86654662—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product5-Amino-7-(cyclopropylamino)pyrazolo[1,5-a]pyrimidine-3-carbaldehydeHCID 5831376385%

Reaction Steps

The above product 5-azido-7-(cyclopropylamino)pyrazolo[1,5-a]pyrimidine-3-carbaldehyde (1.09 g, 4.46 mmol) was subjected to hydrogenation using 10% wt palladium on carbon in ethanol. The reaction was stirred under hydrogen for 6 hours. The mixture was filtered through celite and sonicated with 1:1 mixture of ethyl acetate and hexane. The light yellow solid was filtered and dried to yield 5-amino-7-(cyclopropylamino)pyrazolo[1,5-a]pyrimidine-3-carbaldehyde as product 750 mg (85% yield). LCMS (M+1=218)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09303033B2
Source datasetuspto-grants-2016_04
ORD IDord-fd3287d797384144b105c872522746a1
Source noteuspto-grants-2016_04