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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1754365Generated: November 1, 2026

Diisopropylethylamine → N-[1-(4-chlorophenyl)-5-isopropylpyrazol-4-yl]-2-[5-methyl-3-(trifluoromethyl)-1,2,4-triazol-1-yl]propanamide

https://huagongshe.com/reaction/1754365

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Reactant1-(4-chlorophenyl)-5-(propan-2-yl)-1H-pyrazol-4-amineHCID 66425921—
Reactant2-[5-Methyl-3-(trifluoromethyl)-1,2,4-triazol-1-yl]propanoic acidHCID 86711687—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductN-[1-(4-chlorophenyl)-5-isopropylpyrazol-4-yl]-2-[5-methyl-3-(trifluoromethyl)-1,2,4-triazol-1-yl]propanamideHCID 7690296325%

Reaction Steps

To a solution of 1-(4-chlorophenyl)-5-isopropylpyrazol-4-amine (0.054 g, 0.23 mmol) in DMF (1.0 mL) was added 2-[5-methyl-3-(trifluoromethyl)-1,2,4-triazol-1-yl]propanoic acid (0.051 g, 0.23 mmol), followed by diisopropylethylamine (0.059 g, 0.46 mmol) and HATU (0.105 g, 0.28 mmol). After stirring at room temperature for 1 h, the reaction was diluted with water and the aqueous layer was extracted with ethyl acetate (2×5 mL). The combined organic layers were washed with brine, dried (Na2SO4), filtered, and concentrated in vacuo. The resulting crude product was purified by reverse phase HPLC (C18 column, acetonitrile-H2O with 0.1% TFA as eluent) to give the title compound as a white solid (0.025 g, 0.057 mmol, 25%). 1H NMR (400 MHz, CDCl3) δ 8.25 (s, 1H), 8.03 (d, J=0.6 Hz, 1H), 7.49-7.41 (m, 2H), 7.32-7.23 (m, 2H), 5.12 (q, J=7.2 Hz, 1H), 3.02 (m, 1H), 2.61 (s, 3H), 1.92 (d, J=7.2 Hz, 3H), 1.27 (d, J=7.2 Hz, 3H), 1.10 (d, J=7.2 Hz, 3H); MS: (ES) m/z calculated for C19H20ClF3N6O [M+H]+ 441.1, found 440.9.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09169248B2
Source datasetuspto-grants-2015_10
ORD IDord-dc888aa372a9448b96452698b627c61a
Source noteuspto-grants-2015_10