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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2388629Generated: October 25, 2026

Hydrochloric Acid → N-{3-isobutyl-4-[1-methoxy-2,2,2-trifluoro-1-(trifluoromethyl)ethyl]phenyl}-3-fluoromethylpyrazine-2-carboxamide

https://huagongshe.com/reaction/2388629

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium MethoxideHCID 10942334—
ReactantMethyl 3-fluoromethylpyrazine-2-carboxylateHCID 67039225—
Reactant3-Isobutyl-4-[1-methoxy-2,2,2-trifluoro-1-(trifluoromethyl)ethyl]anilineHCID 86619003—
SolventMethanolHCID 887—
ProductN-{3-isobutyl-4-[1-methoxy-2,2,2-trifluoro-1-(trifluoromethyl)ethyl]phenyl}-3-fluoromethylpyrazine-2-carboxamideHCID 8661900667%

Reaction Conditions

Temperature60 °C

Reaction Steps

Methyl 3-fluoromethylpyrazine-2-carboxylate (390 mg, 2.29 mmol) and 3-isobutyl-4-[1-methoxy-2,2,2-trifluoro-1-(trifluoromethyl)ethyl]aniline (750 mg, 2.29 mmol) were stirred, followed by adding a 28% by weight methanol solution of sodium methoxide (4.4 g, 22.9 mmol), heating at 60° C. for 3 hours while stirring, pouring into a diluted HCl solution, extracting with ethyl acetate and washing with water. The reaction solution was dried over magnesium sulfate, and concentrated under reduced pressure, and then the residue was purified by using silica gel chromatography (hexane:ethyl acetate=3:1) to obtain 0.71 g of the desired compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08269045B2
Source datasetuspto-grants-2012_09
ORD IDord-091b49a4710b47dcbc4bf5615ea1c066
Source noteuspto-grants-2012_09