Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2409104Generated: October 31, 2026

Trifluoroacetic acid → HCID 69093386, compound

https://huagongshe.com/reaction/2409104

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantSodium CarbonateHCID 10340—
Reactant2-Chloro-N-methyl-5-(trifluoromethyl)pyrimidin-4-amineHCID 21077587—
ReactantHCID 69082882HCID 69082882—
SolventWaterHCID 962—
Solvent2-MethoxyethanolHCID 8019—
ProductHCID 69093386HCID 6909338651.1%

Reaction Conditions

Temperature70 °C

Reaction Steps

To a solution of 2-(4-amino-3-methyl-1H-pyrazol-1-yl)-2-methylpropanamide (250 mg, 1.37 mmol) in 2-methoxyethanol (5 mL) was added 2-chloro-N-methyl-5-(trifluoromethyl)pyrimidin-4-amine (290 mg, 1.37 mmol) and trifluoroaceticacid (156 mg, 1.37 mmol), the reaction was stirred at 70° C. for about 0.5 h. The reaction mixture was cooled to ambient temperature followed with the addition of water (10 mL) and the pH of solution was adjusted to 8 with sat. Na2CO3 The aqueous phase was extracted with ethyl acetate (10 mL×3), the combined organic phase was dried over anhydrous sodium sulfate, filtered and concentrated to dry to give a residue which was purified by column chromatography on silica gel (CH2Cl2:MeOH=20:1) to give 2-methyl-2-(3-methyl-4-(4-(methylamino)-5-(trifluoromethyl)pyrimidin-2-ylamino)-1H-pyrazol-1-yl)propanamide (250 mg, 51%) as white solid. LCMS (m/z) ES+358 (m+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08815882B2
Source datasetuspto-grants-2014_08
ORD IDord-4f665e35d3004581beca09f9631afffe
Source noteuspto-grants-2014_08