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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1850673Generated: October 30, 2026

Potassium Hydroxide → Allyl 2-amino-5-(trifluoromethyl)pyrazolo[1,5-a]pyrimidine-3-carboxylate

https://huagongshe.com/reaction/1850673

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
Reactant1-(1,3-Dioxolane-2-yl)-3,3,3-trifluoropropane-2-oneHCID 55296049—
ReactantAllyl 3,5-diamino-1H-pyrazole-4-carboxylateHCID 73554792—
Solvent1,4-DioxaneHCID 31275—
ProductAllyl 2-amino-5-(trifluoromethyl)pyrazolo[1,5-a]pyrimidine-3-carboxylateHCID 9041781479%

Reaction Steps

3-(1,3-Dioxolan-2-yl)-1,1,1-trifluoro-propan-2-one (55.58 g, 301.9 mmol) and allyl 3,5-diamino-1H-pyrazole-4-carboxylate (55 g, 301.9 mmol) were dissolved in 1,4-dioxane (330 mL). KOH (1.694 g, 30.19 mmol) was added and the yellow suspension was stirred at room temperature for 4 h30 min. The reaction mixture was heated at 90° C. for 16 h. The mixture was cooled down to room temperature. The reaction mixture was concentrated onto silica and purified by column chromatography (CombiFlash Companion XL, 1.5 kg column, 0.5 to 40% EtOAc in DCM) to afford allyl 2-amino-5-(trifluoromethyl)pyrazolo[1,5-a]pyrimidine-3-carboxylate 4d as a bright yellow solid (68 g, 79% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08957078B2
Source datasetuspto-grants-2015_02
ORD IDord-e981510f0ee84801ad9bbeebee7ef5cc
Source noteuspto-grants-2015_02