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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 22863생성일: 2026년 10월 24일

Hydrochloric Acid → N-[3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)pyrazole-5-yl]pyrazine-2-carboxamide

https://huagongshe.com/ko/reaction/22863

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Methyl pyrazinoateHCID 72662—
반응물5-amino-1-(2,6-dichloro-4-(trifluoromethyl)phenyl)-1H-pyrazole-3-carbonitrileHCID 3303913—
반응물HCID 178501943HCID 178501943—
용매WaterHCID 962—
용매AcetonitrileHCID 6342—
생성물N-[3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)pyrazole-5-yl]pyrazine-2-carboxamideHCID 1213763177%

반응 단계

Into a mixture of 0.5 g (1.6 mmol) of 5-amino-1-(2,6-dichloro-4-trifluoromethylphenyl)pyrazole-3-carbonitrile, 0.24 g (1.7 mmol) of methyl pyrazinecarboxylate, and 0.5 ml of acetonitrile was gradually added 0.3 g (1.6 mmol) of 28% CH3ONa/CH3OH at room temperature. After 2 hours of stirring at room temperature, 5 ml of water and then concentrated hydrochloric acid were added thereto to make the mixture pH 2, whereby crystals were precipitated. Thereto was added 10 ml of ethyl acetate, followed by extraction. The organic layer was washed with saturated saline and then dried over anhydrous sodium sulfate. After removal of the sodium sulfate by filtration, the layer was concentrated and the resulting crystals were filtrated. The crystals were washed with a small amount of hexane and ethyl acetate and the dried to obtain 0.5 g (yield 77%) of N-[3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)pyrazole-5-yl]pyrazine-2-carboxamide.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06849633B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-682290b21894463a9a4b5061a1ed1e7e
출처 메모uspto-grants-2005_02