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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1641466생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/1641466

반응식

참여 물질

역할이름HCID투입량
반응물Sodium SulfateHCID 24436—
반응물Potassium tert-butoxideHCID 23665647—
반응물2-amino-5-chloro-N-(1-cyclopropylethyl)benzamideHCID 43533096—
반응물S-ethyl 3-bromo-1-(3-chloropyridin-2-yl)-1H-pyrazole-5-carbothioateHCID 86639909—
용매Dimethyl SulfoxideHCID 679—
용매WaterHCID 962—
생성물3-bromo-N-(4-chloro-2-(1-cyclopropylethylcarbamoyl)phenyl)-1-(3-chloropyridin-2-yl)-1H-pyrazole-5-carboxamideHCID 6673619345.6%

반응 단계

0.35 g of S-ethyl 3-bromo-1-(3-chloropyridin-2-yl)-1H-pyrazole-5-carbothioate and 0.24 g of 2-amino-5-chloro-N-(1-cyclopropylethyl)benzamide were dissolved in 5 ml of dimethyl sulfoxide, and 0.85 g of anhydrous sodium sulfate was added, followed by stirring for 5 minutes. 0.14 g of potassium tert-butoxide was added at room temperature, followed by stirring for 1.5 hours. The reaction liquid was added to water, followed by extraction with ethyl acetate. The organic 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 1/1) to obtain 0.24 g of the desired product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08115006B2
출처 데이터셋uspto-grants-2012_02
ORD IDord-03f86ded675b4afea7a5b6b732205db2
출처 메모uspto-grants-2012_02