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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1842574Generated: October 26, 2026

1,2-Dichloroethane → 1-(5-Fluoropyridin-2-yl)-3-(2-methyl-1,3-thiazol-5-yl)-N-{(1R)-1-[1-oxido-6-(trifluoromethyl)pyridin-3-yl]ethyl}-1H-pyrazole-4-carboxamide

https://huagongshe.com/reaction/1842574

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantSodium ChlorideHCID 5234—
ReactantTriethylamineHCID 8471—
ReactantHOAtHCID 181649—
ReactantSodium BicarbonateHCID 516892—
Reactant(1R)-1-[1-oxido-6-(trifluoromethyl)pyridin-3-yl]ethanamineHCID 59539683—
Reactant1-(5-Fluoropyridin-2-yl)-3-(2-methyl-1,3-thiazol-5-yl)-1H-pyrazole-4-carboxylic acidHCID 66679476—
SolventDimethylformamideHCID 6228—
Product1-(5-Fluoropyridin-2-yl)-3-(2-methyl-1,3-thiazol-5-yl)-N-{(1R)-1-[1-oxido-6-(trifluoromethyl)pyridin-3-yl]ethyl}-1H-pyrazole-4-carboxamideHCID 6667984458.5%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of sodium chloride salt of 1-(5-fluoropyridin-2-yl)-3-(2-methyl-1,3-thiazol-5-yl)-1H-pyrazole-4-carboxylic acid (0.14 g, 0.25 mmol) in DMF (2.5 mL) was added (1R)-1-[1-oxido-6-(trifluoromethyl)pyridin-3-yl]ethanamine (66.2 mg, 0.27 mmol), EDC (83.0 mg, 0.43 mmol), HOAT (16.9 mg, 0.12 mmol) and triethylamine (0.21 mL, 1.49 mmol). The mixture was stirred at 50° C. After 2 h, saturated aqueous NaHCO3 were added and the mixture was extracted with dichloromethane (3×). The combined organic extracts was dried over MgSO4, filtered and concentrated. Purification by silica gel chromatography (100% dichloromethane 85% dichloromethane/methanol) gave the title compound (72 mg). HRMS 493.1070 (M+1). 1H NMR (500 MHz, DMSO): δ 9.41 (s, 1H); 8.61 (s, 1H); 8.56 (s, 1H); 8.48 (s, 1H); 8.04-8.02 (m, 2H); 7.94 (d, J=8.4 Hz, 1H); 7.56 (d, J=8.3 Hz, 1H); 5.17-5.14 (m, 1H); 2.67 (s, 3H); 1.51 (d, J=7.1 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946231B2
Source datasetuspto-grants-2015_02
ORD IDord-0bba8f936ffd41c4a58edb98711493e7
Source noteuspto-grants-2015_02