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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 644881Generated: October 30, 2026

Hydrochloric Acid → HCID 17862355, compound

https://huagongshe.com/reaction/644881

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl IsocyanateHCID 12228—
ReactantHCID 17862409HCID 17862409—
SolventEthyl AcetateHCID 8857—
ProductHCID 17862355HCID 1786235562.9%

Reaction Steps

Potassium carbonate (0.83 g, 6.0 mmol) and methyl isocyanate (0.29 g, 5.0 mmol) were added to a solution of 3-(3-chloro-5-trifluoromethylpyridin-2-yloxy)-4-ethyl-5-methylpyrazole (1.83 g, 6.0 mmol) in ethyl acetate (25 ml), and the mixture was stirred at room temperature overnight. After completion of the reaction, the reaction mixture was poured into 2N hydrochloric acid and extracted with diethyl ether (30 ml×3). An organic layer was washed with water, dried over anhydrous magnesium sulfate and filtered to remove a desiccant, and the solvent was distilled off from the filtrate under reduced pressure. The resultant crude product was purified with a silica gel column (ethyl acetate/hexane=1/5), to give a white solid of N-methyl-3-(3-chloro-5-trifluoromethylpyridin-2-yloxy)-4-ethyl-5-methylpyrazole-1-carboxamide (1.14 g, yield: 62.9%). mp: 84-86° C.; 1H-NMR (CDCl3, TMS, ppm): δ 1.04 (t, J=7.6 Hz, 3H), 2.26 (q, J=7.6 Hz, 2H), 2.59 (s, 3H), 2.93 (d, J=5.0 Hz, 3H), 6.80-7.05 (m, 1H), 8.02 (d, J=2.0 Hz, 1H), 8.32 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07700786B2
Source datasetuspto-grants-2010_04
ORD IDord-7effaf8259a6485f88c41774291bd853
Source noteuspto-grants-2010_04