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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 448820생성일: 2026년 10월 26일

Sulfuric Acid → 3-bromo-N-(4-chloro-2-(1-cyclopropylethylcarbamoyl)phenyl)-1-(3-chloropyridin-2-yl)-1H-pyrazole-5-carboxamide

https://huagongshe.com/reaction/448820

반응식

참여 물질

역할이름HCID투입량
반응물Sulfuric AcidHCID 1118—
반응물DimethylformamideHCID 6228—
반응물Potassium PersulfateHCID 24412—
반응물3-bromo-N-(4-chloro-2-(1-cyclopropylethylcarbamoyl)phenyl)-1-(3-chloropyridin-2-yl)-4,5-dihydro-1H-pyrazole-5-carboxamideHCID 44185606—
용매WaterHCID 962—
용매Ethyl AcetateHCID 8857—
생성물3-bromo-N-(4-chloro-2-(1-cyclopropylethylcarbamoyl)phenyl)-1-(3-chloropyridin-2-yl)-1H-pyrazole-5-carboxamideHCID 6673619390.3%

반응 단계

0.24 g of potassium peroxodisulfate and 0.02 g of sulfuric acid were added to 3 ml of an N,N-dimethylformamide solution containing 0.10 g of 3-bromo-N-(4-chloro-2-(1-cyclopropylethylcarbamoyl)phenyl)-1-(3-chloropyridin-2-yl)-4,5-dihydro-1H-pyrazole-5-carboxamide, followed by heating and refluxing. After 1.5 hours, the reaction liquid was left to cool and introduced into 10 ml of water, and then ethyl acetate was added, followed by extraction. The organic layer (the ethyl acetate layer) was washed with a saturated sodium chloride aqueous solution, and dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure, and the residue was purified by silica gel column chromatography (eluent: n-hexane/ethyl acetate=1/0 to 1/2) to obtain 0.09 g of the desired product (melting point: 231-233° C.).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08481744B2
출처 데이터셋uspto-grants-2013_07
ORD IDord-5b2021305ef24e90aa308a488e79064a
출처 메모uspto-grants-2013_07