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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1393653Generated: November 2, 2026

1H-Pyrazol-3-amine, 5-methyl- → 2-methyl-7-(trifluoromethyl)pyrazolo[1,5-a]pyrimidine-6-carboxylic acid

https://huagongshe.com/reaction/1393653

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1H-Pyrazol-3-amine, 5-methyl-HCID 93146—
ReactantEthyl 2-(ethoxymethylene)-4,4,4-trifluoro-3-oxobutanoateHCID 4685753—
CatalystHydrochloric AcidHCID 313—
SolventEthanolHCID 702—
Product2-methyl-7-(trifluoromethyl)pyrazolo[1,5-a]pyrimidine-6-carboxylic acidHCID 276806742%

Reaction Conditions

Temperature70 °C

Reaction Steps

3-Amino-5-methylpyrazole (389 mg) and ethyl (ethoxymethylidene)trifluoroacetoacetate (960 mg) were dissolved in ethanol (10 ml) and stirred for 1.5 hours at 70° C. Conc. hydrochloric acid (1 mg) was added thereto, and the mixture was stirred for additional 1 hour. The mixture was cooled to room temperature and concentrated under reduced pressure. Ethanol (10 ml) and 5 N sodium hydroxide solution (3 ml) were added to the residue and then stirred for 1 hour at 70° C. The mixture was cooled to room temperature, and water was added to the mixture which was then washed with ethyl acetate. 2 N Hydrochloric acid was added to the aqueous phase until it became acidic, and precipitated crystals were collected by filtration and washed with water and n-hexane. The product was dried under reduced pressure to give the title compound (102 mg, Y.:42%) as white crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07345180B2
Source datasetuspto-grants-2008_03
ORD IDord-71317cfbd6c740068595a2333d506f0b
Source noteuspto-grants-2008_03